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dc.contributor.authorKarásková, Kateřina
dc.contributor.authorChromčáková, Žaneta
dc.contributor.authorŠtudentová, Soňa
dc.contributor.authorMatějka, Vlastimil
dc.contributor.authorJirátová, Květa
dc.contributor.authorObalová, Lucie
dc.date.accessioned2012-11-07T13:18:31Z
dc.date.available2012-11-07T13:18:31Z
dc.date.issued2012
dc.identifier.citationCatalysis Today. 2012, vol. 191, issue 1, p. 112-115.cs
dc.identifier.issn0920-5861
dc.identifier.urihttp://hdl.handle.net/10084/95678
dc.description.abstractA series of Co–Mn–Al/TiO2 catalysts with different Co + Mn loading (5–24 wt.%) was prepared by impregnation of TiO2 support. Bulk Co–Mn–Al mixed oxides were prepared by different methods. The prepared catalysts were characterized by chemical analysis, surface area measurement, temperature programmed techniques (TPR, TPD) and tested for N2O catalytic decomposition. TiO2 acted only as a catalytic support and did not contribute to the catalytic activity. The N2O conversion over TiO2-supported Co–Mn–Al catalysts was increasing with Co + Mn loading, and was proportional to the amount of easily reducible components. Comparing the catalysts with identical amount of active components, the highest catalytic activity was achieved on the calcined precursors having carbonates in their molecules (layered double hydroxides Co–Mn–Al-HT-ex and Co–Mn–Al-carb), the lowest one on the calcined Co–Mn–Al nitrates due to the lower surface area, less advantageous porous structure and worse reducibility.cs
dc.language.isoencs
dc.publisherElseviercs
dc.relation.ispartofseriesCatalysis Todaycs
dc.relation.urihttp://dx.doi.org/10.1016/j.cattod.2012.03.046cs
dc.subjectnitrous oxidecs
dc.subjectcatalytic decompositioncs
dc.subjectlayered double hydroxidescs
dc.subjectmixed oxidescs
dc.subjecttitanium dioxidecs
dc.titleA comparative study of TiO2-supported and bulk Co-Mn-Al catalysts for N2O decompositioncs
dc.typearticlecs
dc.identifier.locationNení ve fondu ÚKcs
dc.identifier.doi10.1016/j.cattod.2012.03.046
dc.type.statusPeer-reviewedcs
dc.description.sourceWeb of Sciencecs
dc.description.volume191cs
dc.description.issue1cs
dc.description.lastpage115cs
dc.description.firstpage112cs
dc.identifier.wos000308675000019


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