Preparation method of waterborne polyurethane adhesive for card matrix material
A water-based polyurethane and adhesive technology, applied in the direction of polyurea/polyurethane adhesives, adhesive types, adhesives, etc., can solve the blurring of UV test, the peeling strength of color card is difficult to maintain the value of wet heat aging, and the expected product cannot be achieved. and other problems to achieve the effect of avoiding the use of toxic solvents, good mechanical properties and high strength
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Embodiment 1
[0053] Add 50g of polybutylene adipate, 10g of polyhexamethylene adipate and 10g of polytetrahydrofuran diol into a 500ml four-neck flask, place them in a vacuum oven at 80°C for melting and mixing, and dehydrate After 1 hour, the temperature was lowered to 50°C and removed from the drying oven. Under the protection of dry nitrogen, a mixture of 35 g of isophorone diisocyanate and 3.5 g of dicyclohexylmethane-4,4-diisocyanate was added into the above-mentioned four-necked flask, and then the temperature was gradually raised to 80°C. After reacting for 1.5 hours, lower the temperature to 40°C, add 0.0217g of bismuth-zinc composite catalyst, 4.34g of hydrophilic chain extender dimethylol butyric acid, 2.17g of crosslinking agent 1,4-butanediol, trimethylolpropane 0.868g, 2.17g of β-hydroxyethyl methacrylate, the temperature was gradually raised to 60°C, and then 27.125g of acetone was added, and the reaction was continued for 4 hours. Cool down to 20°C, add 1.736g of triethylam...
Embodiment 2
[0061] Add 50g of polybutylene adipate, 15g of polyhexamethylene adipate and 15g of polytetrahydrofuran diol into a 500ml four-neck flask, place them in a vacuum oven at 85°C for melting and mixing, and dehydrate After 2 hours, the temperature was lowered to 60°C and removed from the drying oven. Under the protection of dry nitrogen, a mixture of 40 g of isophorone diisocyanate and 8 g of dicyclohexylmethane-4,4-diisocyanate was added into the above-mentioned four-neck flask, and then the temperature was gradually raised to 90° C. After reacting for 2 hours, lower the temperature to 50°C, add 0.0512g of bismuth-zinc composite catalyst, 6.4g of hydrophilic chain extender dimethylol butyric acid, 5.12g of crosslinking agent 1,4-butanediol, trimethylolpropane 1.28g, 5.12g of -β-hydroxyethyl methacrylate, gradually warming up to 65°C, then adding 44.8g of acetone, and continuing the reaction for 5 hours. Cool down to 25°C, add 3.2g of triethylamine for neutralization, and continu...
Embodiment 3
[0069] Add 50g of polybutylene adipate, 10g of polyhexamethylene adipate and 15g of polytetrahydrofuran diol into a 500ml four-neck flask, place them in a vacuum oven at 85°C for melting and mixing, and dehydrate 1 hour, then lower the temperature to 60°C and remove from the drying oven. Under the protection of dry nitrogen, a mixture of 37.5 g of isophorone diisocyanate and 7.5 g of dicyclohexylmethane-4,4-diisocyanate was added into the above four-necked flask, and then the temperature was gradually raised to 80°C. After reacting for 1.5 hours, lower the temperature to 40°C, add 0.048g of bismuth-zinc composite catalyst, 6.0g of hydrophilic chain extender dimethylol butyric acid, 4.8g of crosslinking agent 1,4-butanediol, trimethylolpropane 1.2 g, 4.8 g of β-hydroxyethyl methacrylate, gradually warming up to 60°C, then adding 31.25 g of acetone, and continuing the reaction for 5 hours. Cool down to 20°C, add 2.4g of triethylamine for neutralization, and continue the reactio...
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