Water Sample Analysis Methods
Water Sample Analysis Methods
-Microbiological sampling
-Indicator organisms for pathogen presence
Physical sampling
-turbidity, conductivity, total dissolved solids etc
Chemical sampling
- pH, dissolved oxygen, phosphates, chemical oxygen demand,
biological oxygen demand, mineral impurities (iron,
manganese, chloride, lead, sodium etc)
Types of Testing
∗ Mobile laboratories
∗ Advantages:
∗ Controlled environment,
∗ High level of precision and accuracy
∗ Limitations:
∗ Relatively expensive
∗ Requires skilled laboratory technicians
∗ Laboratory testing
∗ Advantages:
∗ Controlled environment,
∗ High level of precision and accuracy
∗ Limitations:
∗ Expensive
∗ Lack of flexibility to conduct own testing
Selecting Test Methods
Depends on:
∗ Objectives
∗ Range of concentration
∗ Required accuracy and precision
∗ Time period between sampling and analysis
∗ Technical skills and equipment required
∗ Familiarity with the method
∗ Availability of resources
WHAT WE’LL COVER TODAY
∗ Calibration
∗ Place the electrode in the solution of pH 7
buffer, allow the display to stabilize and, then,
set the display to read 7 by adjusting cal 1.
Remove the electrode from the buffer. 4.
Rinse the electrode with deionized water and
blot dry using a piece of tissue
CONDUCTIVITY
∗ References
∗ HANNA-
∗ USEPA 120.1
∗ APHA-
∗ Applies to DW & SW
∗ Cell Constant
∗ Determine annually
∗ Verify w/each use w/known [KCl]
∗ RSDs < 1%
TURBIDITY
∗ References
∗ HACH-2100
∗ USEPA 180.1
∗ APHA,
∗ Applies to DW & SW
∗ References
∗ HANNA- free chlorine checker
∗ iodometric method
∗ Applies to DW & SW
Temperature
∗ Applies to DW & SW
∗ Applies to DW & SW
HARDNESS
∗ Ca+2 / Mg+2 sequestered by NaEDTA
∗ Electrometric (Electrode)
∗ More common
∗ Rate of diffusion of molecular O2 across membrane
DISSOLVED OXYGEN (DO)
∗ Winkler
∗ More precise & reliable
∗ Add Mn+2 + strong base, DO oxidizes Mn+2 to higher ordered
Mn(OH)x+2. Add I-/H+; Mn goes back to Mn+2 & equivalent I-
is liberated. Titrate with (S2O3)-2 w/starch indicator. (S2O3)-2
must be standardized at least quarterly. I- takes the place of
O-2
∗ Interferents include oxid.(+) & red. (-) agents; options
include adding azide [(NO2)-], & permanganate [Fe+2]
∗ Fix on-site & run w/i 8 hrs.
BY VIS
∗ HACH 3900 Spectrophotometer
∗ FerroVer® Method1
∗ Method 10249 Powder Pillows
∗ Range: 0.1 to 3.0, mg/L Fe
∗ Scope and application: For water and wastewater.
∗ Carmine Method1
∗ Method 8015 Powder Pillows
∗ Range:0.2 to 14.0 mg/L B
∗ Scope and application: For water and wastewater.
∗ SulfaVer 4 Method1
∗ Method 10248 Powder Pillows
∗ Range: 2 to 70, 20 to 700, 200 to 7000 mg/L SO4 2–
Scope and application: For water and wastewater.
∗ Analytical Options
∗ Colorimetric
∗ Titrimetric
∗ IC
∗ Ion-Selective Electrodes (ISE)
(SM Method 4500)
∗ DW only
ION SELECTIVE ELECTRODES
∗ Measure the activity of free ions in solution
∗ Electrode types:
∗ Crystalline
∗ Gas Sensing
CYANIDE (CN-)
∗ Measurement Options
∗ Titration
∗ Colorimetry
∗ ISE
NITROGEN SPECIES
∗ Forms of N to be measured:
∗ (NO3)-
∗ (NO2)-
∗ NH3
∗ Organic N
∗ Measurement Options
∗ Titration
∗ ISE
∗ Phenate w/ or w/o automation
AMMONIA (NH3 )
∗ Titration
∗ Only used after distillation
∗ H3BO3 added to decrease hydrolysis of organo-N
species
∗ Titrate w/std. H2SO4; end-pt. either w/indicator or
electrometrically
∗ Useful below 5 mg/L
∗ ISE
∗ Gas-permeable membrane to measure NH3(aq) & (NH4)+
converted to NH3(aq) by pH adjust. to 10-11
AMMONIA (NH3 )
∗ Phenate
∗ Indophenol (VERY blue) is made from reaction between
NH3, (ClO3)- & phenol catalyzed by nitroprusside
∗ Measure spectrophotometrically @ 640 nm
∗ Interfering Ca & Mg can be complexed
∗ Can be easily automated
∗ RSD’s much better than titrimetry or ISE
(NO2)- & (NO3)-
∗ (NO3)-
∗ UV-Spec.
∗ ISE
∗ Cd Reduction
ORGANIC (KJELDAHL) N
∗ Method Options
∗ Iodometric: KI titration w/starch indicator
∗ Colorimetric: (easier) Reaction w/1,10-phenanthroline &
vis. detection @ 510 nm.
SULFATE (SO4)-2
∗ Method Options
∗ IC (BEST CHOICE)
∗ Turbidimetry: BaSO4 ppct. light scattering is measured
(MOST COMMON)
∗ Gravimetry: (Ppct. as BaSO4)
∗ Titrimetry: xs. Ba is complexed w/methylthymol blue to
yield blue color
SULFIDE (S-2)
∗ Interferences
∗ [Cl-] > 1000 mg/l
∗ VOCs might be lost prior to oxidation
∗ Method Summary
∗ Most organics & oxidative inorganics are oxidized
by addition of K2Cr2O7 / H2SO4
∗ xs. (Cr2O7)-2 is titrated w/Fe(NH4)2(SO4)2.6H2O
TOTAL ORGANIC CARBON (TOC)
∗ Measurement Options
∗ Non-Dispersive IR (5310B)
∗ Sample is combusted
∗ Measures total C; inorganic C must be subtracted to give
TOC
∗ Reduce to Methane (5310C)
∗ Measure by dedicated FID analyzer
∗ Wet-Oxidative (5310D)
∗ Oxidized with KHSO4 in autoclave
∗ Resulting CO2 measured by non-dispersive IR
∗ UV-Persulfate
GENERAL RULE
Gracias
Merci