Combination of modified polyurethane and aqueous polyurethane adhesive
A composition and polyurethane technology, applied in polyurea/polyurethane adhesives, adhesives, adhesive types, etc., can solve the problems of poor initial bond strength and low peel strength, and achieve good water resistance
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Example 1
After mixing 86g of hydroxyethyl acrylate, 65g of methacrylic acid, 106g of glycidyl methacrylate, 112g of vinyl trimethoxysilane and 60g of glycidyl tertiary carbonate, add benzoyl peroxide and 0.5g Alkyl mercaptan, the mixture is obtained; the mixture is added dropwise to the mixed solution of propylene glycol monomethyl ether and isopropanol at 130°C, the drop is completed within 3 hours, and the temperature is kept for 5 hours; then the benzoyl peroxide is added dropwise to the reaction mixture The isopropanol solution was incubated for 3 hours to obtain an aqueous hydroxy acrylate, in which the total amount of benzoyl peroxide was 2.3 g.
Nuclear magnetic resonance was performed on the polyurethane, and its hydrogen spectrum was as follows: 1 H NMR: 0.96 ppm, 1.11 to 1.53 ppm, 1.69 ppm, 2.27 ppm, 2.73 ppm, 2.96 ppm, 3.26 ppm, 3.98 to 4.15 ppm, 6.38 ppm. It can be seen that the polyurethane has a structure of formula (III), where R 1 Isophorone base, R 2 It is pol...
Example Embodiment
Example 2
Under the protection of nitrogen, add 240g methyl ethyl ketone, 88g dimethylolpropionic acid, 330g polyethylene adipate diol with a molecular weight of 1500 and 0.5g dibutyltin dilaurate to a four-necked flask, and heat to 75℃ Then, add 244g isophorone diisocyanate, after 2h reaction, add 50g 1,4-butanediol, after 2h reaction, cool to 40℃, add 48g dimethylethanolamine, stir for 20min, pressurize to remove butanone, The polyurethane is obtained.
Nuclear magnetic resonance was performed on the modified polyurethane, and its hydrogen spectrum was as follows: 1 H NMR: 1.20~1.51ppm, 1.67ppm, 1.76ppm, 2.18ppm, 2.32ppm, 2.51ppm, 2.67ppm, 3.01ppm, 3.36ppm, 3.56ppm, 3.61ppm, 3.70ppm, 3.98ppm, 4.23ppm, 4.37ppm, 4.60ppm, 5.98ppm, 6.98ppm. It can be seen that the polyurethane is a modified polyurethane with the structure of formula (I), wherein R 1 Is dicyclohexylmethyl, R 2 For polycaprolactone group, R 3 It is a triethanolamine group, n=5.
Example Embodiment
Example 3
Under the protection of nitrogen, add 150g of methyl ethyl ketone, 78g of dimethylolpropionic acid, 195g of polybutylene adipate diol with a molecular weight of 1000, 65g of E-31 type bisphenol A epoxy resin and 0.3g dibutyltin dilaurate, after heating to 77℃, add 256g dicyclohexylmethane diisocyanate, after 3h reaction, add 41g 1,4-butanediol, after 2h reaction, cool to 45℃, add 46g triethylamine , Stir for 25min and remove butanone under pressure to obtain polyurethane.
Nuclear magnetic resonance was performed on the modified polyurethane, and its hydrogen spectrum was as follows: 1 H NMR: 0.93ppm, 1.26ppm, 1.35ppm, 1.56~2.39ppm, 2.65ppm, 2.96ppm, 3.41ppm, 3.54~3.95ppm, 4.06ppm, 4.13ppm, 4.32ppm, 4.61ppm, 5.90ppm, 6.38ppm, 6.68 ppm, 7.48 ppm. It can be seen that the polyurethane is a modified polyurethane with the structure of formula (I), wherein R 1 For tolyl, R 2 It is polybutylene adipate base, R 3 It is a dimethylethanolamine group, n=5.
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