cation-exchange membranes;
transport number between cations in;
electrodialysis;
conducting polymers;
polyethylene glycols;
crown ethers;
D O I:
10.1016/S0376-7388(01)00491-4
中图分类号:
TQ [化学工业];
学科分类号:
0817 ;
摘要:
Recent studies on selective permeation of specific cations through a cation-exchange membrane in electrodialysis, modification of the membrane and electrodialysis method, are reviewed. The studies are classified (1) to prepare the composite of the cation-exchange membrane with other polymers such as conducting polymers and cationic polyelectrolytes, (2) to change cation-exchange groups from sulfonic acid groups, which are used in conventional membranes, to other groups such as phosphonic acid groups, and (3) to electrodialyze the mixed salt solution in the presence of chelate-forming agent such as poly(ethylene glycol), crown ethers, etc. Though the formation of the layers of the conducting polymers on the surface of the cation-exchange membrane is effective on selective permeation of monovalent cations to divalent cations through the membrane, mechanism of the selective permeation is different depending on species of the conducting polymers: due to sieving of sodium ions from multivalent cations by a tight polypyrrole layer and due to stronger electrostatic repulsion force of the cationic charge in a polyaniline layer to multivalent cations than to the monovalent, which is similar to the membrane having a cationic polyelectrolyte layer on the surface. When cation-exchange groups such as phosphonic acid groups, which are strongly interacted with divalent cations, are introduced in the membrane, monovalent cations selectively permeate through the membrane. However, current efficiency in electrodialysis decreases due to strong binding of divalent cations to the groups-inactivation of cation-exchange groups. Electrodialysis in the presence of chelate-forming agents is effective on the selective permeation of specific cations that have low complex formation constants with the agents through the membrane without any decrease in the current efficiency. (C) 2002 Elsevier Science B.V. All rights reserved.
机构:
Univ Paris Est, ICMPE, CNRS, UMR 7182, 2 Rue Henri Dunant, F-94320 Thiais, France
Univ Carthage, Natl Inst Appl Sci & Technol INSAT, BP 676, Tunis 1080, TunisiaUniv Paris Est, ICMPE, CNRS, UMR 7182, 2 Rue Henri Dunant, F-94320 Thiais, France
Bdiri, M.
Dammak, L.
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Univ Paris Est, ICMPE, CNRS, UMR 7182, 2 Rue Henri Dunant, F-94320 Thiais, FranceUniv Paris Est, ICMPE, CNRS, UMR 7182, 2 Rue Henri Dunant, F-94320 Thiais, France
Dammak, L.
Chaabane, L.
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机构:
Univ Paris Est, ICMPE, CNRS, UMR 7182, 2 Rue Henri Dunant, F-94320 Thiais, FranceUniv Paris Est, ICMPE, CNRS, UMR 7182, 2 Rue Henri Dunant, F-94320 Thiais, France
Chaabane, L.
Larchet, C.
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机构:
Univ Paris Est, ICMPE, CNRS, UMR 7182, 2 Rue Henri Dunant, F-94320 Thiais, FranceUniv Paris Est, ICMPE, CNRS, UMR 7182, 2 Rue Henri Dunant, F-94320 Thiais, France
Larchet, C.
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机构:
Hellal, F.
Nikonenko, V.
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机构:
Kuban State Univ, Membrane Inst, 149 Stavropolskaya St, Krasnodar 350040, RussiaUniv Paris Est, ICMPE, CNRS, UMR 7182, 2 Rue Henri Dunant, F-94320 Thiais, France
Nikonenko, V.
Pismenskaya, N. D.
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机构:
Kuban State Univ, Membrane Inst, 149 Stavropolskaya St, Krasnodar 350040, RussiaUniv Paris Est, ICMPE, CNRS, UMR 7182, 2 Rue Henri Dunant, F-94320 Thiais, France
机构:
Kuban State Univ, Fac Chem & High Technol, Phys Chem Dept, Krasnodar 350040, RussiaKuban State Univ, Fac Chem & High Technol, Phys Chem Dept, Krasnodar 350040, Russia