Electrokinetic and Electroconvective Effects in Ternary Electrolyte Near Ion-Selective Microsphere.

The paper presents theoretical and experimental investigations of the behavior of an electrolyte solution with three types of ions near an ion-selective microparticle with electrokinetically and pressure-driven flow. A special experimental cell has been developed for the investigations. An anion-selective spherical particle composed of ion-exchange resin is fixed in the center of the cell. An enriched region with a high salt concentration appears at the anode side of the particle when an electric field is turned on, according to the nonequilibrium electrosmosis behavior. A similar region exists near a flat anion-selective membrane. However, the enriched region near the particle produces a concentration jet that spreads downstream akin to a wake behind an axisymmetrical body. The fluorescent cations of Rhodamine-6G dye are chosen as the third species in the experiments. The ions of Rhodamine-6G have a 10-fold lower diffusion coefficient than the ions of potassium while bearing the same valency. This paper shows that the concentration jet behavior is described accurately enough with the mathematical model of a far axisymmetric wake behind a body in a fluid flow. The third species also forms an enriched jet, but its distribution turns out to be more complex. The concentration of the third species increases in the jet with an increase in pressure gradient. The pressure-driven flow stabilizes the jet, yet electroconvection has been observed near the microparticle for sufficiently strong electric fields. The electrokinetic instability and the electroconvection partially destroy the concentration jet of salt and the third species. The conducted experiments show good qualitative agreement with the numerical simulations. The presented results could be used in future for implementing microdevices based on membrane technology for solving problems of detection and preconcentration, and thus simplifying chemical and medical analyses utilizing the superconcentration phenomenon. Such devices are called membrane sensors, and are actively being studied.

Efficient Anion-Exchange Membranes with Anti-Scaling Properties Obtained by Surface Modification of Commercial Membranes Using a Polyquaternium-22.

Anion-exchange membranes modified with a polyquaternium-22 (PQ-22) polymer were studied for their use in electrodialysis. The use of PQ-22 for modification makes it possible to "replace" weakly basic amino groups on the membrane surface with quaternary amino groups. It was found that the content of quaternary amino groups in PQ-22 is higher than the content of carboxyl groups, which is the reason for the effectiveness of this polymer even when modifying Ralex AHM-PES membranes that initially contain only quaternary amino groups. In the case of membranes containing weakly basic amino groups, the PQ-22 polymer modification efficiency is even higher. The surface charge of the modified MA-41P membrane increased, while the limiting current density on the current-voltage curves increased by more than 1.5 times and the plateau length decreased by 2.5 times. These and other characteristics indicate that the rate of water splitting decreased and the electroconvective mixing at the membrane surface intensified, which was confirmed by direct visualization of vortex structures. Increasing the surface charge of the commercial MA-41P anion-exchange membrane, reducing the rate of water splitting, and enhancing electroconvection leads to mitigated scaling on its surface during electrodialysis.