Title of article
Selective oxidation of CO over model gold-based catalysts in the presence of H2
Author/Authors
Cécile Rossignol، نويسنده , , Sandrine Arrii، نويسنده , , Franck Morfin، نويسنده , , Laurent Piccolo، نويسنده , , Valerie Caps، نويسنده , , Jean-Luc Rousset، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2005
Pages
8
From page
476
To page
483
Abstract
The model catalysts Au/Al2O3, Au/ZrO2, and Au/TiO2 were produced by laser vaporization of a metallic gold rod followed by deposition of the formed clusters onto the support powders. This technique allows to obtain a narrow size distribution of highly dispersed gold particles on the support and, most importantly, similar sizes whatever the support. This makes it possible to accurately study of the influence of the support identity on the catalytic reaction. A detailed investigation of the preferential oxidation of CO in the presence of H2 was undertaken. Catalytic performances in the PROX reaction were compared with those in the oxidation of CO in the temperature range of 25–420 °C. A boost in the conversion of CO was observed in the presence of H2 at low temperature; the extent of this boost is dependent on the support identity. Hence the reactivity order found for CO oxidation (Au/Al2O3 ≪ Au/ZrO2 < Au/TiO2) was changed. In fact, in the presence of H2, the reaction rates for the oxidation of CO become rather similar on all three systems.
Keywords
Zirconia , ceria , N2O chemisorption , Reverse water–gas shift reaction , Long-term stability , CO formation , Kinetic model , Methanol decomposition , Steam reforming of methanol , Copper , Activation energy
Journal title
Journal of Catalysis
Serial Year
2005
Journal title
Journal of Catalysis
Record number
1223736
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