Acrylamide copolymer, preparation method therefor and application of acrylamide copolymer
An acrylamide copolymer and acrylamide copolymerization technology are applied in the application field of acrylamide copolymers, which can solve the problems of polymer application limitation, complicated process operation, small molecular weight of products, etc., and achieve low residual monomer content and preparation method steps. Simple, high molecular weight effect
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[0038] The present invention also provides a method for preparing an acrylamide copolymer, the preparation method comprising: polymerizing a monomer mixture in water under solution polymerization conditions and in the presence of an initiator, wherein the monomer The mixture contains monomer E, monomer F and monomer G, the monomer E is a monomer having a structure shown in formula (8), and the monomer F is a monomer having a structure shown in formula (9)-(12) At least one of the monomers of the structure, the monomer G is a monomer having a structure shown in formula (13), and the weight ratio of the monomer E, the monomer F and the monomer G is 1: 0.001-10: 0.001-10, more preferably 1: 0.001-3: 0.001-0.5, most preferably 1: 0.01-1: 0.01-0.1; the solution polymerization conditions make the obtained polymer after polymerization The viscosity average molecular weight is 30 million-38 million, preferably 32 million-35 million,
[0039]
[0040]
[0041] Among them, R 1 ’...
preparation example 1
[0098] This preparation example is used to illustrate the preparation method of monomer G.
[0099] (1) Under nitrogen protection, dissolve 3-[tris(trimethylsiloxane)silyl]propylamine in 100 mL of dichloromethane, add iodomethane dropwise at 20°C (wherein, 3-[tri( The molar ratio of trimethylsiloxane (trimethylsiloxane) silyl] propylamine to methyl iodide is 1:2), stirred for 3 hours, and then the obtained reaction solution was spin-dried by rotary evaporation, and reconstituted by dichloromethane / petroleum ether. Crystallization to obtain a mixture containing N,N-dimethyl-3-[tris(trimethylsiloxy)silyl]propylamine;
[0100] (2) Mix and dissolve the mixture containing N,N-dimethyl-3-[tris(trimethylsiloxy)silyl]propylamine obtained in step (1) with allyl chloride in 80 mL of ethanol (wherein, the molar ratio of 3-[tris(trimethylsiloxane)silyl]propylamine to allyl chloride is 1:1.5), stirred at 20°C for 5 hours, and removed the solvent by rotary evaporation after the reaction, a...
Embodiment 1
[0103] This example is used to illustrate the preparation method of the acrylamide copolymer provided by the present invention.
[0104] Add 1000 grams of acrylamide (AM), 10 grams of 2-acrylamido-2-methylpropanesulfonic acid, 10 grams of monomer G prepared in Preparation Example 1, and 4080 grams of deionized water into a beaker, and stir. The temperature of the solution was controlled at 5°C with frozen saline, and the pH was adjusted to 7 by adding sodium hydroxide. Transfer the monomer solution to a polymerization bottle, add 10.2 mg of water-soluble azo initiator 2,2'-azobis(2-amidinopropane) dihydrochloride and 10.2 mg of amine N,N,N', For N'-tetramethylethylenediamine, deoxygenate with high-purity nitrogen gas for 0.5 hour, add 10.2 mg of sodium bisulfite and 10.2 mg of ammonium persulfate, continue nitrogen gas flow until the thermocouple in the polymerization bottle starts to heat up, and the reaction time is 8 hours. The colloid is taken out and granulated into 4-6 ...
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