Synthesis and characterization of sulfonated poly(arylene ether) polyimide multiblock copolymers for proton exchange membranes

被引:55
作者
Lee, Hae-Seung [1 ]
Roy, Abhishek [1 ]
Badami, Anand S. [1 ]
McGrath, James E. [1 ]
机构
[1] Virginia Polytech Inst & State Univ, Macromol & Interfaces Inst, Macromol Sci & Engn Program, Blacksburg, VA 24061 USA
关键词
multiblock copolymer; sulfonated poly(arylene ether); polyimide; proton exchange membrane;
D O I
10.1007/BF03218768
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Novel multiblock copolymers, based on segmented sulfonated hydrophilic-hydrophobic blocks, were synthesized and investigated for their application as proton exchange membranes. A series of segmented sulfonated poly(arylene ether sulfone)-b-polyimide multiblock copolymers, with various block lengths, were synthesized via the coupling reaction between the terminal amine moieties on the hydrophilic blocks and naphthalene anhydride functionalized hydrophobic blocks. Successful imidization reactions required a mixed solvent system, comprised of NMP and m-cresol, in the presence of catalysts. Proton conductivity measurements revealed that the proton conductivity improved with increasing hydrophilic and hydrophobic block lengths. The morphological structure of the multiblock copolymers was investigated using tapping mode atomic force microscopy (TM-AFM). The AFM images of the copolymers demonstrated well-defined nanophase separated morphologies, with the changes in the block length having a pronounced effect on the phase separated morphologies of the system. The self diffusion coefficient of water, as measured by H-1 NMR, provided a better understanding of the transport process. Thus, the block copolymers showed higher values than Nation, and comparable proton conductivities in liquid water, as well as under partially hydrated conditions at 80 degrees C. The new materials are strong candidates for use in PEM systems.
引用
收藏
页码:160 / 166
页数:7
相关论文
共 15 条
[1]  
BADAMI AS, 2006, PREPR PAP AM CHEM SO, V51, P612
[2]   Sulfonated naphthalene dianhydride based polyimide copolymers for proton-exchange-membrane fuel cells II. Membrane properties and fuel cell performance [J].
Einsla, BR ;
Kim, YS ;
Hickner, MA ;
Hong, YT ;
Hill, ML ;
Pivovar, BS ;
McGrath, JE .
JOURNAL OF MEMBRANE SCIENCE, 2005, 255 (1-2) :141-148
[3]   Sulfonated naphthalene dianhydride based polyimide copolymers for proton-exchange-membrane fuel cells. I. Monomer and copolymer synthesis [J].
Einsla, BR ;
Hong, YT ;
Kim, YS ;
Wang, F ;
Gunduz, N ;
Mcgrath, JE .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2004, 42 (04) :862-874
[4]   Soluble sulfonated naphthalenic polyimides as materials for proton exchange membranes [J].
Genies, C ;
Mercier, R ;
Sillion, B ;
Cornet, N ;
Gebel, G ;
Pineri, M .
POLYMER, 2001, 42 (02) :359-373
[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]   Novel sulfonated polyimides as polyelectrolytes for fuel cell application. 2. Synthesis and proton conductivity, of polyimides from 9,9-bis(4-aminophenyl)fluorene-2,7-disulfonic acid [J].
Guo, XX ;
Fang, JH ;
Watari, T ;
Tanaka, K ;
Kita, H ;
Okamoto, KI .
MACROMOLECULES, 2002, 35 (17) :6707-6713
[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 and properties of novel sulfonated (co)polyimides bearing sulfonated aromatic pendant groups for PEFC applications [J].
Hu, ZX ;
Yin, Y ;
Chen, SW ;
Yamada, O ;
Tanaka, K ;
Kita, H ;
Okamoto, K .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2006, 44 (09) :2862-2872
[9]  
NOSHAY A, 1977, BLOCK COPOLYMERS OVE, P91
[10]  
ROY A, 2006, PREPR PAP AM CHEM SO, V51, P660