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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 Ce 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 Ce 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.

[EN] Copper and cerium oxide bi-component materials with different Cu/Ce ratio were prepared using ordered SBA-15 silica as a support and compared with their bulk analogs. The samples were characterized by nitrogen physisorption, XRD, UV-Vis, FTIR, XPS, Raman spectroscopy and TPR with hydrogen. Cyclohexanol conversion was used as a catalytic test to obtain more information for the surface properties of the supported materials. The catalytic properties of the samples were studied in VOCs oxidation using toluene and ethyl acetate as probe molecules. A strong effect of mesoporous silica support and samples composition on the formation of catalytic sites was established. (C) 2012 Elsevier B.V. All rights reserved., Financial support of Bulgarian Academy of Science and National Scientific Fond of Ministry of Education Projects DTK 02/64 and ДНTC/Киtай 01/8, financial support from DGICYT in Spain (Project CTQ-2009-14495) and bilateral project Bulgarian-Spain Inter-academic Exchange Agreement (Project 2009BG0002) are acknowledged.