Influence of confinement by smooth and rough walls on particle dynamics in dense hard-sphere suspensions

We used video microscopy and particle tracking to study the dynamics of confined hard-sphere suspensions. Our fluids consisted of 1.1-μm-diameter silica spheres suspended at volume fractions of 0.33–0.42 in water-dimethyl sulfoxide. Suspensions were confined in a quasiparallel geometry between two glass surfaces: a millimeter-sized rough sphere and a smooth flat wall. First, as the separation distance (H) is decreased from 18 to 1 particle diameter, a transition takes place from a subdiffusive behavior (as in bulk) at large H, to completely caged particle dynamics at small H. These changes are accompanied by a strong decrease in the amplitude of the mean-square displacement (MSD) in the horizontal plane parallel to the confining surfaces. In contrast, the global volume fraction essentially remains constant when H is decreased. Second, measuring the MSD as a function of distance from the confining walls, we found that the MSD is not spatially uniform but smaller close to the walls. This effect is the strongest near the smooth wall where layering takes place. Although confinement also induces local variations in volume fraction, the spatial variations in MSD can be attributed only partially to this effect. The changes in MSD are predominantly a direct effect of the confining surfaces. Hence, both the wall roughness and the separation distance (H) influence the dynamics in confined geometries

Measuring Advection and Diffusion of Colloids in Shear Flow

An analysis of the dynamics of colloids in shear flow can be challenging because of the superposition of diffusion and advection. We present a method that separates the two motions, starting from the time-dependent particle coordinates. The restriction of the tracking to flow lanes and the subtraction of estimated advective displacements are combined in an iterative scheme that eventually makes the spatial segmentation redundant. Tracking errors due to the neglect of lateral diffusion are avoided, while drifts parallel and perpendicular to the flow are eliminated. After explaining the principles of our method, we validate it against both computer simulations and experiments. A critical overall test is provided by the mean square displacement function at high Peclet numbers (up to 50). We demonstrate via simulations how the measurement accuracy depends on diffusion coefficients and flow rates, expressed in units of camera pixels and frames. Also, sample-specific issues are addressed: inaccuracies in the velocity profile for dilute suspensions (volume fraction ≤0.03) and tracking errors for concentrated ones (VF ≥ 0.3). An analysis of experiments with colloidal spheres flowing through microchannels corroborates these findings and indicates perspectives for studies on transport, mixing, or rheology in microfluidic environments

Adhesive Hard-Sphere Colloidal Dispersions. A Small-Angle Neutron-Scattering Study of Stickiness and the Structure Factor

Small-angle neutron-scattering structure factor measurements were made on sterically stabilized silica spheres dispersed in benzene up to volume fractions of 0.30. Benzene is only a marginal solvent for the stabilizing layer on the surface of the particles. The particles are made attractive by lowering temperature. This attraction is modeled by a square well potential, the depth of which varies with temperature. At the highest temperature studied, our experimental system behaved effectively as an assembly of hard spheres, whereas at the lowest temperature the system approaches a spinodal. Using Baxter's theory we were able to evaluate the interaction parameters and to calculate the structure factor. Experimental structure factors were satisfactorily reproduced over the entire temperature range studied

Charge inversion and colloidal stability of carbon black in battery electrolyte solutions

Colloids and Surfaces A: Physicochemical and Engineering Aspects is an international journal devoted to the science of the fundamentals, engineering fundamentals, and applications of colloidal and interfacial phenomena and processes. The journal aims at publishing research papers of high quality and lasting value. In addition, the journal contains critical review papers by acclaimed experts, brief notes, letters, book reviews, and announcements. Basic areas of interest include the following: theory and experiments on fluid interfaces; adsorption; surface aspects of catalysis; dispersion preparation, characterization and stability; aerosols, foams and emulsions; surfaces forces; micelles and microemulsions; light scattering and spectroscopy; detergency and wetting; thin films, liquid membranes and bilayers; surfactant science; polymer colloids; rheology of colloidal and disperse systems; electrical phenomena in interfacial and disperse systems. These and related areas are rich and broadly applicable to many industrial, biological and agricultural systems. Of interest are applications of colloidal and interfacial phenomena in the following areas: separation processes; materials processing; biological systems (see also companion publication Colloids and Surfaces B: Biointerfaces); environmental and aquatic systems; minerals extraction and metallurgy; paper and pulp production; coal cleaning and processing; oil recovery; household products and cosmetics; pharmaceutical preparations; agricultural, soil and food engineering; chemical and mechanical engineering

Linear viscoelastic behavior of aggregated colloidal dispersions

The viscoelastic behavior of a depletion-flocculated dispersion of colloidal spheres is investigated at different volume fractions of the spheres, using a controlled stress and a dynamic rheometer. Combining the results, we obtain the storage G′ and loss G′′ moduli over a frequency range of 0.02<ω<200rad/s. The measured G′ gradually increases with increasing frequency, while G′′ almost remains constant, indicating a broad spectrum of relaxation times. To describe and explain the observed behavior of the moduli as a function of frequency and volume fraction in terms of microscopic parameters, a microrheological model based on the fractal concept is proposed. Comparing experimental results with model calculations, we find a good agreement between the two, with physically plausible parameter values

Ion adsorption-induced wetting transition in oil-water-mineral systems

The relative wettability of oil and water on solid surfaces is generally governed by a complex competition of molecular interaction forces acting in such three-phase systems. Herein, we experimentally demonstrate how the adsorption of in nature abundant divalent Ca2+ cations to solid-liquid interfaces induces a macroscopic wetting transition from finite contact angles (≈10°) with to near-zero contact angles without divalent cations. We developed a quantitative model based on DLVO theory to demonstrate that this transition, which is observed on model clay surfaces, mica, but not on silica surfaces nor for monovalent K+ and Na+ cations is driven by charge reversal of the solid-liquid interface. Small amounts of a polar hydrocarbon, stearic acid, added to the ambient decane synergistically enhance the effect and lead to water contact angles up to 70° in the presence of Ca2+. Our results imply that it is the removal of divalent cations that makes reservoir rocks more hydrophilic, suggesting a generalizable strategy to control wettability and an explanation for the success of so-called low salinity water flooding, a recent enhanced oil recovery technology