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Mechanism of hydrodenitrogenation (Part 4) infrared spectroscopy of acidic molybdena catalysts

Technical Report ·
DOI:https://doi.org/10.2172/6355791· OSTI ID:6355791

Mo oxide catalysts supported over a complete series of silica-aluminas have been characterized in the oxidic and reduced states, by means of total acidity measurements and by infrared spectroscopy. Ammonia chemisorption was used to titrate the total acidity of the catalysts, and IR absorption of adsorbed pyridine to distinguish Bronsted from Lewis acid sites. The formation of new acidity upon deposition of molybdena on silica-alumina supports was then explained on the basis of a simple surface model. The new acidity is of both Lewis and Bronsted type, the preponderance of one over the other depending on support composition, as well as loading and state of oxidation of Mo. High-alumina supports and low Mo loading favor dispersed Mo species, in particular bidentate and monodentate di-oxo Mo species. The latter is responsible for the new Bronsted acidity. Coordinative unsaturation of polymolybdates is responsible for the new Lewis acidity, which is increased upon reduction of Mo. High-silica supports favor monodentate species (high Bronsted acidity) up to 4 wt % MoO{sub 3}. Beyond that, polymolybdates species and Lewis acidity predominate. 7 refs., 4 figs.

Research Organization:
Louisville Univ., KY (USA). Dept. of Chemical Engineering
Sponsoring Organization:
DOE/FE
DOE Contract Number:
FG22-89PC89771
OSTI ID:
6355791
Report Number(s):
DOE/PC/89771-4; ON: DE91002496
Country of Publication:
United States
Language:
English