Transport of metal ions across an electrically switchable cation exchange membrane based on polypyrrole doped with a sulfonated calix[6]arene

Abstract

The conducting polymer polypyrrole, PPy, was used as the active component of a cation exchange membrane for transferring a range of metal ions between two solutions by electrical modulation of the polymer between its conducting and non-conducting states. The cation exchange membranes consisted of platinum sputter-coated polyvinylidene difluoride (PVDF) which had been coated with polypyrrole doped with sulfonated calix[6]arene (PPy(C6S)). It was shown that applying a constant potential in the range −0.4 to +0.6 V did not result in any metal ion flux across the PVDF/Pt-PPy(C6S) membrane. However, a gradual but steady increase in metal ion concentration was detected in the receiving cell when −0.8 V was applied to the membrane. To investigate the effect of film thickness on the permeability of metal ions, transport experiments were performed with composite membranes containing 2.0, 3.3, and 5.6 μm thick PPy(C6S) films. The permeability of the metals across the membrane increased as the PPy(C6S) film thickness decreased and was found to decrease in the following order: Ca 2+ > K + > Mn 2+ ≫ Co 2+, when the receiving cell contained deionised water. The PVDF/Pt-PPy(C6S) composite membrane showed significant permeability towards metal ions such as Ca 2+, K + and Mn 2+, with the flux for Ca 2+ higher than that seen for this metal ion with any previously studied PPy films containing other complexing dopants.