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Chemical Modification of Polyethersulfone Nanofiltration Membranes: A Review

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JOURNAL OF APPLIED POLYMER SCIENCE
卷 114, 期 1, 页码 630-642

出版社

WILEY
DOI: 10.1002/app.30578

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polysulfone; poly(ether)sulfone; nanofiltration; membranes; modification; hydrophilicity; surface characteristics; grafting; plasma treatment; blending

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Polysulfone (PS) and poly(ether)sulfone (PES) are often used for synthesis of nanofiltration membranes, due to their chemical, thermal, and mechanical stability. The disadvantage for applying PS/PES is their high hydrophobicity, which increases membrane fouling. To optimize the performance of PS/PES nanofiltration membranes, membranes can be modified. An increase in membrane hydrophilicity is a good method to improve membrane performance. This article reviews chemical (and physicochemical) modification methods applied to increase the hydrophilicity of PS/PES nanofiltration membranes. Modification of poly(ether)sulfone membranes in view of increasing hydrophilicity can be carried out in several ways. Physical or chemical membrane modification processes after formation of the membrane create more hydrophilic surfaces. Such modification processes are (1) graft polymerization that chemically attaches hydrophilic monomers to the membrane surface; (2) plasma treatment, that introduces different functional groups to the membrane surface; and (3) physical preadsorption of hydrophilic components to the membrane surface. Surfactant modification, self-assembly of hydrophilic nanoparticles and membrane nitrification are also such membrane modification processes. Another approach is based on modification of polymers before membrane formation. This bulk modification implies the modification of membrane materials before membrane synthesis of the incorporation of hydrophilic additives in the membrane matrix during membrane synthesis. Sulfonation, carboxylation, and nitration are such techniques. To conclude, polymer blending also results in membranes with improved surface characteristics. (C) 2009 Wiley Periodicals, Inc. J Appl Polym Sci 114: 630-642, 2009

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