A kind of fluorine-containing hydrophobic association surface-active polyacrylamide and its preparation method
A polyacrylamide and hydrophobic association technology, which is applied in the field of water-soluble polymers, can solve the problems of poor water solubility, poor oil displacement effect, and low fluorine content of polyacrylamide, and achieve strong temperature resistance and low cost. Effect
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example 1
[0041] Step 1: Synthesis of Surface Active Fluorinated Polymerizable Macromonomer HAPS
[0042] ①. Synthesis of N-dimethylperfluoroalkylsulfonamide
[0043] Add 0.1mol dimethylamine, 0.08mol triethylamine and 100mL isopropanol into a three-necked flask equipped with a spherical reflux condenser, a thermometer and a stirrer, stir and mix evenly, and slowly pour into the reaction system through a constant pressure dropping funnel. 0.05mol perfluorooctanesulfonyl fluoride was added dropwise, then the temperature was raised to 40°C, and the reaction was continued for 6h. The reaction mixture was washed successively with water, 0.5% hydrochloric acid aqueous solution, and saturated brine, then dried over anhydrous sodium sulfate, and distilled under reduced pressure to obtain the product N-dimethylperfluoroalkylsulfonamide.
[0044] ②, Synthesis of hydroxypropyl chloroacrylate
[0045] Add 0.1mol of hydroxypropyl acrylate and 100mL of dichloromethane into a three-necked flask equ...
example 2
[0054] Step 1: Synthesis of Surface Active Fluorinated Polymerizable Macromonomer HAPS
[0055] ①. Synthesis of N-diethylperfluorobutanesulfonamide
[0056] Add 0.2 mol of diethylamine, 0.2 mol of triethylamine and 100 ml of isopropyl ether into a three-necked flask equipped with a spherical reflux condenser, a thermometer and a stirrer, stir and mix evenly, and slowly pour into the reaction system through a constant pressure dropping funnel. 0.1mol perfluorooctanesulfonyl fluoride was added dropwise, then the temperature was raised to 60°C, and the reaction was continued for 10h. The reaction mixture was washed successively with water, 0.5% hydrochloric acid aqueous solution, and saturated brine, then dried over anhydrous sodium sulfate, and distilled under reduced pressure to obtain the product N-diethylperfluorobutanesulfonamide.
[0057] ②, Synthesis of hydroxypropyl chloroacrylate
[0058] Add 0.5mol of hydroxypropyl acrylate and 150ml of acetone into a three-necked fla...
example 3
[0066] Step 1: Synthesis of Surface Active Fluorinated Polymerizable Macromonomer HAPS
[0067] ①, N-methyl, ethyl perfluorohexylsulfonamide synthesis
[0068] Add 0.6mol of N-methylethylamine, 0.75mol of triethylamine and 150ml of acetone into a three-necked flask equipped with a spherical reflux condenser, a thermometer and a stirrer, stir and mix evenly, and pour into the reaction via a constant pressure dropping funnel. 0.4 mol of perfluorohexylsulfonyl fluoride was slowly added dropwise into the system; then the temperature was raised to 35° C., and the reaction was continued for 5 hours. The reaction mixture was washed successively with water, 0.5% hydrochloric acid aqueous solution, and saturated brine, then dried over anhydrous sodium sulfate, and distilled under reduced pressure to obtain the product N-methyl, ethyl perfluorohexylsulfonamide.
[0069] ②, Synthesis of hydroxypropyl chloroacrylate
[0070] Add 0.5mol of hydroxypropyl acrylate and 130ml of tetrahydrofu...
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