Graft modified polyacrylamide and its preparation method
A technology of polyacrylamide and graft modification, which is applied in the direction of chemical instruments and methods, drilling compositions, etc., can solve the problems of poor displacement efficiency such as temperature resistance, salt resistance and aging resistance, and achieve improved temperature resistance, The effect of increasing the three-dimensional space network structure and improving the displacement efficiency
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Embodiment 1
[0028] Inject 0.14mol2,2,6,6-tetramethyl-4-bromo-1-oxypiperidine sodium and 2.5mol ethylene oxide into the dry reaction flask, react at 47°C for 7 hours, then add 0.14 mol2,2,6,6-tetramethyl-4-epoxypropyloxypiperidine-1-oxyl radical, continue to react at 78°C for 6 hours, add isopropanol to terminate the reaction, and precipitate with ether , to obtain polyethylene oxide with a molecular weight of 760 in the hydrophilic segment X -PEO-NO·. Add 0.07 mol of the functionalized polymer prepared above, 0.6 mol N, N-dimethylacrylamide (NDMAM), and 0.08 mol benzoyl peroxide to the reactor, pass nitrogen to remove oxygen, stir and mix evenly, and place at 98 Reaction at ℃ for 5 hours to obtain a block copolymer with a molecular weight of 800 in the hydrophobic segment X -PEO- b -PNDMAM. 0.05 g of the obtained copolymer and 2.0 g of ultra-high molecular weight polyacrylamide with a viscosity-average molecular weight of 30.5 million were dispersed in 98 g of aqueous sodium bicarbona...
Embodiment 2
[0033] Inject 0.15mol2,2,6,6-tetramethyl-4-chloro-1-oxypiperidine sodium and 2.0mol ethylene oxide into the dry reaction flask, react at 55°C for 6 hours, then add 0.15 mol2,2,6,6-tetramethyl-4-epoxypropyloxypiperidine-1-oxyl radical, continue to react at 80°C for 5 hours, add isopropanol to terminate the reaction, and precipitate with ether , to obtain polyethylene oxide with a molecular weight of 550 in the hydrophilic segment X -PEO-NO·. Add 0.06 mol of the functionalized polymer prepared above, 0.3 mol N, N-dibutylacrylamide (NDBAM), and 0.07 mol tert-butyl peroxide 2-ethylhexanoate to the reactor, pass nitrogen to remove oxygen, Stir and mix evenly, and react at 102°C for 7 hours to obtain a block copolymer with a molecular weight of 900 in the hydrophobic segment X -PEO- b -PNDBAM. 0.06 g of the obtained copolymer and 1.8 g of ultra-high molecular weight polyacrylamide with a viscosity-average molecular weight of 28 million were dispersed in 98 g of aqueous sodium bi...
Embodiment 3
[0036] Inject 0.13mol2,2,6,6-tetramethyl-4-chloro-1-oxypiperidine sodium and 1.8mol propylene oxide into the dry reaction flask, react at 52°C for 6 hours, then add 0.14mol2 , 2,6,6-Tetramethyl-4-epoxypropyloxypiperidine-1-oxyl radical, continue to react at 88°C for 4 hours, add isopropanol to terminate the reaction, and precipitate with ether, Obtaining the polyoxypropylene with the molecular weight of the hydrophilic segment being 800 X -PPO-NO·. Add 0.05 mol of the functionalized polymer prepared above, 0.2 mol N, N-dioctyl acrylamide (NDOAM), and 0.06 mol benzoyl peroxide into the reactor, pass nitrogen to remove oxygen, stir and mix evenly, and set at 100 Reaction at ℃ for 6 hours to obtain a block copolymer with a molecular weight of 900 in the hydrophobic segment X -PPO- b -PNDOAM. 0.05g of the obtained copolymer and 1.2g of ultra-high molecular weight polyacrylamide with a viscosity-average molecular weight of 32 million were dispersed in 102g of sodium hydroxide a...
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