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Thermochemistry and product studies of the isomerization and cracking of hydroaromatic molecules and the reactions of hydrogen atom produced from radical oxidation intermediates of hydroaromatic molecules. [1, 2 dihydronapthalene]

Conference ·
OSTI ID:5722058
The oxidation of hydroaromatic molecules of donor solvents and of hydroaromatic structure of coal during liquefaction occurs in stepwise fashion involving hydroaromatic radicals. For the prototype of hydroaromatic donors, tetralin, the formation of intermediate radicals leads to rearrangements and fragmentations. In addition, the scission of hydrogen atom from intermediate radicals leads to hydrocracking, production of H/sub 2/ and other reactions. In this paper, we present data from two sets of experiments bearing on the mechanism and energetics of hydroaromatic ring opening reactions, and present evidence showing that scission of hydrogen atom occurs in solution at 427/sup 0/C during the decomposition of 1,2-dihydronaphthalene (DHN), an oxidation intermediate in coal liquefaction, in tetralin.
Research Organization:
Pacific Northwest Lab., Richland, WA (USA)
DOE Contract Number:
AC06-76RL01830
OSTI ID:
5722058
Report Number(s):
PNL-SA-11281; CONF-830807-11; ON: DE83016777
Country of Publication:
United States
Language:
English