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Novel sulfonated poly(arylene ether ketone) containing benzoxazole membranes for proton exchange membrane fuel cell

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dc.contributor.authorLi, Jinhuan-
dc.contributor.authorLee, Chang Hyun-
dc.contributor.authorPark, Ho Bum-
dc.contributor.authorLee, Young Moo-
dc.date.accessioned2022-12-21T10:44:40Z-
dc.date.available2022-12-21T10:44:40Z-
dc.date.issued2006-08-
dc.identifier.issn1598-5032-
dc.identifier.issn2092-7673-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/181145-
dc.description.abstractNovel sulfonated poly(aryl ether ketones) containing benzoxazole were directly synthesized by aromatic nucleophilic polycondensation using various ratios of 2,2'-bi[2-(4-flurophenyl)benzoxazol-6-yl]hexafluoropropane to sodium 5,5'-carbonylbis(2-fluorobenzenesulfonate). The copolymers were soluble in polar aprotic solvents such as N-methyl-2-pyrrolidone, N,N-dimethylacetamide, and N,N-dimethylformamide at a relatively high solid composition (> 15 wt%) and formed tough, flexible and transparent membranes. The membranes exhibited a degradation temperature of above 290 degrees C. The exact dissolution times of these membranes at 80 degrees C in Fenton's reagent (3 wt% H2O2 containing 2 ppm FeSO4) were undetectable, confirming their excellent chemical stability in fuel cell application. The membranes showed a moderate increase in water uptake with respect to increasing temperature. The proton conductivities of the membranes were dependent on the composition and ranged from 1.10 X 10(-2) to 5.50x 10(-2) Scm(-1) at 80 degrees C and 95% relative humidity (RH). At 120 degrees C without externally humidified conditions, the conductivities increased above 10(-2) Scm(-1) with respect to increasing benzoxazole content, which suggested that the benzoxazole moieties contributed to the proton conduction.-
dc.format.extent5-
dc.language영어-
dc.language.isoENG-
dc.publisher한국고분자학회-
dc.titleNovel sulfonated poly(arylene ether ketone) containing benzoxazole membranes for proton exchange membrane fuel cell-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.1007/BF03219107-
dc.identifier.scopusid2-s2.0-33748784616-
dc.identifier.wosid000240423300007-
dc.identifier.bibliographicCitationMacromolecular Research, v.14, no.4, pp 438 - 442-
dc.citation.titleMacromolecular Research-
dc.citation.volume14-
dc.citation.number4-
dc.citation.startPage438-
dc.citation.endPage442-
dc.type.docTypeArticle-
dc.identifier.kciidART001022396-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaPolymer Science-
dc.relation.journalWebOfScienceCategoryPolymer Science-
dc.subject.keywordPlusPOLYMER ELECTROLYTE MEMBRANES-
dc.subject.keywordPlusAROMATIC POLYBENZOXAZOLES-
dc.subject.keywordPlusTRANSPORT BEHAVIOR-
dc.subject.keywordPlusCONDUCTIVITY-
dc.subject.keywordPlusCOPOLYMERS-
dc.subject.keywordPlusALCOHOL)-
dc.subject.keywordPlusBLEND-
dc.subject.keywordPlusWATER-
dc.subject.keywordAuthorfuel cell-
dc.subject.keywordAuthormembrane-
dc.subject.keywordAuthorpoly(aryl ether ketone)-
dc.subject.keywordAuthorpolybenzoxazole-
dc.subject.keywordAuthorsulfonation-
dc.identifier.urlhttps://link.springer.com/article/10.1007/BF03219107-
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