Journal
PHYSICAL CHEMISTRY CHEMICAL PHYSICS
Volume 2, Issue 13, Pages 3007-3015Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b000226g
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Ag/Al2O3 catalysts with various Ag contents were characterized by thermal gravimetry (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 groups on alumina have a close relationship with Ag loading either through ion-exchange with the proton of an acidic -OH or bonding with oxygen of a basic -OH species. An Ag loading of less than 240 mu mol g(-1) decreases the Lewis acid sites but increases the Bronsted acid sites with medium NH3 adsorption energy. A greater Ag loading induces interaction between NH3 molecules and Ag oxides, leading to reduction of Ag oxides and dissociation of adsorbed NH3. A large amount of Ag loading produces greatly enhanced basicity. The changes in the loaded form of silver on alumina are discussed. The appropriate acid-base property plays an important role in de-NOx activity using propane as the reductant.
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