Novel anhydrous composite membranes based on sulfonated poly (ether ketone) and aprotic ionic liquids for high temperature polymer electrolyte membranes for fuel cell applications

被引:31
|
作者
Malik, Rajender Singh [1 ,2 ]
Tripathi, Sandeep Nath [1 ]
Gupta, Deeksha [1 ]
Choudhary, Veena [1 ]
机构
[1] Indian Inst Technol Delhi, Ctr Polymer Sci & Engn, New Delhi 110016, India
[2] Deenbandhu Chhotu Ram Univ Sci & Technol Murthal, Dept Chem, Sonepat 131039, India
关键词
SPEK; Aprotic ionic liquid; Proton conductivity; Fuel cell; PROTON CONDUCTING MEMBRANES; OPERATION; ACID; SULFONE)-B-POLYBUTADIENE; POLYBENZIMIDAZOLE; TRANSPORT; HYDROGEN;
D O I
10.1016/j.ijhydene.2014.06.060
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
Novel composite membranes were prepared using imidazolium type aprotic ionic liquids and sulfonated poly (ether ketone) (SPEK) as polymer matrix by solution casting process. All the prepared membranes were characterized for their thermal stability, mechanical properties, ion exchange capacity, proton conductivity and leaching out of ionic liquids in presence of water. Ionic liquid based membranes were more flexible than neat SPEK membrane due to the plasticization effect of ionic liquids. The interactions and compatibility occurring among components were investigated by vibration spectroscopy (FTIR ATR) and scanning electron microscopy respectively. The thermal stability of composite membranes was higher than unmodified membranes. The ion conductivity of composite membranes under anhydrous conditions was found to be dependent on temperature, type and concentration of ionic liquid in SPEK matrix. Ion conductivities of composite membranes under anhydrous condition were found to be up to two orders (similar to 100 times) higher than neat SPEK membrane and it was found to be similar to 5 mS/cm at 140 degrees C for SPEK/OTf-70. These composite membranes can be successfully operated at temperatures ranging from 40 degrees C to 140 degrees C under anhydrous conditions. Copyright (C) 2014, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:12826 / 12834
页数:9
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