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Enhancement of decane-SCR-NOx over Ag/alumina by hydrogen. Reaction kinetics and in situ FTIR and UV-vis study

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    SYSNO ASEP0028528
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JOstatní články
    TitleEnhancement of decane-SCR-NOx over Ag/alumina by hydrogen. Reaction kinetics and in situ FTIR and UV-vis study
    TitleZvýšení selektivní katalytické redukce oxidů dusíku na Ag/alumině vodíkem. Reakční kinetika a in-situ FTIR a UV-Vis studie
    Author(s) Sazama, Petr (UFCH-W) RID, ORCID
    Čapek, Libor (UFCH-W)
    Drobná, H. (CZ)
    Sobalík, Zdeněk (UFCH-W) RID
    Dědeček, Jiří (UFCH-W) RID, ORCID
    Arve, K. (FI)
    Wichterlová, Blanka (UFCH-W) RID
    Source TitleJournal of Catalysis. - : Elsevier - ISSN 0021-9517
    Roč. 232, č. 2 (2005), s. 302-317
    Number of pages16 s.
    Languageeng - English
    CountryUS - United States
    KeywordsSCR-NOx ; hydrogen effect ; Ag clusters ; in situ FTIR
    Subject RIVCF - Physical ; Theoretical Chemistry
    R&D Projects1ET400400413 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    CEZAV0Z40400503 - UFCH-W (2005-2011)
    AnnotationDecane-SCR-NOx oxidation of NO and decane by molecular oxygen, and these reactions enhanced by hydrogen over Ag/alumina were investigated by monitoring of gaseous product composition, surface intermediates (in situ FTIR), and the state of silver (in situ UV-vis) under realistic reaction conditions in the steady-state and transient modes. It has been shown that oxidation of NO or decane by oxygen is greatly affected by the presence of decane or NO. Monodentate nitrates are formed preferentially and are more reactive compared with the bidentate species. Oxidation of decane mostly yields surface acetates, and the presence of NOx favors the formation of formates (acrylates). The reaction steps most enhanced by the addition of hydrogen to the SCR-NOx reaction are the transformations of the intermediate -CN species into -NCO and oxidation of the hydrocarbon to formates (acrylates).
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2006
Number of the records: 1  

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