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Modification of poly(aryl ether ketone) using imidazolium groups as both pendants and bridging joints for anion exchange membranes

机译:使用咪唑鎓基团作为阴离子交换膜的侧基和桥联键修饰聚芳醚酮

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Quaternary imidazolium groups were grafted onto poly(aryl ether ketone) as both pendants and joints of crosslinking by using 1-methylimidazole and C2-substituted imidazole of 2-undecylimidazole in a certain mole ratio. Crosslinking of the imidazolium-functionalized poly(aryl ether ketone) was performed with three dibromoalkane crosslinkers having different alkyl chain-length in order to know the correlation of the structure and property of the crosslinked membranes meanwhile to enhance their mechanical strength. The obtained crosslinked membranes in hydroxide form showed a high tensile strength of about 20 MPa at room temperature with less swelling, and they were thermally stable up to around 230 degrees C according to the data of thermogravimetric analysis. All the crosslinked anion exchange membranes exhibited conductivities in purified water of higher than 0.010 S cm(-1) at 25 degrees C, and over 0.040 S cm(-1) at 80 degrees C, respectively. The durability of the membranes in alkaline medium was tested by monitoring the changes in conductivity, ion exchange capacity (IEC) and tensile strength at break, respectively. The results indicate that the anion exchange membrane crosslinked with a long alkyl spacer demonstrated high tolerance to the nucleophilic attack. In addition, the increase in the temperature could accelerate the degradation of the polymer membrane more than that increase in the concentration of the alkaline solution. (C) 2015 Elsevier Ltd. All rights reserved.
机译:通过以一定摩尔比使用1-甲基咪唑和2-十一烷基咪唑的C 2-取代的咪唑,将季咪唑基团接枝到聚(芳基醚酮)上作为交联的侧基和接头。咪唑鎓官能化的聚(芳基醚酮)的交联是通过三个具有不同烷基链长的二溴代烷烃交联剂进行的,以了解交联膜的结构和性能的相关性,同时提高其机械强度。所获得的氢氧化物形式的交联膜在室温下显示出约20MPa的高拉伸强度且溶胀较少,并且根据热重分析的数据它们在高达230℃左右的温度下是热稳定的。所有的交联阴离子交换膜在25摄氏度时在纯水中的电导率均高于0.010 S cm(-1),在80摄氏度时在0.040 S cm(-1)之上。通过分别监测电导率,离子交换容量(IEC)和断裂拉伸强度的变化来测试膜在碱性介质中的耐久性。结果表明与长的烷基间隔基交联的阴离子交换膜表现出对亲核攻击的高耐受性。另外,温度的增加比碱溶液的浓度增加更能加速聚合物膜的降解。 (C)2015 Elsevier Ltd.保留所有权利。

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