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Title: Chemistry and structure of coal derived asphaltenes and preasphaltenes. Quarterly progress report, January-March 1980

Technical Report ·
OSTI ID:5622367

The following conclusions are drawn: (1) the aromaticity of petroleum-derived asphaltene (f/sub a/ = 0.2-0.5) is lower than that of coal-derived asphaltene (f/sub a/ = 0.6-0.7). (2) The aromatic ring systems within petroleum-derived asphaltene are much more ccondensed (peri) (H/sub aru//C/sub ar/ = 0.3-0.5) than that of coal-derived asphaltene (kata)(H/sub aru//C/sub ar/ = 0.5-0.7). (3) The substituents of the petroleum-derived asphaltenes are longer (n = 4-6) than those of coal-derived asphaltenes (n = 1). (4) The aromatic system of petroleum-derived asphaltene is extensively substituted (70 to 80%), whereas the coal-derived asphaltene is sparingly substituted (35 to 45%). (5) The molecular weight of petroleum-derived asphaltene is ca. 10 times higher than that of the coal-derived asphaltene. (6) Petroleum-derived asphaltene is less reactive to physical or chemical agents than that of coal-derived asphaltene. (7) Petroleum-derived asphaltene is more highly associated (Me = 5-7) than that of coal-derived asphaltene (Me-2-4). This will be reflected in the ease of processing. (8) Petroleum-derived asphaltene is less poplar than the coal-derived asphaltene.

Research Organization:
University of Southern California, Los Angeles (USA)
DOE Contract Number:
EX-76-C-01-2031
OSTI ID:
5622367
Report Number(s):
FE-2031-16
Country of Publication:
United States
Language:
English