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High performance aliphatic-heterocyclic benzyl-quaternary ammonium radiation-grafted anion-exchange membranes

机译:高性能脂族杂环苄基季铵盐辐射接枝阴离子交换膜

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摘要

Anion-exchange membranes (AEM) containing saturated-heterocyclic benzyl-quaternary ammonium (QA) groups synthesised by radiation-grafting onto poly(ethylene-co-tetrafluoroethylene) (ETFE) films are reported. The relative properties of these AEMs are compared with the benchmark radiation-grafted ETFE-g-poly(vinylbenzyltrimethylammonium) AEM. Two AEMs containing heterocyclic-QA head groups were down-selected with higher relative stabilities in aqueous KOH (1 mol dm-3) at 80°C (compared to the benchmark): these 100 μm thick (fully hydrated) ETFE-g-poly(vinylbenzyl-Nmethylpiperidinium)- and ETFE-g-poly(vinylbenzyl-N-methylpyrrolidinium)-based AEMs had as-synthesised ion-exchange capacities (IEC) of 1.64 and 1.66 mmol g-1, respectively, which reduced to 1.36 mmol dm-3 (ca. 17 – 18% loss of IEC) after alkali ageing (the benchmark AEM showed 30% loss of IEC under the same conditions). These down-selected AEMs exhibited as-synthesised Cl- ion conductivities of 49 and 52 mS cm-1, respectively, at 90°C in a 95% relative humidity atmosphere, while the OH- forms exhibited conductivities of 138 and 159 mS cm-1, respectively, at 80°C in a 95% relative humidity atmosphere. The ETFE-g-poly(vinylbenzyl-N-methylpyrrolidinium)-based AEM produced the highest performances when tested as catalyst coated membranes in H2/O2 alkaline polymer electrolyte fuel cells at 60°C with PtRu/C anodes, Pt/C cathodes, and a polysulfone ionomer: the 100 μm thick variant (synthesised from 50 μm thick ETFE) yielded peak power densities of 800 and 630 mW cm-2 (with and without 0.1 MPa back pressurisation, respectively), while a 52 μm thick variant (synthesised from 25 μm thick ETFE) yielded 980 and 800 mW cm-2 under the same conditions. From these results, we make the recommendation that developers of AEMs, especially pendent benzyl-QA types, should consider the benzyl-Nmethylpyrrolidinium head-group as an improvement to the current de facto benchmark benzyltrimethylammonium headgroup.
机译:报道了通过辐射接枝到聚(乙烯-共-四氟乙烯)(ETFE)膜上合成的含有饱和杂环苄基季铵盐(QA)基团的阴离子交换膜(AEM)。将这些AEM的相对性能与基准辐射接枝ETFE-g-聚(乙烯基苄基三甲基铵)AEM进行了比较。在80°C(与基准相比)的KOH水溶液(1 mol dm-3)中具有较高的相对稳定性的条件下,选择了两个含杂环QA头基的AEM:这些100μm厚(完全水合)ETFE-g-poly (乙烯基苄基-N甲基哌啶鎓)和ETFE-g-聚(乙烯基苄基-N-甲基吡咯烷鎓)基AEM的合成后离子交换容量(IEC)分别为1.64和1.66 mmol g-1,降低到1.36 mmol dm碱老化后为-3(约17 – 18%的IEC损失)(基准AEM在相同条件下显示30%的IEC损失)。这些向下选择的AEM在90%的相对湿度为90°C的情况下,合成后的Cl-离子电导率分别为49和52 mS cm-1,而OH-形式的电导率分别为138和159 mS cm-1。分别在80°C和95%相对湿度的环境中,如图1所示。当在60°C的H2 / O2碱性聚合物电解质燃料电池中以PtRu / C阳极,Pt / C阴极,和聚砜离聚物:100μm厚的变体(由50μm厚的ETFE合成)产生的峰值功率密度分别为800和630 mW cm-2(分别具有0.1 MPa和不具有0.1 MPa的背压)和52μm的变体(合成的)在相同条件下,从25μm厚度的ETFE中获得980和800 mW cm-2。从这些结果中,我们建议AEM的开发者,尤其是侧基QA类型的开发人员,应考虑将苄基-N甲基吡咯烷鎓头基作为对当前事实上的基准苄基三甲基铵头基的改进。

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