Preparation and properties of sulfonated poly(phenylene arylene)/sulfonated polyimide (SPA/SPI) blend membranes for polymer electrolyte membrane fuel cell applications

被引:42
|
作者
Zhang, Xuan [1 ]
Chen, Shanshan [1 ]
Liu, Jianmei [1 ]
Hu, Zhaoxia [1 ]
Chen, Shouwen [1 ]
Wang, Lianjun [1 ]
机构
[1] Nanjing Univ Sci & Technol, Sch Environm & Biol Engn, Nanjing 210094, Jiangsu, Peoples R China
关键词
Sulfonated poly(phenylene arylene)s; Sulfonated polyimide; Polymer electrolyte membrane; Fuel cell; Blend membrane; PROTON-EXCHANGE MEMBRANES; WATER STABILITY; ETHER KETONE); SIDE-GROUPS; CONDUCTIVITY; ACID; COPOLYMERIZATION;
D O I
10.1016/j.memsci.2011.01.054
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
A novel series of sulfonated poly( phenylene arylene)s (SPAs) were successfully synthesized from 2,5-dichloro-3'-sulfobenzophenone (DCSB) and 2,2'-bis[4-(4-chlorobenzoyl)]phenoxyl perfluoropropane (BCPPF) by Ni(0)-catalyzed coupling polymerization, and subsequently used as the start materials to prepare blend membranes with sulfonated polyimide (SPI) for polymer electrolyte membrane fuel cell (PEMFC) applications. The miscible structure of the prepared blend membranes was confirmed by scanning electron microscopy (SEM). The properties required for a PEM such as ion exchange capacity, water uptake, solution uptake and dimensional change and/or in water or methanol solutions, proton conductivity and hydrolytic stability were investigated in details. The obtained blend SPA/SPI membranes showed rather high proton conductivities in both the plane and the thickness direction of the membrane. They exhibited slightly anisotropic proton conductivity in water with sigma(perpendicular to/II) values in the range of 0.85-0.90, irrespective of the introduction of SPI (sigma(perpendicular to/II) = 0.73). They also showed significantly enhanced stability in water and methanol solutions compared with the corresponding SPA membranes. All the results indicated that this type of blend membranes were quite promising candidates for PEMFC applications. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:276 / 285
页数:10
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