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dc.contributor.authorPark, Jong-Hwa-
dc.contributor.authorJurng, Jongsoo-
dc.contributor.authorBae, Gwi-Nam-
dc.contributor.authorPark, Sung Hoon-
dc.contributor.authorJeon, Jong-Ki-
dc.contributor.authorKim, Sang Chai-
dc.contributor.authorKim, Ji Man-
dc.contributor.authorPark, Young-Kwon-
dc.date.accessioned2024-01-20T14:31:44Z-
dc.date.available2024-01-20T14:31:44Z-
dc.date.created2021-09-05-
dc.date.issued2012-07-
dc.identifier.issn1533-4880-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/129097-
dc.description.abstractThe catalytic oxidation of a representative volatile organic compound, benzene, with ozone at a low temperature was investigated. A nanoporous MCM-48 material with a high specific surface area was used as the support for the catalytic oxidation for the first time. Mn, which has high activity at a low temperature, was used as the metal catalyst. To examine the effect of the Mn precursor, MCM-48 was impregnated with two different Mn precursors: Mn acetate and Mn nitrate. The characteristics of the synthesized catalysts were analyzed by Brunauer Emmett Teller surface area, X-ray diffraction, X-ray photoelectron spectroscopy, and temperature-programmed reduction. MCM-48 impregnated with Mn acetate showed higher catalytic activity than MCM-48 impregnated with Mn nitrate. This result was attributed to the better dispersion within nanoporous MCM-48 and higher oxygen mobility of Mn oxides produced by Mn acetate. The catalytic activity was also shown to depend closely on the ozone concentration.-
dc.languageEnglish-
dc.publisherAMER SCIENTIFIC PUBLISHERS-
dc.subjectLOW-TEMPERATURE-
dc.subjectOXIDE CATALYSTS-
dc.subjectPYROLYSIS-
dc.subjectREDUCTION-
dc.subjectNO-
dc.titleCatalytic Oxidation of Benzene with Ozone Over Nanoporous Mn/MCM-48 Catalyst-
dc.typeArticle-
dc.identifier.doi10.1166/jnn.2012.6411-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY, v.12, no.7, pp.5942 - 5946-
dc.citation.titleJOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY-
dc.citation.volume12-
dc.citation.number7-
dc.citation.startPage5942-
dc.citation.endPage5946-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000307604700154-
dc.identifier.scopusid2-s2.0-84865125091-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryPhysics, Applied-
dc.relation.journalWebOfScienceCategoryPhysics, Condensed Matter-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalResearchAreaPhysics-
dc.type.docTypeArticle-
dc.subject.keywordPlusLOW-TEMPERATURE-
dc.subject.keywordPlusOXIDE CATALYSTS-
dc.subject.keywordPlusPYROLYSIS-
dc.subject.keywordPlusREDUCTION-
dc.subject.keywordPlusNO-
dc.subject.keywordAuthorMCM-48-
dc.subject.keywordAuthorBenzene-
dc.subject.keywordAuthorOzone-
dc.subject.keywordAuthorMnOx-
dc.subject.keywordAuthorMn Precursor-
dc.subject.keywordAuthorCatalytic Oxidation-
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KIST Article > 2012
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