Abstract
Highly charged porous polymer membranes with adjustable pore size and gradient pore structure along the membrane cross-section were prepared by ammonia-triggered electrostatic complexation between an imidazolium-based cationic poly(ionic liquid) (PIL) and multivalent benzoic acid derivatives. The PIL and the acid compound were first dissolved homogeneously in DMSO, cast into a thin film onto a glass plate, dried, and finally immersed into an aqueous ammonia solution. The diffusion of ammonia from the top to the bottom into the film neutralized the acid and introduced the gradient pore structure and in situ electrostatic cross-linking to fix the pores. The pore size and its distribution of the membranes were found controllable in terms of the multivalency of the acids, the imidazolium/carboxylate ratio, and the nature of the PIL counteranion.
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