Preparation method and application of hyperbranched polyurethane acrylate interpenetrating polymer network waterproof agent
A polyacrylate, interpenetrating network structure technology, applied in the field of textile printing, dyeing and finishing, can solve the problems of poor washing resistance of textiles and short duration of waterproof performance of textiles, and achieves low cost, excellent waterproof performance, and film-forming properties. Good results
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Embodiment 1
[0032] (1) Preparation of water-based polyurethane prepolymer: Weigh 100 grams of polyoxypropylene diol N210 in a four-necked flask, heat it to 110°C, treat it at a vacuum of -0.098MPa for 100 minutes, add 44.46 grams of IPDI, and React at 70°C for 4 hours, lower the temperature of the reaction system to between 40°C and 50°C, add 8.93 g of N-methyldiethanolamine evenly with a dropping funnel within 30 minutes, keep the reaction temperature at 40°C to 50°C, and react for 30 minutes , add 1.3 grams of hydroxyethyl methacrylate and 1.04 grams of phenol to carry out partial capping reaction, and react at 60 ° C for 1.5 hours to obtain a water-based polyurethane prepolymer;
[0033] (2) Preparation of hyperbranched waterborne polyurethane prepolymer: add 3.27 g of hyperbranched polyester BoltornH20 to the polyurethane prepolymer prepared in the above step (1), and react at 75°C for 2 hours to obtain a hyperbranched waterborne polyurethane prepolymer;
[0034] (3) Preparation of hy...
Embodiment 2
[0037](1) Preparation of water-based polyurethane prepolymer: Weigh 200 grams of polybutylene adipate diol (PBA) with a molecular weight of 2000 in a four-necked flask, and heat it to 110°C, at a vacuum of -0.098MPa Treat at low temperature for 100min, add 33.64g of HDI, react at 55°C for 5 hours, cool down the reaction system to between 40°C and 50°C, and add 12.09g of N-butyldiethanolamine evenly with a dropping funnel within 30min to keep the reaction The temperature is 40°C~50°C, react for 30min, add 1.01g of methylolacrylamide and 0.73g of acetone oxime for partial capping reaction, and react at 60°C for 1.5 hours to obtain a waterborne polyurethane prepolymer;
[0038] (2) Preparation of hyperbranched waterborne polyurethane prepolymer: Add 3.43 g of hyperbranched polyester BoltornH30 to the polyurethane prepolymer prepared in the above step (1), and react at 75°C for 2 hours to obtain a hyperbranched waterborne polyurethane prepolymer;
[0039] (3) Preparation of hyperb...
Embodiment 3
[0042] (1) Preparation of water-based polyurethane prepolymer: Weigh 100 grams of polytetrahydrofuran glycol (PTMEG) with a molecular weight of 1000 in a four-neck flask, heat it to 110°C, and treat it under a vacuum of -0.098MPa for 100min, add 31.32 gram of TDI, reacted at 60°C for 2.5 hours, cooled the reaction system to between 40°C and 50°C, added 5.95 g of N-methyldiethanolamine evenly with a dropping funnel within 30 minutes, and kept the reaction temperature between 40°C and 50°C ℃, reacted for 30 minutes, added 2.16 grams of hydroxypropyl methacrylate and 1.3 grams of butanone oxime to carry out a partial capping reaction, and reacted at 50 degrees Celsius for 3 hours to obtain a water-based polyurethane prepolymer;
[0043] (2) Preparation of hyperbranched waterborne polyurethane prepolymer: Add 3.37 g of hyperbranched polyester BoltornH40 to the polyurethane prepolymer prepared in the above step (1), and react at 95°C for 0.5 hours to obtain a hyperbranched waterborn...
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