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Effect of Preparation Method on Catalytic Properties of Co-Mn-Al Mixed Oxides for N2O Decomposition.

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    SYSNO ASEP0467588
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleEffect of Preparation Method on Catalytic Properties of Co-Mn-Al Mixed Oxides for N2O Decomposition.
    Author(s) Klyushina, A. (CZ)
    Pacultová, K. (CZ)
    Karásková, K. (CZ)
    Jirátová, Květa (UCHP-M) RID, ORCID, SAI
    Ritz, M. (CZ)
    Fridrichová, D. (CZ)
    Volodorskaja, A. (CZ)
    Obalová, L. (CZ)
    Source TitleJournal of Molecular Catalysis A-Chemical. - : Elsevier - ISSN 1381-1169
    Roč. 425, DEC 15 (2016), s. 237-247
    Number of pages11 s.
    Languageeng - English
    CountryNL - Netherlands
    KeywordsCo-Mn-Al mixed oxide ; N2O decomposition ; preparation methods
    Subject RIVCI - Industrial Chemistry, Chemical Engineering
    R&D ProjectsGA14-13750S GA ČR - Czech Science Foundation (CSF)
    Institutional supportUCHP-M - RVO:67985858
    UT WOS000390634100027
    EID SCOPUS84992206945
    DOI10.1016/j.molcata.2016.10.014
    AnnotationCo-Mn-Al mixed oxides (Co:Mn:Al molar ratio of 4:1:1) were prepared by three different methods (i) calcination of hydrotalcite-like precursors (Co-Mn-Al-HT-ex), (ii) calcination of corresponding nitrates (Co-Mn-Al-nitr) and (iii) calcination of the product of mechanochemical reaction of Co, Mn, Al nitrates with NH4HCO3 (Co-Mn-Al-carb). Different conditions of synthesis led to the formation of spinel-like phase with different structural properties leading to different catalytic activity.N2O conversions decreased with decreasing specific surface area in order Co-Mn-Al-carb > Co-Mn-Al-HT-ex > Co-Mn-Al-nitr. Highest catalyst activity was determined by the lowest bond strength of active site − oxygen while specific surface area and amount of active sites per unit surface were not decisive parameters for activities order.
    WorkplaceInstitute of Chemical Process Fundamentals
    ContactEva Jirsová, jirsova@icpf.cas.cz, Tel.: 220 390 227
    Year of Publishing2017
Number of the records: 1  

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