Complexometry: Pharmaceutical Analysis For Liquid and Semisolid Preparation
Complexometry: Pharmaceutical Analysis For Liquid and Semisolid Preparation
Complexometry: Pharmaceutical Analysis For Liquid and Semisolid Preparation
2015
DEFINITION
TITRIMETRIC METHODS THAT ARE
BASED UPON COMPLEX FORMATION
REACTIONS
Application :
1)Calcium determination in food using EDTA titration
2)Water hardness (Ca, Mg)
3) Ca or Al content of drugs such as calcium pantothenate or
alumina.
4) Metal content in every kind of matrix
Complexation equilibria
and so on
METAL-CHELATE COMPLEXES
Synthetic Aminocarboxylic Acid Chelating
Ligands
Ethylenediaminetetraacetic acid (EDTA)
Trans-1,2-diaminocyclohexanetetraacetic acid
(DCTA)
Diethylenetriaminepentaacetic acid (DTPA)
Bis(aminoethyl)glycolether-N,N,N,Ntetraacetic acid (EGTA)
- Form 1:1 complexes with metal ions
(but not with monodentate ions like Li +, Na+,
K+)
EDTA
It is hexaprotic in the form H6Y2+
HO2CH2C
CH2CO2H
HNCH2CH2NH
HO2CH2C
CH2CO2H
EDTA
[H
]
[H
Y
]
-2
3
K a1 1.0 10
[H 4 Y]
H 3Y H H 2 Y 2
2
[H
]
[H
Y
]
-3
2
K a2 2.2 10
[H 4 Y]
H 2 Y 2 H HY 3
3
[H
]
[HY
]
-7
K a3 6.9 10
[H 4 Y]
HY H Y
4
[H
]
[Y
]
-11
K a4 5.5 10
[H 4 Y]
Disodium EDTA
EDTA
Complexometric Titration
- Titration based on complex formation
Formation constant (stability constant)
-Equilibrium constant for complex formation (Kf)
Mn+ + Y4- MYn-4
[MY n 4 ]
Kf
[M n ][Y 4 ]
EDTA
- Metal-EDTA complex is unstable at very low pH
-H+ competes with metal ion for EDTA
- Metal-EDTA complex is unstable at very high pH
- OH- competes with EDTA for metal ion
- Unreactive hydroxide complexes may form
- Metal hydroxide may precipitate
Titration Curves
In most cases, a titration is performed by addition of
the titrant (EDTA) to the metal ion solution adjusted to
appropriate pH and in presence of a suitable indicator.
The break in the titration curve is dependent on:
1. The value of the formation constant.
2. The concentrations of EDTA and metal ion.
3. The pH of the solution
As for acid-base titrations, the break in the titration
curve increases as kf increases and as the
concentration of reactants is increased. The pH effect
on the break of the titration curve is such that sharper
breaks are obtained at higher pH values.
15
Example :
Ca 2 Y 4 CaY 2
[CaY 2 ]
Kf
[Ca 2 ] [Y4-]
Kf
Log Kf
Ag+
2.1 x 107
7.32
Mg2+
4.9 x 108
8.69
Ca2+
5.0 x 1010
10.70
Sr2+
4.3 x 108
8.63
Ba2+
5.8 x 107
7.76
Mn2+
6.2 x 1013
13.79
Fe2+
2.1 x 1014
14.33
Co2+
2.0 x 1016
16.31
Ni2+
4.2 x 1018
18.62
Cu2+
6.3 x 1018
18.80
Zn2+
3.2 x 1016
16.50
Cd2+
2.9 x 1016
16.46
Hg2+
6.3 x 1021
21.80
Pb2+
1.1 x 1018
18.04
Al3+
1.3 x 1016
16.13
Fe3+
1.3 x 1025
25.1
V3+
7.9 x 1025
25.9
Th4+
1.6 x 1025
23.2
Titrations
EDTA solution
Sample + indicator+buffer
Using indicator
+ H2Y22+ H
MgY
2-
colorless
colorless
EDTA
MgEDTA
(colorless)
+ In
(colorless)
(blue)
Back titration
many metals cannot be titrated directly; thus they
may precipitate from the solution in the pH range
necessary for the titration or they may form inert
complexes, or a suitable metal indicator is not
available. In such cases an excess of standard EDTA
solution is added, the resulting solution is buffered to
the desired pH and the excess of the EDTA is back
titrated with a standard metal ion solution; a solution
of zinc chloride or sulphate or of magnesium chloride
or sulphate is often used for this purpose. The end
point is detected with the aid of the metal indicator
which responds to the zinc or magnesium ions
introduced in the back titration
Laboratory Modul
Home Works
Home Works
2. Calculate the concentration of Mg 2+ in a solution
prepared by mixing 100 mL of 0,03 M Mg 2+ with
100 mL of 0,05 M EDTA. The mixture is buffer to
a pH of 3.
4 at pH 3 = 2,5 x 10-4. KMg-Y4- = 4,9x 108