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Crossed reaction networks in the catalytic hydrodenitrogenation of synthetic liquid fuels. Final report

Technical Report ·
OSTI ID:5267181

Several of our findings are particularly noteworthy: (1) we have shown that the method of presulfiding of a commercial NiMo/Al/sub 2/O/sub 3/ catalyst can have a significant effect on its activity for hydrodenitrogenation (HDN) of quinoline. Of three methods studied, the most intense resulted in the most active catalyst, whereas in hydrodesulfurization an intermediate degree of presulfiding seems to be best; (2) in addition to the above, addition of H/sub 2/S to the reaction mixture increases the HDN rate and removal of H/sub 2/S decreases it, in a reversible manner; (3) small concentrations of water vapor also increase HDN, especially if H/sub 2/S is also present. An oxygenated compound such as a phenol or furan may decrease the rate of HDN, if it is relatively unreactive, by competitive adsorption. However, water, formed by HDO reactions, will increase HDN; (4) the kinetic behavior of quinoline HDN is remarkably the same in liquid-phase reaction as in vapor-phase reaction. The accelerating effects of H/sub 2/S work similarly in either phase; and (5) addition of NH/sub 3/ markedly reduces the rate of hydrogenation reactions. Although it also reduces HDN rates, this is an interesting lead to a means of reducing overall hydrogen consumption in hydrotreating reactions.

Research Organization:
Massachusetts Inst. of Tech., Cambridge (USA)
DOE Contract Number:
AC22-80PC30075
OSTI ID:
5267181
Report Number(s):
DOE/PC/30075-T1; ON: DE84007714
Country of Publication:
United States
Language:
English