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Kinetic and mechanistic study of CO oxidation over nanocomposite Cu-Fe-Al oxide catalysts

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F20%3A10423829" target="_blank" >RIV/00216208:11320/20:10423829 - isvavai.cz</a>

  • Výsledek na webu

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=ZjphLhgQg9" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=ZjphLhgQg9</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/cctc.202000852" target="_blank" >10.1002/cctc.202000852</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Kinetic and mechanistic study of CO oxidation over nanocomposite Cu-Fe-Al oxide catalysts

  • Popis výsledku v původním jazyce

    The oxidation of CO has been studied over Fe-Al and Cu-Fe-Al oxide nanocomposite catalysts prepared by melting of copper, iron, and aluminum nitrates. It was shown that the addition of copper significantly increases the catalytic activity of the Fe-Al nanocomposites. The catalysts were characterized by low-temperature nitrogen adsorption, X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). It was found that the catalysts contain Fe(2)O(3)with the hematite structure modified by aluminum. Copper in the three-component catalyst is in the Cu(2+)state, forming CuO and CuFeO(x)clusters on the catalyst surface. An increase in the copper content leads to the formation of a Cu(x)Al(y)Fe(3-x-y)O(4)spinel phase.In situXPS study showed that a treatment of the catalysts in a CO flow leads to the reduction of both copper and iron cations into the metallic state. In contrast, a treatment in a CO/O(2)flow leads only to partial reduction of Cu(2+)to Cu1+, while Fe(3+)are not reduced. The tests of catalytic activity performed in a flow fixed bed reactor using a CO pulse technique showed that the light-off temperature in the oxidation of CO over the Cu-Fe-Al nanocomposite catalysts depends on the copper content. The minimal light-off temperature was achieved over the catalyst containing 5 wt% CuO. In addition, we performed kinetic measurements in a differential reactor and obtained the activation energy and the reaction orders with respect to the reactants. The reaction mechanism of the catalytic oxidation of CO and the origin of active species are discussed.

  • Název v anglickém jazyce

    Kinetic and mechanistic study of CO oxidation over nanocomposite Cu-Fe-Al oxide catalysts

  • Popis výsledku anglicky

    The oxidation of CO has been studied over Fe-Al and Cu-Fe-Al oxide nanocomposite catalysts prepared by melting of copper, iron, and aluminum nitrates. It was shown that the addition of copper significantly increases the catalytic activity of the Fe-Al nanocomposites. The catalysts were characterized by low-temperature nitrogen adsorption, X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). It was found that the catalysts contain Fe(2)O(3)with the hematite structure modified by aluminum. Copper in the three-component catalyst is in the Cu(2+)state, forming CuO and CuFeO(x)clusters on the catalyst surface. An increase in the copper content leads to the formation of a Cu(x)Al(y)Fe(3-x-y)O(4)spinel phase.In situXPS study showed that a treatment of the catalysts in a CO flow leads to the reduction of both copper and iron cations into the metallic state. In contrast, a treatment in a CO/O(2)flow leads only to partial reduction of Cu(2+)to Cu1+, while Fe(3+)are not reduced. The tests of catalytic activity performed in a flow fixed bed reactor using a CO pulse technique showed that the light-off temperature in the oxidation of CO over the Cu-Fe-Al nanocomposite catalysts depends on the copper content. The minimal light-off temperature was achieved over the catalyst containing 5 wt% CuO. In addition, we performed kinetic measurements in a differential reactor and obtained the activation energy and the reaction orders with respect to the reactants. The reaction mechanism of the catalytic oxidation of CO and the origin of active species are discussed.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    10305 - Fluids and plasma physics (including surface physics)

Návaznosti výsledku

  • Projekt

    <a href="/cs/project/LM2018116" target="_blank" >LM2018116: Laboratoř fyziky povrchů - Optická dráha pro výzkum materiálů</a><br>

  • Návaznosti

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2020

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    ChemCatChem

  • ISSN

    1867-3880

  • e-ISSN

  • Svazek periodika

    12

  • Číslo periodika v rámci svazku

    19

  • Stát vydavatele periodika

    DE - Spolková republika Německo

  • Počet stran výsledku

    11

  • Strana od-do

    4911-4921

  • Kód UT WoS článku

    000567671800001

  • EID výsledku v databázi Scopus

    2-s2.0-85090060989