Precipitant Effects on Aggregates Structure of Asphaltene and Their Implications for Groundwater Remediation

Asphaltenes generally aggregate, then precipitate and deposit on the surfaces of environmental media (soil, sediment, aquifer, and aquitard). Previous studies have recognized the importance of asphaltene aggregates on the wettability of aquifer systems, which has long been regarded as a limiting factor that determines the feasibility and remediation efficiency of sites contaminated by heavy oils. However, the mechanisms/factors associated with precipitant effects on asphaltene aggregates structure, and how the precipitant effects influence the wettability of surfaces remain largely unknown. Here, we observe the particle-by-particle growth of asphaltene aggregates formed at different precipitant concentrations. Our results show that aggregates for all precipitant concentrations are highly polydisperse with self-similar structures. A higher precipitant concentration leads to a more compacted aggregates structure, while precipitant concentration near to onset point results in a less compact structure. The well-known Smoluchowski model is inadequate to describe the structural evolutions of asphaltene aggregates, even for aggregation scenarios induced by a precipitant concentration at the onset point where the Smoluchowski model is expected to explain the aggregate size distribution. It is suggested that aggregates with relative high fractal dimensions observed at high precipitant concentrations can be used to explain the relatively low Stokes settling velocities observed for large asphaltene aggregates. In addition, asphaltene aggregates with high fractal dimensions are likely to have high density of nanoscale roughness which could enhance the hydrophobicity of interfaces when they deposit on the sand surface. Findings obtained from this study advance our current understandings on the fate and transport of heavy oil contaminants in the subsurface environment, which will have important implications for designing and implementing more effective and efficient remediation technologies for contaminated sites.

Relevance of Hydrodynamic Effects for the Calculation of Outer Surface Potential of Biological Membrane Using Electrophoretic Data

ABSTRACT In this paper, we present the results of a study on the influence of hydrodynamic effects on the surface potentials of the erythrocyte membrane, comparing two different models formulated to simulate the electrophoretic movement of a biological cell: the classical Helmholtz-Smoluchowski model and a model presented by Hsu et al. (1996). This model considers hydrodynamic effects to describe the distribution of the fluid velocity. The electric potential equation was obtained from the non-linear Poisson-Boltzmann equation, considering the spatial distribution of electrical charges fixed in glycocalyx and cytoplasmic proteins, as well as electrolyte charges and ones fixed on the surfaces of lipidic bilayer. Our results show that the Helmholtz-Smoluchowski model is not able to reflect the real forces responsible to the electrophoretic behavior of cell, because it does not take account the hydrodynamic effects of glycocalyx. This charged network that covers cellular surface constitutes a complex physical system whose electromechanical characteristics cannot be neglected. Then, supporting the hypothesis of other authors, we suggest that, in electrophoretic motion analyses of cells, the classical model represents a limiting case of models that take into account hydrodynamic effects to describe the velocity distribution of fluid.