Acrylamide copolymer, and preparation method and application thereof
A technology of acrylamide series and copolymers, which is applied in chemical instruments and methods, mechanical equipment, piping systems, etc., can solve the problems of insignificant water sensitivity, poor temperature and salt resistance, and poor temperature and salt resistance. The effect of monomer conversion
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Embodiment 1
[0093] This example is used to illustrate the preparation of acrylamide copolymer by the solution polymerization method provided by the present invention.
[0094] At room temperature, 37.31 g of acrylamide (AM), 38.86 g of monomer M1 represented by formula (27), 4.17 g of N-vinylpyrrolidone and 0.41 g of M2 monomer represented by formula (28) ( Prepared according to the method of the document Macromolecular Bioscience, 2006, 6(7), 540-554, the same as below) into the reaction flask, add 149.2g of deionized water, stir to completely dissolve the monomer, and stir evenly. 17.94 g of a 1% by weight aqueous EDTA solution, 2.1 g of a 1% by weight azobisisobutylamidine hydrochloride aqueous solution, and 0.12 g of urea were respectively added to the flask, and the mixture was thoroughly stirred to mix uniformly. Use 1% by weight sodium hydroxide solution to pH 7.5, add 1.1 g of 0.5% by weight sodium bisulfite solution, control the initial temperature of the system to 4 ° C, and add...
Embodiment 2
[0103] This example is used to illustrate the preparation of acrylamide copolymer by the solution polymerization method provided by the present invention.
[0104] At room temperature, 34.04g of methacrylamide, 70.63g of monomer M3 represented by formula (30), 8.89g of N-vinylpyrrolidone and 0.01g of M2 monomer represented by formula (28) were added to In the polymerization bottle, add 340.68g of deionized water, stir to dissolve the monomer completely, add 0.1% by weight of sodium citrate aqueous solution 0.24g to the flask, add 1% by weight of 2.2'-azobisisobutylamidine hydrochloride Add 2.13 g of saline solution, add 2.53 g of 0.1% by weight sodium bisulfite solution, add 0.08 g of urea, and stir well to make it evenly mixed. The initial temperature of the system was controlled to 10°C, and after 30 minutes of nitrogen deoxygenation, 1.0 g of 1% ammonium persulfate aqueous solution was added and nitrogen deoxygenation was continued for 10 minutes. Seal the reactor and keep...
Embodiment 3
[0109] This example is used to illustrate the preparation of acrylamide copolymer by the solution polymerization method provided by the present invention.
[0110] At room temperature, 45.95g of methacrylamide, 37.73g of monomer M4 represented by formula (32), 20g of N-vinylpyrrolidone and 0.21g of M2 monomer represented by formula (28) were added to the reaction In the bottle, add 414.72 g of deionized water, stir to dissolve the monomer completely, and stir evenly. 10.03 g of a 1% by weight aqueous EDTA solution, 4.87 g of a 1% by weight azobisisobutylamidine hydrochloride aqueous solution, and 0.03 g of urea were respectively added to the flask, and the mixture was thoroughly stirred to make them uniform. The pH was adjusted to 7.5 with solid sodium hydroxide. Add 1.1 g of 0.5% by weight sodium bisulfite solution, control the initial temperature of the system to 8°C, and pass nitrogen to deoxygenate for 30 minutes, then add 1.1 g of 1% by weight ammonium persulfate aqueous...
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