Selective Oxidation of CO, over Supported Au Catalysts

Abstract

The selective oxidation of CO on Au/Al2O3 and Au/MOx/Al2O3 (M=Mg, Mn) in the presence of H2 was studied. The addition of MgO and MnOx improves the CO oxidation activity and selectivity towards CO2. The beneficial effect of MgO can be ascribed to stabilization of small Au particles, which are intrinsically more active in CO and H2 oxidation. MnOx is thought to be able to supply the active O needed for CO oxidation. Au catalysts containing both MgO and MnOx are extremely active in CO oxidation. In the presence of H2 selectivity towards CO2 higher than 0.90 was observed for Au/MgO/Al2O3 and Au/MnOx/MgO/Al2O3 at 100°C and below. The H2 oxidation at low temperature was affected by adsorbed CO. At temperatures above 50°C the thermal desorption rate of CO was large enough for H2 oxidation to commence, implying a decrease in selectivity. Besides H2, water was also found to have a pronounced effect on the CO oxidation rate even at room temperature. The effect of water is ascribed to a beneficial role of surface OH groups in CO oxidation.