Alkaline Stability of Poly(Phenylene Oxide) Based Anion Exchange Membranes Containing Imidazolium Cations

Abstract

Two modified imidazole bases (1-heptyl-2-methyl-imidazole and 1-dodecyl-2-methyl-imidazole) were synthesized, each with a long alkyl chain (7 or 12 carbon) attached to the N-3 position. Anion exchange membranes (AEMs) were prepared with imidazolium cations derived from these bases that were either grafted directly onto the benzyl position of poly(phenylene oxide) (PPO) or affixed to the PPO using a hexyl spacer chain. First, we reacted 1-methylimidazole with brominated PPO and with PPO with a hexyl spacer chain. By comparing the alkaline stability of the resultant AEMs, we demonstrated that a hexyl spacer chain could improve AEM alkaline stability substantially. Second, by comparing the alkaline stability of PPO-based AEMs obtained by the reaction of brominated PPO with 1-methylimidazole and 1,2-dimethylimidazole, we showed that C-2-substituted (with a methyl group) imidazolium-based AEMs were much more stable in alkali than C-2-unsubstituted imidazolium-based AEMs. Finally, by investigating the alkaline stability of AEMs synthesized by reaction of brominated PPO with 1,2-dimethylimidazole and modified imidazole bases (with 7 or 12 alkyl carbon chain at the N-3 position), we demonstrated that the increase in length of a long alkyl chain affixed to the N-3 position decreases the alkaline stability of the resultant imidazolium-based AEMs.