首页 | 本学科首页   官方微博 | 高级检索  
     

含羧基交联型质子交换膜的制备及其性能
引用本文:魏红,姜虹,倪蕾. 含羧基交联型质子交换膜的制备及其性能[J]. 应用化学, 2012, 29(12): 1428-1432. DOI: 10.3724/SP.J.1095.2013.20171
作者姓名:魏红  姜虹  倪蕾
作者单位:(北华大学化学与生物学院 吉林 132033)
摘    要:合成了一种含酯基的磺化聚合物,利用后水解的方法得到了含有羧基侧基的聚合物;将磺化聚合物与聚乙烯醇通过溶液共混,热处理后得到交联型的共混膜材料。 研究结果表明,膜材料的玻璃化转变温度(Tg)有明显的上升,证明了交联反应的发生;同时,膜的吸水率和溶胀率有一定的下降,力学性能和热稳定性也有一定的提升。 通过共价交联的方法,制备了综合性能优异的磺化聚芳醚质子交换膜材料。 在100 ℃,交联膜的质子传导率为0.072~0.065 S/cm,吸水率为51%~89%,溶胀率为19%~30%。

关 键 词:质子交换膜  交联   羧基  
收稿时间:2012-04-25
修稿时间:2012-08-27

Preparation and Performance of Crosslinked Proton Exchange Membranes Containing Carboxyl Group
WEI Hong , JIANG Hong , NI Lei. Preparation and Performance of Crosslinked Proton Exchange Membranes Containing Carboxyl Group[J]. Chinese Journal of Applied Chemistry, 2012, 29(12): 1428-1432. DOI: 10.3724/SP.J.1095.2013.20171
Authors:WEI Hong    JIANG Hong    NI Lei
Affiliation:(College of Chemistry and Biology,Beihua University,Jilin 132033,China)
Abstract:Excessive water swelling has been an important problem for proton exchange membranes materials, especially for sulfonated poly aryl ether ketone. In this article, a sulfonated polymer containing ester group was hydrolyzed to yield carboxylic side group on its side chain, then the polymer was blended with polyvinyl alcohol and heat-treated to obtain crosslinked blend membranes. The results showed that Tg of the crosslinked membrane was increased significantly suggesting the presence of crosslinking reaction in the polymers. At 100 ℃, the proton conductivity, water uptake and swelling ratio of the crosslinked membranes are in the ranges of 0.072~0.065 S/cm, 51%~89%, and 19%~30%, respectively. Both the water uptake and swelling rate of the membrane decreased in a certain degree. This method is promising for the preparation of sulfonated poly arylene ether based proton exchange membrane with improved overall performance.
Keywords:proton exchange membranes  crosslink  carboxyl group
本文献已被 万方数据 等数据库收录!
点击此处可从《应用化学》浏览原始摘要信息
点击此处可从《应用化学》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号