A kind of acrylamide series copolymer and its preparation method and application
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 effect, permanent damage, etc., and achieve low water-insoluble matter content. , Simple monomer conversion rate, low formation damage effect
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Embodiment 1
[0078] This example is used to illustrate the preparation of acrylamide copolymer by the solution polymerization method provided by the present invention.
[0079] At room temperature, add 21.32g of acrylamide (AM), 66.40g of M1 monomer represented by formula (13) and 20.43g of N-(3-dimethylaminopropyl)methacrylamide into the reaction flask , add 612.85g of deionized water, stir to dissolve the monomer completely, and stir 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 deoxygenati...
Embodiment 2
[0085] This example is used to illustrate the preparation of acrylamide copolymer by the solution polymerization method provided by the present invention.
[0086] Add 29.85g of AM, 45.94g of monomer M2 represented by formula (15) and 10.26g of N-(4-dimethylaminobutyl)acrylate into the polymerization bottle, add 200.78g of deionized water, and stir To completely dissolve the monomer, add 4.65 g of 1% by weight EDTA aqueous solution, 1.23 g of 1% by weight azobisisobutylamidine hydrochloride aqueous solution, and add chain extender N,N'-dimethyl Add 0.002g of ethylenediamine, add 1.15g of 0.1% sodium bisulfite solution, add 0.11g of urea, 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. ...
Embodiment 3
[0090] This example is used to illustrate the preparation of acrylamide copolymer by the solution polymerization method provided by the present invention.
[0091] At room temperature, put 5.11g of methacrylamide, 110.66g of M1 monomer represented by formula (13) and 47.52g of N-(5-dimethylaminopentyl)methacrylamide into the polymerization bottle, and add 244.94 g deionized water, stir to dissolve the monomer completely, add 11.63 g of 1 wt % EDTA aqueous solution, 2.13 g of 1 wt % azobisisobutylamidine hydrochloride aqueous solution, and add chain extender N' , N-dimethylethylenediamine 0.001g, add 0.1% by weight sodium bisulfite solution 1.13g, add urea 0.20g, 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 2°C, and after 30 minutes of nitrogen deoxygenation, 0.8 g of 1% ammonium persulfate aqueous solution was added, and nitrogen deoxygenation was continued fo...
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