Mesoporous copper-ceria-titania ternary oxides as catalysts for environmental protection: Impact of Ce/Ti ratio and preparation procedure
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388980%3A_____%2F20%3A00522956" target="_blank" >RIV/61388980:_____/20:00522956 - isvavai.cz</a>
Výsledek na webu
<a href="http://hdl.handle.net/11104/0307363" target="_blank" >http://hdl.handle.net/11104/0307363</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.apcata.2020.117487" target="_blank" >10.1016/j.apcata.2020.117487</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Mesoporous copper-ceria-titania ternary oxides as catalysts for environmental protection: Impact of Ce/Ti ratio and preparation procedure
Popis výsledku v původním jazyce
Hydrothermally obtained mesoporous ceria-titania mixed oxides with different composition are modified with copper using incipient wetness impregnation and “chemisorption-hydrolysis” techniques. Their catalytic properties in methanol decomposition as a source of hydrogen and total oxidation of ethyl acetate as representative volatile organic pollutant are investigated. The effect of support composition and modification method on the formation of catalytic active sites is studied. The obtained results show that the catalytic behavior is determined by the activity of finely dispersed CuO crystallites and facile electron transfer in the “conjugated” Ti[sbnd]Ce[sbnd]Cu redox centres in the interface layer. The mechanism of the formation of the interface layer and the growth of CuO crystallites during different modification procedures are discussed in details. The mesoporous Cu[sbnd]Ce[sbnd]Ti oxides demonstrate excellent catalytic activity in total oxidation of ethyl acetate. Their catalytic behavior in methanol decomposition is strongly influenced by the reductive transformations, which are provoked by the reaction medium.
Název v anglickém jazyce
Mesoporous copper-ceria-titania ternary oxides as catalysts for environmental protection: Impact of Ce/Ti ratio and preparation procedure
Popis výsledku anglicky
Hydrothermally obtained mesoporous ceria-titania mixed oxides with different composition are modified with copper using incipient wetness impregnation and “chemisorption-hydrolysis” techniques. Their catalytic properties in methanol decomposition as a source of hydrogen and total oxidation of ethyl acetate as representative volatile organic pollutant are investigated. The effect of support composition and modification method on the formation of catalytic active sites is studied. The obtained results show that the catalytic behavior is determined by the activity of finely dispersed CuO crystallites and facile electron transfer in the “conjugated” Ti[sbnd]Ce[sbnd]Cu redox centres in the interface layer. The mechanism of the formation of the interface layer and the growth of CuO crystallites during different modification procedures are discussed in details. The mesoporous Cu[sbnd]Ce[sbnd]Ti oxides demonstrate excellent catalytic activity in total oxidation of ethyl acetate. Their catalytic behavior in methanol decomposition is strongly influenced by the reductive transformations, which are provoked by the reaction medium.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10402 - Inorganic and nuclear chemistry
Návaznosti výsledku
Projekt
<a href="/cs/project/LM2015073" target="_blank" >LM2015073: Nanomateriály a nanotechnologie pro ochranu životního prostředí a udržitelnou budoucnost</a><br>
Návaznosti
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
Applied Catalysis A - General
ISSN
0926-860X
e-ISSN
—
Svazek periodika
595
Číslo periodika v rámci svazku
APR
Stát vydavatele periodika
NL - Nizozemsko
Počet stran výsledku
12
Strana od-do
117487
Kód UT WoS článku
000523558600009
EID výsledku v databázi Scopus
2-s2.0-85080026702