Characterization of Ag/Al2O3 de-NOx catalysts by probing surface acidity and basicity of the supporting substrate

Ag/Al2O3 catalysts with various Ag contents were characterized by thermal g ravimetry (TG), differential thermal analysis (DTA), temperature-programmed desorption (TPD), NH3 and CO2 adsorption calorimetry, FT-IR spectroscopic method, and diffuse reflectance spectra (DRS). It was found that hydroxy gr oups on alumina have a close relationship with Ag loading either through io n-exchange with the proton of an acidic -OH or bonding with oxygen of a bas ic -OH species. An Ag loading of less than 240 mu mol g(-1) decreases the L ewis acid sites but increases the Bronsted acid sites with medium NH3 adsor ption energy. A greater Ag loading induces interaction between NH3 molecule s and Ag oxides, leading to reduction of Ag oxides and dissociation of adso rbed NH3. A large amount of Ag loading produces greatly enhanced basicity. The changes in the loaded form of silver on alumina are discussed. The appr opriate acid-base property plays an important role in de-NOx activity using propane as the reductant.