Diffusiophoresis in Multivalent Electrolytes.

Diffusiophoresis is the spontaneous movement of colloidal particles in a concentration gradient of solutes. As a small-scale phenomenon that harnesses energy from concentration gradients, diffusiophoresis may prove useful for passively manipulating particles in lab-on-a-chip applications as well as configurations involving interfaces. Though naturally occurring ions are often multivalent, experimental studies of diffusiophoresis have been mostly limited to monovalent electrolytes. In this work, we investigate the motion of negatively charged polystyrene particles in one-dimensional salt gradients for a variety of multivalent electrolytes. We develop a one-dimensional model and obtain good agreement between our experimental and modeling results with no fitting parameters. Our results indicate that the ambipolar diffusivity, which is dependent on the valence combination of cations and anions, dictates the speed of the diffusiophoretic motion of the particles by controlling the time scale at which the electrolyte concentration evolves. In addition, the ion valences also modify the electrophoretic and chemiphoretic contributions to the diffusiophoretic mobility of the particles. Our results are applicable to systems where the chemical concentration gradient is comprised of multivalent ions, and motivate future research to manipulate particles by exploiting ion valence.

Armoring confined bubbles in the flow of colloidal suspensions.

We study the process of coating the interface of a long gas bubble, which is translating in a horizontal circular capillary tube filled with a colloidal suspension. A typical elongated confined bubble is comprised of three distinct regions: a spherical front cap, a central body that is separated from the tube wall by a thin liquid film, and a spherical cap at the back. These three regions are connected by transitional sections. Particles gradually coat the bubble from the back to the front. We investigate the mechanisms that govern the initial accumulation of the particles and the growth of the particle-coated area on the interface of the bubble. We show that the initial accumulation of particles starts at the stable stagnation ring on the rear cap of the bubble, and the particles will completely coat the spherical cap at the back of the bubble before accumulating on the central body. Armoring the central interface of the bubble with particles thickens the liquid film around the bubble relative to that around the particle-free interface. This effect creates a rather sharp step on the interface of the bubble in the central region, which separates the armored region from the particle-free region. After the bubble is completely coated, the liquid film around the body of the bubble will adjust again to an intermediate thickness. We show that the three distinct thicknesses that the liquid film acquires during the armoring process can be well described analytically.