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A comprehensive study of the polyaniline influence on mineral scaling on the surface of the heterogeneous MK-40 sulfocationite membrane under electrodialysis has been conducted. Current-voltage curves and chronopotentiograms have been obtained and analyzed for the pristine MK-40 membrane and the MK-40 membrane which is surface-modified by polyaniline. The study of the electrochemical behavior of membranes has been accompanied by the simultaneous control of the pH of the solution outcoming from the desalination compartment. The mixture of NaCO, KCl, CaCl, and MgCl is used as a model salt solution. Two limiting states are observed on the current-voltage curve of the surface-modified membrane. There is the first pseudo-limiting state in the range of small values of the potential drop. The second limiting current is comparable with that of the limiting current for the pristine membrane. It is shown that chronopotentiometry cannot be used as a self-sufficient method for membrane scaling identification on the surface-modified membrane at high currents. A mineral scale on the surfaces of the studied membranes has been found by scanning electron microscopy. The amount of precipitate is higher in the case of the surface-modified membrane compared with the pristine one.
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http://dx.doi.org/10.3390/membranes10070145 | DOI Listing |
Polymers (Basel)
August 2023
Department of Analytical Chemistry, Chemical Faculty, Voronezh State University, Universitetskaya pl. 1, 394018 Voronezh, Russia.
Membranes (Basel)
May 2023
A.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, Leninsky Prospect 29, 119991 Moscow, Russia.
The thermal-oxidative degradation of aqueous solutions of carbonized monoethanolamine (MEA, 30% wt., 0.25 mol MEA/mol CO) was studied for 336 h at 120 °C.
View Article and Find Full Text PDFMembranes (Basel)
January 2023
Faculty of Chemistry, Voronezh State University, 394018 Voronezh, Russia.
The modification of an MB-2 bipolar ion exchange membrane with chromium (III) hydroxide was carried out by a chemical method, namely, by the sequential treatment of the membrane with a solution of chromium (III) salt and alkali. Data on the morphology, phase, and chemical composition of the modified membrane were obtained using scanning electron microscopy and energy-dispersive analysis. In particular, it was shown that the modifier was distributed in a layer 30-50 microns thick at the boundary of the cation- and anion-exchange layers of the bipolar membrane.
View Article and Find Full Text PDFMembranes (Basel)
January 2023
Department of Analytical Chemistry, Voronezh State University, 1 Universitetskaya pl., 394018 Voronezh, Russia.
The alterations in current-voltage and transport characteristics of highly basic and strongly acidic ion-exchange membranes, during the electrodialysis of solutions containing a heterocyclic amino acid and a strong electrolyte, were studied. An increase in the catalytic activity of the water splitting process at the surface of heterogeneous MK-40 and MA-41 membranes upon prolonged contact with proline and tryptophan solutions was found. A significant effect of electroconvection on the components mass transfer through the cation-exchange membrane in the intensive current mode of electrodialysis was revealed for the solution containing a heterocyclic amino acid along with mineral salt (NaCl).
View Article and Find Full Text PDFPolymers (Basel)
November 2022
Physical Chemistry Department, Kuban State University, 350040 Krasnodar, Russia.
Electrodialysis with layer-by-layer coated membranes is a promising method for the separation of monovalent and polyvalent ions. Since the separation selectivity is significantly reduced in the presence of defects in the multilayer system, the stability of the modifiers becomes an important issue. This article reports the i-V curves of layer-by-layer coated membranes based on the heterogeneous MK-40 membrane before and after 50 h long electrodialysis of a solution containing sodium and calcium ions at an underlimiting current density, and the values of concentrations of cations in the desalination chamber during electrodialysis.
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