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Potassium as the best alkali metal promoter in boosting the hydrogenation activity of Ru/MgO for aromatic LOHC molecules by facilitated heterolytic H2 adsorption

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dc.contributor.authorKim, Tae Wan-
dc.contributor.authorKim, Dongun-
dc.contributor.authorJo, Yeongin-
dc.contributor.authorJung, Hwi Ju-
dc.contributor.authorPark, Ji Hoon-
dc.contributor.authorSuh, Young-Woong-
dc.date.accessioned2023-05-03T09:57:28Z-
dc.date.available2023-05-03T09:57:28Z-
dc.date.issued2023-03-
dc.identifier.issn0021-9517-
dc.identifier.issn1090-2694-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/184976-
dc.description.abstractAlkali metals (AM) are frequently used as promoters in a number of reactions. In aromatic hydrogenation over Ru/MgO, their basicity may promote heterolytic H2 adsorption, thereby boosting reaction kinetics. Herein, Ru/AM/MgO catalysts (AM: Na, K, and Cs) with different AM/Ru molar ratios are prepared and evaluated in the hydrogenation of toluene and benzyltoluene. The activity exhibits a volcano-type relationship with the AM/Ru molar ratio, where the optimal AM content decreases in the order Na+ > K+ > Cs+ and the AM showing the best activity is in the sequence Cs+ < Na+ < K+. These results originate from the heterolytic H2 adsorption induced by charge transfer from AM to proximate Ru atoms at the Ru-MgO interface. The degree of charge transfer depends on the AM's ionic radius and electronegativity affecting surface mobility and charge donation ability. Consequently, K+ is the best AM promoter in Ru/MgOcatalyzed aromatic hydrogenation.-
dc.format.extent13-
dc.language영어-
dc.language.isoENG-
dc.publisherAcademic Press-
dc.titlePotassium as the best alkali metal promoter in boosting the hydrogenation activity of Ru/MgO for aromatic LOHC molecules by facilitated heterolytic H2 adsorption-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1016/j.jcat.2023.02.006-
dc.identifier.scopusid2-s2.0-85148575040-
dc.identifier.wosid000944422000001-
dc.identifier.bibliographicCitationJournal of Catalysis, v.419, pp 112 - 124-
dc.citation.titleJournal of Catalysis-
dc.citation.volume419-
dc.citation.startPage112-
dc.citation.endPage124-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryEngineering, Chemical-
dc.subject.keywordPlusRU NANOPARTICLES-
dc.subject.keywordPlusCATALYSTS-
dc.subject.keywordPlusSURFACE-
dc.subject.keywordPlusCO2-
dc.subject.keywordPlusTEMPERATURE-
dc.subject.keywordPlusMGO-
dc.subject.keywordPlusHYDRODEOXYGENATION-
dc.subject.keywordPlusEFFICIENT-
dc.subject.keywordPlusSTORAGE-
dc.subject.keywordPlusOXIDE-
dc.subject.keywordAuthorLiquid organic hydrogen carrier-
dc.subject.keywordAuthorHydrogenation-
dc.subject.keywordAuthorSupported Ru catalysts-
dc.subject.keywordAuthorHeterolytic H 2 adsorption-
dc.subject.keywordAuthorAlkali metals-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0021951723000490?via%3Dihub-
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