In order to improve the alkaline stability of polyarylether-based anion exchange membranes (AEMs), the strategy of attaching a hydrophobic side-chain to the backbone is proposed. A series of AEMs which include three original quaternary ammonia AEMs (QAPSF, QAPPSU, and QAPPO) and three hydrophobic side-chain attached AEMs ( s QAPSF, s QAPPSU, and s QAPPO) are synthesized. Although a gradual enhancement of chemical stabilities for QAPSF, QAPPSU, and QAPPO is observed by reducing backbone polar groups, degradation of the original QA-type AEMs is still obvious. After testing in 1 M N 2 -saturated NaOH solution at 60 °C for 30 days, the weight losses of the original QA-type AEMs exceed 29%; the IEC losses of the AEMs exceed 24%, and the IC losses of the AEMs exceed 25% (IEC, ion exchange capacity). While for s -type AEMs, due to the hydrophobic side-chains endowing the membranes with hydrophilic/hydrophobic microphase separation morphologies, the backbones are protected from OH – attacking; significant improvements of the AEMs’ chemical stabilities are achieved. After the 30 day test, the side-chain attached AEMs exhibit much higher stabilities than those of original AEMs. The weight loss percentages for s QAPSF (IEC = 1.02 mmol g –1 ), s QAPPSU (IEC = 1.05 mmol g –1 ), and s QAPPO (IEC = 2.52 mmol g –1 ) are 8%, 8%, and 10%, respectively. The IECs of s QAPSF, s QAPPSU, and s QAPPO are reduced by 12%, 10%, and 15%, respectively. The ionic conductivities of the membranes are reduced by 15%, 12%, and 8%, respectively. Besides, compared to the original AEMs, the side-chain attached AEMs show enhanced ionic conductivity and suppressed swelling behavior. The results explicitly show that the approach of introducing a hydrophobic side-chain is an effective way to elevate the chemical stabilities of polyarylether-based AEMs.
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Han et al. (2019) studied this question.
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