Please use this identifier to cite or link to this item: https://doi.org/10.1016/S0920-5861(01)00285-1
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dc.titleAdsorption and catalytic combustion of aromatics on platinum-supported MCM-41 materials
dc.contributor.authorXia, Q.-H.
dc.contributor.authorHidajat, K.
dc.contributor.authorKawi, S.
dc.date.accessioned2014-10-09T09:51:32Z
dc.date.available2014-10-09T09:51:32Z
dc.date.issued2001-07-01
dc.identifier.citationXia, Q.-H., Hidajat, K., Kawi, S. (2001-07-01). Adsorption and catalytic combustion of aromatics on platinum-supported MCM-41 materials. Catalysis Today 68 (1-3) : 255-262. ScholarBank@NUS Repository. https://doi.org/10.1016/S0920-5861(01)00285-1
dc.identifier.issn09205861
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/91860
dc.description.abstractAmong a series of Pt-supported catalysts prepared by impregnation, the most hydrophobic Pt-supported on MCM-41 (synthesized in the presence of fluoride anions) with large surface area and pore size is found to be the most active catalyst for the combustion of toluene in air, and its activity is maintained even in the presence of water. However, Pt/ZSM-5 with micropores, the smallest pore volume and the least hydrophobicity has the worst catalytic activity. The high oxidation activity of the catalyst depends mainly on its high hydrophobicity (characterized by selective adsorption for H2O and toluene and by FTIR spectra of surface hydroxyl groups) and partly on its large pore size and high Pt loading. The order of the oxidation activity of a series of aromatics with different molecular weight and different boiling point on Pt-supported MCM-41 catalyst is found to be as follows: toluene > benzene > cumene > ethyl benzene > mesitylene. © 2001 Elsevier Science B.V. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/S0920-5861(01)00285-1
dc.sourceScopus
dc.subjectCatalytic combustion of aromatics
dc.subjectImpregnation
dc.subjectOxidation
dc.subjectPt-supported catalysts
dc.subjectPt/MCM-41
dc.subjectSynthesis of MCM-41
dc.typeArticle
dc.contributor.departmentCHEMICAL & ENVIRONMENTAL ENGINEERING
dc.contributor.departmentCHEMICAL AND PROCESS ENGINEERING CENTRE
dc.description.doi10.1016/S0920-5861(01)00285-1
dc.description.sourcetitleCatalysis Today
dc.description.volume68
dc.description.issue1-3
dc.description.page255-262
dc.description.codenCATTE
dc.identifier.isiut000170859100030
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