Preparation method of aromatic high solid content water-borne polyurethane
A water-based polyurethane and water-based technology, used in textiles and papermaking, can solve the problems of increasing processes, equipment, energy consumption and costs, products without market competitiveness, and acetone cannot be recycled, saving organic solvent resources, The effect of improving the ecological level of products and international market competitiveness and eliminating fire hazards
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Embodiment 1
[0038] A kind of preparation method of high-solid surface layer resin, comprises the following steps:
[0039] (1) Preparation of water-based polyurethane A containing active end groups (-NH2):
[0040] Equipped with electric mixer, reflux condenser, thermometer and N 2 Add 50 parts of polycaprolactone diol with a relative molecular weight of 1000, 50 parts of polypropylene glycol with a relative molecular weight of 2000, 3.0 parts of butanediol, 4,4'-diphenyl Methane diisocyanate is MDI 28.7 parts, toluene diisocyanate is TDI 20 parts, catalyst dibutyltin laurate is DBTDL 0.1 part, in dry N 2 Under protection, react at 80°C for 2 hours, then add 8 parts of dimethylolpropionic acid for chain extension reaction for 2 hours, until the -NCO content reaches the theoretical value, the prepolymer is obtained. The theoretical value is determined by n-butylamine titration method .
[0041] Cool the prepolymer to 55°C and then add 6.0 parts of triethylamine for neutralization for 20...
Embodiment 2
[0048] A preparation method of high-solid foaming resin, comprising the following steps:
[0049] (1) Preparation of water-based polyurethane A containing active end groups (-NH2):
[0050] Equipped with electric mixer, reflux condenser, thermometer and N 2 In the reaction kettle of the import and export, add 100 parts of polycaprolactone diol with a relative molecular weight of 2000, 50 parts of polypropylene glycol with a relative molecular weight of 2000, 2.0 parts of ethylene glycol, and 30 parts of toluene diisocyanate (TDI) after pre-dehydration treatment. , 0.2 parts of catalyst environmental protection silver, in dry N 2 Under protection, react at 80°C for 3 hours, then add 5.0 parts of dimethylolpropionic acid for chain extension reaction for 2 hours, until the -NCO content reaches the theoretical value, the prepolymer is obtained. The theoretical value is determined by n-butylamine titration method .
[0051] Cool the prepolymer to 58°C and then add 3.7 parts of t...
Embodiment 3
[0058] A kind of preparation method of high-solid viscous resin, comprises the following steps:
[0059] (1) Preparation of water-based polyurethane A containing active end groups (-NH2):
[0060] Equipped with electric mixer, reflux condenser, thermometer and N 2 Add 200 parts of polypropylene glycol with molecular weight of 2000, 5.0 parts of hexylene glycol, 70 parts of 4,4'-diphenylmethane diisocyanate (MDI) and 0.1 part of stannous octoate catalyst into the reaction kettle of import and export. in dry N 2 Under protection, react at 70°C for 2 hours, then add 15.0 parts of dimethylolbutyric acid for chain extension reaction for 2 hours, until the -NCO content reaches the theoretical value to obtain a prepolymer. The theoretical value is determined by n-butylamine titration.
[0061] Cool the prepolymer to 51°C and then add 10.3 parts of triethylamine for neutralization for 15 minutes; add the neutralized prepolymer to 676 parts of deionized water containing 15 parts of d...
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