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Calcination Temperature on N2O Conversion in the Presence of H2O and NOx

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    SYSNO ASEP0540440
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleCalcination Temperature on N2O Conversion in the Presence of H2O and NOx
    Author(s) Karásková, K. (CZ)
    Pacultová, K. (CZ)
    Jirátová, Květa (UCHP-M) RID, ORCID, SAI
    Fridrichová, D. (CZ)
    Koštejn, Martin (UCHP-M) RID, SAI, ORCID
    Obalová, L. (CZ)
    Article number1134
    Source TitleCatalysts. - : MDPI
    Roč. 10, č. 10 (2020)
    Number of pages17 s.
    Languageeng - English
    CountryCH - Switzerland
    Keywordsnitrous oxide ; catalytic decomposition ; potassium ; calcination
    Subject RIVCI - Industrial Chemistry, Chemical Engineering
    OECD categoryChemical process engineering
    Method of publishingOpen access
    Institutional supportUCHP-M - RVO:67985858
    UT WOS000583992900001
    EID SCOPUS85091899998
    DOI10.3390/catal10101134
    AnnotationThe effect of calcination temperature (500-700 degrees C) on physico-chemical properties and catalytic activity of 2 wt. % K/Co-Mn-Al mixed oxide for N2O decomposition was investigated. Catalysts were characterized by inductively coupled plasma spectroscopy (ICP), X-ray powder diffraction (XRD), temperature-programmed reduction by hydrogen (TPR-H-2), temperature-programmed desorption of CO2 (TPD-CO2), temperature-programmed desorption of NO (TPD-NO), X-ray photoelectron spectrometry (XPS) and N-2 physisorption. It was found that the increase in calcination temperature caused gradual crystallization of Co-Mn-Al mixed oxide, which manifested itself in the decrease in Co2+/Co3+ and Mn3+/Mn4+ surface molar ratio, the increase in mean crystallite size leading to lowering of specific surface area and poorer reducibility. Higher surface K content normalized per unit surface led to the increase in surface basicity and adsorbed NO per unit surface. The effect of calcination temperature on catalytic activity was significant mainly in the presence of NOx, as the optimal calcination temperature of 500 degrees C is necessary to ensure sufficient low surface basicity, leading to the highest catalytic activity. Observed NO inhibition was caused by the formation of surface mononitrosyl species bonded to tetrahedral metal sites or nitrite species, which are stable at reaction temperatures up to 450 degrees C and block active sites for N2O decomposition.
    WorkplaceInstitute of Chemical Process Fundamentals
    ContactEva Jirsová, jirsova@icpf.cas.cz, Tel.: 220 390 227
    Year of Publishing2021
    Electronic addressfile:///C:/Users/jirsova/AppData/Local/Temp/catalysts-10-01134-v3.pdf
Number of the records: 1  

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