Extraction and separation of metal cations in solution by supported liquid membrane using lasalocid A as carrier

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Abstract

Flat-sheet-supported liquid membranes incorporating lasalocid A (a natural ionophore), were previously shown to be permeable to metal cations (Cd2+ and Zn2+) against a proton gradient (ΔpH), which is the driving force of the process [1]. This transport process has been extended to other metal species such as Pb2+, Na+, and Ag+ and also to the case where two metal species compete for transport. A higher transport flux for Pb2+ as compared to Cd2+ and Zn2+ is observed and partly explained by a higher rate of interfacial complexation owing to the smaller hydration shell of this species. This effect is confirmed by the data obtained with Ag+. However, the size of the metal cation in relation to its hydration shell does not appear as the major parameter to take into account for an estimate of the trans-membrane transport efficiency, as the Na+ ions escape to this behavior, which has been considered until now as a general trend for metal cation ionophores.

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Canet, L., & Seta, P. (2001). Extraction and separation of metal cations in solution by supported liquid membrane using lasalocid A as carrier. In Pure and Applied Chemistry (Vol. 73, pp. 2039–2046). Walter de Gruyter GmbH. https://doi.org/10.1351/pac200173122039

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