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U.S. Department of Energy
Office of Scientific and Technical Information

Chemistry of lignite liquefaction. Quarterly report, July-September 1981

Technical Report ·
OSTI ID:5384386

A series of lignite liquefaction samples were isolated into asphaltene and preasphaltene fractions to determine what structural differences are observed in the resulting asphaltenes and preasphaltenes. The solvent refined lignite samples were prepared using H/sub 2/-CO and H/sub 2/ with different degrees of dryness of the starting lignite coal. Quantitative cleavage of dialiphatic ethers with an excess of boron tribromide gave two moles of alkyl bromide, some rearranged. The deficiencies of quantitative anisole and xanthene cleavage with sodium were overcome by using potassium. Quantitative analysis of ketonic carbonyl remains a problem. Studies have continued on N,N-dimethylaniline(I) and related compounds. In the conversion on I into toluene under liquefaction conditions, the methyl group occupies the carbon site formerly occupied by nitrogen as determined by the conversion of o, m- and p-methyl phenyl dimethylamines. The reaction is H/sub 2/S pressure dependent at lower H/sub 2/S concentrations. Tetralin retards the H/sub 2/-induced conversion of I but not the H/sub 2/-H/sub 2/S reaction. The combination of H/sub 2/ and H/sub 2/S is more effective than either alone. The appendix has been entered separately.

Research Organization:
North Dakota Univ., Grand Forks (USA)
DOE Contract Number:
AB18-78FC02101
OSTI ID:
5384386
Report Number(s):
DOE/FC/02101-19; ON: DE82017361
Country of Publication:
United States
Language:
English