Core-shell type cationic/anionic polyacrylamide profile control oil displacing microsphere and preparation method thereof
A polyacrylamide and acrylamide technology, applied in chemical instruments and methods, drilling compositions and other directions, can solve the problems of high relative molecular mass of products, poor stability of product emulsions, low product purity, etc., and it is easy to achieve the conditions of the preparation process. Control, excellent injectability and flowability, green effect of the preparation process
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Embodiment example 1
[0036] Weigh successively 50g (33.3%) of acrylamide, 10g (6.7%) of acryloxyethyltrimethylammonium chloride, 0.06g (0.1%) of pentaerythritol triacrylate, 0.14g (0.1%) of Tween 60 surfactant ), add propanol to 140g, stir well until the monomer is completely dissolved to obtain solution A; weigh 0.06g (0.1%) of azobisisobutyronitrile, add propanol to 10g, and stir until completely dissolved to obtain solution B ;
[0037] Add 1 / 3 of solution A and solution B into the four-necked flask respectively, control the speed at 200r / min, pass N 2 Exhaust oxygen for 0.5h, heat up to 50°C and react for 3h, white insoluble matter precipitates; then mix the remaining A and B solutions evenly and add to the reaction system, control 50°C, speed 200r / min, N 2 After reacting for 3 hours under environmental protection conditions, the white insoluble solid gradually increased, and a white turbid microsphere core system was obtained.
[0038] Take by weighing acrylamide 10g (33.3%), sodium acrylate ...
Embodiment example 2
[0041] Weigh successively 30g (15%) of acrylamide, 2g (1%) of dimethyldiallyl ammonium chloride, 0.325g (1%) of dimethyldiallyl ammonium chloride, dodecylbenzenesulfonate Add 2g (1%) of sodium nitrate, add cyclohexane to 180g, fully stir until the monomer is completely dissolved to obtain solution A; weigh 0.32g (1%) of azobisisobutyronitrile, add cyclohexane to 20g, fully Stir until completely dissolved to obtain solution B;
[0042] Add 1 / 3 of solution A and solution B into the four-necked flask respectively, control the rotation speed at 300r / min, pass N 2 Exhaust oxygen for 0.5h, heat up to 60°C and react for 3h, white insoluble matter precipitates out; then mix the remaining A and B solutions evenly and add to the reaction system, control 60°C, speed 300r / min, N 2 After reacting for 3 hours under environmental protection conditions, the white insoluble solid gradually increased, and a white turbid microsphere core system was obtained.
[0043] Weigh 7.5g (15%) of acryla...
Embodiment example 3
[0046] Weigh successively 3g (8.8%) of acrylamide, 10.2g (30%) of β-aminoethyl methacrylate sulfate, 1.056g (8%) of polyethylene glycol diacrylate, and 2g of Span 80 surfactant (5.9%), add benzene to 30g, fully stir until the monomer is completely dissolved to obtain solution A; weigh 0.041 (0.3%) g of potassium persulfate, add benzene to 4g, fully stir until completely dissolved to obtain solution B;
[0047] Add 1 / 3 of solution A and solution B into the four-necked flask respectively, control the rotation speed at 400r / min, pass N 2 Exhaust oxygen for 0.5h, heat up to 40°C and react for 3h, white insoluble matter precipitates; then mix the remaining A and B solutions evenly and add to the reaction system, control 40°C, speed 400r / min, N 2 After reacting for 3 hours under environmental protection conditions, the white insoluble solid gradually increased, and a white turbid microsphere core system was obtained.
[0048] Weigh 75g (50%) of acrylamide, 45g (30%) of β-allylsulfo...
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