Styrene compound and acrylamide copolymer and preparation method and application thereof
A technology of acrylamide copolymer and acrylamide copolymerization, applied in chemical instruments and methods, drilling compositions, organic chemistry, etc., can solve problems such as poor salt resistance, and achieve strong temperature and salt resistance, good water solubility , the effect of high thermal stability
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[0026] The preparation method of the above-mentioned styrene compounds provided by the present invention may comprise: mixing the lactam shown in formula II and / or its salt with an alkali agent, and contacting the obtained mixture with vinylbenzyl chloride shown in formula III reaction, and then selectively in the presence of an alkylating agent, the product obtained by the contact reaction is alkylated,
[0027] (m=1 or 2, preferably m=1)
[0028] Wherein, the salt of the lactam shown in formula II may be a salt of various lactams common in the art, including but not limited to hydrochloride, sulfate and acetate. Vinylbenzyl chloride represented by formula III may be at least one of p-vinylbenzyl chloride, m-vinylbenzyl chloride and o-vinylbenzyl chloride, preferably p-vinylbenzyl chloride.
[0029] In the present invention, there is no special requirement on the amount of lactam represented by formula II and / or its salt, alkali agent, vinylbenzyl chloride and alkylating...
preparation Embodiment 1
[0067] Dissolve 11.4g of α-aminovalerolactam in 100m of anhydrous tetrahydrofuran, add 2.4g of sodium metal, react for 30 minutes, dissolve 16g of p-vinylbenzyl chloride in 10ml of anhydrous tetrahydrofuran, and add it dropwise to the above solution. The dropwise addition was completed within 30 minutes. After continuing to react for 60 min, remove the solvent by rotary evaporation, add chloroform to dissolve, wash the organic phase with deionized water three times, and add anhydrous potassium carbonate for drying. After drying to remove the solvent, compound 1 was obtained 20g. The chemical composition of the compound measured by X-ray fluorescence spectrometer is: C, 72.98, N, 12.09, O, 6.97 (theoretical values: C, 73.01; N, 12.16; O, 6.95).
[0068] 24.6 g of Compound 1 was dissolved in anhydrous dichloromethane, 15 g of potassium carbonate was added, and 30 g of iodomethane was slowly added dropwise under ice-bath conditions. After 4 hours of dropwise addition, the tem...
preparation Embodiment 2
[0070] Dissolve 23.0g of compound 1 in dimethylformamide, add 15g of anhydrous potassium carbonate, add 100g of bromooctadecane, react at 100°C for 8h, and then stop the reaction. After the solvent and unreacted bromooctadecane were removed under reduced pressure, the product was dissolved in dichloromethane, washed 3 times with distilled water, and then dried by adding anhydrous sodium sulfate. After drying, the desiccant was filtered off and evaporated to remove Compound B was obtained after solvent The chemical composition of the compound measured by X-ray fluorescence spectrometer is: C, 81.70, N, 3.77, O, 2.10 (theoretical values: C, 81.68; N, 3.81; O, 2.18).
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