Biomedical subjects

Anh V Nguyen

Publications and source records attributed to Anh V Nguyen.

13 recordsLinked to original sources

PubMed2006

A novel technique for improving interferometric determination of emulsion film thickness by digital filtration.

Determination of the thickness of emulsion films by using the film interferometric images is usually less accurate than that of foam films, due to the close values of the refractive indices of the liquid film and adjacent liquid phases (hence, low contrast and high level of noise at high magnification). A new technique was developed to improve the thickness determination by obtaining the interferometric images without directly filtering the illuminating light, as is usually done in the classical Scheludko interferometric technique. The new method then uses digital filtration during the off-line image post-processing to obtain monochromatic interferometric images required for the thickness determination. The technique was tested with foam films stabilised by sodium dodecyl sulfate and successfully applied to determine thickness of toluene-water-toluene emulsion films using the green and red digital filters. Results for emulsion film thickness determined by either the green or red digital filtration are comparable, thus validating the new technique developed here for emulsion films.

Letter↗

PubMed2005

Combining hydrodynamics and molecular kinetics to predict dewetting between a small bubble and a solid surface.

This paper examined the dewetting between a small air bubble and a solid surface in deionised water. Hydrodynamics was used in conjunction with surface molecular kinetics to model and predict the velocity of the moving contact line as a function of the dynamic macroscopic contact angle. The dewetting hydrodynamics was modelled following the approach developed specifically for drops and bubbles using the (absolute) coordinate system with the origin located at the centre of the contact area, which does not move with the moving contact line. The model provides accurate corrections unavailable in the generic hydrodynamic theories developed by Voinov and Cox, and removes the need for a macroscopic length scale employed in their generic theories. Molecular kinetics was used to determine the contact angle of the inner region close to the contact line, where the hydrodynamic approach breaks down due to the singularity. Unlike the generic hydrodynamic theories, the inner (microscopic) angle in our combined model is not a constant (a fitting parameter) but is a function of the moving contact line velocity and other molecular properties of the interfaces. The combined model agreed with the experimental data and produced physically consistent values for the slip length, molecular jumping distance and frequency. The dissolved gases accumulated at the non-wetting solid-liquid interface may influence the slip length.

Journal Article↗

PubMed2005

Hydrophobic attraction as revealed by AFM force measurements and molecular dynamics simulation.

Spherical calcium dioleate particles ( approximately 10 mum in diameter) were used as AFM (atomic force microscope) probes to measure interaction forces of the collector colloid with calcite and fluorite surfaces. The attractive AFM force between the calcium dioleate sphere and the fluorite surface is strong and has a longer range than the DLVO (Derjaguin-Landau-Verwey-Overbeek) prediction. The AFM force between the calcium dioleate sphere and the mineral surfaces does not agree with the DLVO prediction. Consideration of non-DLVO forces, including the attractive hydrophobic force and the repulsive hydration force, was necessary to explain the experimental results. The non-DLVO interactions considered were justified by the different interfacial water structures at calcite- and fluorite-water interfaces as revealed by the numerical computation experiments with molecular dynamics simulation.

Journal Article↗

PubMed2005

Critical thickness of microscopic thin liquid films.

This paper outlines the progress achieved during the four decades of research on the spontaneous destruction of the thinning microscopic liquid films through rupture or black spot formation at the so-called critical thickness. Although most of both experimental and theoretical results are primarily related to the foam films that form between gas bubbles, in many respects they can be principally generalized for emulsion films, as well as the wetting films confined between a bubble and a solid surface. The paper focuses on the validation, application and extension of the theory of the phenomenon. The experimental results are analysed with respect to the frequently observed deviations from the widely used model of a planar circular film with tangentially immobile surfaces. The applicability of the new theory of accelerated drainage due to spatial variation in thickness is expressed. The effects of surface tension, surface mobility, variation of the film size, and spatial thickness heterogeneity on the critical thickness are compared.

Adsorption↗

PubMed2005

Heterocoagulation of chalcopyrite and pyrite minerals in flotation separation.

Heterocoagulation between various fine mineral particles contained within a mineral suspension with different structural and surface chemistry can interfere with the ability of the flotation processes to selectively separate the minerals involved. This paper examines the interactions between chalcopyrite (a copper mineral) and pyrite (an iron mineral often bearing gold) as they approach each other in suspensions with added chemicals, and relates the results to the experimental data for the flotation recovery and selectivity. The heterocoagulation was experimentally studied using the electrophoretic light scattering (ELS) technique and was modelled by incorporating colloidal forces, including the van der Waals, electrostatic double layer and hydrophobic forces. The ELS results indicated that pyrite has a positive zeta potential (zeta) up to its isoelectric point (IEP) at approximately pH 2.2, while chalcopyrite has a positive zeta up to its IEP at approximately pH 5.5. This produces heterocoagulation of chalcopyrite with pyrite between pH 2.2 and pH 5.5. The heterocoagulation was confirmed by the ELS spectra measured with a ZetaPlus instrument from Brookhaven and by small-scale flotation experiments.

Adsorption↗

PubMed2005

Effect of sodium dodecylbenzene sulfonate on the motion of three-phase contact lines on the Wilhelmy plate surface.

The combined approach of the molecular-kinetic and hydrodynamic theories for description of the motion of three-phase gas-liquid-solid contact lines has been examined using the Wilhelmy plate method. The whole dynamic meniscus has been divided into molecular, hydrodynamic, and static-like regions. The Young-Laplace equation and the molecular-kinetic and hydrodynamic dewetting theories have been applied to describe the meniscus profiles and contact angle. The dissipative forces accompanying the dynamic dewetting have also been investigated. The experiments with a Wilhelmy plate made from an acrylic polymer sheet were carried out using a computerized apparatus for contact angle analysis (OCA 20, DataPhysics, Germany). The extrapolated dynamic contact angle versus velocity of the three-phase contact line for Milli-Q water and 5x10(-4) M SDBS solution was experimentally obtained and compared with the combined MHD models with low and moderate Reynolds numbers. The models predict similar results for the extrapolated contact angle. SDBS decreases the equilibrium contact angle and increases the molecular jumping length but does not affect the molecular frequency significantly. The hydrodynamic deformation of the meniscus, viscous dissipation, and friction were also influenced by the SDBS surfactant.

Journal Article↗

PubMed2004

Exact and global rational approximate expressions for resistance coefficients for a colloidal solid sphere moving in a quiescent liquid parallel to a slip gas-liquid interface.

In this paper mathematical expressions have been developed to describe the hydrodynamic resistance force on a colloidal particle as it slides along a slip surface of a gas bubble held stationary in a quiescent liquid. The particle size was considered to be sufficiently small relative to the bubble size so that the bubble surface could be locally approximated to a planar interface. The modeling incorporated a bispherical coordinate transformation to solve the equations governing the liquid creeping flow disturbed by the particle. Exact numerical solutions for the resistance coefficients of the particle-shearing motion parallel to the slip bubble surface were obtained as a function of the separation distance from the bubble surface. Finally, simplified analytical rational approximations for the whole range of the separation distance were presented, which were in good agreement with the exact numerical result. Importantly, the approximations for the modeling and simulation of the bubble-particle interactions are mathematically tractable.

Journal Article↗

PubMed2004

Movement of fine particles on an air bubble surface studied using high-speed video microscopy.

A CCD high-speed video microscopy system operating at 1000 frames per second was used to obtain direct quantitative measurements of the trajectories of fine glass spheres on the surface of air bubbles. The glass spheres were rendered hydrophobic by a methylation process. Rupture of the intervening water film between a hydrophobic particle and an air bubble with the consequent formation of a three-phase contact was observed. The bubble-particle sliding attachment interaction is not satisfactorily described by the available theories. Surface forces had little effect on the particle sliding with a water film, which ruptured probably due to the submicrometer-sized gas bubbles existing at the hydrophobic particle-water interface.

Journal Article↗

PubMed2003

The dynamic nature of contact angles as measured by atomic force microscopy.

Atomic force microscopy appears to be a useful tool for determining the contact angle for small particles. It is shown in this paper that the contact angle of a spherical polyethylene particle changes with the speed of the AFM piezoelectric translator. Such dynamic behavior of the contact angle and other uncertainties such as the position of the three-phase contact on the particle surface during bubble-particle interaction make it difficult to decide whether or not the AFM single-particle contact angle can be used to describe the hydrophobic state of the particle surface.

Letter↗

PubMed2002

Influence of electrical double-layer interaction on coal flotation.

In the early 1930s it was first reported that inorganic electrolytes enhance the floatability of coal and naturally hydrophobic minerals. To date, explanations of coal flotation in electrolytes have not been entirely clear. This research investigated the floatability of coal in NaCl and MgCl2 solutions using a modified Hallimond tube to examine the role of the electrical double-layer interaction between bubbles and particles. Flotation of coal was highly dependent on changes in solution pH, type of electrolyte, and electrolyte concentration. Floatability of coal in electrolyte solutions was seen not to be entirely controlled by the electrical double-layer interaction. Coal flotation in low electrolyte concentration solutions decreases with increase in concentration, not expected from the theory since the electrical double layer is compressed, resulting in diminishing the (electrical double layer) repulsion between the bubble and the coal particles. Unlike in low electrolyte concentration solutions, coal flotation in high electrolyte concentration solutions increases with increase in electrolyte concentration. Again, this behavior of coal flotation in high electrolyte concentration solutions cannot be quantitatively explained using the electrical double-layer interaction. Possible mechanisms are discussed in terms of the bubston (i.e., bubble stabilized by ions) phenomenon, which explains the existence of the submicron gas bubbles on the hydrophobic coal surface.

Journal Article↗

PubMed2002

Liquid drainage in single plateau borders of foam.

This paper reports on an investigation of the influence of the interfacial shear viscosity on the liquid drainage in single Plateau borders of foam. The simplified Navier-Stokes equation governing the liquid flow is solved for the liquid velocity by the numerical computational method. The numerical results show significant influence of the interfacial shear viscosity on the liquid velocity in the Plateau border. Comparison of the numerical results for the average velocity over the cross-section area of the Plateau border to the available analytical solution shows that the available analytical solution underestimates the average velocity. New, simple yet accurate correlations for the dependence of the average velocity on the radius of the cross section of the Plateau border, the pressure gradient, and the interfacial shear viscosity are obtained using the asymptotic analysis and the numerical data.

Journal Article↗

PubMed2002

Empirical equations for meniscus depression by particle attachment.

In this paper the problem of calculating the depression of the gas-liquid meniscus by the particle attachment was solved. The analytical approximate equations obtained for small and large radii, r(tpc), of the three-phase contact were analyzed and compared to the available numerical results. The Derjaguin equation for small r(tpc) and the analytical results for large r(tpc) are accurate for r(tpc)/L< or =0.2 and r(tpc)/L> or =2, respectively, where L is the capillary length. For the meniscus depression with r(tpc)/L from 0.2 to 2, the empirical equations were obtained based on the asymptotic analysis of the analytical approximate solutions. The empirical numerical constants were obtained by fitting to the exact numerical results. The empirical equations together with the analytical approximate equations provide the accurate predictions for the meniscus depression for the whole range of the radius of the three-phase contact and are expected to be useful for modeling the detachment interaction in the flotation separation processes.

Journal Article↗

PubMed2002

The liquid flow force on a particle in the bubble-particle interaction in flotation.

In this paper the problem of calculating the liquid flow force on a particle in interaction with an air bubble with a mobile surface in flotation as a function of the separation distance was solved. The force equation was obtained by first deriving the disturbed flow confined between the surfaces. The model for the force includes the separation distance between the bubble and the particle, the particle size, the bubble's Reynolds number, the bubble rise velocity, and the polar position of the particle on the bubble surface. The proposed equations provide an exact solution to the situation where the particle and the bubble are very close together. The attractive flow force and the surface forces are of similar orders of magnitude. Consequently, the models presented in this paper should provide a better estimate for calculating the forces on particles interacting with air bubbles in mineral flotation and other separation operations involving colloidal interactions.

Journal Article↗