Bi-component high-strength polyurethane waterproofing paint
A polyurethane waterproof, two-component technology, applied in the field of polyurethane waterproof coatings, can solve the problems of low bonding strength, low tensile strength and tear strength, environmental pollution, etc., and achieve the effect of convenient construction and environmental protection
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Embodiment 1
[0015] The preparation process of component A is as follows: Add 200 parts of polyether glycol (propylene glycol polyoxypropylene ether), 150 parts of glycerin polyoxypropylene into a 500ml ground-mouthed three-necked bottle equipped with a stirrer, reflux condenser, and thermometer. Propylene ether, 2.5 parts of dibutyl phthalate, and 0.1 part of tartaric acid are slowly heated up to 120°C while stirring, and placed under a vacuum pressure of -0.098MPa for 2 hours. Lower the temperature below 60°C, add 55 parts of toluene-2,4-diisocyanate (TDI), control the temperature at 70°C, and dehydrate in vacuum for 2 hours under stirring. After the reaction is finished, lower the temperature to below 60°C and discharge the material, and fill with nitrogen to protect to obtain component A.
[0016] The preparation process of component B is as follows: add 50 parts of petroleum resin, 20 parts of chlorinated paraffin, 10 parts of dibutyl phthalate, and 60 parts of polyether trihydric alc...
Embodiment 2
[0018] The preparation process of component A is as follows: 120 parts of polyether diol (polyoxypropylene-refined castor oil diol), 40 parts of Polyether trihydric alcohol (glycerol polyoxypropylene ether), 1.5 parts of dibutyl phthalate, 0.5 parts of tartaric acid, slowly heated up to 110°C while stirring, and placed under vacuum pressure -0.098MPa for 2 hours. Lower the temperature below 60°C, add 47 parts of toluene-2,4-diisocyanate (TDI), control the temperature at 80°C, and conduct vacuum dehydration reaction for 3 hours under stirring. Nitrogen protection is used to protect the discharge to obtain component A.
[0019] The preparation process of component B is as follows: add 60 parts of petroleum resin, 50 parts of chlorinated paraffin, 20 parts of dibutyl phthalate, and 360 parts of polyether trihydric alcohol (GEP-330N) tube and a thermometer with a 500ml ground-necked three-neck bottle, after slowly heating up to 120°C, slowly add 45 parts of 3,3-dichloro-4,4'-diph...
Embodiment 3
[0021] The preparation process of component A is as follows: 150 parts of polyether diol (polybutadiene diol), 3 parts of phthalic acid Dibutyl ester, 180 parts of polyoxypropylene-refined castor oil trihydric alcohol, and 1 part of tartaric acid are slowly heated to 130° C. under stirring, and placed under a vacuum pressure of -0.098 MPa for 2 hours. Lower the temperature below 60°C, add 80 parts of toluene-2,4-diisocyanate (TDI), control the temperature at 90°C, and vacuum dehydration reaction for 3h under stirring. After the reaction is finished, the temperature is lowered to below 60°C, and then the material is discharged, and the A component is obtained for protection with nitrogen protection.
[0022] The preparation process of component B is as follows: add 90 parts of petroleum resin, 30 parts of chlorinated paraffin, 30 parts of dibutyl phthalate, 200 parts of polyether triol (GEP-330N), and dispersant (FA196) into the container In a 500ml ground three-neck flask wit...
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Abstract
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