Kazuhito Sato

Enhanced activity of in and Ga-supported sol-gel alumina catalysts for NO reduction by hydrocarbons in lean conditions

Abstract Nitrogen monoxide was reduced efficiently by hydrocarbons in the presence of oxygen over sol-gel alumina supported indium, gallium, cobalt and tin catalysts. The support alumina prepared by a sol-gel method had high surface area and accordingly active alumina sites for the reaction. Particularly indium/alumina showed a high activity to reduce NO preferably by propene, propane and ethene but also by alcohols in the absence and the presence of water vapor. The activities of alumina supported cobalt, silver and tin catalysts were increased when calcinating the catalysts at 800°C instead of 600°C. In the case of gallium/alumina, NO 2 has higher reactivity than NO to nitrogen when propene was used as a reductant, proving the significance of the oxidation step of NO to NO 2 . The step of NO oxidation was promoted by preparing a physical mixture of 5 wt% Mn 3 O 4 with indium/alumina or gallium/alumina. The NO conversion to nitrogen was increased from 58 to 84% with the manganese oxide promotion over indium/alumina in the presence of water. The reaction mechanistic differences between the alumina supported catalysts and Cu/ZSM-5 were also discussed.

Catalytic performance of silver ion-exchanged saponite for the selective reduction of nitrogen monoxide in the presence of excess oxygen

Abstract The catalytic activity of ion-exchanged saponites for NO reduction with hydrocarbons in the presence of oxygen was investigated. Silver ion-exchanged saponite (Ag-saponite) showed excellent catalytic activity for NO reduction with propene. The highest activity was obtained for Ag-saponite with a silver loading of 7–8 wt%, on which the addition of water vapor to the feed gas promoted NO reduction at temperatures below 400°C. 2-Propanol and acetone served as more efficient reducing agents in the presence of water vapor.