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A chemically stable copolymer [poly(2,6 dimethyl 1,4 phenylene oxide)- b -poly(vinyl benzyl trimethyl ammonium)] with two ion exchange capacities, 3.2 and 2.9 meq g −1 , was prepared as anion exchange membranes (AEM-3.2 and AEM-2.9). These materials showed high OH − conductivities of 138 mS.cm −1 and 106 mS.cm −1 , for AEM-3.2 and AEM-2.9 respectively, at 60°C, and 95% RH. The OH − conductivity = 45 mS.cm −1 for AEM-3.2 at 60% RH and 60°C in the absence of CO 2 . Amongst the ions studied, only OH − is fully dissociated at high RH. The lower E a = 10–13 kJ.mol −1 for OH − compared to F − ∼ 20 kJ.mol −1 in conductivity measurements, and of H 2 O from self-diffusion coefficients suggests the presence of a Grotthuss hopping transport mechanism in OH − transport. PGSE-NMR of H 2 O and F − show that the membranes have low tortuosity, 1.8 and 1.2, and high water self-diffusion coefficients, 0.66 and 0.26 × 10 −5 cm 2 .s −1 , for AEM-3.2 and AEM-2.9 respectively. SAXS and TEM show that the membrane has several different sized water environments, ca. 62 nm, 20 nm, and 3.5 nm. The low water uptake, λ = 9–12, reduced swelling, and high OH − conductivity, with no chemical degradation over two weeks, suggests that the membrane is a strong candidate for electrochemical applications.
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Pandey et al. (2016) studied this question.
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