Acrylamide copolymer, preparation method and application thereof
A technology of acrylamide series and copolymers, applied in the direction of chemical instruments and methods, drilling compositions, etc., can solve the problems of poor fluid loss resistance, not easy to degrade, "water sensitive effect is not significant, etc., and achieve good compatibility properties, low water-insoluble content, and simple monomer conversion
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Embodiment 1
[0081] This example is used to illustrate the preparation of acrylamide copolymer by the solution polymerization method provided by the present invention.
[0082] At room temperature, 4.26g of acrylamide (AM), 74.68g of M1 monomer represented by formula (15), 30.13g of N-(3-dimethylaminopropyl)methacrylamide (purchased from Sigma- Aldrich Company, hereinafter the same) and 1.16g of M2 monomer represented by formula (16) (prepared according to the method described in Example 1 in JP08217755A, hereinafter the same) were prepared, added to the reaction bottle, and deionized water was added 624.64g, stir to dissolve the monomer completely, and stir evenly. Add 5.5 g of 1 wt % EDTA aqueous solution, 2.1 g of 1 wt % 2,2' azobisisobutylamidine hydrochloride aqueous solution, 1.1 g of 0.1 wt % sodium bisulfite solution, urea 0.12g, stir well to make it evenly mixed. The pH was adjusted to 7.5 with 10% by weight sodium hydroxide solution. The initial temperature of the system was c...
Embodiment 2
[0089] This example is used to illustrate the preparation of acrylamide copolymer by the solution polymerization method provided by the present invention.
[0090] 29.85g of acrylamide (AM), 5.80g of M3 monomer represented by formula (18), 25.44g of N-(4-dimethylaminobutyl) acrylate (purchased from Sigma-Aldrich, the same below ) and 0.46g of the M2 monomer represented by the formula (16) were added to the polymerization bottle, 143.62g of deionized water was added, stirred to completely dissolve the monomer, 4.65g of 1% by weight EDTA aqueous solution was added to the flask respectively, and Add 1.23 g of 1% by weight azobisisobutylamidine hydrochloride aqueous solution, add 1.15 g of 0.1% sodium bisulfite solution, add 0.11 g of urea, and stir well to make it evenly mixed. The pH was adjusted to 7.1 with 10% by weight sodium hydroxide solution. The initial temperature of the system was controlled to 10°C, and after 30 minutes of deoxygenation with nitrogen gas, 1.0 g of 1% ...
Embodiment 3
[0095] This example is used to illustrate the preparation of acrylamide copolymer by the solution polymerization method provided by the present invention.
[0096] At room temperature, 25.53 g of methacrylamide, 51.07 g of M3 monomer represented by formula (18), and 7.13 g of N-(5-dimethylaminopentyl) methacrylamide (purchased from Sigma-Aldrich Company , the same below) and 0.002g of the M2 monomer represented by the formula (16) into the polymerization bottle, add 125.55g of deionized water, stir to completely dissolve the monomer, and add 11.63g of 1% by weight EDTA aqueous solution into the flask , add 2.13 g of 1% by weight of azobisisobutylamidine hydrochloride aqueous solution, add 1.13 g of 0.1% by weight of sodium bisulfite solution, add 0.20 g of urea, and stir well to make it evenly mixed. The pH was adjusted to 7.3 with 10% by weight sodium hydroxide solution. The initial temperature of the system was controlled to 8°C, and after 30 minutes of nitrogen deoxygenati...
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