Investigation on the reversibility of asphaltene precipitation

Citation
S. Peramanu et al., Investigation on the reversibility of asphaltene precipitation, ENERG FUEL, 15(4), 2001, pp. 910-917
Citations number
17
Categorie Soggetti
Environmental Engineering & Energy
Journal title
ENERGY & FUELS
ISSN journal
08870624 → ACNP
Volume
15
Issue
4
Year of publication
2001
Pages
910 - 917
Database
ISI
SICI code
0887-0624(200107/08)15:4<910:IOTROA>2.0.ZU;2-E
Abstract
The precipitation and redissolution of asphaltenes upon the addition and re moval of solvent were investigated for Athabasca and Cold Lake bitumens usi ng a flow-loop apparatus. The presence of precipitate was detected through an increase in pressure drop across an in-line filter. These solvent-revers ibility experiments were conducted at 40 and 60 degreesC with n-heptane sol vent. A significant hysteresis was observed for Athabasca bitumen while lit tle or no hysteresis was observed for Cold Lake bitumen. In both cases, the precipitation could be completely reversed. Temperature-reversibility was also investigated with n-dodecane solvent at temperatures ranging from 40 t o 160 degreesC. A hysteresis was observed for both bitumens and only partia l reversibility was achieved. Benchtop solvent-reversibility experiments we re also conducted on the two bitumens at room temperature. In this case, th e precipitate was recovered by centrifugation. The benchtop results were in good agreement with the flow-loop experimental results. Two heavy oils wer e also tested and both exhibited hysteresis and complete reversibility. Pre cipitation and redissolution in n-heptane were measured over time for the A thabasca bitumen. Precipitation increased over time reaching an apparent eq uilibrium after 8 days. Redissolution experiments reached virtually the sam e equilibrium position in less than 1 day. The slow kinetics of precipitati on suggests rate-limiting nucleation, growth, or flocculation of the asphal tenes. Redissolution experiments with their more rapid kinetics are better suited for obtaining equilibrium solubility data.