Solvent-free polyurethane adhesive for compound film
A solvent-free polyurethane and adhesive technology, applied in the direction of polyurea/polyurethane adhesives, adhesives, adhesive types, etc., can solve safety problems, environmental pollution, energy consumption and other problems, and achieve low hydrolysis and high safety , Improve the effect of bonding strength
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Embodiment 1
[0019] ① Preparation of component A: Add 0.01mol dimer acid, 0.18mol adipic acid, 0.14mol terephthalic acid, 0.10mol diethylene glycol, 0.17mol neopentyl glycol, 0.17mol 1,4-butanediol to In the reaction kettle, the temperature was raised with stirring under weak nitrogen flow, and the temperature was controlled at 140-160°C. The inlet temperature of the condenser is controlled at 100°C, and after 5 hours of reaction, the temperature is raised to 200°C; after another 4 hours of reaction, a sample is taken to measure the acid value, and the acid value is less than 30mgKOH / g, and the nitrogen flow is stopped; After 1 hour, take a sample to measure the acid value, the acid value is less than 1mgKOH / g, and the product is discharged, and the product is a light yellow liquid, and the A component is obtained. The viscosity at 25°C is 1100mPa·s, and the hydroxyl value is 140mgKOH / g.
[0020] ②Preparation of component B: first dehydrate polyoxypropylene diol and polytetrahydrofuran di...
Embodiment 2
[0023] ① Preparation of component A: Add 0.10mol of dimer acid, 3.00mol of adipic acid, 1.20mol of diethylene glycol, 2.10mol of neopentyl glycol, and 2.00mol of 1,4-butanediol into the reactor, Under normal circumstances, raise the temperature to 70°C for reaction, take a sample after 2 hours, and measure the NCO group content. When the NCO mass content changes ≤ 0.01%, stop the reaction, lower the temperature, pour the product into a dry storage bottle and seal it, and obtain the B component. The reaction was carried out according to the method described in Example 1 to obtain component A with a viscosity of 830 mPa·s and a hydroxyl value of 178 mgKOH / g at 25°C.
[0024] ②Preparation of component B: After dehydration, take 0.39mol of polyoxypropylene diol with a molecular weight of 700, 0.08mol of polyoxypropylene triol, and 2.73 mol of polyphenylpolymethylene polyisocyanate with a water mass percentage of less than 0.05% after dehydration. mol in a reactor, reacted accordin...
Embodiment 3
[0027] ① Preparation of component A: Add 0.16mol of dimer acid, 1.7mol of sebacic acid, 0.75mol of isophthalic acid, 0.94mol of diethylene glycol, 1.67mol of neopentyl glycol, and 1.68mol of 1,4-butanediol into In the reaction kettle, the reaction was carried out according to the method described in Example 1 to obtain component A with a viscosity of 1150 mPa·s and a hydroxyl value of 174 mgKOH / g at 25°C.
[0028] ② Preparation of component B: take 0.30 mol of polyoxypropylene diol with a molecular weight of 2000 and 1.43 mol of isophorone diisocyanate with a water mass percentage of less than 0.05% after dehydration, and raise the temperature while stirring React at 70°C, add 0.02mol of HDI trimer after 2h to continue the reaction, take a sample after 2h, measure the NCO group content, stop the reaction when the NCO mass content changes ≤0.01%, and get B component, at 25°C The viscosity is 2500mPa·s, NCO%=10.3%.
[0029] ③According to the molar ratio of functional groups NCO...
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