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dc.contributor.authorHarshini, D.-
dc.contributor.authorLee, Dae Hyung-
dc.contributor.authorKim, Yongmin-
dc.contributor.authorNam, Suk Woo-
dc.contributor.authorHan, Jong Hee-
dc.contributor.authorHam, Hyung Chul-
dc.contributor.authorYoon, Chang Won-
dc.date.accessioned2024-01-20T10:02:51Z-
dc.date.available2024-01-20T10:02:51Z-
dc.date.created2021-09-05-
dc.date.issued2014-04-
dc.identifier.issn1011-372X-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/126933-
dc.description.abstractNi/Ce0.65Hf0.25M0.1O2-delta (Ni/CH-M, M = Tb, Sm, Nd, Pr, and La), Ni-based catalysts supported on CeO2-HfO2 materials incorporated with rare earth elements, were prepared by a solvothermal method. The resulting catalysts were found to have surface areas ranging from 41 to 47 m(2)/g, and they proved to possess strong metal-to-support interactions, as evidenced by temperature programmed reduction analyses. Upon utilization of these catalysts for dry reforming of methane (DRM) with a CH4/CO2 ratio of 1 at a range of 600 to 900 degrees C, the Ni/CH-M catalysts were found to have higher activities than the Ni/CH catalyst. In addition, the activities proved to increase in the order of Ni/CH-Pr>Ni/CH-La similar to Ni/CH-Tb>Ni/ CH-Nd similar to Ni/CH-Sm>Ni/CH. With a high CH4/CO2 ratio of 2, these Ni/CH-M materials showed better stabilities than the Ni/CH catalyst in the DRM reaction at 800 degrees C for 150 h. Moreover, the Ni/CH-M (M = Pr, Tb, and La) catalysts exhibited superior durability over other Ni materials. Consistent with the observations, transmission electron microscopy further confirmed that no carbon species were observed in the Ni/CH-M (M = Pr, Tb, and La) catalysts following the reforming reactions.-
dc.languageEnglish-
dc.publisherSPRINGER-
dc.subjectSOLID-SOLUTIONS-
dc.subjectOXIDES-
dc.subjectSTEAM-
dc.subjectCEXZR1-XO2-
dc.subjectBEHAVIOR-
dc.subjectCH4-
dc.titleCatalytic Hydrogen Production via Dry Reforming of Methane Over Ni/Ce0.65Hf0.25M0.1O2-delta (M = Tb, Sm, Nd, Pr and La)-
dc.typeArticle-
dc.identifier.doi10.1007/s10562-014-1192-x-
dc.description.journalClass1-
dc.identifier.bibliographicCitationCATALYSIS LETTERS, v.144, no.4, pp.656 - 662-
dc.citation.titleCATALYSIS LETTERS-
dc.citation.volume144-
dc.citation.number4-
dc.citation.startPage656-
dc.citation.endPage662-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000332866400016-
dc.identifier.scopusid2-s2.0-84900646411-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusSOLID-SOLUTIONS-
dc.subject.keywordPlusOXIDES-
dc.subject.keywordPlusSTEAM-
dc.subject.keywordPlusCEXZR1-XO2-
dc.subject.keywordPlusBEHAVIOR-
dc.subject.keywordPlusCH4-
dc.subject.keywordAuthorMethane dry reforming-
dc.subject.keywordAuthorCarbon dioxide-
dc.subject.keywordAuthorCeria-hafnia-
dc.subject.keywordAuthorRare-earth elements-
dc.subject.keywordAuthorOxygen storage capacity-
dc.subject.keywordAuthorHeterogeneous catalyst-
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