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Issue 15, 2018
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Mechanism of ionic-liquid-based acidic aqueous biphasic system formation

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Abstract

Ionic-liquid-based acidic aqueous biphasic systems (IL-based AcABS) represent a promising alternative to the solvent extraction process for the recovery of critical metals, in which the substitution of the inorganic salt by an acid allows for a ‘one-pot’ approach to the leaching and separation of metals. However, a more fundamental understanding of AcABS formation remains wanting. In this work, the formation mechanisms of AcABS are elucidated through a comparison with traditional aqueous biphasic systems (ABS). A large screening of AcABS formation with a wide range of IL identifies the charge shielding of the cation as the primary structural driver for the applicability of an IL in AcABS. Through a systematic study of tributyltetradecylphosphonium chloride ([P44414]Cl) with various chloride salts and acids, we observed the first significant deviation to the cationic Hofmeister series reported for IL-based ABS. Furthermore, the weaker than expected salting-out ability of H3O+ compared to Na+ is attributed to the greater interaction of H3O+ with the [P44414]+ micelle surface. Finally, the remarkable thermomorphic properties of [P44414]Cl based systems are investigated with a significant increase in the biphasic region induced by the increase in the temperature from 298 K to 323 K. These finding allows for the extension of ABS to new acidic systems and highlights their versatility and tunability.

Graphical abstract: Mechanism of ionic-liquid-based acidic aqueous biphasic system formation

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Publication details

The article was received on 08 Feb 2018, accepted on 08 Mar 2018 and first published on 08 Mar 2018


Article type: Paper
DOI: 10.1039/C8CP00937F
Citation: Phys. Chem. Chem. Phys., 2018,20, 9838-9846
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    Mechanism of ionic-liquid-based acidic aqueous biphasic system formation

    N. Schaeffer, H. Passos, M. Gras, V. Mogilireddy, J. P. Leal, G. Pérez-Sánchez, J. R. B. Gomes, I. Billard, N. Papaiconomou and J. A. P. Coutinho, Phys. Chem. Chem. Phys., 2018, 20, 9838
    DOI: 10.1039/C8CP00937F

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