Acrylamide copolymer, and preparation method and application thereof
An acrylamide-based, copolymer technology, applied in chemical instruments and methods, drilling compositions, etc., can solve the problems of non-degradation, rapid drop in resistance reduction, permanent damage, etc., and achieve low water-insoluble content. , Simple monomer conversion rate, low formation damage effect
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Embodiment 1
[0075] This example is used to illustrate the preparation of acrylamide copolymer by the solution polymerization method provided by the present invention.
[0076] At room temperature, add 21.32g of acrylamide (AM), 66.40g of M1 monomer represented by formula (11) and 13.34g of N-vinylpyrrolidone into the reaction flask, add 572.67g of deionized water, and stir to make The monomer is completely dissolved and stirred evenly. Add 5.5g of 1% by weight of EDTA aqueous solution, 2.1g of 1% by weight of azobisisobutylamidine hydrochloride aqueous solution, chain extender N', 0.002g of N-dimethylethylenediamine, and add 0.1 % sodium bisulfite solution 1.1g, urea 0.12g, stir well to make it evenly mixed. The pH was adjusted to 7.5 with 1% by weight sodium hydroxide solution. The initial temperature of the system was controlled to 4°C, and after 30 minutes of nitrogen deoxygenation, 0.75 g of 1% by weight ammonium persulfate aqueous solution was added, and nitrogen deoxygenation was ...
Embodiment 2
[0082] This example is used to illustrate the preparation of acrylamide copolymer by the solution polymerization method provided by the present invention.
[0083] Add 29.85g of AM, 45.94g of M2 monomer represented by formula (13) and 6.67g of N-vinylpyrrolidone into the polymerization bottle, add 192.41g of deionized water, stir to completely dissolve the monomer, and pour Add 4.65g of 1% by weight of EDTA aqueous solution, add 1.23g of 1% by weight of azobisisobutylamidine hydrochloride aqueous solution, add 0.002g of chain extender N,N'-dimethylethylenediamine, add 0.1% Add 0.11 g of urea to 1.15 g of sodium bisulfite solution, stir well to make it evenly mixed. The pH was adjusted to 7.1 with 1% by weight sodium hydroxide solution. The initial temperature of the system was controlled to 10°C, and after 30 minutes of nitrogen deoxygenation, 0.6 g of 1% by weight ammonium persulfate aqueous solution was added and nitrogen deoxygenation was continued for 10 minutes. Seal th...
Embodiment 3
[0087] This example is used to illustrate the preparation of acrylamide copolymer by the solution polymerization method provided by the present invention.
[0088] At room temperature, put 5.11g of methacrylamide, 110.66g of M1 monomer represented by formula (11) and 26.67g of N-vinylpyrrolidone into a polymerization bottle, add 213.66g of deionized water, and stir to make the monomer Dissolve completely, add 11.63g of 1% by weight EDTA aqueous solution, 2.13g of 1% by weight azobisisobutylamidine hydrochloride aqueous solution, and add chain extender N', N-dimethylethylenediamine to the flask 0.001g, add 1.13g of 0.1% by weight sodium bisulfite solution, add 0.20g of urea, stir well to make it evenly mixed. The pH was adjusted to 7.3 with 1% by weight sodium hydroxide solution. The initial temperature of the system was controlled to 8°C, and after 30 minutes of nitrogen deoxygenation, 0.8 g of 1% ammonium persulfate aqueous solution was added, and nitrogen deoxygenation was ...
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