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Thermally Rearranged Poly(benzoxazole-co-imide) Membranes with Superior Mechanical Strength for Gas Separation Obtained by Tuning Chain Rigidity

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dc.contributor.authorJo, Hye Jin-
dc.contributor.authorSoo, Chye Yang-
dc.contributor.authorDong, Guangxi-
dc.contributor.authorDo, Yu Seong-
dc.contributor.authorWang, Ho Hyun-
dc.contributor.authorLee, Moon Joo-
dc.contributor.authorQuay, Jeffery R.-
dc.contributor.authorMurphy, M. Keith-
dc.contributor.authorLee, Young Moo-
dc.date.accessioned2022-02-03T01:35:17Z-
dc.date.available2022-02-03T01:35:17Z-
dc.date.created2021-05-11-
dc.date.issued2015-04-
dc.identifier.issn0024-9297-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/133966-
dc.description.abstractThermally rearranged polybenzoxazoles (TR-PBO) are some of the most promising materials for gas separation because of their microporous and bimodal cavities that offer high gas transport performance. However, the brittleness of fully converted TR-PBO membranes has impeded their widespread industrial implementation. In this study, we prepared novel, thermally rearranged poly(benzoxazole-co-imide) membranes (TR-PBOI) with improved mechanical strength and good gas separation performance. These membranes are based on two commercially available TR-able diamines and two non-TR-able diamines with various compositions and different polymer rigidities. TR-PBOI membranes with the appropriate ratio of PBO and PI displayed a high fractional free volume and therefore exceptional gas separation properties (CO2 permeability over 300 barrer and CO2/N-2 ideal selectivity above 20); both these values were higher than those of the corresponding original TR-PBO membranes. Furthermore, a substantial improvement in the mechanical properties of TR-PBOI membranes relative to their TR-PBO counterparts was observed.-
dc.language영어-
dc.language.isoen-
dc.publisherAMER CHEMICAL SOC-
dc.titleThermally Rearranged Poly(benzoxazole-co-imide) Membranes with Superior Mechanical Strength for Gas Separation Obtained by Tuning Chain Rigidity-
dc.typeArticle-
dc.contributor.affiliatedAuthorLee, Young Moo-
dc.identifier.doi10.1021/acs.macromol.5b00413-
dc.identifier.scopusid2-s2.0-84927725473-
dc.identifier.wosid000353176900030-
dc.identifier.bibliographicCitationMACROMOLECULES, v.48, no.7, pp.2194 - 2202-
dc.relation.isPartOfMACROMOLECULES-
dc.citation.titleMACROMOLECULES-
dc.citation.volume48-
dc.citation.number7-
dc.citation.startPage2194-
dc.citation.endPage2202-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPolymer Science-
dc.relation.journalWebOfScienceCategoryPolymer Science-
dc.subject.keywordPlusPOSITION FUNCTIONAL-GROUP-
dc.subject.keywordPlusPRECURSOR SYNTHESIS ROUTE-
dc.subject.keywordPlusINTRINSIC MICROPOROSITY-
dc.subject.keywordPlusTROGERS BASE-
dc.subject.keywordPlusFREE-VOLUME-
dc.subject.keywordPlusTRANSPORT-PROPERTIES-
dc.subject.keywordPlusPOLYMER-
dc.subject.keywordPlusPERMEABILITY-
dc.subject.keywordPlusPOLYIMIDES-
dc.subject.keywordPlusPARAMETERS-
dc.identifier.urlhttps://pubs.acs.org/doi/10.1021/acs.macromol.5b00413-
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