4.6 Article

Influence of Naphthenic Hydrocarbons and Polar Solvents on the Composition and Structure of Heavy-Oil Aquathermolysis Products

Journal

INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
Volume 60, Issue 36, Pages 13191-13203

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.iecr.1c02341

Keywords

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Funding

  1. Ministry of Science and Higher Education of the Russian Federation [075-15-2020-931]
  2. Russian Federation [MK1517.2020.3]

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Research shows that naphthenic solvents significantly impact viscosity reduction through destructive hydrogenation of resins and asphaltenes. Among the solvents used, decalin notably increases the amount of evolved gases, particularly C-4-C-10 isomers and aromatics. The maximum evolved gases among all used solvents correspond to formic acid.
Estimates of the conventional proven hydrocarbon reserves show a tendency toward depletion, and in the near future they will be insufficient to meet the ever-growing global energy demand. The problem of crude oil deficiency can be solved by involving unconventional hydrocarbon resources in both recovery and refinery. However, the hydrogen deficiency of heavy oil and natural bitumen requires technical and technological solutions. Therefore, the hydrogen-donating capacity of water and solvents, particularly in reservoir conditions, is very attractive. In this paper, we study the hydrogen-donating capacity of naphthenic and polar solvents during hydrothermal treatment of heavy oil from Ashal'cha reservoir (Republic of Tatarstan, Russia). It was established that naphthenic solvents significantly influence the viscosity reduction due to the destructive hydrogenation of resins and asphaltenes. Among naphthenic solvents, decalin significantly increases the amount of evolved gases, particularly C-4-C-10 isomers and aromatics. However, the maximum evolved gases among all of the used solvents correspond to formic acid. The results of elemental analysis revealed that the H/C ratio rises in crude oil samples after hydrothermal treatment in the presence of cyclohexane and decalin. FTIR spectral indices revealed an increase in crude oil aliphaticity in case of using solvents from the cyclohexane-tetralin- decalin series due to the cleavage of carbon-heteroatom bonds in aliphatic substitutes of resins and asphaltenes. Significant changes in the FT-IR spectra of crude oil are observed in the presence of tetralin.

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