Alkylphenol polyoxyethylene ether hydroxysulfonate betaine and preparation method thereof
A technology of alkylphenol polyoxyethylene ether hydroxysulfonate and alkylphenol polyoxyethylene ether, which is applied in the directions of sulfonate preparation, chemical instruments and methods, drilling compositions, etc., and can solve the problem of corrosion equipment and transportation. Pipeline, poor oil displacement efficiency, formation and oil well damage, etc., to achieve the effect of reducing huge damage, superior salt resistance, and optimal temperature resistance
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Embodiment 1
[0033] Synthesis of Amyl (R=5) Phenol Polyoxyethylene Ether (n=2) Sodium Hydroxysulfonate Betaine
[0034] 1) Synthesis of chloropentyl (R=5) phenol polyoxyethylene ether (n=2)
[0035] Add 100g of pentyl (R=5) phenol polyoxyethylene ether (n=2) and 57g of pyridine into a four-neck round bottom flask equipped with a reflux condensing device, a thermometer, a stirrer and a gas absorption device, and heat to 70 under stirring. °C, slowly add 85 g of thionyl chloride dropwise with a dropping funnel, and react at 90 °C for 10 hours after the dropwise addition is completed. After the reaction, the reactants were left to stand, cooled and separated into layers. The upper organic phase was the target product, and the lower layer was solid pyridinium hydrochloride. Use 30% sodium hydroxide solution to neutralize the upper organic phase to neutral or weakly alkaline, separate the inorganic salt, then wash the upper organic phase with hot saturated saline for 5 to 6 times, and obtain t...
Embodiment 2
[0041] Synthesis of Nonyl (R=9) Phenol Polyoxyethylene Ether (n=10) Sodium Hydroxysulfonate Betaine
[0042] 1) Synthesis of chlorinated nonylphenol polyoxyethylene (n=10) ether
[0043] Add 100g of nonyl (R=9) phenol polyoxyethylene (n=10) ether and 22g of pyridine into a four-neck round bottom flask equipped with a reflux condensing device, a thermometer, a stirrer and a gas absorption device, and heat to 70 32.5 g of thionyl chloride was slowly added dropwise with a dropping funnel, and reacted at 70°C for 8 hours after the dropwise addition was completed. After the reaction, the reactants were left to stand, cooled and separated into layers. The upper organic phase was the target product, and the lower layer was solid pyridinium hydrochloride. Use 30% sodium hydroxide solution to neutralize the upper organic phase to neutral or weakly alkaline, separate the inorganic salt, then wash the upper organic phase with hot saturated saline for 5 to 6 times, and obtain the interme...
Embodiment 3
[0049] Synthesis of dodecylphenol polyoxyethylene ether (n=20) sodium hydroxysulfonate betaine
[0050] 1) Synthesis of chlorinated dodecylphenol polyoxyethylene (n=20) ether
[0051] Add 100g of dodecylphenol polyoxyethylene (n=20) ether and 13g of pyridine into a four-neck round bottom flask equipped with a reflux condensing device, a thermometer, a stirrer and a gas absorption device, heat to 60°C under stirring, and use 18.7 g of thionyl chloride was slowly added dropwise into the dropping funnel, and reacted at 80° C. for 10 hours after the dropwise addition was completed. After the reaction, the reactants were left to stand, cooled and separated into layers. The upper organic phase was the target product, and the lower layer was solid pyridinium hydrochloride. Use 30% sodium hydroxide solution to neutralize the upper organic phase to neutral or weakly alkaline, separate the inorganic salt, then wash the upper organic phase with hot saturated saline for 5 to 6 times, and...
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