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Tuning microcavities in thermally rearranged polymer membranes for CO2 capture

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dc.contributor.authorHan, Sang Hoon-
dc.contributor.authorKwon, Hye Jin-
dc.contributor.authorKim, Keun Young-
dc.contributor.authorSeong, Jong Geun-
dc.contributor.authorPark, Chi Hoon-
dc.contributor.authorKim, Seungju-
dc.contributor.authorDoherty, Cara M.-
dc.contributor.authorThornton, Aaron W.-
dc.contributor.authorHill, Anita J.-
dc.contributor.authorLozano, Angel E.-
dc.contributor.authorBerchtoldf, Kathryn A.-
dc.contributor.authorLee, Young Moo-
dc.date.accessioned2022-02-03T01:37:40Z-
dc.date.available2022-02-03T01:37:40Z-
dc.date.created2021-05-11-
dc.date.issued2012-04-
dc.identifier.issn1463-9076-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/134017-
dc.description.abstractMicroporous materials have a great importance in catalysis, delivery, storage and separation in terms of their performance and efficiency. Most microporous materials are comprised of inorganic frameworks, while thermally rearranged (TR) polymers are a microporous organic polymer which is tuned to optimize the cavity sizes and distribution for difficult separation applications. The sub-nano sized microcavities are controlled by in situ thermal treatment conditions which have been investigated by positron annihilation lifetime spectroscopy (PALS). The size and relative number of cavities increased from room temperature to 230 degrees C resulting in improvements in both permeabilities and selectivities for H-2/CO2 separation due to the significant increase of gas diffusion and decrease of CO2 solubility. The highest performance of the well-tuned TR-polymer membrane was 206 Barrer for H-2 permeability and 6.2 of H-2/CO2 selectivity, exceeding the polymeric upper bound for gas separation membranes.-
dc.language영어-
dc.language.isoen-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleTuning microcavities in thermally rearranged polymer membranes for CO2 capture-
dc.typeArticle-
dc.contributor.affiliatedAuthorLee, Young Moo-
dc.identifier.doi10.1039/c2cp23729f-
dc.identifier.scopusid2-s2.0-84863338295-
dc.identifier.wosid000301235200009-
dc.identifier.bibliographicCitationPHYSICAL CHEMISTRY CHEMICAL PHYSICS, v.14, no.13, pp.4365 - 4373-
dc.relation.isPartOfPHYSICAL CHEMISTRY CHEMICAL PHYSICS-
dc.citation.titlePHYSICAL CHEMISTRY CHEMICAL PHYSICS-
dc.citation.volume14-
dc.citation.number13-
dc.citation.startPage4365-
dc.citation.endPage4373-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaPhysics-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryPhysics, Atomic, Molecular & Chemical-
dc.subject.keywordPlusPOSITRON-ANNIHILATION LIFETIME-
dc.subject.keywordPlusMETAL-ORGANIC FRAMEWORKS-
dc.subject.keywordPlusFREE-VOLUME DISTRIBUTION-
dc.subject.keywordPlusHYDROGEN STORAGE-
dc.subject.keywordPlusGAS SEPARATION-
dc.subject.keywordPlusINTRINSIC MICROPOROSITY-
dc.subject.keywordPlusTEMPERATURE-DEPENDENCE-
dc.subject.keywordPlusCARBON-DIOXIDE-
dc.subject.keywordPlusTRANSPORT-
dc.subject.keywordPlusPOLYBENZOXAZOLE-
dc.identifier.urlhttps://pubs.rsc.org/en/content/articlelanding/2012/CP/c2cp23729f-
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