Particle/wall electroviscous effects at the micron scale: comparison between experiments, analytical and numerical models.

We report a experimental study of the motion of 1 µm single particles interacting with functionalized walls at low and moderate ionic strengths conditions. The 3D particle's trajectories were obtained by analyzing the diffracted particle images (point spread function). The studied particle/wall systems include negatively charged particles interacting with bare glass, glass covered with polyelectrolytes and glass covered with a lipid monolayer. In the low salt regime (pure water) we observed a retardation effect of the short-time diffusion coefficients when the particle interacts with a negatively charged wall; this effect is more severe in the perpendicular than in the lateral component. The decrease of the diffusion as a function of the particle-wall distancehwas similar regardless the origin of the negative charge at the wall. When surface charge was screened or salt was added to the medium (10 mM), the diffusivity curves recover the classical hydrodynamic behavior. Electroviscous theory based on the thin electrical double layer (EDL) approximation reproduces the experimental data except for smallh. On the other hand, 2D numerical solutions of the electrokinetic equations showed good qualitative agreement with experiments. The numerical model also showed that the hydrodynamic and Maxwellian part of the electroviscous total drag tend to zero ash→ 0 and how this is linked with the merging of both EDL's at close proximity.

Transition from diffusive to subdiffusive motion in colloidal liquids.

In this work we report experimental and theoretical results for the motion of single colloidal particles embedded in complex fluids with different interparticle interactions. The motion of particles is found to follow a similar behavior for the different systems. In particular, the transition from the short-time diffusive motion to the subdiffusive intermediate-time motion is found to occur when the square root of its mean squared displacement is in the order of 1 tenth of the neighbors' interparticle distance, thus following a quantitative criterion similar to Lindemann's criterion for melting.

Hydrodynamic interactions between colloidal particles in a planar pore.

The correlation between the motion of pairs of colloidal particles confined in a planar pore is measured using optical microscopy. The systems studied here are aqueous suspensions of polystyrene spheres of diameter 1.9 µm, interacting as effective hard spheres, confined between two parallel planar plates separated by 2.9 µm. The lateral motion, along the plane parallel to the plates, of the particles is recorded with a time resolution of 30 frames s(-1). From the short-time motion, the hydrodynamic diffusion coefficients are determined as functions of the interparticle distance for various particle concentrations. At low concentrations, when the static correlation between particles is also low, the diffusion coefficients exhibit some symmetry, and at higher concentrations they are modulated by the structure of static correlation.

Colloidal diffusion inside a spherical cell.

The hydrodynamic hindering of a single-particle dynamics under total confinement is measured by optical microscopy. The three-dimensional trajectories of single-colloidal particles confined in spherical water globules of sizes only a few times the particle's diameter are tracked as they sample the entire volume of the globule. The hydrodynamic interactions between the particle and the spherical wall produce a dependence of the short-time diffusion on the particle's distance to the surface and an asymmetry in the radial and tangential components of the local diffusion coefficient, with the diffusion along the tangential direction being faster than along the radial direction. The latter decreasing close to the wall while the former being practically constant.

Effective potentials of dissipative hard spheres in granular matter.

We present an experimental study of the spatial correlations of a quasi-two-dimensional dissipative gas kept in a non-static steady state via vertical shaking. From high temporal resolution images we obtain the Pair Distribution Function (PDF) for granular species with different restitution coefficients. Effective potentials for the interparticle interaction are extracted using the Ornstein-Zernike equation with the Percus-Yevick closure. From both the PDFs and the corresponding effective potentials, we find a clear increase of the spatial correlation at contact with the decreasing values of the restitution coefficient.