Controllable degradable terpolymer temporary plugging agent, preparation method and use method
A technology of terpolymer and propylene carbonate terpolymer, which is applied in the direction of chemical instruments and methods, drilling compositions, etc., can solve the problem of difficulty in uniform distribution of acid, unreachable acid solution, and poor effect of acidification transformation and other problems, to achieve the effect of high plugging strength, simple use method and good market promotion value
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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 then 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...
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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