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A study of the mechanism of the solvent extraction of metal ions by carboxylic acids

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posted on 13.08.2018, 16:11 by Alan D. Jones
A study of the species involved in the extraction of metal ions from aqueous solutions into organic solvents with long-chain carboxylic acids has been made. The theoretical analysis of the extraction data in terms of a single equilibrium approach and a multiple equilibria method has been made. The two approaches have been shown to be equivalent in the case of one extracted complex, and an extraction expression has been proposed to describe the extractions. The analysis of the data has been considered in terms of this expression by graphical and regression procedures. Under the equilibrium extraction conditions studied, the extracted species in the case of copper (II), cobalt (II) and nickel (II) systems appear to be predominantly dimeric in nature and are usually solvated with carboxylic acid molecules in the organic phase. Results obtained from the extraction of copper from an aqueous solution into free-falling drops of n-octoic acid dissolved in carbon tetrachloride indicate that the rate of extraction does not vary appreciably over the pH range studied. The measurement of the interfacial tensions in the same system suggests that no abrupt change in the nature of the interfacial region occurs as the pH of extraction increases.

Funding

Great Britain, Ministry of Technology, Warren Spring Laboratory.

History

School

  • Science

Department

  • Chemistry

Publisher

© Alan David Jones

Publisher statement

This work is made available according to the conditions of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) licence. Full details of this licence are available at: https://creativecommons.org/licenses/by-nc-nd/4.0/

Publication date

1967

Notes

A Doctoral Thesis. Submitted in partial fulfilment of the requirements for the award of Doctor of Philosophy at Loughborough University.

Language

en

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