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Cited 6 time in webofscience Cited 6 time in scopus
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dc.contributor.authorAhn, Nak Ho-
dc.contributor.authorShin, Jiho-
dc.contributor.authorRyu, Taekyung-
dc.contributor.authorHong, Suk Bong-
dc.date.accessioned2019-04-07T15:52:14Z-
dc.date.available2019-04-07T15:52:14Z-
dc.date.created2019-01-16-
dc.date.issued2018-12-
dc.identifier.issn1932-7447-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/95464-
dc.description.abstractWe have recently demonstrated that divalent copper ions exchanged into the large-pore zeolite UZM-35 with MSE topology (Cu-UZM-35) when hydrothermally aged at 750 degrees C exhibit a considerably wider operating temperature window for NH3-SCR than those into the small-pore zeolite SSZ-13 with CHA topology (Cu-SSZ-13), the current commercial catalyst for this reaction. Here we report the physical states and locations of copper ions in the fresh and 750 degrees C aged forms of Cu-UZM-35 determined using quantitative EPR measurements and synchrotron powder X-ray diffraction and Rietveld analyses. Among the four different cation sites (Cu1-Cu4) identified in fresh Cu-UZM-35, sites Cu3 and Cu4 are easily accessible via 12-ring and 10-ring channels, respectively, allowing their copper ions to serve as the main active sites for NH3-SCR. It was also found that while the Cu2+ ions at site Cu3 remain unchanged even after hydrothermal aging at 750 degrees C, the [Cu(OH)](+) ions at site Cu4 are transformed into CuOx and/or CuAl2O4 species. This led us to conclude that the Cu2+ ions at the former site are mainly responsible for the wide operating temperature window of Cu-UZM-35.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.relation.isPartOfJOURNAL OF PHYSICAL CHEMISTRY C-
dc.titleExtraframework Cation Locations in Cu-UZM-35 NH3-SCR Catalyst-
dc.typeArticle-
dc.identifier.doi10.1021/acs.jpcc.8b09764-
dc.type.rimsART-
dc.identifier.bibliographicCitationJOURNAL OF PHYSICAL CHEMISTRY C, v.122, no.51, pp.29330 - 29337-
dc.identifier.wosid000454751000026-
dc.citation.endPage29337-
dc.citation.number51-
dc.citation.startPage29330-
dc.citation.titleJOURNAL OF PHYSICAL CHEMISTRY C-
dc.citation.volume122-
dc.contributor.affiliatedAuthorHong, Suk Bong-
dc.identifier.scopusid2-s2.0-85059698215-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.type.docTypeArticle-
dc.subject.keywordPlusZEOLITES-
dc.subject.keywordPlusSITES-
dc.subject.keywordPlusNOX-
dc.subject.keywordPlusCU-ZSM-5-
dc.subject.keywordPlusSSZ-13-
dc.subject.keywordPlusBETA-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalResearchAreaMaterials Science-

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홍석봉HONG, SUK BONG
Div of Environmental Science & Enginrg
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