Number of the records: 1  

Role of active oxygen and NOx species in N2O decomposition over Fe-ferrierite

  1. 1.
    SYSNO ASEP0376640
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleRole of active oxygen and NOx species in N2O decomposition over Fe-ferrierite
    Author(s) Sobalík, Zdeněk (UFCH-W) RID
    Tabor, Edyta (UFCH-W) RID, ORCID
    Nováková, Jana (UFCH-W) RID
    Sathu, Naveen Kumar (UFCH-W)
    Závěta, K. (CZ)
    Source TitleJournal of Catalysis. - : Elsevier - ISSN 0021-9517
    Roč. 289, MAY 2012 (2012), s. 164-170
    Number of pages7 s.
    Languageeng - English
    CountryUS - United States
    KeywordsN2O decomposition ; iron ferrierite ; active oxygen
    Subject RIVCF - Physical ; Theoretical Chemistry
    R&D ProjectsKAN100400702 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    GA203/09/1627 GA ČR - Czech Science Foundation (CSF)
    GAP106/11/0624 GA ČR - Czech Science Foundation (CSF)
    CEZAV0Z40400503 - UFCH-W (2005-2011)
    UT WOS000303788800017
    DOI10.1016/j.jcat.2012.02.007
    AnnotationDirect evidence for the formation of surface Fe–NOx species over iron ferrierites during decomposition of N2O was found with a combination of temperature-programmed desorption of adsorbed surface species and infrared and Mössbauer spectroscopies. Surface NOx species were produced via the conversion of a transiently formed Fe(III)–O by exposing iron ferrierites (Si/Al = 8.7, Fe/Al = 0.07–0.1) to N2O. The transformation of Fe(III)–O into Fe–NOx was time- and temperature- dependent. Below 280 °C, predominantly Fe(III)–O species were formed; these species are known to be highly active in oxidations at low temperatures. A transformation of Fe(III)–O into Fe–NOx species occurred when the reaction temperature was increased or when the reaction time was increased at low temperatures. This resulted in the disappearance of the oxidation activity of iron ferrierite. In contrast, the formation of Fe–NOx species enhanced the rate of N2O decomposition. Once formed, NOx species were stable during the subsequent N2O decomposition.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2013
Number of the records: 1  

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