Cross-Linked, Monovalent Selective Anion Exchange Membrane: Effect of Prealkylation and Co-ions on Selectivity

Abstract

Tuning of hydrophobicity, water uptake, and size of the ion channel is very crucial for the monovalent anion-selective membrane (MASM) preparation. In this work, we report the preparation of MASM from the cross-linked polyacrylonitrile-co-polyvinylimidazole (PAN-co-PVI) copolymer. The copolymer was in situ quaternized and cross-linked using the polyacrylonitrile-co-polychloromethylstyrene (PAN-co-PCMSt) copolymer as cross-linker. The benzyl chloride moiety (Ar-CH2Cl) of PAN-co-PCMSt reacts with imidazolium nitrogen of PAN-co-PVI and provides a positive charge on the membrane matrix, whereas the PAN moiety provides greater compatibility with the PAN-co-PVI copolymer matrix. The faster cross-linking without external prealkylation forms a strong network structure with a low ionic charge on the membrane surface. Judicious extent of prealkylation followed by cross-linking forms a controlled network structure and small-sized ionic channel with moderate water uptake and good mechanical stability. The representative AEM0Q and AEM17Q membranes with 0 and 17% prealkylation exhibited a permselectivity (PSO42–Cl–) value of 4.39 and 15.40, respectively, during the separation of 0.01 M NaCl + 0.01 M Na2SO4 by electrodialysis. Upon further increase of prealkylation to 27 and 32%, the water uptake of the membrane increased, which in turn allowed the passage of SO42– along with Cl– and decreased the PSO42–Cl–value to 4.12 and 2.45, respectively. Similar trends were observed during the separation of NaCl + MgSO4, MgCl2 + Na2SO4, and MgCl2 + MgSO4 mixtures of each 0.01 M concentration.