ABSTRACT

I. Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 465

II. Extraction Systems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 465

III. Reactive Equilibria . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 469

IV. Reactive Mass Transfer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 471

A. Mass Transfer without Electrical Fields . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 471

B. Mass Transfer with Electrical Fields . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 473

1. Surfactants . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 475

2. External Fields . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 479

V. Liquid-Liquid Hydrodynamics in Electric Fields . . . . . . . . . . . . . . . . . . . . . . . . . 483

VI. Summary . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 486

Acknowledgments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 487

References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 488

The first extraction processes were with solid extraction gaining perfumes, waxes, and pharma-

ceutical active oils in an operation quite similar to a modern Soxhlet apparatus. An extraction

pot with an age of about B.C. 3500 was found 250 km north of Bagdad and extraction instructions

were documented by a Sumerian text of B.C. 2100 [1]. The next major improvements were in the

medieval age with new solvents like ethanol, mineral acids, and amalgams used to extract and

purify metals. The first extraction of a metal was reported by Peligot [2] who used diethylether

to extract uranyl nitrate which gave a basis to uranium extraction within the “Manhattan”

project in the 1940s [3]. Reactive solvent extraction was then a niche for pyrometallurgically diffi-

cult to separate metals (Nb/Ta, Zr/Hf) till the 1960s, when there was a breakthrough with copper extraction. Liquid ion exchanger (LIX) chemicals [4] were size-selective extractants for separation

of copper from iron, allowing copper recovery from low-grade ores after a sulfate leaching process.

Meanwhile, the use of LIXs has expanded to a large variety of ionic species and neutral solutes in

hydrometallurgical, environmental, petrochemical, chemical and biochemical industries [5-9].