Method for preparing non-ionic hydrophobic association polymerization water-soluble polymer from reverse micro emulsion
A water-soluble polymer and hydrophobic association technology, which is applied in the field of non-ionic hydrophobic association water-soluble polymers and their synthesis, can solve the problems of product molecular chain damage, performance degradation, asymmetric distribution, etc.
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Embodiment 1
[0021] In the reaction vessel, add 80g of white oil and 40g of surfactant, control the HLB value of the surfactant mixture between 9.2, control the temperature at 40°C, stir at 800rpm, and stir for 1.5h; mix acrylamide according to the amount (Monomer A), dodecyl dimethyl (acryloxyethyl) ammonium bromide (monomer B) is formulated into an aqueous solution, the solution concentration is between 55 wt% (the molar ratio of A and B is 99:1 ). Then, under the condition of stirring again, the aqueous monomer solution was slowly added dropwise, and the stirring was continued for 5 hours, and the temperature of the solution was controlled between 40°C. Continue to stir, control the stirring speed between 300rpm, pass high-purity nitrogen for 30 minutes, add 0.15g of water-soluble free radical initiator V50, and continue to pass nitrogen for 5 hours to obtain a transparent polymer microlatex with bluish light.
Embodiment 2
[0023] In the reaction vessel, add 80g of white oil and 40g of surfactant, control the HLB value of the surfactant mixture between 9.2, control the temperature at 40°C, stir at 800rpm, and stir for 1.5h; mix acrylamide according to the amount (Monomer A), dodecyl dimethyl (acryloxyethyl) ammonium bromide (monomer B) is formulated into an aqueous solution, the solution concentration is between 55 wt% (the molar ratio of A and B is 99:1 ). Then, under the condition of stirring again, the aqueous monomer solution was slowly added dropwise, and the stirring was continued for 5 hours, and the temperature of the solution was controlled between 40°C. Continue to stir, control the stirring speed between 300rpm, pass high-purity nitrogen for 30 minutes, add 0.70 g of water-soluble free radical initiator V50, and continue to pass nitrogen for 5 hours to obtain transparent polymer microlatex with bluish light.
Embodiment 3
[0025] In the reaction vessel, add 80g of white oil and 40g of surfactant, control the HLB value of the surfactant mixture between 9.2, control the temperature at 40°C, stir at 800rpm, and stir for 1.5h; mix acrylamide according to the amount (Monomer A), dodecyl dimethyl (acryloxyethyl) ammonium bromide (monomer B) is formulated into an aqueous solution, the solution concentration is between 55 wt% (the molar ratio of A and B is 99:1 ). Then, under the condition of stirring again, the aqueous monomer solution was slowly added dropwise, and the stirring was continued for 5 hours, and the temperature of the solution was controlled between 40°C. Continue to stir, control the stirring speed between 300rpm, pass high-purity nitrogen for 30 minutes, add 0.50 g of water-soluble free radical initiator V50, and continue to pass nitrogen for 5 hours to obtain a transparent polymer microlatex with bluish light.
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