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Related Concept Videos

Controlled-Current Coulometry: Coulometric Titration01:18

Controlled-Current Coulometry: Coulometric Titration

Coulometric titrations are a form of titrimetric analysis where the reagent is generated electrically, and its amount is evaluated based on current and generating time. The electron serves as the standard reagent. The procedure is similar to conventional titrations, such as endpoint detection.
The fundamental requirements for coulometric titrations are (1) 100% efficiency in the reagent-generating electrode reaction and (2) a stoichiometric and preferably rapid reaction between the generated...
Controlled-Current Coulometry: Overview01:27

Controlled-Current Coulometry: Overview

Controlled current coulometry, also known as amperostatic coulometry, is a technique used in electrochemical analysis to measure the quantity of a substance through the controlled passage of current. It involves the application of a constant current to an electrochemical cell containing the analyte of interest. As the current flows through the cell, the analyte undergoes a redox reaction at the electrode surface, resulting in a charge transfer. By monitoring the time required for a certain...
Coulometry: Overview01:00

Coulometry: Overview

Coulometry is one of the rapid, most accurate, and precise analytical techniques that determine the quantity of an analyte by measuring the electrical charge needed for its complete electrolysis without using any analytical standards. The total charge passed during electrolysis correlates with the analyte amount by Faraday's laws of electrolysis. For accurate coulometric measurements, a charge equal to Faraday's constant multiplied by the number of electrons involved in the relevant...
Titrimetric Methods: Types and Commonly Used Strategies01:08

Titrimetric Methods: Types and Commonly Used Strategies

In chemistry, titrimetric methods are broadly classified into three types: volumetric, gravimetric, and coulometric. Volumetric titrations involve measuring the volume of a titrant of known concentration that is required to react completely with an analyte. In gravimetric titrations, the standard solution reacts with the analyte to form an insoluble precipitate, which is filtered, dried, and weighed. In coulometric titrations, current is applied to an electrochemical reaction until the reaction...
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: 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...

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Isothermal Titration Calorimetry for Measuring Macromolecule-Ligand Affinity
08:45

Isothermal Titration Calorimetry for Measuring Macromolecule-Ligand Affinity

Published on: September 7, 2011

Flow-injection coulometric titrations.

R H Taylor1, J Růzicka, G D Christian

  • 1Center for Process Analytical Chemistry, Department of Chemistry, BG-10, University of Washington, Seattle, WA 98195, U.S.A.

Talanta
|March 1, 1992
PubMed
Summary
This summary is machine-generated.

This study introduces a novel flow-injection analysis system using stop-flow coulometric titrations for automated sample analysis. The technique offers high precision for titrating sodium hydroxide and nitric acid across wide concentration ranges.

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Area of Science:

  • Analytical Chemistry
  • Electrochemistry

Background:

  • Conventional coulometric titrations face challenges with reagent handling, storage, and degradation.
  • Automated analytical methods are crucial for improving efficiency and accuracy in chemical analysis.

Purpose of the Study:

  • To develop and validate a flow-injection analysis (FIA) technique based on stop-flow coulometric titrations.
  • To integrate key components into a single unit for streamlined analysis.
  • To assess the system's performance for titrating strong acids and bases.

Main Methods:

  • A novel flow-injection analysis system was designed, incorporating a gradient chamber, reagent generation chamber, and detector flow cell.
  • Stop-flow functionality enabled automated sample dilution up to 100-fold.
  • Remote spectrophotometric detection was achieved using optical fibers.
  • The system eliminated the need for frits or membranes between electrodes.

Main Results:

  • The system successfully titrated sodium hydroxide (5 x 10(-4)-4M) and nitric acid (5 x 10(-3)-15M).
  • Analyses achieved a relative standard deviation of less than 3% across the entire concentration range.
  • A correlation coefficient of 0.999 was obtained when compared to manual titrations.

Conclusions:

  • The developed stop-flow coulometric titration system provides an accurate and precise method for analyzing strong acids and bases.
  • It retains the advantages of conventional coulometric titration while overcoming reagent handling issues.
  • The integrated design and automated dilution enhance analytical workflow efficiency.