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Title: Development of unique catalysts for hydrodenitrogenation of coal-derived liquids. Ninth quarterly report, September 15, 1980-December 15, 1980

Technical Report ·
OSTI ID:5220315

Catalysts have been prepared and tested with the emphasis on understanding the role of catalyst support on the carbon-nitrogen bond scission reaction. Hydrodenitrogenation of quinoline has been studied using catalysts containing Ni-Mo on several different supports, such as alumina, fluorided alumina, magnesia and titania. Preliminary results from this study indicate that the nitrogen removal activity of titania-supported catalysts is significantly higher than those with alumina or magnesia supports. This difference in activity is probably due to a strong interaction between molybdenum and titania. The basic magnesium oxide catalyst shows very little hydrodenitrogenation activity when compared to an acidic support. Based on these results, we can speculate that the hydrogenolysis site may involve an acidic group adjacent to the transition metal ion on the surface of the catalyst and that the C-N bond scission reaction occurs via a Hoffman E-2 (..beta..-elimination) process. Batch reactions of phenothiazine and an equimolar mixture of dibenzothiophene and acridine in the presence of sulfided CoO-MoO/sub 3//..gamma..-Al/sub 2/O/sub 3/ catalyst were performed at 573/sup 0/K and 7000 kPa. Results show an increased rate of phenothiazine hydrodesulfurization (HDS) over that for dibenzothiophene. The presence of acridine inhibits HDS of dibenzothiophene. These results appear to be contradictory to a mechanism involving one-point sulfur site coordination, but can be explained in terms of a multipoint coordination of reactant Pi electrons with catalytic sites. A complete reaction network for the HDS and subsequent hydrodenitrogenation of phenothiazine is presented.

Research Organization:
Delaware Univ., Newark (USA). Dept. of Chemical Engineering
DOE Contract Number:
AC22-78ET11429
OSTI ID:
5220315
Report Number(s):
DOE/ET/11429-9; ON: DE82020154
Resource Relation:
Other Information: Portions of document are illegible
Country of Publication:
United States
Language:
English