4.6 Article

Effect of the preparation method and calcination temperature on the oxidation activity of CO at low temperature on CuO-CeO2/SiO2 catalysts

Journal

APPLIED CATALYSIS A-GENERAL
Volume 462, Issue -, Pages 56-63

Publisher

ELSEVIER
DOI: 10.1016/j.apcata.2013.04.032

Keywords

Catalysts; Copper; Ceria; Silica; CO oxidation

Funding

  1. Fondecyt [1110184]

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The effect of preparation method, either coimpregnation or sequential impregnation, and of calcination temperature (between 500 degrees C and 700 degrees C) of CuO-CeO2/SiO2 catalysts on the CuO-CeO2 interface and on their activity in the oxidation of CO with O-2 at low temperatures is studied. The catalysts are characterized by BET, XRD, TPR and UV-vis DRS. The results show that the preparation method has a substantial effect on the kind of CuO species formed on the surface. At calcination temperatures in the 500-600 degrees C range, coimpregnation leads to the formation only of Cu species that interact strongly with CeO2, while sequential impregnation leads also to the formation of bulk CuO species that do not interact, or interact weakly, with CeO2. In the case of sequential impregnation the concentration of the different CuO and CeO2 species and of the sites on the interface depends on the impregnation sequence of the support with the precursors of the oxides of both metals. On the other hand, the activity of the catalysts in the oxidation of CO at low temperatures (less than 180 degrees C) does not differ substantially with the preparation method, provided the calcination temperature remains in the 500-600 degrees C range. If the catalysts are calcined at 700 degrees C, the CuO-CeO2 interface, and therefore the activity of the catalysts, is strongly dependent on the preparation method and on the impregnation sequence of both oxides. Using sequential impregnation, impregnating first with the Ce precursor, produces a catalyst whose activity is substantially higher than that of the catalysts prepared by the other methods after calcining at 700 degrees C. (C) 2013 Elsevier B.V. All rights reserved.

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