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Aspahltene reaction pathways. 3. Effect of reaction environment

Journal Article · · Energy Fuel; (United States)
OSTI ID:6272310
Asphaltenes precipitated from an off-shore California crude oil were subjected to pyrolysis and hydropyrolysis, both neat and in solvents, and catalytic hydroprocessing over Co/emdash/Mo/Al/sub 2/O/sub 3/. Reaction products were collected as gases, maltenes, residual asphaltenes, and coke, based on a solvent extraction were protocol. The yield of each product fraction was determined gravimetrically, and selected fractions were further characterized by GC, GC-MS, LC-ICP, and elemental analysis. The reaction environment altered both the kinetics and asphaltene disappearance and the selectivity to the gas, maltene, and coke product fractions. For instance, the apparent first-order rate constants for asphaltene disappearance at 400/degrees/C were between 0.025 and 0.030 min/sup -1/ for neat reactions and pyrolysis in toluene. The corresponding yields of coke were high (approx. 45%), and the selectivities to maltenes at 60 min were between 0.22 and 0.45. However, the rate of asphaltene and disappearance for pyrolysis in tetralin and hydropyrolysis in toluene was slower (k approx. 0.008 min/sup -1/), the selectivities to maltenes were much higher (e.g., approx. 0.8), and the induction time for coke formation was longer. The addition of a hydrotreating catalyst provided disappearance rate constants of about 0.020 min/sup -1/ and high selectivities (approx. 0.8) to maltenes and yields (approx. 60%) of maltenes.
Research Organization:
Univ. of Delaware, Newark (USA)
OSTI ID:
6272310
Journal Information:
Energy Fuel; (United States), Journal Name: Energy Fuel; (United States) Vol. 2:5; ISSN ENFUE
Country of Publication:
United States
Language:
English