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Oxygen adsorption on supported silver catalysts investigated by microgravimetric and transient techniques

Journal Article · · Journal of Catalysis; (United States)
Oxygen adsorption on [alpha]-Al[sub 2]O[sub 3]-supported Ag catalysts was investigated in the temperature range 40 to 400[degrees]C. The adsorption kinetics, studied with a vacuum ultramicrobalance and analyzed with the Elovich equation, indicate that three kinetically distinguishable processes take place, with activation energies of [approximately]1, 10.5, and 24 kcal/mol. Temperature-programmed desorption (TPD) experiments confirm the existence of three adsorbed oxygen species. A weakly adsorbed species, which is found to desorb below 150[degrees]C, is related to the 10.5 kcal/mol adsorption process and is assigned to molecularly adsorbed oxygen. The adsorption peak at 285[degrees]C is related to the almost nonactivated process and is ascribed to atomic oxygen, which is probably multicoordinated on the surface. At high adsorption temperatures (300 and 400[degrees]C) a third peak, desorbing above 400[degrees]C, is observed in the TPD profiles and is related to the highly activated process of 24 kcal/mol which is revealed by the gravimetric experiments. This species is suggested to be subsurface oxygen based on the results of TPD experiment conducted after isotope exchange of preadsorbed [sup 16]O[sub 2] and [sup 18]O[sub 2]. Temperature-programmed reaction (TPR) experiments showed that all three species are active toward ethylene combustion. 36 refs., 9 figs., 1 tab.
OSTI ID:
5154243
Journal Information:
Journal of Catalysis; (United States), Journal Name: Journal of Catalysis; (United States) Vol. 143:2; ISSN 0021-9517; ISSN JCTLA5
Country of Publication:
United States
Language:
English