A method for preparing hydrophilic charged composite ultrafiltration membrane
An ultrafiltration membrane, hydrophilic technology, applied in the field of preparing hydrophilic charged composite ultrafiltration membrane, can solve the problems of high transmembrane pressure, poor permeability, poor hydrophilicity, etc., and achieve enhanced charging properties and performance. Long-lasting, stable and low-cost effects
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[0050] The method for preparing the hydrophilic charged composite ultrafiltration membrane of the present invention adds acrylamide (AM), acrylic acid (AA) and 2-acrylamido-2-methylpropanesulfonic acid (AMPS) to the film-forming liquid. ) three kinds of monomers, and then generate a high molecular copolymer additive by initiating free radical polymerization. Hydrophilic modification and enhanced electronegative performance. The composite ultrafiltration membrane prepared by the non-solvent-induced phase separation method using the film-forming solution containing the high-molecular copolymer additive, the high-molecular copolymer additive molecule with strong hydrophilicity and negatively charged properties is embedded in the membrane, which can effectively Improve the hydrophilicity, membrane flux and anti-fouling ability of the ultrafiltration membrane, and the performance is durable and stable. The method avoids the technical problem that the polymer copolymer additive is ...
Embodiment 1
[0084] (1) Dissolve AM, AA and AMPS monomers with a total weight of 0.1 g in 100 g of DMF solvent at a ratio of 1:1:1, and stir at a high speed at 95°C to fully dissolve. Then add 22 grams of PES special film-making material, stir at 90°C for 12 hours until it is completely dissolved, and prepare a film-forming solution with a mass ratio of monomer, film-making material and solvent of 0.1:22:100.
[0085] (2) Add 0.01 g of initiator azobisisobutyronitrile (ABIN) to the film-forming solution, and carry out free radical polymerization at 5° C. for 12 hours. The film-forming liquid after the reaction was degassed for 12 hours under negative pressure to obtain a film-forming liquid containing AM-AA-AMPS copolymer additive.
[0086] (3) The film-forming solution containing the AM-AA-AMPS copolymer additive prepared by step (2) is passed through a flat-panel film-making equipment using a non-solvent-induced phase inversion method, and water is used as a coagulation bath to prepare a...
Embodiment 2
[0089] (1) Dissolve AM, AA and AMPS monomers with a total weight of 5 grams in 100 grams of DMF solvent at a ratio of 0.1:1:3, and stir at a high speed at 55°C to fully dissolve. Then add 2 grams of PVP and 15 grams of PES special film-making material, stir at 75°C for 12 hours until they are completely dissolved, and prepare a composition with a mass ratio of monomer, other additives, film-making material and solvent of 5:2:15:100. Membrane fluid.
[0090] (2) Add 0.05 g of initiator dicumyl peroxide to the film-forming solution, and carry out free radical polymerization at 5° C. for 12 hours. The film-forming liquid after the reaction was degassed for 12 hours under negative pressure to obtain a film-forming liquid containing AM-AA-AMPS copolymer additive.
[0091] (3) The film-forming solution containing the AM-AA-AMPS copolymer additive prepared by step (2) is passed through a flat-panel film-making equipment using a non-solvent-induced phase inversion method, and water i...
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