Morphological investigations of disulfonated poly(arylene ether sulfone)-b-naphthalene dianhydride-based polyimide multiblock copolymers as potential high temperature proton exchange membranes

被引:35
作者
Badami, Anand S. [1 ]
Roy, Abhishek [1 ]
Lee, Hae-Seung [1 ]
Li, Yanxiang [1 ]
McGrath, James E. [1 ]
机构
[1] Virginia Polytech Inst & State Univ, Dept Chem, Macromol Sci & Engn Program, Macromol & Interfaces Inst, Blacksburg, VA 24061 USA
基金
美国国家科学基金会;
关键词
Proton exchange membrane; Sulfonated polymers; High temperature; Hot stage atomic force microscopy; Water desorption; POLYMER ELECTROLYTE MEMBRANES; PERFLUOROSULFONATE IONOMERS; SULFONE) COPOLYMERS; FUEL-CELL; NAFION; 100-DEGREES-C; STATE; WATER;
D O I
10.1016/j.memsci.2008.12.007
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
A major goal of current proton exchange membrane fuel cell research involves developing high temperature membranes that can operate at similar to 120 degrees C and low humidities. Multiblock copolymers synthesized from 100% disulfonated poly(arylene ether sulfone) (BPSH100) and naphthalene polyimide (PI) oligomers may be an alternative. The high temperature behavior of BPSH100-PI multiblock copolymers was evaluated in terms of morphology and water retention and compared to that of BPSH-based random copolymers, Nafion 112, and new recast Nafion (NRE211). Atomic force microscopy (AFM) performed at elevated temperatures with a hot stage demonstrated that at block lengths of similar to 15 kg/mol the multiblock copolymers displayed no morphological changes up to 120 degrees C or even higher. Water desorption was observed to decrease with increasing block length. The copolymers exhibited little to no water loss during a 200 degrees C isotherm in contrast to random BPSH copolymers and Nafion. A BPSH100-PI multiblock copolymer with large block length appears to have morphological stability and retain water (likely strongly bound) at temperatures exceeding 120 degrees C, suggesting its candidacy as a high temperature PEM. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:156 / 164
页数:9
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