Terpolymer and polymer and preparation method and application thereof
A terpolymer and polymerization technology, applied in chemical instruments and methods, drilling compositions, etc., can solve the problems of large difference in the copolymerization activity of acrylamide, poor water solubility, and use, etc., and achieve high-speed shear resistance. The effect of enhanced oil recovery value, good solubility and injectability, and enhanced oil recovery value
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[0050] The invention provides a method for preparing a polymer, which is characterized in that the preparation method comprises the following steps: under the solution polymerization reaction conditions of olefins, in the presence of an initiator, a monomer mixture is polymerized in water, wherein It is characterized in that the monomer mixture contains monomer D, monomer E and monomer F, the monomer D has a structure shown in formula (17), and the monomer E has the structure shown in formula (18)-formula ( 20) At least one of the monomers of the structure shown in the monomer F is at least one of the monomers of the structure shown in formula (21)-formula (25), and the monomer in the monomer mixture Based on the total number of moles, 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 mol%; preferably Preferably, the content of the monomer D is 10-70 mol%, the content of the monomer E is 20-50 mol...
Embodiment 1
[0081]At room temperature, 50.0 g of acrylamide (AM), 50.0 g of AMPS and 35.3 g of monomers of the structure shown in formula (27) (according to the literature Journal of applied polymer science.1995, Vol.56, 1615-1623 method prepared) into a 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. Into the flask, add 5.5 g of EDTA aqueous solution with a concentration of 1% by weight, 1.1 g of azobisisobutylamidine hydrochloride aqueous solution with a concentration of 1% by weight, and chain extender N, N'-dimethylethylenediamine 0.066 g, 0.11g of urea, fully stirred to make it evenly mixed. The pH of the system was adjusted to 7.5 with a 1% by weight sodium hydroxide solution. The initial temperature of the system was controlled to 4° C., and after 30 minutes of nitrogen deoxygenation, 1.1 g of ammonium persulfate aqueous solution with a c...
Embodiment 2
[0087] The monomer of the structure shown in the AM of 45.0g, the N-vinylpyrrolidone NVP of 34.2g and the formula (29) of 49.1g (according to document J.Chem.Soc., Perkin Trans.1,2000,2091-2103 Method prepared) joins in the polymerization bottle, adds 495g deionized water, stirs and makes monomer dissolve completely, adds the sodium citrate aqueous solution 5.65g that concentration is 0.1% by weight in the flask respectively, adds the 2 that concentration is 0.1% by weight, 1.13g of 2'-azobis[2-(2-imidazoline-2-propane)-dihydrochloride aqueous solution, add 0.01g of chain extender N,N'-dimethylpropylenediamine, the concentration is 0.1 Add 0.01 g of sodium formate to 1.13 g of the weight % sodium bisulfite solution, 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...
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