Interactions of CO and NO with the perovskite-type oxide larho3

Some aspects of the interactions of CO and NO with LaRhO₃ have been studied. The reduction of this oxide with CO occurs where the contracting sphere model is of perovskite structure stable up to a concentration of anion vacancies of ca. 2e^? per molecule. By reduction of LaRhO₃ at 817 K, rhodium was obtained, highly dispersed on a matrix of La₂O_3. After a reduction-oxidation cycle at 871 K the particle size of the perovskite decreased drastically. The activation energy of the reduction (67 kJ mol^?1) was significantly lower than that of other LaMO₃ oxides of group-VIII metals. Coverages of CO(θ_CO) and NO(θ_NO) at room temperature were lower than 3%, θ_NO being substantially higher than θ_CO. The reversibly adsorbed fractions of CO and NO underwent a remarkable decrease after preadsorbing NO and CO, respectively. This competitive adsorption is assumed to be associated with the adsorption of CO and NO on metallic sites. NO preadsorption inhibited the total adsorption of CO more severely than the reverse, indicating that NO is bound more strongly than CO to the LaRhO₃ surface.