The conversion of oil asphaltenes of heavy oil in the supercritical hexane stream within the temperature ranges up to 250 and 250–450°C and at pressure 5 MPa is investigated. Elemental analysis, IR and 1H NMR spectroscopy and chromatography-mass spectrometry are used to characterize the initial asphaltenes and liquid products of their transformation. The C14−C27n−alkanes, C14−C35 alkenes, C27, C29–C35 hopanes and C30 hopene, C27−C29 steranes, C14−C27 mono-, C14−C29 bi-, C13−C25 tri- and C13−C20 tetraalkylsubstituted benzenes, C2–C4 naphthalenes, C2–biphenyls, C0–C3 phenanthrenes, C1–C2 fluorenes, C0–C1 pyrenes and C0–C1 fluorantenes, C3–C4 benzo-, and C1–C2 dibenzothiophenes were identified in the oils of a liquid product of the conversion of asphaltenes. The data obtained suggest the proceeding of reactions of dealkylation and cleavage of associative bonds in the course of thermolysis of asphaltenes in supercritical hexane.

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