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dc.contributor.authorKim, Jongsik-
dc.contributor.authorLee, Somin-
dc.contributor.authorKwon, Dong Wook-
dc.contributor.authorLee, Kwan-Young-
dc.contributor.authorHa, Heon Phil-
dc.date.accessioned2024-01-19T21:01:50Z-
dc.date.available2024-01-19T21:01:50Z-
dc.date.created2021-09-02-
dc.date.issued2019-01-25-
dc.identifier.issn0926-860X-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/120449-
dc.description.abstractSO2 is notorious to poison the catalytic surface during the selective catalytic reduction of NOx with NH3 (NH3-SCR). Nonetheless, the use of poisonous SO2 and O-2 as surface modifiers to generate the surface metal-SOY2- species (Y = 3 or 4) can be one of the viable ways for promoting catalytic NH3-SCR consequence. To develop a novel catalyst that is highly active in and selective to NH3-SCR, we previously explored four catalytic copper vanadates and determined the optimum active phase (i.e., Cu3V2O8, denoted as Cu-3) that revealed the greatest NH3-SCR performance, when combining with a proper Sb quantity of 1.4 wt. %. While using anatase (TiO2) as a support, this study investigated the effect of SOY2- functionalization temperature on the surface property of the optimum catalyst, Sb-promoted Cu3V2O8 on TiO2 (Cu-3-Sb-1.4/TiO2). Cu-3-Sb-1.4/TiO2 was subjected to SOY2- functionalization at 300, 400, and 500 degrees C, leading to the formation of S300, S400, and 5500. Although the catalyst surface was not fully functionalized with the SOY2- species in S300 -S500, various metal sulfate or sulfite species appeared on the surfaces and showed distinct surface features. The SOY2- functionalization of Cu-3-Sb-1.4/TiO2 could not increase the quantity of Lewis acid sites. However, 400 degrees C was deemed as an adequate SOY2- functionalization temperature for increasing the quantity of Bronsted acid sites and the redox behavior of the intact Cu-3-Sb-1.4/TiO2. This could result from the increase in the surface abundance of Cu(SO4) or from a proper combination of the metal-bound SOY2- species with mono-dentate and bi-dentate binding configurations. Apart from exhibiting moderate tolerance to hydrothermal aging, 5400 was also validated to improve its resistance to alkali-metal, H2O, SO2, (NH4)(2)SO4, or (NH4)HSO4 in comparison to its SOY2--unfunctionalized counterpart, S300, and S500.-
dc.languageEnglish-
dc.publisherELSEVIER SCIENCE BV-
dc.subjectAMMONIUM BISULFATE FORMATION-
dc.subjectHIGH-TEMPERATURE STABILITY-
dc.subjectVANADIUM-OXIDE CATALYSTS-
dc.subjectDEACTIVATION MECHANISM-
dc.subjectV2O5/TIO2 CATALYSTS-
dc.subjectEFFICIENT CATALYST-
dc.subjectSO3 DECOMPOSITION-
dc.subjectSCR PERFORMANCE-
dc.subjectANODE MATERIAL-
dc.subjectNITRIC-OXIDE-
dc.titleSO32-/SO42- functionalization-tailorable catalytic surface features of Sb-promoted Cu3V2O8 on TiO2 for selective catalytic reduction of NOx with NH3-
dc.typeArticle-
dc.identifier.doi10.1016/j.apcata.2018.11.024-
dc.description.journalClass1-
dc.identifier.bibliographicCitationAPPLIED CATALYSIS A-GENERAL, v.570, pp.355 - 366-
dc.citation.titleAPPLIED CATALYSIS A-GENERAL-
dc.citation.volume570-
dc.citation.startPage355-
dc.citation.endPage366-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000457661500038-
dc.identifier.scopusid2-s2.0-85057723891-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryEnvironmental Sciences-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaEnvironmental Sciences & Ecology-
dc.type.docTypeArticle-
dc.subject.keywordPlusAMMONIUM BISULFATE FORMATION-
dc.subject.keywordPlusHIGH-TEMPERATURE STABILITY-
dc.subject.keywordPlusVANADIUM-OXIDE CATALYSTS-
dc.subject.keywordPlusDEACTIVATION MECHANISM-
dc.subject.keywordPlusV2O5/TIO2 CATALYSTS-
dc.subject.keywordPlusEFFICIENT CATALYST-
dc.subject.keywordPlusSO3 DECOMPOSITION-
dc.subject.keywordPlusSCR PERFORMANCE-
dc.subject.keywordPlusANODE MATERIAL-
dc.subject.keywordPlusNITRIC-OXIDE-
dc.subject.keywordAuthorCopper vanadate-
dc.subject.keywordAuthorCu3V2O8-
dc.subject.keywordAuthorAntimony-
dc.subject.keywordAuthorSelective catalytic reduction of NOx-
dc.subject.keywordAuthorSO32-/SO42- functionalization-
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