Abstract
Rh/SiO2, as well as Ir/SiO2, catalysts showed excellent activity for NO reduction with H2 in the presence of O2 and SO2. In particular, the coexistence of O2 and SO2 was essential for NO reduction to occur. FT-IR measurements of the adsorbed species on Rh/SiO2 catalyst indicated that NO adsorption was completely inhibited by SO2 in the absence of O2, but the adsorption of NO occurred on the vacant sites formed by the oxidation of SO2 to SO3 in the presence of O2. NO reduction with H2 probably proceeds via NHx intermediate species as for NH3- SCR. SiO2 was the most effective support for rhodium. Other supports such as Al2O3 were not effective, possibly because activation of H2 is hindered on more cationic rhodium (Rhδ+) due to the presence of adsorbed SO3 or NO3 species on the supports.