Phosphoric acid doped sulfonated poly(tetra phenyl isoquinoline ether sulfone) copolymers for high temperature proton exchange membrane potential application

被引:5
|
作者
Seo, Dong Wan [1 ]
Lim, Young Don [1 ]
Hossain, Mohammad Awlad [1 ]
Lee, Soon Ho [1 ]
Lee, Hyun Chul [1 ]
Jang, Ho Hyoun [1 ]
Islam, Md Monirul [1 ]
Kim, Whan Gi [1 ]
机构
[1] Konkuk Univ, Dept Appl Chem, Chungju 380701, Chungbuk, South Korea
基金
新加坡国家研究基金会;
关键词
Fuel cells; Proton exchange membrane; Phosphoric acid; Doping; Proton conductivity; Polymer electrolyte membrane; POLYMER ELECTROLYTE MEMBRANES; FUEL-CELL APPLICATIONS; POLY(ETHER KETONE)S; PHYSICAL-PROPERTIES; POLYBENZIMIDAZOLE; CONDUCTIVITY; WATER;
D O I
10.1016/j.ijhydene.2012.05.162
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
Phosphoric acid-doped sulfonated poly(tetra phenyl isoquinoline ether sulfone)s (PA-SPTPIESs) were successfully synthesized for high temperature proton exchange membrane. Poly(tetra phenyl ether ketone sulfone)s (PTPEKS) were prepared from 1,2-bis(4-fluorobenzoyl)-3,4,5,6-tetraphenyl benzene (BFBTPB) and bis(4-fluorohenyl) sulfone with bis(4-hydroxyphenyl) sulfone. The synthesis of the poly(tetra phenyl isoquinoline ether sulfone)s (PTPIESs), was carried out via an intramolecular ring-closure reaction of dibenzoylbenzene of PTPEKS with benzylamine. The sulfonated poly(tetra phenyl isoquinoline ether sulfone)s (SPTPIESs) were obtained by following sulfonation with concentrated sulfuric acid and doped by phosphoric acid. Different contents of sulfonated unit on PTPIESs (8, 12, 16 mol% of BFBTPB) and PA-SPTPIESs were studied by FT-IR, H-1 NMR spectroscopy, and thermogravimetric analysis (TGA). Strong acid-base interaction effect between poly benzisoquinoline (PBI) and sulfonic acid groups formed ionic crosslinking network between polymer chains. The ion exchange capacity (IEC) and proton conductivity of PA-SPTPIESs were evaluated with degree of sulfonation and doping of phosphoric acid. Copyright (c) 2012, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:667 / 674
页数:8
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