Influence of Metal Oxides and Their Precursors on the Composition of Final Products of Aquathermolysis of Raw Ashalchin Oil

Experiments were conducted simulating hydrothermal conversion of heavy oil in the presence of carbonate, kaolin, Al2O3, Ni2+ and Cu2+, NiO mixed with poly-α-olefins, C6H8O7, C2H4O2 at 290–375 °C and 10–135 bar. Al2O3, carbonate at 375 °C and 135 bar, accelerated the resin degradation. Experiments wi...

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Published inProcesses Vol. 9; no. 2; p. 256
Main Authors Petrov, Sergey M., Safiulina, Aliya G., Bashkirtseva, Natalya Yu, Lakhova, Alfiya I., Islamova, Galiya G.
Format Journal Article
LanguageEnglish
Published 01.02.2021
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Abstract Experiments were conducted simulating hydrothermal conversion of heavy oil in the presence of carbonate, kaolin, Al2O3, Ni2+ and Cu2+, NiO mixed with poly-α-olefins, C6H8O7, C2H4O2 at 290–375 °C and 10–135 bar. Al2O3, carbonate at 375 °C and 135 bar, accelerated the resin degradation. Experiments with carbonate at 350 °C and 10 bar showed no significant composition changes. NiSO4, CuSO4, kaolin mineral, at 350 °C and 78 bar, accelerated decomposition of resins (from 35.6% to 32.5%). Al2O3 and carbonate at 290 °C and 14 bar led to the destruction of asphaltenes (from 6.5% to 4.7% by weight), which were adsorbed on the surface of carbonate. Al2O3, NiO, poly-α-olefins at 350 °C and 78 bar accelerated C–C bond cracking of high-boiling asphaltenes. C6H8O7, rock-forming carbonate, at 360 °C and 14 bar, contributed to the polymerization and polycondensation of hydrocarbons with the formation of additional resins. C2H4O2 and kaolin at 360 °C and 12 bar affected the reduction in the resin content from 35.6% to 31.9% wt. C2H4O2 interacted with the active metals with the formation of acetate salts exhibiting catalytic activity.
AbstractList Experiments were conducted simulating hydrothermal conversion of heavy oil in the presence of carbonate, kaolin, Al2O3, Ni2+ and Cu2+, NiO mixed with poly-α-olefins, C6H8O7, C2H4O2 at 290–375 °C and 10–135 bar. Al2O3, carbonate at 375 °C and 135 bar, accelerated the resin degradation. Experiments with carbonate at 350 °C and 10 bar showed no significant composition changes. NiSO4, CuSO4, kaolin mineral, at 350 °C and 78 bar, accelerated decomposition of resins (from 35.6% to 32.5%). Al2O3 and carbonate at 290 °C and 14 bar led to the destruction of asphaltenes (from 6.5% to 4.7% by weight), which were adsorbed on the surface of carbonate. Al2O3, NiO, poly-α-olefins at 350 °C and 78 bar accelerated C–C bond cracking of high-boiling asphaltenes. C6H8O7, rock-forming carbonate, at 360 °C and 14 bar, contributed to the polymerization and polycondensation of hydrocarbons with the formation of additional resins. C2H4O2 and kaolin at 360 °C and 12 bar affected the reduction in the resin content from 35.6% to 31.9% wt. C2H4O2 interacted with the active metals with the formation of acetate salts exhibiting catalytic activity.
Author Lakhova, Alfiya I.
Bashkirtseva, Natalya Yu
Islamova, Galiya G.
Safiulina, Aliya G.
Petrov, Sergey M.
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