Amphoteric comb block polymer surfactant and preparation method thereof
A technology of surfactants and block polymers, applied in chemical instruments and methods, chemical/physical processes, dissolution, etc., can solve problems such as emulsion coalescence, sedimentation, and water resistance of emulsions
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Embodiment 1
[0022] 1mol 2-acrylamido-2-methyl-propanesulfonic acid (AMPS), 9mol butyl methacrylate (BMA), 0.033g catalytic chain transfer agent (COBF), 1.6mol water-soluble The nitrogen initiator azobisiso(azaminoethyl)butyl ether (AIBA). Stir and mix evenly, blow high-purity nitrogen gas after sealing, and put it in a water bath at 70-80°C for 9-11 hours. Add 0.5 mol butyl methacrylate (BMA), 1.6 mol water-soluble azo initiator azobisiso(azidoethyl) butyl ether (AIBA), 9.5 mol 2-hydroxyhexyl methacrylate (HEMA ), then seal the reactor and blow high-purity nitrogen into it, and react at 70-80° C. for 9-11 hours. After the reaction, it was purified with a mixed solution of methanol and distilled water at a volume ratio of 1:1. The product was dried in a vacuum oven at 40° C. for 24 hrs to obtain a dry product with a yield of 71%.
Embodiment 2
[0024] 2mol 2-acrylamido-2-methyl-propanesulfonic acid (AMPS), 8mol butyl methacrylate (BMA), 0.033g catalytic chain transfer agent (COBF), 1.6mol water-soluble The nitrogen initiator azobisiso(azaminoethyl)butyl ether (AIBA). Stir and mix evenly, blow high-purity nitrogen gas after sealing, and put it in a water bath at 70-80°C for 9-11 hours. Add 0.5 mol butyl methacrylate (BMA), 1.6 mol water-soluble azo initiator azobisiso(azidoethyl) butyl ether (AIBA), 9.5 mol 2-hydroxyhexyl methacrylate (HEMA ), then seal the reactor and blow high-purity nitrogen into it, and react at 70-80° C. for 9-11 hours. After the reaction, it was purified with a mixed solution of methanol and distilled water at a volume ratio of 1:1. The product was dried in a vacuum oven at 40° C. for 24 hrs to obtain a dry product with a yield of 67%.
Embodiment 3
[0026] 2mol 2-acrylamido-2-methyl-propanesulfonic acid (AMPS), 8mol butyl methacrylate (BMA), 0.033g catalytic chain transfer agent (COBF), 1.6mol water-soluble The nitrogen initiator azobisiso(azaminoethyl)butyl ether (AIBA). Stir and mix evenly, blow high-purity nitrogen gas after sealing, and put it in a water bath at 70-80°C for 9-11 hours. Add 0.4mol butyl methacrylate (BMA), 1.6mol water-soluble azo initiator azobisiso(azidoethyl) butyl ether (AIBA), 9.6mol 2-hydroxyhexyl methacrylate (HEMA ), then seal the reactor and blow high-purity nitrogen into it, and react at 70-80° C. for 9-11 hours. After the reaction, it was purified with a mixed solution of methanol and distilled water at a volume ratio of 1:1. The product was dried in a vacuum oven at 40° C. for 24 hrs to obtain a dry product with a yield of 72%.
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