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Enhanced activity of CuO/ZnO catalyst on the decomposition of dimethylhexane-1,6-dicarbamate into dimethylhexane-1,6-diisocyanate

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dc.contributor.authorKim, Jinsung-
dc.contributor.authorJeong, Cheonwoo-
dc.contributor.authorLee, Jae-Hong-
dc.contributor.authorSuh, Young-Woong-
dc.date.accessioned2021-08-03T03:26:12Z-
dc.date.available2021-08-03T03:26:12Z-
dc.date.created2021-05-12-
dc.date.issued2018-06-
dc.identifier.issn0922-6168-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/32949-
dc.description.abstractTo decompose dimethylhexane-1,6-dicarbamate (HDC) to hexamethylene diisocyanate (HDI), mixed CuO and ZnO catalysts with Cu/(Cu + Zn) ratio of 4 and 8% were prepared by coprecipitation (CP), sequential precipitation (SP) and incipient wetness impregnation (IW). The SP-derived CuO/ZnO catalysts showed higher HDC yields than those derived by CP and IW. The IW method produced CuO/ZnO catalysts consisting of larger CuO and ZnO particles compared to the two precipitation methods. The CP method led to substitution of Zn2+ by Cu2+ in the hydrozincite precursor phase, resulting in higher BET and Cu surface areas of CuO-ZnO catalysts due to intimate intergrowth of nano-sized particles. However, the inherent character of ZnO in the CP-derived catalysts was modified by interfacial contact between CuO and ZnO identified by UV-visible and Raman spectra. In contrast, the properties of CuO and ZnO, as well as the relatively large surface areas, were kept in the SP-derived catalysts owing to deposition of Cu precipitates to fully aged Zn precipitates. This is believed to be a benefit of the SP method for the reaction. Therefore, our preparation approach has great potential to be extended to various mixed oxide catalysts.-
dc.language영어-
dc.language.isoen-
dc.publisherSPRINGER-
dc.titleEnhanced activity of CuO/ZnO catalyst on the decomposition of dimethylhexane-1,6-dicarbamate into dimethylhexane-1,6-diisocyanate-
dc.typeArticle-
dc.contributor.affiliatedAuthorSuh, Young-Woong-
dc.identifier.doi10.1007/s11164-018-3382-4-
dc.identifier.scopusid2-s2.0-85043679625-
dc.identifier.wosid000432844000012-
dc.identifier.bibliographicCitationRESEARCH ON CHEMICAL INTERMEDIATES, v.44, no.6, pp.3787 - 3796-
dc.relation.isPartOfRESEARCH ON CHEMICAL INTERMEDIATES-
dc.citation.titleRESEARCH ON CHEMICAL INTERMEDIATES-
dc.citation.volume44-
dc.citation.number6-
dc.citation.startPage3787-
dc.citation.endPage3796-
dc.type.rimsART-
dc.type.docTypeArticle; Proceedings Paper-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusMETHANOL SYNTHESIS-
dc.subject.keywordAuthorCarbamate decomposition-
dc.subject.keywordAuthorCuO/ZnO-
dc.subject.keywordAuthorSequential precipitation-
dc.subject.keywordAuthorCoprecipitation-
dc.identifier.urlhttps://link.springer.com/article/10.1007/s11164-018-3382-4-
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