MDI-base polyurethane electronic pouring sealant as well as preparation method and application method thereof
A potting and polyurethane technology, applied in the direction of polyurea/polyurethane adhesives, adhesives, non-polymer adhesive additives, etc., can solve the problems of difficult to guarantee performance and stability, high prepolymer viscosity and high activity , to achieve the effect of adjustable curing speed, low fogging flame retardant performance and good adhesion
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Embodiment 1
[0023] (1) Preparation of component A: Add 20kg polypropylene glycol (MN=2000) and 30kg hydroxyl-terminated polyphosphate (hydroxyl value 170mgKOH / g) into the reactor and vacuum dehydrate at 110°C for 3h, then cool down to At 65°C, add 20kg of 4,4-diphenylmethane diisocyanate and 30kg of polymethylene polyphenyl polyisocyanate, and gradually raise the temperature to 80°C within 30 minutes to react. During the reaction, pass nitrogen protection and test the NCO% value. When the NCO% value reaches 11%, the reaction is stopped, and the A component is obtained.
[0024] (2) Preparation of component B: Add 75kg of polypropylene glycol (MN=3000), 22kg of castor oil (hydroxyl value 170mgKOH / g), 3kg of 1,4-butanediol, and 119kg of alumina into the reactor and heat at 115°C Stir under vacuum for 2 hours, then lower the temperature to 75°C, add 0.5kg of defoamer, 0.01kg of catalyst, and 0.5kg of antioxidant and stir evenly to obtain component B.
[0025] (3) After weighing, stirring an...
Embodiment 2
[0027] (1) Preparation of component A: Add 20kg polypropylene glycol (MN=2000), 9kg tris(dipropylene glycol) phosphite (hydroxyl value 395mgKOH / g) into the reactor and vacuum dehydrate at 115°C 2h, then lower the temperature to 70°C, add 50kg of liquefied 4,4-diphenylmethane diisocyanate, and gradually raise the temperature to 85°C within 30min to react, protect with nitrogen during the reaction, and test the NCO% value, in the NCO% When the value reaches 15%, the reaction is stopped, and the A component is obtained.
[0028] (2) Preparation of component B: 72kg polypropylene glycol (MN=2000), 17kg castor oil (hydroxyl value 170mgKOH / g), 1kg propylene glycol, 50kg alumina, 59kg aluminum hydroxide were added to the reactor and heated at 120°C Stir under vacuum for 2 hours, then lower the temperature to 80°C, add 0.5kg of defoamer, 0.01kg of catalyst, and 0.5kg of antioxidant and stir evenly to obtain component B.
[0029] (3) After weighing, stirring and defoaming components A...
Embodiment 3
[0031] (1) Preparation of component A: 15g polypropylene glycol (MN=2000), 12.5g N, N-di(2-hydroxyethyl)aminomethylphosphonic acid diethyl ester (hydroxyl value 450mgKOH / g) was added to In the reactor, vacuum dehydrate at 120°C for 2 hours, then lower the temperature to 60°C, add 35g of 4,4-diphenylmethane diisocyanate, 15g of polymethylene polyphenyl polyisocyanate and gradually heat up to 75°C within 30min for reaction , Nitrogen protection during the reaction, and the NCO% value is tested, and the reaction is stopped when the NCO% value reaches 15%, that is, the A component is obtained.
[0032] (2) Preparation of component B: Add 39kg hydroxyl-terminated polybutadiene (hydroxyl value 60mgKOH / g), 29kg castor oil (hydroxyl value 170mgKOH / g), 2kg1,4-butanediol and 129kg aluminum hydroxide In the reaction kettle, stir under vacuum at 110°C for 2 hours, then lower the temperature to 60°C, add 0.5kg of defoamer, 0.01kg of catalyst, and 0.5kg of antioxidant and stir evenly to obt...
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