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Mechanism of hydrodenitrogenation

Technical Report ·
OSTI ID:5532649
Activity and selectivity for hydrodenitrogenation (HDN) of a series of acidic molybdena catalysts have been determined using the pyridine HDN reaction. Measurements of total activity, selectivity for HDN, selectivity towards saturated versus unsaturated hydrocarbons, and selectivity for cracking, as a function of support composition and molybdena loading, provide clear evidence of two predominant types of sites: highly reduced Mo sites and highly acidic Bronsted sites. Both sites chemisorb strongly the heterocyclic aromatics and hydrogenated amines. Highly reduced Mo sites are highly active for denitrogenation, as seen clearly for silica-supported catalysts. The acidic sites also contribute to denitrogenation, probably by Hofmann elimination, and are active in cracking and cyclization. The optimum combination of these two types of sites for maximum HDN selectivity occurs at 4 wt% molybdena loaded on silica-aluminas containing >50 wt% silica. 8 refs., 7 figs., 4 tabs.
Research Organization:
Louisville Univ., KY (United States). Dept. of Chemical Engineering
Sponsoring Organization:
DOE; NSF; USDOE, Washington, DC (United States); National Science Foundation, Washington, DC (United States)
DOE Contract Number:
FG22-89PC89771
OSTI ID:
5532649
Report Number(s):
DOE/PC/89771-6; ON: DE91016595; CNN: R11-8610671
Country of Publication:
United States
Language:
English