Preparation method of novel efficient thickener polyacrylate copolymer
A polyacrylate and thickener technology, which is applied in the field of preparation of new high-efficiency thickener polyacrylate copolymers, can solve the problems of dispersion and post-neutralization, and achieve high alcohol tolerance, high product quality, Huge application prospects and the effect of market economic benefits
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Embodiment 1
[0020] Add 140g of tert-butanol, 10g of deionized water, 35g of sodium bicarbonate, and 0.18g of pentaerythritol triallyl ether to a 500ml four-necked flask in sequence, keeping the temperature below 25°C; blowing nitrogen gas and stirring for 20-30min; heat up To 60°C, add 0.1g of lauryl peroxide, and slowly add 30g of acrylic acid monomer within 1h, about 10-20Min the polymerization reaction starts, the solid precipitates out, and the system gradually thickens; after reacting at 60°C for 4h, the temperature is raised to 65°C, add 0.05g of lauryl peroxide, continue to react for 2h, the reaction is over, the system exists in a viscous form; finally, the temperature is further raised to 90°C, until all the solvent is evaporated, and a white fluffy powder is obtained in a four-necked flask.
Embodiment 2
[0022] Add 145g tert-butanol, 5g deionized water, 32.9g ammonium bicarbonate (other steps of polymerization method 2 are carried out similarly to polymerization method 1) and 0.18g pentaerythritol triallyl ether to a 500ml four-necked flask successively, keeping The temperature does not exceed 25°C; mix and stir with nitrogen for 20-30min; heat up to 60°C, add 0.1g lauryl peroxide, and add 30g acrylic acid monomer within 1h, the polymerization reaction starts in about 10-20Min, and the solid precipitates out. The system gradually thickened; after reacting at 60°C for 4 hours, the temperature was raised to 65°C, 0.05g of lauryl peroxide was added, and the reaction was continued for 2h. The solvent was all evaporated, and a white fluffy powder was obtained in a four-neck flask.
Embodiment 3
[0024] Add 145g of tert-butanol, 5g of deionized water, 32.9g of ammonium bicarbonate, and 0.18g of trimethylolpropane triacrylate to a 500ml four-necked flask in sequence, keeping the temperature below 25°C; blowing nitrogen and stirring for 20-30min ;Heat to 60°C, add 0.1g of azobisisobutyronitrile, and add 30g of acrylic acid monomer within 1h, the polymerization reaction starts in about 10-20Min, the solid precipitates out, and the system gradually thickens; react at 60°C for 4h Finally, raise the temperature to 65°C, add 0.05g of azobisisobutyronitrile (the other steps of polymerization method 3 are similar to polymerization method 1), and continue the reaction for 2 hours. After the reaction is completed, the system exists in a viscous form; to 90°C until the solvent was completely evaporated, and a white fluffy powder was obtained in a four-neck flask.
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