No Arabic abstract
Mixtures of near-symmetric oppositely charged components with strong attractive short range interactions exhibit ordered lamellar phases at low temperatures. In the strong segregation limit the state of these systems can be described by the location of the interfaces between the components. It has previously been shown that these systems are stable against small deformations of the interfaces. We examine their stability in the presence of a uniform electric field. When the field is perpendicular to the lamellae, the system is unstable against long wavelength deformations for all non-zero values of the external field. A field parallel to the lamellae produces deformed but persistent interfaces. In a finite thickness system, onset of an external perpendicular field modifies the ground state. Flow between the old and new ground states requires the destruction of the original interfaces; this destruction proceeds through the instabilities identified in the bulk case. We examine the possibility of dynamical stabilization of structures by means of oscillating fields.
Lattice Boltzmann simulations of liquid-gas systems are believed to be restricted to modest density ratios of less than 10. In this article we show that reducing the speed of sound and, just as importantly, the interfacial contributions to the pressure allows lattice Boltzmann simulations to achieve high density ratios of 1000 or more. We also present explicit expressions for the limits of the parameter region in which the method gives accurate results. There are two separate limiting phenomena. The first is the stability of the bulk liquid phase. This consideration is specific to lattice Boltzmann methods. The second is a general argument for the interface discretization that applies to any diffuse interface method.
Viscoelastic fluids exhibit elastic instabilities in simple shear flow and flow through curved streamlines. Surprisingly, we found in a porous medium such fluids show strikingly different hydrodynamic instabilities depicted by very large sideways excursions and presence of fast and slow moving lanes which have not been reported before. Particle image velocimetry (PIV) measurements through a pillared microchannel, provide experimental evidence of such instabilities at very low Reynolds number (< 0.01). We observe a transition from a symmetric laminar to an asymmetric flow, which finally transforms to a nonlinear aperiodic flow with strong lateral movements. The instability is characterized by a rapid increase in spatial and temporal fluctuations of velocity components and pressure at a critical Deborah number (De). Our experiments reveal the presence of a fascinating interplay between pore space and fluid rheology.
The movement of the particles in a capillary electrophoretic system under electroosmotic flow was modeled using Monte Carlo simulation with Metropolis algorithm. Two different cases, with repulsive and attractive interactions between molecules were taken into consideration. The simulation was done using a spin-like system where the interactions between the nearest and second closest neighbors were considered in two separate steps of the modeling study. A total of 20 different cases with different rate of interactions for both repulsive and attractive interactions were modeled. The movement of the particles through the capillary is defined as current. At a low interaction level between molecules, a regular electroosmotic flow is obtained, on the other hand, with increasing interactions between molecules the current shows a phase transition behavior. The results also show that a modular electroosmotic flow can be obtained for separations by tuning the ratio between molecular interactions and electric field strength.
We consider phase separated states in magnetic oxides (MO) thin films. We show that these states have a non-zero electric polarization. Moreover, the polarization is intimately related to a spatial distribution of magnetization in the film. Polarized states with opposite polarization and opposite magnetic configuration are degenerate. An external electric field removes the degeneracy and allows to switch between the two states. So, one can control electric polarization and magnetic configuration of the phase separated MO thin film with the external electric field.
Charged colloidal dispersions make up the basis of a broad range of industrial and commercial products, from paints to coatings and additives in cosmetics. During drying, an initially liquid dispersion of such particles is slowly concentrated into a solid, displaying a range of mechanical instabilities in response to highly variable internal pressures. Here we summarise the current appreciation of this process by pairing an advection-diffusion model of particle motion with a Poisson-Boltzmann cell model of inter-particle interactions, to predict the concentration gradients around a drying colloidal film. We then test these predictions with osmotic compression experiments on colloidal silica, and small-angle x-ray scattering experiments on silica dispersions drying in Hele-Shaw cells. Finally, we use the details of the microscopic physics at play in these dispersions to explore how two macroscopic mechanical instabilities -- shear-banding and fracture -- can be controlled.