Oil displacing agent containing imidazole ring quaternary ammonium salt polymer and preparation method
A technology of polymer and oil-displacing agent, which is applied in the field of imidazole ring-containing quaternary ammonium salt polymer oil-displacing agent and its preparation, can solve the problems of less research on imidazole ring-containing polymers and oil-displacing agent, and achieves increased rigidity and increased water solubility. The effect of increasing the stability and thermal stability
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Embodiment 1
[0020] Embodiment 1: the preparation of AOAB monomer
[0021] Add 14.1g of oleic acid into the reactor, slowly add 3.4g of phosphorus trichloride under stirring, the feeding temperature is controlled at 10°C, after the addition is completed, the temperature is raised to 55°C, and the lower layer is separated after 6 hours of heat preservation, and the upper layer is removed by evaporation. Unreacted phosphorus trichloride, yield oleoyl chloride with a yield of 99.5%; then dilute 5.0 g of oleoyl chloride prepared in the previous step with tetrahydrofuran solvent and put it into a constant pressure dropping funnel for later use, and add Dissolve 2.0g of imidazole with tetrahydrofuran solvent, then add 0.74gNaH as a catalyst, slowly drip the above-mentioned liquid for use under stirring, then react with a reflux device at 35°C for 10h, wash the reaction solution with water, and wash with 2% sodium hydroxide Wash, wash with saturated salt water, dry and filter, and obtain N-oleoyl...
Embodiment 2
[0022] Embodiment 2: the preparation of polymer AM / AA / AOAB
[0023] First weigh AA and NaOH according to the ratio in Table 1, put them into a 250mL three-necked flask and dissolve them with deionized water, cool to room temperature, add AM and AOAB, and dissolve them completely at room temperature, then adjust the pH of the system to 8 with NaOH solution , blow nitrogen for 20 minutes, add the pre-prepared sodium bisulfite solution, stir for 5 minutes, add ammonium persulfate solution, continue to pass nitrogen for 20 minutes, seal the reaction at a constant temperature of 45 ° C for 12 hours, wash with absolute ethanol precipitation three times, and The precipitate was crushed into small particles, soaked in absolute ethanol for 2 days, and dried at a temperature of 40° C. for 2 days to obtain the polymer AM / AA / AOAB.
[0024] Table 1 Polymer Preparation Drug Dosage
[0025]
Embodiment 3
[0026] Embodiment 3: AM / AA / AOAB copolymer structural characterization
[0027] The infrared spectrogram of the prepared polymer AM / AA / AOAB of embodiment 2 is as figure 1 shown. It is known from the picture that 2923cm -1 and 2846cm -1 for C-H (-CH 3 and -CH 2 -) stretching vibration, -N-H (-NH 2 ) stretching vibration peak at 3430cm -1 , the -C=O stretching vibration peak is at 1665cm -1 .
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