Biomedical subjects

Jacob H Masliyah

Publications and source records attributed to Jacob H Masliyah.

17 recordsLinked to original sources

PubMed2006

Particle deposition onto charge heterogeneous surfaces: convection-diffusion-migration model.

The role of surface charge heterogeneity of planar collectors on particle deposition and distribution was investigated in the vicinity of a heterogeneous surface for a radial impinging jet flow geometry. The charge heterogeneity was modeled as concentric circular stripes bearing different surface charges. Particle deposition was studied employing the Eulerian approach (convection-diffusion-migration equation). It was observed that when the collector was completely unfavorable, the presence of small amounts of charge heterogeneity in the form of a small fraction of favorably charged stripes enhanced the deposition rate substantially. In contrast, when the collector was completely favorable, the presence of small amounts of charge heterogeneity in the form of a small fraction of unfavorably charged stripes did not affect the particle deposition rate significantly.

Journal Article↗

PubMed2006

Colloidal interactions between Langmuir-Blodgett bitumen films and fine solid particles.

In oil sand processing, accumulation of surface-active compounds at various interfaces imposes a significant impact on bitumen recovery and bitumen froth cleaning (i.e., froth treatment) by altering the interfacial properties and colloidal interactions among various oil sand components. In the present study, bitumen films were prepared at toluene/water interfaces using a Langmuir-Blodgett (LB) upstroke deposition technique. The surface of the prepared LB bitumen films was found to be hydrophobic, comprised of wormlike aggregates containing a relatively high content of oxygen, sulfur, and nitrogen, indicating an accumulation of surface-active compounds in the films. Using an atomic force microscope, colloidal interactions between the LB bitumen films and fine solids (model silica particles and clay particles chosen directly from an oil sand tailing stream) were measured in industrial plant process water and compared with those measured in simple electrolyte solutions of controlled pH and divalent cation concentrations. The results show a stronger long-range repulsive force and weaker adhesion force in solutions of higher pH and lower divalent cation concentration. In plant process water, a moderate long-range repulsive force and weak adhesion were measured despite its high electrolyte content. These findings provide more insight into the mechanisms of bitumen extraction and froth treatment.

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PubMed2006

Spherical cell approach for the effective viscosity of suspensions.

In the present paper, the spherical cell approach is employed for addressing the effective viscosity of suspensions of spherical particles. The proposed derivation is based on the only assumption which constitutes the essence of the spherical cell approach: a representative part of the suspension is a spherical cell which contains a particle surrounded by the continuous phase. In contrast with the previous studies on this topic, no additional assumptions are used in the present analysis. The general method of derivation and the final result, which represents the effective viscosity as a function of the solid-phase volume fraction, are compared with earlier studies where the spherical cell approach was applied for describing the effective viscosity.

Biophysics↗

PubMed2006

Adhesion of single polyelectrolyte molecules on silica, mica, and bitumen surfaces.

In a recent study (Energy Fuels 2005, 19, 936), a partially hydrolyzed polyacrylamide (HPAM) was used as a process aid to recover bitumen from oil sand ores. It was found that HPAM addition at the bitumen extraction step not only improved bitumen recovery but also enhanced fine solids settling in the tailings stream. To understand the role of HPAM, single-molecule force spectroscopy was employed for the first time to measure the desorption/adhesion forces of single HPAM molecules on silica, mica, and bitumen surfaces using an atomic force microscope (AFM). Silicon wafers with an oxidized surface layer and newly cleaved mica were used, respectively, to represent sand grains and clays in oil sands. The force measurements were carried out in deionized water and in commercial plant process water under equilibrium conditions. The desorption/adhesion forces of HPAM obtained on mica, silica, and bitumen surfaces were approximately 200, 40, and 80 pN in deionized water and approximately 100, 50, and 40 pN in the plant process water, respectively. The measured adhesion forces together with the zeta potential values of these surfaces indicate that the polymer would preferentially adsorb onto clay surfaces rather than onto bitumen surfaces. It is the selective adsorption of HPAM that benefits both bitumen recovery and tailings settling when the polymer was added directly to the bitumen extraction process at an appropriate dosage.

Acrylic Resins↗

PubMed2005

Acoustic and electroacoustic spectroscopy of water-in-diluted-bitumen emulsions.

Water-in-oil emulsions of Athabasca bitumen diluted with toluene have been studied using the latest advances in acoustic and electroacoustic spectroscopy. From the sound attenuation spectra of emulsions, the water droplet size distribution is measured. The electrical surface charge density of the water droplets is obtained from the colloid vibration current. In the case of freshly prepared water-in-oil emulsions, the droplet size increased while the surface charge density decreased with time. The time-dependent relaxation of the surface charge ranges from several hours to 3 days, and it is probably due to the slow adsorption/desorption kinetics of bituminous components at the water-oil interface. This study illuminates the contribution of the electrostatic interactions to the stability of water-in-oil emulsions.

Journal Article↗

PubMed2005

Adsorption of bituminous components at oil/water interfaces investigated by quartz crystal microbalance: implications to the stability of water-in-oil emulsions.

Silica-gel-coated QCM crystals oscillating in a thickness shear mode are used to measure adsorption of bituminous components in water-saturated heptol (1/1 vol ratio of a heptane/toluene mixture) at the oil/water interface. In addition to the viscoelasticity of the adsorbed film, the effects of the bulk liquid density and viscosity as well as the liquid trapped in interfacial cavities are taken into account for the calculation of adsorbed mass. Asphaltenes in heptol adsorb continuously at the oil/water interface, while resins (the surface-active species in maltenes) show adsorption saturation in the same solvent. For Athabasca bitumen in heptol, two adsorption regimes are observed depending on concentration. At low concentrations, a slow, non-steady-state, and irreversible adsorption takes place. At high concentrations, a steady-state adsorption with limited reversibility results in a quick adsorption saturation. The threshold concentration between these adsorption regimes is 1.5 wt % and 8 wt % for oil/water and oil/gold interfaces, respectively. The threshold concentration, the total adsorbed amount, and the flux of non-steady-state adsorption depend on the resin-to-asphaltene ratio. The threshold concentration is related to the earlier reported critical bitumen concentration characterizing the rigid-to-flexible transition of the interfacial film. We propose a new mechanism based on the change of the effective resin-to-asphaltene ratio with dilution to explain both the adsorption behavior and emulsion stability.

Journal Article↗

PubMed2005

Particle deposition onto micropatterned charge heterogeneous substrates: trajectory analysis.

A trajectory analysis of particles near a micropatterned charged substrate under radial impinging jet flow conditions is presented to investigate the effect of surface charge heterogeneity on particle trajectory and deposition efficiency. The surface charge heterogeneity is modeled as concentric bands of specified width and pitch having positive and negative surface potentials. The flow distribution is obtained using finite element analysis of the governing Navier-Stokes equations. The particle trajectory analysis takes into consideration the hydrodynamic interactions, gravity, van der Waals and electrostatic double layer interactions. The presence of surface charge heterogeneity on the substrate gives rise to an oscillating particle trajectory near the collector surface due to repulsive and attractive forces. As a result of the coupled effects of hydrodynamic and colloidal forces, the particle trajectories and deposition efficiencies are increasingly affected by surface charge heterogeneity as one moves radially away from the stagnation point. The results indicate that it is possible to render collectors with up to 50% favorable surface fraction completely unfavorable by modifying the ratio of the radial to normal fluid velocity. Utilizing the real favorable area fraction of the collector, the patch model expression for calculating the deposition efficiency is modified for impinging jet flow geometry.

Journal Article↗

PubMed2005

Simulations of a dielectrophoretic membrane filtration process for removal of water droplets from water-in-oil emulsions.

A novel separation technique based on simultaneous application of AC dielectrophoresis and preferential transport through a semipermeable hydrophilic membrane is proposed for separation of small amounts of emulsified water droplets from a water-in-oil emulsion. Embedding an array of parallel microelectrodes on a membrane matrix, followed by application of an AC potential to these electrodes, can result in capturing the water droplets onto the membranes from the emulsion during a crossflow filtration process. The present paper describes the theoretical principles underlying such a process, and describes a simple mathematical framework based on trajectory analysis for assessing the separation efficiency of such a technique. The results indicate that superimposition of an AC dielectrophoretic field can significantly enhance the preferential transport of the emulsified water through the membrane in a crossflow filtration device. This can lead to a highly efficient continuous separation process for dilute emulsions.

Journal Article↗

PubMed2005

Fractal structure of asphaltene aggregates.

A photographic technique coupled with image analysis was used to measure the size and fractal dimension of asphaltene aggregates formed in toluene-heptane solvent mixtures. First, asphaltene aggregates were examined in a Couette device and the fractal-like aggregate structures were quantified using boundary fractal dimension. The evolution of the floc structure with time was monitored. The relative rates of shear-induced aggregation and fragmentation/restructuring determine the steady-state floc structure. The average floc structure became more compact or more organized as the floc size distribution attained steady state. Moreover, the higher the shear rate is, the more compact the floc structure is at steady state. Second, the fractal dimensions of asphaltene aggregates were also determined in a free-settling test. The experimentally determined terminal settling velocities and characteristic lengths of the aggregates were utilized to estimate the 2D and 3D fractal dimensions. The size-density fractal dimension (D(3)) of the asphaltene aggregates was estimated to be in the range from 1.06 to 1.41. This relatively low fractal dimension suggests that the asphaltene aggregates are highly porous and very tenuous. The aggregates have a structure with extremely low space-filling capacity.

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PubMed2005

Adsorption isotherms of associating asphaltenes at oil/water interfaces based on the dependence of interfacial tension on solvent activity.

In the Gibbs adsorption equation, the application of solvent activity for the calculation of the surface/interfacial excess is proposed for nonideal or associating or pseudocomponents such as asphaltenes. For the aforementioned systems, only the mass-based phenomenological interfacial excess can be determined based on interfacial tension versus activity data. The use of the mole fraction is compared to the use of the activity when the adsorbed amount of associating asphaltenes is calculated at a water/toluene interface. Langmuir-type isotherms describe the adsorption of asphaltenes at toluene/water interfaces. Asphaltenes were treated to remove the resins and natural surfactants using cyclic precipitation and dissolution of asphaltenes at a fixed aliphatic/aromatic ratio. Different fractions of asphaltenes were obtained by changing the aliphatic/aromatic ratio of the precipitating solvent. The limiting molar masses of asphaltenes measured by vapor pressure osmometry are different for fractions precipitated at different heptane to toluene ratios. The mass-based adsorbed amounts at the water/toluene interface, at a 0.1 asphaltene-to-toluene mass-ratio, varied in the range of 0.8-2.8 mg/m(2), depending on the molar mass of asphaltenes.

Journal Article↗

PubMed2004

Effect of charged colloidal particles on adsorption of surfactants at oil-water interface.

A change of oil/water interfacial tension in the presence of cationic or anionic surfactants in an organic phase was observed due to the addition of charged fine solids in the aqueous phase. The charged fine solids in the aqueous phase adsorb surfactants diffused from the oil phase, thereby causing an increase in the bulk equilibrium surfactant concentration in the aqueous phase, governed by the Stern-Grahame equation. Consequently, surfactant adsorption at the oil-water interface increases, which was demonstrated from the measured reduction of the oil-water interfacial tension. The increased surfactant partition in the aqueous phase in the presence of the charged particles was confirmed by the measured decrease in the surface tension for the collected aqueous solution after solids removal, as compared with the cases without solids addition.

Journal Article↗

PubMed2004

Hydrodynamic dispersion due to combined pressure-driven and electroosmotic flow through microchannels with a thin double layer.

The hydrodynamic dispersion of a nonadsorbed and nonelectrolyte solute is considered for the case of a flow driven through a straight microchannel by pressure and electric potential differences. The analysis is conducted using a thin double layer approximation developed in the previous paper (Zholkovskij, E. K.; Masliyah, J. H.; Czarnecki, J. Anal. Chem. 2003, 75, 901-909). On the basis of this approach, an expression is derived to address the dispersion coefficient for arbitrary electrokinetic potential, electrolyte type, and cross-section geometry. In the derived expression, the influence of cross-section geometry manifests itself through the channel hydrodynamic radius and through three dimensionless geometrical factors. The procedure for obtaining the geometrical factors is presented for an arbitrary cross-section geometry. The geometrical factors are evaluated for several examples of cross section: (i) unbounded parallel planes; (ii) circle; (iii) annulus; (iv) ellipse; (v) rectangle. The dependency of the dispersion coefficient on different parameters is discussed. It is shown that the dependencies are substantially affected by the cross-section geometry, electrolyte type, and electrokinetic potential.

Journal Article↗

PubMed2003

Studies of Athabasca asphaltene Langmuir films at air-water interface.

Asphaltenes are present in heavy oils and bitumen. They are a mixture of hydrocarbons having complex structures of polyaromatic rings and short side chains. In general, the high-molecular-weight asphaltene is the most aromatic fraction with the highest number of side chains and the low-molecular-weight asphaltene contains the lowest number of side chains, while the number of side chains of the whole asphaltene fraction lies in between. In this study, asphaltenes were extracted and/or fractionated from Athabasca oil sand bitumen. Subfractions of high and low molecular weight and the whole asphaltenes were characterized using a Langmuir trough and complementary techniques such as VPO, FTIR, AFM, and contact angle measurements. At an air-water interface, amphiphilic asphaltene molecules can form a monolayer. Various fractions (high, low, and whole) of the asphaltene molecules behave similarly at the air-water interface, characterized by close resemblance of their surface pressure-area, hysteresis, and relaxation isotherms. The high-molecular-weight asphaltene is the most expanded fraction, while the low-molecular-weight asphaltene fraction is the most condensed, with the whole asphaltene lying in between. At the air-water interface a monolayer of the low-molecular-weight asphaltene relaxes at a faster rate than one of the high-molecular-weight asphaltene.

Air↗

PubMed2003

Effect of surface mobility on the particle sliding along a bubble or a solid sphere.

The sliding velocity of glass beads on a spherical surface, made either of an air bubble or of a glass sphere held stationary, is measured to investigate the effect of surface mobility on the particle sliding velocity. The sliding process is recorded with a digital camera and analyzed frame by frame. The sliding glass bead was found to accelerate with increasing angular position on the collector's surface. It reaches a maximum velocity at an angular position of about 100 degrees and then, under certain conditions, the glass bead leaves the surface of the collector. The sliding velocity of the glass bead depends strongly on the surface mobility of a bubble, decreasing with decreasing surface mobility. By a mobile surface we mean one which cannot set up resistive forces to an applied stress on the surface. The sliding velocity on a rigid surface, such as a glass sphere, is much lower than that on a mobile bubble surface. The sliding velocity can be described through a modified Stokes equation. A numerical factor in the modified Stokes equation is determined by fitting the experimental data and is found to increase with decreasing surface mobility. Hydrophobic glass beads sliding on a hydrophobic glass sphere were found to stick at the point of impact without sliding if the initial angular position of the impact is less than some specific angle, which is defined as the critical sticking angle. The sticking of the glass beads can be attributed to the capillary contracting force created by the formation of a cavity due to spontaneous receding of the nonwetting liquid from the contact zone. The relationship between the critical sticking angle and the particle size is established based on the Yushchenko [J. Colloid Interface Sci. 96 (1983) 307] analysis.

Journal Article↗

PubMed2003

Electroosmotic dispersion in microchannels with a thin double layer.

Dispersion of a nonelectrolyte solute due to the electroosmotic flow in long straight microchannels was analyzed theoretically. A version of the Aris-Taylor procedure was employed to predict the dispersion coefficient for arbitrary geometry of the microchannel cross section. The analysis was conducted using a thin double-layer approximation, which is valid when the Debye length is much smaller than the characteristic dimensions of the cross section. For thin double layers, the obtained results describe the electroosmotic dispersion for arbitrary surface potential, electrolyte type, and cross-section geometry. Dispersion for several cases of the cross-section geometries was discussed. It was shown that, for given values of the surface potential and the Debye length, both the cross-section geometry and the electrolyte content of the driven solution substantially affect the dispersion of a nonelectrolyte solute. In the relevant particular cases, the obtained results agree with predictions of the previous theories.

Journal Article↗

PubMed2003

Emulsion stability based on phase behavior in sodium naphthenates containing systems: gels with a high organic solvent content.

Addition of heptane to a sodium naphthenates/toluene/water system at 25 degrees C reduces the lamellar liquid-crystal phase range and increases the microemulsion phase range. Both of these effects result in the extension of the composition range where emulsions have low stability. This effect is even stronger at 40 degrees C. Heptane addition also results in the formation of very stable emulsions within the overlapping phase-existence ranges of aqueous (L1) and organic (L2) phases. Stable non-birefringent gel observed in equilibrium with L1 and L2 phases contains only a small percentage of water and sodium naphthenates. The swelling behavior of an unstable gel, an emulsion previously compressed by centrifugation, appears to be due to a stepwise thickening of the thin liquid films between the droplets.

Journal Article↗

PubMed2002

Sandwich structures at oil-water interfaces under alkaline conditions.

Equilibrium liquid crystal (LC) layer on an interface between crude oils and water was observed at high pH. This layer is composed mainly of sodium naphthenates produced in situ at the water/oil interface. Transient LC layer was also evolved at the interface of aqueous phase of sodium hydroxide solutions and oleic phase of naphthenic acid (NA) solutions as result of a chemical reaction between NaOH and NA. This chemical reaction causes transport process resulting in a disturbance of the interface. Optical observation of this interface disturbance reviled that the interface covered with LC shows considerably lower flexibility as compared to LC free interface. The LC layer eventually dissolves in the water phase at low oil-to-water ratio, while at high oil-to-water ratio it can form an equilibrium phase, which spreads spontaneously at the oil-water interface.

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