Zwitterionic gemini viscoelasticity surfactant, preparing method thereof and clean fracturing fluid with zwitterionic viscoelasticity surfactant as thickening agent
A surfactant and cleaning fracturing fluid technology, applied in chemical instruments and methods, transportation and packaging, drilling compositions, etc., can solve the problems of high cost, complicated preparation process, poor temperature resistance, etc., and achieve low cost , less dosage, good temperature resistance
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Embodiment 1
[0037] 10mmol of 2,2 bis(bromomethyl)-1,3-propanediol was added to a round bottom flask, with tetrahydrofuran as a solvent, 20mmol of erucamide propyl dimethylamine was added, and refluxed at 60°C for 12 hours, wherein n (2,2 bis(bromomethyl)-1,3-propanediol):n(erucamide propyl dimethylamine)=1:2, intermediate A was obtained by distillation under reduced pressure after the reaction was completed. Dissolve the intermediate A obtained in the first step in tetrahydrofuran, add 20-22mmol of sodium hydride, stir at room temperature for about 15min, then dissolve 20mmol of 1,3 propane sultone in 50mL of tetrahydrofuran, and slowly add it dropwise to the intermediate In the reaction solution of A and sodium hydride, reflux at 60°C for 12 hours, wherein n(intermediate A):n(sodium hydride):n(1,3 propane sultone)=1:2~2.2:2, the reaction is over Afterwards, react with hydrochloric acid and excess sodium hydride, filter and distill under reduced pressure to obtain yellow viscous colloidal...
Embodiment 2
[0039]Add 10mmol of 2,2 bis(bromomethyl)-1,3-propanediol into a round bottom flask, use tetrahydrofuran as solvent, add 20mmol of arachidamide propyl dimethylamine, reflux at 60°C for 12 hours, where n (2,2 bis(bromomethyl)-1,3-propanediol):n(arachidic acid amidopropyl dimethylamine)=1:2, intermediate A was obtained by distillation under reduced pressure after the reaction was completed. Dissolve the intermediate A obtained in the first step in tetrahydrofuran, add 20-22mmol of sodium hydride, stir at room temperature for about 15min, then dissolve 20mmol of 1,3 propane sultone in 50mL of tetrahydrofuran, and slowly add it dropwise to the intermediate In the reaction solution of A and sodium hydride, reflux at 60°C for 12 hours, wherein n(intermediate A):n(sodium hydride):n(1,3 propane sultone)=1:2~2.2:2, the reaction is over Afterwards, react with hydrochloric acid and excess sodium hydride, filter and distill under reduced pressure to obtain yellow viscous colloidal Gemini a...
Embodiment 3
[0041] 10mmol of 2,2 bis(bromomethyl)-1,3-propanediol was added to a round bottom flask, with tetrahydrofuran as a solvent, 20mmol of oleic acid amidopropyl dimethylamine was added, and refluxed at 60°C for 12 hours, wherein n (2,2 bis(bromomethyl)-1,3-propanediol):n(oleic acid amidopropyl dimethylamine)=1:2, and intermediate A was obtained by distillation under reduced pressure after the reaction was completed. Dissolve the intermediate A obtained in the first step in tetrahydrofuran, add 20-22mmol of sodium hydride, stir at room temperature for about 15min, then dissolve 20mmol of 1,3 propane sultone in 50mL of tetrahydrofuran, and slowly add it dropwise to the intermediate In the reaction solution of A and sodium hydride, reflux at 60°C for 12 hours, wherein n(intermediate A):n(sodium hydride):n(1,3 propane sultone)=1:2~2.2:2, the reaction is over Afterwards, react with hydrochloric acid and excess sodium hydride, filter and distill under reduced pressure to obtain yellow v...
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