The complex of physicochemical
methods of analysis (elemental analysis,
cryoscopy in benzene, IR and 1H NMR spectroscopies, structural
group analysis, gas chromatography–mass spectrometry, and selective
chemical cleavage of sulfide and ether bonds) is used to comparatively
characterize resins and asphaltenes of light and heavy oils. Attention
is paid to the study of their structural group composition and the
composition of moieties bound in molecules of resin–asphaltene
substances (RAS) through ether and sulfide bridges, as well as the
composition of compounds occluded by asphaltene molecules and nitrogen
bases of resins. It is found that resins and asphaltenes of the heavy
oil are characterized by higher average molecular masses and large
overall sizes of mean molecules, due to the increased content of aromatic
cycles in the naphthenic–aromatic system. The similar sets
of linear and branched alkanes, alkylcyclopentanes, alkylcyclohexanes,
steranes, mono- and disubstituted alkylbenzenes, and dibenzothiophenes
identified in occluded compounds and products of chemolysis of resins
and asphaltenes under study suggest the presence of most of these
compounds as structural fragments in RAS molecules of light and heavy
crude oils under study. Alkyl-substituted quinolines and benzoquinolines
are identified in the nitrogen bases of resins. The feature of the
light oil is the presence of “sulfur-bound” alkenes
and polycycloalkenes in the structure of its asphaltenes. The findings
expand our understanding of the structure of petroleum resins and
asphaltenes. They can be used to simulate their structure in developing
new controlled methods for processing hydrocarbon feedstock.