作者: D LORIMER , A BELL
DOI: 10.1016/S0021-9517(79)80027-5
关键词: Catalysis 、 Carbon monoxide 、 Infrared spectroscopy 、 Inorganic chemistry 、 Chemical reaction 、 Oxidizing agent 、 Reaction rate 、 Dissociation (chemistry) 、 Chemistry 、 Platinum
摘要: The reduction of NO by CO was studied over a Pt/SiO 2 catalyst at 300°C. Reaction rate data were obtained together with in situ infrared spectra species adsorbed on the surface. performance depended strongly ratio CO/NO reactor. For net reducing conditions (CO/NO > 1) deactivated time. Measurements kinetics taken during period slow deactivation showed that first order and inverse second CO. Reactivation both oxidizing pretreatments. Under In bands corresponding to chemisorbed Pt NCO CN groups attached support as Si-NCO Si-CN, respectively. Both more intense under than conditions. product selectivities observed found be good agreement mechanism based upon dissociation rate-limiting step. This further assumes N O is formed reaction an nitrogen atom. It proposed loss activity associated change electronic properties supported crystallites, caused accumulation large concentrations areas adjacent crystallites.