Synthesis and characterization of poly(arylene ether sulfone) copolymers with sulfonimide side groups for a proton-exchange membrane

被引:47
作者
Cho, Chang Gi
Kim, Yu Seung
Yu, Xiang
Hill, Melinda
McGrath, James E. [1 ]
机构
[1] Hanyang Univ, Ctr Adv Funct Polymers, Seoul 133791, South Korea
[2] Los Alamos Natl Lab, MPA11, Los Alamos, NM 87545 USA
[3] Virginia Tech, Dept Chem & Macromol, Blacksburg, VA 24061 USA
[4] Virginia Tech, Interfaces Inst, Blacksburg, VA 24061 USA
关键词
electrochemistry; fuel cells; membrane; poly(arylene ether sulfone); poly(ether sulfones); proton conductivity; proton-exchange membranes; sulfonimides;
D O I
10.1002/pola.21565
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A sulfonimide-containing comonomer derived from 4,4 '-dichlorodiphenylsulfone was synthesized and copolymerized with 4,4 '-dichlorodiphenylsulfone and 4,4 '-biphenol to prepare sulfonimide-containing poly(arylene ether sulfone) random copolymers (BPSIs). These copolymers showed slightly higher water uptake than disulfonated poly(arylene ether sulfone) copolymer (BPSH) controls, but their proton-conductivity values were very comparable to those of the BPSH series with similar ion contents. The proton conductivity increased with the temperature for both systems. For samples with 30 mol % ionic groups, BPSI showed less temperature dependence in proton conductivity and slightly higher methanol permeability in comparison with BPSH. The thermal characterization of the suffortimide copolymers showed that both the acid and salt forms were stable up to 250 degrees C under a nitrogen atmosphere. The results suggested that the presumed enhanced stability of the sulfonimide systems did not translate into higher protonic conductivity in liquid water. (c) 2006 Wiley Periodicals, Inc.
引用
收藏
页码:6007 / 6014
页数:8
相关论文
共 27 条
[1]   CHLOROSULFONATION OF SOME DIPHENYL DERIVATIVES [J].
CREMLYN, R ;
MONTGOMERY, S ;
NG, Y ;
SIMPSON, D .
PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS, 1982, 12 (03) :341-352
[2]   NOVEL PERFLUORINATED IONOMERS AND IONENES [J].
DESMARTEAU, DD .
JOURNAL OF FLUORINE CHEMISTRY, 1995, 72 (02) :203-208
[3]   Novel aromatic polymers with pendant lithium perfluoroalkylsulfonate or sulfonimide groups [J].
Feiring, AE ;
Choi, SK ;
Doyle, M ;
Wonchoba, ER .
MACROMOLECULES, 2000, 33 (25) :9262-9271
[4]   Aromatic monomers with pendant fluoroalkylsulfonate and sulfonimide groups [J].
Feiring, AE ;
Wonchoba, ER .
JOURNAL OF FLUORINE CHEMISTRY, 2000, 105 (01) :129-135
[5]   Stability study of sulfonated phthalic and naphthalenic polyimide structures in aqueous medium [J].
Genies, C ;
Mercier, R ;
Sillion, B ;
Petiaud, R ;
Cornet, N ;
Gebel, G ;
Pineri, M .
POLYMER, 2001, 42 (12) :5097-5105
[6]   STERIC EFFECTS IN THE INTRAMOLECULAR CARBOXYL-CATALYZED HYDROLYSIS OF SULFONAMIDES - ABINITIO QUANTUM CHEMICAL STUDIES OF THE PENTA-COORDINATED SULFUR INTERMEDIATE [J].
GRAAFLAND, T ;
NIEUWPOORT, WC ;
ENGBERTS, JBFN .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1981, 103 (15) :4490-4494
[7]   Alternative polymer systems for proton exchange membranes (PEMs) [J].
Hickner, MA ;
Ghassemi, H ;
Kim, YS ;
Einsla, BR ;
McGrath, JE .
CHEMICAL REVIEWS, 2004, 104 (10) :4587-4611
[8]   Synthesis of polyphosphazenes with sulfonimide side groups [J].
Hofmann, MA ;
Ambler, CM ;
Maher, AE ;
Chalkova, E ;
Zhou, XYY ;
Lvov, SN ;
Allcock, HR .
MACROMOLECULES, 2002, 35 (17) :6490-6493
[9]   Effect of acidification treatment and morphological stability of sulfonated poly(arylene ether sulfone) copolymer proton-exchange membranes for fuel-cell use above 100 °C [J].
Kim, YS ;
Wang, F ;
Hickner, M ;
McCartney, S ;
Hong, YT ;
Harrison, W ;
Zawodzinski, TA ;
McGrath, JE .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 2003, 41 (22) :2816-2828
[10]   Sulfonated poly(arylene ether sulfone) copolymer proton exchange membranes: composition and morphology effects on the methanol permeability [J].
Kim, YS ;
Hickner, MA ;
Dong, LM ;
Pivovar, BS ;
McGrath, JE .
JOURNAL OF MEMBRANE SCIENCE, 2004, 243 (1-2) :317-326