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.

New processes for recycling valuable materials from used lithium-ion batteries (LIBs) need to be developed. This is critical to both meeting growing global demand and mitigating the electronic waste crisis. In contrast to the use of reagent-based processes, this work shows the results of testing a hybrid electrobaromembrane (EBM) method for the selective separation of Li⁺ and Co²⁺ ions. Separation is carried out using a track-etched membrane with a pore diameter of 35 nm, which can create conditions for separation if an electric field and an oppositely directed pressure field are applied simultaneously. It is shown that the efficiency of ion separation for a lithium/cobalt pair can be very high due to the possibility of directing the fluxes of separated ions to opposite sides. The flux of lithium through the membrane is about 0.3 mol/(m² × h). The presence of coexisting nickel ions in the feed solution does not affect the flux of lithium. It is shown that the EBM separation conditions can be chosen so that only lithium is extracted from the feed solution, while cobalt and nickel remain in it.

The entrance of even a small amount of phosphorus compounds into natural waters leads to global problems that require the use of modern purification technologies. This paper presents the results of testing a hybrid electrobaromembrane (EBM) method for the selective separation of Cl⁻ (always present in phosphorus-containing waters) and H₂PO₄⁻ anions. Separated ions of the same charge sign move in an electric field through the pores of a nanoporous membrane to the corresponding electrode, while a commensurate counter-convective flow in the pores is created by a pressure drop across the membrane. It has been shown that EBM technology provides high fluxes of ions being separated across the membrane as well as a high selectivity coefficient compared to other membrane methods. During the processing of solution containing 0.05 M NaCl and 0.05 M NaH₂PO₄, the flux of phosphates through a track-etched membrane can reach 0.29 mol/(m²×h). Another possibility for separation is the EBM extraction of chlorides from the solution. Its flux can reach 0.40 mol/(m²×h) through the track-etched membrane and 0.33 mol/(m²×h) through a porous aluminum membrane. The separation efficiency can be very high by using both the porous anodic alumina membrane with positive fixed charges and the track-etched membrane with negative fixed charges due to the possibility of directing the fluxes of separated ions in opposite sides.