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Eric M V Hoek

Publications and source records attributed to Eric M V Hoek.

3 recordsLinked to original sources

Extended DLVO interactions between spherical particles and rough surfaces.

An "extended DLVO" approach that includes Lifshitz-van der Waals, Lewis acid-base, and electrostatic double layer interactions is used to describe interaction energies between spherical particles and rough surfaces. Favorable, unfavorable, and intermediate deposition conditions are simulated using surface properties representing common aquatic colloids and polymeric membranes. The surface element integration (SEI) technique and Derjaguin's integration method are employed to calculate interaction energy. Numerical simulations using SEI demonstrate that nanometer scale surface roughness features can produce a distribution of interaction energy profiles. Local interaction energies are statistically analyzed to define representative interaction energy profiles-minimum, average, and maximum-for various combinations of simulated particles and surfaces. In all cases, the magnitude of the average interaction energy profile is reduced, but the reduction of energy depends on particle size, asperity size, and density of asperities. In some cases, a surface that is on average unfavorable for deposition (repulsive) may possess locally favorable (attractive) sites solely due to nanoscale surface roughness. A weighted average of the analytical sphere-sphere and sphere-plate expressions of Derjaguin reasonably approximates the average interaction energy profiles predicted by the SEI model, where the weighting factor is based on the fraction of interactions involving asperities.

Journal Article↗

Direct observation of microbial adhesion to membranes.

Direct microscopic observation and an interfacial force model were used to better understand and control microbial adhesion to polymeric ultrafiltration membranes. The model was used to predict a "critical flux", below which cells deposited reversibly, and direct observation was used to visually quantify cell deposition and removal. In preliminary direct observation experiments, permeate reversal (backpulsing) was more effective than cross-flow hydrodynamics at removing deposited cells. In experiments conducted below the critical flux, no cell accumulation was observed over repeated forward-reverse filtration cycles; however, a small fraction of cells deposited irreversibly regardless of the flux, membrane, or solution chemistry. The fraction of irreversibly deposited cells was consistent with the equilibrium surface coverage attained without permeation (i.e., due to heterogeneous adsorption). Although steric forces were not invoked to establish a critical flux, when operating above the critical flux, a balance between permeation drag and steric repulsion appeared to determine the strength of adhesion of cells to membranes. Direct observation also confirmed that above the critical flux fouling occurred and pressure losses accumulated over several backpulse cycles, whereas below the critical flux there were no observable pressure losses or fouling.

Adsorption↗

Cake-enhanced concentration polarization: a new fouling mechanism for salt-rejecting membranes.

Results from well-controlled colloidal fouling experiments with reverse osmosis (RO) and nanofiltration (NF) membranes suggest the existence of a new source of flux decline for salt-rejecting membranes-cake-enhanced osmotic pressure. The physical mechanisms leading to this enhanced osmotic pressure are a combination of hindered back-diffusion of salt ions and altered cross-flow hydrodynamics within colloidal deposit layers, which lead to an enhanced salt concentration polarization layer. A model that accounts for both hindered diffusion of salt ions and altered hydrodynamics within colloidal deposit ("cake") layers is presented. The model successfully links permeate flux and salt rejection to cake-enhanced concentration polarization and provides new insight into the mechanisms through which salt-rejecting membranes foul. Experimental data support the model calculations and highlight the role of enhanced concentration polarization phenomena in the performance (i.e., water flux and salt rejection) of polymeric thin-film composite RO/NF membranes in environmental applications.

Colloids↗