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Selectivity of catalysts towards coal-derived products

Conference ·
OSTI ID:5604211
Reaction of coal, preasphaltene, asphaltene, and oil has been studied with and without CoMo and FeS/sub 2/ to identify the areas of coal liquefaction that can be affected by these catalysts. We have shown that, early in the reaction of coal and solvent, an intermediate product (preasphaltene) is produced which is soluble in the slurry. This reaction appears to proceed to completion, so that all subsequent reactions proceed from this intermediate, and not from the coal. This reaction does not appear to be sensitive to H/sub 2/ in the gas phase, nor does it appear to be very sensitive to the amount of solvent as long as minimum quantity is present. The disappearance of this material is dependent upon H/sub 2/, and hydrogenation catalysts should be able to affect these reactions unless the H/sub 2/ is only retarding cracking. Asphaltene conversion is dramatically affected by catalysts. Conversion of asphaltenes has been increased from 30 to 70 percent in 15 minutes at 400/sup 0/C by the addition of CoMo and FeS/sub 2/. Although preasphaltene conversion was not effected by catalysts under these conditions, more oil, with the same gas production, was observed with catalyst -- this would mean a higher quality product. The production of gases, in general, from the classes of products formed in coal liquefaction is greatest for preasphaltene, less for asphaltene, and least for oils. Both CoMo and FeS/sub 2/ have been found to be active towards asphaltene conversion. Based upon metals loading, unsulfided CoMo is approx. 2.5 times more effective than FeS/sub 2/.
Research Organization:
Sandia Labs., Albuquerque, NM (USA)
DOE Contract Number:
EY-76-C-04-0789
OSTI ID:
5604211
Report Number(s):
SAND-79-1826C; CONF-800303-5
Country of Publication:
United States
Language:
English