Sulfonated PEEK-WC membranes for proton-exchange membrane fuel cell: Effect of the increasing level of sulfonation on electrochemical performances

被引:47
作者
Basile, Angelo
Paturzo, Luca
Iulianelli, Adolfo
Gatto, Irene
Passalacqua, Enza
机构
[1] Univ Calabria, Inst Membrane Technol, ITM, CNR, I-87030 Commenda Di Rende, Italy
[2] CNR, ITAE, Adv Technol Energy Inst, I-98126 Messina, Italy
关键词
PEEK-WC; sulfonation; fuel cell; hydrogen; proton-exchange membrane;
D O I
10.1016/j.memsci.2006.04.006
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Sulfonation of PEEK-WC powder (a glassy poly-ether ether ketone) has been performed at 80 degrees C for 3 h using H2SO4 cone. (96%). The degree of sulfonation varied from 15 to 40%, depending on the reaction time. The sulfonated polymers (S-PEEK-WC) were used to prepare dense membranes for possible fuel cell application. In particular, two membranes were prepared by solvent evaporation technique, using DMA as the solvent for the 2-and 3-h sulfonated polymers. The dense character of both membranes has been confirmed by SEM analysis. The chemical-physical characterization has showed an increasing water solubility of the sulfonated polymers with the increasing level of sulfonation: from 7 to 11% of weight loss at 80 degrees C in pure water. Despite this, a water uptake increase up to 15% has been found for the dense membranes at 80 degrees C. Furthermore, if compared with a commercial Nafion membrane, S-PEEK-WC membranes exhibit comparable electrochemical performances even if at higher temperature, especially the membrane prepared with the 3-h sulfonated polymer. A power density of 284 mW/cm(2) was obtained for S-PEEK-WC membrane at 120 degrees C in H-2/air fuel cell, slightly above the corresponding value found for Nation. At the same temperature, a Tafel slope of 70 mV was reached for the S-PEEK-WC membrane versus 100 mV for the Nation. Finally, the specific conductivity is about 1.7 x 10(-2) S/cm versus 1.4 x 10(-1) S/cm of the commercial Nation membrane. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:377 / 385
页数:9
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