Acrylamide copolymer, as well as preparation method and application thereof
An acrylamide-based, copolymer technology, which is applied in chemical instruments and methods, drilling compositions, etc., can solve the problems of limited use of polymers and small molecular weight of products, and achieves low residual monomer content, high molecular weight, increased molecular weight, etc. The effect of relaxation time
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[0033] The present invention also provides a method for preparing an acrylamide-based copolymer. The preparation method includes the following steps: under solution polymerization conditions and in the presence of an initiator, a monomer mixture is polymerized in water, wherein, The monomer mixture contains monomer E, monomer F and monomer G, the monomer E is a monomer having a structure shown in formula (9), and the monomer F is a monomer having a formula (10) - formula ( 13) At least one of the monomers with the structure shown in the formula (14), and the monomer E, the monomer F and the monomer G The mass ratio is 1: 0.001-3: 0.001-0.5, preferably 1: 0.01-1.5: 0.01-0.2; the solution polymerization conditions make the viscosity-average molecular weight of the polymer obtained after the polymerization reaction 30 million-35 million, Preferably 32 million-34 million,
[0034]
[0035] Among them, R 1 ’, R 2 ’, R 6 ’, R 7 ’, R 10 ’ and R 11 ' each independently hydro...
Embodiment 1
[0072] This embodiment is used to illustrate the preparation method of the acrylamide copolymer provided by the present invention
[0073] Add 1000 grams of acrylamide, 10 grams of 2-acrylamido-2-methylpropanesulfonic acid and 10 grams of silicon-containing surface-active functional monomers with the structure shown in formula (17), 4080 grams of deionized water, and stir In the state, 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 the polymerization bottle, add 10.2 mg of 2,2'-azobisisobutylamidine dihydrochloride and 10.2 mg of N,N,N',N'-tetramethylethylenediamine, pass High-purity nitrogen was deoxygenated for 0.5 hour, 10.2 mg of sodium bisulfite and 10.2 mg of ammonium persulfate were added, and nitrogen was continued until the thermocouple in the polymerization bottle began to heat up, and the reaction time was 8 hours. The colloid is taken out and granul...
Embodiment 2
[0077] This embodiment is used to illustrate the preparation method of the acrylamide copolymer provided by the present invention
[0078] Add 1,000 grams of acrylamide, 1,000 grams of 2-acrylamido-2-methylpropanesulfonic acid, 100 grams of silicon-containing surface-active functional monomers with the structure shown in formula (17), and 4,900 grams of deionized water in a beaker, stirring The temperature of the solution was controlled at 15°C with frozen brine, and the pH was adjusted to 7 by adding sodium hydroxide. Transfer the monomer solution to the polymerization bottle, add 1.05 grams of 2,2'-azobisisobutylamidine dihydrochloride and 1.05 grams of N,N,N',N'-tetramethylethylenediamine, and pass High-purity nitrogen was deoxygenated for 0.5 hour, 1.05 grams of sodium bisulfite and 1.05 grams of ammonium persulfate were added, and nitrogen was continued until the thermocouple in the polymerization bottle began to heat up, and the reaction time was 4 hours. The colloid is...
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