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dc.contributor.authorSun, W.
dc.contributor.authorLi, X.
dc.contributor.authorMu, J.
dc.contributor.authorFan, S.
dc.contributor.authorYin, Z.
dc.contributor.authorWang, X.
dc.contributor.authorQin, M.
dc.contributor.authorTade, Moses
dc.contributor.authorLiu, Shaomin
dc.date.accessioned2018-08-08T04:43:43Z
dc.date.available2018-08-08T04:43:43Z
dc.date.created2018-08-08T03:50:42Z
dc.date.issued2018
dc.identifier.citationSun, W. and Li, X. and Mu, J. and Fan, S. and Yin, Z. and Wang, X. and Qin, M. et al. 2018. Improvement of catalytic activity over Mn-modified CeZrOx catalysts for the selective catalytic reduction of NO with NH3. Journal of Colloid and Interface Science. 531: pp. 91-97.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/70146
dc.identifier.doi10.1016/j.jcis.2018.07.050
dc.description.abstract

A series of MnCeZrOxmixed oxide catalysts were facilely synthesized using the impregnation-NH3·H2O coprecipitation method and tested for selective catalytic reduction (SCR) of NO with NH3. Doping manganese significantly improved the catalytic activity and the best performing SCR catalyst, Mn0.25Ce0.5Zr0.25Ox, was shown to achieve NO conversion > 80% in the temperature range (60–350 °C), with the denitration effect up to 50% at room temperature (conditions: [NO] = [NH3] = 500 ppm, [O2] = 5 vol%, He as balance, flow rate = 100 mL/min, GHSV = 40, 000 h-1). Characterization of the catalyst using BET, XRD, XPS, H2-TPR, and in-situ FTIR proved that the improved SCR activity may be attributed to the large surface area, great reduction ability and increased amount of surface adsorbed oxygen afforded by the introduction of manganese. The SCR reaction mechanisms were also investigated by analyzing in-situ FTIR spectra and the SCR reaction pathway over the Mn0.25Ce0.5Zr0.25Oxcatalyst was shown to mostly follow the E-R mechanism.

dc.publisherAcademic Press
dc.titleImprovement of catalytic activity over Mn-modified CeZrOx catalysts for the selective catalytic reduction of NO with NH3
dc.typeJournal Article
dcterms.source.volume531
dcterms.source.startPage91
dcterms.source.endPage97
dcterms.source.issn0021-9797
dcterms.source.titleJournal of Colloid and Interface Science
curtin.accessStatusFulltext not available
curtin.facultyFaculty of Science and Engineering


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