A novel anion exchange membrane based on poly (2,6-dimethyl-1,4-phenylene oxide) with excellent alkaline stability for AEMFC

被引:25
作者
Liu, Qian [1 ]
Wang, Zhe [1 ,2 ]
Yu, Aijun [3 ]
Li, Jinsheng [1 ,2 ]
Shen, Hongcheng [1 ]
Wang, Hui [1 ]
Yang, Kai [1 ]
Zhang, Hongyu [1 ]
机构
[1] Changchun Univ Technol, Coll Chem Engn, Changchun 130012, Peoples R China
[2] Changchun Univ Technol, Adv Inst Mat Sci, Changchun 130012, Peoples R China
[3] Beijing Shougang Int Engn Technol Co Ltd, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
Anion exchange membrane; Ether bond; Polyphenylene oxide; Alkaline stability; FUEL-CELLS; SIDE-CHAIN; POLY(2,6-DIMETHYL-1,4-PHENYLENE OXIDE); DIMENSIONAL STABILITY; POLYPHENYLENE OXIDE; PROTON CONDUCTIVITY; HYDROXIDE SOLVATION; CHEMICAL-STABILITY; NAFION MEMBRANE; WATER;
D O I
10.1016/j.ijhydene.2021.05.004
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We report a novel comb-shaped anion exchange membrane based on poly (2,6-dimethyl-1,4-phenylene oxide) (PPO) and 4-(dimethylamino)butyraldehyde diethyl acetal (DABDA). The Menshutkin reaction successfully introduced DABDA into the brominated PPO backbone, which was proved through FT-IR and H-1 NMR. The distinct hydrophilic/hydrophobic microphase separation structure observed by transmission electron microscope (TEM). As the increase of grafting degree, so does the water uptake, swelling ratio, hydroxide conductivity and alkaline stability. The membranes also possess good mechanical property with tensile strength from 14.2 to 38.11 MPa. This is due to the increasing number of hydroxide and unique steric hindrance effect caused the higher water uptake and higher dimensional stability. Simultaneously, especially PPO/DABDA-60 in comb-shaped membranes demonstrate an excellent long-term alkali resistance stability. In a 576-h alkali resistance stability test, the retained ionic conductivity of the PPO/DABDA-60 membrane is 96% of the initial value. The PPO/DABDA-60 is a potential candidate material for AEM. (C) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:24328 / 24338
页数:11
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