Acrylamide terpolymer and polymer and preparation method and application thereof
A technology of acrylamide-based terpolymers and polymers, applied in chemical instruments and methods, and drilling compositions, etc., can solve problems such as poor water solubility, inability to fully meet requirements, and failure of tertiary oil recovery agents, etc.
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[0040] The present invention also provides a method for preparing a polymer, which is characterized in that the preparation method comprises the following steps of polymerizing a monomer mixture in water in the presence of an initiator under the solution polymerization reaction conditions of olefins , it is characterized in that, described monomer mixture contains monomer D, monomer E and monomer F, described monomer D is the monomer that has the structure shown in formula (12), and described monomer E has the formula ( 13)-At least one of the monomers of the structure shown in the formula (15), the monomer F is a monomer with the structure shown in the formula (16) and / or formula (17), and the monomer F is Based on the total number of moles of monomers in the mixture, the content of the monomer D is 5-95 mol%, the content of the monomer E is 2.5-90 mol%, and the content of the monomer F is 0.5-90 mole %; preferably, the content of the monomer D is 10-70 mole %, the content of...
Embodiment 1
[0067] At room temperature, the monomer of the structure shown in the acrylamide (AM) of 50.0g, the AMPS of 50.0g and the formula (19) of 63.43g (according to the method of document Macromolecules 1997, Vol.30, No.7, 2016-2020 prepared) into the reaction flask, add 287.0 g of deionized water, stir to dissolve the monomer completely, then slowly add 38.6 g of NaOH aqueous solution with a concentration of 25% by weight, and stir evenly. Add 5.5 g of 1% by weight of EDTA aqueous solution, 1.1 g of 1% by weight of azobisisobutylamidine hydrochloride aqueous solution, chain extender N', 0.066 g of N-dimethylethylenediamine, and 0.11 g of urea into the flask respectively. g, stir well to make it evenly mixed, and adjust the pH of the system to 7.5 with 1% by weight of sodium hydroxide solution. The initial temperature of the system was controlled to 4° C., and 1.1 g of 1% by weight ammonium persulfate aqueous solution was added after 30 minutes of nitrogen deoxygenation, and nitroge...
Embodiment 2
[0073] 45.0g of AM, 34.2g of N-vinylpyrrolidone NVP and 103.2g of monomers of the structure shown in formula (20) (according to the method of document Biomacromolecules, 2009, Vol.10, No.7, 1846-1853 Obtained) join in the polymerization bottle, add 495.2g deionized water, stir to make the monomer dissolve completely, add the sodium citrate aqueous solution 5.65g that concentration is 0.1% by weight respectively in the flask, add the concentration that is 0.1% by weight 2,2 '-Azobis[2-(2-imidazoline-2-propane)-dihydrochloride aqueous solution 1.13g, add chain extender N,N'-dimethylpropylenediamine 0.01g, adding concentration is 0.1 weight % sodium bisulfite solution 1.13g, add sodium formate 0.01g, stir well to make it evenly mixed. The initial temperature of the system was controlled to 4° C., and after 30 minutes of nitrogen deoxygenation, 1.0 g of a 1% by weight potassium persulfate aqueous solution was added and nitrogen deoxygenation was continued for 10 minutes. Seal the...
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