The Role of Lewis and Brønsted Acid Sites in NO Reduction with NH3 on Sulfur Modified TiO2-Supported V2O5 Catalyst

Abstract

V₂O₅/S-doped TiO₂ was prepared by the sol-gel and impregnation methods. The adsorption of NO, NH₃, and O₂ over the catalyst was studied by in situ DRIFTS spectroscopy to elucidate the reaction mechanism of the low-temperature selective catalytic reduction of NO with NH₃. Exposing the catalyst to O₂ and NO, three types of nitrates species appeared on the surface. The introduction of S to TiO₂ could generate large amounts of acid sites for ammonia adsorption on the catalyst, which was believed to be an important role in the SCR reaction and hereby improved the catalytic activity. The results indicated two possible SCR reaction pathways for catalyst. One was that NO was absorbed to form nitrite species, which could react with NH₃ on Lewis acid sites, producing N₂ and H₂O. Another way was that NH₃ was adsorbed, then reacted with gas phase NO (E–R) and nitrite intermediates on the surface (L–H).