Crystallization accelerating agent for crystallization/semi-crystallization polyurethane and preparing method and application thereof
A technology of crystallization accelerator and polyurethane, applied in polyurea/polyurethane adhesives, adhesives, adhesive types, etc. and crystalline/semi-crystalline polyurethane system, and the inability to make the most effective use of the advantages of crystalline/semi-crystalline polymers, etc., to achieve the effects of wide application range, increasing the number of crystal nuclei, and improving hardness
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Embodiment 1
[0025] Stir 1 mol of 2000 molecular weight polybutylene adipate diol and 2 mol of TDI under nitrogen protection, and react at a temperature of 90°C for 2.5 hours to obtain compound A; add 2 mol of methyl ethyl ketoxime under nitrogen protection and stir evenly, React at a temperature of 60°C for 3 hours to obtain a crystallization accelerator.
[0026] Application 1: Dehydrate 50g of 500 molecular weight polybutylene adipate diol at 110°C for 1.5h in vacuum, then cool to 65°C, add 39gTDI, under nitrogen protection, stir for 0.5h, add dibutyltin dilaurate 0.015 g, react at 80°C for 2h; add 2.5g DMPA, 1g 1,4-butanediol, 2g neopentyl glycol, 10g butanone, 5g N-methylpyrrolidone, react at 80°C for 3h, and cool to 50°C , To obtain a clear and transparent viscous prepolymer A, mix 5g crystallization promoter and 116g prepolymer A uniformly, add triethylamine with the same molar ratio of dimethylolpropionic acid contained in the prepolymer to neutralize, Disperse in 150 g of deionized ...
Embodiment 2
[0029] Stir 1mol of 2000 molecular weight polyhexanediol adipate diol and 2mol TDI under nitrogen protection, and react at 60℃ for 4h to obtain compound A; add 2mol caprolactam under nitrogen protection and stir evenly. React at 70°C for 2.5 hours to obtain a crystallization accelerator.
[0030] Application 1: Dehydrate 50g of 500 molecular weight polybutylene adipate diol at 110°C for 1.5h in vacuum, then cool to 65°C, add 50gIPDI, under nitrogen protection, stir for 0.5h, add 0.02g stannous octoate, React at 80°C for 2h; add 3g 2-methylpropanediol, 2g 3-methylpentanediol, 10g butanone, 5g N-methylpyrrolidone, 4g sodium ethylenedihydroxyethanesulfonate, and react for 3h at 80°C. Cool down to 50°C to obtain a clear and transparent viscous prepolymer A. Mix 10g of crystallization accelerator and 114g of prepolymer A uniformly, disperse them in 100g of deionized water under high-speed stirring at 800~2000r / min, and add 2g of acetone. After diamine chain extension, stirring for 1 ...
Embodiment 3
[0033] Mix 1 mol of 1000 molecular weight polycarbonate diol and 2 mol of IPDI under nitrogen protection, and react at a temperature of 80°C for 4 hours to obtain compound A; add 2 mol 3,5-dimethylpyrazole under nitrogen protection and stir evenly, React for 1.5h at a temperature of 90°C to obtain a crystallization accelerator.
[0034] Application 1: 150g of 2000 molecular weight polyethylene adipate diol was vacuum dehydrated at 110°C for 1.5h, cooled to 65°C, 40gIPDI, 30gHDI, under nitrogen protection, stirred for 0.5h, added stannous octoate 0.15 g, react at 80°C for 2h; add 6g diethylene glycol, 2g trimethylolpropane, 30g acetone, 4g dimethylolbutyric acid, react for 3h at 70°C, and cool to 50°C, Obtain a clear and transparent viscous prepolymer A, mix 15g crystallization accelerator and 115g prepolymer A uniformly, add triethylamine with the same molar ratio of dimethylolbutyric acid contained in the prepolymer to neutralize it, Disperse in 100g deionized water under high-...
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