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Enhanced catalysts for hydrodenitrogenation of coal liquids: Appendix A

Conference ·
OSTI ID:6895316
Two approaches to the development of improved HDN catalysts are being investigated. One approach is to synthesize high-activity, highly dispersed, ''surface-confined'' catalysts based on organometallic cluster complexes. The second approach is to examine the hydrotreating activities of metals not currently used in HDN and HDO catalysis. This second method arises from homogeneous modeling studies for the transalkylation reaction and from studies of bulk metals on the HDN of tetrahydroquinoline. From the results of these studies the investigators have found that ruthenium exhibits the highest activity for C-N bond cleavage. In this paper the syntheses and HDN activities of catalysts prepared using these two approaches are described. The conclusion is that both surface-confining techniques and metal-promotion with an active amine transalkylation catalyst such as Ru/sub 3/(CO)/sub 12/ greatly enhances the activity of CoMo or NiMo HDN catalysts. Not only are the activities of the RuCoMo and RuNiMo catalysts greater, but also the selectivity towards aromatic products are higher. Furthermore, unlike with bulk metals, these ruthenium promoted catalysts are sulfur tolerant. The exact mechanism of the promotion will require more detailed work. However, these preliminary results are highly significant with regard to the need to develop improved HDN catalysts that can remove nitrogen with a minimum amount of hydrogen consumption. 6 refs., 1 fig., 1 tab.
Research Organization:
SRI International, Menlo Park, CA (USA)
DOE Contract Number:
FG22-85PC80906
OSTI ID:
6895316
Report Number(s):
CONF-870410-21; ON: DE87009365
Country of Publication:
United States
Language:
English