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dc.contributor.authorJabłońska, Magdalena
dc.contributor.authorArán, Miren Agote
dc.contributor.authorBeale, Andrew M.
dc.contributor.authorGóra-Marek, Kinga
dc.contributor.authorDelahay, Gérard
dc.contributor.authorPetitto, Carolina
dc.contributor.authorPacultová, Kateřina
dc.contributor.authorPalkovits, Regina
dc.date.accessioned2019-04-12T11:19:15Z
dc.date.available2019-04-12T11:19:15Z
dc.date.issued2019
dc.identifier.citationRSC Advances. 2019, vol. 9, issue 7, p. 3979-3986.cs
dc.identifier.issn2046-2069
dc.identifier.issn000457727800053
dc.identifier.urihttp://hdl.handle.net/10084/134622
dc.description.abstractCu-Al-O-x mixed metal oxides with intended molar ratios of Cu/Al = 85/15, 78/22, 75/25, 60/30, were prepared by thermal decomposition of precursors at 600 degrees C and tested for the decomposition of nitrous oxide (deN(2)O). Techniques such as XRD, ICP-MS, N-2 physisorption, O-2-TPD, H-2-TPR, in situ FT-IR and XAFS were used to characterize the obtained materials. Physico-chemical characterization revealed the formation of mixed metal oxides characterized by different specific surface area and thus, different surface oxygen default sites. The O2-TPD results gained for Cu-Al-O-x mixed metal oxides conform closely to the catalytic reaction data. In situ FT-IR studies allowed detecting the form of Cu+center dot center dot center dot N-2 complexes due to the adsorption of nitrogen, i.e. the product in the reaction between N2O and copper lattice oxygen. On the other hand, mostly nitrate species and NO were detected but those species were attributed to the residue from catalyst synthesis.cs
dc.language.isoencs
dc.publisherRoyal Society of Chemistrycs
dc.relation.ispartofseriesRSC Advancescs
dc.relation.urihttps://doi.org/10.1039/c8ra10509jcs
dc.rights© The Royal Society of Chemistry 2019cs
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/cs
dc.titleCatalytic decomposition of N2O over Cu-Al-O-x mixed metal oxidescs
dc.typearticlecs
dc.identifier.doi10.1039/c8ra10509j
dc.rights.accessopenAccesscs
dc.type.versionpublishedVersioncs
dc.type.statusPeer-reviewedcs
dc.description.sourceWeb of Sciencecs
dc.description.volume9cs
dc.description.issue7cs
dc.description.lastpage3986cs
dc.description.firstpage3979cs
dc.identifier.wos000457727800053


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© The Royal Society of Chemistry 2019
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