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Novel bimetallic dispersed catalysts for temperature-programmed coal liquefaction. Technical progress report, April 1994--June 1994

Technical Report ·
OSTI ID:10188424
Coal liquefaction involves cleavage of methylene and dimethylene bridges connecting polycyclic aromatic units. The selected compound for model coal liquefaction reactions is 4-(1-naphthylmethyl)bibenzyl (NMBB). This report describes the synthesis and screening of several iron containing complexes as precursors of dispersed catalysts for hydrocracking of NMBB. Experiments were carried out at 400{degrees}C for 30 min under 6.9 MPa H{sub 2} pressure. All catalyst precursors converted NMBB predominately into naphthalene and 4-methylbibenzyl. Small amounts of secondary products were formed by hydrogenation, isomerization and fragmentation of the primary products. The greatest activity among the tested catalysts was found using superfine iron oxide with added sulfur. An experiment of the high surface Fe{sub 2}O{sub 3} without added sulfur gave only moderate conversion. Organometallics with relatively high volatility show higher activity than the inorganic system iron oxide. The thiocubane type cluster Cp{sub 4}Fe{sub 4}S{sub 4} showed the lowest activity. The beneficial effect of sulfur was also demonstrated in a reaction of iron pentacarbonyl and NMBB. A sulfur-free run showed substantially smaller conversion, whereas an experiment with added sulfur gave 15.6 % higher conversion. The catalytic activity of Cp{sub 2}Fe{sub 2}(CO){sub 4} is the highest among the sulfur-free catalyst precursors.
Research Organization:
Pennsylvania State Univ., University Park, PA (United States). Dept. of Materials Science and Engineering
Sponsoring Organization:
USDOE, Washington, DC (United States)
DOE Contract Number:
AC22-92PC92122
OSTI ID:
10188424
Report Number(s):
DOE/PC/92122--T7; ON: DE95001171
Country of Publication:
United States
Language:
English