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Title: Co-oxidative depolymerization of coal. Final report

Technical Report ·
OSTI ID:5707972

Extensive preliminary experiments have been carried out to investigate the use of an oxidative process for the depolymerization of coal. Chemical methodology from polymer science has been applied in a novel manner to determine the conditions under which mild oxidation of coal, in the presence of a suitable co-solvent, will result in significant depolymerization of the coal matrix. All reactions involved Western Kentucky hvB or hvC bituminous coal. In addition to testing numerous potential co-solvents, other variables considered were reaction temperature, reaction time, oxygen partial pressure, pre-oxidation extraction of the coal, and post-oxidation treatment. The extent of co-oxidative depolymerization was determined by exhaustive Soxhlet extraction. That the otherwise facile oxidation of solvent was inhibited when coal was present was interpreted as an indication that reactive sites within the coal matrix were competing for oxygen up-take. In general, the inability to enhance the extractability of coal by co-oxidation is believed to be the result of the failure to form hydroperoxide species. Rather, spectral analysis of the coal indicated that carbonyl structures were formed either during the co-oxidation reaction, or subsequent to co-oxidation. A literature search has indicated that cleavage (C-C bond scission) of some carbonyl species can be carried out under very mild reaction conditions. As a result, future work carried out along these lines may be promising. 24 refs., 7 figs., 14 tabs.

Research Organization:
Western Kentucky Univ., Bowling Green (USA). Dept. of Chemistry
OSTI ID:
5707972
Report Number(s):
EPRI-AP-4105; ON: TI85920721
Country of Publication:
United States
Language:
English