Abstract

The compositions of extractants containing xylene (G) and n-heptane (P) recovered and reused in the asphaltene extraction process were determined by densimetry and the extracted asphaltenes were analyzed to study the influence of extractant composition on their elemental, spectral and structural properties. With increasing the number of extraction, the G/P ratio in extractant increases, which dissolves more asphaltenes of higher aromaticity and causes a decrease of asphaltene yield, the polarity and aromaticity in molecular structure of the extracted asphaltenes. Asphaltenes extracted at a higher G/P ratio were found to have less fractions of N and O elements as well as higher fractions of H and S elements, a lower C/H atom ratio and molecular unsaturation. Moreover, they have a smaller fraction of aromatic rings and aromatic carbon ratio, a higher substitution rate on aromatic rings, a higher fraction of alkyl chain and free ends in their average molecular structure. Compared with the base asphalt, asphaltenes’ infrared absorptions generally move towards smaller wave numbers owing to more aromaticity in their molecules and subsequent stronger conjugative and inductive effects. The asphaltenes extracted at a higher G/P ratio have a denser packing of alkyl chains and a looser packing of aromatic rings, according to their spectra of X-ray diffraction.

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