Constructing a rigid crosslinked structure for enhanced conductivity of imidazolium functionalized polysulfone hydroxide exchange membrane

被引:37
作者
Dai, Jian [1 ]
He, Gaohong [1 ,2 ]
Ruan, Xuehua [1 ]
Zheng, Wenji [1 ]
Pan, Yu [1 ]
Yan, Xiaoming [1 ,2 ]
机构
[1] Dalian Univ Technol, Sch Petr & Chem Engn, State Key Lab Fine Chem, 2 Dagong Rd, Panjin 124221, LN, Peoples R China
[2] Dalian Univ Technol, Res & Dev Ctr Membrane Sci & Technol, Sch Chem Engn, State Key Lab Fine Chem, 2 Linggong Rd, Dalian 116024, Peoples R China
基金
中国国家自然科学基金;
关键词
Anion exchange membrane; Fuel cell; Imidazolium; Crosslink; ALKALINE POLYMER ELECTROLYTE; FUEL-CELLS; POLY(VINYLBENZYL CHLORIDE); ETHER SULFONE); WATER-UPTAKE; STABILITY; TRANSPORT; CATIONS; LINKING; AEMS;
D O I
10.1016/j.ijhydene.2016.04.059
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
A series of novel bis-imidazolium crosslinked polysulfone membranes (CL-PSf-ImOHs) membranes were prepared through simultaneous quaternization and crosslinking reactions of 4,4'-bis(2-methylimidazole-1-ylmethyl)diphenyl (bis-Im-diPh) and chloromethyl groups on the polymer during the membrane formation. The novel bis-Im-diPh crosslinker possesses a rigid bis-phenyl structure, which creates large free volume and leads to the formation of continuous hydroxide conducting channels in the membrane as demonstrated by TEM. The properties of the crosslinked membrane were controlled by varying the molar ratio (Rats) of bis-Im-diPh and chloromethyl groups from 0.18 to 0.33. With increasing R-d/c, the swelling ratio decreases, and the hydroxide conductivity increases. The CL-PSf-ImOH membrane with R-d/c of 0.33 exhibits the conductivity of 112 mS cm(-1) at 60 degrees C, much higher than that of non-crosslinked membrane (83 mS cm(-1), losing its morphology at 60 degrees C) and those of other crosslinked membranes (17-68 mS cm(-1)) prepared with the similar methods. In addition, the CL-PSf-ImOH membranes show good dimensional stability at elevated temperatures. (C) 2016 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:10923 / 10934
页数:12
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