A novel crosslinking strategy for preparing poly(vinyl alcohol)-based proton-conducting membranes with high sulfonation

被引:99
作者
Tsai, Chun-En [1 ]
Lin, Chi-Wen [2 ]
Hwang, Bing-Joe [1 ,3 ]
机构
[1] Natl Taiwan Univ Sci & Technol, Dept Chem Engn, Nanoelectrochem Lab, Taipei 106, Taiwan
[2] Natl Yunlin Univ Sci & Technol, Dept Chem Engn, Yunlin, Taiwan
[3] Natl Synchrotron Radiat Res Ctr, Hsinchu 300, Taiwan
关键词
Poly(vinyl alcohol); Proton-conducting membrane; Sulfonation; Two-step crosslinking process; SEMIINTERPENETRATING NETWORK; EXCHANGE MEMBRANES; METHANOL TRANSPORT; HYBRID MEMBRANES; POLYMER BLENDS; WATER; IR;
D O I
10.1016/j.jpowsour.2009.10.055
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
This study synthesizes poly(vinyl alcohol) (PVA)-based polymer electrolyte membranes by a two-step crosslinking process involving esterization and acetal ring formation reactions. This work also uses sulfosuccinic acid (SSA) as the first crosslinking agent to form an inter-crosslinked structure and a promoting sulfonating agent. Glutaraldehyde (GA) as the second crosslinking agent, reacts with the spare OH group of PVA and forms, not only a dense structure at the outer membrane surface, but also a hydrophobic protective layer. Compared with membranes prepared by a traditional one-step crosslinking process, membranes prepared by the two-step crosslinking process exhibit excellent dissolution resistance in water. The membranes become water-insoluble even at a molar ratio of SO3H/PVA-OH as high as 0.45. Moreover, the synthesized membranes also exhibit high proton conductivities and high methanol permeability resistance. The current study measures highest proton conductivity of 5.3 x 10(-2) S cm(-1) at room temperature from one of the synthesized membranes, higher than that of the Nafion (R) membrane. Methanol permeability of the synthesized membranes measures about 1 x 10(-1) cm(2) S-1, about one order of magnitude lower than that of the Nafion (R) membrane. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:2166 / 2173
页数:8
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