Controllable sulfonation of aromatic poly(arylene ether ketone)s containing different pendant phenyl rings

被引:15
作者
Li, Zhiliang [1 ]
Liu, Xincai [1 ]
Chao, Danming [1 ]
Zhang, Wanjin [1 ]
机构
[1] Jilin Univ, Alan G MacDiarmid Inst, Changchun 130012, Peoples R China
关键词
Proton exchange membrane; Proton conductivity; Direct methanol fuel cell; PROTON-EXCHANGE MEMBRANES; POLY(ETHER KETONE)S; COMPOSITE MEMBRANES; POLYIMIDES; COPOLYMERS; SULFONE);
D O I
10.1016/j.jpowsour.2009.04.009
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
The sulfonation selectivity of various pendant phenyl groups in poly(arylene ether ketone) (Ph-3F-PAEK) is invested via the postsulfonation approach. The sulfonated Ph-3F-PAEKs with different degrees of sulfonation (DS) are quantitatively synthesized by controlling the length of the segments that cannot be sulfonated. In this study, H-1 NMR and FT-IR are used to confirmed the structures of the polymers and the experimentally DS values were calculated by H-1 NMR. The experimentally observed DSs are corresponding to the theoretical values expected from the monomer ratios. All the sulfonated membranes have excellent mechanical properties (with a Young's modulus > 13 GPa, a tensile strength > 55 MPa and the elongation > 10%). Thermogravimetric analysis (TGA) is used to characterized the thermal stability of these polymers, and all the polymers show excellent thermal properties at high temperatures. The methanol permeability values of Ph-3F-SPAEKs in the range of 0.37 x 10(-7) cm(2) s(-1) to 4.12 x 10(-7) cm(2) s(-1) are much lower than that of Nafion (R) 117 (1.55 x 10(-6) cm(2) s(-1)). It should be noted that the polymer with highest DS, Ph-3F-SPAEK-100 with an ion exchange capacity of 2.16 mequiv.g(-1), exhibits high proton conductivity of 0.187 S cm(-1) at 80 degrees C, which is also higher than that of Nafion (R) 117. (c) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:477 / 482
页数:6
相关论文
共 28 条
[11]   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
[12]   Proton-conducting polymers derived from poly(ether-etherketone) and poly(4-phenoxybenzoyl-1,4-phenylene) [J].
Kobayashi, T ;
Rikukawa, M ;
Sanui, K ;
Ogata, N .
SOLID STATE IONICS, 1998, 106 (3-4) :219-225
[13]   On the development of proton conducting polymer membranes for hydrogen and methanol fuel cells [J].
Kreuer, KD .
JOURNAL OF MEMBRANE SCIENCE, 2001, 185 (01) :29-39
[14]   Proton conducting polysulfone ionomers carrying sulfoaryloxybenzoyl side chains [J].
Lafitte, B ;
Puchner, M ;
Jannasch, P .
MACROMOLECULAR RAPID COMMUNICATIONS, 2005, 26 (18) :1464-1468
[15]  
Lafitte B, 2002, MACROMOL RAPID COMM, V23, P896, DOI 10.1002/1521-3927(20021001)23:15<896::AID-MARC896>3.0.CO
[16]  
2-P
[17]   A novel bisphenol monomer with grafting capability and the resulting poly(arylene ether sulfone)s [J].
Li, Zhao ;
Ding, Jianfu ;
Robertson, Gilles P. ;
Guiver, Michael D. .
MACROMOLECULES, 2006, 39 (20) :6990-6996
[18]   Aromatic poly(ether ketone)s with pendant sulfonic acid phenyl groups prepared by a mild sulfonation method for proton exchange membranes [J].
Liu, Baijun ;
Robertson, Gilles P. ;
Kim, Dae-Sik ;
Guiver, Michael D. ;
Hu, Wei ;
Jiang, Zhenhua .
MACROMOLECULES, 2007, 40 (06) :1934-1944
[19]   Soluble aromatic poly(ether ketone)s with a pendant 3,5-ditrifluoromethylphenyl group [J].
Liu, BJ ;
Hu, W ;
Chen, CH ;
Jiang, ZH ;
Zhang, WJ ;
Wu, ZW ;
Matsumoto, T .
POLYMER, 2004, 45 (10) :3241-3247
[20]   Poly(aryl ether ketone)s with (3-methyl)phenyl and (3-trifluoromethyl)phenyl side groups [J].
Liu, BJ ;
Wang, GB ;
Hu, W ;
Jin, YH ;
Chen, CH ;
Jiang, ZH ;
Zhang, WJ ;
Wu, ZW ;
Wei, Y .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2002, 40 (20) :3392-3398