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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...
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...
Fast Reactions01:27

Fast Reactions

Fast reactions occurring in times shorter than the time needed to mix reactants pose a unique challenge for investigation. In a liquid-phase continuous-flow system, reactants A and B are swiftly pushed into the mixing chamber, where mixing occurs within 1 ms. The reaction mixture then flows through an observation tube, and one measures light absorption to determine species concentrations at various points of the tube. This method is most appropriate when relatively large volumes of reactants...
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...
Complexometric EDTA Titration Curves01:20

Complexometric EDTA Titration Curves

EDTA titration curves determine the free metal ion concentration. The titration curve represents the change in concentration of free metal ions (p function) as a function of the volume of EDTA added. This curve consists of three regions: before, at, and after equivalence points. Excess free metal ions are present before the equivalence point. Equal concentrations of metal ions and EDTA are present at the equivalence point. After the equivalence point, excess EDTA exists. This means slight...
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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Quantitative Detection of Trace Explosive Vapors by Programmed Temperature Desorption Gas Chromatography-Electron Capture Detector
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Automated titrations with an alternate flow exponential speed variation system.

C N Yarnitzky1, N Klein, O Cohen

  • 1Department of Chemistry, Technion, Israel Institute of Technology, Haifa, Israel 32000.

Talanta
|December 1, 1993
PubMed
Summary

This study introduces an automatic titration system with an alternate flow exponential speed variation. The novel twin cycle procedure enables accurate sample concentration calculation without precalibration, improving precision and eliminating tubing wear errors.

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Area of Science:

  • Analytical Chemistry
  • Instrumentation Science

Background:

  • Traditional automatic titration systems can suffer from inaccuracies due to tubing deterioration and require precalibration.
  • Developing precise and robust analytical methods is crucial for accurate chemical analysis.

Purpose of the Study:

  • To describe a novel alternate flow exponential speed variation system for automatic titrations.
  • To demonstrate a method for accurate sample concentration determination without precalibration.
  • To eliminate errors associated with peristaltic pump tubing wear in automated titrations.

Main Methods:

  • The system utilizes two peristaltic pumps and two three-way valves for fluid handling.
  • A twin cycle titration procedure involving forward and reverse cycles with variable pump speeds was employed.
  • A mixing coil and detector facilitate the titration process and measurement.

Main Results:

  • The system achieved an accuracy better than 0.5% for sample concentration determination.
  • The titration process required approximately 2 minutes and 2 ml of sample volume.
  • The alternate flow method effectively compensated for tubing deterioration, eliminating associated errors.

Conclusions:

  • The described alternate flow exponential speed variation system offers a precise and reliable method for automatic titrations.
  • This innovative approach negates the need for precalibration and mitigates errors from system wear.
  • The system demonstrates significant potential for improving efficiency and accuracy in analytical laboratories.