Argentometric Titrations
Argentometric Titrations
Argentometric Titrations
Principle:
Precipitation titrations are based on reactions that yield ionic compounds of limited
solubility.
The most widely used and important precipitating reagent is silver nitrate, which is used for
the determination of the halogens, the halogenlike anions, mercaptans, fatty acids, and several
divalent inorganic anions.
Appratus:
Beaker.
Burette
Iron Stand
Funnel
Volumetric Flask
Dropper
Procedure:
1. Mohr Method, Chromate Ion
In the Mohr method, sodium chromate (Na2CrO4) serves as the indicator for the
argentometric titration of chloride, bromide, and cyanide ions.
Silver ions react with chromate to form the brick-red silver chromate (Ag2CrO4) precipitate
in the equivalence-point region.
• At low pH; the concentration of the chromate ion in the acidic solutions is so low that it can
not form a precipitate with Ag+ at the equivalence point. Because in acidic solutions CrO 42-
is converted to Cr2O72- (Chromate ion is conjugated base of chromic acid).
• At high pH; the silver ions can be precipitated as AgO.
In this method, Fe (III) ion is used as an indicator. The most important application of the
Volhard method is the indirect determination of halide ions.
First, a measured excess of standard silver nitrate solution is added to the sample:
Iron(III) serves as the indicator. The solution turns red with the first slight excess of
thiocyanate ion due to the formation of Fe(SCN)2+.
The strongly acidic environment of the Volhard titration is a distinct advantage over other
titrations of halide ions because such ions as carbonate, oxalate, and arsenate do not interfere.
The silver salts of these ions are soluble in acidic media but only slightly soluble in neutral
media.
Silver chloride is more soluble than silver thiocyanate. As a result, in chloride determinations
using the Volhard method, the reaction
AgCl(s) + SCN- ↔ AgSCN(s) + Cl- occurs to a significant extent near the end of the back-
titration. This reaction causes the end point to fade and results in overconsumption of
thiocyanate ion. The resulting low results for chloride can be overcome by filtering the silver
chloride before undertaking the back-titration. Filtration is not required for other halides
because they form silver salts that are less soluble than silver thiocyanate.
The Fajans method uses an adsorption indicator, an organic compound that adsorbs onto or
desorbs from the surface of the solid in a precipitation titration. Ideally, the adsorption or
desorption occurs near the equivalence point and results not only in a color change but also in
the transfer of color from the solution to the solid or vice versa.
Fluorescein is a typical adsorption indicator useful for the titration of chloride ion with silver
nitrate. In the aqueous solution, fluorescein is partially ionized to hydronium ions and
yellowish green colored negatively charged fluoresceinate ions. The fluoresceinate ion forms
a dark red silver salt.
Before the equivalence point, Cl− is in excess, and the primary adsorbed layer is Cl−. This
repels the indicator anion, and the more loosely held secondary (counter) layer of adsorbed
ions is cations, such as Na+.
Beyond the equivalence point, Ag+ is in excess, and the surface of the precipitate becomes
positively charged, with the primary layer being Ag +. This will now attract the indicator anion
and adsorb it in the counterlayer.
Titrations involving adsorption indicators are rapid, accurate, and reliable, but their
application is limited to the few precipitation titrations that form colloidal precipitates rapidly.
Experimental Procedure:
The solution is titrated until the orange color of Ag2CrO4 precipitate is observed in the solution.