Hydrophobically associating water-soluble polymer (HAWSP) oil displacement agent and preparation method thereof
A hydrophobic association, polymer technology, applied in drilling compositions, chemical instruments and methods, etc., to achieve the effects of enhanced rigidity, enhanced oil recovery, good temperature and salt resistance and shear resistance
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Embodiment 1
[0021] Embodiment 1: the preparation of NAO monomer
[0022] Add 42.3g oleic acid into the reactor, slowly add 10.2g phosphorus trichloride under stirring, the feeding temperature is controlled at 10-15°C, after the addition is completed, the temperature is raised to 55°C, and the lower layer liquid is separated after 4 hours of heat preservation, and the upper layer liquid is passed through Evaporate and remove unreacted phosphorus trichloride to obtain oleoyl chloride with a yield of 98.8%; dilute 18.7 g of oleoyl chloride obtained in the previous step with dichloromethane solvent and put it into a constant pressure dropping funnel for later use, and then dry it in 250ml trichloride Add 4g of allylamine to the neck flask, dilute with dichloromethane solvent, then add 7.6g of triethylamine and 0.02g of hydroquinone, slowly add the ready-to-use oleoyl chloride solution dropwise in an ice bath with constant stirring, and control the 1h drop After the dripping, react at room tem...
Embodiment 2
[0023] Embodiment 2: the preparation of terpolymer AM / NaAA / NAO
[0024] According to the ratio in Table 1, first weigh acrylic acid and dilute it with 10g of deionized water, slowly add sodium hydroxide in an ice bath, and cool to room temperature; add the NAO prepared above into a 250ml three-necked flask, and then add OP-10 to emulsify Add acrylamide after fully emulsifying, then add sodium acrylate solution, adjust the pH to 8 with NaOH solution, and pass nitrogen for 20 minutes; then add initiator sodium bisulfite solution, and then add persulfuric acid Ammonium solution, nitrogen gas for 10 minutes, reacted at a temperature of 30-70°C for 10h; finally washed three times with absolute ethanol, pulverized, and dried at a constant temperature of 40°C to obtain the AM / NaAA / NAO terpolymer.
[0025] Table 1 Addition amount of ternary polymer synthetic drugs
[0026]
Embodiment 3
[0027] Embodiment 3: AM / NaAA / NAO terpolymer structure characterization
[0028] The infrared spectrogram of the ternary polymer AM / NaAA / NAO synthesized by embodiment 2 is as follows figure 1 shown. It is known from the figure that N-H(-NH), C-N(-CH 2 -N-) Stretch vibration peaks are at 3444.24cm -1 and 1121.40cm -1 , the -C=O stretching vibration peak is at 1683.55cm -1 .
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