Government of India

Ministry of Mines
Indian Bureau of Mines
Ore Dressing Division

Manual of Procedure for

Chemical and Instrumental Analysis of
Ores, Minerals, Ore Dressing Products and Environmental Samples

Issued by
Controller General
Indian Bureau of Mines
NAGPUR

Revised Edition
February, 2012

Price : (Inland) A 750; (Foreign) $ 36.35 or 23.70

Printed at IBM Press, 48/500/February, 2012

 INDIAN BUREAU OF MINES
PROJECT CREDIT

OVERALL GUIDANCE

C.S.GUNDEWAR
Controller General

FORMULATION & GENERAL GUIDANCE

MOHAN RAM
Suptdg. Officer (Ore Dressing)

COLLECTION AND COMPILATION OF TECHNICAL DATA

S.M. SHENDE S.R. BHAISARE

Suptdg. Officer (Ore Dressing) (Retired) Suptdg. Chemist (Retired)

V.K. JAIN B.S. MORONEY

Senior Chemist (Retired) Suptdg. Chemist

SHYAMJI SINGH Dr. A.K. SOLANKI

Chemist (Retired) Chemist

REVISION

B.S. MORONEY
Suptdg. Chemist

Mrs. JYOTI SHRIVASTAVA

Chemist

DTP COMPOSING AND PAGE MAKING

M.N. GULKOTWAR
Stenographer Gr.I (Retired)

PUBLICATION SECTION

A.K.SINGH
Chief Editor

N.U.KADU
Asstt. Editor

P.L.MASRAM
A.P.MISHRA
Junior Technical Assistants
 PREFACE

The chemistry of rock/ore is the key to understand the concentration of elements

and presence of other associated elements. There is no doubt that chemical analysis
reveals economic value of any mineral/rock.

The chemical analysis of samples shall guide and aid the future course of
exploration with reference to the quantum, quality and the time frame. Chemical assay is
also very important and helps the beneficiation engineers to plan their test work and do
the required improvement during the beneficiation process. The chemical analysis of
ore/processed products speaks of their suitability for various mineral based industries.

Ores and minerals have variety of elements and radicals, which offer interference
with one another during analysis. The chemist has to choose the exact procedure of
chemical analysis depending upon the nature of ore samples and radicals/elements to be
analyzed. The choice of any analytical procedure or instrumental analytical techniques
also depends on the concentration of elements in parts per million (PPM) or otherwise.
Thus each procedure of chemical analysis has its own merits and demerits and selection
of method is based on desired accuracy.

Instrumental analysis using instruments like XRF, AAS, ICPA, Ion-

chromatograph, FTIR brought a modernization and sophistication to the analytical data.
The analyst needs to develop techniques very carefully for the standardization and
calibration of the instrument for obtaining the reproducibility and accuracy in the results.

The analysis of environmental samples for the various parameters in waste, water,
drinking water, soil and ambient air help in preparing a baseline data and environmental
management plans for the mines. The methods based on ISI procedures and using
modern sophisticated instruments have been selected and mentioned in the manual.

Rapid and accurate analysis of samples holds the key to success in exploration,
mineral based mining, marketing and assess quality of mineral based products.

This revised edition is brought for the industry.

(C.S.GUNDEWAR)
Nagpur Controller General
Dated : 21st February, 2012 Indian Bureau of Mines
 CONTENTS

SL.NO. SUBJECT PAGE NO

1 METHODS OF ANALYSIS USING WET CLASSICAL 1
AND COLOURIMETRIC PROCEDURES
1.1 OPENING OF ORE/MINERAL SAMPLE 1
1.2 DETERMINATION OF MAJOR AND MINOR 5
CONSTITUENTS FROM STOCK SOLUTION
ALUMINIUM ORES 22
ALUMINO SILICATE & OTHER SILICATES 24
ANTIMONY ORES 26
ARSENIC ORES 28
BARIUM ORES 28
BISMUTH ORES 34
CHROME ORES 36
COBALT ORES 39
FLUORSPAR ORES 41
GYPSUM 44
IRON ORES 46
LIMESTONE, DOLOMITE, MAGNESITE AND ALLIED 47
MATERIALS
MANGANESE ORES 48
MOLYBDENUM ORES 51
NICKEL ORES 55
COPPER, LEAD, ZINC (POLYMETALLIC ORES) 58
PYRITES 59
ROCK PHOSPHATE AND APATITE 60
SELENIUM AND TELLURIUM 62
SILICA 64
TIN ORE 65
TITANIUM BEARING ORES 67
TUNGSTEN ORES 70
VANADIUM ORES 73
ZIRCONIUM ORES 75
COAL AND GRAPHITE 77
CEMENT 80
1.3 DETERMINATION OF CaF2 IN FLUORSPAR BY 80
CHEMICAL PHASE TECHNIQUE
1.4 CHEMICAL QUALITY EVALUATION AND 83
STANDARDISATION OF SODIUM OLEATE FOR
APPLICATION AS FROTH FLOTATION REAGENT
1.5 SPECTROMETRIC (COLOURIMETRIC) METHODS OF 87
ANALYSIS
 STANDARD SOLUTION AND STANDARDIZATION 111
GENERAL SAFETY PRECAUTIONS 118
TITRE EQUIVALENT PER ML OF STANDARD 121
SOLUTION
2. METHODS OF ANALYSIS USING X-RAY 123
FLUOROSCENCE (XRF) ANALYSER
2.1 X-RAY FLUOROSCENCE SPECTROMETRY 123
2.2 CHOICE OF INSTRUMENTAL PARAMETERS 132
2.3 SAMPLE PREPARATION TECHNIQUE 144
3. METHODS OF ANALYSIS USING ATOMIC 150
ABSORPTION SPECTROPHOTOMETRY
3.1 ATOMIC ABSORPTION SPECTROPHOTOMETRY 150
3.1.1 ATOMIC ABSORPTION 150
3.1.2 RELATION BETWEEN ATOMIC ABSORPTION & 151
CONCENTRATION
3.1.3 ATOMIZATION OF SAMPLE 152
3.2 SAMPLE PREPARATION FOR AAS 160
3.3 DETERMINATION OF LITHIUM IN LITHIUM, 162
RUBIDIUM, CESIUM IN TUNGSTEN ORES, MINERALS
& BENEFICIATION PRODUCTS AND MICA
3.4 DETERMINATION OF RUBIDIUM IN LITHIUM 164
RUBIDIUM, CESIUM IN TUNGSTEN ORES, MINERALS
BENEFICIATION PRODUCTS AND MICA
3.5 DETERMINATION OF CESIUM IN LITHIUM RUBIDIUM, 165
CESIUM IN TUNGSTEN ORES, MINERALS &
BENEFICIATION PRODUCTS AND MICA,
3.6 DECOMPOSITION AND ANALYSIS OF CHROMIUM IN 168
ORE, MINERALS AND BENEFICATED PRODUCTS FOR
CHROMIUM, IRON, NICKLE & COBALT
3.7 DETERMINATION OF SILVER BY ATOMIC 171
ABSORPTION SPECTROSCOPY IN POLYMETALLIC
ORES & BENEFICIATED PRODUCTS
3.8 DETERMINATION OF MOLYBDENUM IN TUNGSTEN 173
& POLYMETALLIC ORES, MINERALS AND
BENEFICIATION PRODUCTS
3.9 DETERMINATION OF BISMUTH IN TUNGSTEN & 174
POLYMETALLIC ORE, MINERALS AND
BENEFICIATION PRODUCTS BY ATOMIC
ABSORPTION TECHNIQUES
3.10 DETERMINATION OF OXIDISED ZINC IN ZINC ORE, 176
ZINC CONCENTRATE & OTHER BENEFICIATED
FRACTION
3.11 DETERMINATION OF OXIDISED LEAD IN LEAD ORE, 177
LEAD CONCENTRATE & OTHER BENEFICIATED
FRACTIONS
3.12 DETERMINATION OF OXIDISED COPPER IN COPPER 178
ORE CONCENTRATE
 3.13 DETERMINATION OF NIOBIUM & TANTALUM IN 179
ORES AND ORE DRESSING PRODUCTS OF TUNGSTEN
AND TIN
3.14 DETERMINATION OF GALIUM, INDIUM, THALLIUM 181
IN ZINC AND LEAD ORE AND BENEFICIATION
PRODUCTS BY ATOMIC EMISSION ON ATOMIC
ABSORPTION SPECTROPHOTOMETER
4. PRINCIPLE AND PROCEDURE OF CARBON & 184
SULPHUR ANALYSER
5. METHODS OF ANALYSIS USING INDUCTIVELY 186
COUPLED PLASMA (ICP) INSTRUMENT
5.1 ICP(AES)- TECHNIQUES AND APPLICATIONS 186
5.2 ANALYSIS OF PLATINUM GROUP ELEMENTS 192
5.3 APPLICATION OF ICP-OES TO WATER ANALYSIS 195
5.4 THE ICP OES IN ENVIRONMENTAL APPLICATIONS 198
6. METHODS OF ANALYSIS OF ENVIRONMENTAL 199
SAMPLES
6.1 DETERMINATION OF DISSOLVED FLUORIDE, 199
CHLORIDE, NITRATE, ORTHOPHOSPHATE, SULPHATE
IONS USING ION CHROMATOGRAPHIC METHOD
6.2 ANALYSIS OF SODIUM & POTASSIUM IN WATER, 201
WASTE WATER, EFFLUENTS, SOLIDS, SOILS ETC.
USING FLAME PHOTOMETER
6.3 DETERMINATION OF TURBIDITY IN WATER, WASTE 203
WATER USING TURBIDITY METER/NEPHELOMETER
6.4 DETERMINATION OF COLOUR IN WATER AND 204
WASTEWATER (UV-SPECTROPHOTOMETRIC
METHOD)
6.5 DETERMINATION OF SUSPENDED SOLIDS, TOTAL 205
SOLIDS, DISSOLVED SOLIDS, INORGANIC MATTER
AND VOLATILE MATTER IN WATER, WASTE WATER,
EFFLUENT ETC.
6.6 DETERMINATION OF CHEMICAL OXYGEN DEMAND 208
IN WASTE WATER/EFFLUENT
6.7 DETERMINATION OF BIOCHEMICAL OXYGEN 210
DEMAND (BOD) IN WASTE WATER AND EFFLUENTS
6.8 DETERMINATION OF DISSOLVED OXYGEN IN 212
WATER AND WASTEWATER
6.9 DETERMINATION OF PHENOLIC COMPOUNDS AS 214
C6H5OH(DIRECT COLORIMETRIC METHOD)
6.10 DETERMINATION OF OIL AND GREASE IN WATER 216
AND WASTE WATER
6.11 ANALYSIS OF SULPHATE IN WATER AND WASTE 217
WATER/EFFLUENT
6.12 DETERMINATION OF SULPHIDE IN WATER & WASTE 219
WATER
6.13 ANALYSIS OF SILICA IN WATER AND WASTE WATER 221
6.14 ANALYSIS OF PHOSPHOROUS IN WATER AND WASTE 224
WATER
6.14.1 DETERMINATION OF PHOSPHORUS BY 224
STANNOUS CHLORIDE METHOD (SOLUABLE
PHOSPHATE)
6.14.2 DETERMINATION OF PHOSPHORUS BY 225
ASCORBIC ACID METHOD (SOLUABLE PHOSPHATE)
6.15 ANALYSIS OF NITRITE NITROGEN (NO2-N) IN WATER 226
AND WASTE WATER
6.16 DETERMINATION OF NITRATE NITROGEN (NO3-N) IN 228
WATER AND WASTE WATER
6.16.1 DETERMINATION OF NITRATE NITROGEN (NO3- 228
N) IN VISIBLE RANGE at 410 nm
6.16.2 DETERMINATION OF NITRATE NITROGEN (NO3- 229
N) IN ULTRA VIOLET REGION OF
SPECTROPHOTOMETER AT 220 nm & 275 nm
6.17 ANALYSIS OF AMMONICAL NITROGEN (NH3-N) IN 231
WATER AND WASTE WATER
6.18 ANALYSIS OF RESIDUAL CHLORINE IN WATER AND 232
WASTEWATER SAMPLES
6.19 ANALYSIS OF CHLORIDE IN WATER, WASTE WATER 234
AND SOIL SAMPLES
6.20 DETERMINATION OF ACIDITY IN WATER, WASTE 236
WATER
6.21 DETERMINATION OF ALKALINITY IN WATER & 238
WASTE WATER
6.21.1 PROCEDURE FOR THE DETERMINATION OF 239
PHENOLPHTHALEIN ALKALINITY
6.21.2 PROCEDURE FOR THE DETERMINATION OF 240
TOTAL ALAKINITY
6.22 DETERMINATION OF HARDNESS IN WATER 240
SAMPLES
6.23 ANALYSIS OF HEXAVALENT CHROMIUM IN 243
DRINKING WATER, WASTE WATER BY
COLOURIMETRIC METHOD USING 1-5
PHENYLCARBAZIDE
6.24 ANALYSIS OF CYANIDE IN WATER, WASTE WATER 247
AND SOLID WASTES USING ION SELECTIVE
ELECTRODE AND COLORIMETRIC METHODS
6.25 ANALYSIS OF FLUORIDES IN WATER, WASTE 250
WATER, MINERALS, ORES AND SOIL SAMPLES USING
ION-SELECTIVE ELECTRODE AND COLORIMETRIC
METHODS
6.26 ANALYSIS OF MERCURY IN WATER/WASTE WATER, 255
MINERALS, ORES AND SOIL SAMPLES USING
MERCURY ANALYSER
6.27 SOIL ANALYSIS 259
6.28 AMBIENT AIR QUALITY MONITORING 283
Addenda 1 290
BORON ORES
Addenda 2 292
LOSS ON IGNITION
Addenda 3 295
DETERMINATION OF TOTAL SILICA IN SILICATE
MINERAL (A COMBINATION OF GRAVIMETRIC AND
PHOTOMETRIC METHOD)
1. Method of Analysis Using Wet Classical
and Colourimetric Procedures
1.1 OPENING OF ORE/MINERAL SAMPLE

The chemical transformation of any ore/mineral sample into a desired form so

as to facilitate analysis of its constituents is known as opening of the sample i.e.,
conversion of an ore or mineral sample into desired soluble or insoluble species. In
simple words, opening of an ore is its dissolution in suitable solvent or flux depending
upon the aim of analysis. Thus, opening of a sample is a very vital and important step
in ore/mineral analysis. The separation of soluble and insoluble species should be
near 100%. The exact choice of method for opening of an ore depends on the nature
of the ore, the element of interest and its chemical properties. The selection of the
appropriate method of sample decomposition is very important for correct analysis.
To achieve this, an analyst should carefully take into account the chemical properties
of various minerals present in the sample. Owing to the variable characteristics of the
ore, it is not possible to have any one set procedure applicable to all samples. It is
often necessary to combine two or more methods to effect the dissolution of an ore.
There are mainly two methods to open an ore. They are (1) wet method & (2) dry
method.

Wet method constitutes the digestion of an ore sample with an acid or a

mixture of acids to convert the complex ore mineral into simple chemical compounds.
The action of an acid or a mixture of acids is supplemented by heat and pressure. Heat
and pressure hasten the dissolution rate. This is normally preferred over dry method
due to its simplicity and it requires less attention, moreover, the dissolving media
least affects the vessel used.

Dry method constitutes the fusion of an ore with a solid or mixture of solids to
convert complex minerals compound into simple chemical compounds. The reaction
is effected by melting the mass at elevated temperature. The fusion is carried out in
variety of crucibles made of platinum, gold, nickel, iron, zirconium, palladium, silica,
porcelain etc. There are numbers of chemical compounds used for fusion. The choice
of fusion mixture depends on the nature of the ore to be fused and the nature of the
final product needed for further analysis.

Before entering into the further details of use of wet and dry methods, it is
necessary to categorize the ore samples. On the basis of their chemical composition
and chemical properties, the categorization makes the opening of an ore easy and
logical. Following are the main categories of ores on the basis of their chemical
composition.

1. Carbonates
2. Sulphides and Pyrites
3. Oxides
4. Sulphates
5. Silicates
 6. Phosphates
7. Spinel (mixed oxides)

On the basis of chemical properties of an ore, various acids,

combination of acids and acids with some suitable salts are generally
employed for dissolution of an ore sample. Choice and reactivity of various
reagents are given here:

S.No Reagent Material to be treated

1. Water Alkali salts
2. HCl Carbonates and oxides ore of Fe, Ca, Mn, Mg,
P, Sn, Ti, Zn etc., sulphides of various metals
3. HCl with Sulphides/pyrites, ores of Cu, Pb, Mo, Zn, Ni,
Oxidizing agent Fe, As, etc.
4. Nitric Acid Ores of Cd, Cu, Mo, Co, Ni, etc.
5. Aqua regia Ores of Cd, Mg, Rh, W, etc.
6. H2SO4 Ores of Al, Be, Mn, Pb, Th, Ti, V, etc.
7. HF (with HCl, Silicates where SiO2 is not to be determined.
HN03 or H2SO4)
8. Perchloric Acid A powerful oxidizing and also a dehydrating
agent when hot and concentrated. The
solubility of the majority of the perchlorates
in water makes the acid a very desirable
solvent.
9. H2O2 & HCl One of the most promising combination of
reagents
10. Acetic acid For selective dissolution of carbonates
(10%)
11. Ammonium acetic For dissolution of gypsum, PbSO4 etc.
solution
12. Alcohol Used for separation of MgSO4 and CaSO4
13. Sugar solution Estimation of CaO in cement, quick lime etc.
14. H3PO4 In phase analysis of free silica to dissolve
silicates but not quartz.
15. H3PO4& H2SO4 To dissolve fused Al2O3 and chrome ores.

Fusion, dry methods, remains as popular as wet acid decomposition, in spite of their
apparent disadvantages such as increased solid contents in the test solution, greater
reagent requirement, more problems with reagent blank. In making fusion, the sample
is well mixed with six to twenty times its weight with fusion mixture and placed over
a thin layer of the flux in the crucible and then covered by a lid of the material as that
of the crucible. In case of refractory oxides, adding a small piece of filter paper to the
molten mass assists decomposition.

Fluxes can be categorized into the following main categories on the basis of their
chemical properties.

2
 1. Acidic flux : KHSO4, K2S2O7, NaHSO4, Na2S2O7, etc.
2. Basic flux : Na2CO3, K2CO3, KOH etc.
3. Oxidizing flux : Na2O2, KOH KNO3 etc.
4. Reducing flux : Na2CO3 C

Acidic fluxes are commonly used for dissolution of basic oxides, wolframite,
powellite, sulphides/pyrites etc.

Basic fluxes are commonly used for dissolution of acidic oxides, silicates,
amphoteric oxides etc.

Oxidizing fluxes are employed for two reasons; firstly, their dissolution
capacity is higher than acidic and basic flux, secondly for selective conversion of
element of interest into higher oxidation state like sulphide to sulphate, chromic oxide
to chromate.

Reducing fluxes are generally employed for converting element of interest

into lower valency state, like conversion of sulphates to sulphides.

Choices and reactivity of various fluxes are given below:

S.No. Reagent/Flux Material

1. Na2CO3 Silicates of Al, Fe, Ca, Cr etc, halides of Ag,
sulphates of Ba & Pb.
2. Na2CO3 & K2CO3 Silicates of Al, Fe, F, N, Se, Te, etc.
3. Na2CO3 with oxidizing Ores of Sb, As, Cr, Fe, Mo, V, Zr, sulphides, pyrites
agent etc.
4. Na2O2 Ores of Sb, As, Cr, Mo, Ni, V, Sn etc. in sulphide for
sulphur determination.
5. KHSO4, K2S2O7 Ores of Al, Sb, Cu, Cr, Co, Fe, Mn, Ni, Rh, Ta, Ti,
W etc.
6. NaOH, KOH Oxidized Sb ore, ores of Cr, Sn, Zn, Zr, sulphides
and sulphates etc.
7. CaCO3 + NH4Cl Estimation of alkalies in silicates
(J.Lawrence
Smith method)
8. NH4Cl + NH4 NO3 For dissolution and oxidation of sulphide and pyrite.
(Solid aquaregia)
9. NH4NO3 + (NH4)2SO4 Dissolution of sulphide and pyrites.
10. Eshka Mixture For sulphur determination in coal sample.
Na2CO3 + MgO
11. Na2CO3 + C Used for reduction of sulphates to sulphides.
12. Lithium Borate Promising for various silicates
13. Na2CO3 + Borax Estimation of silica in sample containing fluorine.

Broad outline of the ores categorized for chemical analysis can be summerised as
follows:

3
 All carbonates are attacked by mineral acid. Limestone, dolomite etc. are
treated with concentrate hydrochloric acid. Carbonatic material passes into solution
and silicate and other insoluble material are left as insolubles. Insolubles are then
treated with hydrofluoric acid, where silica is hydrofluorised. The remaining
unattacked material is fused with suitable flux (K2S2O7, Na2CO3 etc.) and then
extracted in mother liquor.

Most of the hydrated oxides (Al2O3 2H2O, Al2O3 H2O etc.) and some other
oxides are soluble in concentrated mineral acid; their solubility increases with degree
of hydration. Higher the degree of hydration greater is the solubility. Hence goethite
is more easily soluble than hematite or magnetite. Similarly gibbsite is more easily
soluble than bohemite or diaspore.

Most of the phosphates are easily soluble in mineral acids. Normally a

phosphate sample is dissolved in concentrated hydrochloric acid (with little HNO3).
Sulphuric acid must not be used, as the presence of sulphate ion is not desired in
Wilson method of phosphate estimation.

Mineral acids attack all sulphides. Pyrites are resistant to hydrochloric acid but
presence of nitric acid or sulphuric acid helps their dissolution.

Analysis of silicate is most complicated as the solubility of silicate ranges

from watersoluble (sodium, potassium silicate) to HF resistant (magnesium silicate).
While analyzing silicate, its solubility is taken into account, silicates which contains a
high portion of bases such as calcium, copper, zinc etc. are decomposed by strong
acids such as HCl. Clay, wollastonite etc. are attacked by concentrated hydrochloric
acid and silica separates from the matrix. Silicates, which are acidic in nature, are
only partially attacked by mineral acid and hence they are better analysed after fusing
with suitable flux. If silica is not to be determined, a mixture HNO3, HF and
perchloric acid dissolves the silicate completely. Alternatively, a mixture of NH4F
and hydrochloric acid can be employed for dissolution of silicate rock.

Decomposition is generally hastened by using very finely ground sample (-

200 mesh). Acids should never be added to a dry powder because of danger of loss
due to ferocity of the reaction. The sample should be moistened with water, the acid is
added cautiously and the covered container allowed to stand without additional
heating till the completion of initial reaction.

This manual deals with procedures adopted by/evolved in Chemical analysis

Laboratory of Indian Bureau of mines for analysis of various ores, minerals, ore
dressing products, etc. Preparation of stock solution and determination of silica has
been described ore/mineral-wise highlighting the special treatment or attention to be
given in respect of certain radicals in the ore.

Following pages deal with determination of the content of common elements (major
or minor) present in the stock solution.

4
1.2 DETERMINATION OF MAJOR AND MINOR CONSTITUENTS FROM
THE STOCK SOLUTION

1.2.1 Major Elements

1.2.1.1 Iron (Fe) (Dichromate method)

Pipette out 50 ml from the main stock solution into a 250 ml beaker. Add 2-3
drops of methyl orange (very dilute solution) to impart a very faint red colour to the
solution. Add 2 g ammonium chloride. Stirr and dissolve the solids. Precipitate mixed
oxide (R2O3) by dropwise addition of dilute ammonia till the colour of indicator turns
yellow. Add 2-3 drops in excess. Boil the content on burner. Cool and filter through
Whatman 41 filter paper. Wash the precipitate and beaker 5-6 times with hot water.
Preserve the filtrate for estimation of CaO and MgO. Transfer the precipitate carefully
with jet of hot water into the original beaker. Dissolve the precipitate in concentrated
hydrochloric acid. Wash the sides of the beaker. Now heat the beaker to 80-90 oC on
burner (avoid boiling) and add 10% stannous chloride solution dropwise with
constant stirring to reduce iron. Yellow colour of ferric chloride disappears due to
conversion to ferrous ion. Add 1-2 drops of stannous chloride in excess. Cool the
solution in cold water. Add 10 ml mercuric chloride solution and stir. A silky white
precipitate of mercurous chloride will appear. If the precipitate found is black, discard
the solution and repeat the process with new aliquot. The black colour indicates the
reduction of mercurous chloride to elemental mercury, which adds inaccuracies to the
determination. Add 10-15 ml sulphuric-phosphoric acid mixture and dilute to about
150 ml. Add 2-3 drops of barium diphenylamine sulphonate indicator solution. Titrate
this against standard dichromate solution with constant stirring till a constant stable
violet colour appears. Colour changes from dirty green to violet. Avoid use of excess
of indicator as it imparts intense dirty green colour near the end point and confuses
the actual end point.

1 ml 1 N K2Cr2O7 = 0.05585 g Fe
= 0.07185 g FeO
0.07985 g Fe2O3

1.2.1.2 Calcium Oxide (CaO)-EDTA (Complexometry) Method

Divide the filtrate of iron estimation (1.2.1.1) into two parts. One is used
for estimation of calcium and other is preserved for estimation of MgO.

Take solution for CaO estimation in 250 ml beaker. Add 2-3 drops of tri-
ethanol amine and stir. Now add a pinch of hydroxylamine hydrochloride or ascorbic
acid. Add 50 ml of 20% KOH solution. Add 5-6 drops of Patton and Readers
indicator. The indicator will impart rose red colour to the solution. Titrate this against
standard EDTA solution. Colour changes from rose red to blue. Sometimes 0.5-1 ml
of 10% potassium cyanide solution is added to mask heavy metals (especially in case
of Cu-Pb-Zn ores). Use of cyanide should be avoided and should only be used with
care and caution in case of need. Cyanide must be used in alkaline media only. The
excess of cyanide in waste must be destroyed with bleaching powder before it is
disposed to sewage.

5
 1 ml of 1 M EDTA 0.05608 g of CaO

Oxalate Method (Volumetry)

The silica and mixed hydrated oxides are removed. The solution is acidified
with hydrochloric acid and calcium is precipitated as calcium oxalate. The precipitate
is filtered, washed, dissolved in hot dilute sulphuric acid and titrated against standard
potassium permanganate solution to pink colour.

Take the ammonical filtrate from the mixed oxide precipitation in a 500 ml
beaker; acidify the solution with hydrochloric acid using methyl red as indicator. Add
about 0.5 gm of ammonium oxalate and stir well. Make the solution ammonical and
boil for about 10 minutes. Remove from the flame and allow the precipitate to settle
for about one hour. Filter through No.40 Whatman filter paper and wash the residue
with hot water till free from oxalate (test the filtrate with a drop of dilute
permanganate solution and a drop of dilute sulphuric acid). Collect the filtrate and
the washing for the determination of MgO. Spread out the filter paper containing the
precipitate and wash out the precipitate into the beaker with water. Add about 25 ml
of 1:1 sulphuric acid and warm the solution (70 to 80 oC), titrate with standard
permanganate solution till a permanent pink colour persists. Calculate % CaO as
follows

CaO % = A x B x 0.028 x 100

C
Where
A = volume in ml. of standard permanganate solution used
B = normality of permanganate solution, and
C = weight in gm of the sample representing the aliquot taken
Reactions involved

1. Ca++ + C2O4- = CaC2O4

2. CaC2O4 + 2H+ = Ca++ + H2C2O4
3. Potassium permanganate in the presence of dil. sulphuric acid oxidizes oxalic
acid to carbon dioxide and water.

The following reaction takes place

2KMnO4 + 5H2C2O4 + 3H2SO4 = 10CO2 + 8H2O + K2SO4 + MnSO4

The ionic reaction is

2MnO4- + 5C2O4--+ 16H+ = 2Mn++ + 10CO2 + 8H2O

1.2.1.3 Magnesium Oxide-EDTA Method (Complexometry)

Take part of the iron estimation filtrate preserved for estimation MgO in 250 ml
beaker. Add 2-3 drops of triethanol amine and stir. Now add a pinch of
hydroxylamine hydrochloride or ascorbic acid. Add 50 ml, 10-pH ammonia-
ammonium chloride buffer. Add 5-6 drops Eriochrome Black T indicator solution.

6
The indicator will impart brilliant red colour to the solution. Titrate this against
standard EDTA solution. Colour changes from red to blue. This titration estimates
calcium and Magnesium together. Find magnesium equivalent EDTA by subtracting
volume required for CaO determination. Sometimes 0.5-1 ml of 10% potassium
cyanide solution is added to mask heavy elements (especially in case of Cu-Pb-Zn
ores). Use of cyanide should be avoided and should only be used with care and
caution in case of necessity.

Caution:

Cyanide must be used in alkaline media only. The excess of cyanide in waste
must be destroyed with bleaching powder before it is disposed to sewage.

1 ml 1 M EDTA 0.04030 of MgO

Pyrophosphate Method (Gravimetry)

Determination of MgO

Outline

When a cold acid solution of magnesium is treated with an excess of

diammonium hydrogen phosphate and then excess of ammonia solution is added.
Magnesium ammonium phosphate hexahydrate MgNH4PO4.6H2O is precipitated at
room temperature.

The magnesium ammonium phosphate hexahydrate is ignited at 1000oC to

o
1100 C to magnesium pyrophosphate (Mg2P2O7).

Procedure

Take the filtrate from the precipitation of calcium oxalate in a 500 ml beaker.
Add 50 ml nitric acid and 20 ml. conc. hydrochloric acid and boil vigorously to
destroy the organic salt. When the material is nearly dry, add 10-ml. conc.
hydrochloric acid and 100 ml. water and boil. If the solution is not clear, filter
through No.40 Whatman filter paper and wash the residue with hot water. Discard
the residue and proceed with the filtrate. Add about 0.5 gm. of diammonium
hydrogen phosphate (NH4)2HPO4 and stir well to dissolve the phosphate. Add a few
drops of methyl red indicator. Add conc. ammonia solution slowly, while stirring,
until the indicator turns yellow. Continue to stir the solution for 5 minutes, adding
ammonia solution drop wise to keep the solution yellow, and finally add 5 ml. of
conc. ammonia solution in excess. Allow the solution to stand in a cool place
overnight. Filter through No.40 Whatman filter paper. Wash the precipitate on the
paper with cold 0.1% aqueous ammonia solution until free from chloride ions.

Remove the precipitate into a previously weighed platinum or porcelain

crucible. Char the paper slowly and burn off the filter paper at a low heat and then
ignite to a constant weight in an electric muffle furnace at 1000 to 1100oC and cool in
a desiccators weigh and find out the weight of the residue.

7
Calculate the percentage of MgO from the factor:

Mg2P2O7 x 0.3623 = MgO

MgO % = W1 x 0.3623 x 100

W2
Where
W1 = weight of the Mg2P2O7 in gm. and
W2 = weight in gm. of the sample represented by aliquot.

Reactions involved

1. Mg++ + HPO4 + NH4+ + OH- = MgNH4PO4 + H2O

2. 2MgNH4PO4 = Mg2P2O7 + 2NH3 + H2O

Precautions

1. Precipitation should be done in an excess of ammonia since the precipitate has

a tendency to dissolve in water (56 mg. Per 1000 ml at 20oC).
2. The precipitate should be washed with ammonical water to avoid solubility.
3. Since there is a tendency of coprecipitation, if time permits, the magnesium
ammonium phosphate precipitate should be dissolved in hydrochloric acid and
reprecipitated.

1.2.1.4 Alumina (Al2O3) -(EDTA Complexometry Back Titration)

Pipette out 50 ml. aliquot from the main stock solution in some beaker. Take
50-75 ml 10% NaOH solution in another 250 ml beaker. Neutralize the aliquot with
10% NaOH solution to a tea red colour. No precipitate of iron should appear. Transfer
this to 10% NaOH solution, taken in other beaker with constant stirring. Wash the
beaker with hot water to transfer all contents. Add a few drops of bromine water and a
pinch of sodium carbonate to this. Boil the content on a burner. Cool and filter this
through Whatman 41 filter paper with little filter paper pulp in 500-600 ml beaker.
Wash the residue 5-6 times with hot water. (residue can be used for estimation of
iron, calcium and magnesium after dissolving in hydrochloric acid. But, as per the
experience of Indian Bureau of Mines analytical laboratory, the estimation is not very
accurate). Acidify the filtrate with dilute hydrochloric acid with gradual addition.
Precipitate of aluminium hydroxide will appear. Dissolve this with a drop of
hydrochloride acid. The solution should be clear (actually this is the catch of pH
required for titration). Add measured excess of EDTA solution to this. (Normally 25
ml of 0.05 M EDTA is added for estimation of Al2O3 in bauxite, clay, kyanite etc. and
10 ml. of 0.02 M EDTA is added for estimation of Al2O3 in iron ore, manganese ore,
limestone etc.). Boil this. Cool this and adjust pH to 5.5 pH HCl and NaOH (or NH3).
Add 50 ml, 5.5 pH sodium acetate buffer. Add 5-6 drops of xylenol orange indicator.
The indicator will impart golden yellow colour to the solution. Titrate this against
(0.05 M or 0.02 M as the case may be) standard zinc acetate solution. Colour changes
from yellow to orange red. The colour should be observed on the rim of the titrating
solution. This is a back titration technique. Find zinc acetate equivalent for the

8
volume of standard EDTA added. Find the amount of standard EDTA (or equivalent
zinc acetate) consumed by aluminium ion for complexion.

1 ml 1 M EDTA 1 ml 1 M Zn-Acetate 0.05098 g Al2O3

Note: Zn interferes in this estimation. A modified method for estimation of zinc and aluminium together is given
below.

Al2O3 and Zn (EDTA Complexmetry back titration)

Follow the procedure given above under Al2O3 in toto. The first equivalence
point will indicate the total amount of Al2O3 and zinc. Now add 1-2 g. of sodium
fluoride to the solution after first titration. Boil the solution. Fluoride will complex
aluminium ion and release equivalent amount of EDTA from Al-EDTA complex.
Cool the solution. Titrate this against standard zinc acetate solution. Colour changes
from golden yellow to orange red. Find the volume of EDTA required for complexing
Zn ions.

1 ml 1M EDTA = 1 ml 1 M Zn-acetate = 0.06537 g Zn

Note: If only Zinc is to be estimated, Aluminium can be masked with Sodium fluoride or Ammonium bifluoride at
first boiling stage and thus only Zinc will complex with EDTA.

1.2.1.5 Zinc (Zn)- (EDTA Complexometry Back Titration)

Follow the procedure given above under Al2O3 in toto. The first equivalence
point will indicate the total amount of Al2O3 and zinc. Now add 1-2 g. of sodium
fluoride to the solution after first titration. Boil the solution. Fluoride will complex
aluminium ion and release equivalent amount of EDTA from Al-EDTA complex.
Cool the solution. Titrate this against standard zinc acetate solution. Colour changes
from golden yellow to orange red. Find the volume of EDTA required for complexing
Zn ions.
1 ml 1M EDTA 1 ml 1 M Zn-acetate 0.06537 g Zn.

Note: If only Zinc is to be estimated, Aluminium can be masked with Sodium Fluoride or Ammonium bifluoride
at first boiling stage and thus only Zinc will complex with EDTA. Hence, Zinc can be estimated by direct titration
at 5.5 pH. In this titration colour changes from wine red to golden yellow.

1.2.1.6 Manganese (Mn) (Volhards method)

Pipette out 25 ml solution in 500 ml conical flask. Boil this and remove free
chlorine. Dilute the volume to 150 ml with demineralised water. Add 5-6 g of zinc
oxide. Shake vigorously. Heat this on burner to near to a boiling point (avoid boiling).
Titrate this against standard potassium permanganate solution to a permanent pink
colour. To observe the colour change the flask should be kept in slanting position and
the insoluble should be allowed to settle and observe the colour in clear solution. Best
is to run a control reading to locate the probable end point and finish the
second/parallel titration to an exact end point.

1 ml 1 N KMnO4 0.01648 g of Mn

9
The reactions involved are

3Mn2+ + 2MnO4 + (X+2) H2O = 5MnO2 XH2O + 4H+

Notes on successful performance of Volhards method

There is much criticism about the use of Volhards method but in the Ore
Dressing Laboratory of Indian Bureau of Mines, this process has been in practice for
many years and the results obtained are quite reliable and satisfactory.

The following precautions are needed for the successful application of the method.

1. The titration is made quickly and the solution is not allowed to cool below
80oC during titration.
2. The permanganate causes formation of precipitate, which obscures the end
point. A drop of HNO3 makes the precipitate to settle quickly. The end point
can be easily observed if the conical flask is kept in a slanting position on a
stand.
3. Avoid boiling of the solution while titrating as it may destroy the
permanganate colouration.
4. A chloride, sulphate or nitrate solution may be used for the determination of
manganese but the amount of permanganate used will vary in each case. In
fact many factors influence and the method is reported to be only empirical.
The permanganate must be standardized against a similar ore or steel of
known manganese content. (Ref.pp. 175 and 176 Advanced Quantitative
Analysis LA companion Volume to Elementary).

1.2.1.7 Titanium Dioxide (TiO2) Ferric Ammonium Sulphate Titration Method

(Volumetric)

Pipette out 50 ml aliquot into a 500 ml conical flask; add 25 ml concentrated

hydrochloric acid. Add a strip of aluminium foil to the flask (nearly 2 g). Digest this
on burner in presence of carbon-di-oxide. Boil at least for 30 minutes. All the time a
slow stream of CO2 must be maintained. Remove the flask from the heat. Cool this in
cold water (preferably ice cold water) and slow current of CO2 should be maintained
during the process of cooling. Wash the side of conical flask. Add 5 ml. Ammonium
thiocyanate solution. Titrate this quickly with standard ferric ammonium sulphate
solution to a faint red colour. Run a blank and deduct this reading from the main
reading.

1 ml 1N ferric ammonium sulphate 0.08 g TiO2

1.2.1.8 Phosphorous Peroxide (P2O5) (Wilson Method Quinoline Phospho

Molybdate Method)

Dissolve 0.05 0.2 g of sample (0.05 for phosphorite, apatite etc., high P2O5
and 0.2 g for iron ore, manganese ore etc. with low P2O5) in 25-concentrated
hydrochloric acid and few drops nitric acid (to convert meta phosphate to ortho
phosphate) in 500-ml. conical flask. Cool the content. Neutralise the acid with 10%

10
NaOH solution. Redissolve the precipitate formed in dilute hydrochloric acid. Use
litmus paper for indication. Add about 5 ml dilute hydrochloric acid in excess. Dilute
the solution to 150 ml with DM water. Add a pinch of citric acid. Heat this to boiling
on a burner. Add 30 ml citromolybdate solution, again heat it to boiling and add 25
ml. Quinoline hydrochloride solution very slowly with constant stirring. Boil this for
5-10 minutes. Cool this in cold water bath. Allow the precipitate to settle for 1-2
hours. If time permits, it is better to keep it overnight. Collect this precipitate on a pad
of filter paper pulp under suction. Wash the conical flask thoroughly with cold water
and transfer this to the precipitate collected on the pad. Wash the precipitate 8-10
times with cold water (till it is free from acid). Transfer the precipitate along with
filter paper pad to the original flask. Add 50 ml DM water. Add known excess of 0.1
N NaOH solution to dissolve the yellow precipitate of quinoline phosphomolybdate
completely. Add 2-3 drops of phenolphthalein indicator. Titrate this against standard
hydrochloric acid solution (0.1 N) to a colourless end point.

1 ml 1 N HCl 0.001193 g of P 0.002733 g of P2O5

NB: Phosphorous can be estimated from R2O3 precipitation as R2O3 carries almost all P2O5 along with it, to
ensure complete precipitation of P2O5 add 1-2 drops of concentrated ferric chloride solution before P2O 5
precipitation. Dissolve R2O 3 in HCl and proceed to precipitate P2O5 as detailed above.

1.2.1.9 Copper (Cu)-Copper (Sodium Thiosulphate titration)

Take 50 ml aliquot for copper estimation expel all nitrate, if present, either by
treatment with urea with constant boiling or by fuming the mass with dilute sulphuric
acid. The latter is more preferred as the nitrates are completely expelled out from the
solution. Therefore, the stock solution is preferably prepared after fuming with
sulphuric acid and extracting the mass in dilute sulphuric acid and water.

Neutralize the aliquot with dilute ammonia to neutralize all mineral acid. Add
8-10 ml of glacial acetic acid. Add 2.3 g of sodium fluoride. Boil this and cool in
water bath. Add approx. 2-3 g potassium iodide and titrate the liberated iodine with
standard sodium thiosulphate solution. Add starch near the end point. Finish to a
colourless end point. Colour changes from blue to colourless.

1 ml 1 N Na2S2O3 0.06357 g of Cu.

The copper present in minute quantities in tailings, etc. is determined by the

spectrophotometric method. The limit of Cu for this method is 0.01 to 0.15%.

Zn (Urea Hydrolysis method) (EDTA-Complexometry)

Take 50 ml aliquot in 250 ml beaker and neutralize the acid with dilute
ammonia (precipitate should not appear). Add 2 g of urea and boil vigorously, check
the pH of the solution continuously with pH paper. Adjust the pH to about 5. Remove
the beaker from the flame. Wash the sides of the beaker with water. Cool this in cold
water. Filter this through Whatman 41 with little filter paper plup. Wash the residue
5-6 times with hot water. Collect the filtrate in 400 ml beaker. Add 0.5 1.0 g.
Ascorbic acid. Dissolve the solid. Now add 0.5-1 g. thiourea. Again dissolve all

11
solids. Add 50 ml, 5.5 pH, sodium acetate buffer. Add 2-3 days of xylenol orange
indicator. Indicator will impart purple red colour to the solution. Intensity will depend
on the quantity of Zn in the solution. Titrate this against standard EDTA solution.
Colour changes from purple red to golden yellow. Add a pinch sodium fluoride to
avoid inference of alumina, if left unprecipitated by urea, with the end point.

1 ml 1M EDTA 0.06537 g of Zn.

1.2.1.10 Lead (Pb) - (EDTAComplexometry)

Separate Pb from other element by conversion to sulphate. Take 50 ml aliquot

add 5 ml dil. sulphuric acid fume of the content. Wet the mass left with dil. H2SO4
and add 50 ml. Water. Boil this on burner. Filter this through Whatman 40. Wash the
precipitate with hot water containing 5% sulphuric acid. Transfer the filter paper
along with precipitate to the original beaker. Add 100 ml, 5.5 pH, ammonium acetate
acetic acid buffer. Boil this, cool this in water bath. Add a pinch of ascorbic acid
and a pinch of thiourea. Dissolve the solids. Add 25 ml. Sodium acetate 5.5 pH
buffer. Add 2-3 drops of xylenol orange indicator. Titrate this against standard EDTA
solution. Colour changes from purple red to golden yellow.

1 ml 1 M EDTA 0.2072 g. of Pb

1.2.2 MINOR ELEMENTS

1.2.2.1 TiO2 & V2O5 (Hydrogen Peroxide method)

Titanium and vanadium both forms yellow coloured complex with hydrogen
peroxide. Chloride ion and chlorine affects the colour of the complex, therefore all
chlorides must be expelled before the colour is developed.

Procedure: Take 25 ml. aliquot in 250 ml beaker, add 1-2 ml. dil. Sulphuric acid and
fume off the content on hot plate. Moisten the mass with dilute sulphuric and 50 ml.
DM water. Boil the content. Filter if there is any turbidity. Add 5 ml. dilute sulphuric
acid and 5 ml. ortho-phosphoric acid. Add 10 ml. (1:1) H2O2. Yellow colour of
titanium complex will appear. Make up the volume to 100 ml. in volumetric flask.
Measure the absorbance at 410 nm. This measurement will give the quantity of TiO2
and V2O5 together. Add a pinch of sodium fluoride in the volumetric flask of
titanium-peroxide complex, shake vigorously for few minutes filter through dry filter
paper. Measure the absorbance at 410 nm. This colour will correspond to V2O5
content. Find TiO2 by difference. If V2O5 is absent or negligible, the original reading
(before adding sodium fluoride) of absorbance should be taken for finding equivalent
of TiO2 content.

Graph for TiO2 estimation: Fuse 0.1 g of pure TiO2 with potassium
pyrosulphate (approx. 1 g.) in silica crucible. Extract the mass in 5 ml (1:1) sulphuric
acid and 50 ml. DM water. Cool this and make up to 100 ml. in volumetric flask.
Now each ml. of this solution will be equivalent to 1 mg. of TiO2. Take out 1 ml, 2

12
ml,5 ml, 6 ml, 7 ml, 9 ml, 10 ml, aliquot and develop colour of Titanium-hydrogen
peroxide complex at described above. Measure the absorbance and plot the graph.

1.2.2.2 Manganese (Mn) (Periodate Oxidation Method)

Determination of minute amounts of manganese (Per-iodate method)

(Spectrophotometry)

Method

The sample is decomposed with hydrochloric and nitric acid and fumed with
sulphuric acid. Phosphoric acid is added to complex the iron. Potassium periodate is
added and boiled to develop permanganate colour. Manganese is determined
spectrophotometrically at 545 nm or with a green filter.

Procedure

Take 0.5 gm of the sample in a beaker, add 10 ml. conc. hydrochloric acid and
digest over a hot plate. Filter through No.40 Whatman filter paper. Wash the residue
with hot hydrochloric acid. Burn off the filter paper in a platinum crucible, add a few
drops of sulphuric acid and 5 to 10 ml. hydrofluoric acid, evaporate and fume off
sulphuric acid. Dissolve the residue in hydrochloric acid, and add to the main
solution.
Add 5 to 10 ml. sulphuric acid and 20-ml. nitric acid to the solution of the
sample and evaporate to dryness. Thus, all chloride ions should be removed. Add 50
ml. water and heat until all ferric sulphate has been brought into solution. Filter off
any suspended matter, add 5 to 10 ml. manganese-free phosphoric acid to the filtrate,
and mix. The solution should be colourless.

Add 1 gm. of potassium periodate and heat to boiling (If there is any delay in
the appearance of permanganate colour, the presence of chloride ions is indicated, and
add more periodate). Take the solution in a 100 ml. volumetric flask and measure the
optical density at 545 nm. Compute the percentage of manganese from the calibration
graph prepared with a standard solution.

The reactions involved

2Mn++ + 5IO4- + 3H2O = 2MNO4- + 5IO3 + 6H+

Note:
1. It has been shown that with a low concentration of manganese, an acidity of 2 N, i.e. 5 to 6% by volume
of sulphuric acid is ideal.
2. In this method Phosphoric acid decolorizes ferric iron by complex formation and prevents precipitation
of periodate or iodates of manganese.
3. applicable for samples containing a low amount of manganese (0.02 to 3%).

Reference

E.B.Sandell, Colorimetric Determination of Traces of Metals, Third Edition, Inter Science Publishers, 1959, pp
609.

13
1.2.2.3 Copper (Spectrophotometric)

Decomposition of the sample

Take 0.5 gm. of the sample in a 250-ml. beaker, add 25-ml. conc. hydrochloric
acid and digest for some time over a hot plate. Add 10 ml. conc. nitric acid and
digest, when the reaction subsides, add 5 ml. of 1:1 sulphuric acid. Fume and dry.
Remove from the hot plate. When cool, add 5 ml. conc. hydrochloric acid and nearly
100 ml. distilled water and boil and filter through No.40 Whatman filter paper. Wash
the residue with hot water acidified with hydrochloric acid. Take the filtrate in a 250
ml. volumetric flask and make up to the volume.

Procedure

Take an aliquot equivalent to 0.1 gm. in a 250-ml. beaker; add 5 ml. 10%
hydroxylamine hydrochloride solution and 5 ml. 10% tartaric acid solution. Adjust
the pH at 5 to 5.5 with AR ammonium hydroxide and dilute/AR hydrochloric acid
and transfer it to a 250 ml separating funnel. Add 25 ml. of a solution of 2-2
biquinoline (100 mg. in 500-ml. amyl alcohol), shake vigorously and discard the
aqueous layer. Run the organic layer into the cell of a spectrophotometer. Measure
the absorbance against a reagent blank at 545 nm.

Compute the copper percentage by reference to the graph prepared with

standard copper solutions.

Determination of small amounts of P2O5 in silica sand, carbonate rock

(Spectrophotometry)

Reagents

1. Vanadate reagent Dissolve 2.5 gm of ammonium vanadate in boiling

water and cool the solution. Add 20-ml. conc. nitric acid, cool and dilute to
one litre.
2. Molybdate reagent Dissolve 50 gm. ammonium molybdate in hot water
and dilute to 1000 ml.
3. Standard P2O5 solution Dry potassium dihydrogen phosphate KH2PO4 at
110oC. Weigh 0.9588 gm. and dissolve in water. Add 5-ml. nitric acid and
dilute to 500 ml.

Method

Take 0.1 gm. of finely pulverized sample in a beaker and add 5-ml. conc.
nitric acid and a few drops of HF. Slowly evaporate over a hot plate, then dry and
dehydrate. Add 5-ml. conc. nitric acid and 50-ml. water, boil and filter through No.40
Whatman filter paper. Wash the residue with hot water. Take the filtrate in a 100 ml.
volumetric flask and make up the volume and mix thoroughly.

Take 5 ml. of the solution by pipette from the flask into a 100 ml. volumetric
flask and add 10 ml. colourless nitric acid (1:1), 10 ml. ammonium vanadate solution

14
and 10 ml. ammonium molybdate solution make the volume up to the mark with
water and mix thoroughly. After 30 minutes, measure the absorbance at 400 nm.
Take a reagent blank. Compute the percentage of P2O5 with Reference to the
standard graph prepared using standard solutions containing 0.5, 1.0, 1.5, 2.0 and 2.5
mg per 100 ml. of P2O5 exactly in the manner stated above.

1.2.2.4 Determination of Water of Crystallization in Minerals (H2O+)

Direct determination (Penfields method)

Dry the sample at 110oC for one hour. Take a dry penified tube and weigh.
Pour in the lower bulb about 1 gm. of the sample through a capillary funnel. Take the
weight of the tube again. The difference in weight will give the weight of the sample
taken.
Place a moistened filter paper or cloth, around the second bulbs to ensure
condensation of all water. Hold the tube horizontally, heat the first bulb on flame to
red hot. Finally pull of the heated bulb along with the residue and cut it off with a
flame from the rest of the tubed and seal off the cut end of the tube. Cool the tube,
clean the external portion and take weight (W1). Place the tube inside an electric oven
at 100 oC for 15 minutes. Remove the tube from the oven, cool in a desiccators and
weigh W2. The difference in weight will give the water.

% H2O+ = (W1 W2) x 100

Weight of the sample taken

Note:

1. Water crystallization is combined water in the structure of the mineral. For example, in goethite
(Fe2O3.H2O), the water is inside the crystal structure, which is normally reported as H2O+. Where the
water is due to absorption in the form of moisture it is indicated as H2O-.
2. This method is suitable for minerals easily deprived of their water.
3. The minerals that do not give up their water wholly are talc,topaz, etc. and special methods are to be
applied for them.
4. The Penfields tube for water determination in minerals is available in various forms.

15
1.2.2.5 Sulphur

The methods given below are applicable for the determination of sulphur in
sulphide ores and materials high in sulphur.

Determination of sulphur in ores (Gravimetry)

A. Wet oxidization method

Principle

The finely ground sample is oxidized by means of a mixture of bromine and

potassium bromate followed by nitric acid. The nitric acid is expelled by evaporation
to dryness, followed by a second evaporation with hydro-chloric acid, which
dehydrates the silica. Iron is now reduced to the ferrous condition and the silica and
un-dissolved residue are filtered off. Sulphur is precipitated in a large volume of cold
solution by barium chloride solution as BaSO4, which is ignited and weighed.

Reagents

1. Bromine-potassium bromide solution: 320 gm of potassium bromide is

dissolved in just sufficient water and 200 ml. bromine added. After mixing
well, the solution is diluted to 2000 ml.
2. Carbon tetrachloride saturated with bromine.
3. Barium chloride 10% solution

16
Procedure

The sample is ground to pass 80 mesh sieve. Take 0.1 gm of sample in a 250
ml. beaker and add 10 ml bromine potassium bromide mixture for pyrrhotite ore or
bromine carbontetrachloride reagent for pyrite ores. Cover the beakers and keep in a
fume chamber (caution bromine should be handled carefully and should not be
inhaled, protective glass for eyes should be worn). The beaker should be shaken
occasionally. After one hour, 15 ml conc. nitric acid is added and the mixture
allowed to stand at room temperature overnight. The beakers are kept over a steam
bath and allowed to dry. Ten ml. of conc. hydrochloric acid is now added and the
solution again evaporated to dryness to expel all nitric acid. Silica is dehydrated by
heating in an air-oven at 100oC for one hour.

The beakers are removed and when cool, 5-ml. conc. hydrochloric acid and
nearly 100-ml. water are added and boiled. After cooling, approximately 0.2 gm. of
aluminium powder is added to the solution and stirred. When the iron has been
reduced, the solution becomes colourless. The solution is filtered through No.40
Whatman filter paper into a 600-ml. beaker (preferably one litre beaker). The residue
on the filter paper is washed 5 or 6 times with hot water. The solution in the large
beaker is diluted to 500 ml. with cold water and 6 ml. (1:1) HCl added and mixed by
stirring. Twenty ml. of 10% solution of barium chloride is now added. The solution
is mixed by stirring. The BaSO4 precipitate is allowed to settle overnight.

The clear solution is filtered through No.42 Whatman filter paper (or a filter
crucible using suction).The precipitate is washed with cold water 10 times to remove
the chloride ions.

Take the precipitate along with the filter paper in a weighed platinum crucible
and slowly ignite at 950 to 1000oC for one hour, remove and cool in a desiccator and
weigh again. From the weight of the BaSO4, calculate the percentage of sulphur.

S% = Weight of the BaSO4 x 0.1374 x 100

Weight of the sample taken

B. Fusion Method

Weigh 0.1 to 0.2 gm of sample, depending on whether the sulphur content is

high or low, in a nickel crucible. Add about 2 gm of sodium peroxide and mix with a
thin dry glass rod. Cover the mixture with a thin layer of the peroxide and then heat
gently over a low flame at a temperature just sufficient to produce complete fusion.
Do not hasten, a slow, gradual fusion is more successful as it will avoid loss due to
spattering or burning of a hole in the crucible itself. The maximum temperature
required is dull redness only. To obtain the liquid condition, 10 to 15 minutes heating
would suffice.

Keep the melt over the flame for 5 minutes, and with the aid of tongs give the
crucible a swirling motion 2 or 3 times during that period.

17
 Remove from heat and allow it to cool in air slowly, (do not try to cool in
water, it will cause an explosion), with the aid of a glass rod. Place the crucible in a
500 ml beaker and pour 100 ml water. Cover quickly with a watch glass to prevent
loss by spattering. Remove and wash the crucible with water, policing it out. Boil for
a few minutes with constant stirring to destroy excess of peroxide. If the supernatant
liquid is greenish, it indicates manganese, add 2 to 5 ml. methyl alcohol and boil to
precipitate manganese as MnO2 and allow it to settle. The solution now will be clear.

Filter hot through Whatman No.40 filter paper in a 500 ml beaker (a bigger
size filter paper is preferable) using funnel of large size so that the layer of precipitate
on the filter paper will not be too thick. This will ensure quick filtering and efficient
washing. Wash the residue with hot water 6 to 8 times. Discard the precipitate. The
total filtrate and washings should have a volume of 250 to 300 ml. Add a few drops
of methyl red and make slightly acidic with HCl (about 3 ml in excess). Heat to
boiling and add slowly and with constant stirring 10 20 ml of 10% BaCl2 solution.
Keep it hot for a few minutes. Then remove from the flame and keep overnight to
allow the precipitate to settle.

Filter through No.42 Whatman filter paper and wash the precipitate 8 to 10
times with hot water.

Transfer the residue along with the filter paper in a weighed platinum crucible
and ignite the residue carefully at a temperature of 1000 oC. Cool in a desiccator and
weigh again. From the weight of the BaSO4, calculate the percentage of S in the
sample as follows:

S% = Weight of the BaSO4 x 0.1374 x 100

Weight of the sample taken

Determination of carbon-di-oxide (Gravimetry)

Principle

A known amount of the sample is made to react with an acid and the liberated
carbon dioxide freed from impurities is absorbed in previously weighed sode asbestos
bulb and weighed. From the difference, the percentage of carbon dioxide is
calculated.

Reagents

1. Dilute hydrochloric acid 1:1 V/V

2. Concentrated sulphuric acid.
3. Ascarite solid.
4. Magnesium perchlorate solid.
5. Copper sulphate solution.

Procedure

18
 Weigh 0.5 gm. of the sample to the flask of the CO2 apparatus and cover it
with water. Insert the stopper carrying the separatory funnel and the condenser.
Connect the latter with the absorption vessel. Pass air that is free from CO2 through
the system. Close the stopper cock in the separatory funnel and insert the weighed
absorption bulb in the train and also put the guard tube. Half fill the separatory funnel
with 1:1 hydrochloric acid. Open the stop-cock in the separatory funnel and run acid
into the flask slowly. When effervescence diminishes, start a flow of water in the
condenser and heat the flask slowly so as to secure steady but quiet ebullition. When
it is judged that carbon dioxide has been boiled out of the solution, remove the flame
increase the current of air and sweep out all carbon dioxide. Close the inlet and outlet
tube and disconnect the weighed bulb. Cool in a desiccators and weigh. The ascarite
absorbs the carbon dioxide and the drying agent takes up the water formed in the
reaction.

Reaction involved

2 NaOH + CO2 Na2CO3 + H2O

Calculation

CO2 % = (A B) x 100
C
Where

A = weight in gm. of the bulb after the test

B = weight in gm. of the bulb before the test
C = weight in gm. of the sample taken.

19
1.2.2.6 Determination of minute amount of Arsenic
(Spectrophotometry heteropoly molybdenum blue method)

Principle

Following the separation of arsenic from matrix elements by distilledlation as

the trichloride, the arsenic (III) is oxidized to the pentavalent state with nitric acid and
ammonium molybdate is added to form a heteropolymolybdioarsenate which is then
reduced by a suitable reducing agent to strongly coloured molybdenum blue and
measured at 840 nm.

Reagents

1. Standard arsenic solution Dissolve 0.1320 gm. of Ar arsenic trioxide

As2O3 in the minimum volume of 1 M sodium hydroxide solution, make
slightly acidic with hydrochloric acid, make up to 100 ml in a volumetric
flask.
1 ml. = 1 mg. As
A solution containing 0.001 mg. of As per ml. is prepared by dilution.
2. Ammonium molybdate solution 0.1% W/V, - Dissolve 5 gm. of ammonium
molybdate (NH4)6 Mo 7 O24.4H2O in approximately 200 ml. of 2.5 M sulphuric
acid and dilute to 500 ml. with the same solution, store in a polythene bottle.
3. Ascorbic acid solution, 0.1% W/V prepare fresh solution daily in water.
4. Sulphuric acid 2.5 M Add 130 ml. of conc. sulphuric acid slowly while
stirring to approximately 800 ml. of water. Allow the solution to cool to room

20
 temperature, transfer to a 1 litre volumetric flask, and dilute to volume with
water.

Procedure

Distill arsenic by the method given under arsenic ore and make up in a volumetric
flask, to 250 ml. Take an aliquot of the distillate, add 10 ml. conc. nitric acid and evaporate
to dryness, bake the residue at 130oC for 15 minutes to ensure complete removal of nitric
acid. Cool and add 2 ml. ammonium molybdate, 2 ml. ascorbic acid solution, keep on a
steam bath for 30 minutes. Transfer the solution in a 100 ml. volumetric flask and make it up
to the volume with water and mix well. Determine the absorbance of the solution at 840 nm
or with a red filter with maximum transmission above 700 nm. Prepare a standard curve from
known amounts of arsenic treated in the same way as the unknown, carry out reagent blank,
and measure the optical density against this. Compute the percent or arsenic from the
standard graph.

Note

1. The acid concentration of the solution must be controlled. If the acidity is too low even molybdate alone
will give a blue colour and if it is too high the colour due to arsenic is decreased in intensity.
2. Oxalic, tartaric, citric acids, fluorides and oxidizing agents interfere in this method.

Reference

E.B. Sandell Colorimetric determination of traces of metals. Interscience publishers Inc., New York
1959, Page 279.

1.2.2.7 Determination of minute amount of Chromium (Spectrophotometry)

Diphenylcarbazide method

Principle

Hexavalent chromium reacts with 1-5-Diphenylcarbazide CO(NH.NHC6H5)2

and produces a soluble violet compound in slightly acidic solutions (0.2 N).
Measurement of the amount of reddish purple colour formed yields an estimation of
chromium present (wave length 540 nm) or green filter may be used if a colorimeter
is used.

Reagents

1. 1-5-diphenylcarbazide reagent 0.25% - Dissolve 0.25 gm.

(C6H5NH.NH)2CO in 100 ml. 95% ethyl alcohol or 50% acetone or isopropyl
alcohol.
2. Sulphuric acid 6N Add cautiously 167 ml. concentrated H2SO4 to distilled
water and dilute to one liter.
3. Standard Chromium Solution Dissolve 2.8283 gm. of pure K2Cr2O7 in
water and dilute to a liter in a volumetric flask. Pipette 20 ml. of this solution
into a 2-liter volumetric flask and dilute to the mark with water.
1 ml = 0.01 mg. Cr

21
Determination of Chromium (Minute Quantity)

Fuse 0.5 gm. of very finely ground rock powder with five times its weight of
sodium peroxide in a nickel crucible (free from chromium and vanadium) and cool.
Leach with hot water and filter through number 40 Whatman filter paper. Wash the
residue with hot water. Add a few drops of alcohol and heat for about half an hour to
destroy peroxide, manganate, if any, will be reduced. If any precipitate is there, filter
through No.40 Whatman filter paper. Keep the solution to nearly 50 ml. If the
solution is yellow in colour, it implies a higher percentage of Cr2O3. In such case,
make up the solution in a volumetric flask and take an aliquot. If a very faint colour
or no colour is visible, take the entire solution.

Neutralize the solution with dilute sulphuric acid. Add 2 ml 6 N H2SO4 more,
add 2 ml of 0.25% diphenylcarbazide solution and make up to 100 ml. mix and obtain
the optical density in a spectrophotometer at 540 nm or in a filter photometer using a
green filter.

Compute the percent of Cr2O3 from a standard curve prepared under the same
condition. Run a blank throughout the procedure.

Note :
1. If the ore contains vanadium, it should be separated by 8-hydroxyquinoline extract in chloroform as
V2O3 (C 9H6ON)4 complex at pH of about 4.
2. A suitable acidity for the chromium diphenylcarbazide reaction is 0.05-0.2 N.

1.2.2.8 Determination of Minute Amount of Iron (1:10 Phenanthroline Method)

Take 50 ml aliquot. Adjust the pH to 3.5 by sodium citrate solution.

Add 1 ml of ascorbic acid solution. Stir the content thoroughly. Add 2 ml,
1:10 phenanthroline solution. Make up the volume to 100 ml in volumetric
flask. Take a blank of all the reagents and make the volume to 100 ml.
Measure the absorbance at 500 nm against the blank. Find corresponding
amount of iron from the graph.

1 V2O5 (Spectrometically) see Vanadium ores

2 Arsenic (Spectrometrically) see Arsenic ores
3 Bismuth (Spectrometrically) see Bismuth ores
4 Chromium
5 Copper
6 Cobalt (Spectrometrically) see Cobalt ores
7 Nickel (Spectrometrically) see Nickel ores
8 Tungsten (Spectrometrically) see Tungsten ores
9 Molybdenum (Spectrometriclly) see Molybdenum ores

ALUMINIUM ORES

Bauxite forms the main source of aluminium metal. It contains monohydrates

aluminium oxides and trihydrate aluminium oxides in different proportions. It is
associated with oxides and hydroxides of iron, titanium dioxide, silica, etc.

22
 Bauxite is generally analysed for L.O.I., SiO2 (total), SiO2 (reactive), Al2O3,
Fe2O3, TiO2, CaO, MgO, P2O5 and V2O5 and Mn.

L.O.I. and Al2O3 are determined in separate portions of the sample. SiO2,
Fe2O3, TiO2, CaO, MgO, P2O5 and V2O5 are determined after digestion of the sample
and drawing aliquots from the main solution.

PREPARATION OF SAMPLE

Dry the well-ground sample (100 or 200 mesh) to constant weight at 140 +
o
2 C for one hour and use this for subsequent determination.

Determination of silica (Gravimetry)

Procedure

Take 1 gm. of dried bauxite sample in a 250 ml. beaker. Add 15 to 20 ml.
conc. hydrochloric acid, 1 ml. conc. nitric acid and digest over a hot plate. After
some time, add 5 ml. of 1:1 sulphuric acid, dry and fume off strongly. Moisten the
dry residue with 1:1 sulphuric acid and add nearly 100 ml. of water and boil to
dissolve the soluble salt. Filter the hot solution through What man filter paper No.40.
Wash the residue 5 or 6 times with hot water.

Reserve the filtrate to prepare the main solution and determine the associated
radicals.
Take the residue along with the filter paper in a platinum crucible and burn off
the filter paper and ignite the residue. Cool in a desiccators and weigh. Moisten the
residue with a few drops of 1:1 sulphuric acid and add 10-to 15-ml. hydrofluoric acid
and keep over a hot plate or over a flame placing an asbestos board over it. Slowly
evaporate and finally dry and ignite the residue, cool in desiccators and weigh. The
difference between the two weights will give the silica content. Calculate the silica
percentage as follows:

SiO2 percentage = (W1 W2) x 100

W3
Where
W1 is the weight of the crucible + material after ignition.
W2 is the weight of the platinum crucible + material after hydrofluorization and
W3 is the weight of the sample taken.

Preparation of the main solution

Fuse the residue after hydrofluorization with 0.5 gm. potassium pyrosulphate
and extract the mass in the preserved filtrate by boiling. Cool the solution.

Transfer the solution into a 250 ml. volumetric flask, make up to the mark and
mix the contents well. Treat this as the main solution. An aliquot is taken for the
determination of Fe2O3, TiO2, P2O5, V2O5, CaO, MgO, etc. Follow the procedure

23
given in chapter on determination of Major and Minor Elements from the Stock
Solution.

Determination of reactive silica (Gravimetry)

Outline of the method

The sample is dissolved in mixture of acids (HCl, HNO3 H2SO4) and

evaporated to fumes. HF is added and the solution filtered. The residue is
hydrofluorized. The loss in weight of the residue represents non-reactive silica.

Reactive silica is obtained by deducting the percentage of non-reactive silica

from the percentage of total silica.

Procedure

Transfer 1 gm. of sample into a beaker. Add 25-ml. conc. hydrochloric acid
and 5-ml. conc. nitric acid and keep over a hot plate. After sometime, add 20-ml. 1:1
sulphuric acid. Heat slowly and continue heating until copious fumes are liberated
and finally dry. Cool and add about 100-ml. water and few drops of 1:1 sulphuric
acid and boil till a clear solution is obtained. Add 30 ml. 40% hydrofluoric acid from
a polythene measuring cylinder, boil for one minute and filter at once through No.40
Whatman filter paper using a little pulp. Wash the residue with hot water 5 to 8
times.
Transfer the filter paper along with the residue into a platinum crucible, ignite
it in a furnace at 900 to 1000 oC for one hour, cool and weigh. Add 5 to 10 drops of
1:1 H2SO4 and half a crucible hydrofluoric acid and evaporate slowly to dryness.
When dry, ignite over a flame. Cool in desiccators and reweigh.

Non-reactive silica percentage = A x 100

B
Where
A = loss of weight of the residue after HF, and
B = weight of the sample taken.
Reactive silica percentage = Total silica Non-reactive silica

N.B.:From our experience, it is observed that this method gives a fair idea of reactive silica in routine analysis of
bauxite. This is also corroborated by some of the Indian aluminium companies in their communications. For
accurate determination of reactive silica, the bomb digestion method, specifying temperature and pressure is
recommended.

ALUMINOSILICATES AND OTHER SILICATES

Some silicates are decomposed by strong mineral acid and the silica passes as
insoluble residue. This is then dehydrated and separated by filtration. The silica is
estimated from the insoluble residue by hydrofluorisation.

Many silicates are not completely decomposed by strong mineral acid or they
are not at all affected by strong mineral acid (except hydrofluoric acid). Silica being

24
acidic in nature fusion with alkali salt is most preferred to break a complex silicate.
The choice of flux depends on the properties and presence of certain elements in the
silicate. Anhydrous sodium carbonate is most commonly used to break complex
silicate. Additions of potassium carbonate lower the fusion temperature and
potassium carbonate being more alkaline in nature increase the activity of flux.
Potassium carbonate is hygroscopic and more corrosive than anhydrous sodium
carbonate care must be taken to avoid loss due to sputtering. A small piece of filter
paper is added to molten mass to dissolve the more refractory silicates. Sodium
carbonate with little borax or boric acid is used to dissolve some hard silicate and
when the silicate or the sample contains fluorine. Excess of borate must be removed
before estimation of silica.

A. Estimation of silica (sodium carbonate fusion)

Mix thoroughly 4 to 6 g of anhydrous sodium carbonate with 1 g of rock or

mineral powder in a platinum crucible of 20-30 ml capacity. Place the crucible,
covered at first, over a moderately low flame, increase this gradually to a maximum
(approximately 1000oC) and maintain it there till the mass is quiescent. There should
be no violent action. Cool the crucible. Place the crucible in 250 ml beaker in
horizontal position. Cover the crucible completely with demineralised water. Now
add 10-15 ml concentrated hydrochloric acid. Cover the beaker with watch glass.
Allow the reaction to complete. Now heat the beaker on low flame. Remove the
crucible. Now transfer the beaker to hot plate. Allow all solvent to evaporate. Near
completion the mass should be occasionally stirred to avoid formation of lumps.
After evaporation of all solvent break any lump thus formed. Bake the mass at 110 oC
for 1 hour. Remove the beaker from the hot plate. Cool the beaker. Moisten the
mass with 1-2 ml concentrated hydrochloric acid and add 50 ml demineralised water.
Boil this on burner. Cool this and filter through Whatman 40. Wash the residue 5-6
times with hot water transfer all silica residue from the beaker with policeman or a
small piece of filter paper. Preserve the filtrate for estimation of other radicals.
Transfer the filter paper into a platinum crucible. Ignite this 1000 oC. Cool the mass
in desiccator and weigh. Moisten the mass with DM water. Add 2-3 drops of dil
sulphuric acid. Add 10-15 ml 48% hydrofluoric acid. Place the crucible on asbestos
sheet on a low flame or on a low temperature hot plate. Expel all acid from the
crucible. Now heat the crucible on a low flame initially and finally to a blast flame
(1000oC) for about 5 minutes. Cool the crucible in desiccater. Weigh the mass. The
loss in weight will be silica. Fuse the residue after silica determination with little
potassium pyrosulphate. Extract the mass in preserved filtrate. Cool the filtrate and
make up to 250 ml.

B. Estimation of silica (when the sample contains fluorine) Borate fusion:

Mix thoroughly 4-6 g of anhydrous sodium carbonate & 0.5 g Borax with 1 g
of fine powdered rock or mineral in a 20-30 ml platinum crucible. Place the crucible,
covered at first, over a moderately low flame, increase this gradually to a maximum
(approximately 1000oC) and maintain it there till the mass is quiescent. There should
be no violent action. Cool the crucible. Place the crucible in 250 ml beaker in
horizontal position. Cover the crucible completely with demineralised water. Add

25
10-15 ml concentrated hydrochloric acid. Cover the beaker with watch glass. Allow
the reaction to cease. Wash the watch glass in to the beaker. Now slowly heat the
content on low flame to remove all mass from the crucible. Remove the crucible and
wash it thoroughly.

(Removal of excess borate) Transfer the contents of the beaker completely into 15-
20 cm diameter china clay dish. Evaporate the contents carefully on a low flame.
Expel all liquid from the dish. Remove the dish from the flame. Add 4-5 drops of
dilute sulphuric acid. Add 10 ml methanol. Ignite the methanol with open flame.
Stir the mass. Apple green flame will indicate the presence of borate in the mass.
Cool the dish. Again repeat the process of removal of borate by additional quantity of
sulphuric acid and methanol till all borate is burnt.

Cool the masses add 5 ml concentrated hydrochloric acid and 50 ml

demineralised water. Boil the content on burner. Cool and filter through Whatman
40. Wash the residue 5-6 times with hot water. Preserve the filtrate for estimation of
other radicals. Transfer the filter paper into a platinum crucible. Ignite this at 1000 oC
in muffle furnace. Cool the mass in a desiccator and weigh. Moisten the mass with
little DM water. Add 2-3 drops dilute sulphuric acid. Add 10-15 ml 48%
hydrofluoric acid to the mass. Place the crucible on asbestos sheet on a low flame or
on a low temperature hot plate. Expel all acid from the crucible. Now heat the
crucible initially on a low flame and finally to a blast flame (1000oC) for about 5
minutes. Cool the crucible in desiccator. Weigh the mass. The loss in weight will be
the quantity of silica. Fuse the residue in the crucible with little potassium
pyrosulphate. Extract the mass in the preserved solution. Cool the filtrate and make
up to 250 ml.

Determination of Fe2O3, CaO, MgO, Al2O3, TiO2 etc.: Follow the procedure given
under the chapter on determination of major and minor constituent from the stock
solution.

Determination of Loss on Ignition (L.O.I.)

Loss on Ignition: Weight 1 g of dry sample in silica or platinum crucible. Place this
crucible in muffle furnace at a temperature below 300oC. Raise the temperature of the
furnace to 1000 OC. Keep this at this temperature for about 30 minutes. Cool the
crucible in desicater. Weigh the crucible. Find the loss in weight.

% Loss on Ignition (LOI) = Loss in weight x 100

Weight of the sample

ANTIMONY ORES

The important antimony-bearing mineral is stibnite (Sb2S3), which is the main

commercial source of antimony. A relatively large amount of antimony is present in
the sulphide ores in the form of tetrahedrite (sulphide of Sb), bournonite (sulphide of
Cu, Pb and Sb), etc.

26
Determination of antimony

Procedure

Take 0.5 to 1 gm of finely powdered ore in a 50 pyrex or corning conical

flask. Add 3 to 5 gm. potassium sulphate and 15 ml. conc. sulphuric acid and a piece
of paper to reduce the antimonic compound. Put a clean funnel over the flask and
heat the mixture gradually at low temperature and then with a full flame. Heating is
continued till carbon is completely oxidized, most of the free acid is driven off and a
clear solution is obtained (taking care not to expel all the H2SO4). The melt is
allowed to cool over the sides of the flask by rotating gently during cool.

Add 50 ml 1:1 hydrochloric acid and dissolve the melt by gentle warming.
Transfer the contents of the flask to 500-ml. beakers, rinse the original flask with 25
ml. conc. hydrochloric acid. Pass a rapid current of H2S through strong acidic
solution to precipitate arsenic sulphide through a double filter paper moistened with
(2:1) HCl, the beaker with (2:1) HCl. Wash the precipitate 5 or 6 times with this acid.
Antimony passes into the filtrate together with the other elements present in the ore.

Dilute the filtrate with three times of its volume of warm water and then
saturate with H2S gas. Antimony sulphide together with the other elements of the
hydrogen sulphide group will precipitate. Filter through no.40 Whatman filter paper
and wash the residue with dilute sulphuric acid (1+1) saturated with hydrogen
sulphide till free from chloride ions. Reject the filtrte. Treat the precipitate in the
filter paper with 10 to 20 ml. mixture of AR quality sodium sulphide and sodium
hydroxide (70 gm. of Na2S with 40% of NaOH diluted to 1000 ml.). This operation
will separate antimony sulphide from the sulphide of Cu, Pb, Cd, Bi, etc.

Take the filtrate and the washings containing antimony, add 2 g of potassium
sulphate and 10 ml. conc. sulphuric acid and heat until sulphur is destroyed and most
of the free acid has been expelled. Dissolve the melt in hydrochloric acid and titrate
with 0.1 N potassium permanganate.

The titration is ordinarily carried out in a solution of trivalent antimony,

which contains both sulphuric and hydrochloric acids. In a volume of 200 ml. there
should be progressively less hydrochloric acid. Add hydrochloric acid approximately
in the following proportion to the solution.
10 ml. H2SO4 .. 30 to 35 ml. HCl
20 ml. H2SO4 15 to 30 ml. HCl

Dilute to 200 ml. with water, and cool to 10 20 oC, then titrate with standard
permanganate solution until a decided pink colour persists for 10 to 30 seconds.

Calculate the percent of antimony from the following factor:

1 ml. of 1 N KMnO4 = 0.06057 g. of Sb.

27
ARSENIC ORES

The principal minerals are arsenopyrite (FeAsS), realgar (As2S2) and orpiment
(As2S3) and many arsenides and sulpharsenides of lead, copper, gold and tin.

Determination of arsenic (Volumetry)

Principle of the method

Arsenic is distilled out at 110 oC in the presence of cuprous chloride and

hydrochloric acid as arsenious trichloride (AsCl3). The distillate is trapped in water
and determined volumetrically by titrating with standard iodine solution at a specified
pH.

Procedure (for sulphide minerals)

Weigh 0.5 to 5 g (according to the anticipated amount) of the finely powdered

sample; add 15 ml of fuming nitric acid and digest over hot plate at low temperature.
Add 10 ml 1:1 sulphuric acid and evaporate to dense fumes.

Allow the mass to cool. Add water and transfer the entire mass into a
distillation flask. Wash the beaker thoroughly and pour the washings into the
distillation flask. Add 1 gm of hydrazine sulphate, 0.5 g of cuprous chloride to ensure
reduction of arsenic to the trivalent condition.

Add 70-ml. conc. arsenic free hydrochloric acid, and set up the distillation
apparatus. The end of the condenser should be submerged in 50 ml. of water in the
collecting beaker. Slowly raise the temperature and distilled out nearly 100 ml.
between 100 and 110 oC (at a very slow rate). The collecting beaker can be graduated
to indicate the various volumes of the distillate. Disconnect, wash out the condenser
into the collecting beaker. Transfer the distillate to a 500 ml. beaker for titration.
Cool, add a piece of litmus paper and make it slightly alkaline with 20% NaOH, then
re-acidify slightly with HCl. Cool again. To the cold, slightly acidic solution, add 3-
4 g. of NaHCO3 (in excess), and then a little starch solution. Titrate with standard
iodine solution to permanent blue tinge.

Calculate the percentage of the arsenic in the sample using the following
factor:
1 ml. 1N iodine = 0.03746 gm. of As
= 0.04946 gm. of As2O3
Reaction involved:

H3AsO3 + I2 + H2O = H3AsO4 + 2HI

BARIUM ORES

The chief minerals of barium are barite (BaSO4) and witherite (BaCO3).

28
 Barite is generally analysed for matters soluble in water, BaSO4, SO3, Fe2O3
and Al2O3 (combined), CaO, MgO, VM at 98 o 102oC.

Determination of matter soluble in water

Procedure

Weigh 10 g of the finely powdered materials in 500 ml. beaker, add about 150
ml. of freshly boiled neutral water (pH-7), boil for about 10 minutes, cool the mixture
to room temperature. Make up to 250 ml. with freshly boiled and cooled neutral
water in a volumetric flask. Shake and filter through a dry funnel using No.40
Whatman filter paper in a beaker. Take 100 ml. of the filtered solution in a weighed
platinum dish and slowly evaporate to dryness on a water bath. Dry the residue at a
constant weight in an oven at 105 to 110oC. Cool in a desiccator and weigh.
Difference in weight gives residue in 100 ml. of the solution. Compute the result as
follows:

Matter soluble in water % = W2 x 2.5 x 100

W1

Where- W2 is the weight of the residue in the platinum dish.

W1 is the weight in gram of the material taken.

Note: Test the water-soluble extract with a pH meter and report the acidity or alkalinity, if
any, calculates as H2SO4 or Na2CO3.

Determination of barium sulphate (BaSO4) (Gravimetry)

Principle

The sample is fused with a mixture of sodium and potassium carbonate,

leached with water to remove silica or other soluble sodium compounds. Barium
remains insoluble as carbonate together with other heavy metals. The residue is
washed with sodium carbonate solution to remove the adhering sulphate. The
insoluble carbonates are dissolved in hydrochloric acid. The R2O3 groups are
separated and filtered. The filtrate is acidified with hydrochloric acid and barium is
precipitated from the acidic solution as barium sulphate with the addition of
ammonium sulphate that is ignited and weighed.

Procedure

Weigh 0.2 g. of finely ground sample in a platinum crucible and add 1.5 g. of
Na2CO3 and 1 g. of K2CO3 cover and fuse the mixture over a high temperature burner
or in a furnace at 1000 oC for about 30 minutes. Take the crucible out of the hot zone
and rotate it so that the fusion will solidify in a thin layer by the side of the crucible.
This will shorten the time required for leaching. When cool, leach out the fusion with
200 ml. boiling water in a 500-ml. beaker. Filter through No.40 Whatman filter paper
and wash the filter paper and residue 10 to 12 times with hot sodium carbonate

29
solution and finally with hot water till free from sulphate. (Test the filtrate with
BaCl2 solution). Preserve the filtrate for the determination of SO3.

Dissolve the residue from the filter paper and a small portion of the solid
adhering to the platinum crucible with hot 1:1 hydrochloric acid. Add 1 g ammonium
chloride and neutralize with NH4OH using methyl red as Indicator. Boil and filter
through No.41 Whatman filter paper, wash the residue 4 or 5 times with hot water.
Preserve the filtrate. Dissolve the residue in hot hydrochloric acid and reprecipitate
with NH4OH as before. Wash the residue with hot water 5 to 6 times. This operation
will bring out any barium that might have been occluded in the R2O3 precipitate. Mix
both the filtrates and proceed.

Take the filtrate in a 500 ml. beaker. Add a few drops of methyl red indicator
and neutralize the solution with hydrochloric acid and add 2 ml. more conc.
hydrochloric acid. Dilute to 400 ml. with distill water, bring the solution to boil and
add 20 ml. 10% hot ammonium sulphate solution drop wise with constant stirring,
boil for five minutes, remove from the flame and allow it to stand for a at least 4
hours or preferably overnight. Filter through No.42 Whatman filter paper and wash
the residue thoroughly with warm water containing five drops sulphuric acid per liter
and then with cold water until filtrate is free from chloride ions. Transfer the residue
along with the filter paper in a weighed platinum crucible, slowly burn off the filter
paper and ignite the residue at 850oC to 900oC for 30 minutes. Cool in desiccators
and weigh. Calculate the percentage of BaSO4 as follows:

BaSO4 % = (A-B) x 100

C
Where - A = weight of the platinum crucible and the ignited
Barium sulphate,
B = weight of the empty platinum crucible
C = weight of the sample taken.

Notes :

1. Fusion is started with a low flame, which is gradually raised to the full blast. This precaution is
necessaryto prevent loss by overflowing.
2. To shorten the time for leaching, the melt in the platinum crucible should be solidified by the side
of thecrucible as a thin layer.
3. If the barite contains small amount of iron, the removal of R2O3 group is not necessary as there will
be little co precipitation and this step may be emitted. The residue on the filter paper after removal
of the sulphate ions may be dissolved in hot hydrochloric acid and directly proceed for the
precipitation of BaSO4.
4. Solubility of barium sulphate increases in hot water or in dilute hydrochloric or nitric acid. Hence,
the precipitation must be made in solution that contains preferably not over 1% of the mineral acid.
5. Thewashing of the precipitate should not be excessive. In accurate analysis, the washing should not
be carried out beyond the point at which 20 ml. of the washings give but a faint opalescence with
silver nitrate.
6. Filter paper containing the precipitate of BaSO4 should be burnt below 600oC. At higher
temperature carbon in the paper reduces barium sulphate to barium sulphite. To ensure complete
conversion to BaSO4. Remove the crucible after burning of the paper and add 2-3 drops of nitric
acid and 2-3 drops of dil sulphuric acid and ignite the ppt
7. .Ignition should be done at approximately 900oC although the precipitate suffers no appreciable
dissociation at temperature up to 1400oC.
8. If the analysis is a continuing one, ignite the filter paper along with the NH 4OH precipitate in a
weighed platinum crucible and weigh. Report this as mixed oxide percent.

30
 9. The method given here for BaSO4 determination is for barite sample containing all the barium as
BaSO4 only. If mineralogical studies indicate the presence of other minerals of barium, then
barium from hydrochloric acid leaching should be determined and deducted from the barium
reported as BaSO4.

Determination of SO3

Take the filtrate reserved for the determination of SO3, add few drops of
methyl red indicator and acidify with HCl, make the volume to nearly 300 ml. with
water, and adjust the acidity such that each 100 ml. of solution contain nearly 1 ml. of
HCl. Boil and add 20 ml. of 10% BaCl2 solution drop wise with constant stirring,
boil and allow to settle at least for four hours or preferably overnight. Filter through
No.42 Whatman filter paper and wash the residue five to six times with hot water
only till free from chloride ions. Wrap the precipitate in the paper, place it in a
weighed platinum crucible, dry, char and ignite at 900oC for 30 minutes. Cool in a
desiccators and weigh. Calculate the percentage of SO3 as follows :

SO3 = (A-B) x 0.3430 x 100

C
Where - A = Weight in g. of the platinum crucible
And ignited residue
B = weight in g. of the empty platinum crucible,
C = weight in g. of the sample taken.

Determination of silica (Gravimetry)

Principle

The material is fused with a mixture of sodium carbonate and potassium

carbonate and leached out with hot water and filtered. Silica is recovered from the
residue as well as from the filtrate and the silica is determined by dehydration and
hydrofluorization.

Procedure
Take 0.5 to 1 g. of the finely pulverized sample in a platinum crucible, add
about 3 grams of AR sodium carbonate and about 1 gm. of AR potassium carbonate,
mix with a dry glass rod and fuse in a muffle furnace or over a burner. Take the
crucible out of the hot zone and rotate it so that the fusion will solidify in a thin layer
by the side of the crucible. Cool the melt. Leach out the fusion with 200 ml. of water
by boiling over a flame.
Filter the solution through Whatman filter paper No.40 and wash the residue
ten times with a hot solution of sodium carbonate till free from sulphate ions (Test the
filtrate with BaCl2 solution). Proceed with the filtrate (a) and residue (b) as follows: -

1. Acidify the filtrate (a) with conc. hydrochloric acid, evaporate, dry and
bake the solid material at 115 120 oC for half an hour. Add 10 ml. of dil.
hydrochloric acid and about 50 ml. of water, boil and filter through No.40
Whatman filter paper. Wash the residue with hot 1% hydrochloric acid
and finally 5 times with hot water. Preserve the residue (A) in filter paper
and the filtrate (A).

31
 2. Dissolve the residue (b) in hot hydrochloric acid, also wash the platinum
crucible in which fusion was carried out with hydrochloric acid to remove
the adhering particles. Evaporate, dry and bake. Add 5 ml. of conc.
hydrochloric acid and about 50 ml. of water boil and filter through No.40
Whatman filter paper. Wash the residue with hot 1% hydrochloric acid
and finally with hot water. Preserve the residue (B) in the filter paper and
the filtrate (B).

Take the residue A and B along with the filter paper in a platinum crucible and
slowly burns off the filter paper and ignite the residue. Cool in a desiccators and
weigh. Add few drops of 1:1 sulphuric acid and about 15 ml. of hydrofluoric acid
evaporate to dryness, ignite and weigh.

Calculation SiO2 % = (A-B) x 100

C
Where - A = weight of the crucible along with
Residue before treatment with hydrofluoric acid,
B = weight of the crucible with material
After treatment with Hydrofluoric acid.
C = weight in gm. of the material taken.

Determination of mixed oxides (Gravimetry)

Principle

From the combined filtrate obtained from the determination of silica, Ba is

removed; iron and aluminium hydroxides are precipitated with ammonium hydroxide.
The precipitate is ignited and weighed as oxides of iron and alumina.

Procedure

Mix the filtrate A and filtrate B of the above operation (i.e. filtrate of SiO2
determination), also fuse the small amount of material adhering to the platinum
crucible after hydrofluorization of silica with small amount of potassium
pyrosulphate, take up the hydrochloric acid and mix with the same solution.
Evaporate to reduce the volume of the solution. Adjust the acidity of the solution s
given earlier for BaSO4 precipitation. Add 2 ml. 10% ammonium sulphate solution
and boil and allow the residue to settle for at least two hours. Ammonium sulphate
solution is added to ensure complete precipitation of barium. Filter through No.42
Whatman filter paper; wash the residue with hot water 5 to 6 times. Discard the
residue (BaSO4).

Take the filtrate, add 2 g. of ammonium chloride and precipitate iron and
aluminium with ammonium hydroxide, boil and filter through No.41 Whatman filter
paper. Wash the residue with hot 1 % ammonium nitrate solution till free from
chloride ions. Preserve the filtrate for the determination of CaO and MgO. Ignite the
precipitate in a weighed platinum crucible at 1000oC, cool in desiccator and weigh.
Compute the percent of combined iron and aluminium oxide as follows:

32
 Iron and aluminium oxides % = A x 100
W
Where - A = weight of the mixed oxide.
W = weight of the material taken.

Note: If the sample contains phosphorus and titanium, the same will also be precipitated along with the
ammonia precipitate.

Determination of CaO and MgO (EDTA Complexometry)

Follow the procedure given in chapter on analysis of major and minor

elements from the stock solution.

Determination of barite in Cu-Pb-Zn ores

Some complex Clu-Pb-Zn ores of India contain barite as their associated

mineral. In such case, follow the following procedure for the determination of
BaSO4.

Procedure

Take 0.5 to 1 g. of the material according to the anticipated amount of the

BaSO4 in a beaker; add 10 ml. of conc. hydrochloric acid and 5 ml. of conc. nitric
acid digest over a hot plate. After sometime, add 5-ml. 1:1 sulphuric acid and fume
up cool and add 10 ml of dilute sulphuric acid and about 150 ml. of water boil and
filter through no.40 Whatman filter paper. Wash the residue with hot water. In this
operation, lead will come as lead sulphate along with the barite as residue in the filter
paper. Take the filter paper along with the residue in a beaker; add 50 ml. of a
mixture of acetic acid and ammonium acetate solution and boil. Filter through No.40
Whatman filter paper; wash the residue 5 to 8 times with hot water.

Take the filter paper along with the residue in a weighed platinum crucible,
burn off the filter paper and ignite the residue, add few drops of the sulphuric acid and
about 15 to 20 ml. of hydrofluoric acid and evaporate slowly till finally dry and ignite
at a low heat.

Fuse the remaining residue in the platinum crucible with about 0.5 gm. of
potassium pyrosulphate. Take up the fused material with sulphuric acid and water.
Adjust the acidity of the solution such that every 100 ml. contain 1 ml. of acid. Make
up the volume to nearly 400-ml. boil and allow to settle for at least four hours
preferably overnight. Filter through No.42 Whatman filter paper. Wash the residue
with water till free from chloride ions. Take the residue along the filter paper in a
weighed platinum crucible, burn off the filter paper and finally ignite the residue.
Cool in a desiccators and weigh. Difference in weight will give BaSO4. Compute %
of BaSO4 as follows:

BaSO4 % = (A-B) x 100

C

33
Where - A= weight of the platinum crucible and the Barium sulphate.
B = weight of the empty platinum crucible.
C = weight of the sample taken.
Note:
1. Potassium pyrosulphate fusion will help in decomposing any unattached material and also will supply
sulphate ions for BaSO4 precipitation.
2. It is observed that after hydrofluorization some iron remains in the residue. Fusion and precipitation of
BaSO4 in a large volume will eliminate contamination of iron with BaSO4.

Determination of matter volatile at 98oC

Procedure

Heat a clean empty vitrosil or platinum crucible and lid in the oven at 98oC to
o
102 C for half an hour. Remove the crucible and the lid from the oven and cool in a
desiccator for 10 minutes. Weigh the empty crucible and lid and introduce about 1 g
of the sample. Weigh the crucible and its contents to determine the weight of the
sample. Tap the crucible on a clean hard surface until the content forms an even layer
at the bottom of the crucible. Maintain the oven at a steady temperature of 102 oC.
Place the covered crucible containing the barite in the oven and heat for a period of 15
minutes. Remove, cool in a desiccators and weigh the crucible. Calculate the loss in
weight. Compute as follows:

VM % = W1 x 100
W2

Where - W1 = is the loss in weight of the material

W2 = is the weight of the material taken

BISMUTH ORES

Bismuth is generally found as an associated element in polymetallic ores. It is

specially determined in lead concentrates.

Determination of bismuth (Spectrophotometry)

Principle

Bismuth is determined by spectrophotometric measurement at 460 nm of the

absorbance of the yellow iodobismuthite complex BiI4 formed in a 0.5 M sulphuric
acid 0.12 M potassium iodide in a reducing medium of hypophosphorus acid.

Reagents

1. Standard bismuth solution Dissolve 0.25 g. of pure bismuth metal by

heating with 30 ml. 30% nitric acid. Boil the solution gently for 10 minutes,
then cool, and dilute to 250 ml. with water.
1 ml. = 1 mg. Bi

34
 Dilute this solution to prepare -
1 ml.= 0.1 mg. of Bi
2. Potassium iodide solution 10% /W/V
3. Sodium hypophosphite solution 30% W/V.
4. Sulphuric acid 50% W/V.

Preparation of solution

Take 1 g. to 2 g. of finely pulverized ores according to the anticipated amount

of bismuth in a 500 ml. beaker, add 15 ml of conc. hydrochloric acid and 10 ml. of
fuming nitric acid and keep over a hot plate, when the brisk reaction subsides add 10
ml. of 1:1 sulphuric acid and fume off. Add 5-ml. 1:1 sulphuric acid and 100-ml.
water, boil and filter through No.40 Whatman filter paper. Wash the residue with
water 5 to 10 times. Discard the residue and proceed with the filtrate. Add 1 g. of
ammonium carbonate to the filtrate, make it ammonical, boil and filter through No. 41
Whatman filter paper (this operation will remove copper). Wash the residue with
ammonical hot water till the filtrate is free from the blue colour of ammonia-copper
complex. Reject the filtrate. Dissolve the residue in hydrochloric acid. Warm the
solution to 80oC and pass H2S gas for 30 minutes. Filter through No.40 Whatman
filter paper. Wash the residue with 1% hydrochloric acid saturated with H2S.
Dissolve the residue in the filter paper in a minimum amount of nitric acid. If the
amount of bismuth present is small, use the entire amount of the solution, otherwise
make up the solution and proceed by taking an aliquot for the determination of
bismuth.

Procedure

Take an aliquot or the entire solution if Bismuth presence is less in a 100 ml.
volumetric flask. Add 3 ml. 50% sulphuric acid, 1 ml. 30% sodium hypophosphite
solution and 10 ml. 10% potassium iodide solution, mix thoroughly, and allow the
solution to stand for 10 minutes. Dilute to the required volume with water and mix.
Take reagent blank along with the sample. Determine the absorbance of the solution
at 460 nm against water as Reference solution. Correct the absorbance values
obtained for the blank solution. Compute the percentage of bismuth from the
standard calibration curve prepared from the standard solution.

Notes:

1. Hypophosphorus acid, which is produced by the reaction of the mineral acid

with sodium hypophosphite, eliminates interference from free iodine during
complex formation. This reduction prevents the air oxidation of iodide ion to
iodine.
2. Lead is precipitated as sulphate and copper, iron etc. are removed.
3. As reduction with hypophosphorus acid is slow, a standing period of 15
minutes is recommended to ensure complete destruction of any free iodine
that is formed by the reaction of iodide ions with the oxidizing sample
constituent. Suspended matter, causing turbidity in the final solution, may be
removed by centrifuging or filtering the solution before measuring the
absorbance of the bismuth iodide complex.

35
 4. The coloured product can be extracted with higher alcohols and esters. A
mixture of amyl alcohol and ethyl acetate has been recommended for the
purpose. Extraction enables bismuth to be determined in the presence of
coloured ions such as nickel, cobalt and chromium.

References

1. E.B. Sandell Colorimetric Determination of Traces of Metals, 3rd Edition, Interscience, New York, pp
33 336 (1959).
2. W.F. Hillebrand, G.E.F. Laundell, H.A. Bright and J.I. Hoffman Applied Inorganic Analysis, 2 nd
Edition, John Wiley and Sons, Inc., New York, p 232 (1953).

CHROME ORES

Chromite is the most important ore of chromium. It is a mineral of variable

composition. Theoretically, its composition is FeO, Cr2O3, but in nature, there is
considerable replacement of both Fe and Cr by other elements. Its formation may be
represented as (Fe, Mg) O. (Cr, Al Fe)2O3.

The radicals normally determined are Cr2O3 (total), SiO2, Al2O3, FeO, MgO,
CaO, P and S.

Determination of Cr2O3 (Volumetry)

Principle

The sample is fused with sodium peroxide in a nickel crucible. The sodium
chromate formed is leached out with water and the acidified solution is treated with
known excess volume of ferrous ammonium sulphate. The excess of ferro-
ammonium sulphate is estimated with standard potassium dichromate using barium
diphyenylamine sulphonate as indicator. A blank is taken and the Cr2O3 is
determined from the amount ferrous ammonium sulphate used up.

Reagent

FeSO4(NH4)2SO4.6H2O (0.1N solution) : Dissolve 39.2 g. of the salt in 250

ml. of water, add few drops of sulphuric acid to clear up the solution. Make the
volume one liter.

Procedure
Grind the ore in an agate mortar to the finest possible powder. Weigh 0.2 g.
into a nickel crucible, add about 1 g. of sodium peroxide, mix thoroughly with a glass
rod. Heat the crucible gently over a low flame until the mass melts. Keep fused for a
further 10 minutes at a cherry red heat. Allow the crucible to cool and place it in a
500 ml. beaker containing little water, cover the beaker. Add nearly 100 ml. of water
and after the violent action has subsided remove the crucible with a glass rod and
wash it thoroughly, collecting the washing in the same beaker, boil and filter through
No.40 Whatman filter paper. Wash the residue with hot water till free from chromate
ions. As there are chances of some chromium being held up by the residue, dissolve

36
the residue in the filter paper in minimum amount of hydrochloric acid, dilute, add
sodium peroxide slowly with constant stirring till a permanent precipitate is obtained,
boil and filter through No.40 Whatman filter paper. Wash the residue five to six
times with hot water. Combine this filtrate with the previous filtrate. Boil for half an
hour to decompose hydrogen peroxide. Cool, acidify with 1:1 H2SO4, add 5 ml.
more, cool it and add a measured amount of ferrous ammonium sulphate solution in
excess. The solution becomes green, add 5 ml. of orthophosphoric acid and titrate the
excess of ferrous ammonium sulphate with 0.1 N potassium dichromate solution
using barium diphenylamine sulphonate as indicator until the colour changes to violet.

. Run a blank for the amount of ferrous ammonium sulphate added and from
this, determine the actual volume of the ferrous ammonium sulphate solution, which
was oxidized by the dichromate originating from the chromite. Compute the percent
of Cr2O3 from the following factor:

1 ml. 1 N K2Cr2O7 = 0.02534 g. of Cr2O3

Note: The chromate solution is to be boiled for half an hour to remove the hydrogen
peroxide before it is acidified. This is necessary because the hydrogen peroxide
reduces chromium (VI) to the trivalent state in acid solution.

Reactions involved are:

1. 2FeCr2O4 + 7Na2O2 --- 2NaFeO2 + 4Na2CrO4 + 2Na2O

2. NaFeO2 + 2H2O --- Na+ + Fe (OH)3 + OH-
3. 2H2CrO4 + 6FeSO4 + 6H2SO4 = Cr2 (SO4)3 + 3Fe2(SO4)3 + 8H2O

Determination of Fe2O3 (total) (Volumetry)

Dissolve the residue from the previous operation in hot HCl and precipitate
iron as iron hydroxide with NH4OH. Filter using No.40 filter paper and wash the
precipitate 4 or 5 times with hot water. Dissolve the precipitate in hydrochloric acid,
boil and reduce it with SnCl2. Cool it immediately. Add 10 ml saturated mercuric
chloride solution and 20-25 ml. acid mix and titrate with standard potassium
dichromate solution using barium diphenylamine sulphonate as an indicator.
Compute the percentage of Fe2O3 from the following factor:

1 ml. 1 NK2Cr2O7 = 0.07985 g. Fe2O3

Note: In Analytical Laboratory, Indian Bureau of Mines, chromite ore was fused with
potassium hydroxide in a nickel crucible initially at low temperature and finally to
bright red colour with constant stirring. The mass was extracted in water. The
soluble was estimated for Cr2O3 and insoluble was estimated for Fe. In chromium
determination the filtrate can be directly acidified, as the step of removal of H2O2 (as
in Na2O2 fusion) is eliminated, secondly the insoluble can directly be analysed for
iron after dissolving in concentrated hydrochloric acid as very negligible amount of
nickel is present in the leach. Insoluble, if any, after dissolution of insoluble in
hydrochloric acid is again fused with KOH and the extracts are added to respective
determinations.

37
Determination of SiO2 (Gravimetry)

Take 0.5 g. of finely pulverized sample (all of it should be finer than 200 mesh
for fusion) in a platinum crucible and fuse it with Na2CO3 at about 1000 oC. Dissolve
the fused mass in hydrochloric acid. If black particles remain, filter and wash the
residue with hot water 5 or 6 times. Again fuse the residue after ignition with sodium
carbonate (2 or 3 fusions are required for complete decomposition of the sample).
Keep the solution on the hot plate, dehydrate and bake it for half an hour at 110 oC.
Dissolve the baked mass in dilute HCl. Add 50-75 ml water, boil and filter through
No.40 Whatman filter paper. Wash the residue with hot water 6 to 7 times. Ignite the
residue in a platinum crucible and weigh (W1) and hydrofluorize the residue by
adding 2 or 3 drops of dil sulphuric acid. And 10 ml hydrofluoric acid, ignite and
weigh (W2).

SiO2 % = (W1 W2) x 100

W3

Where - W1 = weight of the residue and the platinum

crucible
W2 = weight of the crucible after
hydrofluorization
W3 = weight of the sample taken.

Fuse the residue with sodium carbonate and take it in the filtrate and make up
the volume to 250 ml. in a volumetric flask and use it for the determination of CaO &
MgO. Follow the procedure given in chapter on determination of major and minor
elements from stock solution.

Determination of Aluminium (Gravimetry)

Fuse 0.2 g of finely powdered sample with 3-4 gm sodium peroxide in nickel
crucible. Treat the fused mass with approximately 150 ml. of water in 250 ml beaker.
Boil vigorously and extract the complete mass. Filter this through Whatman No.40
filter paper in a 500 ml beaker. Wash the residue 5-6 times with hot water. Add 10-
15 g. of ammonium nitrate gradually with constant stirring. Boil the content on
burner. Filter the aluminium hydroxide thus precipitated through Whatman No.41
filter paper. Wash the precipitate 5-6 times with hot water. Ignite the precipitate at
1000oC in silica or platinum crucible. Report the mass quantity of alumina (Al2O3).

Determination of ferrous iron

Principle

Very finely powdered ore is reacted with a solution of V2O5 in a mixture of

sulphuric acid and phosphoric acid at a temperature of nearly 400oC. The un-reacted
V2O5 titrated with a standard solution of ferrous ammonium sulphate and from the
V2O5 used up, FeO is calculated.

38
Reagents

1. V2O5 solution Dissolve 18 g. in 500 ml. of water, acidify with H2SO4 and
make up to the volume of one liter.
2. FeSO4 (NH4)2 SO46H2O(N/10) Dissolve 39.20 g. in water, add 5 ml. of 1:1
sulphuric acid and make up the volume to a liter. Standardize against standard
N/10 K2Cr2O7 solution.

Procedure

Take 0.1 g. of finest possible powder and add 50 ml. of acid mixture
(phosphoric and sulphuric acid in the proportion of 4:1). Add 20 ml. of V2O5 solution
and heat at 350-400oC till the chromite sample is fully digested (3 to 4 hours). Cool
and cautiously add nearly 50 ml. of water, and titrate with standard ferrous
ammonium sulphate solution using sodium diphenylamine barium sulphonate as
indicator. Take a blank of the V2O5 solution and from the difference determine FeO.

1 ml. 1 N FeSO4(NH4)2SO4 6H2O = 0.07185 g. FeO

Note:

1. The determination is difficult and require practice, the strength of acid and temperature should be
rigorously controlled to obtain concordant results.
2. Instead of V2O5 some workers have used ceric sulphate.

References

1. Shin A.V. Determination of ferrous oxide in chromite, Zavodskaya Lab. 6,

1199 1205 (1937), through Chemical Abstract 32, 1211.
2. Journal of Geochemical Society of India, April, 1967

COBALT ORES

The common minerals are linnaeite Co3S4, Carroltite CuCo2S4 and

Cobaltite CoAsS.

Cobalt is estimated in all nickel ores by the gravimetric method using

nitroso naphthol reagent.

Determination of cobalt (Gravimetry)

Principle of the method

When nitroso napthol is added to a hydrochloric acid solution of cobalt, a

brick red precipitate of cobalt nitroso naphthol, Co(C10H6O(NO)3) is formed.
Copper, silver, bismuth, tin, chromium, iron, zirconium, titanium, vanadium and nitric
acid interfere, but mercury, lead, cadmium, arsenic, antimony, aluminium,
manganese, nickel, calcium, manganese, beryllium, zinc and phosphate do not
interfere.

39
 Copper and other Group II metals are removed with H2S and iron together
with the other remaining interfering elements is separated with zinc oxide (refer to
Volhards method for manganese under chapter on manganese ore). The cobalt
precipitate is ignited and weighed as Co3O4.

Reagent

Freshly prepared solution of nitroso naphthol 5% W/V in 1:1 acetic acid.

Procedure

Weigh 0.5 to 1 g finely powdered sample in a 250 ml. beaker. Add 10-25 ml.
conc. HNO3, 10-15 ml. conc. HCl and 10 ml. 1:1 H2SO4 and a few drops of HF, if
necessary, and boil gently over a hot plate and finely evaporate to strong fumes of
SO3. Cool, dilute with water and boil. Adjust the acidity to 5 to 10% with H2SO4 and
pass a strong stream of H2S. Filter through No.40 Whatman filter paper and wash the
residue thoroughly with acidulated H2S water. Reject the residue.

Boil the filtrate for 15 minutes to remove H2S. Add 20 ml. H2O2 to oxidize
the iron and boil to remove the excess of peroxide. Nearly neutralize with Na2CO3
solution and boil to remove all CO2. Add a suspension of zinc oxide until the
precipitate takes the colour of coffee. Boil and filter through No.40 Whatman filter
paper with some pulp. Wash 5 to 10 times with hot water. The filtrate will contain
only Co, Ni, Mn and a few other elements not affecting the nitroso napththol
precipitation. (A turbidity of zinc oxide will appear in the filtrate but will dissolve in
the subsequent acid treatment).

Add 10 ml. conc. HCl to clear the solution. Dilute the solution to 200 ml. (add
enough hydrochloric acid to make a total of 10 ml. in 200 ml. volume). Heat to about
60oC. Add slowly and with constant stirring 1 times, as much reagent as is
required by the anticipated cobalt content, with a minimum of 10 ml. in any case. Stir
vigorously for one minute. Allow the solution to cool to room temperature for several
hours. Filter through No.42 Whatman filter paper, using pulp, and wash the
precipitate several times with warm dilute hydrochloric acid (1+9) (if the solution
passing through the funnel steam is clear, any precipitate subsequent forming in the
filtrate will be free from cobalt). Finally wash the precipitate with hot water until free
of chloride.

Transfer the paper and precipitate to a weighed 30 ml. porcelain crucible of

deep type. Ignite gently at first and finally to constant weight at 750 to 850oC. Cool
in a desiccators and weigh as Co3O4.

% Co = Weight of Co3O4 x 0.7342 x 100

weight of the sample taken

Note: If the determination is done on a high nickel ore, the precipitate may be
dissolved in HCl cobalt is reprecipitated.

40
Determination of Cobalt present in minute quantities (Spectrophotometry)

Principle

The method is based upon the soluble red complex salt formed when cobalt
ions react with an aqueous solution of Nitroso-R salt. The cobalt complex is usually
formed at pH 5.5 to 6. After the formation of cobalt colour, nitric acid is added and
boiled. It decomposes the complexes of most of other heavy metals.

Reagent

Nitroso-R salt (sodium 1 nitroso 2 hydroxy-naphthalene 3, 6

disulphonate) 0.2% aqueous solution.

Procedure

Prepare the solution as prescribed for the gravimetric method and take an
aliquot or take 0.5 g. of the finely pulverized sample in a vitrosil silica crucible (roast
at low temperature if it is a sulphide ore). Add about 2 g. of potassium pyrosulphate
and fuse the sample over a low flame. Dissolve the material in hydrochloric acid by
boiling. If the sample contains copper, dilute the solution add about 1 g. sodium
thiosulphate, boil and filter. If it does not contain copper avoid this step.

Reduce the acidity with ammonia and add pyridine, boil and filter through
No.40 Whatman filter paper. Check the pH of the solution. It should be close to pH
6. Add 2 ml. of 0.2% nitroso-R salt, boil for one minute. Add about 2 ml. of conc.
nitric acid and boil again for one minute. Cool to room temperature, dilute to 100 ml.
in a volumetric flask and determine the optical density at 425 nm against a reagent
blank. Determine cobalt concentration with Reference to a working graph prepared
by the standard cobalt solution treated in the same manner as the sample solution.

Note :
1. If the sample is siliceous then silica should be removed by dehydration and
hydrofluorization.
2. Iron, copper, chromium (III and VI), nickel interfere when present in
appreciable quantities.
3. The use of pyridine to precipitate R2O3 and control the pH has been developed
in the IBM laboratory.

FLUORSPAR

The important commercial source of fluorine is fluorspar or fluorite (CaF2).

The analysis of fluorspar ores is normally done to determine the following radicals:

CaCO3, SiO2 R2O3 (total oxides), S and P2O5, the most important radical is fluorine as
CaF2

41
Determination of CaCO3 (Gravimetry)

Weigh 1.0 g. of sample and transfer it to a 250 ml beaker. Add 20 ml. 20%
(V/V) acetic acid and 100 ml distill water. Heat on a hot plate till it boils. Filter and
wash the residue with hot distill water until free from acid. Ignite the residue with
filter paper in a platinum crucible at 600 oC. Cool in a desiccators and weigh. Loss in
weight represents the CaCO3 content.

CaCO3 % = Loss in wt. x 100

Wt. of the sample

Determination of SiO2 (Gravimetry)

Add to the residue a 15 ml. of 40% hydrofluoric acid (do not add H2SO4).
Evaporate to dryness. Ignite at 600oC. Cool and weigh. Repeat the acid treatment
till there is no further loss in weight. The loss in weight represents the SiO2 content.

SiO2 % = Loss in wt. x 100

Wt. of the sample

Preparation of stock solution for determination of R2O3, CaF2

Add 1 ml concentrate sulphuric to the mass left after determination of silica in

the platinum crucible itself. Fume of the mass carefully. Transfer the crucible to 250
ml beaker. Add 5 ml concentrated hydrochloric acid and 50 ml. DM water. Boil this
to extract the mass from the crucible. Turbidity, if any, indicates the presence of BaO
(as BaSO4). Filter the solution through Whatman 40 filter paper and make up to 250
ml in volumetric flask.

Ignite the residue and the filter paper in silica or platinum crucible. Weigh the
residue and report this as BaSO4.

Determine the other constituent R2O3, Al2O3, MgO and P2O5 as given under
the chapter on determination of major and minor constituents. Convert the Ca thus
determined to CaF2 and report as CaF2 directly. This method gives appreciably
accurate estimation of fluorine in turn CaF2 in fluorspar sample.

More accurate estimation of fluorine can be made by distillation of fluorine as

hydrofluosilicic acid and titrating it against thorium nitrate. The procedure is as given
below:

Method

When a sample of fluoride is boiled with sulphuric acid + phosphoric acid in

the presence of quartz, glass, etc. volatile silicon tetrafluoride is formed. In steam
distillation when the steam vapour is used as a carrier gas, the silicon tetrafluoride
reacts with water vapour and hexaflurosilicic acid is trapped in a dilute solution of
sodium hydroxide. Fluorine in the solution is determined by titrating against standard
thorium nitrate solution using sodium alizarine sulphonate as an Indicator.

42
Procedure

Take 0.1 g. fluorspar, or 1.0 g. of other samples depending on the percentage

of fluorine present in it, in a platinum crucible, mix it with 1-2 g. of Na2CO3 and fuse
it, first on a very low flame and then on just dull red heat. But in a number of cases,
even without fusion, the results are quite satisfactory. Extract the mass with 50-100
ml. water and filter. Transfer it to a Kjeldahl flask. Add 75 ml acid mixture and add
about 1.0 gm. of sodium silicate or quartzite. Heat the flask on an asbestos sheet
making a small hole to expose the bottom of the flask to the flame. When the
temperature reaches 140 oC, flush the steam and collect the distillate in a NaOH
solution (about 25 ml. of 0.1 N). The distillate should be about 300-350 ml. The rate
of distillation should be about 5 to 6 ml. in a minute.

Immediately after distillation, make up the volume to 500 ml. and store it in a
polythene bottle. Take 20 ml. aliquot for each titration and adjust the strength of
Th(NO3)4 solution, so that the titre value lies in the range 5 to 15 ml. The titration is
carried out at pH 2.9 to 3.1 by using monochloro acetic acid (10 ml.) as a buffer and a
few drops of alizarine sulphonate as an indicator. A particular shade is very
important and has to be decided by the worker himself while doing the
standardization of Th(NO3)4 solution and the sample. Compute the percentage of
fluorine from the volume of thorium nitrate used.

The reaction involved is:

2N2SiF6 + 3Th(NO3) 4 + 7H2O 3ThF4 + 12HNO3 + 2H2SiO3 + H2O

Reagents

1. Acid mixture: conc. H2SO4 (Sp. Gr. 1.84) + conc. H3PO4 (85%) : 3:1 parts,
respectively.
2. Standard thorium nitrate solution (0.025 M). Weigh 13.806 g. of thorium
nitrate Th(NO3)4 4H2O, dissolve in water and make up to one litre. Mix well,
standardize against standard fluoride solution.
3. Standard sodium fluoride solution: (1 ml = 1 mg. of F). Dissolve 2.211 g.
of sodium fluoride (AR) previously dried at 120oC to constant weight in one
litre of water in a volumetric flask.
4. Buffer solution (Monochloroacetic acid pH 2.9 3.1). Dissolve 18.9 g. of
monochloroacetic acid in distillled water and dilute to 200 ml, neutralize 100
ml. to phenolpthelein end point with NaOH and add to remaining 100 ml.
Dilute to 500 ml. with distill water. Check the pH meter.
5. Indicator: Sodium salt of alizarin sulphonate (1:1 aqueous solution).

Notes: All of the solutions used in this experiment should be freshly prepared.
Sulphur and P2O5 are determined in the usual way.

Reference

USBM. RI 0314 fluorine analysis by H.E. Blake. Indian Standard IS.

2411-1963.

43
GYPSUM
Gypsum, CaSO4, 2H2O occurs in nature. The deposits are mainly in less rain
fed areas. CaSO4.2H2O is fairly soluble in water, especially rainwater. Presence of
calcium sulphate imparts permanent hardness to water. Gypsum is analysed for CaO,
SO3, Fe2O3, SiO2, MgO, LOI, Al2O3 & CaSO4.2H2O.

1. Drying of Gypsum: Gypsum, CaSO4.2H2O is very sensitive to heat. Hence,

drying of sample should also be done carefully to avoid loss of water of
crystallization. Finely ground powder is dried 45oC for 2 hours. In no case the

44
temperature should exceed 60 oC as it loses one molecule of water of crystallization
around 70oC.
2. Loss on Ignition: LOI in gypsum is mainly contributed by the water of
crystallization. Moreover this water of crystallization is of greater interest to ascertain
the quality of gypsum. Weight about 1 g. of sample in silica crucible. Heat the sample
to 250 oC in muffle furnace for about 30 minutes. The temperature should preferably
below 300 oC. Cool the crucible in desiccators. Weigh the crucible and report the loss
as loss on ignition.

% LOI = Loss in wt. of the sample x 100

Wt. of the sample

3. Determination of SiO2 and preparation of stock solution: Weight 0.5 g. of

dried sample (at 45oC) in 250ml. beaker. Add 25 ml. of Hydrochloric acid. Digest this
on hot plate. Dehydrate and bake the mass at 115-120oC on hot plate. Cool the beaker
add 5 ml concentrated hydrochloric acid and 50 ml. DM water. Boil this and filter this
through Whatman 40 filter paper. Wash the residue 5-6 times with hot water. Preserve
the filtrate. Ignite the residue at 1000 oC in muffle furnace in platinum crucible. Cool
the crucible in desiccators. Weigh the crucible. Add 2-3 drops of dilute sulphuric acid
and 10 ml of hydrofluoric acid. Fume off all acid on an asbestos sheet or low
temperature hot plate. Initially heat the crucible at low flame and finally to bright red
(1000oC) on a maker burner. Cool the crucible in a desicator and weigh. The loss
will correspond to the quantity of silicon dioxide in the sample.

SiO2% = Loss in wt. x 100

Wt. of the sample

Fuse the residue left after hydrofluorisation with little (K2S2O7) potassium
pyrosulphate. Extract the mass into the preserved filtrate by boiling. Cool the
solutions and make up this to 250 ml. in volumetric flask.

4. Determination of CaO, MgO, Al2O3, Fe2O3:

Follow the procedure given under the chapter on determination of major and
minor constituent from the above stock solution. Estimate CaO preferably by calcium
oxalate method if the sample contains phosphate as in phosphogypsum.

5. Determination of SO3: Weigh 0.2 g of sample in 250 ml. beaker. Add 25 ml.
concentrated hydrochloric acid. Digest this on low temperature hot plate for about 30
minutes (till all particles dissolves). Dilute the content of the beaker with 50 ml. DM
water. Boil this. Filter this through Whatman 40 filter paper. Collect the filtrate in
500-600 ml beaker. Wash the beaker and residue 5-6 times with hot water. Add 2-3
drops of methylred indicator to the filtrate. Neutralize the filtrate with dilute
ammonia. Acidify this with dilute hydrochloric acid. Add 5 ml. in excess. Heat the
beaker on burner to boiling. Add 20 ml. 10% barium chloride solution. Continue
boiling for 30 minutes. Cool this for 2-3 hours. Preferably the precipitate should be
allowed to settle overnight. Filter the precipitate through Whatman 42 filter paper.
(To speed up the filtration decant major portion of the solution without disturbing the
precipitate). Wash the precipitate 5-8 times with small fraction of cold water. (till it is

45
free from Ba++ ions). Transfer the filter paper along with precipitate to a silica or
platinum crucible. Ignite the precipitate at 800 oC. The carbon of filter paper should
preferably be burned below 600oC. Add 2-3 drops of dil. H2SO4 and ignite this finally
at 800oC. Weigh the content. This corresponds to BaSO4.

SO3 % = Wt. of BaSO4 ppt x 100 x 0.3430

Wt. of the sample

6. Determination of CaSO4.2H2O: Weigh 1 g. of sample in 500 ml. beaker.

Add 100 ml (10%) alkaline ammonium acetate solution. Maintain the alkalinity with
phenolphthalein and dil. Ammonia through out the experiment. Digest this on
water/steam bath for about 1 hr. Filter this through sintered glass crucible (porosity
G3) under suction. Transfer the residue completely to the crucible. Wash the crucible
5-6 times with cold water. Heat the crucible to a constant weight at 100 oC. Find the
weight of residue. The loss will correspond to the quantity of CaSO4 2H2O (more
precisely CaSO4 x H2O).

CaSO4.2H2O = Loss in wt. x 100

Wt. of the sample.

IRON ORES

The important minerals that constitute iron ore are hematite (Fe2O3) and
magnetite (FeO, Fe2O3). Other associated minerals are hydrates of iron like goethite,
limonite, etc.

The radicals determined in iron ores are Fe (total) FeO, Fe2O3, Al2O3, CaO,
MgO, SiO2, TiO2, P, S, and LOI.

Determination of SiO2 (Gravimetry)

Take 1 g. of sample in a 250 ml. beaker add 30 to 35 ml. conc. hydrochloric

acid. Digest the mixture on a hot plate. Evaporate to dryness and bake the mass for
one hour at 100 to 115oC. Cool the mass and take up with about 10-ml. conc.
hydrochloric acid in about 100-ml. water, boil the solution and filter hot through
Whatman filter paper No.40. Wash the residue thoroughly with hot water containing
a little hydrochloric acid till no yellow colour remains. Finally wash it with hot water
only.

Ignite the residue in a platinum crucible at 950 oC to a constant weight, cool in

a desiccators and weigh (W1). Add 5-8 drops (1:1) H2SO4 to the residue and then 10-
15 ml. HF. Evaporate slowly over a low heat (at the end copious fumes are seen
leaving a dry mass). Ignite the residue over a flame to a constant weight, cool in a
desiccators and weigh the crucible (W2).

% SiO2 = (W1 W2) x 100

Wt. of the sample taken
Where:

46
 W1 = weight of the platinum crucible with the
material before hydrofluorization
W2 = weight of the platinum crucible after hydrofluorization

Fuse the residue in a platinum crucible with potassium pyrosulphate. Dissolve

the fused mass in water containing HCl by heating and add this solution to the main
filtrate. Take the solution in a 250 ml. volumetric flask and make the volume up to
the mark and take aliquots for the determination of other radicals. Follow the
procedure given in chapter on determination of major and minor constituent from
stock solution.

Determination of ferrous iron (Volumetry)

Principle

Ferrous iron is determined by dissolving powdered ore in hydrochloric acid in

the absence of air and titrating with standard K2Cr2O7 solution.

Procedure

To a 500 ml. conical flask, fit a rubber stopper carrying a long inlet tube and a
short outlet tube. Have a ready source of carbon dioxide from a Kipps apparatus.
Accurately weigh by difference into the conical flask about 0.5 g. of powder ore and
connect the inlet tube for CO2 and displace the air in the flask by a current of carbon
dioxide. Now add to the flask 25-ml. 1:1 hydrochloric acid, quickly replacing the
stopper. Dissolve the sample by heating the flask over a wire gauge, meantime
passing a slow stream of carbon dioxide. Heat till there are not black particles (some
insoluble siliceous matter may be observed). Now cool the flask and the contents in
running water while still passing carbon dioxide. When cool, dilute the solution to
nearly 150 ml. with cooled distilled water containing no dissolved oxygen. Add 50
ml. of a mixture of sulphuric and phosphoric acids. Titrate the ferrous iron by
standard N/10 potassium dichromate solution using few drops of barium
diphenylamine sulphonate as indicator to a violet end point.

Repeat the experiment to obtain concurrent results and calculate the

percentage of ferrous iron from

1 ml. 1 N K2Cr2O7 = 0.07185 g. of FeO.

LIMESTONE, DOLOMITE, MAGNESITE AND ALLIED MATERIALS

Calcium is a widely distributed element occurring in nature in the combined

state. It occurs as carbonate, sulphate, phosphate, fluoride, and silicate and in a larger
number of complex compounds associated with silicon, iron, aluminium, boron,
titanium, sodium and potassium.

The main calcium minerals of commercial importance are calcite (CaCO3),

dolomite (CaCO3>MgCO3), magnesite (MgCO3) and gypsum (CaSO4.2H2O).

47
Determination of silica (Gravimetry)

Weigh accurately 1 g. of dried sample in a 250-ml. beaker and add 10 ml

dilute hydrochloric acid (cover the beaker to prevent loss by effervescence) and 1 ml.
conc. nitric acid. Expell all acid. Bake the mass at 100-115oC for one hour. Dissolve
the mass in 5 ml concentrated HCl and 50 ml water by boiling. Cool and transfer all
the residue in the beaker as well as that adhering to the sides of the beaker to a filter
paper by hot water, finally with a rubber policemen or a piece of moist filter paper.
Wash the residue first with 1% hot hydrochloric acid till all yellow colour disappears
and finally wash with hot water till free from chloride ions. Preserve the filtrate for
further determinations. Transfer the residue into a platinum crucible and burn and
ignite the filter paper at 900 to 950 oC. Cool in a desiccators and weigh. Now moisten
the residue with a few drops of 1:1 sulphuric acid and add to it about 20 ml
hydrofluoric acid. Evaporate to dryness, ignite, cool and weigh again. The difference
will be the SiO2 (lost as SiF4 by volatilization).

Calculation :

Silica % = (W2 W3) x 100

W1
Where
W2 =weight of platinum crucible with residue before hydro-fluorization

W3 =weight of the platinum crucible with residue after hydro-fluorization,

W1 =weight of the sample taken.

Preparation of Main Solution

Fuse the residue left over in the platinum crucible after hydrofluorization of
silica with potassium pyrosulphate and extract it in dilute hydrochloric acid and add
the extract to the filtrate reserved for further processing. Take the solution in a 250
ml. volumetric flask and make up to the volume and mix well (if the filtrate is bulky,
reduce the volume by boiling). Aliquots are taken for other determinations. Follow
procedure given in chapter on determination of major and minor constituent from the
stock solution.

MANGANESE ORE

The common minerals constituting our manganese ores are psilomelane

(Ba3(OH)6 Mn8O16), pyrolusite (MnO2) and braunite (3Mn2O3.MnSiO3).Other
associated manganese minerals are manganite, jacobsite, hausmannite, sitaparite,
manganese bearing garnets like spessartite, etc.
Manganese ores are generally analysed for Mn, MnO2, SiO2, Al2O3, Fe2O3,
FeO, P, BaO, CaO, MgO and LOI.

Determination of silica (Gravimetry)

48
Outline

The sample is decomposed with hydrochloric acid in the presence of an

oxidizing agent like nitric acid. The solution is evaporated to dryness and the residue
baked. SiO2 is determined by hydrofluorisation.

Procedure

Take one g. of the sample in a 250 ml. beaker, add 5 ml conc. nitric acid and
25 ml. conc. hydrochloric acid, evaporate slowly over a hot plate to dryness,
dehydrate and bake for 15 to 20 minutes. Cool the beaker and add 10 ml. conc.
hydrochloric acid and 50 ml. water and boil. Filter through No.40 Whatman filter
paper. Wash the residue first with hot 1% hydrochloric acid till no yellow colour
remains and transfer the residue with the filter paper into a clean platinum crucible,
burn off the filter paper and finally ignite the residue. Cool in a desiccators and
weigh (W1). Add few drops of 1:1 sulphuric acid and about 20 ml hydrofluoric acid
and keep over an asbestos board having a flame underneath and slowly evaporate to
dryness, then ignite over a bare flame. Cool in a desiccators and weigh (W2).

% SiO2 = (W1 W2) x 100

Wt. of the sample taken

Fuse the residue in the platinum crucible with sodium carbonate, dissolve in
dilute hydrochloric acid and mix with the filtrate. Take in a volumetric flask and
make up to the volume with water and take aliquots for subsequent determinations.
Follow the procedure given in chapter on determination of major and minor
constituents from the stock solution.

Determination of CaO and MgO

Take 50 ml aliquot in 250 ml beaker. Add 2-3 g. of ammonium chloride and

ammonia. Add 2-3 ml of bromine water. Boil this solution, cool and filter through
Whatman 41. Wash the residue 5-6 times with hot water. Now again add 2-3 ml of
dilute ammonia and 2-3 ml of bromine water. Precipitate manganese left, if any.
Filter this through Whatman 41. Wash the residue 5-6 times with hot water. Repeat
treatment with bromine water till all manganese is precipitated. Divide this filtrate
into two parts estimate calcium in one part and magnesium in other as explained
under the chapter on determination of major and minor element.

Determination of manganese dioxide (Sodium oxalate method) (Volumetry)

Outline

The sample is treated with a known excess of standard sodium oxalate

solution in the presence of sulphuric acid. The remaining oxalate is titrated with
standard permanganate solution. The equivalent manganese dioxide is calculated
from the quantity of oxalate consumed.

49
Reaction involved

MnO2 + H2C2O4 + 2H+ = Mn++ + 2 CO2 + 2 H2O

Reagents

1. Standard sodium oxalate solution 0.1 N

2. Dilute sulphuric acid 4% (V/V).
3. Standard potassium permanganate solution 0.1 N.

Procedure

Take 0.2 to 0.5 g. of the sample in a conical flask; add 50-ml. standard sodium
oxalate solution to which 20 ml. dilute sulphuric acid has been added. Digest over a
steam bath till it is almost free from black particles make the volume to 100 ml. with
hot water (temperature of the solution 70-80oC), titrate with standard potassium
permanganate solution.

Take a blank of an equivalent amount of the standard sodium oxalate solution

that has been added to the sample and from the difference compute the percentage of
MnO2 present as follows:

1 ml. 1 N KMnO4 = 0.04347 g. MnO

Calculation

MnO2 = (A B) x C x 0.04347 x 100

D
Where

A = volume in ml. of standard permanganate solution required for the blank,

B = volume in ml. of standard permanganate solution required for the excess
of the sodium oxalate,
C = normality of the standard permanganate solution, and
D = weight in gm. of the sample.

Determination of FeO in Mn ore by Iodine Monochloride Method (Volumetry)

Reagent

1. Iodine solution Dissolve 10 gm of KI and 6.44 gm. of KIO3 in 25 ml water and

75 ml of concentrated HCl. Little carbontetra chloride is added to the bottle after
shaking CCl4 should be pale violate. If it is colourless add dil. KI drop by drop till
free I2 is present. While CCl4 is distinctly coloured add dil KIO3 till it is
decolourised after shaking.
2. KIO3 Standard Solution : Dissolve 5.35 gm of dry KIO3 in water and dilute to
volume in 1 litre flask. This is M/40 or 0.1 N solution.
3. Conc.HCl
4. Boric Acid

50
Procedure
1 gm of powdered sample is taken in Pt crucible or dish and excess of ICl solution
(1 ml of ICl solution = 0.4 M = 3% FeO) is added. Concentrated HCl (20 ml) is added
and the mixture is stirred with Pt rod. After some time, add 10 ml of 40% AR HF.
Cover the vessel with suitable lid from the beginning. After 5 minutes, pour the
content in 250 ml conical flask containing 2 gm of Boric Acid 50 ml conc. HCl.
Dilute the solution to about 150 ml. Then add 10 ml of CCl4 stopper the bottle and
shake for about 20 seconds. After this stage CCl4 layer, which is deep purple colour
due to liberated I2, is seen. This is obscured if carbonecious matter is there together
at interface. Titrate the solution by adding KIO3 with intermitant shaking of the bottle
until the purple colour almost disappears from the organic layer. Add further CCl4 in
which the end point can be easily detected by disappearing of purple colour. Towards
the end of titration shake the contents of the bottle, after addition of each drop of
KIO3 solution.

2Fe2+ + I2 2Fe+3 + 2I 2Fe2+ + I2 2Fe+3 + 2I

I2 = 2Fe

It should be noted that the total solution should contain atleast 30% conc. HCl by
volume.

MOLYBDENUM ORES

The principal minerals of molybdenum are molybdenite MoS2, wulfenite

PbMoO4 and powallite CaMoO4.

Determination of molybdenum (Volumetry)

Principle

The procedure depends upon the reduction of hexavalent molybdenum to the

trivalent form by passing an acidified solution of it through a column of amalgamated
zinc. The reduced molybdenum compound is sensitive to atmospheric oxygen hence,
the reduced compound is caught in an excess of ferric solution in an atmosphere of
CO2. An equivalent amount of ferrous ion is formed. Titration of the reduced
solution by means of standard permanganate establishes the amount of molybdenum.

Procedure

Weigh 0.2 to 0.5 g. of finely pulverized (-100 mesh) sample depending on the
grade of ore in a nickel or iron crucible and add approximately 5 times its weight of
sodium peroxide, and mix with a dry glass rod. Heats over a low flame to obtain a
clear melt. Keep the melt over the low flame and swirl the crucible form time to time
till no black particle is left un-attacked this generally takes 5 to 10 minutes. Cool the
crucible and place it in a 500 ml. beaker and pour nearly 200 ml. distill water and
boil, remove the crucible and wash well with water, pouring the washings into the
beaker.

51
 Filter through No.40 Whatman filter paper and wash the residue 5 times with
hot water (excess washing should be avoided). Discard the precipitate. Neutralize
the filtrate with 1:1 H2SO4 and add 20 ml. in excess.

Activate the Jones reductor by passing through it about 400 ml. of 4% H2SO4.
Discard the washings. Place in position a 500 ml conical flask containing 25 ml. of
10% ferric ammonium sulphate solution and 5 ml. orthophosphoric acid. CO2 is
passed through the flask having an inlet and outlet for the CO2 gas. Then pass the
solution through the reactor at a slow rate such that 2 or 3 drops fall per second into
the conical flask. At the end, wash the reductor several times with 4% H2SO4
catching all the washings into the conical flask. Pass a stream of CO2 throughout the
operation.

Remove the conical flask add 2 ml. of phosphoric acid and titrate against
standard KMnO4 solution to a pink and point which should persist for at least 5
seconds.

Calculate MoO3 percentage from the following factor :

1 ml. 1N KMnO4 = 0.0320 g. of Mo

The reactions involved are:-

1. 2MoO4- + 3 Zn + 16H+ = 2Mo +3 + 3Zn++ + 8H2O

2. 3Fe2(SO4)3 + Mo2(SO4)3 + 8H2O = 2H2MoO4 + 6H2SO4 + 6FeSO4
3. MnO4- + 5Fe++ + 8H+ = Mn++ + 5Fe+++ + 4H2O

Reagents

1. Ferric Ammonium Sulphate 200 g. Ferric Ammonium Sulphate

1760 ml distilled water 40 ml H2SO4
2. Potassium permanganate N/10.

Alternate method for decomposition of the ore

The procedure mentioned above is suitable for all types of ores. The
following method is suitable for wulfenite and molybdenite:-

Dissolve 0.5 g. of powdered ore by treatment with 25 ml. of fuming nitric acid and 5
ml of sulfuric acid in a 500 ml covered beaker at a temperature just short of boiling.
Evaporate until fumes of SO3 are expelled freely. Cool, add 50 ml water and boil.
Filter through No.40 Whatman filter paper. The residue consists of lead sulphate,
silica and possibly contains small amount so under-composed ore, tungstic and
molybdic acids. Save both the residue and the filtrate.

Dissolve the lead sulphate from the residue in hot ammonium acetate solution
by washing. Ignite the siliceous residue in a platinum crucible and remove silica by
treating it with sulphuric and hydrofluoric acids. Fuse the residue with potassium

52
pyrosulphate and mix with the filtrate. Precipitate R2O3 with ammonia and filter.
Dissolve the precipitate in sulphuric acid and reprecipitate R2O3 with ammonia and
filter. Collect the two filtrates containing all the molybdenum in a beaker. Then
proceed with the solution as above.

Note on application and limitation of Jones reductor

1. The ferric ammonium sulphate should be tested to ensure that all the iron is
present in the trivalent state. If all the iron is not in the trivalent state, drops of
KMnO4 solution are added till a pink colour is obtained (excess should be
avoided). The solution is boiled and if the pink colour persists, a drop of conc.
HCl is added when the colour will disappear.
2. A blank is determined for the Jones reductor as follows and deducted from
the KMnO4 burette readings: 25 ml ferric ammonium sulphate and 5 ml
phosphoric acid are placed in the conical flask, as stated in the experiment,
which is then attached to the apparatus and about 300 ml water containing 4%
H2SO4 solution is passed and titrated with KMnO4. The blank so determined
should not be more than 0.3 to 0.5 ml.
3. Sulphuric acid is generally used as usage of hydrochloric acid may interfere in
the subsequent titration, e.g. with potassium permanganate.
4. Nitric acid must be absent. If nitric acid is present and 3-4 ml of sulphuric
acid and evaporate until fumes of SO3 are evolved. Repeat the operation to
ensure complete removal of nitric acid.
5. Organic matter must be absent.
6. Solution containing compounds of copper, tin, arsenic, antimony and other
reducible metals must never be present. If present, they must be removed
before the reduction by treatment with hydrogen sulphide..
7. Ions which are reduced in the reductor to a definite valency state are those of
titanium to Ti+++, chromium to Cr++, molybdenum to Mo +++, niobium to Nb+++
and vanadium to V++, uranium is reduced to a mixture of U+++ and U++++.

Preparation of amalgamated zinc for reactor

About 300 gm. of AR Zinc, minus 10 +20 mesh size, is covered with 2 percent
mercuric chloride solution in a beaker. The mixture is stirred for 5-10 minutes and
then the solution is decanted from the zinc and washed three to four times with water
by decantation. The resulting amalgamated zinc should have a bright silvery lustre.

The ideal amalgam should give rapid and complete reduction with minimum
of hydrogen evolution.

The reductor containing amalgam is always kept filled with enough water to
cover the surface, otherwise basic salt will form which will tend to clog the column.

Note

1. The quantity of HgCl2 required will be such as to yield Hg equivalent to 1-5% of the zinc used.
2. Use 10, +20 mesh zinc metal. Finer material will clog the reactor.

53
Determination of minute amounts of Molybdenum (Spectrophotometry)

Principle of the method

Molybdenum (VI) in acid solution when treated with a suitable reducing agent
in the presence of a little ferrous iron is converted largely into molybdenum (V). This
forms a complex with thiocyanate ion probably largely due to formation of Mo
(SCN)5, which is red in colour. The latter may be extracted with oxygenated solvents.
The colour depends upon acid concentration (optimum concentration 1 N) and the
concentration of the thiocyanate ion (2 to 10%). The complex has maximum
absorption at 460 nm.

Reagents

1. Potassium thiocyanate, 10%

2. Stannous chloride 10 g. of dihydrate in 100 ml. of 1 N hydrochloric acid.
3. Ferrous ammonium sulphate 1 gm in 100 ml. of 0.2 N. sulphuric acid.
4. Isoamyl alcohol.

54
 5. Standard solution Dissolve 0.075 g of Ar MoO3 in dilute sodium
hydroxide, dilute with water, make slightly acidic with hydrochloric acid, and
make up to 500 ml wit water.
1 ml = 0.0001 g Mo
= 0.1 mg Mo
Procedure

1. If a solution has already been made, proceed with an aliquot for the
determination of Mo. Otherwise prepare the solution as follows and proceed

2. Fuse 0.1 g of finely ground sample with 0.5 g of sodium carbonate in a

platinum crucible. Digest the cake in water containing a few drops of alcohol
until completely disintegrated. Filter through No.40 Whatman filter paper.
Wash the residue with hot water. Reject the residue, take the filtrate which
contains molybdenum as sodium molybdate and acidify with hydrochloric
acid and proceed as follows

Transfer the solution to a separating funnel and add 1 ml of 1% ferrous

ammonium sulphate solution and 3 ml. of 10% potassium thiocyanate and 2 ml. of
10% stannous chloride solution. After 30 seconds, add exactly 25 ml amyl alcohol,
shake vigorously for 2 minutes and allow the coloured phase to separate. Discard the
aqueous phase and take the clear amyl alcohol phase in the cell of a
spectrophotometer and measure the absorbance at 460 nm and determine the
percentage of Mo from the standard curve prepared from a known solution. Run a
reagent blank throughout.

Reference
1. E.B. Sandell, Colorimetric Determination of Traces of Metals. Interscience
Publishers Inc., New York, 1959 p. 641.

NICKEL ORES

The principal nickel bearing minerals are pentlandite (Ni, Fe)S, garnierite (Ni, Mg)
SiO4 .nH2O, and niccolite (NiAs). Nickel is also found associated with copper ore
deposits. In India, Nickel is found associated with laterites in Sukinda, Orissa.

Determination of nickel

Procedure

A. Sulphide ores

Take 0.5 to 1 g. of the finely pulverized sample in an iron crucible and fuse
with sodium peroxide. Dissolve in hydrochloric acid and pass H2S to precipitate
members of the second group. Filter and wash the residue with water saturated
with H2S. Boil the filtrate vigorously to remove H2S, add bromine water and boil
to oxidize iron to the ferric condition. Nearly neutralize with ammonium
hydroxide and finally with pyridine to precipitate iron and boil to coagulate.
Filter through No.40 Whatman filter paper. Wash the residue with hot ammonical

55
 water five to six times. Acidify the filtrate with hydrochloric acid and add 10 ml
of 10% dimethylglyoxime heat and make it ammonical. Keep over a boiling
water bath for two hours and then keep the precipitate overnight. Filter through a
weighed sintered glass crucible, wash with cold water and then dry the precipitate
at 150 oC. Cool in a desiccators and weigh.

Ni % = Weight of the nickel DMG complex x 0.2031 x 100

Weight of the sample taken

B. Oxidized ores

Take 0.5 to 1 g of sample in a beaker, and add 15 to 20 ml conc. hydrochloric

acid and 5-10 ml nitric acid, dry and dehydrate the sample. Take with
hydrochloric acid boil and filter. Ignite the residue in a platinum crucible and
hydrofluorise the residue. Fuse the residue with potassium pyrosulphate and
dissolve in hydrochloric acid and add to the mother liquor. If copper is present,
remove it with H2S. Add bromine water and boil to oxidize the iron. Add 2 g. of
tartaric acid to prevent the precipitation of the hydroxides of iron, aluminium and
chromium by ammonium hydroxode. Then slowly make it ammoniacal to
ascertain if complexing is complete, i.e. no precipitate should appear in the
ammoniacal medium. If a precipitate appears, acidify the solution, add more
tartaric acid and again add ammonium hydroxide. The solution must remain clear
at this point. Add hydrochloric acid until the solution is very slightly acidic, heat
to 60 to 80oC and then add 10 ml of 10% alcoholic solution of dimethyl glyoxime.
Add ammonia solution till a faint smell is perceptible and then add a slight excess.
Keep over hot water bath for two hours and then keep the precipitate overnight.
Filter through a weighed sinter glass crucible wash the precipitate with cold water.
Dry the precipitate at 150oC and weigh. Compute the Ni % as above.
Reaction involved

Ni++ + 2H2 DMG = Ni* (HDMG)2 + 2H+

Ni(C4 H7N2O2)2
Note:

1. Ensure that iron is in the trivalent condition and that no excess oxidizing
agent is present.
2. If the final precipitate is bulky and blackish in colour, filter and dissolve
the residue in hydrochloric acid and reprecipitate nickel under similar
conditions.
3. If iron and alumina are very high and complexing with tartaric acid is not
very efficient i.e. even after the addition of a large amount of tartaric acid,
the precipitate appears when made ammoniacal, then, R2O3 should be
removed by pyridine, (Reference: No.2).
4. The Sukinda nickel ores contain chromium and as such not fully attacked
by acid. Fuse the finely ground ore with sodium peroxide in an iron
crucible and extract with water and filter. Wash the residue with hot water
five or six times. The filtrate will contain sodium chromate and is
rejected. Dissolve the residue in hydrochloric acid and proceed for the

56
 determination of nickel.

References

1. G.E.F. Lund ell, H.A. Bright and J.I. Hoffman Applied Inorganic
Analysis, John Wiley and Sons, Ney York, 1959 p. 409.
2. A.K. Ray at. Al. Use of Pyridine as A Precipitant in Gravimetric
Estimation of Nickel and Cobalt in Low Grade Ores, Indian Journal of
Technology, 1969, Vol. 7 No.4 pp, 129-130.

Determination of minute amount of nickel (Spectrophotometry)

Principle

The sample is brought into solution by treating with nitric, hydrochloric and
hydrofluoric acid. Iron, aluminium, etc. are complexed with sodium citrate. To the
ammonical solution dimethyl glyoxime is added and the red nickel dimethyl glyoxime
complex is extracted with chloroform. The chloroform is stripped off the nickel
complex in acid medium, treat with bromine water and make to a suitable volume in a
volumetric flask and the absorbance measured at 445 nm.

Reagents

1. Dimethyl glyoxime (sodium salt) 1% in water.

2. Sodium citrate 1-% - Dissolve 100 g. in 100 ml water.
3. Chloroform A.R. grade
4. Bromine water Saturated.
Procedure

(A) Preparation of Solution Weigh 0.5 to 1 g. of the sample in a beaker add 5

ml of conc. or fuming nitric acid and 25 ml of conc. hydrochloric acid. Digest and
dry over a hot plate. Cool the beaker add 10 ml of conc. hydrochloric acid and about
50 ml of water, boil, filter through No.40 Whatman filter paper. Wash the residue
with hot water. Take the filter paper along with the residue in a platinum crucible and
slowly burn off the filter paper. Add few drops of 1:1 sulphuric acid and about 20 ml
hydrofluoric acid, evaporate, dry and finally ignite the residue. Fuse the residue with
potassium pyrosulphate, extract in hydrochloric acid and mix with the filtrate. Add
10 ml of sodium citrate solution, heat for 10 minutes and then allow to cool.
Neutralize the solution with aqueous ammonia (1:1), boil and, if any, precipitate, filter
through No.40 Whatman filter paper. Wash the residue with ammoniacal sodium
citrate solution. Make up the volume 250 ml.

(B) Formation of complex and extraction: Transfer 50 ml of the solution to a

separatory funnel and add 1 ml of conc. ammonium hydroxide, adjust the pH at 7.5.
Add 3 ml of 1% dimethyl glyoxime solution. Extract the red compound with
chlorororm.

Shake the chloroform extract vigorously with 5 ml portion of 1 M HCl.

Transfer the aqueous layer to a 50 ml volumetric flask. Add 1 ml saturated solution

57
of bromine water and 2 ml conc.aqueous ammonia. Add 1 ml of 1% dimethyl
glyoxime solution and dilute to volume, stand for 5 minutes and measure the
absorbance at 445 nm. Obtain the percentage of nickel in the sample by Reference to
a graph prepared from the standard nickel solution.

Note :

1. Copper may accompany the nickel in the extraction. But most of the copper is removed from the
chloroform extract when it is shaken with ammonia solution, whereas the nickel remains in the
organic solvent. The nickel dimethyl glyoxime in the chloroform layers may be decomposed by
shaking with dilute hydrochloric acid. Most of the diemthyl glyoxime remains in the chloroform
layers. The nickel is transferred to the aqueous phase.
2. Much manganese may interfere but this is prevented by adding hydroxyl-ammonium chloride,
which maintain the element in the divalent state.
3. Citrate or tartarate is added to prevent the precipitation of iron, aluminium, etc.

Reference

Arthur I. Vogel A Textbook of Quantitative Inorganic Analysis, 3rd Edition,

1962.
The English Language Book Society, pp. 794.

COPPER-LEAD-ZINC (POLYMETALLIC) ORES

Copper minerals viz. chalcopyrite, cuprite, vallerite, Dioptase, Chrysocolla,

etc.zinc minerals sphalerite, Marmatite, Hemimozphite, willenite, etc. and lead
minerals galena, cerussite, Anglesite, Barysilite, etc. are easily attacked by a mixture
of hydrochloric and nitric acid. This is finally converted to sulphate by addition of
sulphuric acid mainly for two reasons, firstly to destroy all nitrate, which interferes in
copper estimation by iodometry, secondly to convert lead into lead sulphate, which
remains as insoluble residue and it is determined from the residue.

The above procedure for analysis of Cu-Pb-Zn, polymetallic ore is developed

in Indian Bureau of Mines and successfully used for analysis of ore dressing products
of these ores.

A) Determination of Silica & Preparation of Stock Solution

1. Take 1 g of the sample in a beaker, add 20 ml conc. hydrochloric acid,

heat this on hot plate for 30 minutes, add 10 ml conc. nitric acid. Keep
over a hot plate and when the brisk reaction subsides, add 5 ml 1:1
sulphuric acid, evaporate and fume to dryness.
2. Treat the resultant dry mass with 10 ml 1:1 sulphuric acid and make the
volume to nearly 100 ml. with water, boil over a hot plate and filter
thoroughly No.40 Whatman filter paper. Wash the residue with hot water
containing a few drops of sulphuric acid.

Preserve the filtrate for estimation of Cu, Zn, CaO, MgO, Fe, Al2O3, etc.

Transfer the insoluble lead sulphate and other insoluble above the original
beaker. Add 100 ml 5.5 pH mixture of ammonium acetate and acetic acid to this.

58
Boil this for 15 minutes. Filter this through Whatman 40 filter paper wash the residue
with hot ammonium acetate-acetic acid buffer 3-4 times with hot water. Determine
Pb in the filtrate as given in the chapter of on determination of major and minor
constituent from the stock solution.

Ignite the filter paper and residue in platinum crucible at 1000oC. Cool the
crucible in desiccators and weigh. Add 2-3 drops of dilute sulphuric acid and 10-15
ml 48% hydrofluoric acid. Heat this on asbestos sheet to fume off all acid slowly.
Heat the crucible initially on a low flame and finally to a blast flame. Cool this in
desiccator and weigh. Loss will correspond to silica in the sample.

Fuse the residue after hydrofluorisation with potassium pyrosulphate and

extract this in the preserved filtrate. Make up the solution 250 ml in volumetric flask.
Determine the other radicals from this stock solution as per the procedure given in
chapter on determination of major and minor radicals from stock solution.

B) Determination of Graphitic Carbon

Weigh 2 g of sample in 250 ml beaker. Add 25 ml concentrated hydrochloric

acid. Digest for 30 minutes to expel hydrogen sulphide gas. Now add 5 ml
concentrated nitric acid and continue digestion for 30 minutes. The content of the
beaker must not dry add occasionally concentrated hydrochloric acid. Dilute this with
100 ml water. Filter this through sintered glass crucible of porosity G4. Wash this 3-
4 times with hot water. Finally give 2 washings with 10 ml carbon-disulphide to
dissolve precipitated sulphur, if any. Dry the crucible at 105oC for 30 minutes. Cool
the crucible in desiccator. Weigh the crucible. Find the weight of insoluble material.
Remove the material carefully on a glaze paper/plastic sheet. Mix this well. Part this
into two parts. Determine volatile matter and ash as given in chapter on coal.

% Graphitic Carbon =100-(%VM +% Ash). Correct the % of graphitic

carbon by a factor (% of insolubles/100).

PYRITES

Determination of pyrite (FeS2)

Take 1 g. sample in a beaker and add 25 ml conc. HCl and digest for about
fifteen minutes (pyretic sulphur is insoluble in conc. HCl). Filter through No.40
Whatman filter paper and wash the residue with hot water. Ignite the residue in a
silica crucible and dissolve in conc. HCl. Reduce with SnCl2 , when hot, cool it and
add 10 ml mercuric chloride. Make the volume to nearly 200 ml. with water add 25
to 30 ml. of sulphuric phosphoric acid mixture and titrate with N/10 potassium
dichromate solution using few drops of barium diphenylamine sulphonate as an
indicator. Calculate percentage of iron. From iron calculate S and FeS2 as follows:

Fe % x 1.143 = S % Pyrite
Fe % x 2.1483 = FeS2 %

59
NOTE:
The above method is only empirical and arsenopyrite (FeAsS) and
chalcopyrite (CuFeS2), if present, will also be counted as pyrite.

ROCK PHOSPHATE AND APATITE

The primary sources of phosphorus and its compounds are phosphate rock and
apatite. They are usually analysed for moisture, LOI, CO2 SiO2, Al2O3, P2O5, Fe2O3,
CaO (free), CaO (total), MgO and F.

Determination of SiO2 and preparation of stock solution for CaO, Al2O3, Fe2O3

Weigh accurately 1 gm (W) of sample in a beaker. Add 15 to 20 ml. conc.

HCl and 5 ml. conc. HNO3, digest over a hot plate and evaporate to dryness. Add
about 50 ml. of water and boil. Filter through No.40 Whatman filter paper. Wash the
residue five to six times with hot water. Preserve the filtrate. Take the residue along
with the filter paper in a platinum crucible, burn off the filter paper and ignite the
residue.

Moisten the residue with 5 drops of 1:1 H2SO4 and add 10 ml. hydrofluoric
acid, evaporate to dryness and finally ignite at a red hot temperature, cool in a
desiccators and weigh (W2). Fuse the residue with sodium carbonate and mix with
the filtrate. Take the filtrate in a 250 ml. volumetric flask and make up to the volume.
Use this solution for the determinations of Fe2O3, Al2O3, CaO.

% SiO2 = (W1 W2) x 100

W
Where
W = weight of the sample
W1 = weight of the crucible and contents before hydrofluorization,
and
W2 = weight of the crucible and contents after hydrofluorization.

Note:

If the phosphorite contains fluorine, some silica will be lost in the above
process. In such case, proceed for the determination of silica in presence of fluorine as
given in chapter on Alumino Silicates. If the fluorine content is very less, then the
lengthy process may be avoided. Alternatively, take 1 g of sample 250 ml beaker
cover the sample with 1 g boric acid; add 25 ml concentrated hydrochloric acid. Heat
this on hot plate to expel all acid. Dry and dehydrate the mass. Moisten the mass
with 1-2 ml concentrate hydrochloric acid and 50 ml of DM water. Boil the content.
Filter this through Whatman 40. Wash the residue 5-6 times with hot water. Ignite
the residue in platinum crucible at 1000 oC. Estimate silica by hydrofluorisation.

Determination of total CaO

Take an aliquot equivalent to 0.1 g. in a beaker, add 0.05 gm. of citric acid,
boil, and add 25 ml. saturated solution of ammonium oxalate solution and few drops

60
of bromophenol blue indicator. Add ammonia until a dirty blue colour develops (pH
3.5), boil and allow the precipitate to settle for at least two hours.

Filter through No.40 Whatman filter paper; wash the residue with hot water till free
from oxalate ions (test with KmnO4 and a drop of 1:1 H2SO4). Dissolve the residue in
10 ml 1:1 sulphuric acid 50 ml DM water, heat to 70-80 oC and titrate hot with 0.1 N
KMnO4 solution to a permanent pink colour. Compute the percentage of total CaO
from the following factor:-

1 ml. 1 N KMnO4 = 0.028 g of CaO

Determination of Fe2O3 and Al2O3

Follow the procedure given under the chapter on determination of major and
minor elements.

Determination of magnesium (Gravimetry)

Procedure
Weigh 1 g sample in 250 ml beaker add 25 ml conc. HCl and 5 ml conc. nitric
acid. Reduce volume to 10 ml, add 5 ml. H2SO4 (1:1) and evaporate to fumes. Cool,
wash down the walls of the beaker with jets of water and evaporate again until all
fumes are evolved. Cool and add 100 ml. absolute methyl or ethyl alcohol. Stir well
and allow tostand for 2 to 3 hours, preferably overnight filter through No.40
Whatman filter paper under suction and wash residue 5 or 6 times with absolute
alcohol.

Evaporate the filtrate on a steam bath as fast as possible and make up the
volume to 100 ml. Add 2 gm. of citric acid and 15 ml. of 25% solution of
diammonium hydrogen phosphate. Make alkaline to litmus by adding ammonium
hydroxide and add 50 ml. conc. ammonium hydroxide in excess. Shake vigorously,
let settle for 4 hours or overnight in a cool place. Filter using Whatman No.42 and
wash with very dilute ammonium hydroxide (1:10). Dissolve the precipitate in hot
dil-HCl and repeat the process to obtain a pure precipitate. Ignite the precipitate at
1000oC and weigh as Mg2P2O7.

% MgO = Wt. of Mg2P2O7 x 0.3623 x 100

Wt. of the sample

Determination of free CaO (volumetry)

Take 0.5 gm. of sample in a volumetric flask, add 25 to 30 gm. cane sugar and
about 200 ml. water, shake occasionally for 2 hours and make up the volume.

Take an aliquot equivalent to 0.1 gm. of sample and titrate with N/10 oxalic
acid solution using phenolphthalein as indicator. Compute the percentage of CaO
from the following factor:

1 ml. 1 N oxalic acid = 0.025 g. of CaO

61
Determination of P2O5

Weigh 0.05 to 0.1 g. of finely pulverized material in 500 ml. conical flask, add
10 ml concentrated hydrochloric acid and digest over a burner till complete
dissolution takes place, add 2 ml con. HNO3 and again digest for about 10 minutes.

Neutralize with NaOH solution till a faint precipitate appears and add 2 ml. of
conc. hydrochloric acid, make the volume to nearly 120 ml. Add 0.5 g. of citric acid,
heat to boiling, then add 30 ml. citromolybdate solution, again heat it to boiling and
add from a burette in a thin stream 25 ml quinoline hydrochloride solution, and again
boil for 5 to 10 minutes. Allow the precipitate to settle at least three hours. If time
permits, it is better to keep it overnight. Filter through a pad of paper pulp under
suction. Wash the precipitate with 30 ml. portion of cold water letting each washing
run through before applying the next, until the washings are acid free (test for acidity
with litmus paper about six washings are required). Transfer the precipitate to the
original flask; add N/10 NaOH solution in multiples of 25 ml. from a pipette till the
precipitate dissolves completely. Add 5 or 6 drops of thymol blue or phenolphthalein
indicator and titrate the excess of alkali with standard N/10 HCl to the appropriate end
point. Take a blank for 25 ml. of NaOH and comparing with this find out the exact
volume of NaOH used up by the precipitate. Compute P or P2O5 from the following
factors:

1 ml. of 1 N HCl = 0.001193 g. of P

= 0.002733 g. of P2O5
Reaction involved:

(C9H7N)3H3PO4, 12 MoO3 + 26 NaOH

Na2HPO4 + 12 Na2MoO4 + 3C9H7N +14H2O

SELENIUM AND TELLURIUM

Se & Te are separated by hydrazine in 9.5 N HCl solution. The method is

based on the interaction of selenious acid with excess standard solution of
thiosulphate.

4Na2S2O3 + H2SeO3 + 4 HCl = Se + 2Na2S4O6 + 4NaCl + 3H2O

The unreacted thiosulphate is titrated with iodine solution.

Tellurium is determined by the reaction between tellurous acid and excess

potassium iodide.

H2TeO3 +4I-+ 4H+ = Te + 2I2 + 3H2O

Small quantities of Se & Te are reported in the presence of collecting agent

Hg2Cl2

62
Reagents

1. HNO3 density 1.42 g/Cu cm.

2. Mixture of bromine & carbon tetrachloride (2:3)
3. H2SO4 conc.
4 HCl density 1.19 g/cu cm. 5% of solution diluted 2:1000, Hg2Cl2, solution
containing 1 mg Hg in 1 ml.
5. Stannous chloride, crystalline SnCl2.2H2O and 20% in 20% HCl
6. Hydrazine hydrochloride, 10% solution.
7. Sodium Thiosulphate, 0.02 N solution
8. Iodine 0.02 N solution
9. KI 03% solution

Procedure

Take 1 to 5 g of fine sample in 600 ml beaker, add 8-25 ml of a mixture of

bromine & carbon tetrachloride and allow to stand for 10-20 minutes. Add 10-50 ml
of HNO3 by small portion with stirring and allow the solution to stand in the cold.
Then heat carefully and evaporate to a small volume. After the sample has been
decomposed, add 10-40 ml of H2SO4 and evaporate the solution to H2SO4 fumes.
Cool the residue, add a small amount of water and evaporate to H2SO4 fumes. Repeat
this operation until all nitrogen oxides and organic substances are completely
removed.

Dissolve the residue 60-200 ml of water and 10-15 ml HCl with boiling in a
beaker (covered with glass) for 5-10 minutes. Add HCl to adjust its concentration
15% (V/V). Heat the solution to boil. Add 5 ml of mercurous chloride and reduce the
ferric iron by small portion of SnCl2, when the solution becomes colourless, add 3-10
ml of the reductant in excess, a small amount of paper pulp, boil for 5 minutes and
allow to stand for 10 minutes at a temperature about the boiling point. Separate the
selenium and tellurium ppt. On a paper pulp filter and wash 3-4 times with hot HCl
(2:100).

Separation of Selenium and Tellurium

Place the selenium and tellurium ppt back in the precipitation beaker; add 20-
25 ml conc. HCl and 4-5 drops of HNO3. Loosen the filter and heat on water bath to
dissolve the ppt (the filter whitens). Add 40 ml conc. HCl and 50 ml of water, heat
the solution almost to boil and add 15-20 ml hydrazine solution. Stir the mixture and
allow to stand for 4 hours in warm place. Separate the selenium ppt on double filter
and wash 7-8 times 5% HCl.

To isolate tellurium, dilute the filtrate with water to 250 ml, add a small
quantity of filter pulp, heat to the boil, add 0.3 g of SnCl2.2H2O and boil until solution
fully clears. Separate the precipitated tellurium on double filter and wash 7-8 times
5% HCl.

63
Determination of Selenium

Transfer the selenium ppt from filter paper into beaker, add 10 ml conc. HCl,
loosen the filter by glass rod, add 3-4 drops HNO3 and heat the mixture on water bath
to dissolve the ppt completely. Add 150 ml water and 4 g of carbamide and boil for
2-3 minutes. Cool the solution at room temperature and 25 ml 0.02 N solution
thiosulphate and titrate its excess with iodine solution in the presence of starch.

Determination of Tellurium

Transfer the tellurium ppt from the filter paper into a flask, add 10 ml conc.
HCl and 3-4 drops HNO3 and heat on water bath to dissolve the ppt. Completely cool
the solution, add 10 ml Kl solution and titrate excess iodine with sodium thiosulphate
solution in the presence of starch until the blue or dark cherry solution (depending on
the tellurium content) turns pale yellow.

SILICA

Determination of minute amounts of silica (Spectrophotometry)

Principle

Silicic acid reacts with a solution of molybdate in the acidic medium to give
an intense yellow coloration due to formation of complex silicomolybdic acid
H4(SiMo 12O40) which can be measured at 400 nm wavelength. It is better to reduce
the complex acid to molybdenum blue. A solution of hydroquinone, aqueous sodium
sulphide, ferrous sulphate, etc. is generally used. But in the I.B.M. Laboratory, the
reduction is done by ascorbic acid. After reduction, the absorbance can be measured
at various wavelengths. For optical density, 600 nm is preferred in our work.

Reagents

1. Ammonium molybdate solution 12% W/V Dissolve 120 g of AR

ammonium molybdate tetrahydrate ((NH4)6Mo7O24) in water and dilute to one
liter. Allow the solution to stand for one day and filter.
2. Oxalic acid solution 5% W/V Dissolve oxalic acid 50 g in 500 ml. water
and dilute to one liter. Filter the solution, if necessary.
3. Ascorbic acid 2% W/V Prepare fresh solution as required.
4. Standard solution of silica Fuse 0.1 gm. of pure silica with 0.5 g. of
anhydrous sodium carbonate in a platinum crucible, cool the melt. Dissolve it
in water and dilute to 1000 ml and store in a polythene bottle.
1 ml. = 0.1 mg of SiO2

Procedure

Preparation of solution

A. If the sample is in solution, dilute the solution.

64
 B. If silica is present in a solid sample, weigh 0.1 gm of the sample in a platinum
dish and add about 10 ml. of conc.hydrochloric acid and keep over a hot plate and
evaporate (do not dry). Dilute to 50 ml. with water, add 1 ml. hydrochloric acid, boil
and filter through No.40 Whatman filter paper. Wash the residue with hot water.
Take the filter paper in a platinum crucible, char the paper and ignite the residue.
Fuse the residue with sodium carbonate, dissolve in conc.hydrochloric acid and mix
with the filtrate. Take the solution in a volumetric flask, make up the volume and
draw an aliquot for the determination of SiO2. Proceed as below :
C. Alternatively, take 0.1 gm. of the sample in a nickel crucible, add a few pellets
of sodium hydroxide and a pinch of sodium carbonate. Heat the crucible over a hot
plate for about 15 minutes followed by fusing over a flame at dull red heat. Cool the
crucible and extract the sodium silicate formed with boiling water. Filter through
No.40 Whatman filter paper and wash the residue with hot water. Take the filtrate
into a volumetric flask and take an aliquot for the determination of SiO2.

Complex formation and measurement

Transfer 25 ml. of an aliquot to a 100 ml volumetric flask and add 2 ml 10%

nitric acid. Then add 5 ml. of 12% ammonium molybdate solution and allow it to
stand for 5 minutes to complete the complex formation. Now add 10 ml. of 5% oxalic
acid solution, 5 ml. of 25% sulphuric acid and 5 ml of 2% ascorbic acid solution in
rapid succession, and mix thoroughly after each addition. Allow the solution to stand
for about minute and dilute with water. Run a blank simultaneously and measure the
absorbance of the sample against the reagent blank solution at 600 nm. Determine the
silica from the standard calibration curve.

Note:

1. This method in various modifications has been used for the determination
of silica in fresh water, sea water in boiler fed water, iron ores, ferrous
alloys and steel.
2. Phosphorus (V) and arsenic (V) form similar yellow heteropolymolybdate
complex under the conditions employed for the formation of yellow
silico-molybdic acid complex. Interference from phosphorus and arsenic
is eliminated by the destruction of this complex with oxalic acid prior to
the reduction of silicon complex.

Reference

A.K. Baleko and A.T. Pilipenko. Photometric Analysis, methods of determining non-metals, 1976, Mir
Publishers, Moscow, pp-83.

TIN ORE

Cassiterite (SnO2) is the chief ore of tin.

Determination of tin (Volumetry)

65
Principle

Finely ground ore is fused with sodium peroxide in a zirconium or iron

crucible and the sodium stannate thus formed is dissolved in hydrochloric acid. Tin is
reduced to the stannous form by lead foil by boiling in an atmosphere of carbon
dioxide and the reduced tin is titrated with standard iodine solution using starch as
indicator.

Reagents

1. Standard N/10 iodine solution Weigh about 12.692 g of iodine

and 26 g of potassium iodide in a 500 m. beaker and agitate with about
400 ml water until they dissolve. Wash the contents into a one liter
graduated flask and make up to the correct volume. Standardize this
solution against a standard Na2S2O3 solution to find out the exact
normality.
2. Starch solution Mix about 1 g of soluble starch with about 20 ml
cold water and add the mixture slowly to 80 ml boiling water. Boil for
a few seconds. Prepare fresh solution when required.

Procedure

A Take 0.1 to 0.5 g of the finely ground (-200 mesh) sample in an iron or
zirconium crucible (see note 1) according to the anticipated amount of tin in the
sample and add about 8 times its weight of sodium peroxide.

Mix the constituents either with a dry glass or platinum rod. Sprinkle a thin
layer of peroxide over the top of the mixture and heat gently over a low flame at a
temperature just sufficient to produce complete fusion. A slow gradual fusion is more
successful and avoids loss due to spattering. Keep the melted mass at a dull redness
for about 5 minutes and with the aid of tongs give the crucible a swirling motion
several times during that period.

Remove from the heat and allow it to cool. Then, with the aid of a glass rod,
upset the crucible in about 100 ml water in a 500 ml beaker and cover with a watch
glass to prevent loss due to spattering. When the disintegration and solution of the
fused mass is complete, remove and wash off the crucible with water. Add
concentrated hydrochloric acid until the precipitate has dissolved. The solution of the
sample should be complete. If any un-decomposed material is present, the
determination should be started again. There may be some iron scales from the
crucible but this can be ignored. Filter the solution through no.40 Whatman filter
paper and wash the filter paper with hot water.

B. Alternatively, the fused mass is boiled with water and filtered (see
Note 2) through No.40 Whatman filter paper. The residue is washed with hot water
and the filtrate containing tin as sodium stannate is taken for reduction and
determination after acidifying with hydrochloric acid.

66
 Transfer the acid solution (either of A or B) in a 500 ml conical flask, add 50
ml conc. hydrochloric acid, about 10 ml of 1:1 sulphuric acid and 15 gm granulated
lead or lead foil. Boil the solution for about an hour in an atmosphere of carbon
dioxide to reduce the Sn4+ to Sn++ state (see Note 3). Remove the flask from the heat
and put it in a cool water bath and cool rapidly while maintaining the carbon dioxide
atmosphere. When the flask and its contents are cooled, remove the stopper and rinse
it off into the flask (see Note 4), add a few ml. of starch solution and titrate
immediately with N/10 iodine solution. The end point is a faint permanent blue tinge.
Compute the percentage of tin from the following factor:

1 ml of 1N iodine = 0.05935 g of Sn.

Take a blank in each batch of operation starting from the fusion stage and
determine the iodine consumed and deduct this blank from each titration (see Note 4).

Reaction involved

SnCl2 + I2 + 2 HCl SnCl4 + 2HI

NOTES :

1. The sample should be finely ground to 200 mesh, the accuracy of the analysis depends largely upon it.
2. The sample may be fused with sodium peroxide and the aqueous extract containing tin as sodium
stannate taken but there are chances of the bulky precipitate holding up tin ions or entrapment of tin due
to hydrolysis, this may give a low result.
3. After reduction with lead, the colour of the solution will be white. It may reasonably be assumed that all
the Sn has been reduced if the solution is boiled for 40 to 50 minutes.
4. A blank should be taken from the very start of the operation of each batch and the consumption of iodine
determined and deducted from each titre value.
5. Water contains dissolved oxygen and hence it should be removed by boiling when used for washing the
conical flask during titration.
6. It is not necessary to remove excess lead prior to titration with iodine since lead has no effect on the cold
solution.
7. If the solution turns blue, brown or purple during reduction, the presence of tungsten, molybdenum or
vanadium is indicated. In such a case, tin is to be precipitated by passing H 2S gas in an acidic solution,
filtered and ignited and fusion with sodium peroxide proceeded with.

TITANIUM BEARING ORES

The principal minerals of titanium are Ilmenite (FeO.TiO2) and Rutile (TiO2).

Determination of TiO2 (Volumetry)

Reagents

1. Standard ferric ammonium sulphate Fe2(NH4)2(SO4)4.3(H2O) Solution

Dissolve 60 g of the salt in 600 ml distilled water acidified with 20 ml of 1 : 1
H2SO4. Add KmnO4 solution until a pink colour begins to appear. Dilute the
solution to 2 litres. Standardize against a 0.1 N K2Cr2O7 solution to find out
the exact strength.
2. Indicator Dissolve 24 g of NH4CNS in 100 ml water.
3. Aluminium foil Commercial grade is satisfactory.

67
Preparation of solution of the sample

Treat 0.2 gm of finely powdered (-200 mesh) ore with 10 to 25 ml of a

mixture of sulphuric and hydrofluoric acids (1:5), add a few drops of HNO3 and
evaporate the solution to fumes to expel HF. If a residue remains upon dissolving
with water containing a little sulphuric acid, filter and fuse it with K2S2O7, dissolve in
H2SO4 and mix with the filtrate.

Alternatively, take 0.2 gm of sample in a silica crucible add approximately 1

gm of potassium pyrosulphate and fuse over a low flame till no black particle
remains. When cool, dissolve in 1:1 sulphuric acid and water and make up in a 250
ml volumetric flask and proceed with an aliquot for the determination of TiO2 .It
hydrolyses easily and as such the acid strength in the volumetric flask should be
approx. 5%).

Procedure

Take the solution in a wide-mounted 500 ml conical flask with a 2-hole rubber
stopper. Add 25 ml conc. HCl. Add a strip of aluminium foil to the flask (nearly 2
gm), close with the rubber stopper and through one hole pass a slow stream of CO2
from a Kipps apparatus, using the other hole as an outlet. The solution in the flask
should be boiled to clarify it and expel the excess H2 (boil for at least half an hour).
All the while, a slow stream of CO2 is to be maintained. When cool, remove the
stopper and the delivery tube. Add 5 ml ammonium thiocyanate solution as an
indicator and titrate quickly with FeNH4(SO4)2.12H2O solution to a faint red colour.
Run a blank and deduct this reading from the main reading. Calculate TiO2 from the
following factor :

1 ml 1 N FeNH4(SO4)2.12H2O = 0.08 g TiO2

Note :

Reduction Procedure

1. The titanium solution should not contain more than 0.15 gm of TiO 2 with 10-15%H2SO4 and it should
have a volume of 125 ml.
2. Reduction with aluminium will not take place unless HCl is present.

Reactions involved

a. 6 Ti(SO4)2 + 2Al = 3Ti2(SO4)3 + Al2(SO4)3

b. Ti2(SO4)3 + Fe2(SO4)3 = 2 Ti(SO4)2 + 2 Fe2SO4

The ionic reactions are:

6 Ti++++ + 2 Al 6Ti+++ + 2 Al+++

Ti+++ + Fe+++ Ti++++ + Fe++

68
Determination of silica (Gravimetry)

Principle

The sample is fused with potassium pyrosulphate. The melt is dissolved and
evaporated with sulphuric acid to fumes, diluted and filtered. Residue is fused with
sodium carbonate and the melt dissolved, evaporated to dryness and baked. The
residue is ignited and the silica is determined by the loss in the weight after
volatilization with hydrofluoric acid.

Procedure

(a) Transfer 0.5 g of the finely pulverized ore in a platinum crucible containing
about 3 g of potassium pyrosulphate, heat it at a low temperature to get a clear melt.
Remove the crucible from the heat, and allow it to cool to the room temperature.

Transfer the crucible with its content to a beaker and extract it with 100 ml 1:1
sulphuric acid. When the fused mass is completely dissolved, remove the crucible
washing down with 1:1 sulphuric acid and evaporate the solution to copious fumes,
cool, add nearly 150 ml of dilute sulphuric acid, boil and filter through No.40
Whatman filter paper. Wash the precipitate in the filter paper with hot dilute
sulphuric acid and finally with hot water. Preserve the filtrate and washing in a
beaker. Transfer the filter paper along with the residue to a platinum crucible and
ignite.

(b) Fuse the residue in the platinum crucible with about 1 gm of sodium
carbonate, dissolve the cake in hydrochloric acid, evaporate to dryness and dehydrate.
Take up in 1:1 hydrochloric acid, boil and filter. Wash the residue with hot dilute
hydrochloric acid and finally with hot water.

Take the filter paper along with the residue in a platinum crucible, burn off the
filter paper and ignite the residue. Cool in a desiccators and take the weight W1. Add
few drops of 1:1 sulphuric acid and about 20 ml of hydrofluoric acid. Evaporate to
dryness, ignite, cool and weigh W2. From the difference of weight, compute the
percent of silica. Fuse the small amount of residue left in the platinum crucible with
potassium pyrosulphate, take up with 1:1 sulphuric acid and mix with the solution
reserved in operation (a). Make up the volume in a 250 ml volumetric flask and take
aliquots for the determination of Fe2O3, Al2O3, Mn, Cr2O3, etc. Follow the procedure
given in chapter on determination of major and minor constituent from the stock
solution.

Determination of FeO (Volumetry)

Principle

The very finely pulverized ore is decomposed with sulphuric acid and
hydrofluoric acid in CO2 atmosphere. Boric acid is added to fix the excess
hydrofluoric acid as fluoboric acid. The solution is titrated with standard KMnO4
solution.

69
Procedure

Pulverize the sample in an agate mortar to the finest possible size, irrespective
of the grain size of the sample supplied. Weigh 0.2 g of the sample for concentrates
and middling and 0.5 g for tailings in a corning or pyrex brand 500 ml conical flask.
There should be an arrangement for the inlet and outlet of CO2 through a rubber bung
fitted with the conical flask. Put the flask over a very low flame and put the CO2
delivery tube on and add the following solutions in sequences and swirl from time to
time.

1. Add 30 ml 1:3 H2SO4 and simmer over the flame for 15 minutes.
2. Add 10 ml HF, simmer over the flame for 10 minutes and swirl the flask
from time to time.
3. Add 10 ml 1:3 H2SO4 and simmer for 15 minutes.
4. Add 3 ml HF, simmer for 5 minutes and swirl from time to time.
5. Add 5 ml 1:3 H2SO4 and maintain a mild heat do not heat to SO3 fumes.

Allow the solution to cool in an atmosphere of CO2. Dilute to nearly 200 ml

with oxygen free water add about 4-5 g. of boric acid and remove the CO2 delivery
tube add 2 ml of phosphoric acid and titrate with N/10 KMnO4 solution to a faint pink
end point. Calculate the percentage of FeO from the following factor:

1 ml 1 N KMnO4 = 0.07185 g FeO

TUNGSTEN ORES

The important tungsten-bearing minerals are Wolframite (FeMn)WO4 and

Scheelite (CaWO4). In the IBM Laboratory, the gravimetric method is used for ores
and ore dressing products containing high tungsten values up to 5% WO3 .
Spectrophotometric method is employed for low tungsten values below 5% WO3.

Determination of WO3 (Gravimetry)

Pulverise the sample in an agate mortar until it is minus 200 mesh.Weigh 0.1
to 0.5 gm of the sample, according to the anticipated amount of WO3 content and add
70 ml. conc. hydrochloric acid and digest over a hot plate at a low temperature till all
black particles dissolve (about 3 hours). Add 20 ml conc. nitric acid to the very hot
boiling solution, digest and evaporate to about 50 ml. Make the volume to nearly
100 ml. with hot water. Stir thoroughly and gently simmer the solution. Add 10 ml
cinchonine hydrochloride solution (10 gm. of cinchonine dissolved in 100 cc of 6 N
HCl) and boil over the hot plate. Allow it to settle and filter through no.40 Whatman
filter paper adding a little pulp. Wash the precipitate 3 times with 0.1% cinchonine
hydrochloride solution. Dissolve the precipitate in the same beaker in hot conc.
ammonia to convert all the tungsten acid to ammonium tungstate. Filter through
No.41 Whatman filter paper and wash the residue with hot water. Take the filtrate
and boil until all free ammonia is expelled and dilute the solution to 100 ml with hot
water. Add to the boiling solution 50 ml conc. HCl and 25 ml conc. HNO3 and boil.
Add 10 ml cinchonine hydrochloride solution and 50 ml hot water and again boil.

70
Allow it to cool at room temperature. Filter through No.40 Whatman filter paper and
wash the residue as before.

Ignite the precipitate in a weighed platinum crucible. The temperature should

not exceed 750 oC (WO3 is volatile above this temperature). Cool the ignited oxide
and moisten with a few drops of water. Pour a few drops of HF and keep over a low
heat to remove silica. When dry, heat to a dull red temperature (not exceeding
750oC). Weigh as WO3. The residue should have a lemon yellow colour.

WO3 % = Weight of the ignited residue x 100

Weight of the material taken
Sources of error

In the gravimetric determination of tungsten, the following points should be

remembered.

1. Good results can be obtained only by careful work and strict adherence to all
details from the preparation of the sample to the final weighing as WO3.
2. The representative sample of ore should be thoroughly dried and ground to
minus 200 mesh.Complete decomposition of the ore might not be obtained if a
coarse sample is used.
3. Volatilization of the silicon with HF before the final weighing is a must,
failure to remove the silica invariably gives high results.
4. A reaction of about 3 hours is required for Scheelite ores.

Determination of small amount of Tungsten (Spectrophotometry)

This method is based on the formation of a yellow tungsten thiocyanate

complex after reduction of tungsten with stannous chloride in an approx. 1.8 M
sulphuric acid and 2.3 M hydrochloric acid medium. Tungsten is determined by
direct spectrophotometric measurement at 400 nm of absorbance of the complex in an
aqueous medium.

Reagents

1. SnCl2 2 M Dissolve 113 gm of SnCl2 (AR), dihydrate in conc. HCl and

make up to 250 ml with conc. HCl.
2. Tartaric acid in one liter of water.
3. Potassium thiocyanate (20%) Dissolve 20 g of potassium thiocyanate in
100 ml water. This reagent should be prepared fresh daily.

Procedure

Weigh 0.1 to 0.2 gm of finely pulverized sample in a silica crucible or hard

test tube. Add 0.5 to 1 gm of potassium pyrosulphate, mix well and fuse to a clear red
hot melt and keep in this condition for at least 10 minutes, remove from the flame and
allow it to cool. Dissolve the cake by boiling with 40-50 ml of 0.5 M tartaric acid.
filter the resultant solution through No.40 Whatman filter paper. Wash the residue
with hot water containing a pinch of tartaric acid. To the filtrate, add 10 ml conc.

71
H2SO4, 20 ml. of 12 N HCl and 5 ml of 2 M stannous chloride solution. Place the
beaker in a boiling water bath for half an hour. Add 10 ml water, mix and finally cool
the beaker to 10-15oC (ice-cold water bath).

Add 10 ml of 20% potassium thiocyanate solution and take the solution in a

100 ml volumetric flask and make up the volume with distilled water. Allow it to
stand at room temperature for 10 minutes. Determine the optical density of the
solution immediately at a wavelength of 400 nm or using a blue filter, if colorimeter
is used, against a reagent blank. Calculate the percentage of WO3 from the calibration
curve prepared by using standard tungsten solutions.

References

1. H.G.. Faye, R.J. Guest and R.C. mc Adam The determination of tungsten in
ores, concentrates and Steels, Deptt. Of Energy, Mines and Resources, Mines
Branch Mineral Sciences Division, Ottawa Technical Bulletin, TB 37, May
1962.
2. E.B. Sandell Colorimetric determination of traces of metals Inter Science
Publishers Inc. New York, 1961, p. 887.
3. A.K. Ray, etc. al. rapid gravimetric method for the estimation of tungsten in
ores and minerals free from tin, niobium and tantalum, Indian Journal of
Technology, 1968, Vol. 6, No. 6, pp 185-188.

Determination of Silica & preparation of stock solution for Tungsten,

Molybdenum, Niobium, Tantalum ores

Weigh 0.5 g. of sample in 500ml. beaker. Add 50 ml. concentrated

hydrochloric acid and 10 ml. concentrated nitric acid. Heat this on high temperature
hot plate; continue addition of small portion of HCl and HNO3 till all black particles
dissolves. If the sample contains black silicate minerals such as horn blend all black
particles will not disappear, 4-5 hours digestion is sufficient. Drive off all nitric acid
by addition of small portions of hydrochloric acid and heating this continuously on
hot plate. Finally dry, dehydrate and bake the mass. Extract the mass in 5ml. conc.
hydrochloric acid and 50ml. water. Filter this carefully through Whatman 40 filter
paper. Wash the beaker and the residue 2-3 times with small volume of hot water.
Preserve the filtrate. Dissolve the residue along with filter paper in dilute ammonia
and water in the same beaker by boiling. Filter through, Whatman 40 filter paper.
Wash the residue 3-4 times with water containing little ammonia. Finally wash the
residue 2-3 times with hot water. Ignite the residue in platinum crucible at 1000 oC.
Cool this in desiccators and weigh. Add 2-3 drops of dilute sulphuric acid and 10-15
ml. hydrofluoric acid.Heat this on asbestos sheet on a low flame or low temperature
hot plate to expel all acid. Heat the crucible initially on a low flame and finally at a
blast flame at 1000oC. Cool the mass in desiccators and weigh. The loss corresponds
to the quantity of silica in the sample.

% Silica = Loss in weight x 100

Weight of the sample

72
 Fuse the residue with potassium pyrosulphate. Extract the mass in the
preserved filtrate by boiling. Follow the procedure given in the chapter on
determination of major and minor constituents from the stock solution for
determination of Ca, Mg, Fe, Mn, TiO2, Al2O2, etc.

Determination of Sulphur in Tungsten, Molybdenum, Niobium and Tantalum

samples:

Weigh 0.2-0.3 g. of sample in 250ml. beaker, add 5ml. bromine water, 25 ml.
concentrated hydrochloric acid and 5 ml. nitric acid. Heat this on hot plate to reduce
the volume to 5 ml. Sample must not dry. Add 50 ml. DM water. Filter this through
Whatman 40. Wash the residue 5-6 times with hot water containing dil.hydrochloric
acid. Collect the filtrate in 250ml. beaker. Add 2-3 g. of finely cut aluminium foil or
granulated zinc to reduce iron. Heat the solution. Filter through Whatman 41 filter
paper. Collect the filtrate in 500ml. beaker. Neutralise the filtrate with dil. Ammonia
and reacidify the solution. Add 5 ml. of dil. Hydrochloric acid in excess. Make
volume to about 250 ml, add 20 ml. 10% barium chloride solution, boil the content
for 5 minute. Cool for 3-4 hours, preferably overnight. Decant the major portion of
liquid without disturbing the precipitate. Finally filter the precipitate through
Whatman 42 filter paper. Wash the precipitate 5-6 times with cold water. Ignite the
precipitate along with the filter paper at 1000oC. Weigh the precipitate of BaSO4.

% Sulphur = Wt. of BaSO4 ppt x 100 x 0.1374

Wt. of the sample.

VANADIUM ORES

Vanadium is widely distributed in nature, being found in ores, hard coal,

limestone, bauxite, phosphorite, etc. Usually, the amount of vanadium present is
extremely small. The following are the more important vanadium minerals,
vanadinite (PbCl) Pb4 (VO4), carnotite K2O.2UO3.V2O5 and titaniferous vanadium
ores.

Determination of chromium and vanadium (Volumetry)

Principle

A solution of vanadium is reduced with ferrous ammonium sulphate and

vanadium is preferentially oxidized with potassium permanganate at room
temperature so as not to oxidize any chromium, which might be present. The excess
permanganate is reduced with sodium nitrite. Urea is added to decompose excess
nitrite and vanadium is titrated with standard ferrous ammonium sulphate using
diphenylamine barium sulphonate as indicator.

Reagents

1. Sodium nitrite 3.5 g/l

2. Ferrous ammonium sulphate 0.1 N 39.216 g/l Standardize
against a 0.1 N K2Cr2O7 solution.

73
Procedure

Fuse 0.2 to 0.5 gm of finely ground ore with 5 times its weight of sodium
peroxide in an iron or nickel crucible. Transfer into a 500 ml beaker, add water and
boil. Filter through No.41 Whatman filter paper, adding some pulp. Wash with hot
water. Reject the residue and proceed with the filtrate. Vanadium in the form of
sodium vanadate will pass into the solution. Boil the solution for 30 minutes to expel
H2O2. Transfer into a 500 ml. beaker, neutralize with (1:1) H2SO4 and then add 4-6
ml. in excess.

Add ferrous ammonium sulphate solution until a drop of the solution shows
blue in a spot test with potassium ferricyanide solution. Add 10-15 ml. H3PO4 (to
prevent Fe interference) and cool to room temperature. Add N/10 KMnO4 until a
slight pink colour is obtained. Let it stand for 2 or more minutes to make sure that all
vanadium is oxidized. Then destroy the excess KMnO4 with 0.05 N NaNO2 solution.
Add 2 gm. of urea and stir. Then, allow it to stand for 5 minutes. Add 15 gm. of
sodium acetate and stir to dissolve. If a precipitate is formed, add a drop of H2SO4 to
clear it. Add 8 drops of diphenylamine barium sulphonate indicator, allow 2 or 3
minutes for the full colour of the indicator to develop. Titrate with 0.10 N ferrous
ammonium sulphate until the disappearance of blue colour. Calculate V or V2O5
from the following factor:

1 ml of 1 N Fe(SO4).(NH4)2SO4 = 0.05094 g. V
= 0.09094 g. V2O5

NOTE: The maintenance of a uniform sulphuric acid concentration of 5 to 7% at the start of the titration and a
uniform speed of titration for all samples are essential.

Determination of small amounts (less than 0.5%) of Vanadium

(Spectrophotometry)

Principle

In approximately 0.5 N sulphuric acid medium, vanadium forms a yellow

phosphotungstovanadic acid complex which can be measured at 400 nm.

Reagents

1. Sodium tungstate 0.5 N Dissolve 16.5 g. of Na2WO4.2H2O in water and

dilute to 100 ml.

2. Standard vanadium solution Dissolve 1.785 g. of pure V2O5 previously

ignited at 500oC in slight excess of sodium hydroxide, add slight excess of
sulphuric acid and dilute to one litre. this solution contains 1 mg. of vanadium
per ml.

74
Procedure

Fuse 0.1 to 0.2 gm of the sample either with sodium carbonate in a platinum
crucible or with sodium peroxide in a nickel crucible and take water extract for the
determination of vanadium.

Neutralize the solution with H2SO4 and make the solution approximately 0.5
N in sulphuric acid. Add 1 ml of 1:2 phosphoric acid and 0.5 ml sodium tungstate
solution for each 10 ml of sample solution and cool. Take in a 100 ml. volumetric
flask, dilute to the volume measure the absorbance of the solution at 400 nm against a
reagent blank and determine the percentage of vanadium from the calibration curve
prepared from the standard solution.

ZIRCONIUM ORES

Determination of Zirconium in Zircon & Eudialite

Zircon ores containing much silicon ore fused with Na2CO3 or a mixture of
Na2CO3 and Na2B407 or KOH fusion in nickel crucible. Zirconium associated with
rare earth element is first treated with concentrated sulphuric acid to dissolve rare
earth element and zirconium remains as insoluble residue and is fused with flux as
described above.

ZrSiO4 + 2Na2CO3 = Na2ZrO3 + Na2SiO3 + 2CO2

ZrSiO4 + 3 Na2CO3 + Na2B407 = Na2ZrO3 + Na2SiO3 + 4NaBO3 + 3CO2

The melt is leached with conc. HCl to preclude hydrolysis of zirconium and
separate silica by dehydrations and extract in concentrated HCl and water. Filter silica
through Whatman 40.

Reagents:

1. HCl Sp.Gr. 1.19, 2N

2. EDTA. 0.01 M & 0.05 M solutions
3. Eriochromeblack T, a mixture with NaCl (1:50)

1 ml of 0.05 M EDTA solution = 4.56 mg. Of Zr.

Fuse a sample of zircon or eudialite containing 5-10 mg. of Zr. With a ten-fold
of the flux in a pt. crucible, heat first on a burner to red heat then in a muffle furnace
at 1000oC for 15-30 mins. Add HCl, density 1.19, cover the crucible with a watch
glass and heat on water bath. When CO2 evolution stops remove the watch glass and
evaporate the solution to dryness. Repeat the process 2 times and finally dissolve the
salt.

Separate the ppt SiO2 x H2O on filter, wash with 2NH4Cl and collect the
filtrate and washings in 50 or 100 ml. volumetric flash. The acidity of the solution
should be 2N. Add a small portion of eriochrome black T to the solution, boil for 7-10

75
minute until a persistent blue violet colour develops and titrate with a 0.01 M EDTA
until the solution turns violet pink. Now heat the solution again and if blue violet
colour is restored, continue the filteration with EDTA until the violet pink colour
persists.

1 ml. of 0.01 M EDTA = 0.9122 mg. Zr.

Determination of Zirconium by Gravimetry

Principle

The mineral is decomposed by two successive fusions (sodium carbonate and

potassium pyrosulphate). The zirconia is precipitated by hydrolysis with thiosulphate.

Reagents

1. Anhydrous Na2CO3
2. K2Cr2O7
3. H2SO4
4. HCl
5. Na 2S2O3
6. Dil .NH3
7. Dil NH4NO2 soln.
Procedure

Fuse 0.5 g of 300# zircon sample with 5 g of anhydrous sodium carbonate in a

platinum crucible, first on a burner to red, heat then in a muffle furnace at 1000oC for
15-20 mins. Cool the crucible and extract the mass in the hot water. Filter this through
What man 40.Wash the residue with hot water. Preserve this filter ate A.

Ignite the residue to burn the paper in a platinum crucible. Fuse this with
potassium pyrosulphate on burner. Cool the mass and extract in 10 ml dilute sulphuric
acid and 50 ml water. Boil this for about 10 mins to dissolve zirconium completely.
Filter this through What man 40 .Wash the residue with hot water. Preserve this filter
ate, B.

Ignite the residue in platinum crucible. Fuse the mass with 3-4 g of anhydrous
sodium carbonate. Cool the crucible and extract the mass in hot water. Filter this
through What man 40 and collect the filterate with preserve filterate A and above C.

Ignite the residue above in platinum crucible to burn off the filter paper. Fuse
this with potassium pyrosulphate. Cool and extract the mass in 10 ml dilute sulphuric
acid and 50 ml water. Filter this through What man 40 and collect the filterate in
filterate B and above D.

Determination of SiO2

Acidify the aqueous extract C above with dilute hydrochloric acid. Evaporate
this on a hot plate to dryness. Continue heating for about one hour to dehydrate the

76
silica. Extract this with 5 ml dil. HCl and water. Filter this through What man 40 .
Wash the residue with hot water. Ignite the residue in platinum crucible. Weigh the
residue. Add 3-4 drops of dilute sulphuric acid and 15 ml 40 % hydrofluoric acid.
Expel all acid on asbestos sheet. Finally, ignite the crucible to red heat. Cool and
weigh the crucible. Calculate percentage loss and report it as SiO2.

Fuse residue after silica with little potassium pyrosulphate and extract this
in preserved filterate D above. Now make up the filterate to 250 ml.

Pipette out 50 ml aliquot from the above solution in a 250 ml beaker.

Neutralize it with NaHCO3. until a slight permanent precipitate is formed. Dissolve
this by adding a few drops of dil.H2SO4..Boil till all CO2 expels.

To this hot solution, add 10 g Na2S2O3.5H2O dissolved in 20 ml of water.

Continue boiling for an hour, replacing water lost by evaporation.

Add filter paper pulp. Filter through What man 41 filter paper. Wash the
precipitate on the paper 15 times with hot water. The precipitate contains ZrO2 (HfO2)
and some Al2O3 and TiO2.Ignite it in a platinum crucible and report this as
ZrO2.Further refining can be done by digesting this crude ZrO2 with HCl. Make this
ammoniacal and again filter through What man 40.Wash the residue this time with
dil.ammonium nitrate solution. Ignite the residue to constant weight and weigh as
ZrO2.

ZrO2% = Weight of the ZrO2 x 100 x dilution

Weight of the sample taken

COAL AND GRAPHITE

Coal, graphite and diamond are the naturally occurring substance, which are
mainly composed of carbon. They are entirely different from each other in physical
look and physical properties. They are the allotropes of carbon. Coke is a by-product
of destructive distillation of coal. Coal, coke and graphite is analysed for the chemical
composition. On the other hand diamond is never subjected to chemical analysis but
its grade is determined from physical properties.

An analytical chemist working in the field of minerals has to analyse coal,

coke and some times graphite for confirming their grade. Therefore, the analysis of
coal, coke and graphite is included here.

Analysis of coal, coke and graphite is divided into three parts namely
proximate analysis, ultimate analysis and analysis of ash. Proximate analysis gives the
rough grade of the coal whereas analysis of ash gives the analysis of combustion
waste. Ultimate analysis and determination of calorific value gives a closer look on
the grade of the coal.
In this Chapter, proximate analysis, analysis of ash and N, S, determinations
are only included as the ultimate analysis and determination of calorific value needs
special apparatus. Hence they are not included in this text.

77
A. Proximate Analysis:

1. Moisture: The common indirect method in which coal is heated for 60

minutes in an air oven at 105 oC and the loss in weight is assumed to be the moisture is
rather inaccurate even with high rank coal and the inaccuracy increase with
decreasing rank. Use of current of nitrogen gives appreciably good determination of
moisture. Hence, the moisture determination should always be carried in current of
nitrogen.

Procedure: Weight 1 g. of coal sample in silica patty dish. Tap the crucible
to spread the sample in uniform thin layer. Place the patty dish in an oven maintained
at 105 oC in current of nitrogen for 60 minutes. Cool the patty dish in desiccators and
weigh. The loss in the weight is the quantity of moisture in the sample.

2. Volatile Matter: Loss in weight of the coal sample at 930 20oC is reported
as volatile matter. Volatile matter is composed of coal gas, gas ammonia, benzene,
toluene, phenol and tar. Though these are combustible their heat energy is rarely
utilized in any furnace and are driven off with waste gases or they burn at the mouth
and the energy released is of little use.

Procedure: Weigh 1 g. of coal sample (preferably dried sample at 105oC) in

volatile matter crucible. Tap the crucible to form a thin layer. Close all air inlet and
outlet of the furnace. Add 2-3 drops of benzene in the crucible and place this in
muffle furnace maintained at 930 20oC for seven minutes. Cool the crucible in
desiccators and weigh. The loss corresponds to the quantity of volatile matter and
moisture if dried sample is not used. Correct the determination for moisture by
multiplying the factor [100/(100 - % moisture)]

C. Ash: Spread 2 g of sample in silica patty dish. Place the patty dish in cold
furnace at 500 oC for 30 minutes and at 75050oC for further 60 minutes. Cool the
patty dish on metal for 5 minutes and cool finally to room temperature in desiccators
and weigh. The weight of the un-burnt residue corresponds to the quantity of ash.
Correct the determination for moisture (if un-dried sample is used) by multiplying the
factor [100 / (100 - % of moisture)].

% Ash = weight of ash x 100

wt. of the sample (100 - % of moisture)

Fixed Carbon % = 100 - (% moisture + % VM +% Ash)

D. Determination of Sulphur in Coal (ESCHKAs Method)

One g of coal is intimately mixed with 3 g. of Eschka mixture consisting of 2

parts of porous, calcined magnesia and 1 part of anhydrous sodium carbonate. The
mixture is taken in a platinum crucible and this is covered about 2 g more of Eschka
mixture. Fuse the mass carefully a low flame, till all black particles burned out. Cool
the crucible. Extract the mass in 100 ml. DM water in 250 ml. beaker by gradual

78
heating on hot plate. Remove crucible and wash it carefully. Filter this through
Whatman 40. Wash the residue 5-6 times with hot water. Add 10 ml. bromine water,
acidify the filtrate with dilute hydrochloric acid. Boil this, add 20 ml, 10% Barium
chloride solution to this. Boil for 30 minutes. Cool this for 3-4 hours preferably leave
this overnight. Decant the water from the beaker without disturbing the precipitate.
Finally filter the precipitate through Whatman 42 filter paper. Wash this 5-6 times
with cold water. Ignite the filter paper along with the precipitate in platinum crucible
at 800oC. The carbon from the filter paper should be burned below 600oC.

% of S = Wt. of BaSO4 x 0.1374 x 100

Wt. of the sample

E. Determination of Nitrogen (Kjeldahl method)

Weigh accurately 0.1 to 0.2 g of the sample and 2 g. of catalyst (87 parts of
K2SO4 and 13 parts of HgSO4) and transfer this into a Kjeldahl flask. Shake to mix,
add 10 ml. concentrated sulphuric acid and shake. Place the flask on a hole in an
asbestos board and incline the neck at an angle of 600. The hole must be such that it
should cover the liquid. Heat gradually to boiling, continue boiling for 15 to 20
minutes, add small volume of concentrated sulphuric acid if required. Cool, carefully
dilute with about 200 ml. of water, add few pieces of cracked porecelain to prevent
from bumping and then add 25 ml. of solution containing 80 g of sodium thiosulphate
or 40 g. of sodium or potassium sulphide per litre. Next add sufficient sodium
hydroxide solution to make the solution strongly alkaline, add alkali solution very
slowly from the side of the flask. Connect the condenser. Place other end of the
condenser dipped in measured solution of standard sulphuric acid. Distill about 150-
200 ml. into the standard sulphuric acid solution. Remove the dipped end of the
condenser. Put off the flame, disconnect the flask, wash the condenser into the
standard sulphuric acid. Add 2-3 drops of methyl red indicator. Titrate this against
standard alkali solution. Find a blank for the standard sulphuric acid solution. Find the
volume of acid consumed by the distilled ammonia. Estimate the quantity of nitrogen
in the sample and the percentage of nitrogen in the sample.

1 ml, 0.5 N, H2SO4 0.007 g of nitrogen.

F. Analysis of Ash: Determination of SiO2 & preparation of stock solution

Fuse 1 g. of ash with 3-4 g. of sodium carbonate in platinum crucible. Cool,

and extract the mass in dilute hydrochloric acid and water. Evaporate the solution on
hot plate to dry. Bake this to dehydrate completely on hot plate for 30 minutes. Add 5
ml. concentrated hydrochloric acid and 50 ml. DM water, boil this, cool and filter this
through Whatman 40. Wash the residue 5-6 times with hot water. Preserve the filtrate
for further determinations. Transfer the residue along with filter paper to a platinum
crucible. Heat this in muffle furnace at 1000oC. Cool, and weigh the mass. Add 2-3
drops of dilute sulphuric acid and 10-15 of 48% hydrofluoric acid. Heat this on
asbestos sheet to fumes. Expel all fumes from the crucible. Now heat crucible on a
low burner initially and finally at 1000 oC in a furnace. Cool, and weigh the residue.
The loss corresponds to the quantity of silica in the ash. Fuse the mass left, after
hydrofluorisation, in the crucible with potassium pyrosulphate. Extract this in the

79
filtrate preserved for further analysis. Make up the filtrate to 250 ml. in volumetric
flask. Follow the procedures given in the chapter on determination of major and
minor constituent from the stock solution.

CEMENT

Portland cement is mainly composed of tricalcium silicate along with

dicalcium silicate, mono calcium silicate, calcium aluminate also small amount of
iron and little calcium sulphate (acting as a retarder). Cement is analysed for SiO2,
Fe2O3, Al2O3, CaO, MgO, SO3, Loss on Ignition, Na2O, K2O on routine basis and also
P2O5, MnO2, TiO2 free CaO at regular interval.

Determination of Silica and preparation of stock solution:

Weigh 1 g. of cement sample in 250 ml. beaker. Add 25 ml. concentrated

hydrochloric acid and 5 ml. concentrated nitric acid. Digest this on hot plate. Expel all
acid. Dry, dehydrate and bake silica for 30 minutes at 115-120oC. Wet the mass with
5 ml. concentrated hydrochloric acid and 50 ml. DM water. Boil this & cool. Filter
this through Whatman 40 filter paper. Wash the residue 5-6 times with hot water.
Preserve the filtrate for determination of other radicals. Transfer the residue along
with filter paper to a platinum crucible. Ignite this at 1000oC. Cool, and weigh the
mass. Add 2-3 drops of dilute sulphuric acid and 10-15 ml. of 48% hydrofluoric acid.
Heat this on asbestos sheet slowly to expel all acid. Heat the crucible on low flame
initially and finally to blast flame at 1000 oC. Cool this in desiccators and weigh. The
loss corresponds to the quantity of silica in the sample.

% SiO2 = loss of wt. x 100

wt. of sample

Fuse the residue left after hydrofluorisation with small amount of potassium
pyrosulphate. Extract this in the filtrate preserved for other radicals. Make up the
filtrate to 250 ml. Follow the procedure given in the chapter on determination of
major and minor constituents from the stock solution.

1.3 DETERMINATION OF CALCIUM FLUORIDE IN FLUORSPAR

SAMPLES BY CHEMICAL PHASE TECHNIQUE.

Scope
The method is suitable for determination calcium fluoride in fluorspar sample
in the range from 0.30 to 96.00% CaF2.

Principle

Finely powdered (-150 mesh) fluorspar sample is digested with 8% aluminium

chloride solution in 0.1 N hydrochloric acid, the loss in weight corresponds to
calcium fluoride (CaF2) after appropriate corrections due for all acid soluble contents
of sample.

Reagents and equipments

80
 All the reagents used were of analytical grade.

1. Hydrochloric acid, 0.1 N

2. Acetic acid, 10% (V/V)
3. Aluminium chloride, 8% - Dissolve 80 g Ar anhydrous aluminium
chloride in one litre ice cold 0.1 N hydrochloric acid. Cool to room
temperature, filter by Whatman filter paper No.40 and keep in a glass
bottle.
4. Platinum crucibles, 25 ml capacity
5. Muffle furnace, Temp.-1000oC range.
6. Electric oven, Temp. 280oC.

Procedure

(A)
Accurately weigh 0.5000 g fluorspar sample (-150 mesh) and
transfer to a 250 ml beaker.
Add 25 ml aluminium chloride solution
Stir with a glass rod.
Digest on a steam bath for 1 hr.
Filter the sample through Whatman filter paper No.40.
Quantitatively transfer the residue to filter paper (Use policeman)
Wash the residue with hot water (8-10 washings)
Transfer filter paper and residue into a tared platinum crucible.
Transfer platinum crucible to a cold furnace and ignite filter paper
at 500 o + 10oC. Give 1 hour soaking time.
Cool crucible to room temperature in an efficient desicator and
weigh.
The % loss in weigh of sample corresponds to calcium fluoride and
other acid soluble matter of sample, viz. carbonates, ferruginous
matter, etc.

% loss in weight (A) = Weight of sample Weight of residue x 100

Weight of sample

(B) Correction for acid soluble matter.

Treat 0.5000 gm finely powdered sample taken in (a) with 25 ml. 10%
acetic acid solution in a beaker
Digest the sample on steam bath for 1 hr.
Filter the residue through Whatman filter paper No.40. Wash 8-10 times
with hot water.
Ignite the filter paper with residue, starting from a cold furnace to 550 +
10oC.
Calculate acid soluble matter from the loss in the weight of sample after
treatment.

81
 % Acid Soluble matter (B) =Weight of sample Weight of residue x 100
Sample weight

(C) Calculation of % CaF2 in sample:

Deduct the % acid soluble matter (B) from the percent loss in weight
(A), the difference corresponds to % CaF2 dissolved in aluminium chloride
solution by forming CaCl2 and AlF63- compounds

% CaF2= % Loss in weigh of sample (A) - % Acid soluble

matter of sample (B)

EXPERIMENTAL

All the reagents used were analytical grade.

Reagents

(a) 0.1 N hydrochloric acid Dilute 100 ml 1N hydrochloric acid to 1 litre with
water.
(b) 10% Acetic acid Dilute 100 ml glacial acetic acid to 1 litre by water
(c) Aluminium chloride reagents: Dissolve 80 grams analytical grade anhydrous
aluminium chloride in 1 litre ice cold 1N hydrochloric acid. Cool to the room
temperature and filter through Whatman filter paper No.40. Preserve in a
glass bottle.

Procedure:
(a) Weight 0.5000 g sample and transfer to a 250 ml. corning beaker. Add 25 ml
aluminium chloride reagents. Digest on a steam bath for one hour. Filter through
sinter glass G-4 crucible. Wash the residue with hot water for 6-7 times. Dry the
residue at 180oC in an electric oven for one hour. Cool it to room temperature in a
desicator and weight it. Alternately, filter the residue through Whatman filter paper
No.40, wash it thoroughly with hot water. Ignite and residue and paper in a platinum
crucible at 550 + 10oC in a furnace for 15 minutes. Cool it to room temperature and
weigh it.

The % loss in weight corresponds to CaF2 and other acid soluble matter in
sample, such as carbonates, ferruginous material, etc.

(b) Correction for acid soluble matter : Treat 0.5000 a sample with 25 ml with 10%
acetic acid or 0.1 N hydrochloric acid in a 250 ml beaker. Digest the sample on steam
bath for one hour. Filter it through tarred sinter glass G-4 crucible. Dry the residue at
180oC and weigh it after cooling to room temperature. Calcuate % loss in weight,
which is the acid soluble matter. Alternately, filter the residue through Whatman
filter paper No.40, wash 6-7 times with hot water, ignite the residue at 550 + 10 oC
and calculate acid soluble matter. Deduct the percent acid soluble matter from the
percent aluminium chloride soluble sample the difference is % CaF2.

82
1.4 CHEMICAL QUALITY EVALUATION AND STANDARDIZATION
OF SODIUM OLEATE FOR APPLICATION AS FROTH FLOTATION
REAGENT.

Scope
The chemical analysis methods are standardized to determine moisture, pH,
total alkalinily, matter soluble in ethylalcohol, Free alkali, free acid, total fatty acid,
free fatty matter, unsaponi fible matter, unsapanified matter, iodine number and
bromine number.

Introduction

Sodium oleate has been a wellknown anionic collector employed in froth

flotation beneficiation. It is a saponified product of oleic acid along chain fatty acid
with one double bond at 9 carbon position. The performance of sodium oleate
depends on the quality of mother oleic acid and impurities present there in. Hence, it
is imperative to evaluate and standardize the quality of commercial sodium oleate to
ensure its optimum performance in froth flotation tests.

Methodology

Moisture

Dry 10 to 15 gms. of homogeneous soap sample in a weighed corning glass

petri dish on a steam bath to constant weight to third decimal. Keep dried sample in
desicator over fleshly heated silica gel. This dried material has been used for all
determination.

Note : This estimation gives loss of moisture and other volatiles at 100 oC.

pH of Soap solution

Dissolve 5 gms. of dried soap sample in 100 ml. Distilled water on steam bath.
Cool it to room temperature and measure pH using a pH meter calibrated and
equilibrated suitably in the pH range 0-14 pH meter. Report as pH of 5% aqueous
solution.

Note : (i) Calibration and setting of the pH meter may be carried out according to the
instrument operation manual. (ii) The pH of 5% solution usually falls in 8.5 to 9.5
range.

Total alkalinity of soap

Dissolve 5 grams of dried soap material in 100 ml distilled water by heating

over low flame of burner. Filter it through Whatman filter paper no. 40, wash it
thoroughly with hot water until the filter paper is free from soap. Titrate the filtrate in
the cold to the methyl orange end point with 0.1 N hydrochloric acid. Report percent
total alkalinity as sodium oxide.

83
Calculation

% Total alkalinity as Na2O = Titration in ml x normality x 0.031 x 100

Weight of soap

Matter soluble in ethyl alcohol

Soap is soluble in ethylalcohol. Added builder such as carbonates, borates,

silicates, phosphates and other contaminants are insoluble.

Procedure

Put 2 to 5 grams of the dried soap sample into a covered beaker and add 200
ml of absolute ethyl alcohol and digest it on a steam bath for two hours. Filter
through a weighed lG 4 sinter glass crucible under mild suction in a clean area free
from carbon dioxide and other acid fumes. Wash the residue with warm absolute
ethyl alcohol until it is free from soap usually six to eight perfect washings are
sufficient. Reserve the filtrate and washings for estimation of free alkali/free acid.
Dry the residue by heating sinter glass crucible at 100oC for one hour in an oven.
Cool and weight the total matter insoluble in alcohol. Calculate matter soluble in
ethyl alcohol.

Free alkali/Free acid in soap

Heat the clear filtrate reserved from the ethyl alcohol soluble matter to
incipient boiling and add 0.5 ml. of one percent phenolphthalein indicator. If the
colour of the solution is pink, hints the presence of free alkali, titrate from pink to
colourless end point with 0.10 N hydrochloric acid. Calculate free alkali present. If,
the reaction of the alcoholic solution of soap with phenolphthalein is acidic, titrate it
with 0.10 N sodium hydroxide to pink end point. Calculate free acid as oleic.

Calculation

(i) % Free alkali as sodium hydroxide =Titration ml x Normality of acid x 0.040 x 100
Weight of soap

The free alkali is also expressed as sodium oxide or sodium carbonate with the
factor 0.031 or 0.053 respectively.

(ii) % Free alkali as sodium hydroxide =Titration mlxNormality of acid x 0.02825 x 100
Weight of soap
Total fatty matter (TFM)

Transfer 2 to 5 grams of dried soap sample to 250 ml covered beaker. Add

150 ml. distilled water to the sample and dilute nitric acid until slightly acidic, heat on
a steam bath for one hour. The fatty matter collects on the top and the solution below
appears perfectly clear. Cool to the room temperature in ice water. Transfer the
liberated fatty matter along with the solution and 50 ml chloroform to a 500 ml
separatory funnel. Shake it for one minute, let the two layers separate and transfer the

84
lower chloroform extract to a beaker. Again, similarly extract the fatty matter in
solution with 25 ml of chloroform for two to three times and transfer it to the beaker.
Then transfer the whole chloroform extract to a 200 ml separatory funnel, rinse the
beaker with chloroform. Wash the chloroform extract with 25 ml of water for two to
three times. Now transfer the chloroform extract to a weighed 100 ml beaker.
Evaporate off the chloroform on a steam bath and dry on it for 30 minutes. Cool in a
desicator and weigh as total fatty matter.

Calculation

% TFM = Weight of fatty matter x 100

Weight of soap

Free fatty matter (unsaponified and unsaponifiable matter FFM)

Take 2 to 5 grams of the dried soap in a 250 conical flask and add 0.1 to 0.2
gram of sodium bicarbonate. Dissolve sample in 100 ml of 50% ethyl alcohol. Warm
on a steam bath to dissolve it. Filter it through Whatman filter paper No.40 and wash
the filter thoroughly with 50% ethylalcohol and a little petroleum ether (60-80 oC).
Shake it vigorously for one minute. Let the two clear layers separate and then draw
off upper petroleum ether layer into another 250 ml separatory funnel. Repeat the
above extraction for 2-3 times with 25 ml portion of petroleum ether. Wash
petroleum ether fraction in separatory funnel with 0.1 N sodium hydroxide and
ethylalcohol mixture (one to one by volume) for two to three times. Evaporate the
petroleum ether in a weighed beaker on a steam bath and dry the residue on steam
bath for 30 minutes. Weight of the residue corresponds to free fatty matters.
Calculation

% FFM = Total weight of residue x 100

Weight of soap

Unsaponifiable matter

Put 2 to 5 grams of dried soap in a 250 ml. beaker. Add 30 ml of ethylalcohol

and 5 ml of 50% potassium hydroxide solution and then heat it on a steam bath for
two hours and then boil over a low flame of burner for 15 minutes. Transfer the
solution to a 250 ml separatory funnel, add 20 ml ethyalcohol and 80 ml of distilled
water. Mix it well. Now add 50 ml petroleum ether (60-80oC) and shake vigorously
for 30 seconds. Allow the two layers to separate perfectly clear. Draw upper
petroleum ether layer in another separatory funnel. Continue extraction with fresh 25
ml portion of petroleum ether for three to four times and collect all extraction
fractions in the separatory funnel. Wash the petroleum ether extract with ethylalcohol
water mixture (1:5 by volume) until the washing is just acidic or neutral to the
methylorange indicator. Transfer petroleum ether layer to a weighed beaker and
evaporate on a steam bath and then dry the residue for 30 minutes. Cool and weigh it
corresponds to unsaponifiable matter.

85
Calculation

% Unsaponifiable matter = Weight of residue x 100

Weight of soap

Unsaponified matter

The unsaponified matter is computed by deducting the percent of

unsaponifiable matter from the percent of unsaponified and unsaponifiable matter
(FFM).

Examination of fatty matter for unsaturation Determination of iodine number

and bromine number

The total fatty matter separated from soap has been employed as sample for
estimation of iodine number and bromine number. In iodine number the total iodine
consumed by the sample is estimated which may be either the addition at a double
bond or the substitution on the chain. While in bromine number a less common
determination, envisages the correction for any substitution and hence only
demonstrate the degree of unsaturation. However, both the methods have been used.

(i) Iodine number Wijs method

Weigh 0.1 to 0.2 grams of fatty matter into an iodine conical flask. Dissolve it
by mixing in 25 ml of chloroform. Now add from a pipette 245 ml of wijs iodine
solution or standard iodine monochloride solution. Just moisten the stopper with 15%
potassium iodide solution and let stand the flask in dark closed for one hour at room
temperature. The above steps can be conducted in a 500 ml conical flask nicely cover
with a watch glass or a glass stopper. After one hour add 20 ml of 15% potassium
iodide solution and 100 ml of distilled water, boiled and cooled. Titrate it
immediately with 0.10 N sodium thiosulphate solution to disappearance of blue
colour of starch indicator. Run blank of wijs solution.

Calculation

Iodine value = ml. of thiosulphate consumed by sample x normality of thiosulphate x 12.629

(Iodine number) Weight of sample

The iodine number represents the number of centigrams of iodine absorbed by 1 gram
of fatty matter, i.e. the percent of iodine absorbed.

Note : Wijs solution : Dissolve 13 gms of pure analytical grade iodine in 1 litre of
in 1 litre of analytical grade acetic acid. Titrate 25 ml with 0.10 N sodium
thiosulphate using potassium iodide and starch. Put aside about 10 ml of iodine
solution and in the rest of the solution pass pure chlorine gas until the red colour of
the solution just turns to the yellow colour and the original sodium thiosulphate
titration just doubled. Then add the original solution to neutralize any free chlorine.
Preserve in amber-coloured bottle and use only in one month period.

86
Bromine value

Take 0.1 to 0.2 grams of fatty matter in a 250 ml iodine flask or alternately to
a 500 ml. conical flask. Dissolve fatty matter in 25 ml of carbontetra-chloride.
Pipette 25 ml of 0.33 N bromine reagent into the flask containing the sample. Put the
stopper and let it stand for two minutes at room temperature. The immerse the flask
in ice water and quickly add 30 ml of 25 percent potassium iodide solution.
Restopper and shake the solution to absorb vapors of bromine and then wash down
the walls of flask with distilled water. Add 75 ml of 10 percent sodium chloride
solution to overcome emulsification of the solvent. Titrate the iodine liberated with
0.10 N sodium thiosulphate solution to disappearance of blue colour of starch
indicator. Run a blank. The difference in litre value for blank and residual free
bromine is the measure of percent total bromine absorbed.

When the end point for total bromine absorbed reached and recorded add 5 ml
of potassium iodate solution the hydrobromic acid liberated from substitution reaction
is transformed into the equivalent free iodine. Mix well and titrate liberated iodine
with 0.10 N hyposolution. The difference of milliliters of hypo solution consumed
for liberated hydrobromic acid and blank is the bromine substitution value. The
difference of the percent total bromine absorbed and bromine substitution value is
reported as bromine addition value.

Calculation

(i) Bromine substitution = (Ml. of hypo equivalent to liberated hydrobromic

acid-Blank) x Normality of hypo x 0.0799 x 100
Weight of sample

(ii) Percent total = (Blank-ml. of hypo equivalent to residual free bromic

acid ) x Normality of hypo x 0.0799 x 100
Weight of sample

(iii) Bromine addition = Percent total bromine absorbed

value (2 x bromine substitution value)

Note

(A) Bromine reagent (0.33 N) Dilute 26.6 gms of bromine to one litre with carbon tetrachloride.

(B) Potassium iodate solution Dissolve 21.4 gms of potassium iodate in one litre distilled water.

1.5 SPECTROMETRIC (COLOURIMETRIC)METHODS OF ANALYSIS

General Consideration

The technique is based on the fact that when visible (380-800 nm), ultraviolet
(200-400 nm), etc. electromagnetic radiations passes through a colour solution, the
quantity of light absorbed (or transmitted) varies depending upon the concentration of
the colour component (absorbing species) of the solution. The intensity of the colour

87
of the unknown is compared against a solution of known concentration by following
the same procedure and the concentration/percentage of the colour component present
in the sample is determined.

Law of the absorption of light

The colourimetric analysis is based upon Lambert and Beers law :

(i) Lambert Law: When mono-chromatic light passes through a transparent

medium, the rate of decrease in intensity with the thickness of medium is proportional
to the intensity of the light or that the intensity of the emitted light decreases
exponentially as the thickness of the absorbing medium increases arithmetically.

Thus, the law by Briggsian logarithm :

It = Io 10-k.t

Where Io is the intensity of the incident light, it is the thickness of the

medium. It is the intensity of the transmitted light, and K is extinction coefficient.

(ii) Beers law: The intensity of a beam of monochromatic light decreases

exponentially as the concentration of the absorbing medium increases arithmetically.

Thus,
It = Io. 10-kc

Where C is concentration and K is a constant. These two laws are combined

to obtain following exponential form:

It = Io. 10E.C.t.
Or log Io = E.C.t. = A (absorbance)
It
Where E is molar extinction coefficient.

This is the fundamental equation of colourimetry and termed as Lambert-Beer

Law.
The concentration of an unknown solution can be calculated knowing A,E,t
provided the Lambert = Beer law is applicable.
C = log Io/It = A
E.t. E.t.
If a coloured system does not show conformity to Lambert Beer Law, a
standard calibration graph is prepared by plotting other transmittance or absorbance
value (ordinate0 against concentration using a series of standard solution. From this
graph, concentration of unknown solution can be computed corresponding to its
absorbance reading. An identical procedure must be followed in preparing the
coloured solution of unknown sample and the standard colour solution. However, a
calibration graph is applicable to specific instrument only.

88
Instrumentation

Absorption measurements are made with various instruments, i.e.

colourimeter, photoelectric colourimeter, and spectrophotometer which are
constructed according to the following scheme

Source of Mono Blank

continuous chromator
radiation Sample Sample Detector Recorder
solution solution

Table- Photometric analytical method

Method Region of Monochromator Technique of recording of

spectrum light absorption
(Detector)
Colourimetry Visible Absent Visual
Photoelectric Visible Colour filters PMT
colourimetry
Spectrophotometry Visible Diffraction PMT
Ultraviolet grating
Prism

Operation

In using a single beam spectrophotometer, the wavelength set to the

absorption maximum of the analyte to be determined. The instrument is adjusted to
red zero transmittance when no light passes to detector. The reagent blank is then
positioned into the light path and adjust the read out to a 100 percent transmittance or
zero absorbance setting. The light is then passed through the sample to obtain the
absorbance or transmittance and related to concentration either through the use of
calibration graph or by the use of algebriae method.

W1 x A2 x 100 = % concentration
A1 W2

A1 = Absorbance of standard solution

W1 = Weight of standard (in mg or gm)
A2 = Absorbance of the sample
W2 = Weight of sample taken (in mg or gm)

In a double beam spectrophotometer, a monochromatic light beam is split into

two components. The instrument is adjusted to zero by placing reagent blank in both
the component beam after wavelength setting to the absorption maximum. Then one
of the reagent blank is replaced by sample solution (absorbing solution) and the
difference of absorbance between the two is determined simultaneously. This
absorbance value is used for calculating percent analyte in solution.

89
Method

i. Tungsten:

Principle

Tungsten is preferentially extracted in tartaric acid solution after fusion with

potassium pyrosulphate. The WVI is reduced to WV by stannous chloride in strongly
acidic medium followed by reaction of thiocyanate ion to form a WV green-yellow
complex, which absorbs at 400 nm.

Reagents

(i) Standard Tungsten solution: Dissolve 1.7940 g. of reagent grade

Na2WO4. 2H2O in water. Add one pellet of sodiumhydroxide dissolve
and dilute to one litre. 1 ml -= 1 mg of tungsten with a pipette, transfer 10
ml of this stock solution to a 100 ml volumetric flask and dilute to the
mark. 1 ml = 0.10 mg of tungsten.
(ii) Stannous chloride 2M: Dissolve 113 g stannous chloride dihydrate in
concentrated hydrochloric acid. Make volume to 250 ml with
concentrated hydrochloric acid.
(iii) Tartaric acid : 7.5% - Dissolve 7.50 gm of tartaric acid in 100 ml water.
(iv) Potassium thiocyanate 20% - Dissolve 20 gm of potassium thiocyanate
in 100 ml water.

Procedure

Transfer 0.10 0.40 g sample in dry test tube and mix with five fold of
potassium pyrosulphate.
Fuse over a burner and keep it red hot for 10-15 minutes.
Spread melt over the walls of test tube and allow it to cool.
Add 10-15 ml of tartaric acid solution in the test and put a glass rod.
Heat the tube gently in a hot water bath until the cake breaks up.
Remove the test tube from water bath and filter solution in 100 ml.
Volumetric flask using Whatman No.40 filter paper, wash tube and
residue with 1% hot tartaric acid solution. Usually five to six washings are
sufficient.
To the filtrate, add 10 ml of concentrated sulphuric acid, 20 ml of
concentrated hydrochloric acid, and 5 ml of stannous chloride solution in
that order.
Mix well and digest on a steam bath for 10 minutes.
Remove from heat and immediately chill in an ice bath to 10oC or less
(minimum time should be given at this point) and then quickly add 10 ml
of potassium thiocyanate solution, dilute to the mark and mix well. Return
to the ice bath for 5 to 10 minutes.
Remove the flask from ice bath and allow it to stand at room temperature
for 10 minutes (The colour is stable for at least one hour).

90
 Measure the absorbance in a spectrophotometer at 400 nm using reagent
blank for a null.
Compute tungsten concentration from calibration graph.

Standard absorption concentration graphs Transfer 1,2,5,7,10,15 and 20 ml

of 0.10 mg tungsten per ml stock solution to 100 ml volumetric flasks. The aliquots
represent 0.10, 0.20, 0.50, 0.70, 1.00, 1.50 and 2.00 mg of tungsten respectively.
Dilute to 25 ml and follow steps 5-12 plot the absorbance versus mg of tungsten on
co-ordinate paper.

ii. Silica

Principle

A yellow coloured 12-molybdo-silicic acid forms reaction of silicate ion with

molybdate ion in pH range of 1.6-4.90. The heteropoly blue of silicon is produced by
the reduction of the molybdenum (vi) in the 12-molybdosilicic acid to the
molybdenum (v) State. The intensity of the blue colour is measured at 650 nm.

Reagents

(i) Standard silica solution Fuse 2.1393 g SiO2 with 4.60 gm anhydrous
sodium carbonate, maintaining melt for 15 minutes in platinum crucible
dissolve in water, and dilute to 1 litre 1 mg SiO2 per ml.
(ii) Standard silica 0.1 mg SiO2/ml : Dilute 10 ml of 1 mg SiO2/ml solution
to 100 ml by water, store in polythene bottle.
(iii) Ammonium molybdate solution, 5% - Dissolve 5 g ammonium
molybdate in warm water (60 aC) and make volume 100 ml.
(iv) Oxalic acid, 8% - Dissolve 8.00 g of oxalic acid in 100 ml of water.
(v) Ascorbic acid, 5% - Dissolve 5.00 g of ascorbic acid in 100 ml of water

Procedure

Transfer 2.5 ml aliquot of 19 sample solution in 250 ml volume obtained

in decomposition of silicates by sodium carbonate fusion, after usual
separation of silica (SiO2) by dehydration and baking and
dehydrofluorisation.
Add 20 ml distilled water and mix.
Then neutralize acid by adding dilute sodium hydroxide solution using pH
paper externally.
Now add 0.40 ml dilute hydrochloric acid (1:1) to bring pH of solution
around 2.2.
To this add 5 ml of ammonium molybdate solution mix well and stand
for10 minutes.
Then add 10 ml of oxalic acid solution. Mix well by swirling, and add
immediately 2 ml of ascorbic acid solution and again mix.
Dilute solution to 100 ml by water and keep aside for 30 minutes at room
temperature.

91
 Measure absorbance of the blue complex at 650 nm.
Run a reagent blank.
Calculate SiO2 percentage using calibration graph.

Standard calibration graph Transfer 0, 0.5, 1.0, 1.5, 2.0, 2.5, 3, 4 and 5 ml of the
0.1 mg SiO2 per ml stock solution to 100 ml volumetric flask, dilute to about 20 ml by
water and follow steps 3-18. Plot absorbance values versus mg silica per ml and use
this graph for calculation of percent SiO2 in unknown solution.

iii. Molybdenum in tungsten mineral

Principle

Thiocyanate ion react with Mo(V) in an acid solution to form coloured complex the
maximum absorbance is read at 540 nm. The interfering effect of tungsten is
overcome by adding tartaric acid which percents then formation of its thiocyanate
complex.

Reagents

(i) Molybdenum Standard solution, 1 ml equivalent to 0.1 mg of

molybdenum. Dissolve 2.0425 g ammonium molybdate in water dilute to
1 litre volumes Mo = 1 mg/ml. Dilute 10 ml of above solution to 100 ml
to prepare 0.1 mg Mo/ml solution.
(ii) Dilute sulphuric acid 1:1 and 1:4
(iii) Tartaric acid 10% : Dissolve 10 g of tartaric acid in 100 ml water.
(iv) Stannous chloride : 35% - Dissolve 350 g of SnCl2 2H2O in 100 ml of
concentrated hydrochloric acid by heating, dilute the clear solution with
900 ml water and add a few pieces of tin metal.
(v) Ferric sulphate, 8% - Dissolve 8 gm of ferric sulphate in 100 ml of N
sulphuric acid.
(vi) Potassium thiocyanate, 5% - Dissolve 5 gm of potassium thiocyanate in
100 ml water (freshly prepared).
(vii) Butyl acetate : The extracting solution is prepared by shaking 250 ml of
butyl acetate in a separating funnel with 5 ml of 5% potassium thiocyanate
solution and 25 ml of 25% solution of stannous chloride. The solutions
are allowed to settle and the aqueous solution is drawn off and discarded.
The extracting solution deteriorates and must be prepared every 24 hours.

Procedure

Decomposition : Mix 0.1 0.5 g of mineral with a five fold quantity of sodium
carbonate and fuse it over the flame, leach the melt with 50 ml of hot water, separate
the residue on a What man No.40 filter paper, wash with 25-50 ml of 1% sodium
carbonate solution and neutralize the filtrate with hydrochloric acid using pH paper
externally. Add 10 ml of the acid in excess and make to 250 ml volume for taking
aliquot.

92
 Alternately the sample can be decomposed by treating 0.1 g of sample (Mo ~
0.5%) with dilute perchloric acid (1:1), warm until the sample has dissolved. Heat to
boiling, cover and fume. Cool somewhat and add 25 ml of water, boil a few minutes
to expel free chlorine filter and use aliquot.

Transfer appropriate aliquot to a 250 ml separatory funnel.

Add 25 ml of dilute sulphuric acid (1:1) and mix.
Now add 3 ml of ferric sulphate solution and shake for 30 seconds.
Then add 5 ml of tartaric acid solution and shake for 30 seconds.
Now add 10 ml of potassium thiocyanate solution and shake for 11
minutes.
Add 10 ml of stannous chloride solution and shake vigorously for one
minute.
Add 20 ml of butylacetate from a pipette, stopper and shake for one
minute.
Allow the funnel and contents to cool and repeat the shaking.
Allow the layers to separate and draw off and discard the lower acid layer.
Add 50 ml of dilute sulphuric acid (1/1), 10 ml of potassium thocyanate
solution and 5 ml of stannous chloride solution and shake well.
Allow the layers to separate and draw off and discard lower acid layer.
Transfer the butylacetate layer to a volumetric flask and stopper.
Take butylacetate extract in an absorption cell and measure absorbance at
540 nm using a blank run to set the zero. Compute percentage of
molybdenum from calibration curve. (The absorption maxima of the
molybdenum thiocyanate complex is ~ 470 nm, but the measurement is
made at a longer wavelength to avoid interference by tungsten).

Standard curve

Transfer 3 ml of ferric sulphate solution and 25 ml of dilute sulphuric acid

(1:1) to separatory funnel and add 0.5, 1.0, 2.0, 4.0 and 5.0 ml of the 0.1 mg/ml
molybdenum standard solution into each funnel, respectively and proceed as in steps
4 to 12. Construct a standard curve plotting absorbance against mg of molybdenum.

iv. Bismuth in polymetallic ore

Principle
Yellow bismuth diethyl dithiocarbonate is extracted over 9-11 pH in chloform. The
formation of the diethyl dithiocarbonates of metals such as iron (iii), mercury, silver
and copper is prevented by the use of an ammonical solution in the presence of
cyanide and disodium enthylene diamine tetra acetate. The absorption maximum of
the yellow complex is 400 nm.

Reagents

1. Bismuth Standard : 1000 mg of Bi per ml : Dissolve 1.0 gm of bismuth

metal in 8 ml of 10 N nitric acid, boil gently to expel brown fumes and dilute

93
 to one liter. Bismuth standard 10 ppm. Dilute 1 ml of the 1000 ppm Bi/
solution to 100 ml with water containing 5 ml concentrate nitric acid.
2 Potassium bisulphate fused powder
3. Ethylene diamine tetracetic acid, disodium salt
4. pH paper range 5-12
5. Sodium diethyl dithiocarbonate solution 1% - Dissolve 1.0 g sodium
diethyl dithiocarbonate in 100 ml of water.
6. Chloroform

Procedure

Decomposition of Sample : Dissolve 1.00 5.00 gm sample in a mixture of 3

parts of concentrate nitric acid and 1 part of concentrated hydrochloric acid.
Evaporate to dryness, bake and take up with 1:10 hydrochloric acid. Dilute to a
known volume for the use of aliquots.

For siliceous samples or tailings, the sample is decomposed by fusion with

potassium bisulphate or potassium pyrosulphate. Bring sulphates in solution by
boiling fused cake with 2 ml nitric acid and 8 ml water.

Take aliquot equivalent to 0.50 gm.

Add water to make volume around 20-50 ml.
Add 1 gm of ethylene diamine tetraacetic acid disodium salt and mix
well to get clear solution.
Add ammonia solution drop wise until the pH of the solution is
between 5 and 6 using a pH test paper externally.
Add 5 ml of sodium cyanide solution (5% aqueous solution), mix well
and filter through a Whatman No.40 filter paper into a 250 ml
separatory funnel.
Add 1 ml of ammonia to the filtrate and mix.
Add 1 ml of sodium diethyl dithiocarbonate solution and shake.
Add 5 ml of chloroform and shake the stoppered separatory funnel for
one minute.
Place a plug of cotton in the steam of the funnel and transfer organic
phase to an absorption cell.
Read absorbance at 400 nm.
Compute bismuth concentration using standard calibration curve.

Standard Calibration curve : To five separatory funnels each containing 8 ml of

water and 1 gm of EDTA add respectively, 10, 20, 40, 60 and 80 mg of bismuth per
ml using the standard solution containing 10 mg of bismuth per ml. Continue as
described in steps 4-10. Construct a calibration curve using absorbance and mg of
bismuth.

v. Determination of Fluorine in water sample

Principle

94
 The method is based on decolorisation of zirconium-alizarin dye by fluoride
ions. Colourless ZrF2-6 is formed in this reaction. With progressive increase in
fluoride ion concentration, the colour changes from pink-yellow to bright yellow.
Maximum absorbance is at 520 nm.

Reagents

(i) Standard fluoride solution : Dissolve 0.221 gm of NaF in 1 litre

distilled water. 100 mg of fluorine per ml.
(ii) Acid Zirconylalizarin reagent (Sauchis method). To 0.30 g
zirconium oxychloride octathydrate or 0.25 g zirconium nitrate
octahydrate, dissolved in 50 ml water, add 50 ml alizariureds water
solution containing 0.07 g of the dye with swirling. To above
solution add 900 ml acid mixture, prepared by mixing 1123 ml
concentrated hydrochloric acid diluted to 500 ml and 37 ml
concentrated sulphuric acid diluted to 500 ml.
Procedure

Take 50 ml clear water sample in 100 ml volumetric flask.

Add 10 ml zirconium alizarin reagent. Mix the solution well.
Make volume to the mark using water sample.
Wait for one hour and then compare colour with standards or read
absorbance at 520 nm.
Calculate fluoride concentration from calibration curve.

Calibration curve : Transfer 0.5, 1.0, 1.5, 2.0, 3.0, 4.0 and 5 ml of 100 mg
fluorine per ml stock solution to 100 ml volumetric flask containing 25 ml deionized
water and then follow steps 2-4 under procedure. Plot absorbance against mg of
fluorine. A graph of inverse slope is obtained. A standard graph must be prepared
each time a fresh batch of zirconium alizarin reagent is prepared.

vi. Antimony

Principle

Antimony (V), in a medium of 1 M hydrochloric acid, forms red-violet

coloured complex with rhodamin-B dye. Absorbance of the red-violet coloured
complex is measured at 550 nm. Antimony (V) is preferentially extracted in
isopropylether to overcome interference of other cations in sample.

Reagents

1. 1 M hydrochloric acid
2. 6 M hydrochloric acid
3. Aquous hydroxylamine hydrochloride 1% - Dissolve 1 gm of
NH2OH.HCl in 100 ml water.
4. Acidic hydroxylamine hydrochloride 1% - Dissolve 1 gm of
NH2OH.HCl in 100 ml 1 M. hydrochloric acid.

95
 5. Cericsulphate, 3.3% - Dissolve 16.5 g of ceric sulphate in 500 ml of 0.5
M sulphuric acid.
6. Sodium bi sulphite 1% - Dissolve 1 g of sodium bi sulphite in 100 ml of
water.
7. Rhodamine-B-0.02% - Dissolve 0.02 g of rhodamine B in 100 ml of 1 m
hydrochloric acid. Warm and filter, if necessary.
8. Isopropylether : Shake in a 500 ml separating funnel, sufficient
isopropylether with successive 25 ml portions of ceric sulphate solution
until the yellow colour remain after shaking for 1 minute. Then destroy
the excess ceric sulphate with 1 ml 1% aqueous NH2OH. HCl and discard
the aqueous phase. Shake with two 25 ml. portion of water followed by 25
ml of 1 M HCl. Stopper the funnel and leave the ether standing over the
hydrochloric acid, until required. This treatment should be repeated daily.
9. Standard antimony stock solution Sb-1000 mg/ml Dissolve 0.11979
of antimony (iii) oxide, Sb 2O3 in 100 ml of 6 M hydrochloric acid.
Prepare antimony standard 100 mg Sb/ml by dilution of 10 ml of 1000
Mg/ml antimony solution to 100 ml with 6 M hydrochloric acid. Prepare
an antimony solution containing 5 Mg.Sb/ml by dilution of 5 ml of 100 mg
Sb/ml to 100 ml by 6 M hydrochloric acid (Prepare fresh).

Procedure

Weigh 0.2 g sample into the test tube.

Add 1 g potassium pyrosulphate and mix well.
Heat in a flame until frothing ceases remove from the flame and spread
melt in a thin layer on the wall of the tube.
Allow to cool and add 5 ml of 6 M hydrochloric acid.
Heat the tube gently in a steam bath untill the melt breaks up, taking care
that the solution does not boil.
Remove the tube and add 1 ml of 1% sodiumbisulphite solution.
Make up to 10 ml with 6 M hydrochloric acid. Mix the contents and allow
to settle overnight.
Decant the solution into a 125 ml. Separating funnel. Wash the sides of
the tube and residue in the 3 ml warm 6 M hydrochloric acid, allow to
stand a few minutes and decant in the separatory funnel.
Repeat above step with 3 ml of warm 6 M hydrochloric acid and then with
2 ml. of hot water.
Cool the solution to below 25oC.
Add 5 ml of ceric sulphate solution, mix and leave for 30 seconds.
Add 1 ml 1% aqueous NH2OH.HCl and leave for 1 minute.
Add 45 ml of cold water.
Now add 5 ml isopropylether, shake for 1 minute and allow to stand 5
minutes.
Drain off all but 0.5 ml of the aqueous phase and add 2 ml of 1%
NH2OH.HCl in 1 M hydrochloric acid shake for 30 seconds.
Allow the phases to separate, discard the aqueous phase. Add 2 ml of 1 M
hydrochloric acid and shake for 30 minutes.

96
 Discard the aqueous phase. Add 2 ml of the 0.02% rhodamin-B solution
and shake for 30 seconds.
Discard the aqueous phase and transfer the ether phase to an absorption
cell.
Measure the optical density of the solution at 550 nm against a Reference
solution isopropylether. If the reading is greater than the highest
calibration standard, pipette a suitable volume of the ether solution into an
absorption cell and dilute as necessary with a known quantity of
isopropylether record the dilution.
From the optical density reading, determine the concentration of antimony
from the calibration curve.

Preparation of standard curve

Add 15 ml of 6 M hydrochloric acid to each separating funnel containing 1,2,3

and 4 ml of 5 mg Sb/ml followed by 1 ml of 1% sodium bi-sulphite solution. Mix.
Follow step (11) to (19). Record the optical density reading of each standard. Run-
identical reagent blank. Construct the calibration curve by plotting absorbance against
antimony concentration.

vii. Determination of small amounts of Vanadium ((V2O5) in Silicate rocks,

Bauxite, Vanadium mineral, Iron ore, Red mud and Bayer plant liquored)

Principle

Estimation of vanadium (V) is based on the formation of yellow soluble

phosphotungsto vanadic acid on treatment with phosphoric acid and sodium tungstate
(tungstic acid) to an acid vanadate solution. The maximum absorption is at 400 nm.

Reagents

1. Sodium tungstate 0.5 N : Dissolve 16.5 gm of Na2WO4.2H2O in water

and dilute to 100 ml.
2. Standard vanadium solution : 1 ml = 1 mg of V. Dissolve 1.785 gm of
vanadium penta oxide (V2O5) in slightly excess of sodium hydroxide then
add slight excess of dilute sulphuric acid and dilute to 1 liter.
3. Sulphuric acid : (A.R. grade)
4. Phosphoric acid : (A.R. grade)

Method of Decomposition : (Iron ore, Bauxite, Vanadium & Red mud) : Finally
ground sample (0.10 to 0.20 gm) is fused with sodium carbonate in a platinum
crucible and the sintered mass is leached with hot water. The filtered leach solution is
fumed with perchloric acid for estimation of silica. The aliquot is used for
determination of vanadium.

97
Alumina hydrate

The vanadium present as soluble salt is leached with hot water. The filtrate is
acidified with sulphuric acid and used for determination of vanadium.

Calcined Alumina

The sample is fused with a mixture of borax and sodium carbonate and the
sintered mass is leached with hot water and filtered. The filtrate is acidified with
sulphuric acid and used as aliquot.

Bayer plant process liquors

The filtered sample is acidified with sulphuric acid and used as aliquot.

Procedure

Transfer approximate aliquot (about 0.1 gm sample) in a 250 ml beaker.

Add approximately 3 ml dilute 1:1 sulphuric acid and some water to bring
volume about 40 ml and heat to 90-95oC (do not boil the solution). Add 2-
3 drops acid in excess, adjust pH around 2-2.5.
Add 5 ml 1:1 orthophosphoric acid.
Keep for 5 minutes then add 0.5 ml of tungestic acid and again heat to 90-
95oC.
Allow the solution to stand for two minutes, cool to room temperature.
Transfer the solution into 100 ml volumetric flask and make with water up
to the mark.
Measure the absorbance of solution at 400 nm.
If titanium content is high as expected in bauxite read the absorbance after
standing coloured solution for about an hour. During this course, colour of
titanium complex fades completely.
Calculate percentage of vanadium by using standard calibration curve.

Standard calibration curve

Place 0.5, 1.0, 2.0 and 2.5 ml of the vanadate standard solution, 1 mg
vanadium/ml into fine 100 ml volumetric flasks. Then follow the procedure step 2 to
8. Construct the calibration curve using the data obtains.

viii. Determination of small amounts of Iron (In clay, quartz, silica sand/calcite
samples, etc.)

Principle

Iron is determined by the complex formation of orange, red coloured complex

with 1.10 phenathroline at pH about 3.5 in sodium citrate medium containing ascorbic
acid as reducing a gent.

98
Reagent

1. Standard solution: Dissolve 1.00 gm of iron metal in 20 ml of 1:1 HCl

and dilute 1 litre to get 1 ml = 1 mg iron solution.
2. Ascorbic acid : A.R. grade, 1% solution in water.
3. Sodium citrate : A.R. grade, 20% solution in water.
4. 1,10 phenanthroline : A.R. grade 0.25% solution in water.

Decomposition (Silicate rocks)

Finally powdered sample (0.1-0.2 gm) is fused with sodium carbonate and
potassium carbonate (5:1) ratio mixture in a platinum crucible. Extract in water,
dissolve in 1:1 hydrochloric acid if any insoluble matter. Bake, dry the solution, filter
through No.40 filter paper, dis-card silica.

Alternately sample can directly be kept for hydrofluorisation. Weigh 0.1 gm

sample in platinum crucible, add 5 ml water, 5 ml 1:1 H2SO4 and 1 ml hydrofluoric
acid. Evaporate to dryness. Fuse with potassium pyrosulphate. Extract with 1:10
sulphuric acid, proceed with aliquot.

Iron : Add concentrate hydro chloric acid 20 ml to 0.4 gm sample. Add more from
time to time as required till complete digestion. Make up the volume to 1 litre and
appropriate aliquot.

Silica sand, quartz Take 0.1 gm sample in a platinum crucible, add 2-3 drops 1:1
sulphuric acid and 10 ml HF. Hydrofluorise till dryness. Repeat the process twice.
fuse with potassium pyrosulphate and extract in 1:1 hydrochloric acid. Take aliquot
for iron determination.

Procedure

Take appropriate aliquot 10 ml. Neutralizxe the solution with 10% NaOH
solution using phenolpthalien indicator exactly.
Add 5-6 drops conc. hydrochloric acid with mixing to adjust the pH 3.0-
3.5.
Add 5 ml sodium citrate solution to set pH exactly 3.5-4.0.
Add 2 ml of ascorbic acid to reduce Fe3 to Fe2.
Add 5 ml of 1,10 phenanthroline solution.
Keep the solutions for an hour. Make up the volume in 100ml.
Volumetric flasks with water.
Measure the absorbance at 500 nm. Run a reagent blank.

Standard calibration curve

Take 0.3, 1.0, 1.5, 2.0 and 4.0 ml of standard iron solution in 100 ml
volumetric flask and follow the steps from 1 to 6. Plot the calibration curve and
compute the results.

99
ix. Determination of small amount of manganese

Principle

The sample is decomposed with hydrochloric and nitric acid and fumed off
with sulphuric acid. Phosphoric acid is added to complex with iron and it prevents
precipitation of periodates or iodatas of manganese. Permanganate colour is
developed by addition of potassium per iodata in boiling state. The absorbance is
measured at 545 nm.

Reagent

1. Standard Manganese Solution Dissolve 1.00 gm of electrolytic

manganese metal in dilute nitric acid by heating and make up in 1 litre.
Alternately weigh 1.2255 gm. manganese dioxide in a 250 ml beaker,
decolourize it by 15 ml HCl. add 20 ml 1:1 sulphuric acid, fume off
completely. Extract in 10% sulphuric acid and make up to 1 litre in
measuring flask to get 1 ml = 1 mg. MnO in solution.
2. Potassium periodate : Solid A.R. grade
3. Hydrochloric acid : A.R. grade
4. Nitric Acid : A.R. grade
5. Sulphuric acid : A.R. grade
6. Orthophosphoric acid : Manganese free (A.R. grade)

Procedure: Decomposition (silicate rocks, Mn ore, Bauxite) To, a 0.5 gm sample

add 10 ml conc. hydrochloric acid and 2.0 ml conc. nitric acid, digest on hot plate.
Extract in dilute HCl and filter through No.40 Whatman filter paper. Ignite the
residue and hydrofluorise silica. Fuse the mass with potassium pyrosulphate and
extract in hydrochloric acid and mix with main solution.

Alternately sample can directly be kept for hydrofluorisation in presence of 2

ml conc. sulphuric acid and 10 ml of hydrofluoric acid. Fuse with K2S2O7. Extract in
1:10 H2SO4.

Alternately take suitable aliquot 10-25 ml.

1. From mother liquor, add 10 ml. conc. H2SO4, fume it off completely till
syrapy mass, remains.
2. Extract in 10% sulphuric acid solution. (Filter off if any suspended
matter).
3. Add 5 ml 1:1 orthophosphoric acid. The solution should be colourless at
this stage.
4. Heat the solution to boiling, add at pinch (0.2-0) of potassium per iodata.
5. Develop permangate colour.
6. Cool the solution and make up 100 ml in measuring flask. Measure
absorbance at 545 nm.
7. Run a reagent blank. Calculate percentage of MnO by using standard
calibration curve.

100
Standard Calibration Curve

Take 0.10, 0.15, 0.20, 0.30 and 0.40 ml of standard MnO solution in 100 ml
volumetric flasks. Follow the procedure from step 2 to 6. Plot the calibration curve
and compute the results.

x. Determination of Small amounts of Phosphorous (P2O5 in Iron ore, Mn

ore, Limestone, Silicate rocks)

Principle

A yellow mixed heteropoly acid molybdovanado phosphoric acid is formed

when an excess of molybdate solution is added to an acidic (0.05 N HNO3) solution
of orthophosphate and vanadate ion. The absorbance is measured at 460 nm.

Reagents

1. Standard phosphorus solution : Dissolve 0.4263 gm diammonium hydrogen

phosphate, (NH4)2 HPO4 in water and make up the solution up to 1.0 liter to get
0.1 mg = 1 ml of phosphorus.
2. Vanadate reagent : Dissolve 2.5 gm ammonium vandate in 500 ml boiling
water. Cool the solution and add 20 ml conc. nitric acid. Cool and dilute to 1
litre. Store in polythene bottle.
3. Molybdate reagent : Dissolve 50 gm ammonium molybdate tetrahydrate in
warm water (50 oC). Cool and dilute to 1 litre. Store in polythene bottle.

Decomposition (Iron ore, Manganese ore & Limestone etc.)

Take 1.0 gm sample add 10 ml of conc. Hydrochloric acid heat on a hot plate
to dissolve the sample. Add more acid if necessary. Cool and add 0.5 ml nitric acid,
evaporate to dryness and bake carefully. Cool, add 3 ml conc. hydrochloric acid
dilute with water boil and filter. Make the volume 100 ml use aliquot for further use.

Silicate Minerals : Take 0.10 gm sample in a teflon beaker. Moist the sample with
2-3 drops of water add 2 ml conc. HNO3 and 10 ml hydrofluoric acid (40%). Heat at
low temperature (~100 oC) and slowly evaporate to dryness. Add 1 ml nitric acid and
evaporate to dryness (repeat this step once more time). Then take up the residue in 5
ml nitric acid and make up the volume 100 ml by water. Use appropriate aliquot for
determination of phosphorus. Alternately sample can also be decomposed by fusion
with potassium pyrosulphate at very controlled temperature (i.e. it should not go
above 300 oC). Otherwise phosphorus may escape along with fumes. Take 0.1 gm
sample, add 0.5 gm K2S2O7 and fuse in temperature controlled conditions. Extract in
4M HNO3 and proceed as follows.

Procedure

Take 25 ml aliquot (~ 5 mg phosphorus per 25 ml) to a 100 ml.

Volumetric flask.

101
 Add 5 ml of 1:2 nitric acid solution.
Add 5 ml of ammonium vanadate solution.
Add 5 ml of ammonium molybdate solution, dilute with water up to the
mark and mix thoroughly and develop the colour.
Keep the solutions for 10 minutes and measure the absorbance at 460 nm.
Run a reagent blank.

Standard Calibration Curve

Take 1.0, 2.0, 3.0, 5.0 and 10.0 ml standard phosphorus solution (1 ml = 0.10
mg) in 100 ml volumetric flasks and run a blank also. Follow the steps 2 to 5. Plot
the calibration curve and compute the results.

xi. Determination of Small amount of Titanium

(TiO2 in silicate rocks, bauxite, clay, etc.)

Principle

A yellow coloured complex is formed by Ti(iv) with hydrogen peroxide in

sulphuric acid and phosphoric acid medium. The absorbance is measured at 400 nm.

Reagents

1. Standard TiO2 solution. Roast 1.0 gm of titanium dioxide (TiO2) at

900oC for 30 minutes. Transfer TiO2 to 400 ml beaker. Add 20 ml conc.
H2SO4 and 5.0 gm ammonium sulphate. Heat on hot plate at moderate
temperature till a clear solution forms. Cool to room temperature and add
100 ml of water carefully and dilute to 1 litre. 1 ml = 1 mg TiO2.
Alternately, fume 3.5005 gm of K2TiF6 with 20 ml H2SO4 cool to room
temperature and add 100 ml of water carefully. Finally make volume to 1
litre 1 ml = 1 mg TiO2.

2. Sulphuric acid : A.R. grade

3. Orthophosphoric acid : A.R. grade
4. Hydrogen per oxide solution : 20 volume

Decomposition

1.0 gm sample is fused with 0.5 gm of potassium pyrosulphate in a test tube.

Extract the mass with 1:10 sulphuric acid solution.

Alternately take direct appropriate aliquot from mother liquor after silica
estimation add 10 ml 1:1 sulphuric acid, fume off completely till syrapy mass remains
cool and extract in 1:10 sulphuric acid solution.

Procedure

Take suitable aliquot in 100 ml volumetric flask in sulphuric acid medium.

102
 Add 10 ml of 1:1 orthophosphoric acid which forms colourless complex
with iron.
Add 2 ml of hydrogen peroxide (30% solution)
Develop the colour. Make up the volume to 100 ml with water.
Measure the absorbance at 400 nm. Run a reagent blank.

Standard Calibration Curve

Take 0.5, 1.0, 1.5, 2.0, 4.0, 6.0 and 10.0 ml standard TiO2 solution in 100 ml
volumetric flasks. Follow the steps from 2 to 5. Plot the calibration curve and
compute the results.

xii. Spectro-photometric method for the Determination of traces of Germanium

in ore and beneficiation products of Lead and Zinc.

Scope

This method is applicable to sulphide ores and beneficiation products of zinc

and lead. The lowest level of GeO2 determinable is 100 ppm.

Reagents and Standards

1. Quality of reagents : Unless otherwise specified analytical grade reagents

and distilled water should be used.
2. Standard germanium solution - Dissolve 0.1000 gm pure GeO2
(99.99%) in 20 ml of 10% sodium hydroxide dilute to 100 ml with water.
Prepare the 10 mg GeO2/ml from the above stock solution by adopting
suitable dilution in 50% hydro chloric acid.
3. Hydroxylamine hydrochloride (10%) solution Dissolve 10 g.
hydroxylamine hydrochloride in 100 ml. water.
4. Gum arabica (0.5%): To boiling water add 0.500 g gum-arabica, stir till
it is completely dissolved cool and filter it, if necessary. This solution
should be prepared fresh.
5. Phenyl fluorine reagent (0.06%) To 60 mg. of phenyl fluorine in a
beaker (250 ml) add 80 ml Ethyl alcohol followed by 5 ml. 1 : 6 sulphuric
acid. Dissolve and transfer quantitatively to 100 ml. Volumetric flask.
Make up the volume with alcohol.

Spectrophotometer: UV = visible spectrophotometer with tungsten lamp source is

used.

Procedure

(A) Decomposition of Sample.

Heat a sample weighing 0.5-1.0 g in a porcelain dish in a muffle furnace at

400-500oC. Trnasfer the residue to a platinum dish. Treat the sample with
5 ml sulphuric acid, 1 ml conc. nitric acid and 10 ml of hydrofluoric acid.

103
 Heat it and evaporate to fumes, avoid prolonged or strong fuming with
sulphuric acid. Cool and add 20 ml water and heat to near boiling for a
few minutes. Cool and filter through Watman filter paper No.42, wash
residue (lead sulphate and barium sulphate, etc.). with 1% sulphuric acid
solution. Use filtrate for spectro-photometric determination.
Alternatively, transfer 1.000 g sample (ground to 150 mesh) into a nickel
crucible containing 4-5 g sodium peroxide. Keep the crucible on a wire
gauge and heat by a burner till peroxide melts. Fuse the sample with flux
for 5-7 minutes. Cool the melt in crucible. Transfer crucible to a 250 ml
beaker containing 50 ml hot water. Boil, remove the crucible from beaker
and wash with water. Evaporate the solution to 20 ml volume and transfer
to the distillation flask. Assemble distillation unit and keep the receiving
cylinder in ice-bath. Add 60 ml conc. hydrochloric acid. Boil and collect
45 ml of the distillate in a 6 N hydrochloric acid in cylinder. Make the
volume 100 ml.

(A) Development of colour

For (i) Take sufficient aliquot containing 10-50 mg. Germanium in a 150
ml separating funnel. Add conc. hydrochloric acid to attain an acid concentration
of 9 M, mix and cool. Add 10 ml of carbontetrachloride, shake vigorously for two
minutes. Transfer the organic layer to a 50 ml beaker, and repeat the extraction
twice with 10 ml portion of carbontetrachloride. Combine the organic extracts in
a 150 ml separatory funnel. Add 5 ml water containing 1-2 drops of 0.01 M
sodium hydroxide shake for 2 minutes. Transfer aqueous phase to a 50 ml
volumetric flask. Repeat extraction of organic phase twice with 5 ml water
containing 1-2 drops of sodium hydroxide (0.01 M) and transfer to volumetric
flask. Add 10 ml 6 M hydrochloric acid to the solution and mix.

For (ii) Take 10 ml aliquot into a 50 ml volumetric flask.

Add 10 ml hydroxylamine solution and 5 ml gum arabica solution to the

solution in 50 ml volumetric flask. Dilute to 40 ml with water and cool in an ice bath
for 15 minutes. Add 2.5 ml phenyl fluorine solution and mix. Allow the solutin to
attain room temperature (1 hour) and make up to the mark with water and mix.
Measure the absorbance of the complex at 510 nm against reagent blank. Compute
the GeO2 content present in the sample from the calibration curve.

Calibration curve :

Take 1.0, 2.0, 3.0, 4.0 and 5 ml. of standard GeO2 (10 Mg/ml) in 50 ml
volumetric flask. Add 10.0, 9.0, 8.0, 7.0, 6.0 and 5.0 ml of 6 N hydrochloric acid,
respectively. Add 10 ml hydroxylamine solution, 5 ml. Gum arabica solution and
dilute to 40 ml. Cool in ice-bath. Remove the flask from ice bath. Add 2.5 ml of
phenyl fluorine solution, mix and allow to cool to room temperature (1 hour). Make
up the volume with water and measure the absorbance of the standards against the
reagent blank at 510 nm. Draw the calibration curve by plotting the absorbance

104
against the GeO2 content. An absorbance of 0.149 unit observed for 10 Mg GeO2/50
ml solution.

Calculation

% GeO2 = GeO2 Mg x Dilution factor x 100

106 x Weight of sample (g)

or GeO2 (ppm) = GeO2 Mg Reading x Dilution factor

Sample Weight (g)

Dilution factor = Volume of solution made up

Volume of aliquot taken

xiii. Spectrophotometric Determination of Gallium in Zinc and Lead ores and

beneficiation products.

Scope

The method is applicable for determination of gallium in ore and mineral

dressing products of lead and zinc.
Principle

Rhodamine-B reacts with chlorogallate anion to produce red-colour complex

extractable in 3:1 chloroform carbon tetrachloride. The optical density of red
chlorogallate-rhodamine-B complex in organic phase is measured at 565 nm.

Reagents and Standards

1. Titanous chloride solution (20%) Treat pure titanium metal piece with
hot conc. hydrochloric acid. Keep solution over titanium metal.
2. Chloroform: Carbon tetrachloride (3:1) : Mix 150 ml chloroform with
50 ml carbon tetrachloride.
3. Rhodamine-B : Dissolve 0.500 g rhodamine-B in 100 ml 6N hydrochloric
acid.
4. Di-isopropyl ether : Pre extracted with 6N hydrochloric acid.
5. Standard gallium stock solution Dissolve pure gallium chloride in 10
ml 6N hydrochloric acid. Transfer to a 100 ml volumetric flask, add 5 ml
conc. hydrochloric acid and dilute to mark with water. This solution
contains 1.0 mg Ga/ml in 6N hydrochloric acid.
6. Standard Gallium working solution Prepare a dilute solution
containing 1 Mg Ga/ml by serial dilution of the stock solution with 6N
hydrochloric acid.
7. Sodium chloride solution (1%) : Dissolve 10 g sodium chloride in 100
ml water.

Procedure

(i) Decomposition of Sample :

105
 Weigh 1-2 g of sample (-150 mesh) into a porcelain dish and roast at 500 oC
for 3 hours in a muffle furnace. Cool the dish transfer the sample into a 250 ml
beaker. Add 50 ml aquaregia, cover the beaker and keep aside for half an hour.
Digest on steam bath for half an hour. Remove the watch glass. Wash with water
and evaporate the solution to dryness with occasional mixing. Add 50 ml of 6 M
hydrochloric acid, boil to dissolve the residue. Filter through Whatman filter paper
No.40 containing a little pulp into a 100 ml volumetric flask. Wash the residue with 6
M hydrochloric acid make up the volume 100 ml maintaining 7 N hydrochloric acid
concentration.

(ii) Separation of Gallium

Take 10 ml aliquot in a 100 ml separatory funner, add 2 ml titanous chloride

solution, mix after 5 minutes, add 10 ml di-isopropylether and shake for 1 minute.
Run the lower aqueous phase into another separatory funnel and shake aqueous phase
with 5 ml of di-isopropylether. Repeat extraction twice with 5 ml portion of di
isopropyl ether. Discard aqueous phase. Wash combined organic extract with a
mixture of in hydrochloric acid and 0.5 ml titanous chloride solution twice. Transfer
organic layer to a 100 ml beaker. Add 0.3 ml of sodium chloride solution and
evaporate ether on steam bath. Take up residue in 5 ml M HCl and transfer to a 100
ml separating funnel. Dilute it to 25 ml keeping acid concentration to 6N
hydrochloric acid. Add 0.4 ml rhodamine solution and 10 ml of 3:1 chloroform
carbonate trachloride. Shake for 1 minute. The lower organic layer is transferred to
an absorption cell of spectrophotometer. Read absorbance of red complex at 56 nm
against a reagent blank in organic phase. Calculate gallium content from calibration
curve.

Calibration Graph

Take 0.0, 1.0, 2.0, 3.0, 4.0 and 5 ml of standard gallium solution (1 Mg/ml) in
separatory funnels. Add 25, 24, 23, 22, 21 and 20 ml of 6 M HCl, respectively. Add
0.4 ml rhodamine-B solution and 10 ml of chloroform carbon tetrachloride mixture.
Shake for 1 minute. Let separate organic layer, filter and read absorbance at 565 nm.
Construct a calibration graph by plotting absorbance against Mg gallium
concentration. An absorbance of 0.08 units is found for 1 mg gallium/10 ml volume.
Calculation

Gallium Mg/ml = Mg gallium reading x Dilution

Sample weight (g)

106
Preparation of Reagents

1. Acid mixture - To 60 ml water, add 15 ml conc. H2SO4 and 15 ml

H3PO4, cool and dilute to 1 litre.

2. Acetic Acid Ammonium Acetate Buffer solution pH 5.5 -Take 200 g. Of

ammonium acetate and 30 ml. acetic acid, make the volume to one litre. Check the pH
with pH meter or pH paper and adjust the pH 5.5 either by acetic acid or ammonia.

3. Ammonium Molybdenum solution 12% (W/V)-Dissolve 12 g. Ammonium

molybdate tetrahydrate (NH4)6 MO7O24.4H2O in a water and dilute to one litre. Allow
the solution to stand for one day and filter.

4. Bromine tetrachloride solution -Carbon tetrachlorite saturated with bromine.

5. Bromine potassium bromide solution -320 g of potassium bromide is

dissolved in just sufficient water and 200 ml bromine added. After mixing well, the
solution is diluted to 2 litre.

6. Buffer solution pH 9.5 -Dissolve 67.5 g of AR NH4 Cl in 300 ml water, add

570 ml NH4OH and dilute to one liter with distilled water.

7. Buffer solution (Monochloroacetic acid pH 2.9 3.1) Dissolve 18.9 g of

monochlora acetic acid in distilled water and dilute to 200 ml., neutralize 100 ml. to
phenolpthelein end point with NaOH and add to remaining 100 ml. Dilute to 500 ml.
with distilled water, check the pH with pH meter.

8. 2-2 biquindine 100 g in 500 ml. amyl alcohol

9. Citromolybdate reagent - Stir 54 g of AR MoO3 with 200 ml. distilled water,

add 11 g of NaOH gradually and stir it while heating until Molybdic anhydride is
dissolved. Dissolve 120 g of pure citric acid in 250-300 ml water and 140 ml. pure
HCl of Sp.Gr. 1.19 and add molybdate solution to the acid solution while stirring,
cool and filter through a pulp pad, if necessary, and dilute to one litre. The solution is
blue or green in colour. Add drop wise a dilute 0.5-1%. solution of KBrO3 until the
blue colour disappear.

10. Diphenyamine barium sulfonate -Dissolve 0.25 g in 100 ml. water

11. Dimethyglyoxime (sodium salt) 10% (W/V) in water

12. 1-5 diphenyl carbazide 0.25% -Dissolve 0.25 g of (C6H5NH.NH)2CO in 100

ml. 95% ethyl alcohol or 50% acetone or isopropyl alcohol.

13. H2SO4 2.5 M Add 130 ml. of conc. H2SO4 slowly while stirring to 800 ml.
of water. Allow the solution to cool and make up to one litre in a measuring
flask.

107
14. H2SO4 6 N Add cautiously 167 ml. of conc. H2SO4 to distilled water and
dilute to one litre.

15. Hydroquinone 1% (W/V) in water.

16. -nitroso- B naphthol solution is prepared in 1:1 acetic Acid.

17. Mercuric chloride Saturated solution in water (60-80 gm./litre)

18. 5% Mercuric chloride 50 g of HgCl2 in 1 litre.

19. Molybdate reagent Dissolve 50g of ammonium molybdate in water and

dilute to one litre.

20. Orthophenonthroline 0.25% in distilled water.

21. Oxalic acid 5% W/V Dissolve 50 g of oxalic acid in 500 ml. water and
dilute to one litre. Filter the solution if necessary. Always prepare fresh
solution.

22. Nitroso R salt (Sodium nitroso 2.hydroxy naphthalene 3, 6

disulphonate 0.2% aquous solution.

23. Potassium Thiocyanate (20%) Dissolve 20 g of potassium thiocyanate

in100 ml. water. This reagent should be prepared fresh daily.

24. Potassium hydroxide(20%) Dissolve 20 g of AR quality of AR KOH in

100ml. water.

25. Quinoline hydrochloride solution Take 60 ml. conc. HCl and 300-400 ml.
water in one litre beaker and warm it to 70-80 oC. Pour 50ml. synthetic pure
quinoline (free from reducing agent) in a thin stream into the dilute acid.
When quinoline has dissolved cool the solution and dilute to one litre, filter
through paper pulp.

26. Stannous chloride solution Dissolve 5 g of stannous chloride pure AR

quality in 25ml. conc. HCl and dilute to 100 ml.

27. Sodium citrate 250 g in one litre of distilled water.

28. SnCl2 2M Dissolve 113 gm of SnCl2(AR) dihydrate in conc. HCl and make
up to 250 ml. with conc. HCl.

29. Starch Solution Mix about 1 g of soluble starch with about 20 ml. of cold
water and add the mixture slowly to 80 ml. boiling water. Boil for a few
seconds. Prepare fresh solution when required.

30. Tartaric Acid Dissolve 75 g of tartaric acid in one litre of water.

108
31. Vanadate solution Dissolve 25 g of ammonium vanadate in boiling water
and cool the solution. Add 20 ml. conc. HNO3, cool and dilute to one litre.

32. Xylenol orange (0.2%) Dissolve 0.2 g of reagent in water, add 1 drop of
1:1 HCl and make up the volume to 100 ml.

109
Common acids and alkalies Useful data

HCl HBr HNO3 HF HClO4 H2SO4 H3PO4 CH3COOH NH4OH

Molecular 36.46 80.92 63.02 20.01 100.46 98.07 98.00 60.03 35.04
weight
Average 1.19 1.49 1.42 1.15 1.68 1.84 1.69 1.06 0.90
Sp.Gr. of
conc.reagent
Average % 36.0 48.0 69.5 48.0 71.0 96.0 85.0 99.5 58.6
present in
conc.reagent
Concentration 11.7 8.8 15.6 27.6 11.8 18.0 14.7 17.6 15.1
of
concentrated
reagent
(MOLARITY)
Ml. of 85.5 113.6 64.0 36.2 84.4 55.6 68.2 56.9 66.5
concentrated
reagent per
litre of 1 M
soln.
Grams of 0.715 0.985 0.552 1.19 1.77 1.44 1.0555 0.527
active 0.426
ingradient per
ml.
Standard Solution and Standardization

1. Alumnium solution Dissolve 0.2646 g of very thin aluminium foil or wire

in 10 ml. conc. HCl and make up to 500 ml.

1 ml = 1 mg. Al2O3

2. Arsenite solution 0.1N Dissolve 4.9455 g of As2O3 in a warm solution 2-3

gm. of pure NaOH in 30-40 ml. water. The solution is made slightly acidic
with HCl or H2SO4.

3. Bismuth solution Dissolve 0.25 g of bismuth (pure) metal by heating with

30 ml. of 30 of HNO3. Boil the solution gently for 10 min, then cool and
dilute to 250 ml. with water.

4. Calcium standard solution Weigh 1.7857 g of AR CaCO3 dried at 150oC

in a beaker, add 50 ml. water and dissolve in 10.6 ml. HCl added in small
increment. When dissolution is complete, boil the solution to remove CO2.
Cool the solution to room temperature, transfer to a litre volumetric flash and
dilute to the volume with water.

1 ml = 1 mg. CaO

5. Chromium solution Dissolve 2.8283 g of pure K2Cr2O7 in water and dilute

to a litre in a volumetric flash. Pipette 20 ml. of this solution into a 2 litre
volumetric flash and dilute to the mark with water.

1 ml = 0.01 mg. Cr.

6. EDTA solution (0.05 M) Dissolve 327.24 g of di-sodium salt of EDTA in a

water finally make up the volume to 20 l. It is advisable to allow EDTA
solution standing for couple of days.

7. Ferrous Ammonium sulphate (0.1 N) (NH4)2SO4 FeSO4 6H2O

Dissolve 39.213 g of ferrous ammonium sulphate in a water and add enough

H2SO4 to prevent hydrolysis (aliquot 10 ml. per litre). Standardize by
titration with standard dichromate solution.

8. Ferric Ammonium sulphate solution Fe2 (NH4)2SO4.24H2O

Dissolve 60 gm. of the salt in 600 ml. water acidified with 20 ml. of 1.1
H2SO4. Add KMnO4 solution until a pink colour begins to appear. Dilute the
solution to 2 litres. Standardize against 0.1N K2Cr2O7 solution to find out the
exact strength.

111
9. Fluoride solution Dissolve 2.211 g of sodium fluoride (AR) previously
dried at 120oC to constant weight in one litre of water in volumetric flash.

1 ml = 1 mg. of F

10. Hydrochloric Acid 0.1 N Take 9 ml. conc. HCl sp.gr. 1.19 and dilute to one
litre with DM water. This will give approximately 0.1 N hydrochloric acid
solution.

11. Iodine solution 0.1 N- Dissolve 20-25 g of KI in minimum water and add
12.7 g of Iodine (resublimed, theoretical value 12.692 gm) and dilute to 1000
ml. after all of the iodine has been dissolved in the small volume of KI
solution. Preserve in dark bottle.

12. Magnesium standard solution Dissolve 0.6033 g of Magnesium ribbon in

conc. HCl in a beaker and make up to one litre with distilled water.

1 ml = 1 mg. MgO

13. Manganese standard solution Dissolve electrolytic manganese metal in 40

ml conc. HNO3 by heating cool dilute to one litre in volumetric flask. Transfer
50 ml. of this solution to a one litre volumetric flask, add 50 ml HNO3 and
dilute to the volume.

1 ml = 0.05 mg of manganese

14. Molybdenum standard solution

Dissolve 0.075 g of AR MoO3 in dilute sodium hydroxide, dilute with water

and make slightly acidic with HCl and make up to 500 ml. with water.

1 ml = 0.0001 g of Mo
= 0.1 mg. of Mo

15. P2O5 standard solution Dry potassium hydrogen phosphate KH2PO4 at

110oC. Weight 0.9588 g and dissolve in water. Add 5 ml. HNO3 and dilute to
500 ml.

16. Potassium dichromate solution 0.1 N

Dry AR quality potassium dichromate at 105-110oC cool in a desiccators and

weigh 4.904 g dissolve in water, add 0.5 ml dil.H2SO4 and make it one litre in
a volumetric flask.
It is necessary to standardize K2Cr2O7 solution against standard iron ore
solution.

112
17. Potassium permangnate solution Take 3.2 to 3.25 g of potassium per
mangnate and dissolve in one litre of hot water. After standing 12 hrs. or
longer the solution is filtered through glass wool in order to free it from
manganese dioxide which catalyzes the decomposition of the reagent.

18 Silica standard solution Fuse 0.1gm.of pure silica with 0.5 g of anhydrous
sodium carbonate in a platinum crucible, cool the melt. Dissolve in water and
dilute to one litre and store in polythene bottle.

1 ml = 0.1 mg. of SiO2

19 Sodium thiosulphate standard solution

Dissolve 25 g of sodium thiosulphate in hot distilled water that has been just
boiled to expel CO2. Add 0.1 g of sodium carbonate. Cool and make up to 1
litre. Addition of sodium carbonate increases the life of solution. Actually as
per the reaction i.e.

I2 + 2Na2S2O3 = 2 NaI + Na2S4O6

24.815 g of Na2S2O3 is required to prepare 0.1 N solution.

20 Silver nitrate standard solution

This solution contains 10.788 gm. of silver or 16.989 g of silver nitrate per
litre. The silver nitrate dried at 120 oC. The required weight of the latter may
be dissolved in HNO3 and make up to one litre. It is standardized against pure
NaCl solution (0.1 N).

21 Sodium Tungstate solution (0.5 N)

Dissolve 16.5 gm of Na2WO4.2H2O in water and dilute to 100 ml.

22 Thorium nitrate standard solution

Weigh 13.806 g of thorium nitrate Th(NO3)4.4H2O dissolve in water and

make up to one litre. Mix well standardize against fluoride solution.

23 Vanadium standard solution

Dissolve 1.785 g of pure V2O5 previously ignited at 500 oC in a slight excess

of sodium hydroxide, add slight excess of H2SO4 and dilute to one litre. This
solution contains 1 mg. of vanadium per ml.

24 Zinc Acetate solution (Approximately 0.05 M)

113
 Dissolve 50 g of AR quality zinc acetate in 500 ml. of hot water and make up
the volume to one litre with distilled water. Add two or three drops of dilute
acetic acid to make the solution clear.

Standardization of HCl solution

Weigh 0.2g of dried sodium carbonate (at 105oC for 30 minutes) in 250ml.
beaker. Add 100 ml. DM water. Shake with glass rod to dissolve the solids. Add 2-3 drips
of methyl orange indicator solution. Titrate this against the hydrochloric acid solution.
The colour changes from yellow to orange.

Normality of HCl = weight of Na2CO3 x 1000

Equivalent wt. of Na2CO3 x titer value(ml)

Al2O3 equivalent of zinc acetate solution

Take 5ml standard aluminium solution (equivalent of 5 mg. of Al2O3) in a beaker.

Add 25 ml. EDTA solution and make up the volume to nearly 200 ml.Adjust the pH to 5-
5.5 by adding buffer and boil for 10 minutes. After cooling add 50 ml, 5.5 pH sodium
acetate buffer boil for 10 minutes and after cooling add a few drops of xylenol orange
indicator when yellow colour will develop. Titrate with zinc acetate solution to the purple
end point.

1 ml zinc acetate solution = 5 g Al2O3

(A-B) X 1000

Where

A = ml zinc acetate equivalent to 25 ml. of EDTA soln.

B = ml zinc acetate solution required for titration after adding 25 ml. EDTA
solution to the 5 ml standard Al2O3 solution.

Standardization of EDTA (0.05 M) for Pb:

The lead value of 1ml. EDTA solution is determined either from a synthetic or
Cu-Pb-Zn standard sample.

Standardization of EDTA for CaO & MgO

114
 Take 20-25 ml standard Ca solution in a beaker. Add a pinch of hydroxylamine
hydrochloride and 10ml. triethanal amine solution and 10-20 ml KOH solution and a few
drops of Patton and Reeders indicator. Also add 1 ml. standard magnesium solution. A
rose red colour will develop. Titrate the resulting solution with standard EDTA solution
till a blue colour is detained. Note the reading. The EDTA used up is due to CaO only.

Molarity of EDTA solution (M EDTA) = Mass of calcium in aliquot taken (g)

0.04008 x V

Where V = volume (ml) of EDTA solution required by the calcium.

Calcium equivalent (mg/ml) of EDTA solution

(Ca) Eq = M EDTA x 40.08

or

Mass of calcium in aliquot taken (mg)

V

Where V is as stated above

% Ca in a sample

= Vs x Ca(Eq) x 100
S

where Vs = volume (ml) of EDTA solution required for the titration of Ca.

S = Mass of the sample with aliquot.

V Mg = Vt-Vs

Where VT = Volume (ml) of EDTA solution required for the titration of calcium
plus magnesium.

Vs & S are as described above.

Similarly for magnesium take standard magnesium solution (20-25 ml) in a

beaker. Add nearly 50 ml. distilled water and 25 ml. buffer solution. Add a spetula of
hydroxylazmine hydrochloride and 5-10 ml. triethanolamine and then a few drops of
Eriochrome black T indicator. A port wise colour will develop. Titrate with EDTA till a
blye black colour end point is obtained. Take the reading.

The EDTA used up is due to CaO + MgO

Magnesium equivalent (mg/ml) of EDTA solution

115
 (Mg)Eq = M EDTA x 24.31

Or

= Mass of Magnesium in aliquot taken (mg)

Vmg

Where Vmg = Volume of EDTA solution required by magnesium.

It is preferable to find out 1 ml. EDTA equivalent of CaO & MgO by taking
standard sample of dolomite or limestone.

KMnO4 Standardization against Sodium Oxalate

Eq.Wt. = 67 dried at 105oC

Transfer 0.1 gm. of pure sodium oxalate dried at 105-110oC for 1-2 hr. to a 250
ml. beaker or conical flask containing 15-20 ml. 10 of H2SO4 and about 100 ml. water
which was previously boiled for 10 minutes and cool to room temperature. Shake with
glass rod or swirl if it is in a flask until the oxalate is dissolved, then heat the resulting
solution 70-80oC and titrate with standard potassium permanganate solution until a faint
pink colour persists for about 30 seconds.

N = Wt of sodium oxalate x 1000

Eq. Wt. of sodium oxalate x T.V.
T.V. = Titre value.

Standardization of Iodine solution:

Aliquot portion are titrated with standard thiosulphate or with standard arsenite.
Alternatively separate weighed portion of primary standard arsenious oxide may be
dissolved and titrated.
As2O3 Eq.wt. = 49.455 gm.

Sodium thiosulphate solution: (0.1 N)

Sodium thiosulphate reacts with iodine as follows:

I2 + Na2S2O3 = 2 NaI + Na2S4O6

So 24.815 gm. of Na2S2O3.5H2O is required to prepare 0.1 N solution

116
 Standardization of Sodium thiosulphate solution:

It is standardized against standard dichromate solution.

Take 4.9035 gm of K2Cr2O7 per litre. Take an appropriate volume of this 0.1 N
solution into water containing 2-3 gm. of KI and 10 ml. dil. HCl per 200 ml. The acid
solution should be freed of dissolved air. The iodine liberated is titrated with thiosulphate
solution and the normality is determined.

117
 Appendix 1
1.7 General safety precautions

Precautions for safety are essential in an analytical laboratory, where corrosive

acids, caustic alkalies, hazardous chemicals, brittle glassware, etc. are handled as a daily
routine. It is the responsibility of every worker to be cautious and vigilant to avoid acts
that may lead to injury to himself or to his colleagues. An attempt is made to provide a
few basic guidelines for safety.

A. Personal wear

Loose clothing should not be worn, as it may knock down glassware, spurting
acids and chemicals or catch fire from the numerous burners in the laboratory.
Laboratory coats or aprons should be used as they protect the dress from acid holes or
contamination with chemicals. Ladies should wear long overcoats to protect their saris.
The hair should be well tied up and should not hang loosely. Plastic or rubber apron may
be used, when handling large quantities of acids or corrosive chemicals.

It is advisable to use rubber gloves when handling corrosive liquids like bromine,
fuming nitric acid, hydro-fluoric acid, etc. Asbestos gloves should e used, while
removing crucibles from furnaces. If, by accident, some acids or chemicals spill over the
dress, the clothing should be removed and a shower taken to guard against the possibility
of reaction with skin. Safety glasses are also recommended for eye protection. Shoes are
to be worn as footwear.

B. Handling of glassware

Glassware presents an hazard due to the ease with which it is broken by thermal
or physical shock and the razor-sharp edge which the broken glass presents. Small
beakers should be carried by gripping around the sides and not by the top edge. While
using pipette, the worker should be very attentive not to draw the solution inside the
mouth. In case of poisonous chemicals, the pipette should be filled by vacuum suction
and not by mouth. While heating the test tube, the proper holder should be used and test
tube mouth should not point at anyone, as the material may spurt out. Rubber tubing on
glass tubes should not be pulled out with hand. Instead it should be cut out with a sharp
knife. Stiff stopcock of burettes should be removed by light tapping or by warming it
over gentle heat and not by application of force. Patience is essential if breakage and
injury are to be avoided. All the broken glassware should be discarded into a separate
metal container for disposal.

C. Handling of chemicals

Virtually, all chemicals react with human system. Hence, the analyst should
handle the chemicals with great care.

118
 Strong oxidizing agents such as perchlorates, sodium peroxide can cause fire or
explosion when reacted with some organic materials. These reagents must be handled
carefully. Do not use per chlorate for drying organic materials.

While fusing with sodium peroxide in a nickel crucible, a tray containing thick
layer of sand should be kept nearby. If during fusion, the crucible develops a hole, it
should be plunged into the sand. It should not be thrown away or plunged into water, as
serious explosion may occur. Fuming with acids should Invariably be done in the fume
cupboard and not on the work benches.

Acids should not be stored along with alkalis like ammonia. Concentrated
sulphuric acid bottles should be kept separate and handled with care. Perchloric acid
which is commonly used nowadays, should be kept in a lead lined box filled with sand
and away from any organic materials. If fuming nitric acid is splashed over inflammable
materials such as straw, wood, etc., they will immediately catch fire. Such acids should
be kept in a box containing sand. Finely divided zinc or sulphur, if thrown in
wastebasket, may cause delayed fire due to spontaneous combustion.

Potassium cyanide is widely used for limestone analysis. It should always be kept
under lock and key. Cyanide solution should always be used in the alkaline medium.
Cyanide solution should never be used in acidic medium. The waste solution should be
collected in a bucket and cyanide ions should be destroyed by adding either bleaching
powder or chlorine in alkaline medium, before disposal. On disposal, it should be
flushed with plenty of water. Under no circumstance, cyanide solution should be drawn
by mouth into a pipette.

Every container of chemicals must be clearly labeled. Abbreviation should be

avoided as far as practicable. The label should be on the container itself, not on the lid.

D. Handling of compressed gas cylinders

Acetylene and Nitrous oxide gases are used with atomic absorption
spectrophotometer. While installing a new cylinder, the leakage of the gas should always
be tested with a solution of soap. Cylinder having leakage should immediately be
returned. The room should be provided with adequate exhaust arrangements.

While using nitrous oxide, ice condenses in the tube after a while. This may
block the gas and lead to explosion. A heating tape should be wound round the outlet of
the gas. Great precautions should be taken while working with this gas, as its inhalation
is dangerous. Stiff valves should be opened with care. If the cylinder valve cannot be
operated by hand, it is unwise to resort to the use of hammers. On no account should oil
or grease be used in an attempt to ease the working of the valve.

119
E. Eating and drinking in the laboratory

Food and beverage should never be consumed or stored in an analytical

laboratory. Warming the lunch in an oven or over burners or taking cold water from the
refrigerator wherein chemicals are stored should never be practiced. Beaker, conical
flask, etc. should never be used for tea, coffee, or other beverages. Such beakers and
conical flasks might be contaminated with poisonous chemicals. Smoking in a laboratory
is also inadvisable and particularly in airconditioned rooms, where sophisticated
instruments are in use.

F. Working along in the laboratory

Working alone in a laboratory is not desirable as an injury or illness could occur

and help might not be available readily. Even the simplest of experiments have been
known to cause serious accidents.

120
 Appendix II

Titre equivalents per ml. of standard solution

1 ml N KMnO4 0.05585 gm. Fe

1 ml N K2Cr2O7 0.07185 gm. FeO
0.07985 gm. Fe2O3
1 N KMnO4 0.01648 gm Mn (Volhards 3/10 Mn)
0.01029 gm. Mn (Bismuthete per sulphate
calorimetric per iodate)
0.04347 gm. MnO2 (FeSO4, Oxalic acid
Method MnO2/2)
0.02804 gm. CaO
0.032 gm. Mo by Jones reductor Mo vi -
Moiii
0.02534 gm. Cr2O3 (Cr2O3/6)
0.06057 gm Sb
0.0435 gm MnO2
0.07490 TiO2
1 ml. N Na2S2O3 0.06357 gm. Cu
0.06907 gm. Pb (Pb/5)
0.01603 gm S By evolution method
0.04395 gm FeS
1 ml. of N Iodine 0.05955 gm. Sn
0.03746 gm. As
1 ml. of N HNO3 0.001349 gm. P Nitromolybdate
0.003086 gm. P2O5 method
1 ml. of N HCl 0.001193 gm. P Citromolybdate
0.002733 gm. P2O5 method
1 ml. of N Ferric Amm. Sulphate 0.08 gm. TiO2

121
 Appendix III

Conversion factors

FROM TO MULTIPLY BY
Al2O3 Al 0.5293
AlPO4 Al 0.2212
AlPO4 Al2O3 0.4180
BaCO3 Ba 0.6960
BaSO4 S 0.1374
CaC2O4.H2O CaO 0.3838
Fe Fe2O3 1.430
Fe FeO 1.286
FeO Fe2O3 1.111
Mg2P2O7 MgO 0.3623
Mg2P2O7 P 0.2783
P P2O5 2.2914
WO3 W 0.7930
ZnS Zn 0.6709
ZnS ZnO 0.8351
Mn MnO2 1.582
Mn MnO 1.29
ZnO Zn 0.8030
FeO Fe 0.7773
Fe S(for FeS2) 1.145
Fe FePO4 0.1508
BaSO4 SO3 0.3430
BaSO4 BaO 0.6570

122
2. Methods of Analysis Using X-Ray
Fluorescence(XRF) Analyser

2.1 X-RAY FLUORESCENCE SPECTROMETRY

In recent years X-ray fluorescence (XRF) technique has emerged as a most potent
analytical tool in research as well as continuous production control. Hardly any other
analytical technique is so universally suited for qualitative as well as quantitative
determination as the XRF analysis.

In modern X-ray fluorescence analysis sample is irradiated by polychromatic

radiation from a x-ray tube. In this process, elements in the sample are excited to emit
their characteristic x-ray radiations. The secondary (fluorescence) radiation consists of
several lines, which are diffracted by a crystal (analyzing crystal) and separated into
individual wavelengths in wavelength dispersive XRF spectrometer. In energy dipersive
XRF spectrometer the quality and quantity of the radiation is simultaneously measured by
a special type detector such PIN-Si and Si-Li detectors.

In qualitative analysis, X-ray fluorescence analysis has proved to be a very

versatile tool. An X-ray scan requires less than two hours to identify the element present
in an unknown sample in WDXRF and few minutes in EDXRF.

In quantitative analysis not only the wavelength but also the intensity of emitted
radiation has to be measured, larger the relative intensity of the radiation higher is the
content of respective element in the sample. For accurate quantitative analysis matching
standards (mineralogical/structural match) are used to establish the relationship between
the concentration and the fluorescent intensity. The relation is not very linear.Due to the
interference of various elements; it may reduce or enhance the intensity of an element
under examination. Thus, a good linear relationship between fluorescent radiation and
concentration is not possible unless the inter-element correction is incorporated for
correcting the fluorescent yield of the element under examination.

X-ray fluorescence technique is suitable to analyse as low as a few parts per

million (ppm) to 100%. Pre-concentration technique helps to handle samples in parts per
billion concentration. Now the commercially available instruments can analyse all
elements from lithium to plutonium. This technique can analyse solid as well as liquids.

X-ray fluorescence technique is very useful for elemental analysis and is

becoming popular with it qualities of simplicity, utility, versatility, flexibility
reproducibility, speed accuracy and reliability.

123
Interaction of X-rays with matter

When a specimen is irradiated with X-rays the following interaction takes place
and the remainder of x-rays emerges out.

(a) Absorption
(b) Ionization, photoelectric effect
(c) Scatter
(d) Diffraction

All these effects take place at the same time.

a. Absorption : In case of absorption Lamberts Law is obeyed and then.

I = Ioe- d

Where Io = Incident X-ray

I = Emergent X-rays
= Mass absorption coefficient
= Density
d = Thickness of absorber

Mass absorption co-efficient is dependent on wavelength and atomic number of the

element.

124
 a. Ionization, photoelectric effect: Ionization is a process where an electron is
removed from, or added to, the electronic cloud of an atom. X-ray photons are capable
of entering the inner orbit of an atom and eject out an electron due to its impact. In this
process the electron is removed from K, L or M orbit, and this gap is immediately filled
by an electron from the adjoining orbit. During the process of filling up of vacancy of
the electron which is in the higher energy orbit, it losses its excess energy in the form of
electromagnetic radiation. As the energy difference between the two orbits of an atom is
always constant, hence the radiation given out, which corresponds to the energy
difference, will also be same. Therefore, this radiation becomes a primary characteristic
of an atom. The loss of energy and it conversion into its characteristic radiation is given
by the equation.
E = (E-E1) h
Where E E1 = the energy difference
h = Plancks constant
= Frequency of radiation given out.
The reason for several spectral lines from an element is due to filling up of the vacancy

by an electron from one of the higher orbits according to certain selection rules.
The two major emission spectra are distinguished namely, the K spectrum (or K
series) and the L-spectrum (or L series). These spectra are named, respectively, after K
and L orbits. An element emits K spectrum when it s K orbit is excited. The K spectrum
has two major lines K and K. The L spectrum has two major lines L and L and series
of several other lines which are detected when the heavier element, which gives L lines is
in major quantity. The probability diagram below gives a picture of radiation likely to be
named and sources of its occurrence.

125
 K and L lines are more intense than their respective K and L lines. They also
bear a constant ratio between themselves, i.e.

K = constant or
K

L = constant
L

The fluorescent yield depends on the intensity of primary X-rays, which are
striking the sample and the atomic number. Maximum fluorescent yield for a particular
element can be obtained by proper choice of kVmA setting, is discussed in the following
paragraph.

The relative fluorescent yield for the same intensity of incident X-rays is given
below:

126
b. Scatter : It should be noted that no mention has been made of continuous
spectrum emitted by fluorescence. There is no continuous spectrum excited because the
primary X-rays do not lose their energy in a continuous fashion analogous to deceleration
of electron in X-ray production by an X-ray tube. If this is true, then, there should be
discrete peak at the characteristic position but it is not so, but a continuous background
intensity is present. This is due to the scatter of primary radiation by the specimen. The
collision between the X-ray photons and specimen may be elastic or non-elastic,
consequent to which coherent scattering (Rayleigh scatter) and incoherent scattering
(Compton scatter) are observed. When the collision is elastic, there is no loss of energy
and hence, the wavelength of coherent scattering will be that of incident (primary) X-
rays. In case of non-elastic collision there is a slight loss of energy, mostly in the form of
heat energy, hence an incoherent scattering will follow the Rayleigh scattering and
wavelength of this scatter will be slightly longer than the primary incident X-rays.

Intensity of Compton scattering increases for shorter wavelength and decreasing mass
absorption co-efficient. Therefore, in case of Cr tube the Compton scatter will be small
compared with that in Rh-tube, this illustrated below :

127
 Rayleigh scatter is also recognized as tube line. Second order lines of the tube are
also observed. In case of quantitative estimation, for line overlap by a tube line, other
less prominent peak is used for analysis or preferably a tube where this line is free
from overlap by tube line.

d. Diffraction : Diffraction is a phenomenon observed due to bending of light

around an edge. In X-ray diffraction, a crystal is used for the purpose. The tiny
nucleons act as an edge and subsequently the light is bent. In an X-ray diffractometer
the sample is irradiated with X-rays of known wavelength and sample is observed,
subsequently, d and h,k,l, values are obtained and consequently the crystal structure of
the sample is found out. An X-ray fluorescence spectrometry is exactly a reverse
analytical technique where the polychromatic beam of X-ray falls on a crystal of known
geometry, d value and then, in quantitative estimation the intensity of such is
measured. When a crystal is irradiated with a polychromatic beam of X-rays a
diffraction pattern is observed. It obeys Braggs Law.

n = 2dSin
, is the wavelength.
d, is the interplainer space,
, is the Braggs angle
n, is the order of spectrum

128
In qualitative estimation wavelength is found out.

In X-ray fluorescence technique first order spectrum is used. Hence, n will be equal to
one. Then

= 2dSin

In the above equation, if any of the two parameters is known then the unknown can be
calculated.

In quantitative X-ray fluorescence technique angle is used for setting a gonimeter and
then to measure the intensity (I) of the radiation.

Resolution in case of EDXRF

In an EDXRF the X-ray detector itself acts as the depressive agent. The detector is
generally a lithium drifted silicon (Si-Li) detector, which is a proportional detector of
high intrinsic resolution. The resolution of the detector is typically 160-180 eV. When
an X-ray photon is stopped by the Si-Li detector a cloud of ionization is generated in the
form of electron-hole pairs, the number of electron-hole pairs or charge produced is
proportional to the energy of X-ray photon, the charge is amplified to produce a voltage
pulse that is proportional to the original X-ray photon energy.

Thus, when a range of photon energies is incident upon the detector an equivalent range
of voltage pulses are produced as detector output. A multichannel analyzer (MCA) is
used to sort the arising pulse to produce a histogram representation of the X-ray energy
spectrum.

QUALITATIVE ESTIMATION

Qualitative estimation of a geological sample by X-ray fluorescence technique is

very fast and accurate. Even relative quantities of various elements present can be
estimated. As the geological sample is not a discrete sample which may have elements of
particular origin, so the exact presence of any element cannot be predicted. Therefore, an

129
X-ray fluorescence qualitative identification is of great interest. A careful study and a
gradual experience help in accurate qualitative estimation. X-40 software developed by
Philips, Netherlands or Uniquont is very useful for identification of various elements in
simple samples such as exploration sample. These automatic recorders use K . K or L .
L lines for identification of the elements present. Complex samples or concentrates pose
problems to these systems. In analysis of complex samples careful observation of the
scan is required and the analyst has to use his skill for it interpretation.

A simple procedure for peak identification in qualitative analysis is described

below :

1. Mark tube lines and Compton scatter before identifying elemental peaks.
2. Start with highest intensity or angle of the scan and mark K or L peak with
respect to its angular position about presumed element.
3. Verify the correctness of this presumed identification by presence of other peak
of the same element (K and K lines L . L and L lines M lines). Take into
consideration the relative intensity of various lines of the same element. If these
peaks are not present or the relative Intensities (after making correction for
abnormalities discussed latter) are not comparable then the presumed element is
absent. Repeak from step 2 to identify the peak with a different presumed
element. The probable associations in geological samples, ore dressing products
and concentrates should also be taken into account for the above purpose.
4. If the identification is positive, mark all peaks of that element in the spectrum.
5. Continue with step 2 for the next highest intensity or angle, until all peaks are
identified.

A simple X-ray scan where there is no interference from other elements present will
have relative K , K , L and L peaks. The intensity of K line is approximately four
times more than that of K line. A simple scan of a sample containing iron, copper and
zinc will appear as

130
Abnormalities in the intensity of peak In interpreting a qualitative X-ray scan the
following factors must be taken into account for accurate identification of the peak:

1. Source of the sample and earlier findings.

2. Line overlap by the tube line.
3. Line overlap by the line of other element.
4. Quantitative presence of heavy element.
5. Tube used (effect of target element).
6. Absorption edge of the counter gas.

Absorption co-efficient of argon as a function of wavelength. Cadmium recorded with an

argon filled proportional counter, the spectrum of cadmium, the absorption edge of the
counter gas is located between the K and L1 lines and hence L line is registered less
effectively than L1 line.

Sample preparation for XRF scan

Pressed powder samples are used for XRF scan. As there is no dilution, elements
present in trace level can easily be detected. Pre-concentration techniques are rarely
employed to eliminate the interfering elements and elements present in large quantities.
Pre-concentrations are usually accompanied with chemical changes in the sample but
they do not affect the detection of element of interest.

Generally, 5 to10 gm. of sample in 300 mesh is mixed with suitable binder and
then is pressed into a pellet of suitable diameter in a suitable holder (such as boric acid
cup, aluminum cup, cellulose cup, etc.).

131
2.2 CHOICE OF INSTRUMENTAL PARAMETERS

Detection limit and accuracy of analysis depends mostly on the choice of

instrumental parameters. Separation of interfering lines or analysis of two adjacent lines
largely depends on the instrumental parameters. Thus, instrumental parameters are very
important for a precise and accurate analysis. Choice of instrumental parameters depends
on the element to be analysed, choice of spectrometer alternatives, etc. This can be
illustrated in following way :

Choice of instrumental parameters

Element specific Application specific Instrument

Adjustment
KvmA X-ray tube Detector high
voltage
Filter Collimator mask
Collimator Spectrometer medium
Crystal, angle Flow detector window
Detector Selection of off
position
Window, PHS

Assembling of a channel includes all above parameters. Initially a channel can be

assembled as suggested by the operating manual. The ideal condition required for a
particular element for a particular unit can be achieved by following the instruments
operating manual.

1. kV & mA selection : A heavy element requires high kV and a lighter element

requires high mA. Accordingly, the selection of kV/mA close to the most possible
setting is first made and enter optimized in actual experiments.

Procedure : Set the channel for the element to be studied, increase mA gradually, and
measure counts for each setting. In no case, the power applied should exceed the power
of the tube. Now change kV by 5 units either side and repeat the observation with
increasing mA setting. Find the maximum for a set of kV. mV and include this value in
the channel setting

132
2. Filter : Filter selection is necessary for removal of interfering characteristic tube
lines, suppression of spectral impurities from the tube spectrum and attenuation of

133
intensities. A filter reduces the intensity of primary X-ray and proportionally the
secondary. Filter should be used only when essential.

3. Collimator : Normally, a coarse and fine collimator choice is available with the
various marketed instruments. A fine collimator gives a better line separation compared
to a coarse collimator, but it will yield a lower intensity. A coarse collimator can be
used for lighter elements (B to Ca) and a fine collimator for heavier elements (Ti to U).
This is only broad determined recommendation. Each case, however, is to be recording
the spectrum of a representative sample and thus containing the collimator choice. If
there is no interference from adjoining line, coarse collimator can well be used it will
also considerably improve the lowest detection limit.

Collimator, serves to select a parallel beam of radiation and is used to accurately provide
the angle which the resident fluorescent radiation forms with the analyzing crystal. The
longer and the finer the collimator, the smaller is the divergence of the selected beam
and the better is spectral resolution.

INFLUENCE OF COLLIMATOR CHOICE ON DISPERSION & INTENSITY

A fine collimator gives better separation of close lines, but yields a lower intensity.
Thus, the choice of collimator depends on the nature of element and also the various
interferences.

4. Crystals & angles : The fluorescent spectrum emitted by a sample contains

lines of different wavelengths. Analysis of spectrum according to wavelength and its
intensity is carried out with the aid of an analyzing crystal of known lattice parameter.
The wavelength of radiation can be determined by measuring the angle of diffraction,
2. According to Braggs equation.

n = 2dSin
In this equation n = 1, 2, 3 .. represents the order of diffraction. First order
diffraction is of greater interest and is generally used for analysis. Then, n = 1, and
Braggs equation reduces to.

n = 2dSin

134
 By measuring the Braggs angle, for a crystal of known d value, of the
radiation measured at an angle can easily be calculated. Now-a-days, JCPDS tables
are available and hence, no calculations are needed. In latest series of instruments with
JCPDS cards (computer) , the angle is automatically converted into its corresponding ,
the wavelength. The qualification of is of greater interest in qualitative analysis, but in
quantitative determinations, the intensity of such wave length, is measured at
corresponding angle and used for quantification of the element corresponding to the
characteristic value.

Inter-layer distance d lattice parameter is much significant in respect of crystal

and its capability to theoretically can have a maximum value of 90 o, and Sin90 = 1.
Thus, the Braggs equation reduces to.
= 2d

Therefore, a crystal can analyse only radiation of wavelength shorter than 2d

or equal to 2d, which is the limit. In commercial spectrometer, the maximum angle
which a gonimeter can attain is around 150 oC ( = 75o and Sin75 = 0.9659) and,
therefore, the practical ability of any crystal will be.

= 2d x 0.9659

= 1.9318 d.

Therefore, ability of any crystal will be slightly less than the theoretical one. In
case of crystal of larger d the shorter wavelengths will be concentrated near = 0o,
hence, they are generally used for larger wavelengths only. The crystal selection
depends on the nature of the element to be analysed, consequently, the wavelength of the
characteristic radiation.

The ability of crystal depressive power is illustrated in the following figure

135
Large number of crystals with flat and curved surface are available commercially and
their choice depends on users need. A list of commercially available crystals with their
d values and elemental range is given below:

Crystal type 2d in nm. Elemental range

LiF420 0.180 Ni-U
Topaz 0.271 V-U
LiF220 0.285 V-U
LiF200 0.402 K-U
NaCl 0.564 -
Si 0.627 -
Ge111 0.653 P-Cl
Graphite 002 0.671 P-Cl
InSb111 0.748 Si
PE002 0.874 Al-Cl
EddT020 0.880 Al-Cl
ADP-101 1.064 Mg
T1AP-100 2.575 O-Mg
*Px-1 5.1 O-Mg
*PX-2 12.0 B-C
*PX-3 20.0 B
*PX-4 12.0 C-(N.O)

136
 * Synthetic crystal developed by Philips, Netherlands. Similar synthetic crystals are available with
the instruments manufactures by other companies.

Depressive power of a crystal is inversely proportional to inter-planar distance d.

Higher the inter-planar distance lowers is the depressive power and vice versa.e.g.: 1
and 2 are the characteristic wavelengths of two elements and 1 and 2 are
corresponding Braggs angles.

Then 1 = 2dSin1
2 = 2dSin2

(1 - 2)= 2d (Sin1 - Sin2)

1 - 2 = Sin1 - Sin2
2d

As Sin is directly proportional to , then the difference of Sin 1 and Sin 2,

which will indirectly represent the depressive power of the crystal wavelength 1 and 2.
The ratio ((1 - 2) /d) will be higher for small value of d. Hence the depressive power
of crystal will be higher for smaller value of d.

Reflectivity is another significant character of a crystal. It is very important for

quantitative measurements and depends on the imperfections in a crystal. A truly
perfect crystal would give a very low diffracted intensity because of primary extinction
and would almost be of no use as an analyzing crystal. Natural and synthetic crystals
vary in their imperfections. As is explained in texts on crystallography, the imperfection
reduces the primary extinction and makes for far greater diffracted intensity. Higher the
reflectivity greater will be the diffracted intensity. Hence, it will improve the lower
detection limit. A comparison of depressive power and reflectivity of LiF220 (0.285
nm). and Li200 (0.402 nm.) is given in Figure.
.

137
 The choice of crystal depends on following three primary factors and a proper
choice can be made out of available crystals on the basis of element to be analysed and
its matrix (presence of other elements). (1) Element detection range, (2) Depressive
power and (3) Reflectivity.

Calibration of an angle : All commercially available instruments have facilities

to calibrate the angle for a particular element, which may slightly vary with the
instrumental condition and setting. This can be experimentally found out and used for
analysis. The angle position normally should not change with concentration but in many
cases such deviation is observed. In such cases, two different angles should be used for
these two different concentration range.

5. Detectors : Three types of counters are employed in modern X-ray fluorescence

analysis, namely, proportional, flow proportional and scintillation counters.

Because of the low dead time of proportional counters, high counting rates may be
recorded. The spectral sensitivity of proportional counter depends upon the wavelength
and is usually limited to 0.15 to 0.23 nm.

Flow proportional counter is basically a proportional counter whose window

consists of a very thin Mylar film (1 to 6). Thinner the Mylar film lesser will be the
absorption of incident X-rays. Flow counters are useful for detection of X-rays in the
range from 0.15 to 1 nm. They have very poor sensitivity below 0.05 nm. Analyzing
crystal and flow detectors are normally located in vacuum in order to reduce strong
absorption in air of the long wavelength radiation.

Scintillation counters have almost 100% theoretical sensitivity for all the X-ray
wavelengths. For the range from say 0.2 nm. and shorter they attain almost their
theoretical sensitivity. For longer wavelength, they are limited because of hygroscopic
nature of NaI which is the most common crystal presently used.

Solid state detectors have also appeared on the horizon of detection. Instruments
are now available with Si-Li detectors. These detectors need liquid nitrogen for storage
and because of this requirement they could not yet replace the conventional counters in

138
WDXRF spectrometers. Their sensitivity and response are better than the above other
counters.

L.S. Birks has recently developed HgI2 detectors as X-ray detector for low energy
radiation. No commercial instrument is available with this new type of detector. The
flow counter is efficient for low energy radiation (<9KeV) and the scintillation counter
for high energy radiation (>9KeV). For longer fluorescent radiation, flow counter is
normally recommended for middle range a combination of two can be used but for
shorter wavelength the scintillation counter is most suited.

6. Window Pulse Height Distribution : Amplitude of electrical pulse obtained

from proportional, flow proportional and scintillation counters are proportional to the
energies of the absorbed photons. Pulse height distribution of radiation may easily be
experimentally determined. Only a narrow range of pulse height is allowed to enter the
counting electronics and then the position of window is gradually varied and a graph is
plotted between the intensity and window position. From the graph the position of
window is fixed so as to include the whole wave for detection. There is a phenomenon
observed in case of flow-counter, for pulse height distribution curve known as escape
peak. Relative position of escape peak depends on atomic number of element. When
the energy of the entering X-ray is high enough, it may knock out one of the K electrons
of the noble gas rather than just ionize the atoms. When this happens, a K series X-ray
quantum of noble gas is emitted and, because the gas is quite transparent to its own
radiation, this emitted X-ray quantum must be subtracted from that of original X-ray
quantum and thus, the amplitude of that particular pulse is reduced. For practical
purposes the escape peak is included in determination. Thus, the window position
should be fixed in such a way so as to include the escape peak.

139
7. X-ray tube : The ability of an X-ray tube to excite fluorescent radiation depends
on the position of the emitted wavelength relative to the absorption edge of the elements
contained in a sample. The tube radiation consists of K and L lines that are
characteristic of the anode material employed. The wavelengths and the intensities of
emission must be considered in determining the choice of tube for a given application.

Performance of some of the commercially available tubes is discussed below:

1. Chromium : A general purpose tube with good light element capability also
suitable for some heavy elements. For sample containing chromium this tube can be
used with the insertion of a primary X-ray filter.

2. Scandium : This tube gives optimal excitation of atomic number below 21 (Sc).
Preferable to chromium tube where chromium and manganese need to be determined.
Gives comparable performance for heavy elements. Can be used to take over the
general role of chromium tube.

3. Rhodium tube : Another useful general purpose fully programmable tube,

combining good light element performance with high sensitivity for heavy elements.

4. Molybdenum tube : Useful for heavy elements and specially suitable for
rubidium, strontium, yttrium, uranium, thorium and the rare earth elements.

140
5. Gold and tungsten : These two tubes are for measurement of heavy elements
from atomic numbers 43 (technetium) to 71 (lutetium) and also for specific excitation,
such as, gold tube for Cu and Zn and tungsten for Fe and Ni.

6. Silver : Exhibits sensitivity comparable to rhodium tube for heavy elements.

Offers a useful alternative for elements where rhodium causes spectral interferences.

7. Dual Anode tubes : A significant break-through was the introduction of dual

anode tubes (DAT). It comprises a layer of chromium deposited on a gold substrate or
scandium on a molybdenum substrate. At low kV, DATs functions as a conventional
chromium or scandium tubes. But at higher voltage, radiation produced from the under
laying anode materials gives most efficient excitation of heavy elements. This enables a
single X-ray source to be used without any compromise over a very broad atomic
number range.

7. Collimator mask : Collimator mask, a metallic cover on the entrance of the

collimator, is a small opening. It cuts the radiation given by the collar of the holder or
from the sample mount (used for small diameter samples). It reduces the intensity of
secondary radiation entering the collimator. Different opening masks in sets are
commercially available.

In many commercial instruments a choice of mask is possible.

9. Spectrometer medium : Crystals and flow-detector are placed inside the

vacuum chamber and scintillation detector is mounted in open. Heavy elements (with
fluorescent radiation shorter than 2 nm.) can be analysed in air and lighter elements
should be analysed in vacuum. Solids are generally analysed in vacuum. A helium
medium is used for analyzing liquids. A high vacuum improves the lower detection
limit of the analysis, especially for lighter elements.

10. Flow detector window : At the entrance (for X-rays) of flow-detector a

polypropyline film/Mylars film is fitted. Films of various thickness are available
commercially. Thinner the film greater will be the chances of its rupture due to the gas
pressure inside and vacuum outside, and hence, frequent replacement will be required. 6
micron window is suitable for medium and heavy elements, and 1 or 2 micron window
for lighter elements.

141
11. Selection of off position : Selection of the off-position is very important for
.better and accurate analysis of an element. The rise and fall of intensity of any
wavelength may be gradual or sudden. This rise and fall gives an idea regarding off
selection. This can be experimentally found out by tracing the scan of the particular
element for different concentration on the same position on the chart recorder for small
range of angle . This is explained in the figures given below:

Rise and fall is gradual,

Hence, no off correction is required

Rise is not gradual, hence, negative off position

can be selected at a suitable position

142
 Here rise is gradual but fall is not gradual,
Hence, a positive off can be selected at a suitable position

Here neither rise nor fall is gradual,

Hence, a positive and negative off should be selected at suitable position

143
12. Detector high voltage selection : Adjust the detector high voltage so that the
maximum position of the pulse height distribution occurs at 50%. Procedure for high
voltage selection is normally given in one operation manual. The maximum voltage,
which can safely be applied must not be exceeded, otherwise, it may damage the
electronics or the detector. A general procedure for selection of detector which voltage
is,
1. Select window 49 to 51
2. Adjust high voltage to obtain the highest possible reading on the slip-chart
recorder.
3. Select normal window setting by PHD.

2.3 SAMPLE PREPRATION TECHNIQUE

Claisse, as early as in 1956, traced the importance of breaking of matrix for

accurate XRF analysis. Simple pressed powder pellets may lead to inaccurate
determination. But, where the product produced is consistent and similar then, simple
pressed powder technique is most suited due to its speed and simplicity. The choice of
sample preparation technique is rather more an art than a science. A careful study on
many aspects of the sample to be analysed may suggest some methods for analysis. Out
of these methods, the suitable one for a particular type of analysis can be chosen
experimentally.

Analysis of ores, minerals and especially ore dressing products by XRF is indeed
a challenging one. Ores, minerals and ore dressing products have a variety of elements
and radicals, which interfere with one another during XRF analysis. Moreover, no two
ores are alike. The work of an X-ray analyst is, thus, exacting, interesting, challenging
and at time tedious. But once he acquires mastery over the sample preparation
technique his work becomes most simple. As far as instrumental ability is concerned it
is fixed and optimal (even maximum) can be set by experiments and it will not deviate
from design and manufacture. Therefore, the sample preparation technique is the
cornerstone of XRF analysis. Once it is mastered, the XRF analysis is simple and easy.
And if this task is not accomplished the XRF unit becomes a white elephant. Therefore,
it is necessary that a sample preparation technique should be chosen for a given
requirement only after careful observation and experimentation.

The producibility of the method selected for sample preparation must be

sufficiently good. This means, that the error due to sample preparation must be smaller
than the acceptable total analysis error. Therefore, it is recommended that even the
simplest method of sample preparation should be tested for its reproducibility. Only
then one should start preparing the (expensive) calibration standards.

In the following paragraphs sample preparation techniques for ores, minerals and
ore dressing products are discussed. Other materials are either excluded from the
discussion or are cursorily dealt like metals, alloys, etc.

144
 There are many sample preparation techniques, which are employed for analysis
of ore, minerals and ore dressing products. Most important among these are listed below
and discussed in detail in the following paragraphs.

1. Freshly cut rock by diamond saw.

2. Pressed powder pellets.
3. Glass beads.
4. Solvent extraction.
5. Ion exchange.
6. Solvent impregnated papers.
7. Fire assay beads.
8. Co-precipitation and cementing.

Freshly cut rock or fresh powder pellets of powdered rock do not change the
mineralogical composition of the rock. Sample preparation and analysis is very fast by
this procedure. However, its drawback, render it unsuitable for accurate analysis in
many cases. Pressed powdered pellets of solid solutions, glass beads, solvent extraction,
ion exchange, solvent impregnated papers and fire assay beads are those techniques
where the matrix of the sample to be analysed is broken with the action of suitable
chemicals and converted into a matrix where the matrix effect will be considerably
reduced.

The advantage and disadvantage of all these techniques mentioned above

are discussed in following paragraphs.

1. Freshly cut rock : This sample preparation technique is mostly used for
qualitative estimation, semi-quantitative analysis is also possible. In this technique rock
is cut into a piece of suitable size and then analysed. Therefore, this technique can be
employed at mine site. If the rock matrix is more or less similar reliable quantitative
results are obtained. This technique requires minimum time as compared to other
techniques of sample preparation, and can be employed for analysis of metals and
alloys.

2. Pressed powdered pellets : A popular and widely employed technique in XRF

analysis can be categorized broadly into two classes.

(a) Powder rock without matrix breaking

(b) Solid solution.

(a) Powdered rock is pressed into a pellet with or without binder. Finely
powdered rock, less than minus 300 mesh, reduces the interferences due to grain size. If
the pressed powdered pellet of powdered rock has sufficient strength then no binder is
required. But where it is difficult to have good strength for a pellet without any addition
then suitable binder is added to it. These binding material can further be categorized
into two different categories :

145
 Additive binders Non-additive binders
Starch Polyvinyl acetate
Boric acid Polybutyl methacrylate, etc.
KCl
Cellulose, etc.

In case of additive binders a known small quantity of binder is added and mixed
with known quantity of the sample and then pressed into a pellet. In case of non-
additive binder a very small (negligible) quantity of binder is added to the sample and
then mixed and pressed into a pellet.

Freshly cut rock, pressed powdered pellet with non-additive binder are techniques
of sample preparation where no weighing is required. Hence XRF analysis involving
these samples preparation techniques outweigh the other analytical techniques as in all
quantitative techniques weighing is the first step of analysis. But where the matrix
changes considerably, such as, ore dressing products etc., these simple pressed
powdered techniques are either applicable to limited extent (lower range of
concentration) or lead to inaccurate analysis. For trace analysis simple pressed
powdered technique is most recommended, as the quantity of the element present is not
diluted, hence detection of very low concentration is possible.

Ores and minerals analysed by pure pressed powder technique.

1. All ores for determination of trace quantities of elements.

2. Silica sand and quartz.
3. Magnesite
4. Talc
5. Soapstone

(b) Pressed powdered solid solutions emerge as the most promising sample preparation
technique for its speed and accuracy in XRF analysis. Moreover, this does not suffer
from problems normally faced in glass bead preparation (such as cracks and fractures,
etc.). Number of fluxes can be employed for preparation of solid solution. Most
important is that the melt after cooling must be stable in open for considerably long
period. Hence, hygroscopic fluxes such as KOH, Na2O2, etc. cannot be employed for
preparation of solid solutions. Some of the commonly used fluxes are listed below.
Sodium Pyrosulphate Na2S2O7
Potassium pyrosulphate K2S2O7
Lithium tetraborate Li2B4O7
Lithium metaborate LiBO2
Sodium carbonate Na2CO3
Potassium carbonate K2CO3
Lithium carbonate Li2CO3
Mixture of fluxes such as K2S2O7 +NaF, etc.

146
The choice of flux should be made on the chemical nature of the sample to be analysed.
The melt is carefully removed, ground to a powder and pressed into a pellet of suitable
size. Normally no binder is required but where glass is formed non-additive binder such
as PVA, etc. may be added. The choice of flux is most important step in solid solution
analysis and is based on chemical properties of the material to be analysed. The choice
of fluxes can be made as suggested below for various ores and minerals.
A. Potassium pyrosulphate Sodium pyrosulphate

1. Bauxite 12. Tungsten ores, & concentrates, etc.

2. Manganese ore 13. Molybdenum ores & concentrate, etc.
3. Cobalt ores 14. Vanadium ores
4. Copper ores 15. Niobium ores and concentrate, etc.
5. Iron ores 16. Tantalum ores and concentrate, etc.
6. Nickel ores 17. Tin ores and concentrate, etc.
7. Zinc ores 18. Cadmium ores
8. Indium, Thallium Gallium ores 19. Glauconite
9. Lanthanides ores, concentrates 20. Corundum
and middling
10. Lead ores 21. Chromium ores
11. Titanium ores

B. Lithium metaborate/Lithium tetraborate

1. Aluminium ores 9. Hafnium ores

2. Alumino silicates 10. Wollastonite
3. Clays 11. Slags
4. Chromium ores 12. Cements
5. Limestone/Dolomite/Magnesite 13. Fly ash
6. Rock phosphate 14. Soils
7. Zirconium ores 15. Silica sand/Quartz
8. Thorium ores

C. Sodium/Potassium/Lithium carbonates :
For silicates

D. Potassium pyrosulphate with little NaF

Chromite and high refractories

3. Glass beads : Glass bead technique is a most important and popular technique
for accurate analysis of various refractory samples. Non-wetting agents such as alkali
halides and non-cracking agents such as sodium sulphate, etc. are normally added to
obtain a good bead. Beads can be manually prepared on a blast Makers burner, in
muffle furnace, now automatic bead machines are available in market. Muffle furnace
and bead machines can attain higher temperature so that the fusion is complete, the
molten mass is less viscous, and can be poured easily into a casting dish. Glass beads of

147
30 mm or 40 mm and 2-3 mm thick are normally casted and used for XRF analysis.
Glass beads of the material listed under the table B on the previous page can be cast.

Loss on ignition correction is very important in this analysis. Therefore,

either a calcined sample is used or the weight of the bead cast is used for correction.
Loss on ignition correction, how it is employed is illustrated below:

a) Where calcined sample is used for bead preparation

Initial weight 100

Final weight S {X = (100 LOI%)}
Dilution factor X
100

b) Where uncalcined sample is used for bead preparation

Initial weight Actual wt. of the sample say A gm.

Final weight Actual wt. of the bead, say X gm.
Dilution factor X
A

The calibration programmes should be prepared in the similar manner and used for
analysis. Commercial instruments utilizing computer softwares facility allow entering
dilution factor directly to correct the analysis.

4. Solvent Extraction : This technique is very rarely used in XRF unit.However, a

very potent technique where preconcentration and elimination of other interfering
material can be done. A sample is dissolved in a suitable medium, such as, acids or
dissolution of fused mass in aqueous solutions and the element of interest is extracted in
organic layer. This organic loaded solvent is transferred into a liquid sample cup and
then measured for desired elements. Care should be taken to test the solubility of
polypropylene film with the solvent to be stored in it. Alternatively the organic layer is
stripped in water and then analysed. No corrosive solution should be used for analysis,
as it will damage the spectrometer chamber. Alternatively, measured quantity of organic
or aqueous solution is absorbed on a filter paper or pad and then dried and used for
quantitative analysis.

5. Ion Exchange : Solution containing small amounts of element of interest is

adsorbed on the ion exchange resins. These resins are then dried or stripped and used
for quantitative analysis.

6. Solvent impregnated papers : As explained above under Solvent Extraction, a

known quantity of solution is dried on a filter paper and this paper is fixed on suitable
mount and then analysed. Alternatively a small tablet of filter paper is added to solution
and then the solvent is evaporated. The residue is then pressed into a pellet and used for
analysis.

148
7. Fire Assay Beads : Fire assay beads can be analysed for its constituents by XRF
without further destruction. Fire assay technique serves as a preconcentration technique;
therefore, quick and accurate analysis of these beads can be undertaken.

8. Co-precipitation & Cementing : The chemical process of selective co-

precipitation and cementing can conveniently be employed to separate the desired ions
from the solution and then these precipitates/ cements can be analysed directly or by
employing fusion technique.

149
 3. Methods of Analysis Using Atomic Absorption
Spectrophotometery
___________________________________________________

3.1 ATOMIC ABSORPTION SPECTROPHOTOMETERY

3.1.1 ATOMIC ABSORPTION

Atomic Absorption Spectrophotometry utilizes the phenomenon that atoms absorb

radiation of particular wavelength.

Atoms are either in the low energy state (ground state) or in the high energy state
(excited state).

The atoms in the ground state can be excited by absorbing energy from an external
source. For e.g. Sodium have two levels of excited states, 2.2 eV and 3.6 eV higher than
the ground state. (The unit eV reads electron volt and is used to show the level of
energy. ) When sodium atoms in the ground state are excited by energy of 2.2 eV or
3.6eV they make transitions from the ground level to the upper level of II or I. (Fig. I)
This energy is applied in the form of light. The energy differences of 2.2 eV and 3.6 eV
correspond to the energy of lights having wavelength of 5890 A0 and 3303 A0
respectively. Sodium atoms absorb only the lights having these wavelengths. The light of
any other wavelength is not absorbed at all

Since the difference of the energy level between the ground state and the excited state is
specific to each element, the wavelength of the light absorbed is decided by the element.
In Atomic Absorption Spectrophotometry, hollow cathode lamps are used as the light

150
source. They emit light of a wavelength specific to each element. Thus the concentration
of the atoms of the element, under study can be calculated from the amount of the light
that has been thus absorbed.

3.1.2 RELATION BETWEEN ATOMIC ABSORPTION AND

CONCENTRATION.

When a light beam passes through a medium containing many atoms in the
ground state, the light will be partly absorbed. The degree of absorption depends on the
concentration of the atoms.
When a light of an intensity Io is made incident upon a closed medium, with
a length l , which contains atoms of a concentration C , the intensity of the light will be
reduced to I. The next equation holds for the relation between the I and the Io

I = Io x e - K. l. C.
I
Or -log /Io = K. l. C.

Where K: proportional constant

This equation is called the Lambert - Beers Law.

The term - log I/Io is called absorbance. The equation tells us that absorbance is
linearly proportional to the concentration of atoms.

When the absorbance of Standard samples the concentration of which are say
1, 2, and 3 ppm are plotted against the concentrations, a straight line as shown in Fig. will
be obtained. This line is called the calibration curve for the particular element. The
concentration of the element in an unknown sample can be determined from the
absorbance by means of the concentration curve as shown in the following Fig.

151
3.1.3 ATOMIZATION OF SAMPLE

The principle so far described applies only to the light absorption of free
atoms. Free atoms are those atoms that are not combined with other atoms. No atoms
exist in sample matrices in free state they are combined to form molecules. For e.g.
Sodium atoms in seawater, are combined with chlorine atoms to form sodium chloride
(NaCl) molecules. Since molecules do not absorb light, it is necessary to break their
combination to produce free sodium atoms. This process is called atomization.
The most popular method of atomization by heat samples is heated to a
high temperature, so that molecules are converted into free atoms. This method is
classified into the flame method in which a chemical flame is used as the heat source, and
the flameless method in which a very small electric furnace is used.

a) Flame Atomization Method ----

Molecules are atomized in a flame produced on a burner. The burner as shown in Fig..
In this for e.g. the object of analysis is calcium, which exists as calcium chloride in the
sample solution. First, the sample is nebulized by the nebulizer. Large droplets of
sample solution are exhausted as drain, and only the fine mist is fed into the flame after
being mixed with fuel and support gases. In the flame, the mist is instantaneously
vaporized and small particles remain in the flame. As the small particles of calcium
chloride travel further through the flame, they are decomposed in to free calcium atoms.
If a light beam of 4227 A0 (wavelength for calcium) is introduced through this part of
the flame, atomic absorption can be measured. If the light should pass through the upper
part of the flame, where some of the calcium atoms combine with oxygen to produce

152
calcium oxide or some are ionized, the absorption sensitivity will decrease because of
the reduced amount of free calcium atoms.

Flame Atomisation

Various types of flames have been used in atomic absorption spectroscopy, and
now the following four types are most commonly used, not only because of their high
sensitivity but also because of the safety, ease of operation, and low cost. These four
types of flames, having different temperature and gas characteristics, are selectively used
for different types of elements.

Air Acetylene ( Air C2H2 ) flame ----

This flame is most widely used. About 30 elements are analysed with this flame.

Nitrous oxide Acetylene ( N2O C2H2 ) flame ---

The N2O-C2 H2 flame provides the highest temperature of all the flames used in
atomic absorption spectroscopy. Hence it is most effectively applied to analyses of
refractory elements like Al, V , Ti etc., which form very stable oxide molecules and
are hardly atomized in lower temperature atmosphere as in air acetylene flame.

Also, its high temperature minimizes the interferences of coexisting elements.

This flame, therefore, is sometimes used in analysis of those elements which are usually
analysed with an air-acetylene flame.

153
Air Hydrogen (Air H2) flame and Argon Hydrogen (Ar H2) flame ---

Flames using Hydrogen as the fuel have the advantage that the absorption
by the flame alone is extremely small in the short wavelength region.

These flames, therefore, ensure lower noise level, compared with the air-
acetylene flame, in analysis of such elements as As, Se, Zn, Pb, Cd and Sn in which
short wavelength analytical lines are used.
When the analytical line is shorter than 2000Ao in analysis of As (1937 Ao) or Se
(1960 Ao), it is usual to use an argon-hydrogen flame which has a still smaller
absorption.

The disadvantage of hydrogen flame is that since the flame temperature is low, the
interference of the co-existing elements is relatively large.

154
 FLAME TEMPERATURE

Flame Temperature Maximum

Ar-H2 1577oC
Air-N2 2045 oC
Air-C2H2 2300 oC
N2O-C2H2 2955 oC

Flameless Atomization Method

The flame atomization method is now used as standard method, because it ensures
good repeatability and ease of operation. It has a big disadvantage that only about 10%
of sample is atomized and about 90% of it is exhausted as drain. This poor atomization
efficiency is claimed to be the main restriction of sensitivity given by the flame method.

The flameless atomization method has recently gained a wide popularity which
consists of heated graphite tube and it ensures 10~200 times higher sensitivity than the
flame atomization.

Sample is placed in a graphite tube and an electric current about 300 amperes at the
maximum is allowed to flow through this tube. Thus the tube heated to a high

temperature and the sample is atomized.

The temperature of the graphite tube can be freely adjusted by changing the current
supplied to the tube. Thus, the optimum temperature condition can be attained required
for the type of sample and the element to be determined.

Inert gas such as oxygen and nitrogen is allowed to flow through the graphite tube to
purge the air to prevent oxidation loss of graphite tube.

155
 The biggest advantage of the flameless atomization method is that since the sample
injected is almost completely atomized, the sensitivity is extremely high. It is very
effectively used when sample concentration is extremely low and when sample volume
available is very small.

The flameless atomization method, has also some drawbacks. First, the interference
of co-existing compounds is greater than in the case of flame atomization method. When
the background absorption by the co-existing molecules is especially great, it is necessary
to adjust the temperature and period of ashing so that the background absorption does not
overlap the atomic absorption.

Next, the variation in the volume of sample injected (5~20 ml) and in the position of
injection may cause variation in the photometric values. As the result, the repeatability is
3~10 times worse compared with the flame atomization method. To obtain high
repeatability, it is necessary that the operator is skilled to some extent.

Construction of Atomic Absorption Spectrophotometer

An Atomic Absorption Spectrophotometer mainly consists of a light source, an

atomizer, a monochromator and a detector. Besides this, the instrument required an
optical system that combines these components, a processing system that converts
detector signals into a form that can be easily quantitated, and a power supply.

Fig. shows a typical layout of an atomic absorption spectrophotometer.

An Atomic Absorption Spectrophotometer is different from other spectrophotometers in

the following points.

a) Atomic Absorption occurs only at the wavelength, which is strictly specific to the
element under study with the slightest shift in the wavelength, the atomic
absorption will cease to occur. In A.A.S., it is necessary to use a light source that
emits a line spectrum, the wavelength of which exactly coincides with that of the
element under study. The light source is called Hollow Cathode Lamp.

156
 If a deuterium lamp, which emits wide wavelength light, should be used in atomic
absorption, a very expensive, high-resolution monochromator would become
necessary in order to isolate a 1/100 angstrom wide radiation. Even if this is
accomplished, the sensitivity and accuracy obtained would be inferior to those
provided by a hollow cathode lamp,.

b) Very intense light is emitted from the flame or the graphite furnace in the
atomizer. If this light should directly hit the detector, the detector may be broken
or its accuracy may be greatly lowered. To prevent this trouble, a monochromator
is placed between the atomizer and detector, so that most of the light from the
atomizer is kept away from the detector.

Light Source Unit

The light source unit for an Atomic Absorption Spectrophotometer consists of

Hollow Cathode Lamp and its holder and a power supply.

157
A Hollow Cathode Lamp and an anode are enclosed in a glass tube, which is filled with
neon or argon gas of around 10 Torr. in pressure. The Cathode is made of the element to
be measured or its alloy.

Deuterium Lamp for Automatic Background Correction

A deuterium lamp is generally used for automatic background absorption.

Deuterium lamps are available in two types of, hot cathode type and cold cathode
type.

A cold cathode type deuterium lamp has the same construction as an ordinary
hollow cathode lamp. It encloses deuterium gas and is turned on by the same power
supply as that for a hollow cathode lamp.

A Hot Cathode type Deuterium Lamp, which is used as the UV light source of a
UV- VIS spectrophotometer, is turned on by a power supply having a capacity of 300
milliamperes.

158
 A hot cathode type deuterium lamp, by contrast provides highly intense light,
and moreover, its light is well balanced with the light of hollow cathode lamps. The
influence of noise is much reduced. It can be used in the range up to 4300 Ao

For all reasons, hot cathode lamps are very widely used for automatic correction
of background absorption.

2 Atomizer Unit ( Burner and Gas Controller )

Burner -- The flame atomization method is more popular than the flameless atomization
method. All atomic absorption spectrophotometers are equipped with a burner as
standard.

There are two types of burners, premix type laminar flow burner and total
consumption burner.

Premix Type Laminar Flow Burner

This burner is used for air acetylene, nitrous oxide acetylene, air hydrogen and
argon hydrogen flame. A Laminar flame is given out of a slot, 0.5 mm wide and 50 mm
or 100 mm long, on the burner head.

The nebulizer is a precision sprayer which takes up sample solution through the
capillary and feeds it into the atomizer chamber as a fine mist. In the atomizer chamber, a
glass bead (disperser) is placed near the outlet of the nebulizer, so that the mist collides
with it at a great speed to be further dispersed into finer mist. The large drops produced in
the atomizer chamber are exhausted as drain.

The mist is mixed with acetylene and air and fed to the flame on burner head.

Samples of atomic absorption spectrophotometry often contain strong acids or

alkalies, so the burner, and especially the nebulizer, must be corrosion resistant.

The burner head has a slot, 5cm long or 10cm long. The 5cm- long slot burner head
is used for nitrous oxide- acetylene flame, and the 10cm-long slot burner head for the
other three flames. The 10cm slot burner head can not be used for nitrous oxide-acetylene
flame since it may cause a flash-back due to a very high combustion speed of this gas
mixture.

It is necessary that the position of burner head can be adjusted vertically and
horizontally, so that the light will pass the part of the flame where the excited atoms are
most concentrated. It is possible to lower the sensitivity by rotating the burner head to
shorten the path length in the flame that the light travels.

159
Total Consumption Burner

The total consumption burner produces a cylindrical flame of hydrogen gas. The
sample solution is aspirated by air and directly sprayed into the center of the flame. The
name, total consumption means that it uses total volume of the solution aspirated
through the capillary.

Although it is useful for a viscous sample, the total consumption burner is not
used frequently because of its high audible noise and its lower sensitivity than the premix
burner.

Gas Controller

This unit selects and controls the flow rates of the fuel gas ( acetylene or
hydrogen ) and the support gas ( air nitrous oxide or argon ).

3.2 SAMPLE PREPARATION FOR AAS

Weigh about 0.1 to 0.5 g sample (dry or roasted where necessary) in a 250 ml
beaker. Add about 10-15 ml aqua regia (AR) and digest the sample for half an hour, add
4 to 5 drops of HF and then dehydrate slowly to dryness and finally dissolve the dried
mass in nitric acid. Dilute it with a little water and filter it with Whatman paper No.40 in
100 ml flask, make up the volume to 100 ml with distilled water.

Aspirate the solution to AAS. Dilute the solution if required.

Lead
For higher concentration of lead, after dissolution of dried mass in nitric acid
(AR) add a pinch of tartaric acid and 10 ml of saturated solution of ammonium acetate
and boil it for 10 minutes and filter and make up.

Manganese

For manganese ore sample preparation should be in HCl (AR).

Cesium

For cesium weigh about 0.1 g of sample in 100 ml Teflon beaker and treat it with
aqua regia 15-20 ml on hot plate. Cover with watch glass for some time. After removing
watch glass and when red fumes ceases add 2-5 ml HF and 2 ml perchloric acid. Heat it
to dryness and extract in diluted HNO3 and filter with Whatman filter paper No.40.
Make up (after adding KCl to have final concentration of solution to 2 mg/ml of K) to
100 ml. in 100 ml plastic volumetric flask and aspirate it to AAS.

160
Silver
For silver, weigh about 0.5 g of sample in a graduated digestion tube; add 10 ml
of aqua-regia. Digest it on hot plate and keep it for overnight. Add 10 ml diluted
ammonia (1:1) slowly, cool it in ice cold water, and add little excess. Dilute it to nearest
volume shake well and allow ppt to settle for 1 to 1 hours and aspirate the supernatant
solution to AAS.
Gold
For gold weigh about 10 g of sample (sulphide ore) in silica petridish. Roast in
furnace at 640oC for 1 hour. Transfer the cooled mass in a 250 ml glass beaker add 50 ml
aqua regia and digest and dehydrate. Add 20 ml HCl (AR) and dry. Repeat twice-thrice
to remove nitrate ions. Add 20 ml of HCl and 50 ml distilled water boil and filter with
Whatman filter paper No.40 with pulp. Wash the residue 5-6 times with hot water. Heat
filtrate to boiling to reduce volume. Add 1.5 mg of potassium tellurite (3-4 drops of
saturated solution). And add 20% of stannous chloride solution till tellurium (black ppt)
gets ppted. Add 2-3 drops in excess boil and cool.
Transfer the entire solution with ppt in a separating funnel. Add 10 ml toluene
shake well. Allow to settle and discard the aqueous layer. Wash solution with 2N HCl
twice-thrice. Add 3 ml of 1:4 HBr solution and 2 ml 1%KBrO3 solution shake and allow
to settle.

Element Wavelength (nm) Flame Type

(Hollow Cathode Lamp)
Ag 328.1 Air/Acetylene
Au 242.8 Air/Acetylene
Bi 223.1 Air/Acetylene
Cd 228.8 Air/Acetylene
Co 240.7 Air/Acetylene
Cs 852.1 Air/Acetylene
Cu 324.7 Air/Acetylene
Fe 248.3 Air/Acetylene
Mn 279.5 Air/Acetylene
Ni 232.0 Air/Acetylene
Pb 217.0 Air/Acetylene
Rb 780.0 Air/Acetylene
Zn 213.9 Air/Acetylene
Al 396.2 N2O/acetylene
Ba 553.6 N2O/acetylene
Cr 357.9 N2O/acetylene
Ga 403.3 N2O/acetylene
Ge 265.1 N2O/acetylene
Mo 313.3 N2O/acetylene
Se 196.0 N2O/acetylene
Sn 235.5 N2O/acetylene
Sr 460.7 N2O/acetylene
Ti 364.3 N2O/acetylene
V 318.4 N2O/acetylene

161
 Take out aqueous layer in graduated digestion tube. Make up to nearest volume and
aspirate to AAS instrument

3.3 DETERMINATION OF LITHIUM IN LITHIUM, RUBIDIUM, CESIUM IN

TUNGSTEN ORES, MINERALS AND BENEFICIATION PRODUCT AND
MICA.

Scope

This procedure is applicable for determining the lithium in lithium rubidium

cesium and tungsten ores, minerals and beneficiation product and mica by means of
flame emission atomic spectrometric technique.

Principle

The sample is decomposed by acid attack involving hydrofluoric acid, perchloric

acid and oxalic acid. Potassium chloride is added as ionization buffer to stabilize
emission signal (kaschloride 800 mg/ml).

Reagents and standards

1. Hydrofluoric acid AR, 40%
2. Hydrochloric acid AR
3. Perchloric acid, AR
4. Nitric acid AR
5. Oxalic acid, 1% solution Dissolve 1 g. of AR oxalic acid in 100 ml
distilled water
6. Potassium chloride solution, K-40 mg/ml Dissolve 7.63 g of AR
potassium chloride in 100 ml distilled water.
7. (A) Standard lithium solution 1000 ppm : Dissolve a slurry of 0.5323 g.
lithium carbonate in 30 ml. of water by addition of 1.5 ml. Conc. hydrochloric
acid. After release of carbon dioxide by swirling dilute to 100 ml.
(B) Standard lithium solution 100 ppm Dilute 10 ml of (A) to 100 ml
containing 2 ml conc. hydrochloric acid (Add by pipette)
(C) Standard lithium solution 10 ppm Transfer 10 ml of (B) to 100 ml
volumetric flask. Add 2 ml conc. hydrochloric acid by pipette and make
volume to the mark by distilled water.
(D) Standard lithium solution 5 ppm Transfer 50 ml. of (C) to 100 ml.
volumetric flask. Add 1 ml of conc. hydrochloric acid and 2 ml. of potassium
chloride using pipette and make volume to the mark by distilled water.

162
 (E) Standard lithium solution 2 ppm Transfer 20 ml. of (C) to 100 ml
volumetric flask. Add 1.6 ml conc. hydrochloric acid and 2 ml potassium
chloride solution by pipette and make volume to the mark by distilled water.
(F) Standard lithium solution 1 ppm Transfer 10 ml. of (C) to 100 ml
volumetric flask. Add 1.8 ml. Conc. hydrochloric acid and 2 ml potassium
chloride by pipette and then make volume to the mark by distilled water.

Procedure

Take an appropriate weight of minus 200 mesh particle size mineral sample in
a clean Teflon beaker (100 ml capacity). Record the weight to the nearest
0.0001 gram (The appropriate weight of sample (Step-1) and appropriate size
volumetric flask (Step-6) are dependent on the concentration of the oxide in
the sample, the sensitivity of instrument used for analysis and the range of the
calibration curves or standard solutions used for comparison. The suggested
sample weight and final volume for mineral 0.1-0.2% lithium is 1 gram and
100 ml, respectively. For mineral samples yielding concentrations outside the
working range of the calibration solutions, appropriate changes should be
made in the sample size (say 0.1 gm) and /or final volume or dilution to 10,
50, 100, 500 fold volumes.
Moisten with water; add 5 ml nitric acid, 5 ml hydrofluoric acid and 2 ml
perchloric acid.
Cautiously evaporate the solution to dryness on a hot plate (Temp. 125-
150oC).
Allows the beaker to cool, add 2 ml hydrochloric acid, 10 ml oxalic acid
solution and 5 ml hydro fluoric acid and warm to digest the residue, and then
finally evaporate to dryness.
Now cool the beaker, add 2 ml conc. hydrochloric acid, 2 ml potassium
chloride solution and 20 ml distilled water and heat to digest residue to a clean
solution.
Filter if necessary through filter paper into the appropriate size volumetric
flask washing the filter paper thoroughly.
Cool the solution to room temperature, dilute to volume with water and mix
well.
Determine the lithium content by flame emission at operational instrument
parameters given below using a flame atomic absorption spectro-photometer
in emission mode.
Wavelength 670.8 nm
Slit width 0.5 nm
Instrument mode Emission mode
Calibration parameters 1 ppm, 2 ppm and 5 ppm.

Calculation
Li ppm = Li ppm reading x Final volume (ml)
Weight of sample (g)

163
3.4 DETERMINATION OF RUBIDIUM IN LITHIUM, RUBIDIUM, CESIUM
INTUNGSTEN ORES, MINERALS AND BENEFICIATION PRODUCT AND
MICA.

Scope

The method is designed to estimate rubidium in lithium, rubidium, cesium and

tungsten ores, minerals and beneficiation products and mica using flame emission atomic
spectroscopy.

Principle

The sample is decomposed by acid treatment. Potassium ion (800 mg/ml) as

potassium dihydrogen orthophosphate is added to the sample solution as ionization buffer
to stabilize and condition the emission signal.

Reagents and Standards

1. Hydrofluoric acid AR, 40%

2. Hydrochloric acid AR
3. Perchloric acid, AR
4. Nitric acid AR
5. Oxalic acid, 1% solution Dissolve 1 g. of AR oxalic acid in 100 ml distilled
water
6. Ionisation buffer, potassium dihydrogen ortho phosphate, potassium 40
mg/ml Dissolve 13.95 g of potassium dihydrogen orthophosphate in 100 ml
distilled water.
7. (A) Standard Rubidium solution 1000 ppm Rb - Dissolve 0.1415 g. rubidium
chloride in 100 ml distilled water.
8. (B) Standard Rubidium solution 100 ppm Rb Dilute 10 ml of (A) to 100 ml
by distilled water.
(C) Standard Rubidium solution 10 ppm Rb Dilute 10 ml of (B) to 100 ml
by distilled water.
(D) Standard Rubidium solution 5 ppm Rb Add 50 ml. of (C) to 100 ml.
volumetric flask. Add 2 ml of potassium buffer and 2 ml. of conc. hydro-chloric
acid and dilute to 100 ml. by distilled water. Prepare fresh daily.
(E) Standard Rubidium solution 2 ppm Rb Take 20 ml. of (C) to 100 ml
volumetric flask. Add 2 ml potassium buffer and 2 ml. conc. hydrochloric acid.
Make volume to the mark by distilled water.
(F) Standard Rubidium solution 1 ppm Rb Transfer 10 ml. of (C) to 100 ml
volumetric flask. Add 2 ml. Potassium buffer and 2 ml con. Hydrochloric acid.
Mix and make volume to the mark by distilled water.

164
Procedure

Transfer to the nearest 0.0001 gram, the 0.1-1.0 of a dry (110 oC for 30
minutes) minus 200 mesh mineral sample to a Teflon beaker (100 ml.
Capacity).
Moisten with distilled water; add 5 ml nitric acid, 5 ml HF and 2 ml perchloric
acid.
Place the beaker on a hot plate (Temp. 125-150oC) and evaporate to complete
dryness.
Allows the beaker to cool, add 2 ml conc. hydrochloric acid, 10 ml oxalic acid
solution and 5 ml hydro fluoric acid
Heat to digest and finally evaporate to dryness
Add 2 ml. Conc. hydrochloric acid, 2 ml.Potassium dihydrogen
orthophosphate buffer and 25 ml. distilled water. Heat to dissolve residue
completely.
Quantitatively transfer the contents of the beaker to a 100 ml. volumetric
flask.
Cool to room temperature and dilute to volume with distilled water.
Using an atomic absorption spectrophotometer in emission mode measure the
radiation for rubidium in calibration standard range.
On higher concentration of rubidium in sample solution compared to
calibration standard range dilute original solution to 10/50/100 fold stage.
The operational parameters of instrument are as under.

Wave length 780 nm

Slit width 0.2 nm
Instrument mode Emission mode
Calibration parameters 1 ppm, 2 ppm and 5 ppm.

Calculation

Rb ppm = Rb ppm reading x Final volume (ml)

Weight of sample (g)

3.5 DETERMINATION OF CESIUM IN LITHIUM, RUBIDIUM, CESIUM IN

TUNGSTEN ORES, MINERALS AND BENEFICIATION PRODUCT AND
MICA.

Scope

The method is standardized to analyse cesium in lithium, rubidium, cesium and

tungsten ores, minerals and beneficiation products and mica by atomic absorption
spectroscopy in emission mode.

165
Principle

The cesium is brought in solution by acid attack. The potassium dihydrogen

orthophosphate and ammonium chloride has been used as ionization buffer to stabilize
emission signal and severe background problems due to the formation of cesium
molecular species in flame and the position of the cesium emission line in near infra-red
region.

Reagents and Standards

1. Hydrofluoric acid AR, 40%

2. Hydrochloric acid AR
3. Perchloric acid, AR
4. Nitric acid AR
5. Oxalic acid, 1% solution Dissolve 1 g. of AR oxalic acid in 100 ml distilled
water
6. Ammonium chloride - Dissolve 50 g of ammonium chloride in 100 ml distilled
water.
7. Potassium dihydrogen orthophosphate K-40 mg/ml. Dissolve 13.95 g AR
potassium dihydrogen orthophosphate in 100 ml distilled water.
8. (B) Standard cesium solution

Daily prepare fresh 1 ppm, 2 ppm and 5 ppm cesium standard for calibration of
atomic absorption spectrometer scale.

166
 Cesium Concentration Procedure
Standard ppm
solution
A 1000 Dissolve 0.1267 g cesium chloride in 100 ml. Distilled
water
B 100 Dilute 10 ml. of (A) to 100 ml. with distilled water
C 10 Daily dilute 10 ml of (B) to 100 ml. with water
D 5 Take 50 ml. of (C) in a 100 ml. volumetric flask. Add 2
ml. Potash buffer and 2 ml. Ammonium chloride. Mix
Add 2 ml. Conc. HCl and make volume to the mark
with distilled water.
E 2 Take 20 ml. of (C) in a 100 ml. volumetric flask. Add 2
ml. Conc. HCl, 2 ml. Potash buffer and 2 ml.
Ammonium chloride and make volume to the mark by
distilled water.
F 1 Take 10 ml. of (C) 2 ml. of conc. HCl, 2 ml. Potash
buffer, and 2 ml. Ammonium chloride in a 100 ml.
Volumetric flask and make volume to the mark with
distilled water.

Procedure
Weigh appropriate quantity of sample (0.1 to 1.0 g). Transfer to a clean 100
ml. Capacity Teflon beaker. Record the weight to the nearest 0.0001 gm.
Moisten with distilled water. Add 5 ml. nitric acid, 2 ml perchloric acid, and
5 ml hydrofluoric acid (40%) in that order.
Carefully evaporate on a hot plate to dryness (Temp. 125-150oC). Allow to
cool to room temperature.
Rinse inner walls of beaker with a little distilled water; add 2 ml. Conc.
hydrochloric acid, 10 ml oxalic acid solution and 5 ml. Hydro fluoric acid.
Mix by Teflon rod.
Digest on a hot plate and then finally evaporate to dryness.
Cool to room temperature, add 2 ml. Conc. hydrochloric acid, 2 ml potassium
buffer, 2 ml ammonium chloride buffer and 25 ml distilled water and digest
on a hot plate for 15 minutes.
Filter the solution through Whatman filter paper No.40 into the 100 ml.
volumetric flask.
Wash the filter paper, cool to room temperature and dilute to volume.
Calibrate the atomic absorption spectro-photometer as operational parameters
of instrument given below :
Wavelength 852.1 nm
Slit width 0.2 nm
Instrument mode Emission mode
Calibration parameter 1 ppm, 2 ppm, 5 ppm
Flame Air, Acetylene

167
 1. Atomise the standard solutions to calibrate concentration of cesium of
unknown solutions.
2. When reading is not in calibration scale dilute original solution of sample to
10/20/50 fold volume

Calculation

Cs ppm = Cs ppm reading x final volume (ml)

Sample weight (g)

3.6 DECOMPOSITION AND ANALYSIS OF CHROMIUM IN ORE, MINERAL

AND BENEFICIATED PRODUCTS FOR CHROMIUM, IRON, NICKEL
AND COBALT.

Scope

Chromite mineral in general are not very easy to decompose and often present
serious problems in obtaining reliable analytical results. The following procedure is
rapid, accurate and precise for decomposition of chromite and estimation of chromium,
iron, nickel and cobalt.

Principle

The chromite ore is decomposed by perchloric acid and hydrogen peroxide under
reflux. The final measurement is performed by flame atomic absorption spectroscopy for
determination of chromium, iron, nickel and cobalt.

Reagents and standards

1 Perchloric acid AR,

2 Hydrogen peroxide 30% V/V AR
3 Round bottom flask corning 200 ml.
4 Reflux condenser, 45-60 cm. Length
5 Glass bubbler
6 Perchloric acid, 1%
7. Standard Chromium Solution

168
 Standard Concentration Procedure
solution ppm
A 1000 Dissolve 2.829 potassium dichromate in 100 ml.
water
B 100 Dilute 10 ml. of (A) to 100 ml by water
C 10 Dilute 10 ml of (B) to 100 ml. by water containing
2 ml. of perchloric acid and 88 ml water
D 5 Dilute 50 ml. of (C) in a 100 ml. by water
containing 1 ml perchloric acid and 49 ml. Water.
E 1 Dilute 10 ml. of (C) in a 100 ml. by water
containing 1.9 ml. Perchloric acid and rest water.

8. Standard Iron Solution

Standard Concentration Procedure

solution ppm
A 1000 Dissolve 7.025 gm. ferrous ammonium sulphate in
1 litre. Water containing 20 ml. Perchloric acid
B 100 Dilute 10 ml. Of (A) to 100 ml by distilled water
maintaining acidity 2% as perchloric acid
C 30 Dilute 30 ml of (B) to 100 ml. by maintaining
acidity 2% perchloric acid
D 20 Dilute 20 ml. of (B) in a 100 ml. by maintaining
acidity 2% perchloric acid
E 10 Dilute 10 ml. of (B) to 100 ml. having 2%
perchloric acid.

9. Standard Nickel Solution

Standard Concentration Procedure

solution ppm
A 1000 Dissolve 1.000 gm. Nickel material or nickel nitrate
2.48 g in 10 ml. Conc. nitric acid and dilute to 1
litre.
B 100 Dilute 10 ml. of (A) to 100 ml keeping acidity 1%
as HNO3.
C 10 Dilute 10 ml of (B) to 100 ml maintain acidity 1%
as HNO3
D 5 Dilute 50 ml. of (C) in a 100 ml. By maintaining
acidity 1% as HNO3
E 3 Dilute 30 ml. of (C) to 100 ml. Keeping nitric acid
1% (V/V).
F 1 Dilute 10 ml of (C) to 100 ml by 1% nitric acid
(V/V)

169
10. Standard Cobalt Solution

Standard Concentration Procedure

solution ppm
A 1000 Dissolve 1 gm cobalt metal or 1.97 g. of cobalt
chloride (CO Cl2.6H2O) in 10 ml. Conc. nitric acid
and dilute to 1 litre.
B 100 Dilute 10 ml. of (A) by adding 1 ml nitric acid and 89
ml. Water.
C 10 Dilute 10 ml of (B) to 100 ml keeping 1% nitric acid
D 5 Dilute 50 ml. of (C) in a 100 ml. By maintaining
acidity 1% as HNO3
E 3 Dilute 30 ml. of (C) to 100 ml. Keeping nitric acid
1% (V/V).
F 1 Dilute 10 ml of (C) to 100 ml by maintaining acidity
1%, as HNO3

Procedure

Transfer about 0.1000 g. finely powder (200 mesh) chromite sample to a

borosil round bottom flask.
Fit a vertical condenser (Water) to the flask. Cautiously add 10 ml. Perchloric
acid and 5 ml hydrogen peroxide.
Second end of the condenser is connected to a glass bubbler immersed in a
deep receptacle (50 ml. Measuring cylinder containing 20 ml of 1% perchloric
acid.
The contents of round bottom flask are heated to copious fumes of perchloric
acid for three hour.
The flask is cooled to room temperature
Add 5 ml of perchloric acid and 2 ml hydrogen peroxide
Again reflux the contents of the flask to copious fumes for one hour
The black particles of chromite are dissolved completely, and then cool to
room temperature.
The glass bubbler and condenser are rinsed with water. The abosorbing 1%
perchloric acid in measuring cylinder is added to the flask.
The solution is filtered through Whatman filter paper No.40 (pretreated with
dilute perchloric acid solution) washed.
Filtrate is cooled to room temperature and quantitatively transferred to a 100
ml. volumetric flask and make volume to the mark by distilled water. Mix
thoroughly.
Calibrate the atomic absorption spectrometer as per the manufacturers
instruction for chromium, iron, nickel and cobalt. The operating parameters
of instrument are as below

170
 Parameters Cr Fe Ni Co
Wave length (nm) 357.9 372.0 232.0 240.7
Slit width (nm) 0.2 0.2 0.7 0.2
Lamp current (mA) 6 7 25 25
Instrument mode Absorbance Absorbance Absorbance Absorbance
Standards for 1,5,10 10,20,30 1,3,5 1,3,5
Scale calibration
(ppm)
Flame Acetylene/N2O Acetylene/Air Acetylene/Air Acetylene/Air

1. Atomise the standards solutions and sample solution and record the reading in
calibration scale range.
2. Dilute the sample solution as per requirement to D/10, D/50, D/100 fold
volume by water keeping acidity 2% as perchloric acid.

Calculation

% Cr or
% Fe or
% Ni or = Metal ppm reading x Total vlume (ml) x 100
% Co 106 x sample weight (g)

3.7 DETERMINATION OF SILVER BY ATOMIC ABSORPTION

SPECTROSCOPY IN POLYMETALLIC ORES AND BENEFICIATED
PRODUCTS

Scope

This method has been designed to determine silver in polymetallic ores and
beneficiated products by atomic absorption spectroscopy.

Summary of method

A sample is treated with reverse aquaregia (3 HNO3 : 1 HCl), which breaks down
the sample converting the silver to soluble nitrate compound. The syrupy mass is treated
with aqueous ammonia solution, the silver dissolves as silver ammonia complex and is
separated from flocculent precipitate of iron, etc. The silver is analyzed by atomic
absorption spectrophotometry calibrated by silver standards containing same quantity of
reagent matching to unknown samples.

Reagents and standards

1. Nitric acid Ar
2. Hydrochloric acid AR
3. Standard solution

171
 Standard Concentration Procedure
solution ppm
A 1000 Dissolve 1.5748 g silver nitrate in water and dilute to
1 litre
B 100 Prepare fresh by diluting 10 ml of (A) to 100 ml with
distilled water
C 10 Prepare fresh by diluting 10 ml of (B) to 100 ml with
distilled water
D 3 Prepare fresh by diluting 30 ml of (C) to 100 ml by
adding 15 ml NH3 (1:1) and 55 ml distilled water
E 2 Prepare fresh by diluting 20 ml of (C) to 100 ml by
adding 15 ml NH3 (1:1) and 65 ml distilled water
F 1 Prepare fresh by diluting 10 ml of (C) to 100 ml by
adding 15 ml NH3 (1:1) and 75 ml distilled water

Procedure

Transfer 2.0 gram sample into a 250 ml beaker and moisten the sample with
water.
Add 20 ml reverse aqua regia (3HNO3 : 1HCl).
Carefully stir this mixture with the glass rod and place the beaker on the hot
plate (maximum surface temperature 100-150oC) and allow to evaporate to a
syrupy mass.
Remove the beaker from the hot plate, allow to cool to room temperature, add
15 ml of 1:1 ammonia solution and stir with glass rod.
Quantitatively transfer the total content to a clean 100 ml volumetric flask,
dilute to volume and mix thoroughly.
Dry filter it into a 50 ml volumetric flask (using dry funnel and dry flask).
Determine silver by reading absorbance by atomic absorption spectrometer
calibrated by standards of silver containing matching quantity of reagents used
for sample preparation.

Other instrumental parameters are as mentioned below :

Wavelength 328.1 nm
Slit width 1.00 nm
Lamp current 15 mA
Instrument Mode Absorbance BC
Calibration range 1 ppm 3 ppm

Calculation

Ag ppm = Ag ppm Reading x Volume (ml) x Dilution factor

Weight of sample (g)

172
3.8 DETERMINATION OF MOLYBDENUM IN TUNGSTEN AND
POLYMETALLIC ORES, MINERALS AND BENEFICIATION
PRODUCTS.

Scope

The method is standardized for determination of molybdenum in tungsten and

polymetallic ores, minerals and beneficiation products. The application can be extended
to other types of minerals and ores by essential modification in decomposition pattern.

Principle

The method involves decomposition of finely powdered sample by aqua-regia.

The acidity of the solution is maintained at 20% with respect to hydrochloric acid. The
aluminium chloride or sodium sulphate is added as ionization corrector/modifier to
stabilize absorption signal and baseline.

Reagents and standards

1. Nitric acid, Ar
2. Hydrochloric acid, AR
3. Aluminium chloride solution (10%) Dissolve 10 gm of anhydrous
aluminium chloride in 0.1 N 100 ml hydrochloric acid cool to room
temperature.
4. Sodium sulphate (10%) Dissolve 10 gm of AR sodium sulphate in 100
ml distilled water.
5. (A) Standard molybdenum solution 1000 ppm Dissolve 2.0425 g
ammonium molybdate ( (NH4)2 Mo O4 ) in distilled water and dilute to one
litre
(B) Standard molybdenum solution 100 ppm Dilute 10 ml of (A) to 100
ml by distilled water.
(C) Standard molybdenum solution 10 ppm Dilute 10 ml of (B) to 100
ml by distilled water.
(D)Standard molybdenum solution 5 ppm Daily prepare fresh by taking
50 ml of (C), 10 ml of aluminium chloride buffer, 20 ml conc. hydrochloric
acid and 20 ml distilled water in 100 ml volumetric flask. Mix well.
(E) Standard molybdenum solution 3 ppm Daily prepare fresh by taking
30 ml of (C), 10 ml of aluminium chloride buffer, 20 ml conc. hydrochloric
acid and 40 ml distilled water in 100 ml volumetric flask. Mix well.
(F) Standard molybdenum solution 1 ppm Take 10 ml of (C) in a 100
ml volumetric flask. Add 10 ml aluminium chloride buffer and 20 ml. Conc.
hydrochloric acid. Mix. Make to the mark by distilled water. Daily prepare
freshly.

173
Procedure

Transfer 0.2000 to 0.5000 g finely powdered sample to a clean 250 ml beaker.

Add 10 ml concentrate hydrochloric acid; mix the content by glass rod. Cover
by a watch glass.
Digest on a hot plate (temperature range 125-150oC) for about half an hour
cool.
Carefully add 20 ml aquaregia by measuring cylinder. Cover and digest on
hot plate for two hours.
Remove watch glass and slowly evaporate the acid to a syrupy residue.
Cool. Add 20 ml concentrate hydrochloric acid and 25 ml water. Heat just to
boil. Filter in a 100 ml volumetric flask wash beaker and residue with 1% hot
hydrochloric acid. Cool the filtrate. Add 10 ml aluminium chloride buffer.
Make volume to mark by distilled water. Mix well.
Read absorbance of molybdenum by atomic absorption spectrophotometer
calibrated by molybdenum standards.
The instrument parameters for operation are as under :

Wavelength 313.3 nm
Slit width 0.2 nm
Lamp current 7.0 mA
Instrument mode Absorbance BC ON
Calibration parameter 1 ppm, 3 ppm, 5 ppm
Flame N2O Acetylene

Calculation

Mo ppm = Mo ppm reading x volume (ml) x Dilution factor

Wt. of sample (g)

3.9 DETERMINATION OF BISMUTH IN TUNGSTEN AND POLYMETALLIC

ORE, MINERALS AND BENEFICIATION PRODUCTS BY ATOMIC
ABSORPTION TECHNIQUE.

Scope
This procedure is used for the quantitative measurement of bismuth, which is
present in tungsten and polymetallic ores, minerals and beneficiation products.

The sample is treated with aqua regia (3HCl : 1 HNO3), which breaks down the
mineral converting the elements to soluble chloride compounds. The syrupy mass is
dissolved in hydrochloric acid, and the potassium chloride is added as ionization
buffer/conditioner to stabilize absorption signal.

174
Reagents & Standards

1. Nitric acid AR
2. Hydrochloric acid AR
3. Potassium chloride (ionization buffer) Dissolve 16.3 gm AR potassium in
100 ml distilled water.
4. Standard solution of Bismuth :
A. Bismuth standard 1000 ppm : Dissolve 1.000 g bismuth metal
(99.999%) in 8 ml of 10 M nitric acid, boil gently to expel brown fumes of
nitrates, and dilute to 1 litre volume by distilled water and 250 ml
hydrochloric acid.
B. Standard Bismuth solution 100 ppm : Dilute 10 ml of standard (A) to
100 ml by adding 24 ml concentrated hydrochloric acid and 66 ml water.
C. Standard Bismuth solution 10 ppm : Dilute 10 ml of standard (B) to
100 ml by adding 24 ml concentrated hydrochloric acid and 66 ml water.
D. Standard Bismuth solution 5 ppm : Dilute to 50 ml of standard (C) to
100 ml by adding 12.5 ml concentrate hydrochloric acid and 37.5 ml of
water.
E. Standard Bismuth solution 1 ppm : Dilute 10 ml of standard (C) to
100 ml by adding 24 ml of concentrate hydrochloric acid and 66 ml of
water.

Procedure

Transfer 0.1000 to 0.5000 g of finely powdered sample to a 250 ml beaker.

Moisten the sample with water.
Add 100 ml concentrate hydrochloric acid, carefully stir this mixture with
glass rod and place the beaker on the hot plate (max. temperature 125-150oC)
and digest for 30 minutes.
Using a graduated cylinder, carefully add 10 ml of aqua-regia, mix and
evaporate on hot plate to a syrupy mass.
Cool and add 25 ml hydrochloric acid. Heat to boil and add some distilled
water.
Filter it in a 100 ml volumetric flask quantitatively; wash the residue
thoroughly with hot 5% hydrochloric acid.
Add 10 ml potassium chloride ionization buffer and make volume to 100 ml
by water. Mix well.
Read absorbance of bismuth by atomic absorption spectrometer
The instrumental parameters are as under :

Wavelength 223.1 nm
Slit width 0.2 nm
Lamp current 12 mA
Instrument mode Absorbance BG ON
Calibration range 1 ppm, 5 ppm, 10 ppm
Flame Air Acetylene

175
Calculation

Bi ppm= Bi ppm reading x volume (ml) x Dilution factor

Weight of sample (g)

3.10 DETERMINATION OF OXIDIZED ZINC IN A ZINC ORE, ZINC

CONCENTRATE AND BENEFICIATED FRACTION.

Scope

The method is standardized for estimation of oxidized zinc in zinc ore, its
concentrate and beneficiated fraction by atomic absorption spectroscopy.

Principle

An appropriate weight of the representative sample is digested with ammonium

chloride and ammonium acetate. The zinc is analyzed by atomic absorption
spectroscopy. An identical reagent blank is run for correction of reagent absorbance.

Reagents and Standards

1. Ammonium chloride Dissolve 25 gm AR ammonium chloride in 100 ml

distilled water.
2. Ammonium acetate Saturated solution in distilled water.
3. Stock standard for Zinc
(A) 1 ml of solution = 1 mg of zinc (1000 ppm) Dissolve 1.0000 gm zinc
metal in 10 ml of hydrochloric acid, dilute to 1 litre by distilled water.
(B) Zinc standard stock solution 100 ppm: Dilute 10 ml of A to 100 ml
with 1% (V/V) nitric acid.
(C) Zinc standard stock solution 10 ppm: Daily dilute 10 ml of B to 100
ml with 1% nitric acid (V/V).
(D) Zinc Standard 1 ppm: Daily dilute 10 ml of C to 100 ml with 1%
nitric acid (V/V).
(E) Zinc Standard Solution 0.5 ppm: Prepare daily by diluting 50 ml of D
to 100 ml with 1% nitric acid (V/V).

Procedure

To 1.000 gm of sample in a 250 ml beaker, add 20 ml of ammonium chloride

solution and 10 ml of ammonium acetate solution by pipette. Add 25 ml of
distilled water.
Cover, digest on hot place for 10 minutes, filter by Whatman filter paper
No.40 and wash with hot water containing ammonium chloride (0.2 gm/litre).
Add 2 ml nitric acid just boil.

176
 Cool to room temperature and transfer to a 100 ml volumetric flask.Add
distilled water to mark.
Run an identical reagent blank for absorbance correction.
Read the absorbance on atomic absorption spectrometer. The operating
conditions of instruments are as under.

Wavelength 213.9 nm
Slit width 0.7 nm
Lamp current 5.0 mA
Calibration range 0.5 ppm 1.5 ppm

Calculation

% Zn = Zn ppm reading x volume (ml) x Dilution x 100 factor

106 x sample weight (gm)

3.11 DETERMINATION OF OXIDIZED LEAD IN LEAD ORE, LEAD

CONCENTRATE AND OTHER BENEFICIATION FRACTIONS.

Scope

The method has been standardized for the determination of oxidized lead in its
ore, concentrate and beneficiation fractions. In this method all but the sulfide and
chromate of lead are soluble.

Principle

An appropriate weight of the finely ground sample is digested with saturated

ammonium acetate solution. The extracted lead salts are estimated by an atomic
absorption spectrophotometer running an identical reagent blank.

Reagents and Standards

1. Ammonium acetate saturated water solution.
2. Nitric acid AR
3. (A) Stock standard solution of Lead 1000 ppm : Dissolve 1 gm lead
metal (99.999%) in 10 ml nitric acid and dilute to 1 litre.
(B)Lead standard solution 100 ppm : Dilute 10 ml of (A) to 100 ml with
1% nitric acid (V/V).
(C) Lead standard solution 10 ppm : Prepare daily by diluting 10 ml of B
to 100 ml with 1% nitric acid (V/V).
(D) Lead standard solution 5 ppm : Prepare daily by diluting 50 ml of
(C) to 100 ml with 1% nitric acid.
(E)Lead standard solution 1 ppm : Prepare daily by diluting 20 ml of (D)
to 100 ml with 1% nitric acid.

177
Procedure
To 1 gm of the 100 mesh 150 mesh sample in a 250 ml beaker, add 10 ml of
saturated solution of ammonium acetate and 50 ml of water.
Digest on a steam bath for 1 hour and then boil for a while.
Cool and filter through Whatman filter paper No.40, wash with hot water.
Add 2 ml nitric acid, boil.
Cool and transfer to a 100 ml volumetric flask. Make volume to mark. Run a
reagent blank.
Measure absorbance on atomic absorption spectrometer calibrated to 1.0, 5.0
and 10 ppm.
Other operation parameters of instruments are as below :

Wavelength 217 nm
Slit width 1.0 nm
Lamp current 4.0 mA
Instrument mode Absorbance BG ON
Calculation

% Pb = Pb in ppm reading x volume (ml) x Dilution factor x 10

106 x Weight of sample (gm)

3.12 DETERMINATION OF OXIDIZED COPPER IN COPPER

ORE/CONCENTRATES.

Scope

This method has been standardized for the determination of oxidized copper in
copper ore/concentrates and beneficiated fraction by atomic absorption spectroscopy.

Principle

This method provides a separation of the copper in oxidized form as in cuprite,

tenorite, malachite, and chrysocolla from that in the sulphide form as in chalcocite,
covellite and chalcopyrite. An appropriate weight of the representative sample is
digested with sulphurous acid. The digested copper is analysed in filtrate by atomic
absorption spectroscopy.

Reagents and Standards

1. Sulphurous acid (H2SO3) 3%

2. Stock standards for copper 1 ml of solution = 1 mg of copper (1000 ppm).

178
Procedure

Weigh exactly to 2.5 g of the representative sample, ground to fineness of 100

to 150 mesh in a bottle and add 50 ml of 3 per cent solution of sulphurous
acid. Cork the bottle tightly and agitate by wrist type shaker for 15 minutes.
Then transfer the content of the bottle to a beaker, cover with watch glass, and
digest on steam bath for 5-10 minutes.
Filter by Whatman filter paper No.40, wash the residue with sulphurous acid
solution for at least for to five times, add the washings to the filtrate, which
will contain in solution all oxides, carbonates and silicates of copper, and all
metallic copper.
Boil the filtrate to remove sulphurous acid. Then add 2 ml nitric acid and just
boil, cool and make 100 ml in a volumetric flask.
Read the absorbance on atomic absorption spectrophotometer GBC-932
model calibrated in working range 1 ppm to 5 ppm.

Operating condition for instrument are :

Wavelength 324.7 nm
Slit width 0.5 nm
Lamp current 4.0 mA
Instrument mode Absorbance BG On
Flame Air-Acetylene Blue flame

Calculation

% Cu = Cu ppm reading x volume (ml) x 100 x Dilution factor

106 x weight of sample (gm)

3.13 DETERMINATION OF NIOBIUM AND TANTALUM IN ORES AND ORE

DRESSING PRODUCTS OF TUNGSTEN AND TIN.

Principle

The niobium and tantalum are co-precipitated with titanium in presence of 10%
zinc-ethylene tetramine acetate complex to isolate and separate from tungsten, tin,
zirconium, chromium, molybdenum and iron. The estimation is finished by AAS in
presence of iron as ionization/stabilization buffer in fluoride media.

Reagents and standards

1. Niobium standard 1000 ppm Transfer 1.000 g niobium metal (or 1.4305 g
Nb2O5) to a platinum dish, add 20 ml hydrofluoric acid, and heat gently to
complete dissolution, dilute to 1 litre. Prepare 100 ppm niobium standard by
proper dilution maintaining 2 ml HF/100 ml. volume (Use Teflon ware).

179
 2. Tantalum standard 1000 ppm - Take 1.000 g tantalum metal (or 1.2210 g
Ta2O5) in platinum dish (or Teflon dish), add 20 ml HF, gently heat to
dissolve. Dilute it to 1 litre with water. To prepare 100 ppm tantalum
standard, dilute 10 ml of 1000 ppm stock standard to 100 ml keeping 2 ml.
HF/100 ml volume.
3. Zinc solution (1 M) Dissolve 21.937 g of zinc acetic acid and dilute to 100
ml.
4. Ethylene diamine tetracetate sodium salt solution (1 M) : Dissolve 37.31 g
of AR EDTA sodium salt in warm water and dilute to 100 ml.
5. Zinc-EDTA Complex (1:1) (10%) Mix 10 ml zinc solution with 10 ml
EDTA solution and dilute to 100 ml with water.
6. Ammonia solution - 1:1
7. Instrumental parameters :

An atomic absorption spectrometer equipped with nitrous oxide acetylene burner.

The instrumental operating parameters are as under:

Parameters Niobium Tantalum

Wavelength 334.9 nm 271.5 nm
Slit width 0.2 nm 0.2 nm
Lamp current 20 mA 20 mA
Flame Nitroous oxide Acetylene Nitrous oxide Acetylene

The flame should be adjusted to a slight yellowness where absorption of niobium and
tantalum is optimum.

Procedure

Decomposition of sample: Fuse a sample weighing 0.5000 to 1.0000 with 5 g

sodium hydroxide in an iron crucible at 550 oC in muffle furnace. Cool the
crucible, leach the melt with water, and boil for few minutes. Filter the
precipitate using Whatman filter paper No.40 and wash with 1% sodium
hydroxide solution. The chromium, tungsten, tin, molybdenum, silicon and
aluminium pass in the filtrate, and the precipitate contains iron, titanium,
niobium and tantalum. Transfer precipitate into a 400 ml beaker. Wash filter
several times with 5% sulphuric acid containing a few drops of hydrogen
peroxide. Heat to boil to dissolve precipitate.
Separation : Add 5 ml 1:1 sulphuric acid ot the solution and boil it to destroy
hydrogen peroxide. Add 20 ml of titanium solution (1 mg TiO2/ml) and 10 ml
of zinc EDTA solution. Heat the solution just to boil and neutralize with
dilute ammonia solution adding a few drops in excess. Just boil the precipitate
of Ti, Nb and Ta, separate the precipitate on Whatman filter paper No.41.
Wash the precipitate with very dilute hot ammonia solution. Transfer the
precipitate to a platinum dish by a small quantity of water. Carefully wash the
filter paper with 5 ml. of hydrofluoric acid to dissolve and bring any niobium

180
 and tantalum adhered to filter paper. Add 1 ml 1:1 sulphuric acid and heat to
dissolve precipitate. Cool the solution, add 2.5 ml iron solution (50 mg/ml
prepared in 10% HF (V/V) and dilute to 25 ml in a Teflon volumetric flask.
Mix.
Measurement: Set atomic absorption spectrophotometer to the instrument
operation parameters mentioned above. Calibrate instrument scale by 1, 3 and
5 ppm. Matching standard solution of niobium and tantalum containing 2.5 ml
iron solution and 2.5 ml titanium solution (20 mg/ml) in 25 total volume. The
clear sample solution is aspirated into the flame to measure atomic absorption
and metal concentration in ppm.

Calculation

ppm Nb or Ta = ppm Nb/Ta reading x volume (ml)

Sample weight (g)

3.14 DETERMINATION OF GALIUM, INDIUM, THALLIUM IN ZINC AND

LEAD ORE AND BENEFICIATION PRODUCT BY ATOMIC EMISSION
ON ATOMIC ABSORPTION SPECTROPHOTOMETER.
Scope

The method is optimized for estimation of gallium, indium and thallium in ores
and ore dressing products of lead and zinc by atomic emission technique involving
separation and pre-concentration by tributyl phosphate. The method is also applicable to
bauxite, aluminium metal and its alloys.

Principle

The sample is brought in solution by acid treatment the gallium indium and
thallium are separated and preconcentrated by solvent extraction in tributyl phosphate
containing sodium nitrite. The emission is measured by atomic absorption spectrometer.

Reagents and standards

1. Tributyl phosphate, AR
2. Hydrochloric acid, AR 6 M
3. Nitric acid 1 M
4. Sodium nitrite, crystalline
5. Gallium, indium and thallium standard Prepare gallium, indium and
thallium standard 100 mg/ml and by serial dilution 1 mg metal/ml.
6. Ionisation buffer 2 mg Cs/ml. Dissolve 0.2543 g CsC1 in 100 ml water.
7. Ionisation buffer 5 mg Na/ml. Dissolve 1.275 g NaCl in 100 ml water.

181
Instrumental parameters: The emission intensity is measured on atomic absorption
spectro photometer in emission mode.

Instrumental parameters Gallium Indium Thallium

Wavelength, nm 403.3 451.1 535.1
Slit width, nm 0.20 0.20 0.50
Instrument Mode Emisstion Emission Emission
Calibration Standards 1, 3, 5 1, 3, 5 1, 3, 5
mg/ml
Flame AC:N2O AC:N2O AC:N2O

AC = Acetylene

Procedure

Decomposition of sample :

Sulphides of lead and zinc : Roast 2.000 g sample (-150 mesh) in a porcelain
dish at 600oC for 3 hours in a muffle furnace Transfer roasted sample to a 250
ml beaker, add 25 ml aquaregia. Keep beaker initially at room temperature
for one hour and then slowly heat at low temperature on a hot plate. Finally
evaporate the acid, bring residue in solution by 25 ml 6N hydrochloric acid.
Boil, filter, wash residue with 6 N hydrochloric acid. Use this solutin for
further steps.
Aluminium metal: Treat clean 2.000 g aluminium metal with 6 M
hydrochloric acid. Boil to dissolve it and make it to 50 ml. Use an
appropriate aliquot for further steps.
Bauxite: Fuse sample weighting 0.5000 to 1.0000 g with 2 gm of sodium
hydroxide and 0.5 g Na2O2 in an iron/zinconium crucible at ~ 550 oC. Leach
the cake with hot water. Dissolve precipitate in hydrochloric acid. Maintain
acidity by conc. hydrochloric acid.

Separation, preconcentration and measurement:

Preconditioning of tributyl phosphate: Take 150 ml tributyl phosphate in a

500 ml separating funnel. Add 50 ml 5% sodium carbonate solution. Shake
well for two minutes. Let separate layers, discard lower aqueous layer. Now
add 50 ml 6M hydrochloric acid shake it for 2 minutes and discard acid layer.
Pre-concentration: Transfer the sample to a 125 ml. separatory funnel; add
hydrochloric acid to keep 3M hydrochloric acid concentration for extraction.
Now add 25 ml of tributyl phosphate and a few crystals of sodium nitrite
shake the solution for 2 minutes. Let two phases separate transfer aqueous
phase to another separating funnel extract it two times more with 10 ml
portion of fresh tributyl phosphate. Mix all the three extracted portions of
organic phases and transfer to 125 ml separatory funnel. Wash the tributyl
phosphate twice with 10 ml portions of 6M hydrochloric acid by shaking.

182
 Now strip down gallum, thallium and indium from tributyl phosphate extract by
shaking with 10-15 ml 1% hydrochloric acid (V/V) for two minutes. Collect the aqueous
phase in 100 ml beaker. Repeat extraction with 10 ml 1% hydrochloric acid containing
0.1 g of sodium sulphite. Combine all the three aquous extracts and evaporate on a steam
bath to about 5 ml. Cool and transfer to a 25 ml volumetric flask, add 5 ml cesium or
sodium ionization buffer solution and make it to volume mix.

Measurement

Aspirate the solution into the nitrousoxide acetylene flame red zone and
measure the emission intensity and ppm reading of gallium, indium and thallium.

Calculation

ppm Ga or In or Tl = Metal ppm reading x volume (ml)

Sample weight (g)

Note:

1. A little sodium nitrite should be added to the solution to oxidize thallium (I) to thallium (III), which is
readily extracted into tributyl phosphate at 3.6 M hydrochloric acid concentration.
2. The thallium is readily stripped into aquous phase under reducing conditions and so a few crystals of
sodium sulphite should be added.

183
4. Principle And Procedure of Carbon and Sulphur
Analyser
_______________________________________________________________________________________________________

Principle

A sample held in a ceramic crucible is pyrolysed in the RF furnace. The

combustion atmosphere is technical grade oxygen, which flows through a guide tube to
the sample after being free from water vapour and carbon dioxide in a filtration system.
The C and S contained in the sample are oxidized to carbon dioxide and sulphur dioxide
respectively in the pyrolysis. The oxygen flow serves both as oxidizing agent and as
system carrier gas.

The entrained gaseous combustion products leaving the furnace are passed
through dust and water vapour filters and through a thermostatic pressure regulator and
flow rate regulator system and into the analysis cells of IR analyzer which provides
output signals which are proportional to the respective concentration of CO2 and SO2 in
the carrier gas flow and finally the concentration of C and S contained in each sample
will be shown in percent by weight on Visual Display UnitVDU.

Procedure

Switch on the instrument and connect the compressed air supply at the instrument
rear panel by using polyamide tubing provided, open the compressed air supply. The
required overall pressure is 4 to 6 bar. Open the oxygen cylinder and O2 pressure of (6 to
10 bar) is to be adjusted by means of external pressure regulator. Let the instrument on in
Stand by mode for 30 minutes to warm up.

Fire the crucibles (sample holders) for approximate 45 minutes at 950 oC in the
furnace before analysis then keep it in a desiccators for cooling. Weigh around 1 part
Iron accelerator and 3 parts tungsten accelerator and afterwards take 0.15 g to 0.2g of
standard in the crucible and enter the weights from balance to VDU then select
Calibration Mode. Select the standard range which one is suitable for the sample and
calibrate the instrument. After this the same procedure is to be followed for the sample
and sample is pyrolysed in the RF furnace and C&S contained in the sample are oxidized
to CO2 & SO2 respectively by means of oxygen and fed to the analysis cells of IR
analyzer where the intensity is measured and converted into C&S concentration in
percent by weight and finally display on VDU.

Application

In steel and cast samples for complete combustion tungsten accelerator as additive
material is required.
In non-metallic samples, high purity iron plus tungsten as additive is to be added.
Samples in the form of shavings or chips yield optimal conditions for the
measurement, since their relatively large surface areas promote oxidation.

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 For sample in the form of dust or fine powders, there exists the possibility that the
O2 flow from the guide tube will blow samples particles from the crucible, thus
falsifying the sample weight. The result will be measured concentrations, which
are too low or non-reproducible. Thus the sample surface be well covered by the
diluent material.

Precautions

It is necessary to add to the sample a metallic additive material in order to

guarantee a complete combustion of the sample material and for complete
oxidation.
The additive material should be free from the element to be analysed.
It must not form stable chemical compounds with the element of the sample to be
analysed.
Combustion tube and dust traps should be cleaned after every 30-50 analysis.
For reproducibility of the results one should take precaution that sample as well as
diluent material or accelerator should not be contaminated and it should be
homogeneous.
Check the leakage in the gas flow, combustion tube should be clean and the
carrier gas should be moisture free.

185
5. Method of Analysis Using Inductively Coupled
Plasma ICP ) Instrument
______________________________________________
5.1 ICP (AES) TECHNIQUES AND APPLIICATIONS

ABSTRACT

Plasma Spectrometry is one of the most popular and versatile techniques of

geological and environmental samples, including rocks and minerals, waters, dust,
vegetation, soils and sediments. Inductively coupled plasma is used as emission source
in ICP-atomic emission spectrometry (ICP-AES) and due to wide dynamic range of ICP,
it can measure elements over an extremely wide range of concentrations. Plasma
spectrometry is primarily a solution-based techniques and the dissolution step controls
both the range of elements quantifiable and the limits of determination considering the
detection limit and spectral interferences. However, chemical separation and
preconcentration steps are required for the Rare Earth Elements, precious metals and
several other elements, which enable determination to be made at ppb levels. ICP-AES is
best used for major, minor and trace elements determinations.

INTRODUCTION

ICP-AES instruments are based on the principle that by viewing the appropriate
region in an Ar-Plasma tail flame, the atomic and ionic emission lines of analytes can be
measured against very low background emission intensities. The very high temperature
(up to 10,000oK) in the ICP ensures for more efficient atomization and consequently the
chemical interferences are very less. ICP-AES exhibits very wide linear response range
of more than 5 order of magnitude, making it possible to determine major, minor, and
trace and ultra-trace elements in a single preparation.

Plasma Formation

A water-cooled gold or silver plated copper tube is coiled around the upper part of
the plasma torch. The coil is connected to a RF-Generator, which creates an oscillating
RF magnetic field within the Ar flowing through the torch. RF-Generators operate within
the industrial frequency bands of 27.12 MHz or 40.68 MHz and most systems are
operated at forward powers of 0.9 to 1.5 KW.

The Ar stream passing through the torch is initially seeded with electrons,
generally using a high-voltage spark. The electrons are subjected to intense oscillations
of the RF magnetic fields generated by the induction coil and collide with Ar atoms
causing ionization. Each charged particle formed in the gas stream is controlled by the
magnetic fields, which force it to flow in a closed annular path within the torch.
Resistance to the induced motion of the charged particles causes ohmic heating of the gas
stream, which rapidly rises in temperature to approximately 10,000oK. This transfer of

186
energy by inductive coupling to form high temperature plasma is the definitive
characteristic of an ICP.

SAMPLE PREPARATION METHODS

1. Water and Biological Samples

Plasma spectrometry is primarily a solution technique. Dissolved samples like

natural waters, biological fluids, beverages, oils, etc. require minimum sample
preparation. For waters, acidification with HNO3 and then filtration or centrifuging to
remove particulate matter is normally required. Biological fluids and beverages require
dilution but are then ready for direct analysis. Botanical samples must first be ashed to
ensure their complete decomposition. This will involve wet or dry ashing of the samples.

2. Geological Samples

Geological samples dissolution procedures are divided into three broad groups
Leaching of the sample with mineral acids e.g. HCl-HNO3-HClO4 etc.
HF-HClO4 acid attack of the sample
Fusion methods

i. Acid Leaching

For many elements in geological samples, the complete dissolution of the sample
is not necessary. In many cases, a simple leaching of the elements of interest by some
combination of mineral acids (HCl-HNO3-HClO4) is quite adequate. Some elements
such as As and Sb will be lost if HCl is used without HNO3.

ii. HF-HClO4 Dissolution

The samples are attacked with HNO3-HF-HClO4 mixture in Teflon beakers on hot
plate, which are then evaporated to dryness, followed by final dissolution of samples in
dilution HNO3. But the Si, Se & B will be lost.

iii. Fusion Method

Of these methods, the fusion methods are considered the most rigorous and
complete. The type of flux used will be dependant on the analytical requirement, the
nature of the samples and the range of elements to be determined. The most popular flux
is lithium meta-borate (LiBO2), sodium carbonate, potassium carbonate, sodium
hydroxide, sodium peroxide, potassium hydroxide and potassium-bi-fluorite (KHF2).

The major disadvantage of all fusion procedures is that they introduce large
quantities of total dissolved solids (TDS), which necessitate increased dilution. These
increased dilutions will push some trace element concentrations below the limit of

187
quantitative analysis. The fusion procedures may also lead to increased loss of volatile
elements.

SEPARATION AND PRECONCENTRATION PROCEDURES

Despite low instrumental detection limits, spectral interferences and /or other
matrix effects preclude the determination of several trace elements in samples. These
difficulties may be overcome by using chemical procedures, which separate groups of
analyte from their matrix. Elemental groups, which are routinely analysed in this way
include the

1. Hydride forming elements e.g. As, Bi, Ge, Pb, Sb, Se, Sn, Te & Hg.
2. REEs e.g. La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb & Lu.
3. Platinum Group Elements Ir, Os, Pd, Pt, Rh & Ru.

1. HYDRIDE ELEMENTS

A number of elements will readily form gaseous hydrides at ambient

temperatures. Many of these hydride elements are toxic in the environment and are
important mineral exploration targets or pathfinders. However, they occur at very low
concentrations in samples and are subject to major spectral interferences from other
matrix elements and their determination requires separation procedure.

Hydride formation is achieved by reacting samples with aqueous NaBH4, as the

reducing agent and the element in hydride form directly goes to the Plasma and the
interference elements remains in the solution. Therefore, hydride generation allows
100% efficient injection of these elements into dry Plasma without the use of
nebulisation. Thus very low concentration of these elements can easily be determined by
this method due to the high efficiency of analyte transfer via. hydride generation and the
removal of interference caused by matrix elements.

Recommended wavelengths and typical detection limits

Element Wavelength Detection limit in mg/L

(ppm)
As 189.04 0.5
Se 196.09 0.5
Hg 184.95 0.1
Sn 189.98 0.2
Te 214.30 1.0
Bi 223.06 0.7
Sb 206.83 0.5
Ge 303.91 0.06

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2. RARE EARTH ELEMENTS

The lanthanum group elements from atomic number 57 to 71 are found in nature
in stable form and the analysis of rare earth elements is very important in ores and other
geological samples. For the determination of the rare earth elements, it is essential that
all the minerals that contain the rare earths have been fully dissolved. The mineral zircon
contains large number of REE, with a concentration of the heavier rare earths and it is not
quantitatively dissolved in the standard HF/HClO 4 attack. It is essential that the sample
must be completely dissolved, either using an acid attack followed by a mini fusion of the
insoluble residue with NaOH, LiBO2 or K2S2O7 or fusion of the complete sample.

Procedure

(1) Weigh 0.5 gm sample in a Teflon beaker and add 5 ml HClO4 and 12 ml. HF in it.
After stirring, the solution is evaporated on hot plate to dryness, cooled and dissolved in
20 ml. 3 N HCl. The solution is filtered and the residue is ignited at 800 oC in a silica
crucible. Transfer the residue in nickel crucible and fuse it with NaOH on burner. After
cooling, the flux is dissolved in 25 ml (25% HCl) and the solution is added to the filtrate.
The whole solution is evaporated on the hot plate till dry. Then add 10 ml. 2N-HCl
solution and heat it on hot plate for about 20 minutes to dissolve the residue. This
solution is poured in the column charged with Biograd AG50W-X8 H-form, 200 to 400
mesh, conditioned in 2N-HCl.

(2) Weigh 3.0 gm. sample in Teflon beaker and add 30 ml conc. HCl and 10 ml
concentration HNO3 in it. Keep the beaker on hot plate and digest it for 30 minutes. Add
10 ml. HF and dry the contents on hot plate. Extract the residue in 30 ml 6N HCl, boil
and filter with 40 No. Whatman filter paper. Preserve the filtrate, ignite the residue in
platinum crucible at 800oC. Take out the platinum crucible from furnace and fuse the
residue with K2S2O7 on burner. Dissolve the fused mass in the mother liquor and keep it
on hot plate to reduce the volume till about 1 ml. and then add 50 ml. of 1N HCl in to it.

SEPARATION OF REE

Prepare a column of resin height 20 cm of 200-400 mesh, Biograd AG 50W x 8

H-form, conditioned in 1N HCl.

1. Load 50 ml of the above sample solution in the ion exchange column.

2. Elute it with 50 ml. 2N HCl and then 50 ml. 2N HNO3 and discard the treated
solution coming out from the column which will contain Na, Fe, Mg, Rb, Ca, Sr,
Ba, etc.
3. Elute 2 times with 50 ml. 6N HNO3 each time and collect the treated solution
coming out from the column.
4. Elute 2 times with 50 ml. 8N HNO3 each time and collect the treated solution
coming out from the column.

189
 Combine both (3 & 4) elutes (reated solution) and evaporate to dryness. Make the
volume to 50 ml or 100 ml with 1% HNO3 in a measuring flask and determine REE & Y
in it with ICP (AES).

Regenerate the resin column by washing with 150 ml 1N HCl.

Rare earth element spectral lines for ICP analysis

Lanthanum. Recommended line 398.85 nm

This is a sensitive element in the ICP, and also one of the more abundant in
geological samples. It has several lines of almost equal sensitivity and there does not
appear to be any clear evidence to show which lines are the best. The 398.85 line has
been widely used and gives good results. It has a small interference from Ca but usually
this is too small to be significant.

Cerium Recommended line (418.66 nm)

This is almost invariably the most abundant rare earth element in geological
samples and it is rarely necessary to measure at levels close to the detection limit. The
418.66 nm line has been used by several authors and good results obtained. It does suffer
from interferences from Zr and Dy. Normally the levels of these elements are too low
relative to Ce concentrations for the interferences to be significant. However, in a few
rock samples with very high Zr values (5000 g/g in the sample or more) the Zr may be
eluted from the resin with the Ce. Here the interference corrections must be critically
evaluated and possibly other Ce lines might be better.

Praesodymium-Recommended line (422.29 nm)

This line has minor spectral interferences from Ce and also Sr and Ca for which
corrections can be made. Other spectral line (some of which have slightly better
sensitivity) have been studied but appear to have more severe spectral interferences.
Thus the adjacent 422.54 nm Pr line has a serious interference from Sm. Since the levels
of Pr and Sm might well be comparable in geological samples such interference would be
very difficult to correct.

Neodymium-Recommended line (430.36 nm)

This is a more abundant rare earth element and its determination should be
relatively straightforward. The only interference of note on the 430.36 nm line is a very
small interference from Ba and this is rarely significant. Good results are usually
reported for Nd. However, for samples with Ba present at percent levels there could be
problems. Ba (together with Sr and Sc) is one of the few elements that are not separated
from the rare earth elements using the procedure described above.

190
Samarium-Recommended line 359.26 nm

Interferences from the two most abundant rare earths Ce or Nd (and sometimes
both) cause serious problems for the selection of the best line for Sm. On balance the
most sensitive Sm line (359.26) is preferred although it too has a modest interference
from Nd. The Sm 373.92 line is one of the few other Sm lines that could be used; it is
free from Ce and Nd interference although it has some interference from Pr.

Europium-Recommended line 381.97 nm

The chondritic abundance of Eu is only 0.077 g/g and it is therefore very

fortunate that its detection limit in the ICP is quite exceptionally low. All authors appear
in agreement that the 381.97 is the preferred line for analysis. It has trace interference
from Nd but this is small enough to be readily corrected. There is also a very small
interference from Fe that is not significant when the separation technique described above
is used.

Gadolinium-Recommended line (335.05 nm)

The most sensitive line 342.25 nm has interference from Ce. The next most
sensitive line is the 336.22 line, but this has Y interference. Another sensitive Gd line
376.85 has interference from both Ce and Nd. All these interferences would present
serious problems for geological use. The line recommended (335.05) has a small Ca
interference and Zr interference. Normally these will not present a serious problem when
the separation method described above is used.

Dysprosium-Recommended line 353.17 nm

This is much the most sensitive line for Dy and appears to be almost entirely free
from spectral interferences. There is a small interference from manganese but this would
not be present using the separation technique outlined above. Excellent results are
reported for this element.

Holmium-Recommended line 345.6 nm

This is the most sensitive Ho line and almost invariably used. The low
concentration of Ho found in most geological samples make the use of this line almost
obligatory. The only interference recorded is a very small Zr interference and this is
rarely likely to be significant.

Erbium-Recommended line (390.63)

Erbium is a comparatively low abundance rare earth in geological samples. Thus

its sensitivity in the ICP is adequate. The 390.63 is only one of several lines than can be
used and it does give reasonable results.

191
Ytterbium-Recommended line 328.94 nm

This line is the most sensitive, having no significant interferences and excellent
results are obtained.

Lutetium-Recommended line 261.5 nm line

This line has excellent sensitivity and this enables good Lu values to be obtained
in spite of its low abundance in geological samples. The 261.5 line is almost ten times
more sensitive than the next most sensitive line; consequently its use is virtually
obligatory. No serious interferences are recorded.
5.2 ANALYSIS OF PLATINUM GROUP ELEMENTS

Platinum group elements occur in most natural materials at very low concentrations
and are very heterogeneously distributed so their determination almost invariably requires
a separation and preconcentration step.

The names of Platinum Group Elements are given below:

1. Ruthenium (Ru)
2. Rhodium (Rh)
3. Palladium (Pd)
4. Osmium (Os)
5. Iridium (Ir)
6. Platinum (Pt)

To obtain the low detection limit upto ppb level, the preconcentration of PGE is
very essential. Fire assay is the most common sample preparation procedure for PGE
analysis. The basic reason for the continued use of this technique is that a large sample
size can be treated (typically 25 gm, 50 gm or 100 gm), which is to some extent
compensates for nugget effects during sub-sampling. Smaller sample sizes are generally
considered to be inadequate for assessing low grade ores. Fire assay procedures vary
considerably from laboratory to laboratory and their reliability depends to a large extent
on the skill of the analyst, sample composition and the fusion flux mixture used.

Nickel sulphide fire assay is preferred to lead fire assay for multi-element analysis
because it provides efficient collection for most of the noble metals. Only it is less
effective for Au collection and hence lead fire assay is preferred for Au collection.
Special technique is necessary to avoid the loss of volatile Os compounds (OsO4)
particularly at button dissolution stage.

The low detection limit upto 5 to 10 ppb is desirable while analyzing the PGE and
suitable instruments like AAS (Graphite Furnace), ICP (AES) or ICPA (MS) are
preferable.

192
 To obtain the low detection upto ppb level, the preconcentration and separation of
PGE is very essential.

PRECONCENTRATION PROCEDURE:

Since 1970s, the nickel sulphide collection procedure has been documented and
used for the preconcentration of platinum group elements.

PROCEDURE

During the analysis all the reagents of recognized analytical grade are used unless
otherwise specified and only distilled water or deionised water is used.

FUSION AND NICKEL-SULPHIDE BUTTON PREPARATION:

25 to 50 gms of sample (depending upon the PGE present) are taken on glazed
sheet. The flux containing following reagent in proper proportion has been added to the
sample.

Borax (anhydrous) 90 gms

Sodium Carbonate (anhydrous) 45 gms
Nickel Carbonate (LR Grade) 37 gms
Sulphur Powder (Commercial) 12 gms
Silica (LR Grade) 16 gms

The quantity of flux can be changed depending upon the mineralogy of the sample.

The flux is properly mixed with the sample. The mixture is transferred in a free
clay pot and fused in the furnace at 1000oC and the sample with flux is kept at this
temperature for about 1 hr. 15 minute (75 minutes).

The pot is taken out from the furnace using a furnace tong while it is hot and melt
is poured into an iron mould and allowed to cool.

When it is cooled the whole mass is taken out and nickel-sulphide button is taken
out by breaking the slag. The slag is again fused in the same fire clay crucible using the
flux having following proportion.

Borax 10 gms
Sodium carbonate 5 gms
Nickel carbonate 14.3 gms
Sulphur 3.5 gms

The whole mass is fused at 1200oC in the furnace for an hour. The melted mass is
poured in an iron crucible white it is hot and allowed to cool. When it is cooled the slag

193
is removed and nickel-sulphide button is taken out. Both the buttons obtained are then
crushed and ground to powder form using chromium pot in ring grinder mill (Avoid to
grind using tungsten pot).

PREPARATION OF TEST SOLUTION

The crushed nickel sulphide sample is added in conical flask and 500 ml
concentrate HCl is added to it. The flask is sealed using rubber cork and it is warmed on
the hot plate at moderate heat at 130 oC and the solution is aerated. So that the nickel-
sulphide button is completely dissolved and clear dark green solution is obtained. Then
H2S gas through Kipps apparatus is passed through the solution so that the entire nickel-
sulphide button is dissolved. The solution is allowed to cool while passing H2S through
it.

The solution is filtered using 0.8 micron 47 mm dia Millipore filter paper under
suction. The flask is rinse with dil. HCl till the filtrate is colourless. The flask is rinse
and washed with distilled water.

The filter paper is placed in 150 ml beaker, 20 ml aqua regia is added and beaker
is covered with watch glass. It is gently heated till the paper is decomposed. The
solution is filtered using 40 No. Whatman filter paper. It is washed initially with dil. HCl
and then with distilled water.

The filtrate in the beaker is evaporated on hot plate upto 1 to 2 ml. It is poured in
10 ml volumetric flask and diluted to 10 ml using distilled water (A).

The solution obtained (A) is coloured. Therefore, it is passed through Ion

exchange column. (If the solution is colourless, then it is not necessary to pass through
the Ion exchange column).

ION EXCHANGE COLUMN

The biored resins AG-50 W-X8 50 to 100 mesh size is gently heated with dil. HCl
and filtered.

It is washed several times with water. A Dacron wool is placed at the bottom of
column (50 ml capacity burette) and at the base the washed resin is added to it upto 10
cm height. Dacron wool is again kept under top of resin in the burette. The column is
washed with water till the eluate has a pH equal to the water.

SOLUTION SEPARATION

The sample solution from the last step (A) is added in a beaker. 50 ml of 0.1
molar HCl and 0.2 molar HNO3 is added and it is warmed to dissolve precipitated salt. It
is allowed to cool and then passed through the column keeping the flow rate about one

194
drop per second. The solution is collected in 400 ml beaker. The column is washed with
50 ml of distilled water. The volume of this solution is reduced keeping on hot plate. 2
ml of HCl and 3 ml of water is added to dissolve the residue and it is diluted in 10 ml
volumetric flask upto the mark using distilled water.

This solution is used for the estimation of platinum group elements using ICP
(AES).

PREPARATION OF CALIBRATION SOLUTION

The calibration solution is prepared as individual solution of each element or

composite solution. The metal of each platinum group of elements used for preparing
standard solution must be 99.99% pure and free from all contamination.

The instrumental conditions and the wavelength selected for each platinum group
elements are as under:

Sl.No. Name of Element Wavelength in nm Lower Detection Limit (ppm)

1. Iridium 224.268 0.027
212.681 0.030
205.222 0.061
2. Osmium 225.585 0.00036
228.226 0.00063
189.900 0.0012
3. Palladium 340.458 0.044
363.470 0.055
229.651 0.068
4. Platinum 214.423 0.030
203.646 0.055
204.937 0.071
5. Ruthenium 240.272 0.030
245.657 0.030
267.376 0.036
6. Rhodium 233.477 0.044
249.077 0.057
343.489 0.060
7. Gold 242.795 0.0017
267.595 0.031
197.619 0.038

5.3 APPLICATION OF ICP-OES TO WATER ANALYSIS

Water is a valuable commodity even though it is abundant, and its quality in

respect of dissolved or suspended material is of great importance in many areas. The
effect of industrial pollution on the aqueous environment needs regular monitoring, and

195
this in turn implies knowledge of the composition of the water, and the mode of entry and
ultimate fate of any contaminants. In addition, industries are subject to legislative control
on the quality of water they discharge into national water systems and sewers.

Being a liquid, water is already in the most favourable form for injection into the
ICP. No chemical pretreatment beyond stabilization is required.

Again because of the low concentrations involved, interference effects from

troublesome elements such as calcium, magnesium, aluminum, iron etc. are either
negligible or can be dealt with very simply. Some of these elements, which are otherwise
somewhat troublesome or expensive to determine, can be easily and very accurately dealt
with by ICP for example, boron, sulphur, silicon and phosphorus.

Inductively coupled plasma emission spectrometry provides reliable information

on chemical composition of natural waters. The four interdependent stages of sample
collection, sample storage, laboratory analysis and data interpretation will all influence
significantly the accuracy and precision of the final values obtained.

Advantages

Samples in an ideal form for presentation

Minor and trace element determinations possible simultaneously.
Minimum chemical interference.
Good data processing facilities.

Disadvantages

High concentrations of some elements, e.g. Ca and Mg, may interfere with minor
and trace element determinations.
Suspended matter may block some nebulisers.
Low sensitivity for some trace element.
Spectral interferences must be overcome.

Calibration, Standard Solutions and Accuracy

The wide and nearly linear calibration range characteristic of the ICP permits
calibration graphs covering several orders of magnitude in concentration to be used.
Multi-elemental standard solutions should be planned and prepared with care. Thus, it is
usual to group elements together having regard for purity of reagents, relative
concentrations of analytes, spectral interferences, chemical compatibility and stability.
The US National Bureau of Standards produces SRM 1643a, which is a synthetic solution
certified for its trace element content.

This Standard Reference Material is intended primarily for evaluating the

accuracy of trace element determinations in filtered and acidified fresh water and for
calibrating instrumentation used in these determinations.

196
Wavelength Selection and Spectral Interferences

A typical wavelength program is used for water analysis on a simultaneous ICP

fitted with a Nitrogen Generator. Problems can arise where a line of a major component
lies close to a line used to detect a trace element. Variations in the intensity of the
background signal can become critical in the accurate determination of trace elements in
natural water matrices. A small shift in the background signal could generate a totally
spurious value. Subtraction of spectra is a very useful tool in the interpretation of
emission signals arising from analyte concentrations close to the detection limit.

WAVELENGTH FOR ICP JY 180 IN INDIAN BUREAU OF MINES

LABORATORY
Elt WV Low Limit High Limit
Ca 3179.33 0.2 mg/l 400 mg/l
Mg 2790.79 0.2 mg/l 300 mg/l
Na 5895.92 0.1 mg/l 2,500 mg/l
K 7664.9 0.3 mg/l 400 mg/l
Si 2516.11 0.5 mg/l 100 mg/l
Li 6707.76 0.1 mg/l 10 mg/l
Sr 4077.71 0.01 mg/l 10 mg/l
B 2496.78 20 g/l 1 mg/l
Be 3130.42 5 g/l 1 mg/l
Fe 2599.4 20 g/l 100 mg/l
Mn 2576.1 5 g/l 5 mg/l
Al 3082.15 20 g/l 10 mg/l
Co 2286.16 2 g/l 1 mg/l
Cr 2677.16 5 g/l 10 mg/l
Cu 3247.54 2 g/l 5 mg/l
Ni 2316.04 5 g/l 5 mg/l
Zn 2138.56 5 g/l 5 mg/l
Ag 3280.68 5 g/l 1 mg/l
Cd 2265.02 2 g/l 5 mg/l
As 1890.42 10 g/l 1 mg/l
Ce 4186.6 5 g/l 1 mg/l
La 4086.6 10 g/l 1 mg/l
Mo 2020.32 10 g/l 5 mg/l
Nb 3163.4 10 g/l 1 mg/l
Pb 2203.53 2 g/l 5 mg/l
Sb 2068.33 5 g/l 1 mg/l
Se 1960.9 5 g/l 1 mg/l
Sn 1899.89 5 g/l 1 mg/l
Ti 3349.41 10 g/l 5 mg/l
V 3102.3 10 g/l 1 mg/l
W 2079.11 20 g/l 5 mg/l
Y 3710.29 10 g/l 1 mg/l
P 1782.87 50 g/l 5 mg/l
Ba 4554.04 5 g/l 5 mg/l

197
5.4 THE ICP-OES IN ENVIRONMENTAL APPLICATIONS

The ICP-OES is an efficient analytical process for the determination of inorganic

pollutants in environmentally relevant matrices. The application of this technique has
been scheduled as the standard method of analysis for water, waste water and sludge.
The ICP-OES method is distinguished by the following advantageous qualities.

Larger linear dynamic range (3-4 orders)

Little chemical interference
Higher sample throughput (particularly for simultaneous instruments)
Lower Limits of Detection multi-element capabilities
Small calibration expense (as a rule, 2 point calibration)
High degree of automation

Interferences

ICP-OES can be regarded as an interference free method. Spectral Interferences

can be eliminated only through accurate line selection and background correction. The
chemical matrix effects are extraordinarily small for ICP-OES.

Applications in Environmental Analyses

ICP-OES is used for environmental analysis as given below:

1. Waste water : The standardization of the spectrometer occurs for all elements
using a blank sample and a 1 mg/liter standard solution.

2. Air particulates : 250 mg of an air particulate sample were dissolved in 5 ml

HNO3 and 1 ml HF. The clear solution was diluted to 250 ml after filtration. The
sample is analysed by using ICP.

3. Sewage sludge : The sewage sludge dissolution depends on the sewage sludge
procedure with aqua regia. Because of the high content of alkali earth elements
(particularly Ca) and Fe, it is convenient to dilute the sample and to make a matrix
adjustment. The spectrometer was standardized with a blank sample and a
1mg/liter multi-element standard for Cd, Cr, Cu, Ni and Pb and with a 10 mg/liter
standard for Zn.

It is important to note that the use of ICP-OES for determining environmental

analysis and the results obtained are characterized as good with the certified values of
SRM.

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 6. Methods of Analysis of Environmental Samples
_______________________________________________________________________________________________________

6.1 DETERMINATION OF DISSOLVED FLUORIDE, CHLORIDE,

NITRATE, ORTHOPHOSPHATE, SULPHATE IONS USING ION
CHROMATOGRAPHIC METHOD

Determination of common ions such as fluoride, chloride, nitrate, phosphate,

sulphate, etc., which are soluble in water can be analysed using various methods for
individuals. But all above ions can be determined on a single ion chromatograph
instrument.

Principle

A water sample is injected into a stream of carbonate-Bicarbonate eluent and

passed through a series of ion exchangers. The ions of interest are separated on the basis
of their relative affinities for a low capacity, strongly basic anion exchanger (guard &
separator column). The separated anions are directed onto a strong basic cation
exchanger (packed bed suppressor). In the suppressor the separated anions are converted
to their highly conductive acid forms and carbonate-bicarbonate eluent is converted to
weakly conductive carbonic acid. The separated anions in their acid forms are measured
by conductivity and are identified on the basis of retention time as compared to standards
and quantitatively calculated considering the peak area or peak height of the spectra.

Interferences

Substance that has a retention time coinciding with that of any anion to be
determined will interfere such as low molecular weight organic acids interfere at high
concentration for the determination of chloride and fluoride.

Reagents

i. Distilled water filtered through 0.45 um fibre membrane filter.

ii. Eluent solution: Sodium carbonate-sodium bicarbonate solution. Dissolve
1.0176 gm Na2CO3 (0.0024M Na2CO3) + 1.008 gm NaHCO3 (0.003 M,
NaHCO3) in distilled water and dilute to 4000 ml with distilled water.
iii. Stock solutions of standard anions : Prepare 1000 mg/l solution containing
of each anions. F, Cl, NO3, PO4, SO4, etc.
iv. Mixed standard solutions: As per your requirements prepare standard
solutions of different anion composition from the stock solutions. Use
polyethylene vessels for storing of samples and standards.

199
COMPONANTS OF ION CHROMATOGRAPH APPARATUS

Eluent Reservoir
Pump having a very low pulsation effect
Sample injection system (i.e. sample loop : 50 ml. solution)
Precolumn
Separating column with the required separating performance.
Conductivity detector with or without a suppressor device.
Recording device (i.e. integrator with plotter)

Eluent Pump Sample Injection

Separating
Precolum Detector Waste
column
n

Recorder

(Schematic Digram of Ion Chromatograph System)

Procedure

Set up Ion-Chromatograph instrument according to the manufacturers

instructions.

Calibration

Identify the anions by comparing the retention times with those of the standard
solutions. The retention time is dependant on concentration and matrix. The area of peak
(or height) is proportional to the concentration of anion.

Prepare calibration and blank solutions and feed through Ion-Chromatograph

establish the calibration function.

If the ion concentration of sample to be analysed exceeds the range of validity,

dilute the sample. Sometimes, it may be necessary to establish a new calibration
function for the lower concentration range.

Measurement of Sample Solutions

Filter the sample solution through 0.45 membrane filter to prevent adsorption of
the anions and also prevent from contamination of sample.

Feed filtered sample through Ion-Chromatograph in a similar manner.

200
Calculations

Calculate the mass concentration in mg/l of anion in solution using the peak area
or peak height according to the equation.

Anion, mg/l = Ci x ao
bi

Where Ci = measured value in terms of peak height, mm or peak area in l mm2

bi = slope of calibration function, mm.l/mg, mm2/mg.
ao = ordinate intercept of calibration function, mm or mm2

6.2 ANALYSIS OF SODIUM & POTASSIUM IN WATER, WASTE WATER,

EFFLUENTS, SOLIDS, SOILS ETC. USING FLAME PHOTOMETER

Sodium & potassium are normally found in water, wastewater, in solids and soils
also. These can be analysed quantitatively using Flame Photometer at ppm to
percentage levels.

PRINCIPLE OF FLAME PHOTOMETRY

Flame photometry is based on the fact that of alkali metals can be thermally
excited in a low temperature flame and when the atoms return to the ground state they
emit radiation which lies in the visible range of the spectrum. Each element emits a
characteristic radiation at a wavelength specific to that element.

For example : Na = 589 nm, K = 766.5 nm.

Over a certain range of concentration the intensity of the emitted radiation is

directly proportional to the number of atoms returning to the ground state. This in turn is
proportional to the absolute quantity of species volatilised in the flame i.e. light emitted
is proportional to the sample concentration at its characteristics wavelength is isolated by
an optical filter and intensity of that light is measured by a photodetector which provides
a signal proportional to the sample concentration.

Reagents

1. Stock Sodium Chloride Solution : Dissolve 0.2544 gm sodium chloride (AR)

(NaCl) in water and dilute to 1000 ml with distilled water.

1 ml = 100 mg/l = 100 ppm Na

2. Stock Potassium Chloride Solution : Dissolve 0.1910 gm potassium chloride

(KCl) (AR) in distilled water and dilute to 1000 ml with distilled water.
1 ml = 100 mg/l K = 100 ppm K

201
A. DETERMINATION OF SODIUM AND POTASSIUM IN LIQUID
SAMPLES

i. Standard sodium chloride solution : Dilute 10 ml, 100 ppm Na solution to 100
ml with distilled water.

(1 ml = 10 ppm Na)

ii. Standard Potassium chloride solution : Dilute 10 ml, 100 ppm K solution to
100 ml with distilled water.

(1 ml = 10 ppm K)

Prepare standard mixture of sodium and potassium taking suitable aliquots

ranging from 0 to 10 ppm, Na & K in 100 ml volumetric flask and dilute up
to the mark.
Set up an instrument as per the manufacturers operation instructions.
Feed the standard mixture solution of sodium and potassium into the
instrument for standardization.

a. Determination of soluble sodium and potassium in liquid samples.

Filter sample through Whatman No.40 filter paper (in case of removal of
suspended solids).
Take filtrate for the determination of soluble sodium and potassium in liquid
sample.
Feed above filtrate into the Flame Photometer which is standardized as per
instructions.
Find out the concentration obtained either from graph or directly from
instrument itself.
Calculate concentrations of sodium and potassium and express in mg/l.

b. Determination of total sodium and potassium in liquid samples.

Take suitable aliquot of sample in 250 ml beaker.

Add few drops of hydrochloric acid (in case of suspended solids are present)
to dissolve suspended solids.
Warm on hot plate if needed, cool.
Filter through Whatman filter paper No.40, wash.
Make up the volume to 100 ml with distilled water.
Feed this filtrate in the Flame Photometer as usual manner.
Calculate the concentrations of sodium and potassium and express in mg/l.

202
B. DETERMINATION OF SODIUM AND POTASSIUM IN SOLID
SAMPLES

Take 0.1-1 gm fine powdered sample in platinum crucible (wt. can be varied
depending upon conc. of Na & K).
Add 1-2 drops of con. Sulphuric acid so that all sample should be wet.
Add 2-5 ml hydrofluoric acid.
Evaporate to dryness on either hot plate or on burner.
Extract residue with little volume of hydrochloric acid.
Warm on hot plate for few minutes. Cool.
Filter through Whatman filter paper No.40. Wash.
Transfer filtrate in 100 ml volumetric flask and dilute to 100 ml with distilled
water.
Feed this solution in flame photometer as usual.
Calculate the concentration of sodium and potassium and express in
percentage or ppm.

6.3 DETERMINATION OF TURBIDITY IN WATER, WASTE WATER

USING TURBIDITY METER/NEPHELOMETER

Turbidity in water/waste water is occurred due to presence of suspended matter.

It can be measured using turbidity meter.

Principle

Turbidity is based on comparison of the intensity of light scattered by a sample

with the intensity of light scattered by standard reference suspension under similar
conditions.

Reagents

i. Stock hydrazine sulphate solution : Dissolve 1 gm hydrazine sulphate

(NH2)2.H2SO4) in water and dilute to 100 ml with distilled water.
ii. Stock hexamethylene tetramine solution : Dissolove 10 gms
hexamethylene tetramine {(CH2)6 N4)} in distilled water and dilute to 100 ml
with distilled water.
iii. Standard mixture suspension solution : Mix 5 ml of stock hydrazine
sulphate solution and 5 ml of hexamethylene tetramine solution in 100 ml
volumetric flask and dilute to 100 ml with distilled water.
(Turbidity of this solution = 400 NTU).
iv. For less than 400 NTU, dilute 10 ml 400 NTU solution to 100 ml in
volumetric flask.
(Turbidity of this solution = 40 NTU).

203
Preparation of Standards

Take suitable aliquots of standard suspension turbidity solution ranging from

0-40 NTU in 100 ml volumetric flasks and make up to the mark.
Calibrate the instrument as per manufacturers instructions.

Measurement of Turbidity in samples

Place the sample in absorbing tube of the meter and compare with the standards.
(Note Dilution may be done in case of reading is out of calibration range)
Calculations :

NTU = A X (B+C)
C

Where A = NTU found in diluted sample

B = Volume of dilution water, ml
C = Sample volume taken, ml.

Interpretation of results

Turbidity readings may be reported as follows :

Reading Range NTU Report to the nearest NTU

0-1.0 0.05
1-10 0.10
10-40 1
40-100 5
100-400 10
400-1000 50
>1000 100

6.4 DETERMINATION OF COLOUR IN WATER AND WASTEWATER

(UV-SPECTROPHOTOMETRIC METHOD)

Colour may be due to presence of soluble ions in water such as iron and
manganese or any other material by some activities.

Principle

Colour can be determined with comparing with that of known standards of colour
units.

204
Reagents

Potassium chloroplatinate solution : Dissolve 0.2492 gm potassium

chloroplatinate (K2PtCl6) and 0.2 gm cobaltous chloride (CoCl2.6H2O) in 10 ml conc.
HCl and dilute to 100 ml with distilled water.

(1 ml = 1 mg Pt = 1000 g Pt = 1000 Hazen)

Preparation of Standard Graph

Take suitable aliquots of standard potassium chloroplatinate solutions ranging

from 0-70 Hazen units in 100 ml volumetric flasks and dilute to 100 ml.
Measure absorbance/transmittances at 288 nm.
Plot standard graph between absorbance and hazen units.

Measurement of sample solutions

Measure absorbance of sample directly at 288 nm.

If absorbance exceeds 70 Hazen, sample solution is to be diluted accordingly
so that absorbance should come in range of 70 Hazen units.

(Note In case of turbid solution, sample is to be centrifused to remove turbidity before taking
absorbance).

6.5 DETERMINATION OF SUSPENDED SOLIDS, TOTAL SOLIDS,

DISSOLVED SOLIDS, INORGANIC MATTER AND VOLATILE
MATTER IN WATER, WASTE WATER, EFFLUENT ETC.

Water, wastewater, effluent etc. always contain solids either suspended or

dissolved, may be organic or inorganic.

A. SUSPENDED SOLIDS

Take suitable aliquot of the sample in which suspended solids is to be

determined
Filter through pre-weighed sintered glass crucible of G-4 porosity on vacuum
pump.
Keep sintered crucible in oven at 105oC for drying purpose.
Weigh up to constant weight is obtained.

Calculations :

S.S., mg/l = mg,S.S. (in aliquot) x 1000

ml. aliquot of sample

205
 if aliquot = 50 ml, then

S.S., mg/l = mg, S.S. (in aliquot) x 20

B. TOTAL SOLIDS : (SUSPENDED SOLIDS + DISSOLVED SOLIDS)

Take suitable aliquot of homogeneous sample in pre-weighed platinum dish.

Keep on hot plate to evaporate completely
Dry at 105oC.
Weigh repeatedly up to constant weight is obtained.

T.S., mg/l = mg, T.S. (in aliquot) x 1000

ml, aliquot.

If aliquot = 50 ml, then

T.S., mg/l = mg, T.S. (in aliquot) x 20

C. DISSOLVED SOLIDS :

Take suitable filtered (through Whatman No.40 filter paper) aliquot in

platinum dish.
Evaporate on hot plate
Dry at 105oC
Weight repeatedly up to constant weight obtained.

Calculations :

D.S., mg/l = mg, wt (in aliquot) x 1000

ml. aliquot of sample

If aliquot = 50 ml, then

D.S., mg/l = mg, wt. (in aliquot) x 20

D. TOTAL INORGANIC MATTER AND ORGANIC MATTER

Take suitable aliquot of homogeneous sample in pre-weight platinum dish.

Evaporate on hot plate

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 Dry at 105oC
Take weight of dish and total solids up to constant weight.
Ignite platinum dish along with solids on 550 oC in muffle furnace for half
an hour.
Take out dish, cool in desicator
Weigh up to constant weight is obtained.

Calculations

a. Inorganic matter, mg/l = mg (wt. of residue) in aliquot after 550 oC x 1000

ml, aliquot of sample

b. Organic Matter, mg/l = mg, loss in mass after 550oC x 1000

ml. aliquot

If aliquot = 50 ml, then

Mg/l = mg (in aluquot) x 20

E. DISSOLVED ORGANIC AND INORGANIC MATTER

Take suitable aliquot of filtered (through Whatman No.40 filter paper) in

pre-weighed platinum dish.
Evaporate on hot plate.
Dry at 105oC in oven.
Weigh repeatedly up to constant weight obtained.
Ignite platinum dish along with solids obtained at 550 oC in muffle furnace
for half an hour.
Take out, cool in desicator.
Weigh up to constant weight is obtained.

Calculations

Inorg.Matter, mg/l = mg. of residue after 550oC x 1000

ml. aliquot sample

Org.Matter, mg/l = mg. mass loss at 550oC x 1000

ml. aliquot sample

If aliquot = 50 ml, then

Mg/l = mg, (in aliquot) x 20

207
6.6 DETERMINATION OF CHEMICAL OXYGEN DEMAND IN WASTE
WATER/EFFLUENT

Chemical Oxygen Demand (COD) test provides the oxygen required for the
chemical oxidation of organic matter using a strong chemical oxidizing reagent.

Chemical Oxygen Demand determination has an advantage over BOD

determination; the results can be obtained in 5 days while COD can be obtained within 5
hours. Moreover, the test is much easier, gives reproducible results and less effect of
interferences as compared with B.O.D. test.

Principle

Organic matter present in sample gets oxidized quantitatively by Potassium

Dichromate (K2Cr2O7) in presence of sulphuric acid (H2SO4) added in excess. The
excess potassium dichromate (K2Cr2O7) remaining after the reaction is then titrated
against ferrous ammonium sulphate solution {(Fe(NH4)2.SO4)2.} The volume of
potassium dichromate consumed for oxidation of organic matter gives the oxygen
required for the reaction.

Reagents

i. Standard potassium dichromate solution (0.25 N) : Dissolve 12.259 gms

K2Cr2O7 in water and dilute to 1000 ml with distilled water.
ii. Standard Ferrous Ammonium Sulphate Solution (0.25 N) : Dissolve 97.5
gms. Ferrous Ammonium Sulphate {(Fe(NH4)2.(SO4)2.6H2O)} in 50 ml conc.
H2SO4 and dilute to 1000 ml with distilled water.
iii. Sulphuric acid reagent : Dissolve 10 gm silver sulphate (Ag2SO4) in about
1000 conc. H2SO4 and keep for dissolution.
iv. Ferroin Indicator : Dissolve 1.485 gm 1-10-phenonthrolene + 0.695 gm
Ferrous Sulphate (FeSO4.7H2O) in water and dilute to 100 ml with distilled
water.
v. Mercuric sulphate : HgSO4 (AR/GR).

Standardization of ferrous ammonium sulphate

Take suitable aliquot of standard potassium dichromate solution in 250 ml

beaker.
Add about 15-20 ml conc. H2SO4.
Dilute to about 100 ml with distilled water, Cool.
Add 2-3 drops of Ferroin indicator.
Titrate against ferrous ammonium sulphate solution. Change of blue-green
colour to reddish brown shows the end point.

208
Calculation

NFAS = ml,K2Cr2O7 x N K2Cr2O7

ml,F.A.S. consumed
Procedure

Take 0.4 gm HgSO4 in 250 ml refluxing flask

Add suitable aliquot of sample in the flask
Add few glass bead to avoid bumbling/bumping
Add excess 0.25N dichromate solution. (can be known by observing yellow
colour of dichromate remain in the flask)
Add about 30 ml conc. H2SO4 containing silver sulphate mix thoroughly.
Place refluxing flask on heating mentles or on burner and reflux for about 2
hours.
Stop heating; allow to cool, wash a condenser with distilled water.
Transfer the content in 250 ml conical flask with careful washing.
Dilute if necessary. Cool.
Add 2-3 drops of Ferroin indicator.
Titrate the excess dichromate against ferrous ammonium sulphate solution.
Change of blue green colour to reddish brown shows the end point.
Carry out the blank in a similar manner.

Calculations

COD, mg/l = (mlb mls) x NFAS x 8000

ml aliquot of sample

Where mlb =Volume of Ferrous Ammonium Sulphate required for blank.

mls =Volume of Ferrous Ammoninum Sulphate required for sample
N =Normality of Ferrous Ammonium Sulphate

If aliquot = 20 ml, then

COD,mg/L = (mlb mls) x N x 50 x 8

1 ml 1 N K2Cr2O7 = 8 mg COD

(Note : (i) Ag2SO4 acts as a catalyst, (ii) HgSO4 masks halides)

209
6.7 DETERMINATION OF BIOCHEMICAL OXYGEN DEMAND (BOD) IN
WASTE WATER AND EFFLUENTS

Biochemical Oxygen Demand is defined as the amount of oxygen required by

micro-organisms while stabilizing biologically decomposable organic matter in waste
water, effluents under aerobic conditions. The test is carried out at 20 oC for 5 days is
considered as the standard. BOD provides a data for the determination of an efficiency of
wastewater treatment procedures and pollution load of wastewater.

Normally two methods are used for the determination of BOD.

a. Direct Method : BOD is determined by measuring dissolved oxygen

of waste water/effluent before and after incubation period of 5 days at
20oC.
b. Seeded Dilution Method : In seeded dilution method, dilute water is
seeded with proper kind and number of organisms before the BOD
test. It is important that a mixed group of organisms is called seed.
In absence of toxic substances all necessary nutrients such as nitrogen
and phosphorous should be present.

Interference : Heavy metals & residual chlorine are commonly observed as interference
in this process. Residual chlorine can be removed by the addition of equivalent amount
of sodium sulphite solution.

Reagents

i. Phosphate Buffer Solution (pH = 7.2) : Dissolve 8.5 gms potassium

dihydrogen phosphate (KH2PO4) 21.75 gms dipotasium hydrogen phosphate
(K2HPO4) + 33.4 gms disodium hydrogen phosphate (Na2 HPO4.7H2O) 1.7
gm ammonium chloride (NH4Cl) in water and dilute to 1000 ml with distilled
water.
ii. Magnesium sulphate solution (2.25%) : Dissolve 22.5 gms Magnesium
Sulphate (MgSO4.7H2O) in water and dilute to 1000 ml with distilled water.
iii. Calcium chloride solution (2.75%) : Dissolve 27.5 gms calcium chloride
(CaCl2) in water and dilute to 1000 ml with distilled water.
iv. Ferric Chloride Solution (0.025%) : Dissolve 0.25 gms ferric chloride
(FeCl3.6H2O) in water and dilute to 1000 ml with distilled water.
v. Sodium Sulphite Solution (0.025 N) : Dissolve 1.575 gm sodium sulphite
(Na2SO3) in water and dilute to 1000 ml with distilled water.
vi. Potassium iodide (KI) : Crystal (AR/GR)
vii. Starch indicator: (0.2%) solution.
viii. Acetic acid : Glacial acetic acid.

210
Procedure

A. Preparation of dilution water

a.
Aerate the required volume of distilled water in a PVC container by bubbling
compressed air for 1-2 days to attain saturation.
Add 1 ml phosphate buffer
Add 1 ml magnesium sulphate solution
Add 1 ml calcium chloride solution
Add 1 ml ferric chloride solution.
Dilute to 1000 ml with aerated water and mix thoroughly

b. In case of waste water/effluent, which are not expected to have sufficient bacterial
population, add 2 ml seed into dilution water. (Normally, 2 ml settled sewage is
considered sufficient for 1000 ml dilution water).

c. Neutralise the sample to pH = 7 if it is highly alkaline or acidic accordingly.

d. Removal of residual chloride

Take suitable aliquot of sample in 250 ml beaker/volumetric flask.

Add 10 ml of 1:1 acetic acid solution.
Dilute with distilled water if necessary
Add about 1 gm KI solid (yellow colour appears if R-Cl2 is present).
Titrate the content against standard sodium sulphite (Na2SO3) solution using
starch as an indicator.
Calculate the volume of sodium sulphite required for aliquot taken.
Add calculated volume/amount of sodium sulphite in aliquot sample taken for the
determination of BOD.

e. If samples having high dissolved oxygen i.e. above 9 mg/l due to algal, reduce
dissolved oxygen. by agitating the sample

f. Several dilutions of prepared sample are to be done so as to obtain about 50%

depletion of Dissolved oxygen in dilution water but not less than 2 mg/l, dissolved
oxygen.

g.
Siphon out seeded dilution water in a volumetric flask/measuring cylinder half the
required volume.
Add required quantity of mixed sample solution.
Dilute the desired volume by siphoning dilution water and mix thoroughly.

h. The following dilutions are suggested for better results.

211
 For strong trade waste : 0.1% to 1%
Raw or settled sewage : 1% to 5%
Treated effluent : 5% to 15%
River Water : 25% to 100%

i. Siphon the dilution prepared as above in 4 labeled BOD bottles (300 ml capacity) and
stopped immediately.

j. Keep one bottle for determination of initial dissolved oxygen and incubate
3 bottles at 20oC for 5 days.

(Note : Confirm that bottles have a water sealed)

k. Prepare a blank in duplicate by siphoning plain dilution water (without seed) to

determine the oxygen consumption in dilution water.

l. Fix the bottles kept for immediate D.O. determination and blank.

Add 2 ml MnSO4 solution in each bottle.

Add 2 ml Acid Reagent (500 gm NaOH + 150 gm KI +10 gm NaN3 in 1 lit. D.M.
water) (NaOH + KI + NaN3) solution
Determine D.O. in sample and in blank on initial day as usual manner.
Determine D.O. in samples. Kept in incubator after 5 days at 20oC.

Calculations

Determine D.O. in the sample and in blank on initial day and after 5 days, when
dilution water is not seeded:

BOD5 mg/L = (Di Df) (Bi Bf) x decimal volumetric fraction of samples used
When dilution water is seeded:
BOD5 mg/L =
(Di Df) (Bi Bf) x Vol.of seed in diluted sample x decimal fraction of sample used
Vol.of seed in seed control

Where Di = D.O. of sample for initial day

Df = D.O. of sample for final day (i.e. 5 day)
Bi = D.O. of blank for initial day
Bf = D.O. of blank for final day (i.e. 5 day)

6.8 DETERMINATION OF DISSOLVED OXYGEN IN WATER AND

WASTEWATER

Oxygen is the most important for all living organisms, which is taken from air or
taken from water in case of aquifers who consume dissolved oxygen in water/wastewater.

212
Dissolved oxygen can be analysed either using titrimetric method or using membrane
electrode method.

TITRIMETRIC METHOD : IODOMETRIC AZIDE MODIFICATION METHOD

Principle :

In this process, manganous sulphate oxidized to manganous hydroxide (brown

precipitate) in strong alkaline medium further iodine ions in an acidic solution, oxidized
manganese reverts to its divalent state liberating of iodine equivalent to dissolved oxygen
present in the sample. Liberated iodine is then determined by titrimetric method using
sodium thiosulphate as a titrant and starch as an indicator.

Inference : NO2-N and ferrous iron interefers, addition of KF solution before

acidification, ferrous iron can be masked up to 200 mg/l.

Reagents

i. Manganous sulphate solution : Dissolve 480 gms MnSO4.4H2O or 400 gm

MnSO4.2H2O or 364 gm MnSO4.H2O in distilled water and dilute to 1000 ml
with distilled water.
ii. Alkali-iodide-azide solution : Dissolve 500 gm NaOH or 700 gm KOH +
135 gm NaI (OR 50 gm KI) in distilled water + 10 gm NaN3, mix & dilute to
1000 ml with distilled water.
iii. Sulphuric acid : concentrated.
iv. Starch solution : about 2% solution in boiling water.
v. Standard sodium thiosulphate solution (0.025 M). Dissolve 6.205 gm
Na2S2O3.5H2O in distilled water, add 2-4 palletes of NaOH, mix and dilute to
1000 ml with distilled water.
vi. Standard potassium bi-iodate solution : Dissolve 0.8124 gm KH(IO3)2 in
distilled water and dilute to 1000 ml.
vii. Potassium fluoride solution : (40%) : Dissolved 40 gm KF.2H2O in 100 ml
distilled water.

STANDARDIZATION OF SODIUM THIOSULPHATE SOLUTION

Take suitable aliquot of standard bi-iodate solution in 250 ml conical

flask.
Add about 2 gms of KI solid
Add about 1 ml conc. H2SO4
Dilute to about 100 ml with distilled water.
Titrate liberated iodine against standard sodium thiosulphate solution
using starch as an indicator. Disappearance of blue colour shows the end
point.
N sod.thio. = ml.aliquot (St.pot.bi-iodate) x N
ml. (vol. of thio.sulphate)

213
DETERMINATION OF DISSOLVED OXYGEN

Procedure

Take suitable volume (150 ml) of sample in 150 ml BOD bottle (Normally
300 ml full bottle sample is to be taken).
Add 1 ml MnSO4 solution (Note: tip of pipette should be below the surface of
sample solution)
Add 1 ml alkali-iodide-azide solution as above, mix well.
Stand for few minutes to settle precipitate.
Add 1 ml conc. H2SO4
Mix the content by inverting the bottle several times till precipitate is
completely dissolved.
Take a suitable aliquot from above solution considering added reagents and
loss of solution.
For example if we take 100 ml aliquot we should take 101.5 ml for titration.
Titrate against sod.thiosulphate solution using starch as an indicator as usual
manner.

Calculations

D.O., mg/L = ml(thio) x N(thio) x 1000 x 8

ml aliquot

If aliquot = 200 ml, then

D.O., mg/L = ml(thio) x N(thio) x 5 x 8

Note: 1 ml, 1N thiosulphate = 8 mg D.O.

6.9 DETERMINATION OF PHENOLIC COMPOUNDS AS C6H5OH

(DIRECT COLORIMETRIC METHOD)

Phenol (C6 H5OH) is a hydroxy derivative of benzene. It may occur in

industrial as well as in drinking water. During chlorination process it produces some
peculiar objectionable taste and can be removed giving treatment with chloramines,
ozonization, activated carbon adsorption etc.

Principle

Phenolic compounds react with 4-aminoantipyrine at pH about 8-10 in

presence of pot. ferricyanide to form a coloured antipyrine dye which can be measured at
510 nm.

214
Interference :

Interferences can be eliminated using distillation method at the initial stage.

Reagents

i. Stock phenol Solution : Dissolve 0.10 gm phenol in distilled water and dilute to
1000 ml with distilled water.
(1 ml = 0.1 mg phenol = 100 g phenol).
ii. Standard phenol solution : Dilute 10 ml, 100 g phenol solution to 1000 ml with
distilled water.
(1 ml = 1 g phenol)
iii. Ammonium chloride solution : (5%) : Dissolve 5 gm NH4Cl in water and
dilute to 100 ml with distilled water.
iv Ammonia solution : Concentrated solution.
v. Aminoantipyrine solution : (2%) : Dissolve 2 gm 4-amino-antipyrine in
distilled water & dilute to 100 ml with distilled water.
vi. Potassium ferricyanide solution : (8%) : Dissolve 8 gm potassium ferricyanide in
water and dilute to 100 ml with distilled water.

PREPARATION OF STANDARD GRAPH:

Take suitable aliquots from standard phenol solution from range of 0 to 10

mg/lit. phenol in 100 ml volumetric flask.
Add 2 ml NH4Cl solution in each volumetric flask mix.
Adjust pH around 8-10 using ammonia solution, mix.
Add 2 ml aminoantipyrine solution. Mix.
Add 2 ml pot.ferricyanide solution mix again and dilute to 100 ml with
distilled water. Mix thoroughly.
Measure absorbances/transmittances at 510 nm. after 15 minutes.
Carry out blank in a similar manner.
Plot a standard graph between absorbance and concentrations of phenol.

PROCEDURE FOR WATER/ WASTEWATER/EFFLUENT SAMPLES

Take suitable aliquot (without distillation) of sample in 100 ml. volumetric

flask.
Add 2 ml NH4Cl solution. Mix.
Adjust pH around 8-10 with ammonia solution. Mix.
Add 2 ml aminoantipyrine solution. Mix again.
Add 2 ml pot. ferricyanide solution. Mix and dilute to 100 ml with distilled
water and mix thoroughly.
Measure absorbance/transmittance at 510 nm after 15 minutes.

215
Calculations

Phenol, g/L = g phenol (in aliquot) x 1000

ml, aliquot
If aliquot = 100 ml then

Phenol, g/L = g phenol (in 100 ml) x 10

6.10 DETERMINATION OF OIL AND GREASE IN WATER AND WASTE

WATER

Oil and grease are the material that dissolved in trichlorotrifluroethane in

acidified solution along with sulphur compounds. Organic dyes, chlorophyls etc. It can
be determined by gravimetric method.

Principle

Oil and grease are extracted with trichlorotrifluoroethane and separated

from the aquous phase of sample. The extracted oil and grease present in
trichlorotrifluoroethane is evaporated and the residue is weighed and reported as oil and
grease.

Reagents

i. Hydrochloric acid : Dilute 1 : 1.

ii. Sodium sulphate crystals (Na2SO4), (anhydrous)
iii. Trichlorotrifluoroethane : boiling point 47oC.

Procedure :

Take suitable aliquot in a separating funnel of suitable volume.

Add about 2-5 ml dil. Hydrochloric acid, Mix.
Add about 25-30 ml trichlorotrifluoroethane in the funnel.
Shake gently for about 5-10 minutes.
Allow to stand for separating into two layers.
Run the trichlorofrifluoroethane layer in a platinum dish weighed previously.
Again add 25-30 ml trichlorotrifluoroethane into the separating funnel.
Shake for 5-10 minutes.
Allow to stand for separating two layers.
Drain the organic layer in the same dish.
Place the dish either on water bath or in oven to dry or evaporation.
Dry on 105-110oC for 10-15 minutes.
Take weight after drying.
Carry out blank.

216
Calculations

Deduct the blank mass, if any

Oil & Grease, mg/L = wt. of dish after drying wt. of emply dish x 1000
ml, sample aliquot

if 1000 ml sample is taken, then,

Oil & Grease, mg/L = Final wt. of dish Initial wt. of dish

6.11 DETERMINATION OF SULPHATE IN WATER/WASTE

WATER/EFFLUENT

Sulphate ions (SO4-2) occur in natural water and also in industrial waste. Sulphate
compounds are easily soluble in water. Mine drainage wastes may contribute large
amount of SO4-2 through pyrite oxidation.

Two methods are described for the determination of sulphate.

a. TURBIDIMETRIC METHOD

Principle

Sulphate ion (SO4-2) is precipitated in an acidic medium with (BaCl2) barium chloride
so as to form (BaSO4) barium sulphate crystal of uniform size and absorbance is
measured at 420 nm comparing with standards.

Inferences

Colour and suspended solids in large amounts interfere. Suspended solids can be
removed by filtering a sample solution.
Reagents :

i. Buffer solution : Dissolve 30 gms magnesium chloride (MgCl.6.H2O) + 5

gms sodium acetate (CH3COONa.3H2O) + 1 gm pot. nitrate (KNO3) + 20 ml
acetic acid in water and dilute to 1000 ml with distilled water.
ii. Barium chloride crystals.
iii. Standard sulphate solution : Dissolve 0.2219 gm Na2SO4 in distilled water
and dilute to 1000 ml.

1 ml = 0.1 mg SO4-2 = 100 ug SO4-2

Preparation of Standard Graph

217
 Take suitable aliquots of standard sulphate solution ranging from 0-500 g
SO4 in 100 ml volumetric flasks.
Add 20 ml buffer solution in each flasks mix thoroughly.
Add a pinch of barium chloride crystals (BaCl2)
Stir for about one minute
Measure the absorbance/transmittances at 420 nm.
Plot a standard graph between absorbance and concentrations of sulphate.

Measurement of sample solution

Take suitable aliquot of filtered sample solution in 100 ml volumetric flask.

Add 20 ml buffer solution, mix thoroughly.
Add pinch of barium chloride crystals.
Stir for about 1 minute.
Measure absorbance/transmittance at 420 nm.
Carry out blank in a similar manner.
Find the concentration from standard graph.

Calculations

SO4, mg/l = mg SO4 in aliquot x 1000

ml aliquot

if aliquot = 50 ml, then

SO4, mg/l = mg, SO4 in 50 ml aliquot x 20

B. GRAVIMETRIC METHOD

Principle

Sulphate (SO4-2) is precipitated in hydrochloric acid (HCl) solution as

(BaSO4) barium sulphate by adding barium chloride (BaCL2).

Interference

Commonly suspended solids are noticed as inference in this method and

can be remove by filtering a sample solution before starting analysis.
Reagents

i. Hydrochloric acid solution 1:1 diluted.

ii. Barium chloride solution (10%) : Dissolve 10 gms barium chloride (BaCl2)
in 100 ml distilled water.

218
 iii. Methyl red indicator solution : (0.1%) : Dissolve 0.1 gm methyl red in 100
ml distilled water.
iv. Silver nitrate solution (1%) : Dissolve 1 gm AgNO3 in 100 ml distilled
water.

(Note : Solution is used to check the presence of chloride ions in washings of BaSO4 residue)

Procedure : Removal of Silica

Take suitable aliquot of sample solution in 100 ml platinum dish.

Add 1-2 ml hydrochloric acid.
Evaporated to dryness.
Ignite at 180oC to burn out organic matter if present.
Extract residual mass with 2 ml hydrochloric acid. Boil and allow to cool and
settle insolubles.
Dilute to about 100 ml, boil and filter through Whatman No.40 filter paper
after cooling.
Take filtrate in 250 ml beaker.
Adjust pH = 4-5 using methyl red indicator and adding hydrochloric solution.
Add 2 ml hydrochloric acid in excess.
Boil solution on burner.
Mean time warm barium chloride solution also.
Add about 5 ml barium chloride solution in boiling condition.
Continue boiling for about 15 minutes to coagulate BaSO4 precipitate.
Allow to settle precipitate for over night.
Filter barium sulphate through Whatman No.42 filter paper.
Wash with hot water till absence of chloride ions. (can be checked by adding
AgNO3 solution, white precipitate appears if chloride ions present).
Ignite residue (precipitate) of BaSO4 at 900-950oC in muffle furnace.
Weigh BaSO4 mass up to constant weight obtained.

Calculations

SO4, mg/L = Wt. of BaSO4 (in aliquot) x 0.4116 x 1000

ml aliquot of sample

if aliquot = 50 ml, then

SO4, mg/l = mg, BaSO4 (in aliquot) x 0.4116 x 20

6.12 ANALYSIS OF SULPHIDE IN WATER AND WASTE WATER

Sulphide normally present in wastewater from the decomposition of

organic matter or from industrial wastes and from the bacterial reduction of sulphate.

219
Sulphide forms H2S which is toxic. It attacks metals and caused corrosion of concrete
sewers because it is oxidized biologically to form H2SO4 on the pipe walls.

Determination of sulphide : Iodometric Method

Principle

Excess of standard iodine solution is added in the acidic media to get

oxidize sulphide. Residual iodine is then titrated against standard sodium thiosulphate
solution using starch as an indicator and sulphide is calculated accordingly.

Reagents

i. Standard iodine solution : (0.01 N) : Dissolve 10-15 gms KI in little

distilled water, add 1.28 gms iodine crystals. Allow to dissolve completely,
dilute to 1000 ml with distilled water. This solution should be standardized
against standard sodium thiosulphate solution using starch as an indicator.
ii. Standard sodium thiosulphate solution :(0.01 N) Dissolve 2.482 gms
sod.thiosulphate in distilled water and dilute to 1000 ml with distilled water.
iii. Hydrochloric Acid solution : 6 N.
iv. Starch Solution : Prepare about 5% with boiling water.

Standardization of iodine solution

Take suitable aliquot of iodine solution in 250 ml conical flask.

If necessary dilute with distilled water.
Add 2 ml, 6N HCl solution, mix.
Titrate against standard sodium thiosulphate solution, near the end point, add
2-3 ml starch solution and continue titration till blue colour disappears.

Calculation

N (Iodine) = N (thio) x vol. of thio

Vol..of iodine solution taken

Procedure for samples: Without precipitation with Zn

Take suitable aliquot of iodine in 250 ml conical flask.

If necessary dilute with distilled water.
Add 2 ml, 6N HCl solution.
Pipette out a suitable aliquot of the sample and discharge it under a surface of
solution present in conical flask. Observe the colour of iodine which must be
present at this stage, if not add more standard iodine solution so that colour of
iodine remains (brown colour).
Titrate the content of conical flask against standard sodium thiosulphate
solution using starch as an indicator.

220
 Disappearance of blue colour shows the end point.

Calculations

S-2, mg/l = {(ml Iodine x N Iodine) (ml,thio x N thio)} x 16,000

ml.sample aliquot

(1 ml 1 N Iodine Solution = 16 mg S-2)

6.13 ANALYSIS OF SILICA IN WATER AND WASTE WATER

The silica (SiO2) content in natural water is found in various

concentrations. Silica in water is undesirable component for a number of industrial uses
because it forms silica and silicate scale, which is very difficult to remove.

A. DETERMINATION OF SILICA USING SPECTROPHOTOMETRIC

METHOD

Principle

In acidic pH, ammonium molybdate reacts with silica forming

molybdosilicic acid gives yellow colour which further treated with reducing agent amino-
2-naphthol-4-sulphonic acid forming blue colour and can be measured at 690 nm.

Interference
Colour, turbidity, sulphide & phosphate interfere. Colour and turbidity can
be removed using aluminium hydroxide suspension solution and treatment, while
phosphate can be removed by treatment of oxalic acid solution.
Reagents

i. Ammonium molybdate solution: (10% solution): Dissolve 10 gm

(NH4)6Mo7O24.4H2O in distilled water and dilute to 100 ml with distilled
water.
ii. Oxalic acid solution: (7.5% solution): Dissolve 7.5 gms oxalic acid
(C2H2O4.H2O) in distilled water and dilute to 100 ml with distilled water.
iii. Reducing agent solution: Dissolve 0.50 gm amino-2-naphthol-4-sulphanic
acid. Add 1 gm sod.sulphite (Na2SO3) in 50 ml distilled water, warm, prepare
30 gm NaHSO3 solution in 150 ml distilled water and mix both. Filter in
polythene bottle.
iv. Sodium bicarbonate : Powder
v. Hydrochloric acid : 1:1 diluted
vi. Sulphuric acid: 1 N solution.
vii. Stock silica solution: Dissolve 0.4734 gm sod. Metasilicate nonanhydrous
(Na2SiO3.9H2O) in distilled water and dilute to 1000 ml with distilled water.
1 ml = 100 g SiO2 = 46.67 g.Si

221
 viii. Standard silica solution: Dilute 10 ml, 100 g SiO2 solution to 100 ml
with distilled water (1 ml = 10 g SiO2 = 4.676 g Si)

Preparation of standard graph

Take suitable aliquots of standard silica solution ranging from 0-10 g SiO2 in
100 ml volumetric flasks.
Add 1 ml (1:1) hydrochloric acid solution in each volumetric flask. Mix.
Add 2 ml ammonium molybdate solution, Mix.
Add 1.5 ml oxalic acid solution. Mix again.
Add 2 ml reducing agent solution, mix and dilute to 100 ml with distilled
water. Mix thoroughly.
Measure the absorbance at 690 nm after 10 minutes.
Plot a graph between absorbance and concentrations.

Determination of silica in samples

Take suitable aliquot of the sample in 100 ml volumetric flask.

Add 1 ml (1:1) hydrochloric solution. Mix.
Add 2 ml ammonium molybdate solution. Mix.
Add 1.5 ml oxalic acid solution. Mix.
Add 2 ml reducing agent solution, mix, dilute to 100 ml with distilled water.
Mix thoroughly.
Measure absorbance at 690 nm after 10 minutes.
Carry out blank in a similar manner.

Calculations

SiO2, g /l = g SiO2(in aliquot) x 1000

ml aliquot

If aliquot = 50 ml, then

SiO2, g = g SiO2 (in 50 ml) x 20

B. DETERMINATION OF SILICA BY GRAVIMETRIC METHOD

Principle

Decomposition of silica in presence of HCl and then dehydration by drying the

sample and extraction with dil. HCl, residue which contains crude silica after ignition at

222
900-950oC, followed by hydrofluorization in presence of H2SO4, again igniting at 900-
950oC and the difference can be obtained by weighing procedure in this process.

Reagents

i. Dilute/con. Hydrochloric acid.

ii. Conc. sulphuric acid.
iii. Hydrofluoric acid (40%).

Procedure

Take suitable aliquot of sample in 250 ml beaker.

Add 10-15 ml hydrochloric acid.
Keep a beaker on hot plate.
Allow to evaporate and dry the sample
Allow to cool and add 10-15 ml hydrochloric acid.
Boil the content for 10 minutes.
Cool the content.
Filter through Whatman filter paper.
Wash residue with hot water for 2-5 times.
Place the residue in platinum crucible along with a filter paper.
Ignite at 900-950oC for an hour (in furnace).
Take out the crucible, allow to cool and weigh the ignited residue.
Add 1-2 drops of sulphuric acid in the platinum crucible so that residue
becomes wet.
Add 5-6 ml hydrofluoric acid.
Place platinum crucible on low flame burner or on hot plate and allow to
evaporate to dryness.
Take out the platinum crucible and ignite at 900-950oC for 2-5 minutes.
Allow to cool.
Take weight of remaining residue.

Calculations

Wt. of SiO2 = Weight of crucible before HF Wt. of crucible after HF.

SiO2 g /l = g SiO2(in aliquot) x 1000

ml aliquot

If aliquot = 50 ml, then

SiO2, g = g SiO2 (in 50 ml) x 20

223
6.14 ANALYSIS OF PHOSPHOROUS IN WATER AND WASTE WATER

Various forms of phosphorous are found in water and waste water.

Phosphorous is essential constituent of nutrient for growth of plants. It can be
determined by colorimetry at the low level.

6.14.1 DETERMINATION OF PHOSPHOROUS BY STANNOUS CHLORIDE

METHOD (SOLUBLE PHOSPHATE)

Principle

A blue colour is developed as molybdophosphoric acid in presence of stannous chloride

as a reducing agent, which can be measured at 690 nm.

Reagent

i. Ammonium molybdate solution: Dissolve 25 gm ammonium molybdate

{(NH4)6 Mo7)24.4H2O)} in 150 ml distilled water. Add 280 ml conc. H2SO4,
allow to cool and dilute to 1000 ml with distilled water.
ii. Stannous chloride solution: Dissolve 2.5 gm SnCl2 in 100 ml glycerol by
heating on water bath with constant stirring.
iii. Stock phosphate solution: Dissolve 0.439 gm KH2PO4(AR) in distilled water
and dilute to 1000 ml with distilled water. (1 ml = 100 g PO4).
iv. Standard phosphate solution: Dilute 10 ml, 100 g PO4 solution to 100 ml
with distilled water in volumetric flask. (1 ml = 10 g PO4).

Preparation of standard graph

Take suitable aliquots from standard phosphate solution in the range of 0-10
g PO4 in 100 ml volumetric flask.
Add 4 ml ammonium molybdate solution in each flask, mix.
Add 0.5 ml stannous chloride solution, mix again.
Dilute to 100 ml with distilled water, mix thoroughly.
Measure absorbances/transmittances at 690 nm after 10 minutes.
Carry out blank in a similar manner.
Plot a graph between concentrations and absorbances/transmittances.

Procedure for samples

Take suitable aliquot of sample in 100 ml volumetric flask. (If turbidity
present, filter through 0.45 um filter).
Add 4 ml ammonium molybdate solution, mix.
Add 0.5 ml stannous chloride solution, mix well.
Dilute to 100 ml with distilled water and mix thoroughly.
Measure absorbance/transmittance at 690 nm after 10 minutes.
Carry out blank in a similar manner.

224
Calculations :

P, g /l = g P(in aliquot) x 1000

ml, aliquot

If aliquot = 50 ml, then

P, g /l = g P (in 50 ml) x 20

P X 3.06 = PO4 OR PO4 = P

3.06

(Note : In case of coloured samples, treat with aluminium hydroxide suspension to decolorise and then proceed usually)

6.14.2 DETERMINATION OF PHOSPHOROUS BY ASCORBIC ACID METHOD

(Soluble Phosphate)

Principle
Ammonium molybdate reacts with potassium antimonyl-tartrate in acid
medium to give phosphomolybdic acid which is blue in colour and can be measured at
880 nm.

Reagents

i. Potassium antimonyl-tartrate solution: Dissolve 0.2743 gms potassium

antimonyl-tartrate {K(SbO) C4H4O6.2H2O} in water and dilute to 100 ml with
distilled water.
ii. Ascorbic Acid Solution: (0.01 M): Dissolve 1.76 gm ascorbic acid in 100 ml
flask & dilute to the mark.
iii. Ammonium molybdate solution: Dissolve 4 gm ammonium molybdate
(NH4)6 Mo7O24.4H2O) in water and dilute to 100 ml with distilled water.
iv. Sulphuric acid solution: (5N): Dilute 14 ml conc. H2SO4 to 100 ml with
distilled water.
v. Combined Reagent Solution

a. Take 50 ml 5N H2SO4 solution in 100 ml flask.

b. Add 5 ml potassium antimonyl tartrate solution, mix.
c. Add 15 ml ammonium molybdate solution, mix.
d.Add 30 ml ascorbic acid solution, mix thoroughly. Allow to stand for few
hours to stabilize the mixture (mixture to be prepared feshly).
vi. Stock phosphate solution: Dissolve 0.439 gm KH2PO4(AR) in distilled water
and dilute to 1000 ml with distilled water. (1 ml = 100 g PO4).

225
 vii. Standard phosphorous solution: Dilute 10 ml, 100 g, PO4 solution to 100
ml volumetric flask. (1 ml = 10 g PO4).

Preparation of standard graph

Take suitable aliquots of standard phosphate solution ranging from 0-10 g

PO4 in 100 ml volumetric flasks.
Add 8 ml combined reagent solution in each flask.
Dilute to 100 ml with distilled water, mix thoroughly.
Measure absorbances/transmittances at 880 nm. after 10 minutes.
Carry out blank in a similar manner.
Plot a graph between concentrations and absorbance.

Procedure for samples

Take suitable aliquot of sample in 100 ml volumetric flask.

Add 8 ml combined reagent solution, mix.
Dilute to 100 ml with distilled water.
Take absorbance at 880 nm after 10 minutes.Carry out blank in a similar
manner.

Calculations:

P, g /l = g P(in aliquot) x 1000

ml, aliquot

If aliquot = 50 ml, then

P, g/l = g P (in 50 ml) x 20

Note: for the determination of total phosphate, sample is to be treated with HCl + HNO3 upto dryness. Extract with
water and proceed as usual).

6.15 ANALYSIS OF NITRITE NITROGEN (NO2-N) IN WATER AND WASTE

WATER

Nitrite is another form of nitrogen generally found in water and waste

water sample in small quantity and can be analysed through formation of reddish purple
azo dye at pH 2-2.5 using sulphanilamide & N-(1-naphthyl)-ethylenediamine
hydrochloride at 520 nm.

226
Reagents

i. -naphthylamine hydrochloride solution: Dissolve 0.6 gm naphthylamine

in 1 ml hydrochloric acid and dilute to 100 ml with distilled water.
ii. Sulphanilic acid solution: Dissolve 0.6 gm sulphanilic acid in about 70 ml
hot water. Add 20 ml conc. hydrochloric acid dilute to 100 ml with distilled
water.
iii. Sodium acetate buffer solution: Dissolve 27.2 gms. Sodium acetate in water
and dilute to 100 ml.
iv. EDTA Solution: Dissolve 0.5 gm EDTA in distilled water, add one pallet of
NaOH and dilute to 100 ml with distilled water.
v. Stock Nitrite Solution: Disolve 0.4929 gm NaNO2(AR) in water and dilute
to 1000 ml with distilled water. (1 ml = 100 g NO2-N).
vi. Standard Nitrite Solution: Dilute 10 ml, 100 g NO2 solution to 1000 ml
with distilled water. (1 ml = 1 g NO2-N).
OR dilute 1 ml, 100 g NO2-N solution to 100 ml. with distilled water (1 ml =
g NO2-N)

Preparation of standard graphs

Take suitable aliquots from the standard stock solution of NO2 in the range of
0-10 g NO2-N in 100 ml volumetric flask.
Add 2 ml EDTA solution in each of the volumetric flasks.
Add 1 ml sulphanilic acid solution, mix well and allow to stand for 3-5
minutes.
Add 1 ml -naphthylamine hydrochloride solution.
Add 1 ml sod.acetate buffer and dilute to 100 ml with distilled water and mix
thoroughly.
Measure absorbances/transmittances of each solution at 520 nm.
Carry out blank in similar manner
Plot a graph between concentrations against absorbances.

Procedure for samples

Take suitable aliquot from the sample in 100 ml volumetric flask.
Add 2 ml EDTA solution, mix.
Add 1 ml sulphanilic acid solution, mix again.
Add 1 ml -naphthylamine hydrochloride solution.
Add 1 ml sod.acetate solution and dilute to 100 ml with distilled water, mix
thoroughly.
Measure absorbance at 520 nm.

Calculations:

NO2-N, g/l = g NO2 (in aliquot) x 1000

ml, aliquot

227
 If aliquot = 50 ml, then

NO2-N, g /l = g NO2-N(in 50 ml) x 20

N x 3.29 = NO2

6.16 ANALYSIS OF NITRATE NITROGEN (NO3-N) IN WATER AND WASTE

WATERS

NO3 is one of the compounds of nitrogen family and found in water and wastewater. It
can be determined using spectrophotometer in the range of ultraviolet and visible too.

6.16.1 Determination Of Nitrate Nitrogen (No3-N) In Visible Range At 410 Nm

Principle

In alkaline condition, nitrate gives yellow colour with phenol disulphonic acid solution,
which can be measured at 410 nm and compared with standards.

Reagents

i. Phenol disulphonic acid solution: Dissolve 25 gms phenol in 150 ml conc.

sulphuric acid. Heat for 2 hours, cool and store in coloured bottle.
ii. Potassium permanganate solution: (0.05 N): Dissolve 0.2 gm KMnO4 in
water and dilute to 1000 ml with distilled water.
iii. Standard silver sulphate solution: Dissolve 4.4 gm Ag2SO4 in distilled
water and dilute to 1000 ml distilled water. (1 ml = 1 mg Cl.)
iv. Oxalic acid solution: (0.05N): 0.265 gm/100 ml.
v. Ammonia solution: 30% solution.
vi. Nitrate stock solution : Dissolve 0.7218 gm KNO3(AR) in distilled water and
dilute to 1000 ml. (1 ml = 0.1 mg NO3-N = 100 g NO3-N)
vii. Standard nitrate solution: Dilute 10 ml, 0.1 mg NO3-N solution to 100 ml
with distilled water. (1 ml = 10 g NO3-N).

Preparation of standard graph

Take suitable aliquots from the standard NO3-N solution ranging from 0 to 10
g NO3-N in 100 ml volumetric flask.
Add calculated ml of Ag2SO4 solution (before this take aliquot of sample and
determine equivalent of chlorine if present in sample by precipitating chloride
as (Ag Cl) and warm.
If precipitate is formed, filter through Whatman No.40 filter paper.

228
 Add 2-5 drops of KMnO4 solution to remove nitrites if present.
Remove excess KMnO4 colour by adding oxalic acid dropwise till colour
disappears.
Add 2 ml phenol disulphonic acid solution.
Adjust pH to around 7 by using ammonia solution, mix thoroughly and dilute
to 100 ml with distilled water.
Measure absorbances/transmittances at 410 nm.
Plot a graph between concentrations and absorbances.

Determination of nitrate-nitrogen (NO3-N)

Take suitable aliquot of sample in 250 ml beaker.

Add calculated volume of Ag2SO4 solution (equivalent to chloride) to
precipitate chlorides as AgCl. Warm the solution, cool and filter through
Whatman No.40 filter paper.
Add 3-5 drops of KMnO4 solution to remove nitrite if present in sample.
Remove excess KMnO4 by adding oxalic acid solution dropwise.
Keep the beaker on water bath and allow to evaporate to dryness. Remove
beaker and allow to cool.
Add 2 ml phenol disulphonic acid solution and extract with about 25-30 ml
distilled water.
Adjust the pH around 7 by adding ammonia solution and make up to 100 ml
with distilled water.
Measure the absorbance/transmittance at 410 nm.

Carry out blank in a same manner.

Calculations:

NO3-N, g/l = g NO3 (in aliquot) x 1000

ml, aliquot

If aliquot = 50 ml, then

NO3-N, g /l = g NO3-N(in 500 ml) x 20

(Note : In case of coloured sample, treat aliquot with aluminium hydroxide suspension to remove colour).

6.16.2 Determination of Nitrate Nitrogen (No 3-N) In Ultra Violet Region Of

Spectrophotometer At 220 Nm & 275 Nm

The method is applicable in case of clear drinking water where organic

material is in less quantity. In acidic condition (in HCl) the measurements are carried out
at 220 nm and at 275 nm.

229
 Absorbance at 220 contributes the concentration of nitrate and organic material
while at 275 nm absorbance due to only organic material. The method is purely
impirical. Suspended solids are removed by filtration while addition of hydrochloric acid
prevents from hydroxides and carbonates.

Preparation of standard graph

Reagents

i. Hydrochloric acid: 1N.

ii. Stock Nitrate Nitrogen (NO3-N) solution: Dissolve 0.7218 gm KNO3(AR)
in water and dilute to 1000 ml with distilled water (1 ml= 100 g NO3-N).
iii. Standard Nitrate Nitrogen (NO3-N) solution: Dilute 10 ml, 100 g NO3-N
solution to 100 ml with distilled water. (1 ml = 10 g NO3-N).

Procedure
Take suitable aliquots of NO3-N solution ranging from 0-10 g NO3-N in
100 ml volumetric flask.
Add 2 ml 1 N HCl solution, in each flask mix thoroughly.
Measure absorbances/transmittances at 220 nm and 275 nm respectively.
If absorbance at 220 nm = A and absorbance at 275 nm = B.
Then, absorbance for NO3-N = A 2B.
Plot standard graph between absorbances as calculated above against the
concentrations.

Procedure for samples

Take suitable aliquot of sample in 100 ml volumetric flask.

Add 2 ml, 1N hydrochloric acid, mix thoroughly (remove turbidity if any by
filtering before addition of hydrochloric acid solution).
Dilute to 100 ml with distilled water, mix thoroughly again.
Measure absorbances at 220 nm and 275 nm.

Calculations:

Abs220 nm 2Abs275 mm = Abs (NO3-N)

NO3-N, g/l = g NO3-N(aliquot) x 1000

ml, aliquot

If aliquot = 50 ml, then

NO3-N, g /l = g NO3-N (in aliquot) x 20

N x 4.43 = NO3

230
6.17 ANALYSIS OF AMMONICAL NITROGEN (NH3-N) IN WATER
ANDWASTE WATER

In natural as well as in wastewaters ammonia is generated due to the

microbiological activities of mostly organic nitrogeneous matter.

Principle

Alkaline Nesslers reagent reacts with ammonia present in water/waste

water and develops a yellow colour compound, which can be measured at 410 nm.

Reagents

i. Nesslers Regaent: (a) Dissolve 100 gms mercuric iodide (HgI2) and 70 gms
potassium iodide (KI) in distilled water. (b) Dissolve 160 gms. Sodium
hydroxide in water and mix with solution of (HgI2+KI) prepared above. (c)
Allow to stand for overnight. Filter if precipitate is formed. Keep clear
solution in coloured bottle.
ii. Zinc Sulphate Solution (10%): Dissolve 10 gm ZnSO4.7H2O in distilled
water and dilute to 100 ml with distilled water.
iii. Sodium Hydroxide Solution (6N) : Dissolve 240 gms NaOH in distilled
water and dilute to 1000 ml with distilled water.
iv. EDTA Solution: Dissolve 50 gms EDTA and 10 gms NaOH in water and
dilute to 100 ml with distilled water.
v. Stock Ammonium Solution : Dissolved 0.3819 gm NH4Cl (AR) in water
and dilute to 1000 ml with distilled water (1 ml = 0.1 mg N = 0.122 mg NH3).
vi. Standard Ammonium solution: Dilute 10 ml stock solution to 1000 ml with
distilled water. (1 ml = 1 g N = 1.22 g NH3).

Preparation of standard graph

Take suitable aliquots of standard ammonium solution i.e. from 0 to 10 g N

in 100 ml beaker.
Add 1 ml zinc sulphate solution in each beaker, mix.
Add 0.5 ml NaOH solution to attend a pH around 10, mix again.
Allow to settle the precipitate.
Filter through Whatman No.42 filter paper.
Add 1-2 drops of EDTA solution, in filtrate, mix.
Add 2 ml Nesslers reagent, mix thoroughly and dilute to 100 ml with distilled
water.
Measure absorbance/transmittances at 410 nm.
Plot a graph between concentration and absorbance/transmittances.

Procedure for samples

Take suitable aliquot of the sample in 250 ml beaker.

231
 Add 1 ml ZnSO4 solution, mix.
Add 0.5 ml NaOH solution, mix again.
Allow to settle precipitate.
Filter through Whatman No.42 filter paper.
Add 1-2 drops of EDTA in the filtrate, mix.
Add 2 ml Nesslers reagent solution, mix thoroughly and dilute to 100 ml with
distilled water.
Measure absorbance/transmittance at 410 nm.

Calculations :

NH3-N, g/L = g NH3-N x (in aliquot) x 1000

ml, aliquot

If aliquot = 50 ml, then

NH3-N, g/L = g NH3-N (in 50 ml ) x 20

OR
NH3-N x 1.21 = NH3 NH3 = N
1.21

6.18 ANALYSIS OF RESIDUAL CHLORINE IN WATER AND WASTEWATER

SAMPLES

To supply a good quality of drinking water in view point of health, chlorination is

essential. As the process of chlorination destroy the disease producing bacteria i.e.
micro-organisms. The chlorination procedure has some adverse effects also. During this
process the chances of the formation of chloroform, which is harmful to the health. To
minimize any adverse effects, it is essential that proper testing procedures to be adopted.

Various methods are available for the determination of residual chlorine.

Iodometric method is adopted in I.B.M. laboratory.

Principle

At acidic pH, chlorine liberates equivalent amount of iodine with addition

of pot.iodide, which can be determined after titration against standard sod.thiosulphate
solution using starch as an indicator.

232
Interference

Organic sulphides and manganese, ferric and nitrite ions interfere along
with some forms of combined chlorine. At acidic pH the effect of interfering parameters
is minimized. Acetic acid is preferably used while titrating with sod.thiosulphate
solution.

Reagents

i. Standard Sodium Thiosulphate Solution: (0.01N): Dissolve 2.5 gms

sod.thiosulphate (AR) Na2S2O3.5H2O in distilled water and dilute to 1000 ml.
ii. Standard potassium dichromate solution (0.01N) : Dissolve 0.49 gm
K2Cr2O7 in distilled water and dilute to 1000 ml distilled water.
iii. Starch solution: Dissolve 5 gm starch in 100 ml boiling water.
iv. Potassium iodide : Crystals (AR)
v. Sulphuric Acid: 1:1 dilute.

Procedure: Standardization of Sod.Thiosulphate

Take 25 ml aliquot of 0.01 N K2Cr2O7 solution in 250 ml beaker.

Dilute to 100 ml with distilled water.

Add 10-15 ml sulphuric acid.

Titrate against sod. thiosulphate.

Near an end point add 1 ml starch solution.

Continue titration till colourless solution obtained (i.e. disappearance of blue
colour).
Calculations

N. Na2S2O3 = ml K2Cr2O7 x NK2Cr2O7

ml Na2S2O3

Procedure for determination of residual chlorine in water and waste water

Take suitable aliquot of water/ wastewater in 250 ml beaker.

Add 5-10 ml acetic acid to make acidic.
Dilute to about 100 ml with distilled water.
Add 1-2 gm pot.iodide crystals to liberate iodine.
Titrate liberated iodine against standard sod.thiosulphate solution.
Near an end point add 1-2 ml starch solution.
Continue titration till disappearance of blue colour.
Carry out blank and deduct from total volume.

Calculations:

R.Cl2, mg/L = ml Na2S2O3 x N Na2S2O3 x 1000 x 35.45

ml, aliquot

233
 If aliquot = 50 ml, then

R.Cl2, mg/L = ml Na2S2O3 x N Na2S2O3 x 20 x 35.45

6.19 ANALYSIS OF CHLORIDES IN WATER, WASTEWATER AND SOIL

SAMPLES

Chloride is always found in water and wastewater. The concentration of

chloride may be higher in wastewater than raw water because sodium chloride is most
essential article of human diet and passes unchanged through a digestive system.

DETERMINATION OF CHLORIDE BY ARGENTOMETRIC METHOD

A. PRINCIPLE

In an almost neutral or in slightly alkaline solution, potassium chromate

can indicate the end point against titration of silver nitrate solution (yellowish to dirty
orange).

Interference

Substances normally found in potable waters will not interfere. Sulphide,

thiosulphate and sulphite ions interfere and can be removed giving treatment with
hydrogen peroxide solution. Colour and turbidity also interfere and can be removed
using aluminium hydroxide suspension.

Reagents

i. Standard chloride solution : Dissolve 0.16486 gm NaCl(AR) in distilled

water & dilute to 1000 ml with distilled water (1 ml = 100 g Cl)
ii. Standard silver nitrate solution: Dissolve 1.6987 gm AgNO3 (AR) in
distilled water and dilute to 1000 ml distilled water. Store in a brown bottle or
wrap a carbon paper to the bottle or volumetric flask.
iii. Potassium chromate indicator solution: Dissolve 5 gm (K2CrO4) potassium
chromate in water and dilute to 100 ml.
iv. Aluminium hydroxide suspension solution: Dissolve 125 gm aluminium
pot.sulphate or aluminium ammonium sulphate in water. Warm and add 55
ml conc. ammonia solution with stirring. Allow to stand for 1 hour. Decant
supernatant. Repeat for 2-3 times to remove chloride ions. Make up to 1000
ml. Use this for removal of interference like colour.
v. Hydrogen peroxide: Use 30% H2O2 solution.
vi. Sulphuric acid solution: 1 N solution to adjust pH.

234
 vii. Sod. Hydroxide solution: 1 N solution to adjust pH.

B. PROCEDURE : FOR COLOURLESS AND NO INTERFERING SUBSTANCES

Take suitable aliquot of solution (water, wastewater) in 250 ml beaker.

Adjust pH to around 7 to 10, by adding H2SO4/NaOH solutions.
Add 1 ml potassium chromate solution.
Titrate against 0.1 N AgNO3 (silver nitrate) solution.
Dirty orange colour shows the end point.

C. PROCEDURE : FOR COLOURED AND INTERFERING SUBSTANCES

a. i. Take suitable aliquot of the sample in 250 ml beaker.

ii. Dilute to about 100 ml with distilld water.
iii. In case of coloured sample add 3-4 ml aluminium hydroxide suspension,
mix thoroughly. Allow to settle and filter.
iv. Use above filtrate for determination of chlorides.
v. Add 1 ml potassium chromate solution.
vi. Titrate against 0.1 N Silver Nitrate (AgNO3) solution.
vii. Dirty orange colour shows the end point.

b. i. In case of sulphide, thiosulphate and sulphite are present in the solution.

ii. Add 1 ml H2O2 solution.
iii. Stir well for about 2 minutes
iv. Adjust pH 7-10 by adding H2SO4/NaOH solution.
v. Add 1 ml pot.chromate solution.
vi. Titrate against 0.1 N silver nitrate solution (AgNO3).
i. Dirty orange colour shows the end point.

STANDARDIZATION OF SILVER-NITRATE SOLUTION

Take suitable aliquot of standard sodium chloride solution in 250 ml beaker.

Dilute to about 100 ml with distilled water.
Adjust pH 7-10 using H2SO4/NaOH solutions.
Add 1 ml potassium chromate solution.
Titrate against 0.1 N silver-nitrate solution.
Dirty orange colour shows the end point.
Carry out blank in a same manner.

Calculations of standard silver nitrate solution.

N AgNO3 = (ml NaCl ml Blank) x N NaCl

ml, AgNO3 consumed

235
Calculations for determination of chloride concentration

Cl, mg/L = ml, AgNO 3 (for aliquot) x N AgNO3 x 35.46 x 1000

ml, aliquot taken

If aliquot = 50 ml, then,

Cl, mg/L = ml AgNO3 x N AgNO3 x 35.46 x 20

OR
Cl, mg/L = Cl, mg (in 50 ml) x 20

(Note: Blank is to carried out every time and must be deducted from the volume obtained for experimental aliquot)

D. PROCEDURE FOR DETERMINATION OF CHLORIDE IN SOIL SAMPLES

Take 5-10 gms soil in 250 ml beaker.

Add about 50 ml distilled water.
Stir occasionally for about 1-2 hours.
Filter through Whatman No.40 filter paper. Wash 2-3 times with distilled
water.
Take filtrate for determination of chloride.
Adjust pH 7-10 by adding H2SO4/NaOH solutions.
Add 1 ml potassium chromate solution.
Titrate against standard silver nitrate solution.
Dirty orange colour shows the end point.

Calculations

% Cl = ml AgNO3 x N AgNO3 x 0.03546 x 100

wt. of sample taken (gms)

(Note: Carry out blank and deduct vol. of AgNO3 required for blank).

6.20 DETERMINATION OF ACIDITY OF WATER & WASTEWATER

Acidity is defined as a capacity of neutralization of alkaline materials and

expressed in terms of CaCO3.

236
Reagents

i. Sodium Hydroxide Solution : (0.01 N) : Dissolve 4.0 gm (appr.) NaOH in

distilled water and dilute to 1000 ml.
ii. Sodium Carbonate (Na2CO3) AR/GR: Solid.
iii. Phenolphthalein Solution: 0.1% solution in methanol or in distilled water.
iv. Methyl Orange solution: 0.1% solution in distilled water.
v. Sodium Thiosulphate Solution: 0.1 N (appr.) Dissolve 25 gm
Na2S2O3.5H2O in distilled water and dilute to 1000 ml.

STANDARDIZATION OF SODIUM HYDROXIDE SOLUTION

A. Procedure

Weigh 0.20 gm Na2CO3 in 250 ml beaker.

Add about 100 ml distilled water to dissolve Na2CO3
Add 2-5 drops of Methyl Orange indicator.
Titrate against hydrochloric acid.
Note the reading and calculate the normality of HCl.

N HCl =Weight of Na2CO3 x (gms) x 1000 = Wt. of Na2CO3

equi. Wt. of Na2CO3 x ml HCl 53 x ml, HCl

(equivalent wt. of Na2CO3 = 53)

B
Take suitable aliquot of NaOH solution in 250 ml beaker.
Dilute to about 100 ml with distilled water.
Add 2-5 drops of phenolphthalein indicator.
Titrate against above N HCl solution.
Colourless solution is the end point of the reaction.
Note the volume of HCl and calculate normality of NaOH solution as follows.

N NaOH = NHCl x ml, HCl

ml, NaOH
Interferences

Residual chlorine, colour, turbidity, iron, aluminium etc. are the common
interferences in analysis of acidity.

Residual chlorine can be removed by addition of calculated amount of

sodium thiosulphate solution while others can be avoided by carrying out potentiometric
titrations.

Procedure : Determination of Acidity In Water, Waste Water

237
 Take suitable aliquot of sample in 250 ml beaker.
Dilute to about 100 ml distilled water.
Add 2-5 drops of methyl orange indicator.
Titrate against standard sod.hydroxide solution.
Note down the reading (ml) of colour change (x ml).
Add 2-5 drops of phenolphthalein in the same solution.
Continue titration against same standard NaOH solution.
Red purple colour shows the end point of reaction.
Note down the volume of NaOH require.

Calculations :

Acidity is calculated and is expressed in terms of mg/l of calcium carbonate.

Acidity as CaCO3, mg/l, =ml(NaOHM.O.) + ml (NaOHP) x N x 50 x 1000

ml. aliquot

if aliquot = 50 ml, then

Acidity as CaCO3, =ml, NaOH (Methyl Orange) + ml NaOH (phenol) x 20 x 50

Mg/L ml, aliquot

(1 ml 1 N NaOH = 50 mg CaCO3)

6.21 DETERMINATION OF ALKALINITY IN WATER & WASTE WATER

Alkalinity is defined as the capacity of an aquous medium to neutralize

acid contents. The alkalinity commonly occurs due to dissolved salts of carbonates,
bicarbonates, borates, silicates, phosphates and hydroxyl ions.

Alkalinity is determined as phenolphthalein alkalinity at pH 8.3 and total

alkalinity with methyl orange at pH 4.5 by titrating against standard hydrochloric or
sulphuric acid.

Interference

Likewise in acidity determination, in alkalinity also there is interference of

colour, turbidity, iron aluminium and residual chlorine. Residual chlorine can be
removed by addition of calculated amount of sodium thiosulphate solution while colour
and turbidity can be avoided by titrating potentiometric method.

Reagents

238
 i. Standard hydrochloric or sulphuric acid solutions (0.01 N): Dilute 0.9 ml
(appr.) concentration, HCl or 0.3 ml (appr.) conc. H2SO4 to 1000 ml with
distilled water.
ii. Solid Na2CO3 (AR/GR).
iii. Phenolphthalein indicator solution: Dissolve 0.1 gm in methanol and dilute
to 100 ml.
iv. Methyl Orange indicator solution: Dissolve 0.1 gm in distilled water dilute
to 100 ml.
Standardization of HCl OR H2SO4 solutions

Procedure

Weigh 0.20 gm Na2CO3 (AR/GR) in 250 ml beaker.

Dissolve in water and dilute to about 100 ml with distilled water.
Add 2-5 drops of methyl orange indicator.
Titrate against 0.01 N HCl or H2SO4.
Purple colour shows the end point of reaction.

Calculations

N HCl OR N H2SO4 = Weight of Na2CO3 x 1000

Equi. Wt. of Na2CO3 x ml HCl/ml H2SO4

= Wt. of Na2CO3 x 1000

53 x ml, HCl/H2SO4

6.21.1 Procedure for The Determination Of Phenolphthalein Alkalinity

Take suitable aliquot of the sample in 250 ml beaker.

Dilute to about 100 ml with distilled water.
Add 2-5 drops of phenolphthalein indicator soloution.
Titrate against standard HCl or H2SO4 solutions.
Disappearance of purple colour shows the end point.
Note the volume of acid required.

Calculations

Alkalinity (phenolphthalein) = ml (acid) x N acid x 1000

ml, aliquot

OR Alkalinity (phenol) as CaCO3, = ml (acid) x N (acid) x 1000 x 50

Mg/l ml, aliquot

(1 ml 1N HCl/H2SO4 = 50 mg Ca CO3)

239
6.21.2 PROCEDURE FOR THE DETERMINATION OF TOTAL ALKALINITY

Take suitable aliquot of sample in 250 ml beaker.

Dilute to about 100 ml distilled water.
Add 2-5 drops of phenolphthalein indicator solution.
Titrate against standard acid solution.
Disappearance of purple colour shows the end point.
Add 2-5 drops of methyl orange in the same solution.
Continue titration till pink colour appears which shows the end point of the
reaction.
Note down the volume of acid required.

Calculations

Total Alkalinity= ml(acid for phen.) + ml (acid for methyl orange) x N (acid) x 1000
ml. aliquot

Total Alkalinity, as CaCO3, mg/L

= ml(acid for phen.) + ml (acid for methyl orange)x N(acid) x 50,000
ml. aliquot

Relationship of Alkalinity & Expression of Results

i. Alkalinity of phenolphthalein = P
ii. Total Alkalinity (Methyl Orange) = T

Then the relationship as under:

Sl.No. Values of P & T OH CO3 HCO3

01 P=0 O O T
02 P<T O 2P T-2P
03 P=T O 2P O
04 P>T 2P T 2(T-P) O
05 P=T T O O

6.22 DETERMINATION OF HARDNESS IN WATER SAMPLES

Hardness occurs due to soluble ions mostly of calcium and magnesium,

which affects the quality of water. Hardness of water is measured as the capacity of
water to precipitate soap. It can be defined as a characteristic of calcium and magnesium
ions expressed as calcium carbonate (CaCO3) and magnesium carbonate (MgCO3) and is
determined by EDTA titrimetirc method.

240
 Few metal ions such as Fe, Al, Mn interfere in this method up to some
extent but can be masked by the addition of hydroxylamine hydrochloride and
triethanolamine solutions Cu, Ni & Pt can be masked by addition of potassium cyanide
(KCN) solution before starting a titration.

Reagent

i. Buffer solution : (10 pH) : Dissolve 67.6 gms NH4Cl in 568 ml ammonium
hydroxide solution and dilute to 1000 ml with distilled water.
ii. Buffer solution : (12 pH) : Dissolve 200 gms KOH in water and dilute to
1000 ml with distilled water.
iii. Hydroxylamine Hydrochloride solution : Dissolve 50 gms in water and
dilute to 1000 ml with distilled water.
iv. Triethanol Amine Solution : Mix 100 ml triethanolamine in water and dilute
to 1000 ml with distilled water.
v. Potassium Cyanide Solution : Dissolve 10 gm potassium cyanide (KCN) in
water and dilute to 100 ml (Note : Deadly poison).
vi. Erio-chrome Black-T solution : Dissolve 0.2 gm E.B.T. in methanol
methanol and dilute to 100 ml.
vii. Pattons & Reader Reagent : Dissolve 0.2 gm R. & P. reagent in methanol
and dilute to 100 ml.
viii. Standard EDTA Solution : (0.01 M) : Dissolve 3.723 gm EDTA in water,
add 2-5 drops of acetic acid if turbidity appears and dilute to 1000 ml with
distilled water.
ix. Zinc Acetate Solution : (0.01 M) : Dissolve 0.2195 gm Zinc Acetate
(AR/GR) in water and dilute to 100 ml with distilled water.
x. Buffer Solution : (5.5 pH) : Dissolve 200 gms ammonium acetate in 30 ml
acetic acid and dilute to 1000 ml with water.
xi. Xylenol Orange Solution : Dissolve 0.2 gm xylenol orange in 100 ml
methanol.

STANDARDIZATION OF EDTA SOLUTION AGAINST ZINC ACETATE

SOLUTION

Procedure

Take 25 ml aliquot of 0.01 M Zinc Acetate Solution in 250 ml beaker.

Dilute to about 100 ml with distilled water.
Add 5-10 ml buffer solution (5.5 pH) using measuring cylinder.
Add 2-5 drops of xylenol orange indicator.
Titrate against 0.01 M EDTA solution.
Purple colour shows the end point of the titration.

241
Calculation of Molarity of EDTA

M Zn-Ac x 25 = M EDTA x ml EDTA

MEDTA = M Zn-Ac x 25
ml EDTA

A. DETERMINATION OF TOTAL HARDNESS IN WATER SAMPLES

Procedure

Take suitable aliquot of the water sample in 250 ml beaker.

Add 5-10 ml hydroxylamine hydrochloride solution.
Add 5-10 ml triethanol amine solution, mix well.
Add 5-10 ml. cyanide solution if Cu, Ni, Pt ions suspected.
Add 15-25 ml buffer (pH-10) solution.
Mix thoroughly the contents.
Add 5-10 drops of Eriochrome Black T indicator. (Note: A red wine colour
shows a correct pH i.e. 10).
Dilute the content to about 100-150 ml with distilled water and mix
thoroughly.
Titrate the above content against 0.01 M EDTA solution.
Greenish-blue colour appears at the end of reaction.

Calculations

Total Hardness as CaCO3, mg/l = ml EDTA x M EDTA X 1000 X 100

ml, aliquot

Hardness (Total), mg, CaCO3/L = 2.497 {Ca, Mg/L} + 4.118 {Mg, mg/L}

(Note : 1 ml 1 MEDTA = 100 mg CaCO3)

B. DETERMINATION OF CALCIUM HARDNESS

Procedure

Take suitable aliquot (equal to total hardness aliquot) of sample in 250 ml beaker.
Add 5-10 ml hydroxylamine hydrochloride solution.
Add 5-10 ml triethanolamine solution.
Add 5-10 ml cyanide solution (if Cu, Ni, Pt suspected).
Add 15-25 ml buffer (pH = 12) i.e. 20% KOH solution.
Mix thoroughly.

242
 Add 5-10 drops of Patton & Readers reagent.
Dilute the contents to 100-150 ml with distilled water.
Titrate against 0.01 M EDTA solution.
Greenish-blue colour shows the end point.

Calculations

Calcium hardness as Ca, mg/l = ml EDTA X M EDTA x 1000 x 40

ml, aliquot

OR
Calcium Hardness as CaCO3, mg/L = ml EDTA X M EDTA x 1000 x 40 x 2.497
ml, aliquot

C. DETERMINATION OF MAGNESIUM HARDNESS

Calculation

Mg-hardness as = {ml EDTA (Total) ml EDTA for Ca} x 1000 x 24 x 4.118

CaCO3 ml, aliquot.

6.23 ANALYSIS OF HEXAVALENT CHROMIUM IN DRINKING WATER,

WASTE WATER BY COLORIMETRIC METHOD USING 1-5
PHENYLCARBAZIDE

Chromium may exist in water supplies in both hexavalent & trivalent state
although trivalent state rarely found in potable water.

Hexavalent chromium is determined colorimetrically by using 1, 5-

diphenylcarbazide as a coloring reagent. A red-violet colour is produced can be
measured at 540 nm.

Reagents

i. Chromium stock solution : Dissolve 0.2828 gm K2Cr2O7 in water and dilute

to 1000 ml with distilled water. ( 1 ml = 100 g Cr.)
ii. Standard chromium solution : Dilute 1 ml of 100 g Cr solution to 100 ml
volumetric flask. (1 ml = 1 g Cr).
iii. 1,5 Diphenylcarbazide solution : Dissolve 0.50 gm 1,5- diphenylcarbazide in
100 ml acetone.
iv. Sulphuric acid (0.2N) : Dilute 5.6 ml conc. H2SO4 to 1000 ml.
v. Potassium permanganate solution : Dissolve 4 gm KMnO4 in 100 ml
distilled water.
vi. Phosphoric acid : concentrated and 70% solution.

243
 vii. Sodium azide solution : Dissolve 0.5 gm NaN3 in 100 ml distilled water.

Preparation of Standard graph

Take a suitable aliquot from standard chromium solution in the range of 2 g

Cr to 10 g Cr in 100 ml volumetric flask.
Add 2 ml (70%) phosphoric acid solution, in each volumetric flask mix.
Add 2 ml diphenylcarbazide solution, mix.
Make up the volume with 0.2N H2SO4, mix thoroughly.
Allow to stand for 5-10 minutes to develop a colour.
Take absorbance/transmittance at 540 nm.
Plot a graph of concentrations against absorbances obtained as above.

Measurement of chromium hexavalent in water and wastewater samples.

A. Procedure in absence of oxidizing or reducing substances

Filter water, wastewater sample through 0.45 um filter if any suspended

solids/particles present in sample.
Take suitable aliquot of filtered sample in 100 ml volumetric flask.
Add 2 ml phosphoric acid solution, mix (70%).
Add 2 ml diphenylcarbazide solution, mix.
Dilute to 100 ml with 0.2N H2SO4 solution, mix thoroughly.
Allow to stand for 5-10 minutes to develop a colour.
Take absorbance/transmittance at 540 nm.
Find out the concentration of chromium from a standard graph.

B. Analysis of Chromium Hexavalent in presence of oxidizing or reducing

substances

Reagents

i. Sodium hypochlorite solution : Dilute 70 ml sodium hypochlorite solution

(NaOCl) to 1000 ml with distilled water.
ii. Potassium iodide starch test paper.
iii. Phosphoric acid solution : Dilute 700 ml (H3PO4) phosphoric acid to 1000
ml with distilled water.
iv. Sodium chloride : AR grade NaCl.
v. 1,5-diphenylcarbazide solution : (1%) : Dissolve 1 gm of 1.5-
diphenylcarbazide in acetone and dilute to 100 ml.

Procedure

Take suitable aliquot of the filtered sample in 100 ml volumetric flask.

Add 1 ml sodium hypochlorite solution, mix.

244
 Check the excess of chlorine using potassium iodide starch paper. If there is
no excess of chlorine, then add more sodium hypochlorite solution until
excess is obtained.
Add 2 ml phosphoric acid solution, mix.
Add 10 gm NaCl. Dissolve and mix.
Pass air through the solution as obtained above at the rate of 40 l/h (appr.) for
about 40 minutes (Process may be done in fuming chamber).
Add 2 ml 1,5-diphenylcarbazide solution, mix thoroughly and dilute to 100
ml.
Take absorbance after 5-10 minutes at 540 nm.

Procedure : Removal of Molybdenum, Vanadium, Iron & Copper

Reagents

i. Cupferon solution : Dissolve 5 gms. cupferon (C6H5N(NO)ONH4) in 95 ml

water.
ii. Chloroform : CHCl3
iii. Nitric Acid : Concentrated
iv. Sulphuric acid.

Take suitable aliquot of sample in 125 ml separating funnel

Cool on ice bath.
Add 5 ml ice-cold cupferon solution, shake well and keep on ice bath for 1-
2 minutes.
Add 5 ml CHCl3. Shake vigorously with aquous solution.
Stand for separating two phases.
Discard CHCl3 layer.
Repeat above process of CHCl3 extraction for three times.
Take aquous extract in 250 ml conical flask. Wash separating funnel with
small amount of distilled water.
Boil content for 5 minutes to volatile chloroform, cool.
Add 5 ml concentrate HNO3.
Add 3 ml concentrate H2SO4.
Boil solution upto appearance of SO3 fumes, cool.
Add 5 ml con. HNO3 again and boil up to all NO3 fumes evolved
(escaped). Cool and use this solution for the determination of chromium
hexavalent as described earlier.

C. Oxidation of Trivalent Chromium

Reagents

i. Sulphuric Acid : 1:1 H2SO4 solution.

ii. Ammonium solution : 1:1 Ammonia solution.

245
 iii. Potassium permanganate solution : (1N) : Dissolve 3.6 gm KMnO4 in 100
ml volumetric flask and dilute with distilled water.
iv. Sodium azide solution (0.5%) : Dissolve 0.5 gm NaN3 in water and dilute
100 ml with distilled water.
v. Phosphoric acid solution : Use con. H3PO4.
Procedure
Take suitable aliquot of sample in 100 ml conical flask.
See the pH of solution using pH paper.
Add ammonia solution to make it just alkaline.
Add dil. H2SO4 dropwise just to make it acidic and add 2 ml excess.
Heat to boiling.
Add 2 drops KMnO4 solution until red colour persists.
Boil for 2 minutes.
Add 1 ml sodium azide solution and boil.
If red colour does not fade completely after boiling add another 1 ml sodium
azide solution and continue boiling till there is no colour.
Add 5 drops H3PO4 solution.
Transfer the content in 100 ml volumetric flask.
Adjust pH to 1-1.5 using pH meter or pH paper.
Add 2 ml diphenylcarbazide solution, mix thoroughly.
Stand for 5-10 minutes to develop a colour.
Measure absorbance at 540 nm.

Calculations

Cr+6, mg/L = gCr in aliquot x 1000

ml, aliquot

If aliquot = 50 ml, then, Cr+6, mg/L = gCr+6 in aliquot x 20

ANALYSIS OF CHROMIUM HEXAVALENT IN SOLID SAMPLES

Procedure
Weigh 0.5-1 gm solid sample in silica crucible (-100 mesh)
Ignite at 550oC to destroy carboneous matter, if any.
Digest residue in 10 ml H2SO4 to dissolve chromium hexavalent for about
hour.
Cool.
Filter through Whatman No.40 filter paper.
Take filtrate in 100 ml volumetric flask and make to 100 ml with distilled
water.
Take suitable aliquot from above solution.
Add 2 ml phosphoric acid, mix.

246
 Add 2 ml diphenylcarbazide solution, mix thoroughly.
Make the volume with 0.2 N H2SO4 solution, mix again thoroughly.
Stand for 5-10 minutes to develop a colour.
Measure absorbance at 540 nm.
Find out the concentration from standard graph.

Calculations :

%Cr+6 = gCr+6 (in aliquot)

Wt.of sample in gms (in aliquot) x 10,000

OR %Cr+6 = Cr+6 (gms) in aliquot x 100

Wt.of sample (gms) in aliquot

6.24 ANALYSIS OF CYANIDE IN WATER, WASTE WATER AND SOLID

WASTES USING ION SELECTIVE ELECTRODE AND COLORIMETRIC
METHOD

A. ION SELECTIVE ELECTRODE METHOD

Cyanide as CN can be analysed quantitatively by using Ion Selective Electrode and

colorimetric method. To avoid interferences, Ion Selective Method is usually preferred.
Cyanide is measured using Cyanide Standard Electrode and Double Junction Reference
Electrode immersed in the same solution containing cyanide ions.

The electrical potential of an Ion Selective Electrode is a function of the

logarithm of the activity of the ions to be measured. The relationship is given by Nernst
Equation.

E(measured) = Eo (constant) + S log ACN

Where E = measured electrode potential
Eo = Reference electrode potential (constant)
A = Cyanide ion activity in solution
S = Electrode Slope (constant)
(A) = y x c = concentration
Where y = activity coefficient (constant)

If the activity coefficient is constant then activity is directly proportional to the

concentration of cyanide ions present in the solution at pH >12. This can be easily
achieved by adding 0.2 M NaOH solution as an Ionic Strength Buffer in a 1:1 ratio of
solution and buffer.

Reagents
i. Standard Cyanide solution : Dissolve 1.88 gm NaCN (AR) in water and dilute to
1000 ml with distilled water in polythene volumetric flask. (1 ml = 1000 mg/l =1000
PPM CN).

247
ii. Ionic Strength Buffer : (0.2 M NaOH) : Dissolve 8 gm NaOH in water with constant
stirring. Cool and dilute to 1000 ml in polythene volumetric flask.

Preparation of Standard Graph

Take suitable volume of standard stock solution of cyanide and prepare series
of 4-5 solutions of 0.2 PPM, 0.4 PPM, 0.6 PPM, 0.8 PPM & 1.0 PPM CN
solution in 100 ml volumetric flasks.
Take aliquot (25 ml) of above solutions in 100 ml polythene beaker.
Add equal volume (25 ml) 0.2 M NaOH (ionic strength buffer in the same
beaker).
Place one magnetic stirrer bar in the solution.
Place a beaker containing solution on a magnetic stirrer.
Immerse cyanide and Reference electrodes in the solution.
Switch on the main instrument and magnetic stirrer.
Allow to equilibriate the reaction i.e. to stabilize a reading on the meter.
Note a reading on the meter.
Replace first beaker and repeat a process for other solutions of higher
concentrations as prepared above.
Plot a standard graph between concentrations and readings shown by the
meter for each concentrations.

Measurement of cyanide concentration in water and wastewater

Take suitable aliquot of water, wastewater (25 ml or 50 ml) in 100 ml

polythene beaker.
Add equal volume of 0.2 M NaOH buffer (25 ml or 50 ml) in the same beaker
Place one magnetic stirrer bar in the beaker.
Place this beaker on the magnetic stirrer.
Immerse the cyanide and Reference electrode in the solution.
Switch on the main instrument and magnetic stirrer.
Allow to equilibrate the reaction i.e. allow to stabilize a reading on the meter.
After stabilization note down the reading on the meter.
Find out the concentration of cyanide obtained from the standard graph.

Calculations

CN, mg/l = mg CN (in aliquot) x 1000

ml, aliquot

If aliquot = 50 ml then

CN, mg/l = mg, CN( in 50 ml) x 20

248
Measurement of cyanide in solid waste

Take 50 gm of solid waste or more in a polythene beaker of suitable size.

Add about 50 ml distilled water. Stirrir the content occasionally for about one
hour.
Filter in 100 ml polythene volumetric flask, wash with distilled water.
Make up the volume to 100 ml with distilled water.
Take suitable aliquot (25 ml or 50 ml) from above solution.
Add equal volume of 0.2 M NaOH buffer and measure the concentration of
cyanide as mentioned above.

Calculations

CN, mg/Kg = mg CN(in 1 gm) x 1000

Wt. of sample in aliquot (gms)

OR %CN = mg CN (in aliquot) x 100

Wt. sample in aliquot (gm) x 1000

B. ANALYSIS OF CYANIDE BY COLORIMETRIC METHOD

Principle

Cyanide is converted to CN Cl by reaction with chloramines-T at pH < 8,

which forms a red-blue dye on addition of pyridine-barbituric acid reagent and
absorbance can be measure at 578 nm. For better results distillation of samples may be
carried out before analysis by above method.

Reagents

i. Chloramine-T : Dissolve 1 gm chloramines-T powder in water and dilute to

100 ml.
ii. Standard solution of cyanide : Dissolve 1.88 gm NaCN (AR) in water and
dilute to 1000 ml in polythene volumetric flask with distilled water. (1 ml =
1000 mg/l = 1000 PPM CN) OR Dissolve 0.1880 gm NaCN(AR) in water and
dilute to 1000 ml. (1 ml = 100 PPMCN).
iii. Dilute above 1000 PPM CN solution so that 1 ml = 1 g CN.
iv. Pyridine barbituric acid solution : Dissolve 6 gm barbituric acid in
minimum quantity of water. Add to this 30 ml pyridine and 6 ml concentrate
HCl. Mix thoroughly, cool and dilute to 100 ml in polythene volumetric flask.
v. Sodium dihydrogen phosphate (1M): Dissolve 138 gms NaH2PO4 in water
and dilute to 1000 ml in polythene volumetric flask.
vi. Sodium Hydroxide solution : Dissolve 1.6 gm NaOH in water, cool and
dilute to 1000 ml in polythene volumetric flask.

249
Procedure

Prepration of standard graph :

Take appropriate volume of the standard stock solution to prepare series of

standards ranging from 2 g CN to 10 g CN in 100 ml polythene volumetric
flask.
Add 4 ml sodium dihydrogen phosphate buffer in each flask. Mix.
Add 2 ml chloramines-T solution, mix again.
Add 5 ml pyridine-barbituric acid solution. Mix thoroughly and dilute to 100
ml with distilled water. Mix thoroughly again.
Measure the transmittances/absorbance at 578 nm using spectrophotometer of
1 cm cell path.
Plot a graph between concentrations of cyanide and absorbance obtained.

Measurements of cyanide in samples

Take suitable aliquot of sample in 100 ml polythene volumetric flask.

Add 4 ml phosphate buffer, mix.
Add 2 ml chloramines-T solution, mix again.
Add 5 ml pyridine-barbituric acid solution, mix thoroughly.
Make up the volume to 100 ml with distilled water. Mix thoroughly.
Take absorbance at 578 nm using spectrophotometer. Calculate CN
concentration from the standard graph.

Calculations

CN, mg/l = mg CN(in aliquot) x 1000

ml, aliquot

If aliquot = 50 ml, then

CN, mg/l = mg CN(in 50 ml) x 20

6.25 ANALYSIS OF FLUORIDES IN WATER, WASTE WATER, MINERALS,

ORES AND SOIL SAMPLES USING ION-SELECTIVE ELECTRODE
AND COLORIMETRIC METHOD

A. ION SELECTIVE ELECTRODE METHOD

Whenever a sensing element is in contact with a solution containing

fluoride ions, an electrode potential develops across the sensing element. This potential,

250
which depends on the concentration of free fluoride ions in solution is measured against a
constant Reference potential with a digital pH/mv meter or specific ion meter.

According to Nernst equation:

E = Eo + S log (A)

Where E = measured electrode potential

Eo = Reference electrode potential (constant)
A = fluoride ion activity in solution
S = electrode slope (about 57 mv/decade)

(A) = yxc = ionic concentration

Where y = activity coefficient (constant).

If the activity coefficient is constant then activity is directly proportional to

the concentration of ions present in an ionic high strength of background solution.

Total Ionic Strength Adjustor Buffer (TISAB) is added to all fluoride

standards and samples so that the background ionic strength should be high.

Reagents
1.
a. Standard Fluoride Solution : Dissolve 0.221 gm NaF (AR/GR) in water
and dilute to 1000 ml with distilled water in a polythene volumetric flask.
(1 ml = 100 PPM F).
b. Dilute 1 ml of 100 PPM F solution to 100 ml in polythene volumetric flask
with distilled water. (1 ml =1 PPM F).
2.
i. Total Ionic Adjustor Buffer (TISAB) : Dissolve 58 gms NaCl in 57 ml
glacial acetic acid.
ii. Add 0.2 gm CDTA (1, 2-diamino cyclohexane N, N, N, N-tetra acetic acid)
in TISAB solution.
iii. Mix the contents thoroughly.
iv. Add 125 ml 6N NaOH in TISAB solution, mix again.
v. Make up the volume to 1000 ml.
vi. Check the pH of this TISAB solution. It should be around 5.3-5.5
(otherwise adjust it).

Interferences

Fluoride forms complexes with several polyvalent cations such as Al & Fe.
The extent of complexation takes place depends on solution pH, concentration of fluoride
and complexing species. CDTA (cyclohexylene diamine tetra acetic acid) a component
of buffer, will complexed interfering cations and release free fluoride ions, hence at the
pH maintained by buffer, no interference occur.

251
Procedure for analysis of fluoride in water, waste water samples

A. Standardization of instrument

Take aliquot of 1 PPM, 2 PPM, 3 PPM, and 4 PPM standard solution of

fluoride in 100 ml polythene volumetric flask.
Make up to 100 ml with distilled water. Mix thoroughly.
Take suitable aliquot (25 ml) of each standard solution in 100 ml polythene
beaker.
Add equal volume of TISAB buffer in each of the standards.
Immerse standard and Reference electrodes in to the standard solution.
Place a beaker on magnetic stirrer.
Place a stirring bar in the beaker.
Switch on the main instrument and magnetic stirrer.
Allow to equillibriate the contents in the beaker and take the measurement of
concentrations of standard calibration graph.

(Note: Today most of ISE are having the facilities to calibrate in the instrument itself. If the facilities are not in the
instrument graph may be drawn on graph paper).

B. Measurement of Fluoride in water, waste water

Take suitable aliquot of water, waste water sample in 100 ml polythene beaker.
Add equal volume of TISAB solution in the beaker.
Place a stirring bar in beaker.
Place beaker on the magnetic stirrer.
Immerse a standard and Reference electrode in the solution.
Switch on the instrument and magnetic stirrer.
Allow to stabilize/equillibrate the solution.
Take reading at constant point (steady state).
Find out the concentration from the standard graph.

Calculations

F, mg/l = mg F (in aliquot) x 1000

ml, sample taken

If aliquot = 50 ml, then

F, mg/l = mg F(in 50 ml) x 20

252
ANALYSIS OF FLUORIDE IN MINERALS, ORES, ORE DRESSING
PRODUCTS AND SOIL SAMPLES

Procedure

Fuse 0.1 gm (-100 mesh) (for rich fluoride) or 1 gm sample (for low fluoride)
in platinum crucible.
Add about 5 gm sodium carbonate.
Place the crucible in Muffle Furnace.
Fuse the content at 900oC for about 10-15 minutes.
Take out a crucible and allow to cool at room temperature.
Extract fused mass in 250 ml Teflon beaker with addition of minimum
quantity of hydrochloric acid.
Make up the volume in 100 ml polythene volumetric flask.
Take 1 ml of above solution (in case of rich fluoride content) in 100 ml
polythene volumetric flask and dilute to the mark OR Take 10 ml aliquot (in
case of low fluoride content) and dilute to 100 ml in polythene volumetric
flask.

Measurements

Take suitable aliquot of above solution in 100 ml polythene beaker (i.e. 25 ml

aliquot).
Add equal volume of TISAB buffer.
Place one bar of magnet in a beaker.
Place beaker on magnetic stirrer.
Switch on instrument and magnetic stirrer.
Immerse fluoride and Reference electrode in the solution.
Allow to equillibriate the reaction and stabilize the reading on a meter.

Calculations

%F = Reading (ppm) x dilution factor x 100

Wt. of sample (gms) x 10,000

B. ANALYSIS OF FLUIORIDE BY COLORIMETRIC METHOD : SPADNS

METHOD

The SPADNS method is useful for the determination of fluoride in a range

of 0 to 1.4 mg F/L, which gives instantaneous colour with zirconic oxychloride forming a
zirconium dye lake in acidic condition. Fluoride reacts with above dye lake, dissociating
a portion of it into a colourless complex. Hence as the amount of fluoride increases, the
colour intensity of the complex decreases. This intensity obeys Beers Law in a reverse
manner.

253
Reagents :

a. Standard Fluoride Solution : Dissolve 0.221 gm NaF in water and dilute to 1000 ml.
(1 ml = 100 ppm F).

b.SPADNS Solution : Dissolve 0.1916 gm SPADNS reagent {2-(parasulphophenylazo)-

1, 8-dihydroxy 3, 6-naphthalene disulphonate) in water and dilute to 100 ml with
distilled. Water

c. Zirconyl-acid reagent : Dissolve 0.133 gm Zirconyl oxy-chloride octahydrate

(ZrOCl2.8H2O) in distilled water. Add 350 ml conc. HCl and dilute to 500 ml with
distilled water.

d. SPADNS-Acid Zirconyl Solution : Mix equal volume of SPADNS solution and

zirconyl acid reagent.

e. Reference Solution : 10 ml SPADNS reagent solution prepared earliest is diluted to

100 ml. Then 7 ml conc. HCl is diluted to 10 ml. Now add this solution to diluted
spadns solution. Mix the solution thoroughly. Use this for setting a zero of the
spectrophotometer to be used for the measurement of colour intensity.

f. Arsenite solution : Dissolve 0.5 gm Sod. Arsenite (NaAsO3) and dilute to 100 ml with
distilled water.

Procedure

Preparation of standard graph

Take suitable aliquot from the stock solution of fluoride in 100 ml polythene
flasks in the range of 0.2 PPM to 1.4 PPM F (i.e. 0.2 PPM, 0.4 PPM, 0.6
PPM, 0.8 PPM, 1 PPM, 1.2 PPM and 1.4 PPM F).
Add 10 ml mixed acid zirconyl spadns reagent in each of the volumetric flask.
Make up the volume with distilled water and mix thoroughly.
Measure the absorbance/transmissions at 570 nm of each solution.
Plot a graph, concentrations against absorbance/transmittances.

Measurement of fluoride in water, wastewater samples

Confirm the presence of residual chlorine. If sample contains residual
chlorine, it can be removed by adding 1drop (0.05 ml) NaAsO2 solution which
is equivalent to 0.1 mg R.Cl2. Avoid to add excess of NaAsO2 solution.
Take suitable aliquot of sample in 100 ml polythene volumetric flask (i.e. 50
ml).
Add 10 ml mixed acid zirconyl-SPADNS reagent.
Make up the volume with distilled water and mix thoroughly.
Take absorbance/transmittance at 570 nm.
Find out the Fluoride concentration from the standard graph.

254
Calculations:

F, mg/L = mg.F (from graph in aliquot) x 1000

ml.aliquot

If aliquot = 50 ml , then

F, mg/L = mg.F (in 50 ml) x 20

6.26 ANALYSIS OF MERCURY IN WATER/WASTE WATER, MINERALS,

ORES AND SOIL SAMPLES USING MERCURY ANALYSER

Mercury is the only element, which occurs in liquid form at room temperature. It is
toxic and hence we have to be very much careful about its presence in drinking water.
Mercury can be analysed at the trace level using mercury analyzer.

The technique of mercury analysis is known as cold vapour atomic absorption

spectrophotometry. It is based on the principle that mercury vapour (atoms) absorbs
resonance radiations at 253.7 nm at room temperature.

An instrument consists of

1. Low pressure mercury lamp emitting 253.7 nm resonance line.

2. An absorption cell.
3. A filter
4. Vapour generation system and
5. A detector with associated electronic devices.

The carrier air is bubbled through the vapour generation system, which carries
elemental mercury from the solution and then passes through an absorption cell. This can
be measured on either optical density meter or on transmission meter.

Preparation of Standard Graph

Reagents
a.
i. Pot.permanganate solution (1%) : Dissolve 1 gm KMnO4 in distilled water.
ii. Add 10 ml conc. H2SO4 and dilute to 100 ml.
b.
i. Sodium Hydroxide solution : (20%) : Dissolve 20 gm NaOH in distilled
water
ii. Dilute to 100 ml with distilled water.

255
c.
i. Stannous chloride solution : (20% in 10% HCl) : Dissolve 20 gm SnCl2
(AR/GR) in 10 ml conc. HCl with warming.
ii. Cool and dilute to 100 ml with distilled water.

d. Sulphuric acid solution : Prepare 1:1 dilution.

e. Nitric Acid Solution : Prepare 10% HNO3 solution. (i.e. 10 ml conc. HNO3 is
diluted to 100 ml with distilled water).

f.
i. Standard Mercury Solution : Dissolve 0.1354 gm HgCl2 in 2% HNO3.
ii. Dilute to 1000 ml with 2% HNO3 solution ( 1 ml = 0.10 mg Hg = 100 g Hg).
iii. Dilute 10 ml of 100 ug Hg solution to 100 ml with 2% HNO3 solution.
(1 ml = 10 g Hg = 10,000 ng Hg).
iv. Dilute 10 ml of 10 ug Hg solution to 100 ml with 2% HNO3 solution.
(1 ml = 1 g Hg = 1000 ng Hg).
v. Dilute 10 ml of 1000 ng Hg to 100 ml with 2% HNO3 solution.
(1 ml = 0.1 g Hg = 100 ng Hg).

(Note: Stock solution of Hg is to be maintained with 2% HNO3 and 0.01% K2Cr2O7 solution).

Standard Graph using BOD Bottle

Take aliquots of 1 ml, 2 ml, 3 ml, 4 ml, 5 ml & 6 ml from 100 ng Hg stock
solution in BOD bottles. (This each solution contains 100, 200, 300, 400, 500
& 600 ng Hg).
Add required volume of distilled water to maintain the total volume = 100 ml.
(Before adding any reagents in BOD bottles).
Add 5 ml of 10% HNO3 acid solution in BOD bottle.
Add 2 ml SnCl2 solution and stopped the BOD bottle immediately. (Up to
this stage the total volume in BOD bottle should be 100 ml.).
Keep this BOD bottle (Mercury vapour generator) on magnetic stirrer and
continue for 5 minutes.
Keep a filter rod on open position and mode switch to Hold position.
Adjust absorbance 0 to 2 by moving adjacent switches or transmission
between 0 to 100 by moving adjustment switches of the instrument, as per
manufacturers instructions.
After 5 minutes, start the pump and allow mercury vapours to purge through
the BOD bottle (i.e. vapour generation bottle).
Note an absorbance/transmittances on a meter at Hold position.
Plot a standard graph between concentration of Hg and
absorbance/transmittances.

256
DETERMINATION OF MERCURY IN WATER/WASTEWATER/EFFLUENT
ETC.

Procedure

Take suitable aliquot of sample in BOD bottle (for example, 50 ml)

Take distilled water so that the total volume including other reagents should not
be more than 100 ml.
Add 5 ml of 10% HNO3 acid solution in BOD bottle.
Add 2 ml SnCl2 solution and stopper BOD bottle immediately (upto this stage the
total volume of BOD content should be 100 ml.)
Keep BOD bottle as prepared above on magnetic stirrer.
Start the magnetic stirrer and continue for five minutes.
Take absorbance/transmittance after 5 minutes.
Carry out blank in a similar manner and deduct from sample reading.
Find out the concentration of mercury from the standard graph.

Calculations :

Hg, mg/L = Hg, ng (in aliquot) x 1000 = Hg, ng (in aliquot)

ml, (aliquot) x 1000 x 1000 ml, aliquot x 1000

If aliquot = 50 ml, then

Hg, mg/L = Hg, ng (in 50 ml) x 20

1000

(Note : At the end of every reading, allow mercury vapour to absorb in KMnO4 solution by continuing pump up to a
condition that meter shows zero reading).

ANALYSIS OF MERCURY IN MINERALS/ORES AND SAND SAMPLES

Procedure: Preparation Of Solution/Dissolution Of Mercury

Weigh 1.0 gm finely powdered sample (-100 mesh) in 250 ml beaker.

Add 10 ml acid mixture (1:1 HNO3 : H2SO4) in the above beaker and cover
with watch glass.
Keep beaker on water bath at about 60 oC and allow to digest for two hours
with swirling occasionally.
Remove beaker from the water bath and allow to cool at room temperature.
Dilute the content with 20-25 ml distilled water. Allow to cool again.
Add 5 ml of 6% KMnO4 solution and leave for over night.
Next day, add 5% hydroxylamine hydrochloride solution dropwise until all
brown manganese dioxide and excess of permanganate are reduced. (Almost
colourless solution appears).

257
 Allow the reaction complete for keeping about one hour. During this period
all gases are escaped.
Filter if some turbidity or residue is noticed in the solution.
Make up a volume to 100 ml in volumetric flask.
Take suitable aliquot from this solution for the determination of mercury.

ANALYSIS OF MERCURY

Take suitable aliquot from above solution in B.O.D. bottle (Mercury vapour
generation system).
Add required volume of distilled water to maintain total volume to 100 ml.
Add 5 ml of 10% HNO3 solution.
Add 2 ml of SnCl2 solution (20% in 10% HCl).
Immediately close the system and keep on a magnetic stirrer with magnetic
bids and allow to continue for 5 minutes and take the measurement as
described in earlier procedure.
Run blank in a similar manner and deduct from main reading

Reaction : HgCl2 + SnCl2 = Hg + SnCl4

At room temperature vapour of mercury is generated, which can be measured on optical

density/transmission meter.

Calculations

% Hg = (A-B) ng, Hg x 1000

Wt. of sample in aliquot (gms) x 1000 x 1000 x 1000

%Hg = (A-B) ng, Hg = (A-B) ng Hg x 10-7

Wt. of sample in gm x 107 Wt. of sample in gm

Where A = concentration of Hg in ng for sample.

B = concentration of Hg in ng for blank.

NON-SPECIFIC ABSORPTION

Vapour of organic compounds such as alcohols, ketones and ester, acids

and water vapour will absorb UV radiation and hence will interfere seriously, as
absorption of UV (ultraviolet) radiation by mercury atoms occurs in this technique. All
substances, which absorbs UV radiation will decrease the transmittance and cause
positive bias. The absorption due to these substances is knows as Non-specific
absorption.

258
DETERMINATION OF NON-SPECIFIC ABSORPTION

The traps of alkali and acid will remove acid and water vapour respectively and
therefore will minimize non-specific absorption. However, if non-specific absorption is
suspected in unknown sample, it can be measured by adopting the following procedure.

Remove the trap of H2SO4 (R4)

Place another trap containing 4 ml of 1% KMnO4 solution (1:1 H2SO4
solution) say it as R6.
Now repeat the analysis on a separate aliquot of sample as usual manner.
Note the absorbance obtained, which is of non-specific absorbance and not
due to mercury as R6 absorb all mercury vapour before going to absorption
cell.
The difference of two absorbances will give absorbance due to that of
mercury alone.

Calculations

AHg = AR4 AR6

Where AHg = absorbance due to Hg alone

AR4 = absorbance due to Hg + other organic materials
AR6 = absorbance due to other organic materials.

AR6 = AR4 AHg = Non-specific absorbance

6.27 SOIL ANALYSIS

Soil is the upper layer of earth crust. Most of the plants growth depends upon the
type of soil from which they take water and nutrients. The quality of soil is decided by
taking some factors into considerations and is to be determined using appropriate
methods of analysis such as physical and chemical properties on which the fertility of soil
can be decided. Due to some man made activities the soil has been disturbed and needs
to take proper care to achieve the effectiveness of its origin.

Some important soil parameters can be analysed using the following procedures.

A. Physical parameters

Particle size analysis

Water holding capacity

B. Chemical parameters
pH
Soluble salts

259
 Organic carbon
Cation exchange capacity
Calcium carbonate
Available phosphorous
Available sulphur &
Nitrogen, etc.

Soil testing involves the following steps

1. Sampling of soil to be tested

2. Analysis of various physical and chemical parameters.

SAMPLING

The principal object of this step is to collect the representative samples of the
entire area. Some criteria is to be followed while collecting soil samples such as an area
can be considered as a single sampling unit only if it is appreciably uniform in all
respects. The spots located near bunds, channels, marshy tracts and spots near trees,
wells, compost piles or any other location that can be considered non-representative of
the general area should be avoided.

Sampling depth is another important aspect. It is usually advised to take sample

at the depth of 15 cms from the surface of top soil, which can be extended up to 22 cms
in some cases.

Keeping the above points in mind, the following steps must be followed while
collecting the soil samples.

1. First of all, visually inspect the area to be sampled. If considerable differences in

colour, texture, elevation etc. are existing, divide entire area into sampling units or
if there are no considerable differences noticed then the whole area can be treated
as a single sampling unit.
2. Take as many as possible 10-20 samples from spots distributed covering the entire
area. At each spot scrap away any surface little and collect in a clean cloth or
plastic bags using appropriate instrument and collect enough quantity as per
requirements for the testing purposes.

Collected samples are to be air dried and crush into desired size, either by
hammering or using any mechanical instrument. Crushed samples are then subjected
to coning and quartering process so that a representative sample can be obtained from
the original sample.
Thus the sample obtained as above should properly labeled and preserved from
being contaminating with other materials such as chemicals, fertilizers, etc.

260
 If possible sample may be divided into two separate portions so that one can be
used for physical tests, while other can be crushed into fine powder and used for the
analysis of chemical parameters.

The samples must be analysed as early as possible since some parameters having
the tendency to change with passing of time.

ANALYTICAL PROCEDURES : PHYSICAL PARAMETERS

DETERMINATION OF SOIL TEXTURE : GRAVIMETRIC METHOD

The objective of textural analysis of soil is to determine the percentage of solid

material contained in different size fractions. This can be done either gravimetric or
mechanical method.

Reagents

1. Hydrogen peroxide : 20 ml (30%) hydrogen peroxide is diluted to 100 ml

with distilled water.
2. Hydrochloric acid : (2N) : 83 ml conc. HCl is diluted to 500 ml with distilled
water.
3. Sodium Hydroxide Solution : (2N) : Dissolve 40 gms NaOH in water and
dilute to 500 ml with distilled water.
4. Silver Nitrate Solution (1%) : Dissolve 1 gm AgNO3 in water and dilute to
100 ml with distilled water.
Procedure

Take 10 gm of 2 mm soil sample in 500 ml beaker.

Add 125 ml distilled water, boil for about 10 minutes.
Allow to cool and to settle suspension.
Decant supernatant and discard it.
Add 20 ml H2O2 solution and digest on water bath adding more H2O2 Solution
till no froathing is evolved.
Add about 20-30 ml 2N HCl and dilute to about 100 ml distilled water.
Allow to stand about one hour with occasional stirring to make the soil free
from carbonates.
Filter through Whatman No.41 filter paper. Wash residue with distilled water
till free from chloride ions. (Test with AgNO3 solution).
Transfer residue of soil in beaker.
Add 5 ml, 2N NaOH solution and shake for about an hour.
Transfer the content in 1000 ml measuring cylinder and make up the volume
to 1000 ml with distilled water.
Shake the above contents thoroughly for about 1 minute, and allow to stand.
Take 25 ml volume with pipette at 10 cm depth after 4 minutes in preweighed
platinum dish or in preweighed beaker.

261
 Evaporate at 105oC in oven and weigh to constant weight.
The difference in weight is contributed by clay+silt.
Shake remaining content in the measuring cylinder for about 1 minute and
keep for settlement.
Take 25 ml volume with pipette at 10 cm depth in preweighed platinum
crucible/dish or in beaker after 6 hours.
Evaporate at 105oC in an oven and find out the weight after it is dried
completely.
Weight difference gives the weight of clay alone.

Calculations

1. Calculate % of clay alone obtained.

2. Calculate % of clay + silt as obtained above.
3. Substract weight of clay from weight of clay+silt, which gives only silt %.
4. Substract weight of clay + silt from 100%, which gives sand percentage. i.e. Sand
% = 100 (% clay + % silt).
Let wt. of sample = W0 gms.
Of clay alone = W1 gms
Wt. of clay + slit = W2 gms
Aliquot = 25 ml
Total volume = 1000 ml.
Then % of clay = (W1) gm x Total Volume x 100
Wt. of soil sample x ml. aliquot
= (W1) x 1000 x 100 = (W1) x 4000
W0 x 25 W0
% Slit = (W2 W1) x 4000
W0

% Sand = 100 [ (W ) x 4000 + (W

1 2 W1) x 4000 ]
W0 W0
(Note: If soil containing MnO2, add few drops of acetic acid before treatment of H2O2.
In case of calcareous soil, use H2O2 slightly acidified with HCl.
The pulp density of suspension should not be more than 2% to have a good result

SOIL TEXTURE (MECHANICAL METHOD)

Different methods are used for the determination of sand (coarser than 0.062 mm)
and silt + clay (finer than 0.062mm). Samples are dried and sieved on series of sieves
starting from highest diameter at the top and finest at the bottom. The method of analysis
of particle size distribution of sediments/soils depends on whether sediment/soil is
relatively coarse or fine.

The soil/sediment samples are sieved through different pore sizes for separating
different fractions of soil/sediment.

262
Procedure
Dry soil/sediment samples at 105oC in an oven.
Take 100-500 gms of soil/sediment sample in a tray.
Arrange sieves of 2 mm (at the top), 1 mm, 500 mesh, 250 mesh, 125 mesh
and 63 mesh with decreasing aperture size .
Place the weighed sample on the top of the sieve shaker.
Start the sieve shaker and allow to run for 10-15 minutes.
Collect sample from each sieve.
Take weight of each fraction of collected sample.
+2 mm may be weighed and calculate percentage which is called granules.

Calculations
The distribution of particle size of sample can be represented as below
Sl.No. Size of Particle Grain Name
1. +2 mm Granules
2. -2 mm+500 mesh Very coarse sand
3. -500+250 mesh Coarse sand
4. -250+125 mesh Medium sand
5. -125+63 mesh Fine sand
6. -63 mesh Silt and clay

% of each fraction of soil = Wt. of each fraction x 100

Wt. of sample taken
B. CHEMICAL PROPERTIES

DETERMINATION OF pH

The measurement of hydrogen ions (or hydroxyl ions) activity of soil-water

system is known as soil pH. This indicates the nature of soil reaction.

Procedure

Take 10 gm of soil sample in 100 ml beaker.

Add 50 ml distilled water.
Mix and occasionally stir for about 30 minutes.
Measure pH of above suspension using standard pH meter
(Note : pH meter can be standardized using standard pH solutions of 4.0, 7.0 & 9.2).

DETERMINATION OF ELECTRICAL CONDUCTIVITY

Conductivity is a measurement of current carrying capacity, which gives idea

about the soluble salts present in soil samples.

263
Procedure

Take 10 gms soil sample in 100 ml beaker.

Add 50 ml distilled water.
Stir for about 1 hour with intervals.
Measure the conductivity of above suspension using standardized conductivity
meter.
Conductivity meter can be standardized using KCl (AR) of suitable
concentration.
Calculations

Conductivity (us/cm OR mhos/cm) = Cell constant x meter reading

(Or as per the instructions of instrument manufacturer).

DETERMINATION OF WATER HOLDING CAPACITY OF SOIL SAMPLES

Water holding capacity of soil depends upon the physical and chemical nature of
it. When the soil is absolutely saturated with water so that water fills all the pores
between particles of soil and there is no air space, the soil is said to be at its maximum
Water Holding Capacity.

Procedure
Dry sample in oven at 105oC
Place a filter paper (Whatman No.1) in a rectangular perforated box at the
bottom.
Take weight of box.
Fill perforated box with soil to be tested.
Take weight of box with filled soil.
Place above box in petri dish/tray or suitable pot.
Fill water in petri dish/tray just below the edges of perforated box.
Allow to stand for 12 hours to saturate the soil by entering water through
holes.
Take out box after 12 hours.
Dry box on outside using tissue paper.
Take weight of the box with saturated soil.

Calculations

W.H.C. % = (W2 W1) (W1 W0) x 100

(W1 W0)

= (Wt. of water saturated soil) (Wt. of dried soil) x 100

Wt. of dried soil

264
Where W0 = Wt. of empty box
W1 = Wt. of box with dried soil
W2 = Wt. of box with water saturated soil

DETERMINATION OF ORGANIC CARBON

For the determination of organic carbon (matter) in soil samples, sample digested
with excess of potassium dichromate solution in presence of sulphuric acid and excess of
dichromate is determined by titrating against ferrous ammonium sulphate solution.

Reagents

1. Potassium dichromate solution (1N) : Dissolve 49 gms K2Cr2O7 in distilled

water and dilute to 1000 ml with distilled water.
2. Sulphuric acid with silver sulphate : (5%) : Dissolve 5 gm silver sulphate
(Ag2SO4) in 100 ml conc. H2SO4.
3. Phosphoric acid : 85%
4. Ferrous Ammonium Sulphate Solution (1N) : Dissolve 392.2 gm Ferrous
Ammonium Slulphate {Fe(NH4)2 (SO4), 6H2O} in 20 ml conc. H2SO4 and dilute
to 1000 ml with distilled water.
5. Barium diphenylamine sulphonate indicator : 0.5% : Dissolve 0.5 gm Barium
diphenylamine sulphonate in water and dilute to 100 ml. with water.

Procedure

Take 0.5-1.0 gm soil sample in 500 ml conical flask. Moisten with few ml of
distilled water.
Add 10 ml potassium dichromate (1N) solution using pipette.
Add 20 ml sulphuric acid silver sulphate mixture solution.
Mix gently and allow to stand for an hour.
Dilute mixture to about 200 ml with distilled water.
Add 10 ml phosphoric acid, mix thoroughly. Cool.
Add 1 ml Barium diphenylamine sulphonate indicator.
Titrate above solution with 1 N Ferrous Ammonium sulphate solution.
Brilliant green colour shows the end point of the reaction.
Carry out the blank in a similar manner.

Calculations

Organic Carbon % = ml (Blank) ml (Sample) NFAS x 0.003 x 100

Wt. of sample

= ml (Blank) ml (Sample) x NFAS x 0.3

Wt. of sample
Organic Matter = % C x 1.724
(Note: The factor 1.724 is based on the assumption that carbon is only 58% of organic matter)

265
(1 ml 1 N K2CR2O7= 0.003 gm Organic Carbon = 1N FAS)

DETERMINATION OF CATION EXCHANGE CAPACITY

For the determination of cation Exchange Capacity 1 N.Sodium acetate solution

of pH 8.2 is used. In this technique, sodium replaces all the exchangeable cations of soil
when leached thoroughly and excess sodium ions are removed using ethyl alcohol. These
sodium ions can be easily determined using flame photometer.

Reagents

1. Sodium acetate solution : (1N, pH = 8.2) : Dissolve 40.0 gm sod. hydroxide in

distilled water. Add 58 ml acetic acid and dilute to 1000 ml with distilled water.
Adjust pH = 8.2 using NaOH.
2. Ethyl alcohol : 95%
3. Ammonium acetate : (1N, pH = 7.0) : Mix 58 ml acetic acid and 68 ml conc.
ammonium hydroxide solution and dilute to 1000 ml. Adjust pH to 7.0 using
NH4OH or Acetic Acid.

Procedure
A.
Take 5 gms of soil (powder) in 50 ml centrifuge tube.
Add 30 ml 1 N sodium acetate solution.
Stopper and shake for 5 minutes.
Centrifuge the suspension. Till supernatant is clear.
Decant the supernatent and discard
Repeat above process for three times using 30 ml sodium acetate solution
every time.

B.
Sodium saturated sample is then washed thrice with 30 ml of 95% ethyl
alcohol with shaking 5 minutes each time.
Wash with 20 ml ethyl alcohol till the supernatent shows conductivity
between 55-40 us/cm.
C.
The absorbed sodium is replaced from the sample with 30 ml volume of 1 N.
Ammonium acetate solution.
Repeat for thrice.
Decant the supernatent in 100 ml volumetric flask.
Make upto the mark with ammonium acetate solution.
Determine sodium using Flame Photometer.
Carry out a blank in a similar manner.

266
Calculations :

Cation Exchange Capacity (meq/100 gms) = A x V ml x 100 x 100 ml

W x 23 x 1000 ml

= A x Vml x 10
23 x Wt. of soil sample
Where A = Na content in ammonium acetate extract (meg/L)
V = ml volume of extract, ml
W = Wt. of soil sample taken in grams.

(1 meq/100 gm = 1 mg. Eq./100 gm For sod. Na = 23)

(1 meq/L of Na = 0.023 gms of Na)

(Note: ppm = Atomic mass of atom x meq

Valency of atom

(i.e. 1 meq of Na = 23 ppm = 0.023 gms Na)

DETERMINATION OF EXCHANGABLE CATIONS

EXCHANGEABLE CALCIUM AND MAGNESIUM : EDTA METHOD

Calcium and magnesium can be determined by complexometric titration with

EDTA using Reader & Pattons reagent and Eriochrome Black-T as indicators at pH 12
and 10 respectively.

Reagents

1. Hydrochloric acid (conc.)

2. Nitric acid (conc.)
3. EDTA Solution : 0.01 M : Dissolve 3.722 gm EDTA in distilled water and dilute
to 1000 ml with distilled water.
4. Standard zinc acetate solution (0.01 M) : Dissolve 0.2195 gm zinc acetate (AR)
in water and dilute to 100 ml with distilled water.
5. Buffer Solution (pH = 10) : Dissolve 67.5 gm NH4Cl in 510 ml ammonia
solution and dilute to 1000 ml with distilled water.
6. Buffer Solution (pH = 12) : Dissolve 200 gm KOH in water and dilute to 1000
ml with distilled water.
7. Buffer Solution (pH = 5.5) : Dissolve 200 gms ammonium acetate in 30 ml
acetic acid and dilute to 1000 ml with distilled water.
8. Patton & Readers Reagent : Dissolve 0.1 gm in 100 ml methanol or water.
9. Eriochrome Black-T : Dissolve 0.1 gm in 100 ml methanol or water.
10. Xylenol orange solution : Dissolve 0.1 gm xylenol orange in 100 ml
methanol/distilled water.
11. Hydroxylamine hydrochloride solution : 5% in distilled water.
12. Triethanolamine solution : 5% in distilled water.

267
Procedure
A.
Take suitable aliquot from Ammonium acetate extract from Cation Exchange
Capacity solution in 250 ml beaker.
Evaporate to dryness on hot plate.
Add 5 ml conc. HCl and dilute to 20 ml with distilled water.
Add 1 ml conc. HNO3.
Allow to complete the reaction.
Evaporate to dryness on hot plate.
Extract with 1 ml conc. HCl, wash with distilled water, warm to dissolve any
matter.
Filter through Whatman No.40 filter paper if residue is present.
Make up the volume of filtrate to 100 ml in volumetric flask.

(Note : Add 2 ml, 5% hydroxylamine hydrochloride and triethenolamine solutions to mask some interfering cations
like Fe, Mn, Al, etc. before starting EDTA titration).

B. DETERMINATION OF CALCIUM AND MAGNESIUM

a. DETERMINATION OF CALCIUM + MAGNESIUM

Take suitable aliquot of above solution in 250 ml beaker.

Dilute to about 100 ml with distilled water.
Add 20-25 ml buffer solution (pH = 10).
Add 2-5 drops of Erio-chrome Black-T indicator.
Titrate again 0.01 M EDTA solution.
Peacock blue colour shows the end point of the reaction.
Run blank in a same manner and deduct from sample titration.

b. DETERMINATION OF CALCIUM ONLY

Take equal aliquot from the above solution in 250 ml beaker.

Dilute to about 100 ml with distilled water.
Add 20-25 ml buffer solution (pH=12).
Add 2-5 drops of Patton & Readers reagent indicator solution.
Titrate against 0.01 M EDTA solution.
Peacock blue colour shows the end point of reaction.
Carry out blank in a similar manner and deduct from sample titration.

c. STANDARDIZATION OF EDTA AGAINST ZINC ACETATE SOLUTION

Take suitable aliquot of standard zinc acetate solution (0.01 M) in 250 ml

beaker.
Dilute to 100 ml with distilled water.

268
 Add 20-25 ml buffer solution (pH=5.5).
Add 2-5 drops of xylenol orange indication solution.
Titrate against 0.01 M EDTA solution.
Golden yellow colour shows the end point of the reaction.

Calculations

Calculate molarity of EDTA from standard formula of N1V1 = N2V2

Exchangeable calcium : = ml EDTA x MEDTA x ml aliquot x 100

(meg/100 gm soil) ml(original aliq.) x Wt. of sample

OR Ca,(meg/100 gm) soil = ml EDTA x MEDTA x ml aliquot x 100

ml(original aliq.) x Wt. of sample x 20.04

(1 ml 1 MEDTA = 40.8 mg Ca = 24.3 mg Mg.)

Exchangeable magnesium

ml EDTA for Ca+Mg ml EDTA for Ca = ml EDTA for Mg

Exchangeable +Mg = ml EDTA for Mg x MEDTA x ml aliquot x 100

(meg/100 gm soil) ml aliq. taken (original) x wt. x 12.15

DETERMINATION EXCHANGEABLE SODIUM & POTASSIUM

Reagents

Ammonium acetate (1N) pH = 7 : Dissolve 68 ml ammonium hydroxide

solution in 58 ml acetic acid and dilute to 1000 ml with distilled water. Adjust pH to 7.
Procedure

Take 5 gm soil sample in 100 ml conical flask.

Add 25 ml 1N ammonium acetate buffer solution.
Shake for about 5 minutes.
Filter through Whatman No.41 filter paper.
Use this filtrate for the determination of sodium and potassium.
Feed above extract (filtrate) in Flame Photometer as per the instructions of
instrument manufacturer and calculate comparing with standards.

Calculations

Exchangeable sodium (meg/100 gm soil) = conc. from meter x aliquot x 100

Wt. of sample x 23

{Note: (1 meg/L of Na = 0.023 gms of Na)

(1 meg/L of K = 0.019 gms of K)

269
DETERMINATION OF CALCIUM CARBONATE : (CaCO3) (ACID
NEUTRALIZATION METHOD) AND CALCIUM-BICARBONATES METHOD
(CaHCO3)

This is a rapid method for the determination of calcium carbonate in soil samples.
Reagents

1. Sulphuric acid solution (0.4 N) : Dilute about 11.12 ml of concentrated

sulphuric acid (AR) and make up to 1000 ml with distilled water.
2. Sodium hydroxide solution (0.4 N) : Dissolve 16 gms of sodium hydroxide
(AR) in water and dilute to 1000 ml with distilled water (Solution is to be
standardized against standard acid solution).
3. Phenolphthalein indicator : Dissolve 0.1 gm in 100 ml distilled water.
4. Methyl orange : 0.1% solution in water.

STANDARDIZATION OF SULPHURIC ACID SOLUTION

Take 0.1-0.2 gm sodium carbonate (AR) in 250 ml beaker.

Add about 100 ml distilled water to dissolve it.
Add 2-3 drops of methyl orange.
Titrate against sulphuric acid solution.
Purple colour shows the end point of the reaction.

NH2SO4 = Wt. of Na2CO3 x 1000

Equi. Wt. of Na2CO3 x ml, H2SO4

= Wt. of Na2CO3 x 1000

53 x ml, H2SO4
Procedure

Take about 1-2 gm soil sample in 250 ml flask.

Add 25 ml 0.4 N H2SO4 solution.
Dilute to about 100 ml with distilled water.
Boil for 5-10 minutes.
Cool and titrate against standard NaOH solution using phenolphthalein as an
indicator.
Carry out blank in a similar manner.

Calculations
% CaCO3 = {(ml (Blank) ml (exp)} x NNaOH x 0.05 x 100
Wt. of soil

Where : ml NaOH for blank sample

ml NaOH for experimental sample
(1 ml 1 N H2SO4 =0.05 gm of CaCO3 = 1 ml 1 H NaOH)

270
DETERMINATION OF CALCIUM BICARBONATES (Ca HCO3)

Procedure

Take same solution from which calcium carbonate has been titrated.
Add 2-4 drops of methyl orange indicator.
Titrate further against same sulphuric acid solution till solution becomes red.
Carry out blank in a similar manner and deduct from volume required for
determination of CaHCO3

Calculations

(1 ml 1 N H2SO4 = 0.101 gm of CaCO3)

CaHCO3(meg/100 gm soil) = ml CaHCO3 ml CaCO3 x N1 x 0.101 x 100

Wt. of soil

DETERMINATION OF TOTAL NITROGEN IN SOIL SAMPLES

Total nitrogen can be determine in soil samples using salicylic acid method for
the reduction of nitrogenous substances such as nitrite and nitrates into ammonium
sulphate, which further converts into ammonia can be distilled off into boric acid solution
and determined by titrimetric method.

Reagents

1. Sulphuric acid : conc. H2SO4

2. Salicylic acid (AR/GR).
3. Sodium thiosulphate : (AR/GR).
4. Potasium sulphate : (AR/GR).
5. Copper sulphate : (AR/GR).
6. Sodium hydroxide : 40% solution
7. Methyl red indicator : 0.05% in methanol/water
8. Oxalic acid solution (0.1 N) : Dissolve 0.63 gm oxalic acid (AR/GR) in water
and dilute to 100 ml with distilled water.
9. Sodium hydroxide solution (0.1 N) : Dissolve 4 gm NaOH in water and dilute
1000 ml with distilled water.
10. Sulphuric acid solution (0.1 N) : Dilute 3.6 ml conc. H2SO4 in water and make
up to 1000 ml with distilled water.

Procedure
Take 4-5 gm finely powdered soil sample in Kjeldahl flask.
Add 30 ml conc. H2SO4 containing 1 gm salicylic acid, mix thoroughly for 2-
3 minutes and allow to stand for about half an hour to complete the reaction
where formation of nitro salicylic acid is takes place.

271
 Add 5 gms sodium thiosulphate in above flask to reduce nitro-salicylic acid
into amino-salicylic acid which further produces into ammonia. This
ammonia is then absorbed by sulphuric acid producing ammonium sulphate.
Add 5 gms potassium sulphate and 0.5 gm copper sulphate into the flask after
5-6 minutes.
Digest the content of flask slowly on a heating divice until all the carbon gets
oxidized.
After completion of digestion, cool the mixture and dilute to 100-150 ml with
water.
Transfer the mixture into 500 ml round bottom flask.
Pour 40 ml of 40% sodium hydroxide solution into above mixture and close it
immediately.
Distilled the content upto about its (1/3) one third of original volume.
Collect distillate (ammonia) evolved during distillation in a measured quantity
of standard sulphuric acid/boric acid solution.
Titrate excess sulphuric acid/boric acid solution against standard sodium
hydroxide solution using methyl red indicator.
Carry out blank for the same volume.

Calculations

Total Nitrogen % in soil = ml NaOH consumed x NNaOH x 0.014 x 100

Wt. of soil

(ml NaOH consumed = ml NaOH for blank ml NaOH for soil samples)
(ml 1 N NaOH = 0.014 gms of Nitrogen)

DETERMINATION OF AMMONIUM NITROGEN IN SOIL SAMPLES

Ammonium nitrogen in soil sample can be determined by converting it into

ammonia by the action of alkali solution and thus evolved ammonia is absorbed in dilute
sulphuric acid solution taken in excess. The excess sulphuric acid can be titrated against
standard sodium hydroxide solution from which a consumed volume of acid is calculated
and ammonium nitrogen can be determined.

Reagents

1. Magnesium oxide : MgO (AR/GR)

2. Potassium chloride : Cl (AR/GR)
3. Sulphuric acid (2%) : 2 ml in 98 ml water.
4. Standard sulphuric acid solution (0.1 N) : 3.6 ml sulphuric acid is diluted to
1000 ml. (can be standardized against standard sodium hydroxide solution using
phenolphthalein indicator).
5. Oxalic acid solution (0.1 N) : 0.63 gm oxalic acid in 100 ml distilled water.

272
 6. Methyl red indicator : (0.05%) in methanol/water.
7. Phenolphthalein indicator : (1%) in water/methanol.

Procedure

Take 10-20 gm finely powdered soil sample in 250 ml Erlenmeyer flask.

Add 5 gms magnesium oxide, mix.
Add 0.5 gm potassium chloride, mix again.
Add about 100 ml distilled water into the flask.
Fix immediately to the Kjeldahl distillation unit to prevent ammonia to
escape.
Shake the flask carefully and distilled ammonia using heating device.
Collect distillate (ammonia) in 50 ml 2% sulphuric acid solution.
Titrate collected ammonia in excess of sulphuric acid solution against
standard sodium hydroxide solution using methyl red indicator.
Carry out blank of same volume of sulphuric acid against same standard
sodium hydroxide solution.
Sodium hydroxide can be standardized by titrating against standard oxalic
acid solution using phenolphthalein as an indicator.

Calculations

Amm.Nitrogen % = ml NaOH(Blank) - ml NaOH (sample) x NNaOH x 0.014 x 100

in soil Wt. of soil sample

(ml NaOH consumed = ml NaOH (Blank) Ml NaOH (Sample)

(1 ml 1 N NaOH = 0.014 gms of Nitrogen & N x 1.2143 = NH3)

DETERMINATION OF NITRATE NITROGEN IN SOIL SAMPLE

In this method nitrate has been converted to ammonia, which is absorbed in

excess dil. Sulphuric acid and remaining excess acid can be determined by titrating
against standard alkali solution (i.e. sodium hydroxide solution).

Reagents
1. Sodium hydroxide : (1%) Dissolve 1 gm in 100 ml distilled water.
2. Standard sodium hydroxide solution (0.1 N) : Dissolve 4 gm NaOH in water
and dilute to 1000 ml with distilled water. Standardized with standard oxalic acid
(0.1 N) using phenolphthalein as an indicator.
3. Sulphuric acid solution (2%) : Add 2 ml sulphuric acid in distilled water and
dilute to 100 ml.
4. Standard sulphuric solution (0.1 N) : 3.6 ml conc. sulphuric acid is diluted to
1000 ml and standardized against standard alkali solution.
5. Oxalic acid solution (0.1 N) : Dissolve 0.63 gm oxalic acid in water and dilute
to 100 ml distilled water.
6. Devardas Alloy (Cu:50%, Al:45% and Zn:5%)

273
 7. Phenolphthalein indicator : 1% in water/methanol
8. Methyl red indicator : 0.1% in water/methanol.

STANDARDIZATION OF SODIUM HYDROXIDE SOLUTION AGAINST

STANDARD OXALIC ACID SOLUTION

Take aliquot of 0.1 N NaOH solution in 250 ml beaker.

Dilute to about 100 ml with distilled water.
Add 2-3 drops of phenolphthalein indicator.
Titrate against 0.1 N oxalic acid solution.
Disappearance of red colour shows the end point.

Calculations

NNaOH = N oxalic acid x ml oxalic acid required

ml NaOH taken (aliquot)

STANDARDIZATION OF SULPHURIC ACID AGAINST STANDARD SODIUM

HYDROXIDE ACID SOLUTION

Take suitable aliquot of sodium hydroxide solution in 250 ml beaker.

Add distilled water to dilute to about 100 ml.
Add 2-3 drops of phenolphthalein indicator.
Titrate against sulphuric acid solution.
Disappearance of red colour shows the end point.

Calculations

NH2SO4 = NNaOH x ml (NaOH aliquot)

ml H2SO4 required
Procedure

Take residue remained after the determination of ammonium nitrogen in the

same flask.
Add 1 gm Devardas alloy.
Add 25 ml 1% NaOH in to the flask.
Keep this mixture on a distillation unit and allow to stand for over night.
Evolved ammonia is absorbed in 50 ml of 2% H2SO4 through condenser of
kjeldahl distillation unit.
Next day, distill the mixture. Allow ammonia evolved to absorb in sulphuric
acid as mentioned above.
Take sulphuric acid (ammonia absorbed) or make up the volume as you feel
suitable.
Add 2-3 drops of phenolphthalein indicator.

274
 Titrate against standard sodium hydroxide solution.
Disappearance of red colour shows the end point.
Carry out blank titration of the same volume of sulphuric acid taken for
sample.

Calculations

NO3-N % = ml NaOH (Blank)-ml NaOH (sample) x N x 100 x 0.014 x 100

Wt. of sample (gms)

Where N = Normality of NaOH

OR If aliquot is taken then

NO3-N % = ml NaOH (A) - ml NaOH(B) x gms NO3-N aliquot x N x 100 x 0.014

Wt. of sample in aliquot(gms)

A=ml NaOH in blank

B=ml NaOH in sample
OR
NO3-N%= ml H2SO4 (for Sample)-ml H2SO4 (for Blank) x N x 0.014 x 100
Wt. of sample (gms)

DETERMINATION OF AVAILABLE PHOSPHOROUS IN SOIL SAMPLES

A portion of phosphorous, which is utilized by the plant directly, is known as

available phosphorous. This can be determined by two methods i.e. phosphorous soluble
in sodium bicarbonate and phosphorous soluble in dilute acid-fluoride.

DETERMINATION OF PHOSPHOROUS SOLUBLE IN SODIUM

BICARBONATE (OLSEN-BICARBONATE METHOD)

Here phosphorous can be extracted from soil with sodium bicarbonate solution at
pH = 8.5.

Reagents

1. Extracting solution (sodium bicarbonate solution) (0.5 M) : Dissolve 42 gms

NaHCO3 (sodium bicarbonate) in water and dilute to 1000 ml with distilled water,
adjust pH = 8.5.
2. Sulphuric acid (5N) : Add 141 ml conc. H2SO4 in 500 ml water and dilute to
1000 ml after cooling.
3. Stannous chloride solution (0.1%) : Dissolve 0.1 gm stannous chloride in 5 ml
conc. HCl and dilute to 100 ml with distilled water.

275
 4. Ammonium Molybdate solution (1% in 4 N H2SO4) : Dissolve 10 gm
ammonium molybdate (AR) in 25 ml distilled water with warming. Cool and add
about 110 ml conc. H2SO4. Dilute to 1000 ml.
5. P-nitrophenol solution (0.25%) : Dissolve 0.25 gm P-nitrophenol in water and
dilute to 100 ml with distilled water.
6. Standard stock phosphate solution : Dissolve 0.4393 gm pot. dihydrogen
phosphate KH2PO4 (AR) in water and dilute to 1000 ml with distilled water. (1
ml = 0.1 mg P).
7. Standard phosphate solution : Dilute 10 ml of stock phosphate solution of 1000
ml with distilled water. ( 1 ml = 1 ug P).

PREPARATION OF STANDARD GRAPH

Take suitable aliquots from standard phosphate solution ranging from 0-10 ug
P in 100 ml volumetric flask.
Adjust pH = 5 ( can be checked using universal pH indicator paper).
Add 5 ml ammonium molybdate solution in each flasks mix.
Add 0.25 ml stannous chloride solution, mix again.
Make the volume to 100 ml with distilled water and shake thoroughly.
Measure absorbances/transmittances at 660 nm and blank solution.
Plot graph between absorbances/transmittances against concentrations of
phosphorous.

Procedure

Take 2-5 gms of soil sample in 250 ml conical flask.

Add 100 ml sodium bicarbonate solution into the conical flask.
Shake a flask for about 30 minutes.
Filter after 30 minutes through Whatman No.40 filter paper.
If filtrate has colour, add a pinch of carbon black. Shake for some time to
remove colour and filter again through Whatman No.40 filter paper.
Make up the volume of filtrate in 100 ml volumetric flask.
Take suitable aliquot from the above prepared solution in 100 ml volumetric
flask.
Adjust pH = 5 by adding acid/alkali solutions.
Add 5 ml ammonium molybdate solution, mix.
Add 0.25 ml stannous chloride solution, mix again.
Make the volume to 100 ml with distilled water and mix thoroughly.
Allow to stand for 10 minutes.
Measure the absorbance/transmittance at 660 nm.
Carry out blank in a similar manner.
Find the concentration of phosphorous from the standard graph.

276
Calculations

P% = mg. P (from graph) in aliquot x 100

Wt. of sample (gm) x 1000 (in aliquot)

= g.P (in aliquot) x 100

Wt. of sample in aliquot (gms) x 1000 x 1000

DETERMINATION OF PHOSPHOROUS SOLUBLE IN DILUTE ACID

FLUORIDE (BRAYS METHOD)

The method is suitable for the determination of phosphorous in acidic soil

samples.

Reagents

1. Ammonium Fluoride Solution (1 N NH4F) : Dissolve 37 gms of NH4F in

distilled water and dilute to 1000 ml with distilled water.
2. Hydrochloric acid (0.5M): Dilute 40.4 ml conc. hydrochloric acid to 1000 ml
with distilled water.
3. Extracting solution : Mix 32.60 ml of 1N NH4F solution and 54.4 ml of 0.5 HCl
solution and dilute to 1000 ml with distilled water.
4. Stannous chloride solution : Dissolve 0.12 gm stannous chloride in 2.5 ml conc.
hydrochloric acid by warming and dilute to 100 ml with distilled water.
5. Standard phosphorous solution : Dissolve 0.4393 gm KH2PO4 in distilled water
and dilute to 1000 ml with distilled water (1 ml = 0.1 mg P = 100 ug P).
6. Dilute 10 ml. 100 ug P to 100 ml with distilled water.( 1 ml = 0.01 mg P = 10 ug
P).
7. Ammonium Molybdate Solution : (1.5% in 35% HCl) : Dissolve 15 gm
ammonium mylybdate in 350 ml conc. HCl and dilute to 1000 ml with water.
PREPARATION OF STANDARD GRAPH

Take suitable aliquots from the standard phosphorous solution ranging from 0-
10 ug P in 100 ml volumetric flask.
Add 2 ml ammonium molybdate solution in each flask, mix.
Add 1 ml of stannous chloride solution, mix again.
Make up the volume to 100 ml with distilled water, mix thoroughly.
Measure absorbances/transmittances at 660 nm. after 10 minutes
Carry out bank in a similar manner.
Plot standard graph between absorbances/transmittances and the
concentrations of phosphorous.

Procedure

Take 1-2 gm soil sample into a 100 ml beaker.

Add 7-14 ml extracting solution into beaker.

277
 Shake for 1-2 minutes.
Filter through Whatman No.40 filter paper.
Take filtrate for determination of phosphorous. (Make up the volume if
phosphorous content is more and take aliquot from this solution).
Take suitable aliquot from extracted solution in l00 ml volumetric flask.
Add 2 ml ammonium molybdate solution, mix.
Add 1 ml stannous chloride solution, mix again.
Make up the volume to 100 ml with distilled water, mix thoroughly.
Measure absorbance at 660 nm after 10 minutes.
Carry out blank in a similar manner.

Calculations

%P = mg. P (from graph) in aliquot x 100

Wt. of sample in aliquot (gm) x 1000

= g.P (in aliquot) x 100

Wt. of sample in aliquot (gms) x 1000 x 1000

DETERMINATION OF TOTAL SULPHUR IN SOIL SAMPLES

Total sulphur can be determined by converting sulphur into sulphate by using

oxidizing agent and analysed by colorimeteric method.

Reagents

1. Digesting Solution : Dissolve 100 gms pot. Nitrate (KNO3) in water and add 350
ml conc. nitric acid and dilute to 1000 ml with distilled water.
2. Nitric Acid Solution : (25%) : 250 ml conc. nitric acid is diluted to 1000 ml with
distilled water.
3. (a) Hydrochloric acid (6N): Dilute 484 ml conc. hydrochloric acid to 1000 ml
with distilled water.
(b) Sulphate Sulphur (SO4-S) Solution : (10 PPM) : Dissolve 0.0544 gms
pottasium sulphate (K2SO4) in 1000 ml 6 N HCl.
4. Barium Chloride BaCl2 (AR/GR) : Crystals.
5. Standard Stock Solution : Dissolve 0.4218 gm K2SO4 in water and dilute to
1000 ml with distilled water (1 ml = 0.10 mg SO4-S = 100 g SO4-S).
6. Standard SO4-S Solution : Dilute 10 ml 100 ug SO4-S solution to 100 ml with
distilled water (1 ml = 10 g SO4-S).

PREPARATION OF STANDARD GRAPH

Take suitable aliquot of above standard SO4-S solution in the range of 0 to

100 g SO4-S in 100 ml volumetric flask.
Add 0.25 gm barium chloride (AR), in each volumetric flask, swirl to
dissolve.

278
 Add 1 ml (6N HCL + 10 ppm SO4-S) (seed) solution and allow to stand for 1
minute.
Again swirl the content in the flask.
Make up the volume to 100 ml with distilled water.
Take absorbances/transmittances at 420 nm after 3 minutes.
Plot a graph between absorbances and SO4-S concentrations.

Procedure

Take 1-2 gm dried fine soil sample in 250 ml beaker.

Add 10 ml digesting solution.
Keep on water bath and allow to evaporate upto dryness.
Replace beaker and allow to cool.
Add 5 ml of 25% Nitric acid solution.
Digest the content for one hour on steam bath.
Dilute to about 50 ml with distilled water.
Filter through Whatman No.40 filter paper.
Transfer the filtrate into 100 ml volumetric flask and make up with distilled
water.
Take suitable aliquot of above filtrate or whole solution for determination of
SO4-S as you feel convenient.
Add 0.25 gm barium chloride (AR) crystals, swirl to dissolve.
Add 1 ml of (6 N HCl + 10 ppm SO4-S solution (seed).
Swirl contents for about 1 minute.
Make up the volume to 100 ml, mix well.
Take absorbance at 420 nm after 3 minutes.
Carry out blank in a similar manner.

Calculations

% SO4-S = g, SO4-S in aliquot

wt. of sample in aliquot (gms) x10 9

OR % SO4-S = . g, SO4-S in aliquot

wt. of sample in aliquot (gms) 107

DETERMINATION OF AVAILABLE SULPHUR IN SOIL SAMPLE

Sulphur can be determined using turbidimetric/colorimetric methods by formation

of suspension with barium chloride to form barium sulphate.

Reagents
1. Phosphorous Extraction Solution (500 ppm) : Dissolve 2.195 gms potassium
dihydrogen orthophosphate (KH2PO4) in water and dilute to 1000 ml with
distilled water.

279
 2. Nitric acid (25%) : 25 ml conc. HNO3 is diluted to 100 ml water.
3. Acetic acid phosphoric acid mixture : 300 mlAcetic acid and 100 ml phosphoric
acid is mixed together.
4. Gum-Acacia-Acetic Acid Solution : Dissolve 5 gms. Gum-acacia in hot water.
Cool filter through Whatman No.42 filter paper if precipitate appears. Dilute
filtrate to 1000 ml with distilled water.
5. Standard stock sulphate solution : Dissolve 0.545 gms potassium sulphate
(AR/GR) in water and dilute to 1000 ml with distilled water. (1 ml = 0.10 mgS =
100 gS).
6. Standard working solution : Dilute 10 ml 1000 ugs solution to 1000 ml with
distilled water. (1 ml = 10 gS).
7. Barium chloride : BaCl2 (AR/GR) Crystals.
8. Barium sulphate seed suspension : Dissolve 20.45 gm of Barium Chloride in
50 ml hot distilled water. Add 0.5 ml stock sulphate solution, mix. Heat to
boiling, cool. Add 5 ml of Gum acacia-acetic acid solution, mix again.

(Note this suspension) is not stable hence it should be prepared freshly).

PREPARATION OF STANDARD GRAPH

Take suitable aliquots of standard sulphur solution ranging from 0-20 gS in

25 ml volumetric flask.
Add 2.5 ml of 25% nitric acid in each flask, mix.
Add 2 ml acetic acid-phosphoric acid solution, mix well.
Add 0.5 ml barium sulphate seed suspension, mix well.
Add 0.2 gm (or pinch) barium chloride crystals in mixture and shake for about
5 minutes.
Add 1 ml gum-acacia solution after 5 minutes and make up the volume to 25
ml with distilled water, mix well again. Allow to stand for about hour.
Measure the absorbances/transmittances at 440 nm.
Plot a graph between absorbances/transmittances and concentrations of
sulphur.

Procedure

Take about 20 gm dried fine soil sample in 250 ml conical flask.

Add 100 ml of 500 ppm phosphate extraction solution, shake for about an
hour.
Filter through Whatman No.42 filter paper.
Take above filtrate for determination of sulphur content in soil using complete
filtrate or making up volume of it.
Take suitable aliquot (if volume is make up) in 25 ml volumetric flask.
Add 2.5 ml of 25% nitric acid solution, mix.
Add 2 ml acetic acid-phosphoric acid solution, mix again.
Add 0.5 ml barium sulphate acid suspension, mix well.
Add 0.2 gm (pinch) barium chloride (AR). Shake the contents for 5 minutes.

280
 Add 1 ml gum-acacia solution after 5 minutes.
Make up the volume with water and mix well again.
Allow to stand for an hour.
Take absorbance/transmittance at 440 nm.
Carry out blank in a similar manner and deduct from sample reading.

Calculations
%S = g S (from graph in aliquot) x 100
Wt. of sample in aliquot (gm) x 109

= g S (in aliquot from graph)

Wt. of sample in aliquot (in gm) x 107

DETERMINATION OF MERCURY IN SOIL SAMPLES

Mercury can be determined by using Mercury Analyser at the trace level in soil
samples.

Reagents
1. Aqua-Regia : Mix 1 part of Nitric acid and 3 parts of Hydrochloric acid (conc.
HNO3 + : Conc. 3HCl).
2. Potassium Permanganate Solution (5%) : Dissolve 5 gms KMnO4 (Pot.
permanganate) in 100 ml distilled water.
3. Potassium Persulphate Solution (5%) : Dissolve 5 gm pottasium persulphate
(K2S2O8) in 100 ml distilled water.
4. Hydroxylamine hydrochloride solution (20%) : Dissolve 20 gm hydroxylamine
hydrochloride (NH2OH HCl) in 100 ml conc. hydrochloric acid.
5. Stannous chloride solution (20% in 50% HCl) : Dissolve 30 gms stannous
chloride in 50 ml conc. hydrochloric acid and dilute to 100 ml with distilled
water.
6. Standard Stock Mercury Solution : Dissolve 0.1354 gms mercuric chloride
(HgCl2) in 2% HNO3 and dilute to 1000 ml, (1 ml = 100 ppm Hg.).
7. Dilute 10 ml 100 ppm stock mercury solution to 1000 ml add 2% HNO3 solution.
(1 ml = 1 ppm = 1000 g Hg).
8. Dilute 10 ml 1000 g Hg solution to 1000 ml adding 2% HNO3 solution (1 ml =
10 g Hg). OR Dilute 10 ml, 1000 g Hg solution to 100 ml adding 2% HNO3
solution (1 ml = 100 g Hg)

This solution can be taken for standardization.

PREPARATION OF STANDARD GRAPH

Take suitable aliquot of standard mercury solution ranging from 0-500 ug Hg

in 300 ml B.O.D. bottle (Mercury generator bottle).
Add distilled water so that the total volume of solution should be 100 ml
(including all reagents).

281
 Add 5 ml stannous chloride, which includes in 100 ml total volume of BOD
bottle.
Place a magnetic bar inside the bottle.
Keep the BOD bottle on magnetic stirrer and allow to stir for a fixed period (5
minutes).
Before this check mercury analyzer as per the manufacturers instructions and
keep ready for taking the readings.
After fixed period, i.e. 5 minutes, start the pump and measure the absorbances
of mercury shown on the meter.
Feed blank and deduct from every reading.
Plot a graph between absorbances and the concentrations of mercury in ug of
Hg.

Procedure

Take about 1-5 gm finely powder soil sample in 100 ml beaker.

Add 25 ml aqua-regia in beaker.
Keep for about an hour by swirling occasionally.
Heat on water bath for about 2 hours with swirling occasionally.
Cool at room temperature.
Add 25 ml, 5% KMnO4 solution, mix.
Add 2 ml, 5% K2S2O8 solution, mix again.
Allow to stand for overnight for reaction.
Next day add 20% hydroxylamine hydrochloride solution drop wise to oxidize
KMnO4 solution completely.
Filter through Whatman filter paper No.40.
Wash with distilled water.
Make up the volume to 100 ml or take complete solution for the determination
of mercury depending upon the quantity of mercury present in soil sample.
Take aliquot or complete solution as prepared above in 300 ml BOD bottle.
Add distilled water to make fixed volume as done in standard graph.
Add 5 ml stannous chloride solution which includes in fixed volume (total
volume = 100 ml.).
Place one stirring bar inside the BOD bottle.
Keep on magnetic stirrer and allow to continue for fixed time (5 minutes).
After five minutes take absorbance on meter.
Find out the concentration of mercury from the standard graph.
Carry out blank and deduct from reading.

Calculations

% Hg in soil = conc. Hg (g) in aliquot x 100

Wt. of soil in aliquot (gms) x 109

282
DETERMINATION OF TRACE/HEAVY ELEMENTS IN SOIL SAMPLES

Soil samples (fine powder 100 mesh) is used for the dissolution of trace/heavy
elements in aqua-regia solution and can be analysed using appropriate instruments for
analysis of them.

Reagents

1. Hydrochloric acid : Conc. Hydrochloria acid (AR) grade.

2. Nitric acid : Conc. Nitric acid. AR grade.
3. Nitric acid 0.5 M : Dilute 32 ml conc. HNO3 to 1000 ml with distilled water.

Procedure

Take about 5 gms of finely powder soil sample in 250 ml beaker.

Add 21 ml conc. hydrochloric acid, swirl.
Add 7 ml conc. nitric acid, swir well again.
Digest the content on hot plate for about 1-2 hours with covering in fume
cupboard.
Cool and filter through Whatman No.40 filter paper.
Wash with hot distilled water.
Collect the filtrate and make up the volume in 100 ml volumetric flask with
distilled water.
Use above volume for determination of trace/heavy elements using
appropriate instrument such as Atomic Absorption Spectrophotometer,
Inductively coupled plasma Analyser, etc.

Calculations

Calculate the concentrations of each trace heavy elements and express either in
ppm or percentage as applicable.

6.28 AMBIENT AIR QUALITY MONITORING

In a system of Ambient Air Quality monitoring commonly High volume

Sampler (HVS) is used. Using this instrument (HVS) Suspended Particulate Matter
(SPM), i.e. Respirable SO2 and NOx can be determined in a single instrument.

For the sampling purpose HVS are installed around dust producing sources/points
and measurements are carried out for a fixed period depending upon the concentration of
dust so that the sufficient amount of dust is collected on initially weighed filter paper
(Whatman Glass Micro Fibre Filter Paper) GF/A of size 203 x 284 mm. The time period
can be varied if the concentration of dust is very less, then 16 or 24 hours can sampled
and if the concentration of dust is much more 4-6 hours but commonly 8 hours has been
considered as a standard for the collection of Suspended Particulate Matter (SPM).

283
 After collection of a sufficient dust for the specific period, the filter paper is re-
weighed and the difference in both weights are calculated. At the same time we have to
note the initial, final volume of air passed through the instrument to calculate the
concentration of SPM per cubic meters of air passed during the sampling.

After removal of dust (SPM) in a same instrument clean air is passed through the
impingers containing NaOH solution and sod.tetra-chloromercurate solution in series so
that NOx and SO2 gases can be absorbed respectively. After absorption of NOx and SO2
gases in the solutions these can be analysed using appropriate methods of analysis.
Generally, spectrophotometric methods for analysis are most suitable.

Calculations : Suspended Particulate Matter (SPM)

The volume of air sampled can be calculated using a formula :

V = (Qi + Qf) x T
2
Where V = Volume of air sampled, m3/min
Qi = initial flow rate of air m3/min
Qf = final flow rate of air m3/min
T = Total time of sampling in minutes

and the mass concentration of SPM can be calculated as :

SPM ug/m3 = (Wf Wi) x 10-6, g/m3

V
Where, Wf = final weight of paper + sample
Wi = initial weight of paper
V = total volume of air sampled, m3

GASEOUS POLLUTANTS ANALYSIS

Gaseous pollutants (NOx & SO2) are absorbed in specific absorbing reagents at an
average flow rate of 0.6 to 1.l/min. NOx is absorbed in 0.10 M NaOH solution while SO2
is absorbed in 0.10 M sod.tetra-chloromurcurate solution. 30 ml of respective absorbing
solutions are taken in each impingers.

ANALYSIS OF NITROUS OXIDES (NOX) :

A sample is collected by bubbling air from HVS through 30 ml of 0.10 M

sod.hydroxide solution. Loss in volume due to evaporation is make up to 30 ml and an
aliquot is taken for analysis.

284
Principle

Oxides of Nitrogen as NO2 (Nitrogen dioxide) is absorbed quantitatively by

bubbling air through a NaOH solution (Sod.Hydroxide) which form a stable sodium
Nitrite NO2 + NaOH ---- NaNO2 (stable sod.nitrite solution).

Thus NaNO2 (sod.nitrite) produced as above can be determined

spectrophotometric method by developing coloured complex by adding appropriate
reagents and measurement taken is at 540 nm and compared with standards from which a
concentration of NOx present in the sampled air is calculated.

Reagents

1. Absorbing Reagent : (0.10 N NaOH) : Dissolve 4.0 gms sod.hydroxide in

distilled water and dilute to 1000 ml.
2. Sulphanilamide solution : 20 gm sulphanilamide is dissolved in 700 ml
distilled water, add to this 50 ml of H3PO4 (Phosphoric acid 85%) slowly
while stirring and dilute to 1000 ml with distilled water. Keep in refrigerator.
This can be used up to one month.
3. NEDA solution : Dissolve 1.0 gm N (1-naphthyl) ethylene diamine
dihydrochloride (NEDA) in 1000 ml distilled water. Keep in refrigerator to
protect from sunlight. This solution can be used up to one month.
4. Hydrogen Peroxide : 1 ml of 30% hydrogen peroxide is diluted to 1000 ml.
Keep in refrigerator to protect from light.
5. Standard Sodium Nitrite Solution : Dissolved 0.135 gm sodium Nitrite
(AR/GR) in water and dilute to 1000 ml with distilled water.

1 ml of above solution = 90 g NO2 = 100 g NO2 gas

PROCEDURE FOR COLOUR DEVELOPMENT

10 ml aliquot from the original solution is taken in 30 ml graduated cylinder.

Add 1 ml H2O2 solution. Mix the content.

Add 10 ml sulphanilamide solution Mix again.
Add 1 ml NEDA solution. Mix/shake the contents thoroughly, make up
volume to 25 ml, and allow to develop a colour for about 10 minutes.

Take a blank in a same manner. Measure an absorbance after 10 minutes at 540 nm

using spectrophotometer. Find out the concentration from the standard/calibration graph
and calculate the concentration of NO2/ml.

STANDARDIZATION AND CALIBRATION FOR NO2 :

Take 1.0, 2.0, 3.010.0 ml standard solution of sod. Nitrite in 30 ml graduated

cylinders.

285
 Add 1 ml H2O2 solution in each cylinder.
Add 10 ml sulphanilamide solution.
Add 1 ml NEDA solution. Mix thoroughly and make up the volume to 25
ml of each cylinder. Allow to develop a colour for 10 minutes and
measure an absorbances at 540 nm using Spectrophotometer against
reagent blank.

Plot a graph of concentrations (g) against absorbance and find the concentration
of the experimental solutions.

Calculations

NO2, ug/ml = NO2, g/ml

10 ml (i.e. aliquot)

and NO2, ug/m3= NO2, g/ml x 30 (i.e. Volume taken for absorbing reagent)
V (i.e. total volume of air)

V= (Qi + Qf) x T
2

Where V = Volume of air sampled, m3

Qi = Initial flow rate of air, m3/min
Qf = Final flow rate of air, m3/min.
T = Total time in minutes.

{Note :- If the weights are taken in grams, then

NO2, ug/m3 = NO2, g/ml x 30 x 10-6}

V

ANALYSIS OF SULPHUR DIOXIDE

For the determination of SO2 (sulphur dioxide) a sample is collected by bubbling

through an aqueous solution of sodium tetra-chloro-mercurate, which can absorb SO2
quantitatively.

Principle

Sodium tetra-chloromercurate (TCM) absorbs SO2 quantitatively and formed a

dichlorosulphito mercurate complex, after addition of formaldehyde and P-rosaniline at a
controlled pH = 1, a coloured complex of P-rosaniline-methylsulphonic acid is formed
which can be measured at 560 nm.

286
 H2N
HgCl2SO3-2 + H2CO + 2H+ + C= = NH2,

H2N

which gives

H2N CH2SO3 H

C= =N + 2Cl- + H2) + Hg+2

H2N H

Reagents

1. Absorbing Reagent : 0.10 M sodium tetra-chloromercurate (TCM).

Dissolve 27.2 gms Mercuric chloride and 11.7 gms sodium chloride in water
and dilute to 1000 ml with distilled water.
2. Para-Rosaniline Hydrochloride : Dissolved 0.2 gm of P-rosaniline
hydrochloride in water and dilute to 100 ml with distilled water. Allow to
stand for 48 hours. Filter if precipitate appears.
3. Take above 20 ml of P-rosaniline hydrochloride solution, add 6 ml conc. HCl,
allow to stand for 5 min. and make up the volume to 100 ml.
4. Formaldehyde solution : (0.2%) : Dissolve 5 ml of 40% formaldehyde
solution to 1000 ml with distilled water.
5. Sulphamic Acid Solution : Dissolve 0.6 gm sulphamic acid in 100 ml
distilled water.

PROCEDURE FOR COLOUR DEVELOPMENT

A 10 ml aliquot is taken from the original solution in 30 ml graduated cylinder.

Add 1 ml sulphamic acid solution (masking agent for NOx).

Add 1 ml p-rosaniline solution. Mix well.
Add 1 ml formaldehyde solution. Mix thoroughly the contents and allow to
stand for 10 minutes to stabilize the colour of the complex.

Measure the absorbance/concentration after 10 min. at 560 nm using

spectrophotometer. Concentration of SO2 can be calculated from the standard graph.

STANDARDISATION AND CALIBRATION

A. Preparation of standard sulphite solution

287
 Dissolve 0.4 gm Na2SO3 (Sod.Sulphite) in water and dilute to 500 ml.
Take 25 ml aliquot from above solution in 250 ml conical flask. Dilute it
to about 100 ml with distilled water.
Add 50 ml of 0.01 N iodine solution and cover immediately and allow to
stand for five minutes.
Titrate the content with 0.01 N sod.thiosulphate solution using starch as
an indicator. Change of blue colour to colourless shows the end point of
the reaction.
Carry out a bank in a same manner.

Calculate the concentration of SO2 in ug/ml using a formula :

SO2, ug/ml = (A-B) ml x N x 32,000

Aliquot of standard solution

Where : A = Volume in ml of thiosulphate for blank

B = Volume in ml of thiosulphate for sample
N = Normality of sod.thiosulphate
32,000 equivalent for SO2

B. Preparation of calibration graph :

Dilute 2 ml of above standard solution to 100 ml with TMC solution.

Take aliquots of 1 ml, 2 ml, 3 ml, 4 ml & 5 ml from above solution in a
graduated cylinder of 30 ml capacity.
Add 1 ml of sulphamic acid solution to each cylinder.
Add 1 ml P-rosaniline solution.
Add 1 ml formaldehyde solution, mix the contents thoroughly and make up
the volume to 20 ml with TMC (Tetra-chloromercurate) solution. Mix
again and allow to stand for 10 minutes to develop and stabilize the colour.

Measure Absorbance/concentrations using a spectrophotometer at 560 nm against

a blank prepared in a same manner.

Plot a standard graph between Absorbance and concentrations.

Calculations

SO2, g/ml = SO2, g/ml

10 ml (i.e. aliquot taken)

and SO2, g/m3 = SO2, g/ml x 30 (i.e. Total vol. Taken of Absorbing Reagent)
V (Total Volume of air)

V = (Qi + Qf) x T
2

288
Where V = Volume of air sampled, m3
Qi = Initial flow rate of air, m3
Qf = Final flow rate of air, m3
T = Total time in minutes.

(Note : If weights are taken in grams, then

So2, g/m3 = SO2, g/ml x 30 x 10-6)

V

289
Addenda 1

BORON ORES

The chief minerals of Boron are Ascharite (MgHBO3), Sassolite B(OH)3 ,

Ludwigite (MgFe)2Fe[BO3]O2, Borax Na2B4O7.10H2O, Inderite Mg2B6O11.15H2O,
Colemanite CaB6O11.5H2O and Calcioborite Ca5B8O17, Boronatrocalcite
NaCaB3O9.8H2O .

Boron is generally analysed for B2O3, Fe2O3 ,Al2O3 ,CaO, MgO, Na2O ,K2O and
LOI.

Determination of SiO2 and preparation of Stock solution

Weigh 0.5 g of sample in a 200 ml silica dish. Add 10 ml of HCl and 2 ml

HNO3.Digest and evaporate over a moderately low flame. Expel all liquid from the dish.
Remove the dish from the flame and cool it. Add 4-5 drops of dilute sulphuric acid. Add
10 ml methanol. Ignite the methanol with open flame. Stir the mass. Apple green flame
will indicate the presence of borate in the mass. Cool the dish. Again repeat the process
of removal of borate by additional quantity of sulphuric acid and methanol till all borate
is removed.
Cool the mass; add 5 ml concentrated hydrochloric acid and 50 ml demineralised
water. Boil the content on burner. Cool and filter through Whatman 40.Wash the residue
5-6 times with hot water. Preserve the filtrate for estimation of other radicals. Transfer
the filter paper into a platinum crucible. Ignite this at 1000oC in a muffle furnace. Cool
the mass in a desiccator and weigh .Moisten the mass with little DM water. Add 2-3
drops dilute sulphuric acid. Add 10-15 ml 48% hydrofluoric acid to the mass. Place the
crucible on asbestos sheet on a low flame or on a low temperature hot plate. Expel all
acid from the crucible. Now heat the crucible initially on a low flame and finally to a
blast flame (1000oC) for about 5 minutes. Cool the crucible in a dessicator. Weigh the
mass. The loss in weight will be the quality of silica. Fuse the residue in the crucible with
little potassium pyrosulphate. Extract the mass in the preserved solution. Cool the filtrate
and make up to 250 ml .Use this solution for the determination of major and minor
elements.

Determination of CaO, MgO (EDTA Complexometry), Fe2O3, Al2O3

Follow the procedure given under the chapter on determination of major and
minor constituent from the stock solution.

Determination of Na2O, K2O by Flame Photometry

Weigh 0.1 g of sample. Add 0.5 ml HCl and 50 ml of water. Boil. Cool. Transfer
the contents in a 100 ml volumetric flask. Add ammonium carbonate and ammonia.
Allow to stand for sometime. Feed this filtrate in the flame photometer and determine

290
concentrations of Na2O ,K2O as given in analysis of sodium and potassium in water ,
waste water effluent solids soils etc.

Determination of Boron

Reagents

1. Sodium Hydroxide Solution (0.1N): Dissolve 40.0 gm NaOH in distilled water

and dilute to 1000 ml
2. Mannitol
3. Phenolphthalein solution: 0.1 % solution in methanol or in distilled water
4. Methyl Orange Solution: 0.1 % solution in distilled water

Procedure

Weigh 0.1 g of sample. Add 0.5 ml HCl and 100 ml water in a 250 ml in a beaker.
Boil. Cool adjust the pH to 5.2 preferably by pH meter or using methyl orange
indicator solution. Add 2-3 g of mannitol and titrate with sodium hydroxide using
phenolphthalein as indicator. Color changes from colorless to light pink.

1ml 1N NaOH = 0.03480 g B2O3

291
Addenda 2

LOSS ON IGNITION

Some Special Cases of Loss on Ignition

Loss on ignition of a mineral sample is very important parameter. It approximately

indicates the quality and quantity of minerals present. Differential thermal analysis is
totally based on thermal behavior of minerals. The data obtained can be used to estimate
the quantity of the mineral. In certain samples, loss on ignition is not so simple and the
sample gains the gases, especially oxygen from the atmosphere and here loss obtained
needs correction. Such special cases are dealt hereunder.

1. Iron Ore

Ferrous iron present in iron ore, especially Magnetite, is oxidized during the
process of loss on ignition. Many a time weight after ignition is higher than the initial
weight. Here needs a correction of gain of oxygen to get correct loss of ignition.

a. Procedure

Weigh 1 g of dried iron ore (at 105 0 C) sample in a preweighed platinum

crucible. Place the crucible in a muffle furnace and heat this at 3000 C for 30 minutes.
Now raise the temperature to 10000 C and heat the crucible for 30 minutes. Find the
apparent loss or gain. Keep the ignited mass in dessicator for further analysis.

b. Correction for Ferrous Iron

Determine the ferrous iron on originally dried sample and on the residue
obtained after loss on ignition as per procedure given under iron ore. Reduction in
quantity of ferrous iron will indicate the gain of oxygen. Find the gain of oxygen. Correct
the loss of ignition obtained above by this gain of oxygen. The final quantity is true loss
of oxygen.

2 Manganese Ore

Manganese dioxide when heated loses oxygen very slowly. Manganese dioxide
is converted to manganous oxide when heated at 700 0 C for about 23 hour. Therefore the
determination of loss of ignition is a tedious job and also to estimate the loss of ignition
from other species present in manganese ore is not possible. A procedure given below
can overcome the difficulty.

1. Procedure

Find loss on ignition as detailed in 1 (a) above. Store the ignited mass for further
analysis.

292
b. Correction for Manganous Oxide

(A) Weigh 0.5 g powdered sample in a 250 ml glass beaker. Add 100 ml of 10% (w/w)
sulphuric acid to this. Boil this for 10 minutes on a low flame. Cool this and filter
through What man No.40.Wash the residue with acidulated (H2SO4) hot water.
Make up the filterate to 250 ml.
Take 25 ml aliquot in a conical flask and determine manganese by Volhards
method.
(B) Determine manganese on the ignited sample in the similar manner. Find the loss of
oxygen by manganese dioxide from above A and B. Correct the loss of ignition
obtained above in 2 (a) above. This value will correspond to loss of ignition to the
other species present in manganese ore.

3. Sulphide Ores

Sulphide ore when heated sulphur from sulphide and pyrite is lost as either sulphur
dioxide or the species are converted into their respective sulphates (Sulpahting roasting)
This gain of oxygen due to conversion to sulphate need be used for obtaining trace value
of loss of ignition.

Procedure

Weigh 1 g of dried sulphide sample in pre ignited and preweighed silica crucible
(do not use platinum crucible). Place the crucible in cold muffle furnace, now raise
temperature to 3000 C. Keep this temperature for 30 minutes. Now further raise the
temperature to 9000 C and heat the crucible for 30 minutes. Cool, the crucible in a
dessicator and weigh. Find the apparent loss. Keep the ignited mass in a dessicator for
further analysis.

Determination of Sulphate

2. Weigh about 0.5 g sample in 250 ml glass beaker. Add 50 ml dilute hydrochloric
(1:1) acid. Heat this on hot plate for about 30 minutes. Now add 50 ml oxygen free
distilled water to this. Boil this on a burner to expel hydrogen sulphide gas. Cool this
and filter through Whatman 40.Wash the residue with hot water.
b. Take the filterate in 600 ml beaker. Add few pieces of freshly cut aluminum foil and
boil this to reduce iron. Cool and adjust acidity with methyl red indicator .Add 5 ml
excess of dil.HCl. Now add 10 ml of 10% barium chloride solution in cold condition.
Allow the precipitate thus formed to stand for overnight.
Decant the solution by siphon. No precipitate should pass during this process. Filter
the precipitate through Whatman 42.Wash the precipitate 8-10 times with cold water.
Ignite the precipitate initially at 6000 C and finally at 8000 C. Find quantity of SO4.
c. Determination of SO4 on ignited sample
Determine the quantity of SO4 on the residue obtained after ignition as detailed under
3(a) and 9(b).

293
Correction for oxygen gained during sulphate formation

Find gain of oxygen from the difference of sulphate determination under 3( c) and 3
(b).Correct the loss on ignition obtained under Procedure for sulphide ores

294
Addenda 3

Determination of Total Silica in Silicate Mineral (A combination of Gravimetric

and Photometric Method)

The precision of the photometric determination of silica is controlled to a large

extent by the limitations inherent in spectrophotometry. Such determinations cannot by
their nature be as precise as those obtained by good gravimetric methods, although of
course the possibility of systematic errors exists in both methods. In order to combine the
advantages and avoid some of the disadvantages of both methods Jeffery and Wilson
have suggested a new procedure based upon a single dehydration with hydrochloric acid,
giving a major silica fraction as an insoluble residue and a minor fraction the filtrate that
can be determined photometrically. As only one dehydration is made, this procedure is
more rapid than the classical method and as all the silica not collected in the residue is
determined photometrically, it is also more accurate. Moreover, since the photometric
determination is now or a minor constituent (2-8mg, equivalent to less than 1 per cent of
the rock composition) the limiting accuracy of photometric methods is no longer
restrictive.
A disadvantage that has been introduced is that in the filtrate from the collection
of the major silica fraction, all the remaining elements have been increased in
concentration relative to silica. Under these circumstance elements that are not usually
present in amounts sufficient to interfere may be concentrated up to and beyond this
point. Interference has been noted from titanium and phosphorus, although up to 5%
TiO2 in the rock material does not have a significant effect and upto 10% P2O5 can also
be tolerated.
Fluorine in trace amounts does not interfere, although if present in major amounts,
some of the silica may be lost by volatilization during the dehydration stage, as in the
classical method for determining silicon. Three per cent fluorine in the rock material is
likely to give rise to a loss of as much as 0.5% silica.

Method

Reagents

1. Ammonium molybdate solution Dissolve 10g of crushed ammonium

molybdate in N aqueous ammonia and dilute to 10ml with N ammonia.

2. Oxalic acid solution Dissolve 10 g in water and dilute to 100 ml.

3. Reducing solution Dissolve 0.15g of 1-amino-2-naphthol-4-sulphonic acid,

0.7g of anhydrous sodium sulphite and 9 g of sodium metabisulphite in 100 ml
of water. Prepare freshly each month.

4. Standard silica stock solution Fuse 0.20 g of pure crushed and dried crystal
quartz with 1 g of anhydrous sodium carbonate in a platinum crucible.

295
 Dissolve in water and dilute to 1 litre. This solution contains 200 g silica per
ml. Dilute with water to give a solution containing 20 g per ml as required.

Procedure

Fuse 1 g of rock material with 5 g of anhydrous sodium carbonate in a platinum

crucible and digest the melt with water. Acidify with concentrated hydrochloric acid,
adding approximately 10ml in excess and evaporate to dryness in a large platinum dish.
When completely dry add a further 10 ml of concentrated hydrochloric acid and
sufficient water to dissolve all soluble material. Collect the silica residue on a filter,
wash well with hot water and determine the major silica by hydro-fluorisation. Collect
the filtrate and washings from the silica residue in a 250ml volumetric flask and dilute to
volume with water.
Using a pipette, transfer 5ml of this solution to a 100ml volumetric flask and add 10
ml of water. Now add 1ml of ammonium molybdate solution and set aside for 10
minutes to complete the formation of the silicomolybdate complex. After exactly 10
minutes, add 5 ml of the oxalic acid solution, gently swirl the flask to mix the contents,
and then add 2 ml of the reducing solution. The addition of the reducing solution should
not be delayed. Dilute the solution to volume with water and set aside for at least 30
minutes, but preferably for 1 hour, and then measure the optical density of the solution in
2-cm cells with the spectrophotometer set at a wavelength of 650 nm.

Calibration

Transfer aliquots of the standard silicate solution containing 0-200 g of silica to

separate 100 ml volumetric flasks, dilute to 15ml with water and add 1 ml of 3 N
hydrochloric acid to each. Now add 1 ml of ammonium molybdate solution to each,
allow to stand for 10 minutes and then reduce the silicomolybdate to molybdenum blue as
described above. Dilute each solution to volume with water and measure the optical
density in 2-cm cells with the spectrophotometer set at a wavelength of 650 nm. Plot the
relation of optical density to silica concentration. As the calibration graph is a straight
line passing through the origin, a single point method can be used for subsequent
calibrations.

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