Abstract

Pulsed field gradient nuclear magnetic resonance technique was applied to investigate the self-diffusion mechanism of water, alcohol molecules and Li− counterions in sulfocation exchangers with different structures of the polymeric matrix. It was shown that in the homogeneous perfluorinated sulfocation exchange membranes the ionic and water translation motions are controled by the hydrogen bond network forming in ionogenic channels at the high water content. At the low solvent content, the self-diffusion coefficients of methanol and ethanol are higher than the water self-diffusion coefficients. The influence of non-ion-exchange sorbed electrolyte on Li+ self-diffusion coefficients was observed in the heterogeneous sulfocation exchanger KU-23.

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