Search PubMed⌕ Search

Biomedical subjects

Subir Bhattacharjee

Publications and source records attributed to Subir Bhattacharjee.

3 recordsLinked to original sources

Electrostatic double-layer interaction between spherical particles inside a rough capillary.

Predictions of electrostatic double-layer interaction forces between two similarly charged spherical colloidal particles inside an infinitely long "rough" capillary are presented. A simple model of a rough cylindrical surface is proposed, which assumes the capillary wall to be a periodic function of axial position. The periodic roughness of the wall is characterized by the wavelength and amplitude of the undulations. The electrostatic double-layer interaction force between two spherical particles located axially inside this rough capillary is determined by solving the nonlinear Poisson-Boltzmann equation employing finite element analysis. The effect of surface roughness of the cylindrical enclosure on the interaction force between two particles is extensively studied on the basis of this model. The simulations are carried out for dimensionless amplitudes (amplitude/particle radii) ranging from 0.05 to 0.15 and scaled wavelengths (wavelength/particle radii) ranging from 0.4 to 4.0. The interaction force between the particles is significantly modified by the proximity of the rough capillary wall. Generally, the interaction force for rough capillaries oscillates around the corresponding interaction force in a smooth capillary depending on the magnitudes of the scaled amplitude and wavelength of the roughness. The influence of roughness on the electrostatic interactions becomes more pronounced when the surface potential of the cylinder wall is different from the sphere surface potentials. When the cylinder and the particle surfaces have large potential differences, the axial force experienced by a particle is dominated by the capillary roughness. There are dramatic oscillations of the force, which alternately becomes repulsive and attractive as the particle moves from the crest to the trough of the rough capillary wall. These results suggest that manipulation of colloidal particles in narrow microchannels may be subject to significant force variations owing to the roughness inherent in microfabricated channels etched on metal films.

Journal Article↗

Colloid transport in a geochemically heterogeneous porous medium: aquifer tank experiment and modeling.

To examine colloid transport in geochemically heterogeneous porous media at a scale comparable to field experiments, we monitored the migration of silica-coated zirconia colloids in a two-dimensional layered porous media containing sand coated to three different extents by ferric oxyhydroxides. Transport of the colloids was measured over 1.65 m and 95 days. Colloid transport was modeled by an advection-dispersion-deposition equation incorporating geochemical heterogeneity and colloid deposition dynamics (blocking). Geochemical heterogeneity was represented as favorable (ferric oxyhydroxide-coated) and unfavorable (uncoated sand) deposition surface areas. Blocking was modeled as random sequential adsorption (RSA). Release of deposited colloids was negligible. The time to colloid breakthrough after the onset of blocking increased with increasing ferric oxyhydroxide-coated surface area. As the ferric oxyhydroxide surface area increased, the concentration of colloids in the breakthrough decreased. Model-fits to the experimental data were made by inverse solutions to determine the fraction of surface area favorable for deposition and the deposition rate coefficients for the favorable (ferric oxyhydroxide-coated) and unfavorable sites. The favorable deposition rate coefficient was also calculated by colloid filtration theory. The model described the time to colloid breakthrough and the blocking effect reasonably well and estimated the favorable surface area fraction very well for the two layers with more than 1% ferric oxyhydroxide coating. If mica edges in the uncoated sand were considered as favorable surface area in addition to the ferric oxyhydroxide coatings, the model predicted the favorable surface area fraction accurately for the layer with less than 1% ferric oxyhydroxide coating.

Colloids↗

Virus transport in physically and geochemically heterogeneous subsurface porous media.

A two-dimensional model for virus transport in physically and geochemically heterogeneous subsurface porous media is presented. The model involves solution of the advection-dispersion equation, which additionally considers virus inactivation in the solution, as well as virus removal at the solid matrix surface due to attachment (deposition), release, and inactivation. Two surface inactivation models for the fate of attached inactive viruses and their subsequent role on virus attachment and release were considered. Geochemical heterogeneity, portrayed as patches of positively charged metal oxyhydroxide coatings on collector grain surfaces, and physical heterogeneity, portrayed as spatial variability of hydraulic conductivity, were incorporated in the model. Both layered and randomly (log-normally) distributed physical and geochemical heterogeneities were considered. The upstream weighted multiple cell balance method was employed to numerically solve the governing equations of groundwater flow and virus transport. Model predictions show that the presence of subsurface layered geochemical and physical heterogeneity results in preferential flow paths and thus significantly affect virus mobility. Random distributions of physical and geochemical heterogeneity have also notable influence on the virus transport behavior. While the solution inactivation rate was found to significantly influence the virus transport behavior, surface inactivation under realistic field conditions has probably a negligible influence on the overall virus transport. It was further demonstrated that large virus release rates result in extended periods of virus breakthrough over significant distances downstream from the injection sites. This behavior suggests that simpler models that account for virus adsorption through a retardation factor may yield a misleading assessment of virus transport in "hydrogeologically sensitive" subsurface environments.

Adsorption↗