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Al-MIL-53 metal-organic framework supported Ru catalyst for selective hydrodeoxygenation of lignin-derived phenols into cyclohexane

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dc.contributor.authorKhani, Yasin-
dc.contributor.authorKumar, Avnish-
dc.contributor.authorBu, Sung Kang-
dc.contributor.authorChang, Hyun Ko-
dc.contributor.authorMoonis, Ali Khan-
dc.contributor.authorJeon, Byong-Hun-
dc.contributor.authorPark, Young-Kwon-
dc.date.accessioned2024-11-28T08:27:30Z-
dc.date.available2024-11-28T08:27:30Z-
dc.date.issued2024-06-
dc.identifier.issn1385-8947-
dc.identifier.issn1873-3212-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/195065-
dc.description.abstractCatalytic hydrodeoxygenation (HDO) of guaiacol, as a bio-oil model compound, was investigated employing Ru/Al-MIL −53 Metal-Organic Framework and Ru/γ-Al2O3 catalysts under external molecular hydrogen. Notably, the HDO results attributed the remarkable potential of the Ru/Al-MIL −53 MOF toward the comparatively high conversion of guaiacol (70%) together with a high proportion of cyclohexanol (23%) at a catalyst/feed (C/F) ratio of 1:5. However, only a 30% conversion was found with only 3.5% cyclohexanol for Ru/γ-Al2O3 for the same C/F ratio. This was due to the high porosity and presence of numerous vacancies in the MOF, which directly affects the H2-dissociation/ spillover that assists the transfer of produced H-radicals for further conversion of the adsorbed guaiacol molecules. Notably, the activity of Ru/Al-MIL −53 was remarkably increased by decreasing the amount of guaiacol. The maximum conversion was achieved (100%) for a C/F ratio of 1:1, with a higher (96.2%) selectivity for cyclohexane. The reusability test for the spent catalyst did not show any significant change in catalyst performance for up to five successive cycles.-
dc.format.extent15-
dc.language영어-
dc.language.isoENG-
dc.publisherElsevier BV-
dc.titleAl-MIL-53 metal-organic framework supported Ru catalyst for selective hydrodeoxygenation of lignin-derived phenols into cyclohexane-
dc.typeArticle-
dc.publisher.location스위스-
dc.identifier.doi10.1016/j.cej.2024.151637-
dc.identifier.scopusid2-s2.0-85191468916-
dc.identifier.wosid001285743500001-
dc.identifier.bibliographicCitationChemical Engineering Journal, v.490, pp 1 - 15-
dc.citation.titleChemical Engineering Journal-
dc.citation.volume490-
dc.citation.startPage1-
dc.citation.endPage15-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalWebOfScienceCategoryEngineering, Environmental-
dc.relation.journalWebOfScienceCategoryEngineering, Chemical-
dc.subject.keywordPlusBIO-OIL-
dc.subject.keywordPlusCOKE FORMATION-
dc.subject.keywordPlusMIL-53 AL-
dc.subject.keywordPlusH-BETA-
dc.subject.keywordPlusGUAIACOL-
dc.subject.keywordPlusNI-
dc.subject.keywordPlusDEOXYGENATION-
dc.subject.keywordPlusPYROLYSIS-
dc.subject.keywordPlusMECHANISM-
dc.subject.keywordPlusZEOLITES-
dc.subject.keywordAuthorCyclohexane-
dc.subject.keywordAuthorGuaiacol-
dc.subject.keywordAuthorHydrodeoxygenation-
dc.subject.keywordAuthorHydrogenation-
dc.subject.keywordAuthorRu/Al-MIL −53-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S1385894724031243?via%3Dihub-
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