Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Kim, Jongsik | - |
dc.contributor.author | Lee, Somin | - |
dc.contributor.author | Kwon, Dong Wook | - |
dc.contributor.author | Lee, Kwan-Young | - |
dc.contributor.author | Ha, Heon Phil | - |
dc.date.accessioned | 2024-01-19T21:01:50Z | - |
dc.date.available | 2024-01-19T21:01:50Z | - |
dc.date.created | 2021-09-02 | - |
dc.date.issued | 2019-01-25 | - |
dc.identifier.issn | 0926-860X | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/120449 | - |
dc.description.abstract | SO2 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.language | English | - |
dc.publisher | ELSEVIER SCIENCE BV | - |
dc.subject | AMMONIUM BISULFATE FORMATION | - |
dc.subject | HIGH-TEMPERATURE STABILITY | - |
dc.subject | VANADIUM-OXIDE CATALYSTS | - |
dc.subject | DEACTIVATION MECHANISM | - |
dc.subject | V2O5/TIO2 CATALYSTS | - |
dc.subject | EFFICIENT CATALYST | - |
dc.subject | SO3 DECOMPOSITION | - |
dc.subject | SCR PERFORMANCE | - |
dc.subject | ANODE MATERIAL | - |
dc.subject | NITRIC-OXIDE | - |
dc.title | SO32-/SO42- functionalization-tailorable catalytic surface features of Sb-promoted Cu3V2O8 on TiO2 for selective catalytic reduction of NOx with NH3 | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/j.apcata.2018.11.024 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | APPLIED CATALYSIS A-GENERAL, v.570, pp.355 - 366 | - |
dc.citation.title | APPLIED CATALYSIS A-GENERAL | - |
dc.citation.volume | 570 | - |
dc.citation.startPage | 355 | - |
dc.citation.endPage | 366 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.wosid | 000457661500038 | - |
dc.identifier.scopusid | 2-s2.0-85057723891 | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Physical | - |
dc.relation.journalWebOfScienceCategory | Environmental Sciences | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalResearchArea | Environmental Sciences & Ecology | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | AMMONIUM BISULFATE FORMATION | - |
dc.subject.keywordPlus | HIGH-TEMPERATURE STABILITY | - |
dc.subject.keywordPlus | VANADIUM-OXIDE CATALYSTS | - |
dc.subject.keywordPlus | DEACTIVATION MECHANISM | - |
dc.subject.keywordPlus | V2O5/TIO2 CATALYSTS | - |
dc.subject.keywordPlus | EFFICIENT CATALYST | - |
dc.subject.keywordPlus | SO3 DECOMPOSITION | - |
dc.subject.keywordPlus | SCR PERFORMANCE | - |
dc.subject.keywordPlus | ANODE MATERIAL | - |
dc.subject.keywordPlus | NITRIC-OXIDE | - |
dc.subject.keywordAuthor | Copper vanadate | - |
dc.subject.keywordAuthor | Cu3V2O8 | - |
dc.subject.keywordAuthor | Antimony | - |
dc.subject.keywordAuthor | Selective catalytic reduction of NOx | - |
dc.subject.keywordAuthor | SO32-/SO42- functionalization | - |
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