Coal liquefaction using ore catalysts
โ Scribed by Virendra K. Mathur; Emanuel P. Fakoukakis; John A. Ruether
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- English
- Weight
- 562 KB
- Volume
- 63
- Category
- Article
- ISSN
- 0016-2361
No coin nor oath required. For personal study only.
โฆ Synopsis
Oresand oreconcentratescontaining
mineralsof Co, MO, Ni, Fe, and otherpotentiallyactivemetals have been investigated as slurry catalysts for liquefaction of Blacksville mine, Pittsburgh seam, bituminous coal. The tests were conducted batchwise in a stirred autoclave for 30 min at 425ยฐC and 13.79 MPa (2000 psig) hydrogen pressure according to a two-cycle scheme. In the first cycle, the reaction charge consisted of ground coal, catalyst, hydrogen, and SRC-II heavy distillate. The product of the first cycle was hot-filtered, and the liquid product served as a vehicle for the second cycle, which was otherwise run identically to the first. Reaction products from each cycle were analysed to determine conversion of coal, yield of liquids, liquid product viscosity, and group type (preasphaltene, asphaltene, and oil). Mixtures of ores containing iron pyrites and minerals containing other catalytically active transition metals were compared to pyrites alone and to a pulverized supported Co-MO-alumina
catalyst. An ore catalyst containing both Fe and Ni was superior to another that contained an equivalent mass of iron alone. The best ore catalysts tested, in terms of high liquid yields and low product viscosities, were mixtures of pyrites and molybdenum-and cobalt-containing ores. The latter yielded results that approached those obtained with an equivalent mass of cobalt and molybdenum on an alumina support.
๐ SIMILAR VOLUMES
Iron and molybdenum complexes were studied as precursors to high dispersion catalysts for coal liquefaction. The precursors were either organometallic complexes or water-soluble salts and were impregnated into coals of various ranks. The molybdenum catalysts were found to be very effective for conv
A commercial coal liquefaction catalyst, Amocat lA, has been subjected to a deactivation study in a laboratory catalytic coal liquefaction microreactor. Carbonaceous and metal deposits were the two major factors causing catalyst deactivation. The carbonaceous material deposited primarily in the inte