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Journal ArticleDOI

Kinetics of metal solvent extraction. [160 references]

P.R. Danesi, +1 more
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TLDR
In this article, a review of solvent extraction of metal species by organic solution of acidic, basic, and neutral reagents has been conducted by considering the contribution of both chemical reactions and transport processes on the rate of extraction.
Abstract
The kinetics of solvent extraction of metal species by organic solution of acidic, basic, and neutral reagents has been reviewed by considering the contribution of both chemical reactions and transport processes on the rate of extraction. The relative predominance of slow chemical reactions and diffusion processes has been shown to depend, in a critical way, both on the hydrodynamic conditions present in the extracting apparatus and on the specific nature and composition of the chemical system involved in the extraction. The general criteria that can help to distinguish between extraction kinetics controlled either by mass transport or chemical reactions have been reviewed. These criteria involve the experimental determination of the influence of a rather large number of physical and chemical variables on the rate of extraction and do not always lead to unambiguous conclusions. The reviewed literature has allowed to draw the following conclusions: (1) because of a lack of complete characterization (especially in terms of hydrodynamics, interfacial pressure, and sufficiently wide concentration ranges), much of the early work on solvent extraction kinetics has rarely led to the definite identification of the rate determining processes; as a consequence, correct extrapolation to the different experimental conditions that are met in practicalmore » analytical or technological separations has been often impossible; and (2) more recently a certain number of extraction kinetics studies have appeared which have been carried out in hydrodynamically controlled conditions, exploring a large range of compositions of the species and with knowledge of the interfacial properties of the biphasic system; such studies have contributed to the emergence of a general pattern for the solvent extraction kinetics which is summarized.« less

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Solvent microextraction into a single drop.

TL;DR: An analytical technique is described which combines solvent extraction with gas chromatographic (GC) analysis in a simple and inexpensive apparatus involving very little solvent consumption and is in good agreement with a convective-diffusive kinetic model.
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Separation of Metal Species by Supported Liquid Membranes

TL;DR: In this article, a review of the works performed in the Separation Chemistry Group of the Chemistry Division of Argonne National Laboratory on the transport and separation properties of supported liquid membranes (SLM) is presented.
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Analytical applications of organized molecular assemblies

TL;DR: In this article, a review of micelles and their applications in many types of analytical methods is presented. But the focus of the review is not on the performance of the mouselles, but on the micro-emulsions in shifting acid-base equilibria.
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Solvent bar microextraction.

TL;DR: A new and simple microextraction method, the organic extractant solvent was confined within a short length of a hollow fiber membrane that was placed in a stirred aqueous sample solution that provided very high enrichment and good reproducibility.
Journal ArticleDOI

Solvent Microextraction with Simultaneous Back-Extraction for Sample Cleanup and Preconcentration: Quantitative Extraction

TL;DR: In this article, a solvent microextraction technique was developed to perform simultaneous forward and back-extraction across a microliter-size organic liquid membrane, where the solvent phase (o) consisting of 40 or 80 μL of n-octane, is layered over 0.5 or 1.0 mL of aqueous sample phase (a1) contained in a 1- or 2-mL microreaction vial and is stabilized against mechanical disruption by a small Teflon ring, even when the a1 phase is stirred at a speed of 2000 rpm.
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