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Solubility and diffusion of vanadium compounds and asphaltene aggregates

  • Author / Creator
    Dechaine, Greg Paul
  • Most crude oils contain traces of vanadyl porphyrins within their asphaltene fraction. Although these metals are only present in trace quantities, they have a significant detrimental impact on crude oil processing units; therefore, their selective removal is highly desirable. The current work studied the interaction of these vanadyl porphyrins with asphaltenes using two approaches: 1) equilibrium solubility measurements of model porphyrins and 2) membrane diffusion measurements in dilute solution. Solubility measurements with model porphyrins showed that simple model porphyrins fit the operational definition for asphaltenes, exhibiting negligible solubility in n-heptane and orders of magnitude higher solubility in toluene. Measurement of the melting point properties enabled modeling of their solubility behaviour and showed that simple models incorporating solubility parameters (Regular solution and Flory-Huggins) were not capable of describing the observed behaviour. Diffusion measurements were done using model vanadyl porphyrins, asphaltenes, and petroporphyrins in toluene using a stirred diffusion cell equipped with ultrafiltration membranes (Ultracel YM® and Anopore®). The pore sizes were varied between 3-20 nm to retain aggregates while allowing free molecules to diffuse. The permeate was continuously monitored using in situ UV/Visible spectroscopy. These experiments determined that the size of the asphaltene aggregates at 1 g/L in toluene at 25°C were in the range of 5-9 nm. An increase in temperature results in an increase in asphaltene mobility but does not reduce the size of the asphaltene structures below 5 nm. Likewise, a decrease in concentration to 0.1 g/L did not result in a decrease in size. It was also observed that the exclusion of a large portion of the total asphaltenes by pores < 5 nm eliminates the absorbance of visible light (>600 nm) indicating the presence of Rayleigh scattering for the aggregated species in solution. The petroporphyrins are larger than the model vanadyl porphyrins as indicated by pore hindrance effects within smaller pores. An increase in temperature results in an increase in petroporphyrin mobility, although decreasing the asphaltene concentration does not. The mobility of the vanadyl petroporphyrins is affected by the origin of the sample (Safaniya, Venezuela, Athabasca) and is therefore not universal.

  • Subjects / Keywords
  • Graduation date
    2010-06
  • Type of Item
    Thesis
  • Degree
    Doctor of Philosophy
  • DOI
    https://doi.org/10.7939/R34P9D
  • License
    This thesis is made available by the University of Alberta Libraries with permission of the copyright owner solely for non-commercial purposes. This thesis, or any portion thereof, may not otherwise be copied or reproduced without the written consent of the copyright owner, except to the extent permitted by Canadian copyright law.
  • Language
    English
  • Institution
    University of Alberta
  • Degree level
    Doctoral
  • Department
    • Department of Chemical and Materials Engineering
  • Supervisor / co-supervisor and their department(s)
    • Gray, Murray R. (Chemical and Materials Engineering)
  • Examining committee members and their departments
    • Choi, Philip Y. K. (Chemical and Materials Engineering)
    • Shaw, John M. (Chemical and Materials Engineering)
    • Smith, Kevin J. (Chemical and Biological Engineering, University of British Columbia)
    • Stryker, Jeffrey M. (Chemistry)