Controllable-degradability terpolymer temporary plugging agent and preparation method and application method thereof
A terpolymer and degradable technology, which is applied in the field of controllable degradable terpolymer temporary plugging agent, can solve the problems of difficult to distribute acid evenly, the acid solution cannot be achieved, and the acidification transformation effect is not good, and the method of use can be achieved. Simple, high blocking strength, good marketing value effect
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Embodiment 1
[0053] Pour caprolactone, 0.1% lactide and 0.1% glycolide with a mole fraction of 99.8% into a three-necked flask, and heat the oil bath to 80°C to make the three reaction monomers in a molten state. Vacuum for 15 minutes, the vacuum degree in the bottle is 1-2 Torr, and dry nitrogen gas is passed at the same time to remove the oxygen and moisture in the bottle; then add 0.01% ethylene glycol and 0.01 % stannous octoate, the oil bath was heated to 150°C, and the reaction was continued for 4h to obtain a crude product; the crude product was completely dissolved in dichloromethane, and excess ethanol was added thereto, and the upper solvent was poured off to obtain a precipitate I, which was Precipitate I was dissolved in dichloromethane again, and excess ethanol was added again, the upper solvent was poured off, the precipitate was collected, and the above dissolution-precipitation process was repeated to finally obtain precipitate II, which was vacuum-dried at room temperature ...
Embodiment 2
[0059] Pour mole fractions of 33.3% caprolactone, 33.3% lactide and 33.4% glycolide into a three-necked flask, and heat the oil bath to 80°C so that the three reaction monomers are in a molten state, and stir Vacuumize for 15 minutes, the vacuum in the bottle is 1-2 Torr, and dry nitrogen at the same time to remove the oxygen and moisture in the bottle; then add 0.5% of dipentaerythritol and 0.1 % stannous octoate, the oil bath was heated to 120°C, and the reaction was continued for 8 hours to obtain a crude product; the crude product was completely dissolved in dichloromethane, and excess ethanol was added thereto, and the upper solvent was poured off to obtain a precipitate I. Precipitate I was dissolved in dichloromethane again, and excess ethanol was added again, the upper solvent was poured off, the precipitate was collected, and the above dissolution-precipitation process was repeated to finally obtain Precipitate II, which was vacuum-dried at room temperature for 48 hour...
Embodiment 3
[0065] Pour mole fractions of 0.1% caprolactone, 0.1% lactide and 99.8% glycolide into a three-necked flask, and heat the oil bath to 80°C to make the three reaction monomers in a molten state, stirring Vacuumize for 15 minutes, the vacuum degree in the bottle is 1-2 Torr, and dry nitrogen at the same time to remove the oxygen and moisture in the bottle; then add 0.1% trimethylol to the three-necked flask, accounting for the total molar weight of the three reaction monomers Propane and 0.05% stannous octoate, the oil bath is warmed up to 130 ° C, and the reaction is continued for 6 hours to obtain a crude product; the crude product is completely dissolved in dichloromethane, and excess ethanol is added thereto, and the upper solvent is poured off to obtain Precipitate I, dissolve the precipitate I in dichloromethane again, then add excess ethanol again, pour off the upper solvent, collect the precipitate, repeat the above dissolution-precipitation process, finally obtain the pr...
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