Solvation of extracted substituted ammonium salts in nitrobenzene-benzene mixtures

Date

1970

Contributor

Advisor

Department

Instructor

Depositor

Speaker

Researcher

Consultant

Interviewer

Narrator

Transcriber

Annotator

Journal Title

Journal ISSN

Volume Title

Publisher

University of Hawaii at Manoa

Volume

Number/Issue

Starting Page

Ending Page

Alternative Title

Abstract

The extraction of iron(III) from aqueous hydrochloric acid by tri-n-octylamine hydrochloride (TOAHCl) in nitrobenzene-benzene mixtures ranging from pure benzene to pure nitrobenzene has been studied as a function of amine salt concentration, solvent composition, and temperature. A less extensive extraction study of iron(III) by tetra-n-heptylammonium chloride (THACl) in nitrobenzene-benzene mixtures was also performed. In addition, a brief study was made of the degree of aggregation of both amine salts in benzene. The results of the extraction study using TOAHCl are interpreted in terms of a phenomenological thermodynamic model which includes the solvation of the primary extracted species by nitrobenzene and by additional TOAHCl molecules in the organic phase. This extraction system was found to be metal concentration independent. It is postulated that the organic phase contains the following metal species: TOAHFeCl4•TOAHCl, TOAHFeCl4•(TOAHCl)2, (TOAH+ + FeCl4) solvated, and TOAHFeC14•nøN02, where n was found to be ca. 3.0. The thermodynamic quantities, ΔG° , ΔH° , and Δ5° , were calculated from the various equilibrium constants and are discussed in terms of molecular interactions. The extraction study carried out using THACl was found not to fit the extraction model proposed for TOAHCl and provided little information because of gross non-ideality of the organic solutions of this salt. On a qualitative basis, the results suggest that the nitrobenzene solvation observed in the TOAHCl system may be due to cation solvation only. The aggregation studies demonstrated that TOAHCl exists as an equilibrium monomer and dimer mixture in dilute solutions (≤ 0.05 molar) in benzene, while the THACl is very highly aggregated even in dilute benzene solutions (0.01M).

Description

Keywords

Citation

Extent

Format

Geographic Location

Time Period

Related To

Theses for the degree of Doctor of Philosophy (University of Hawaii (Honolulu)). Chemistry; no. 298

Related To (URI)

Table of Contents

Rights

All UHM dissertations and theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission from the copyright owner.

Rights Holder

Local Contexts

Email libraryada-l@lists.hawaii.edu if you need this content in ADA-compliant format.