Cyclic voltammetry of highly hydrophilic ions at a supported liquid membrane

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• 作者：Sorina M Ulmeanu^a ; Henrik Jensen^a ; Zdenek Samec^a ; ¹ ; Gé ; raldine Bouchard^b ; Pierre-Alain Carrupt^b ; Hubert H Girault^a ; ^{hubert.girault@epfl.ch}
• 关键词：Liquid  ; ?#xA0 ; liquid interfaces ; Membrane ; Ion transfer ; Simulation ; Cyclic voltammetry ; Alkali metal ions
• 刊名：Journal of Electroanalytical Chemistry
• 出版年：2002
• 出版时间：26 July 2002
• 年：2002
• 卷：530
• 期：Complete
• 页码：10-15
• 全文大小：200 K

文摘

Cyclic voltammetry has been used to study the coupling of ion transfer reactions at a liquid membrane. The liquids are either supported by a porous hydrophobic membrane (polyvinylidene difluoride, PVDF) when the organic solvent is non-volatile (o-nitrophenyloctylether) or are merely a free standing organic solvent layer such as 1,2-dichloroethane comprised between two hydrophilic dialysis membranes supporting the adjacent aqueous phases. The passage of current across the liquid membrane is associated with two ion transfer reactions across the two polarised liquid ?#xA0;liquid interfaces in series. It is shown that it is possible to study the transfer of highly hydrophilic ions at one interface by limiting the mass transfer of the other ion transfer reaction at the other interface. Indeed, for systems comprising an ion M in one aqueous phase and a reference ion R partitioned between the membrane and the other aqueous phase, the observed and simulated cyclic voltammograms have a half-wave potential determined by the Gibbs energy of transfer of M transferring at one interface and by the limiting mass transfer of R at the other interface. This new methodology opens a way to measure the Gibbs energy of transfer of highly hydrophilic or hydrophobic ions, which usually limits the potential window at single liquid ?#xA0;liquid interfaces (ITIES).