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Coprocessing through fundamental and mechanistic studies in hydrogen transfer and catalysis. Quarterly report, March 28, 1992--June 30, 1992

Technical Report ·
DOI:https://doi.org/10.2172/10133142· OSTI ID:10133142

Hydrogen transfer from naphthenes to aromatics, coal, resid, and coal plus resid has been investigated at 430{degree}C in a N{sub 2} atmosphere. The reaction of perhydropyrene (PHP) with anthracene (ANT) resulted in the formation of pyrene (PYR) and dihydroanthracene. The weight percents of the products formed varied according to the initial ratio of ANT/PHP with a minimum appearing at a 2:1 weight ratio. Increased reaction times and high ANT/PHP ratios also yielded tetrahydroanthracene (THA). Reactions of Illinois No. 6 coal from the Argonne Premium Coal Sample Bank with PHP, ANT, and PYR resulted in higher coal conversion with PHP and lower with ANT and PYR. Reactions of PHP with resid resulted in less retrogressive reactions occurring in the resid than with either PYR or ANT. Apparent hydrogen transfer from coal or resid to ANT and PYR was observed. Combining PHP with ANT or PYR with coal, resid or coal plus resid yielded higher conversions and less retrogressive reactions. Hydrogen transfer occurred from PHP to ANT or PYR and to the coal and resid as evinced by the increased conversion.

Research Organization:
Auburn Univ., AL (United States). Dept. of Chemical Engineering
Sponsoring Organization:
USDOE, Washington, DC (United States)
DOE Contract Number:
AC22-88PC88801
OSTI ID:
10133142
Report Number(s):
DOE/PC/88801--T14; ON: DE94008150; BR: AA2515150
Country of Publication:
United States
Language:
English