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

Chemistry and structure of coal derived asphaltenes and preasphaltenes. Quarterly progress report, January-March 1981

Technical Report ·
OSTI ID:5839021
Pyrolysis residues from Catalytic Incorporated and FM-COED asphaltenes were investigated by solvent fractionation to ascertain the reaction mechanism during pyrolysis. The residues were fractionated into oil and resin, asphaltene, preasphaltene and mesophase fractions. Elemental analyses for each fraction were made for the Catalytic Incorporated fractions and for the FMC-COED fractions. When the FMC-COED asphaltene is pyrolyzed, it breaks apart to give a more stable three ring radical which probably condenses to preasphaltene and two smaller molecules which react to form oil and resin and then break down to be evolved as gas. When all the oil and resin is depleted, the remaining preasphaltene molecules continue to form pyridine insoluble chars. When the Catalytic Incorporated asphaltene cracks apart, it forms two stable aromatic molecules which can condense to form preasphaltenes. The general conclusions of this study are: a precursor that can nucleate and grow and coalesce to mesophase is a highly aromatic, condensed material with a few aliphatic or hydroxyl functional groups; the key to mesophase growth appears to be the formation of a preasphaltene intermediate that can condense to form the pre-order and be incorporated into the mesophase so that the mesophase can continue to grow and remain fluid to a higher temperature.
Research Organization:
University of Southern California, Los Angeles (USA)
DOE Contract Number:
AC22-75ET10626
OSTI ID:
5839021
Report Number(s):
DOE/ET/10626-T3; FE-2031-20; ON: DE82002638
Country of Publication:
United States
Language:
English

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