Polyurethane resin for solvent-free leather and preparing method and application thereof
A polyurethane resin and solvent-free technology, which is applied in the field of solvent-free leather polyurethane resin and its preparation and application, can solve the problems of limited influence on the physical properties of synthetic leather products, and achieve improved production operability, high production efficiency, and excellent physical and mechanical properties Effect
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Embodiment 1
[0057] 20.00kg of polyetherester polyol-toluene diisocyanate prepolymer (number-average molecular weight is 10,000, functionality is 2), 73.35kg of polyethylene propylene adipate (number-average molecular weight is 1000), 1.65kg The polydiethylene glycol glycerol adipate (functionality of 2.80, number-average molecular weight of 2000) was heated to 120 ° C, dehydrated under vacuum conditions of -0.01 MPa for 6 h, and then cooled to 30 ° C, Add 2.10kg ethylene glycol, 0.90kg trimethylolpropane, 0.70kg organosilicon foam stabilizer, 0.3kg deionized water, 0.65kg ultraviolet absorber UV-320, 0.30kg light stabilizer 292, 0.05kg of antioxidant 245 and 0.30kg of organotin metal catalyst were mixed and stirred for 2 hours, and the hydroxyl value and moisture content were detected. When the hydroxyl value reached 153.8mgKOH / g and the moisture content was 0.3%, the resin A component was obtained and sealed. stand-by.
[0058] Drop into the reaction kettle the toluene diisocyanate of 3...
Embodiment 2
[0061] 35.00kg of polyetherester polyol-isophordione polyisocyanate prepolymer (number-average molecular weight is 10,000, functionality is 4), 58.00kg of poly(diethylene glycol butylene adipate) (number-average molecular weight is 4) The average molecular weight is 5000), 2.00kg of polydiethylene glycol glycerol adipate (functionality 2.05, number average molecular weight is 5000), heated to 140°C, dehydrated under vacuum conditions of -0.06MPa for 5h, After cooling to 50 ℃, add 2.47kg 1,4-butanediol, 0.13kg trimethylolpropane, 0.30kg organosilicon foam stabilizer, 0.30kg deionized water, 0.45kg ultraviolet absorber UV- 320, 0.36kg of light stabilizer 292, 0.09kg of antioxidant 245 and 0.90kg of organotin metal catalyst were mixed and stirred for 2 hours, and the hydroxyl value and moisture content were detected. When the hydroxyl value reached 125.4 mgKOH / g and the moisture content was 16%, That is, the resin A component is prepared, which is sealed and packaged for use.
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Embodiment 3
[0065] 33.40kg of polyetherester polyol-diphenylmethane diisocyanate prepolymer (number-average molecular weight is 30,000, functionality is 3), 40.00kg of polyethylene adipate (number-average molecular weight is 3) 3000), 15.00kg of poly(diethylene glycol trimethylolpropane adipate) (functionality of 2.3, number-average molecular weight of 3000) was heated to 130°C, dehydrated under vacuum conditions of -0.04MPa for 5h, and then Cool to 40 ℃, add 4.50kg ethylene glycol, 0.50kg trimethylolpropane, 2.00kg silicone foam stabilizer, 2.00kg deionized water, 0.64kg ultraviolet absorber UV-320, 0.64kg Light stabilizer 292, 0.32kg antioxidant 245 and 1.00kg organotin metal catalyst were mixed and stirred for 3 hours, and the hydroxyl value and moisture content were detected. When the hydroxyl value reached 235.7 mgKOH / g and the moisture content was 2.0%, resin A was obtained. components, sealed and packaged for use.
[0066] Drop into the reaction kettle the methane diisocyanate of ...
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