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Complexometric Titration: Overview00:39

Complexometric Titration: Overview

Complexometric titration involves the formation of a complex by reacting a metal ion with one or more ligands. A visual indicator often detects the end point of a complexometric titration. It is added to the metal solution before the titration, forming a stable metal–indicator complex and imparting color to the solution. As the titration approaches the equivalence point, the excess of the added ligand displaces the indicator from the metal–indicator complex, releasing the free indicator. The...
EDTA: Auxiliary Complexing Reagents01:26

EDTA: Auxiliary Complexing Reagents

EDTA titrations are usually carried out in highly basic conditions, where the fully deprotonated form of EDTA, Y4−, actively complexes with the free metal ions in the solution. Several metal ions precipitate as hydrous oxide (hydroxides, oxides, or oxyhydroxides) under these conditions, lowering the concentration of free metal ions in the solution. For this reason, auxiliary complexing agents or ligands such as ammonia, tartrate, citrate, or triethanolamine are used in EDTA titrations to...
Precipitation Titration: Endpoint Detection Methods01:19

Precipitation Titration: Endpoint Detection Methods

In argentometric precipitation titrations, endpoints can be detected visually by the Mohr, Volhard, and Fajans methods. In the Mohr method, adding a soluble chromate indicator gives an initial yellow color to the analyte solution. As the titrant is added, the first excess of silver ions forms a red silver chromate precipitate, marking the endpoint. The solution pH should be maintained at about 8 by adding solid CaCO3.
In the Volhard method, a standard excess of AgNO3 is first added to the...
EDTA: Indirect and Alkalimetric Titration01:23

EDTA: Indirect and Alkalimetric Titration

Unlike direct titration, back-titration, and displacement titration, indirect titration is an EDTA titration method for quantifying anions. In the indirect titration method, anions are precipitated as their insoluble salts with excess metal ions. The filtrate containing the excess metal ions is directly titrated with standard EDTA until the endpoint is achieved. Another approach involves extracting the metal ion and back-titrating with standard EDTA to obtain the endpoint. In this way, the...
Precipitation Titration Curve: Analysis01:21

Precipitation Titration Curve: Analysis

The precipitation titration curve demonstrates the change in concentration of one reactant with the volume of titrant added. During the titration of chloride ions with silver nitrate, the precipitation titration curve is divided into three regions: before, at, and after the equivalence point. Before the equivalence point, low redissolution of the sparingly soluble silver chloride precipitate gives a low silver ion concentration. However, in the second region, representing the equivalence point,...
EDTA: Direct, Back-, and Displacement Titration01:30

EDTA: Direct, Back-, and Displacement Titration

The EDTA titration types for metal ion analysis include direct titration, back-titration, and replacement titration.
Direct titration involves buffering the metal ion solution to the desired pH and directly titrating with standard EDTA until the endpoint. The optimum pH ensures a large conditional formation constant of metal−EDTA and visibility of the free indicator color in the solution. In addition, auxiliary complexing reagents are used to prevent the precipitation of metal hydroxides and...

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Related Experiment Video

Updated: Jun 28, 2026

Determination of Thermodynamic Properties of Alkaline Earth-liquid Metal Alloys Using the Electromotive Force Technique
12:02

Determination of Thermodynamic Properties of Alkaline Earth-liquid Metal Alloys Using the Electromotive Force Technique

Published on: November 3, 2017

Amperometric complex-formation titrations with a dropping bismuth amalgam electrode in halide medium.

J W Dieker1, W E van der Linden, G den Boef

  • 1Laboratory for Analytical Chemistry, University of Amsterdam, Nieuwe Achtergracht 166, Amsterdam, The Netherlands.

Talanta
|October 1, 1977
PubMed
Summary

This study demonstrates selective metal ion determination using a dropping bismuth amalgam electrode and amperometric titration. Accurate analysis is achieved even with high halide concentrations, showcasing a novel analytical method.

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Last Updated: Jun 28, 2026

Determination of Thermodynamic Properties of Alkaline Earth-liquid Metal Alloys Using the Electromotive Force Technique
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Area of Science:

  • Analytical Chemistry
  • Electrochemistry

Background:

  • Accurate determination of metal ions is crucial in various chemical analyses.
  • High halide concentrations often interfere with standard metal ion detection methods.

Purpose of the Study:

  • To investigate the selective determination of metal ions.
  • To assess the efficacy of a dropping bismuth amalgam electrode in complex matrices.
  • To explore amperometric complex-formation titrations coupled with normal pulse polarography.

Main Methods:

  • Utilized a dropping bismuth amalgam electrode.
  • Employed amperometric complex-formation titrations.
  • Applied normal pulse polarography for analysis.
  • Compared experimental and calculated current-voltage curves.

Main Results:

  • Achieved selective determination of metal ions.
  • Quantified metal ion concentrations as low as 3 x 10(-7)M.
  • Demonstrated accuracy in the presence of 0.1M chloride or 0.01M bromide.
  • Found reasonable agreement between experimental and calculated data.

Conclusions:

  • The dropping bismuth amalgam electrode is effective for selective metal ion analysis.
  • The method allows for accurate quantification in the presence of significant halide interference.
  • Normal pulse polarography enhances the utility of amperometric titrations for complex sample analysis.