Characterization of cation-exchange membranes prepared from poly(vinyl alcohol) and poly(vinyl alcohol-b-styrene sulfonic acid)

被引:18
作者
Higa, Mitsuru [1 ]
Nishimura, Megumi [1 ]
Kinoshita, Kota [1 ]
Jikihara, Atsushi [1 ]
机构
[1] Yamaguchi Univ, Grad Sch Sci & Engn, Ube, Yamaguchi 7558611, Japan
关键词
Poly(vinyl alcohol); Cation-exchange membrane; Cross-linking conditions; Ionic transport property; Block copolymer; FUEL-CELL APPLICATIONS; POLYMER ELECTROLYTE MEMBRANES; IODINE-SULFUR PROCESS; PROTON CONDUCTIVITY; HYBRID MEMBRANES; METAL IONS; WATER; ELECTRODIALYSIS; TRANSPORT; COMPOSITE;
D O I
10.1016/j.ijhydene.2011.06.003
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
Block-type cation-exchange membranes (CEMs) have been prepared by blending poly(vinyl alcohol) (PVA) and the polyanion poly(vinyl alcohol-b-styrene sulfonic acid) at various molar percentages of cation-exchange groups to vinyl alcohol groups, C-pa, and by cross-linking the PVA chains with glutaraldehyde (GA) solution at various GA concentrations, C-GA. The characteristics of the block-type CEMs were compared with random-type CEMs prepared in a previous study from the random copolymer, poly(vinyl alcohol-co-2-acrylamido-2-methylpropane sulfonic acid). At equal molar percentages of the cation-exchange groups, the water content of the block-type CEMs was less than that of the random-type CEMs. The charge density of the block-type CEMs increased with increasing C-pa and reached a maximum value. Further, the maximum value of the charge density increased with increasing C-GA. The maximum charge density value of 1.3 mol/dm(3) was obtained for the block-type CEM with C-pa = 3.1 mol% and C-GA= 0.10 vol.%, which is almost two thirds of the value of a commercially available CEM [CMX: ASTOM Corp. Japan]. A comparison of the block-type and random-type CEMs with almost the same membrane resistance showed that the block-type CEMs had higher dynamic transport numbers than the random-type ones. The dynamic transport number and membrane resistance of the block-type CEM with C-pa = 4.0 mol% and C-GA = 0.10 vol.% were 0.96 and 4.9 Omega cm(2), respectively. Copyright (C) 2011, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:6161 / 6168
页数:8
相关论文
共 34 条
  • [1] Brandrup J, 1999, POLYM HDB, pV/14
  • [2] Sulfonated polyimides bearing benzimidazole groups for direct methanol fuel cell applications
    Chen, Kangcheng
    Hu, Zhaoxia
    Endo, Nobutaka
    Fang, Jianhua
    Higa, Mitsuru
    Okamoto, Ken-ichi
    [J]. JOURNAL OF MEMBRANE SCIENCE, 2010, 351 (1-2) : 214 - 221
  • [3] Control of the fixed charge distribution in an ion-exchange membrane via diffusion and the reaction rate of the monomer
    Choi, Eun-Young
    Bae, Byungchan
    Moon, Seung-Hyeon
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2007, 111 (23) : 6383 - 6390
  • [4] Electrospinning of hydroxyapatite fibrous mats
    Dai, Xiaoshu
    Shivkumar, Satya
    [J]. MATERIALS LETTERS, 2007, 61 (13) : 2735 - 2738
  • [5] Proton conductivity of phosphoric acid doped polybenzimidazole and its composites with inorganic proton conductors
    He, RH
    Li, QF
    Xiao, G
    Bjerrum, NJ
    [J]. JOURNAL OF MEMBRANE SCIENCE, 2003, 226 (1-2) : 169 - 184
  • [6] Alternative polymer systems for proton exchange membranes (PEMs)
    Hickner, MA
    Ghassemi, H
    Kim, YS
    Einsla, BR
    McGrath, JE
    [J]. CHEMICAL REVIEWS, 2004, 104 (10) : 4587 - 4611
  • [7] Design and preparation of a novel temperature-responsive ionic gel. 1. A fast and reversible temperature response in the charge density
    Higa, M
    Yamakawa, T
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (43) : 16703 - 16707
  • [8] Poly(vinyl alcohol)-based polymer electrolyte membranes for direct methanol fuel cells
    Higa, Mitsuru
    Sugita, Mikinori
    Maesowa, Shin-ichi
    Endo, Nobutaka
    [J]. ELECTROCHIMICA ACTA, 2010, 55 (04) : 1445 - 1449
  • [9] Improvement of the thermochemical water-splitting IS (iodine-sulfur) process by electro-electrodialysis
    Hwang, GJ
    Onuki, K
    Nomura, M
    Kasahara, S
    Kim, JW
    [J]. JOURNAL OF MEMBRANE SCIENCE, 2003, 220 (1-2) : 129 - 136
  • [10] Thermal efficiency evaluation of HI synthesis/concentration procedures in the thermochemical water splitting IS process
    Kasahara, S
    Kubo, SJ
    Onuki, K
    Nomura, M
    [J]. INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2004, 29 (06) : 579 - 587