There is currently great interest in the use of polyaniline (PAni) to impart particular properties to anion exchange membranes, employed in several fields. This special polymeric material can be obtained both chemically and electrochemically; however, the latter affords better control of morphology, which could be used to promote some properties of PAni-based membranes, such as their selectivity or hydrophobic/hydrophilic balance. In this work, commercially available membranes were electrochemically modified with PAni to improve their hydrophobic/hydrophilic balance, and this was achieved by cyclic voltammetry in acidic solutions. The performance of the modified membranes in the electrodialysis process of a nitrate-chloride mixture in neutral solutions was then evaluated. The impregnation imparts specific selective properties to the commercial membrane that lead to a greater retention of chloride ions. This property derives from the higher hydrophobicity of the PAni deposited on the membrane, which leads to a more effective exclusion of the more hydrated chloride anions.
We report a experimental study of the motion of 1μm 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 distance h was similar regardless the origin of the negative charge at the wall. When surface charge was screened or salt was added to the medium (10mM), 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 small h. 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 as h → 0 and how this is linked with the merging of both EDL’s at close proximity.
Nonhomogeneous evaporation fluxes have been shown to promote the formation of internal currents in sessile droplets, explaining the patterns that suspended particles leave after the droplet has dried out. Although most evaporation experiments have been conducted using spherical-cap-shaped drops, which are essentially in an axisymmetric geometry, here we show an example of nonhomogeneous evaporation in asymmetric geometries, which is visualized by following the motion of colloidal particles along liquid fingers forming a meniscus at square corners. It is found that the particle's velocity increases with the diffusive evaporation factor [Formula: see text] for the three tested fluids: water, isopropyl alcohol (IPA), and ethanol (EtOH). Here, [Formula: see text] is the vapor diffusivity in air, RH is the relative amount of vapor in the atmosphere, and cs is the saturated vapor concentration. We observed that in IPA and EtOH the internal currents promote a 3D spiral motion, whereas in water the particle's trajectory is basically unidirectional. By adding 0.25 critical micelle concentration (CMC) of sodium dodecyl sulfate (SDS) surfactant in water, a velocity blast was observed in the whole circulation flow pattern, going from [Formula: see text] to nearly [Formula: see text] in the longitudinal velocity component. To assess the effect of breaking the axisymmetric condition on the evaporation flux profile, we numerically solved the diffusive equation in model geometries that preserve the value of the contact angle θ but introduce an additional angle ϕ that characterizes the solid substrate. By testing different combinations of θ and ϕ, we corroborated that the evaporation flux increases when the substrate and the gas-liquid curves meet at corners with increasing sharpness.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.