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5.12:

Precipitation Titration: Overview

JoVE Core
Analytical Chemistry
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JoVE Core Analytical Chemistry
Precipitation Titration: Overview

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In precipitation titrations, the analyte mixed with visual indicators reacts with the titrant to form a colored precipitate or a soluble, colored complex at the endpoint. A popular precipitating reagent is AgNO3 used in silver or argentometric titrations. A precipitation titration curve monitors the analyte or titrant concentration—plotted as the p function—against the titrant volume. Consider the titration of Cl- with AgNO3. In the beginning, the free analyte concentration is high. With the addition of titrant, some analyte is consumed, and AgCl is precipitated. The titration plot defines three regions. In the pre-equivalence region, the concentration of the unreacted analyte is determined from the moles of excess analyte and the total volume. At the equivalence point, the partial redissolution of the precipitate generates equal concentrations of silver and chloride ions, and the analyte concentration is calculated from the solubility product. Beyond the equivalence point, the analyte concentration is determined from the solubility product, where the Ag+ concentration is obtained from the excess moles of the titrant.

5.12:

Precipitation Titration: Overview

Precipitation titration involves the reaction of a titrant and an analyte to generate an insoluble precipitate. While precipitation titration uses various precipitating agents, silver nitrate is the most common precipitating reagent; titrations involving Ag+ are called argentometric titrations. Usually, the endpoint in a precipitation titration can be detected by visual indicators.

A precipitation titration curve demonstrates the change in concentration of the titrant or analyte upon adding the titrant. Titration curves are plotted with the volume of the analyte on the x-axis and the p function of the analyte or titrant concentration on the y-axis. A titration curve has three significant regions: before, at, and after the equivalence point. Before the equivalence point, the analyte concentration is in excess. The concentration of the unreacted analyte is calculated from a ratio of the moles of excess analyte in the solution to the total volume of the solution.

At the equivalence point, a stoichiometric amount of titrant has reacted with the analyte to form the precipitate (e.g., AgCl). However, some redissolution of the precipitate gives equal concentrations of Ag+ (titrant) and Cl(analyte). The analyte concentration can be estimated from the square root of the solubility product.

Beyond the equivalence point, the solution contains excess Ag+. Here, the analyte concentration can be estimated using the solubility expression, where the concentration of Ag+ is obtained from the ratio of moles of excess titrant to the total volume.