Reactive aqueous polyurethane fabric finishing agent, its preparation method and application
A technology of water-based polyurethane and fabric finishing agent, which is applied in the preparation of fabric finishing agents, and in the field of fabric finishing agents composed of water-based polyurethane, which can solve the problems of non-washing resistance and long-lasting effect of water-based polyurethane, and achieve high washing resistance and excellent recovery Functionality, good flattening and crease retention
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Embodiment 1
[0036] Put 100g polypropylene glycol (molecular weight 2000, dried), 40g isophorone diisocyanate and 6.7g dimethylolpropionic acid into a four-necked round-bottomed flask equipped with reflux condenser, thermometer and stirrer in turn, and pass nitrogen protection , Stirring, adding 30ml of dimethylformamide solvent, reacting at a constant temperature of 75°C for 2-3 hours to prepare a PU prepolymer. The temperature was increased to 85° C., 6 g of methyl ethyl ketoxime was added, and two drops of dibutyltin laurate catalyst were added, and the reaction was carried out for 2 hours. Lower the temperature of the reactant to 50°C, add 4.5 g of triethylamine for neutralization, and add water to stir and invert phases to obtain a blocked waterborne polyurethane with a solid content of 25%.
Embodiment 2
[0038] Put 50g polytetrahydrofuran (molecular weight 2000, dried), 22g diphenylmethane diisocyanate and 6g dimethylolpropionic acid into a four-necked round-bottomed flask equipped with reflux condenser, thermometer and stirrer in turn, and pass nitrogen protection. Stir, add 50ml methyl ethyl ketone solvent, react at a constant temperature of 80°C for 2-3 hours to prepare a PU prepolymer. The temperature was raised to 85°C and 2 g of hydroxyethyl methacrylate was added, and the reaction was performed until the characteristic absorption peak of NCO radical (2270 cm-1) disappeared. Lower the temperature of the reactant to 50°C, add 4.5 g of triethylamine for neutralization, add water and stir to invert the phase, and finally extract the methyl ethyl ketone under reduced pressure to obtain a water-based polyurethane with a solid content of 30% containing double bonds.
Embodiment 3
[0040] Put 95g polycaprolactone (molecular weight 4000, dried), 21g diphenylmethane diisocyanate, 5.5g dimethylolpropionic acid and 100ml dimethylformamide solvent into a reflux condenser, thermometer and agitator in turn The four-neck round-bottomed flask was filled with nitrogen, stirred, and reacted at a constant temperature of 80°C for 2-3 hours to prepare a PU prepolymer. The temperature was raised to 90°C and 4g of benzyl alcohol was added to the reaction until the characteristic absorption peak of NCO radical (2270cm-1) disappeared. Lower the temperature of the reactants to 50°C, and add a small amount of acetone or no solvent. Add 4g of triethylamine to neutralize, and add water to stir and invert phases to obtain a blocked waterborne polyurethane with a solid content of 15%.
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