张守海

个人信息Personal Information

教授

博士生导师

硕士生导师

性别:男

毕业院校:大连理工大学

学位:博士

所在单位:化工学院

学科:高分子材料. 高分子化学与物理. 膜科学与技术

联系方式:0411-84986107

电子邮箱:zhangshh@dlut.edu.cn

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Functionalized 4-phenyl phthalazinone-based polybenzimidazoles for high-temperature PEMFC

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论文类型:期刊论文

发表时间:2013-09-01

发表刊物:JOURNAL OF MEMBRANE SCIENCE

收录刊物:SCIE、EI、Scopus

卷号:442

页面范围:160-167

ISSN号:0376-7388

关键字:Functionalized polybenzimidazole; Phthalazinone; Proton exchange membrane; Acid doped

摘要:A series of novel polybenzimidazoles containing 4-phenyl phthalazinone moieties and functional hydroxyl groups (PPBIOH) were synthesized from 4-(4-(4-(4-carboxyphenoxy)phenyl)-1-oxophthalazin-2(1H)-yl)benzoic acid (CPPBC), 2,5-dyhydroxyterephthalic acid (TPA-OH) and 3,3'-diaminobenzidine (DAB) in polyphosphoric acid (PPA). The resultant polymers showed good solubility in 98% H2SO4 and NMP. The inherent viscosities of the polymers in 98% H2SO4 at 25 degrees C were in the range of 0.33-2.10 dL/g, increasing obviously with decreasing hydroxyl content in the main chain. The corresponding acid doped membranes were prepared directly from the polymerization solution by the PPA process. The chemical structures of PPBIOH polymers and membranes were characterized by FT-IR. These membranes showed reasonable doping levels (10.1-12.2 mol H3PO4), high proton conductivities (0.10-0.21 S cm(-1) above 120 degrees C), good mechanical properties (stress of 1.7-2.9 MPa and strain of 28.1-68.0%) and high oxidative stability (breaking time in the range of 52-155 h). The structures of PPBIOH membranes were analyzed by the Wide-angle X-ray diffraction (WAXD) and polarized optical microscopy (POM). The WAXD and POM results indicate the acid doped PPBIOH membranes exhibit semi-crystalline character, from which the mechanism of proton conduction can be further investigated. The combination performance makes these PPBIOH membranes promising candidates for potential applications in high-temperature proton exchange membrane fuel cells (PEMFCs). (C) 2013 Elsevier B.V. All rights reserved.