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Influence of adjusted hydrophilic-hydrophobic lengths in sulfonated multiblock copoly(ether sulfone) membranes for fuel cell application
Sulfonated multiblock copoly(ether sulfone)s applicable to proton exchange membrane fuel cells (PEMFCs) were synthesized by the coupling reaction of the hydroxyl-terminated hydrophilic and hydrophobic oligomers with different lengths in the presence of highly reactive decafluorobiphenyl (DFB) as a c...
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Published in: | Journal of polymer science. Part A, Polymer chemistry Polymer chemistry, 2008-11, Vol.46 (22), p.7332-7341 |
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container_title | Journal of polymer science. Part A, Polymer chemistry |
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creator | Nakabayashi, Kazuhiro Matsumoto, Kazuya Higashihara, Tomoya Ueda, Mitsuru |
description | Sulfonated multiblock copoly(ether sulfone)s applicable to proton exchange membrane fuel cells (PEMFCs) were synthesized by the coupling reaction of the hydroxyl-terminated hydrophilic and hydrophobic oligomers with different lengths in the presence of highly reactive decafluorobiphenyl (DFB) as a chain extender to investigate the influence of each length on the membranes' properties, such as water uptake, proton conductivity, and morphology. Multiblock copolymers with high molecular weights (Mn > 50,000, Mw > 150,000) were obtained under mild reaction conditions. The resulting membranes demonstrated good oxidative stability for hot Fenton's reagent and maintained high water uptake (7.3-18.7 wt %) under a low relative humidity (50% RH). Proton conductivity of all membranes at 80 °C and 95% RH was higher than that of Nafion 117 membrane, and good proton conductivity of 7.0 x 10⁻³ S/cm was obtained at 80 °C and 50% RH by optimizing the oligomer lengths. The surface morphology of the membranes was investigated by tapping mode atomic force microscopy (AFM), which showed that the multiblock copolymer membranes had a clearer surface hydrophilic/hydrophobic-separated structure than that of the random copolymer, and contributed to good and effective proton conduction. |
doi_str_mv | 10.1002/pola.23038 |
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Multiblock copolymers with high molecular weights (Mn > 50,000, Mw > 150,000) were obtained under mild reaction conditions. The resulting membranes demonstrated good oxidative stability for hot Fenton's reagent and maintained high water uptake (7.3-18.7 wt %) under a low relative humidity (50% RH). Proton conductivity of all membranes at 80 °C and 95% RH was higher than that of Nafion 117 membrane, and good proton conductivity of 7.0 x 10⁻³ S/cm was obtained at 80 °C and 50% RH by optimizing the oligomer lengths. The surface morphology of the membranes was investigated by tapping mode atomic force microscopy (AFM), which showed that the multiblock copolymer membranes had a clearer surface hydrophilic/hydrophobic-separated structure than that of the random copolymer, and contributed to good and effective proton conduction.</description><identifier>ISSN: 0887-624X</identifier><identifier>EISSN: 1099-0518</identifier><identifier>DOI: 10.1002/pola.23038</identifier><identifier>CODEN: JPLCAT</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Applied sciences ; atomic force microscopy ; Exact sciences and technology ; Exchange resins and membranes ; Forms of application and semi-finished materials ; morphology ; multiblock copolymers ; Organic polymers ; Physicochemistry of polymers ; poly(ether sulfone) ; Polymer industry, paints, wood ; Polymers with particular properties ; Preparation, kinetics, thermodynamics, mechanism and catalysts ; proton conductivity ; proton exchange membrane fuel cells ; Technology of polymers ; transmission electron microscopy</subject><ispartof>Journal of polymer science. 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Part A, Polymer chemistry</title><addtitle>J. Polym. Sci. A Polym. Chem</addtitle><description>Sulfonated multiblock copoly(ether sulfone)s applicable to proton exchange membrane fuel cells (PEMFCs) were synthesized by the coupling reaction of the hydroxyl-terminated hydrophilic and hydrophobic oligomers with different lengths in the presence of highly reactive decafluorobiphenyl (DFB) as a chain extender to investigate the influence of each length on the membranes' properties, such as water uptake, proton conductivity, and morphology. Multiblock copolymers with high molecular weights (Mn > 50,000, Mw > 150,000) were obtained under mild reaction conditions. The resulting membranes demonstrated good oxidative stability for hot Fenton's reagent and maintained high water uptake (7.3-18.7 wt %) under a low relative humidity (50% RH). Proton conductivity of all membranes at 80 °C and 95% RH was higher than that of Nafion 117 membrane, and good proton conductivity of 7.0 x 10⁻³ S/cm was obtained at 80 °C and 50% RH by optimizing the oligomer lengths. 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Proton conductivity of all membranes at 80 °C and 95% RH was higher than that of Nafion 117 membrane, and good proton conductivity of 7.0 x 10⁻³ S/cm was obtained at 80 °C and 50% RH by optimizing the oligomer lengths. The surface morphology of the membranes was investigated by tapping mode atomic force microscopy (AFM), which showed that the multiblock copolymer membranes had a clearer surface hydrophilic/hydrophobic-separated structure than that of the random copolymer, and contributed to good and effective proton conduction.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><doi>10.1002/pola.23038</doi><tpages>10</tpages></addata></record> |
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subjects | Applied sciences atomic force microscopy Exact sciences and technology Exchange resins and membranes Forms of application and semi-finished materials morphology multiblock copolymers Organic polymers Physicochemistry of polymers poly(ether sulfone) Polymer industry, paints, wood Polymers with particular properties Preparation, kinetics, thermodynamics, mechanism and catalysts proton conductivity proton exchange membrane fuel cells Technology of polymers transmission electron microscopy |
title | Influence of adjusted hydrophilic-hydrophobic lengths in sulfonated multiblock copoly(ether sulfone) membranes for fuel cell application |
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