Composition for improving recovery ratio substantially and preparation method thereof
A technology of recovery factor and composition, which is applied in the field of composition and its preparation that can greatly increase recovery factor, can solve the problems of alkali corrosion, high use concentration and poor oil displacement efficiency in ASP flooding, and achieve The ability to reduce interfacial tension, high salinity resistance, and the effect of enhancing oil recovery
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Embodiment 1
[0030] 1) Synthesis of chloropentyl (R=5) phenol polyoxyethylene (n=2) ether
[0031] Into a four-necked round bottom flask equipped with reflux condenser, thermometer, stirrer and gas absorption device, add 100g amyl (R=5) phenol polyoxyethylene (n=2) ether and 57g pyridine, and heat to 70g under stirring. °C, slowly drip 85 g of thionyl chloride with a dropping funnel, and react at 90 °C for 10 hours after the addition is complete. After the reaction is over, the reactants are allowed to stand and cool to separate layers, the upper organic phase is the target product, and the lower layer is solid pyridine hydrochloride salt. Use 30% sodium hydroxide solution to neutralize the upper organic phase to neutral or weakly alkaline, separate out inorganic salts, and then wash the upper organic phase with hot saturated brine for 5-6 times, and dry to obtain the intermediate product chlorine Pentyl (R=5) phenol polyoxyethylene (n=2) ether, the yield was 88%.
[0032] 2) Synthesis of pen...
Embodiment 2
[0038] Synthesis of nonyl (R=9) phenol polyoxyethylene ether (n=10) sodium carboxylate betaine
[0039] 1) Synthesis of chlorononyl (R=9) phenol polyoxyethylene (n=10) ether
[0040] Into a four-necked round bottom flask equipped with reflux condenser, thermometer, stirrer and gas absorption device, add 100g nonyl (R=9) phenol polyoxyethylene (n=10) ether and 22g pyridine, and heat to 70g under stirring. At 0°C, 32.5 g of thionyl chloride was slowly added dropwise with a dropping funnel, and after the addition, the reaction was carried out at 70°C for 8 hours. After the reaction is over, the reactants are allowed to stand and cool to separate layers, the upper organic phase is the target product, and the lower layer is solid pyridinium hydrochloride salt. Use 30% sodium hydroxide solution to neutralize the upper organic phase to neutral or weakly alkaline, separate out inorganic salts, and then wash the upper organic phase with hot saturated brine for 5-6 times, and dry to obtain ...
Embodiment 3
[0047] Synthesis of Dodecylphenol Polyoxyethylene Ether (n=20) Sodium Carboxylate Betaine
[0048] 1) Synthesis of chlorododecylphenol polyoxyethylene (n=20) ether
[0049] Into a four-necked round bottom flask equipped with reflux condenser, thermometer, stirrer and gas absorption device, add 100g dodecylphenol polyoxyethylene (n=20) ether and 13g pyridine, and heat to 60℃ with stirring. 18.7 g of thionyl chloride was slowly added dropwise to the dropping funnel, and after the addition, the reaction was carried out at 80° C. for 10 hours. After the reaction is over, the reactants are allowed to stand and cool to separate layers, the upper organic phase is the target product, and the lower layer is solid pyridinium hydrochloride salt. Use 30% sodium hydroxide solution to neutralize the upper organic phase to neutral or weakly alkaline, separate out inorganic salts, and then wash the upper organic phase with hot saturated brine for 5-6 times, and dry to obtain the intermediate prod...
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