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Surface Potassium Promotion of Co4MnAlO x in Direct NO Decomposition Generates the Same Type of Active Sites as Bulk Promotion

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    SYSNO ASEP0574284
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleSurface Potassium Promotion of Co4MnAlO x in Direct NO Decomposition Generates the Same Type of Active Sites as Bulk Promotion
    Author(s) Bílková, T. (CZ)
    Pacultová, K. (CZ)
    Karásková, K. (CZ)
    Fridrichová, D. (CZ)
    Jirátová, Květa (UCHP-M) RID, ORCID, SAI
    Koštejn, Martin (UCHP-M) RID, SAI, ORCID
    Slowik, G. (PL)
    Ritz, M. (CZ)
    Haneda, M. (JP)
    Obalová, L. (CZ)
    Source TitleIndustrial and Engineering Chemistry Research. - : American Chemical Society - ISSN 0888-5885
    Roč. 62, č. 31 (2023), s. 12133-12151
    Number of pages19 s.
    Languageeng - English
    CountryUS - United States
    KeywordsAl mixed-oxide ; alkali-metal promoters ; N2O decomposition ; reaction-mechanism
    OECD categoryChemical process engineering
    Method of publishingOpen access
    Institutional supportUCHP-M - RVO:67985858
    UT WOS001034659700001
    EID SCOPUS85167775788
    DOI10.1021/acs.iecr.3c01011
    AnnotationK/Co4MnAlO x mixedoxidesare active in direct NO decomposition. This work investigates theeffect of the preparation method and K precursor type. Using the incipientwetness impregnation method, the modification by the required amountof K was ensured. Regardless of the K precursor type, similar NO conversionswere reached for samples modified by 4 wt % K. The optimal amountof K from the KNO3 precursor was evaluated as 2-6wt %. The physicochemical properties were carefully explored usingatomic absorption spectroscopy, X-ray photoelectron spectroscopy,X-ray diffraction, Fourier transform IR spectroscopy, N-2 physisorption, H-2 temperature-programmed reduction, CO2 and NO temperature-programmed desorption, scanning electronmicroscopy, and transmission electron microscopy, correlated withcatalytic properties in transient and steady state and compared withthe results obtained in our previous study using bulk modified samples.The present study underlines the effect of the preparation methodon the Brunauer-Emmett-Teller surface area (S (BET)) of prepared catalysts and thus the amountof active sites available for catalytic reaction. Moreover, the resultsemphasize the importance of catalyst basicity, which affects the amountof adsorbed NO2 (-) species, the key intermediatesin the direct NO catalytic reaction.
    WorkplaceInstitute of Chemical Process Fundamentals
    ContactEva Jirsová, jirsova@icpf.cas.cz, Tel.: 220 390 227
    Year of Publishing2024
    Electronic addresshttps://pubs.acs.org/doi/epdf/10.1021/acs.iecr.3c01011
Number of the records: 1  

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