Selectivity in the coextraction of cation and anion by electrochemically modulated liquid-liquid extraction

Electrochemistry at the interface between two immiscible electrolyte solutions has been presented as a method of electrochemically modulated liquid-liquid extraction, where ions in a mixture can be selectively partitioned as a function of the applied interfacial potential difference. In this study, a mixture comprising 4-octylbenzenesulfonate (4-OBSA(-)) and tetraethylarnmonium (TEA(+)) ions was evaluated. The application of negative potential differences enabled the selective extraction of 4-OBSA-into the organic phase, and more positive potential differences enabled the selective extraction of TEA(+). However, intermediate potentials lead to the coextraction of both ions into the organic phase, with apparent selectivity for TEA(+) over 4-OBSA(-). An increased concentration of either ion in the mixture inhibited the extraction response of the other ion, but the order of the extraction at these intermediate potentials was always TEA(+) followed by 4-OBSA(-). The reasons for the selectivity for the cation over the anion are discussed.