Title of article :
Synthesis of novel sulfonated polybenzimidazole and preparation of cross-linked membranes for fuel cell application
Author/Authors :
Xu، نويسنده , , Hongjie and Chen، نويسنده , , Kangcheng and Guo، نويسنده , , Xiaoxia and Fang، نويسنده , , Jianhua and Yin، نويسنده , , Jie، نويسنده ,
Issue Information :
دوهفته نامه با شماره پیاپی سال 2007
Pages :
9
From page :
5556
To page :
5564
Abstract :
A novel sulfonated polybenzimidazole, sulfonated poly[2,2′-(p-oxydiphenylene)-5,5′-bibenzimidazole] (SOPBI), was successfully prepared by post-sulfonation reaction of the parent polymer, poly[2,2′-(p-oxydiphenylene)-5,5′-bibenzimidazole] (OPBI), using concentrated and fuming sulfuric acid as the sulfonating reagent at 80 °C, and the degree of sulfonation (DS) could be regulated by controlling the reaction conditions. No significant polymer degradation was observed in the post-sulfonation processes. Direct polymerization of 4,4′-dicarboxydiphenyl ether-2,2′-disulfonic acid disodium salt (DCDPEDS) and 3,3′-diaminobenzidine (DABz), however, resulted in insoluble gels either in polyphosphoric acid (PPA) or in phosphorus pentoxide/methanesulfonic acid (PPMA) in a ratio of 1:10 by weight reaction medium. The SOPBIs prepared by the post-sulfonation method showed good solubility in dimethyl sulfoxide (DMSO), high thermal stability, good film forming ability and excellent mechanical properties. Cross-linked SOPBI membranes were successfully prepared by thermal treatment of phosphoric acid-doped SOPBI membranes at 180 °C in vacuo for 20 h and the resulting cross-linked membranes showed much improved water stability and radical oxidative stability in comparison with the corresponding uncross-linked ones, while the proton conductivity did not change largely. Highly proton conductive (150 mS cm−1, 120 °C in water) and water stable SOPBI membrane was developed.
Keywords :
Sulfonated polybenzimidazole , Synthesis , Cross-linking
Journal title :
Polymer
Serial Year :
2007
Journal title :
Polymer
Record number :
1730666
Link To Document :
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