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dc.contributor.authorAtes, A
dc.contributor.authorReitzmann, A
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T10:22:01Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T10:22:01Z
dc.date.issued2005
dc.identifier.issn0021-9517
dc.identifier.urihttps://dx.doi.org/10.1016/j.jcat.2005.07.023
dc.identifier.urihttps://hdl.handle.net/20.500.12418/10954
dc.descriptionWOS: 000232147500016en_US
dc.description.abstractThe interaction of N2O with MFI zeolites was investigated by a multipulse transient response method at 250 degrees C with subsequent temperature-programmed desorption. It was shown that the active sites for the formation of a surface oxygen species can be determined quantitatively using this method under the conditions of catalytic applications. Iron content and several pretreatment procedures influenced the formation of surface oxygen and molecular N2O sorption. For example, fresh zeolites with high and low iron content formed significantly more surface oxygen than zeolites that had been pretreated in N2O. The calcination at higher temperatures had an effect only on the activity of the zeolites with high iron content, which was not as pronounced as has been reported in the literature. The adsorption of molecular N2O as an elementary step of N2O activation in iron-containing zeolites cannot be neglected, because it was found to be thermally quite stable. All results indicate that in these zeolites not only one, but several oxygen species were formed that differ in thermal stability and thus in reactivity. (c) 2005 Elsevier Inc. All rights reserved.en_US
dc.language.isoengen_US
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCEen_US
dc.relation.isversionof10.1016/j.jcat.2005.07.023en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectiron-containing MFI zeolitesen_US
dc.subjectsurface oxygenen_US
dc.subjecttransient response methoden_US
dc.subjectnitrous oxide decompositionen_US
dc.subjectN2O sorptionen_US
dc.titleThe interaction of N2O with ZSM-5-type zeolites: A transient, multipulse investigationen_US
dc.typearticleen_US
dc.relation.journalJOURNAL OF CATALYSISen_US
dc.contributor.departmentCumhuriyet Univ, Fac Engn, Dept Chem Engn, TR-58140 Sivas, Turkey -- Univ Karlsruhe, Inst Chem Verfahrenstech, D-76128 Karlsruhe, Germanyen_US
dc.identifier.volume235en_US
dc.identifier.issue1en_US
dc.identifier.endpage174en_US
dc.identifier.startpage164en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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