Ultraviolet-curable extinction resin and preparation method thereof
A technology of matting resin and ultraviolet light, which is applied in coatings, polyurea/polyurethane coatings, etc., can solve problems such as uneven gloss, decreased coating film hardness, and excessive viscosity of the system, achieving good matting effect and good antifouling performance Effect
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[0042] The present invention also provides a preparation method of ultraviolet curable matting resin, including:
[0043] A) Remove water from poly-1,4-butanediol adipate diol and trimethylolpropane, and react with diisocyanate to obtain the first intermediate;
[0044] B) The first intermediate is reacted with hydroxy silicone oil, hydroxy phenyl sulfide and hydroxy-terminated acrylate under the action of a catalyst and a polymerization inhibitor to obtain a UV curable matting resin.
[0045] The present invention first removes water from poly-1,4-butanediol adipate diol and trimethylolpropane. The number average molecular weight of the poly-1,4-butanediol adipate diol is preferably 1000 to 3500 Daltons; the present invention has no limitation on the water removal method, and the water removal method well known to those skilled in the art is sufficient, preferably 105°C to 115°C, vacuum distillation for 1 to 1.5 hours; The sources of the poly-1,4-butanediol adipate diol and trimeth...
Example Embodiment
[0057] Example 1
[0058] Mix 252 g of poly-1,4-butanediol adipate diol with a number average molecular weight of 1000 Daltons and 128 g of trimethylolpropane in a three-necked flask, raise the temperature to 110°C, and reduce pressure for 1 hour; Under the protection of nitrogen, the reaction system was cooled to 75° C., and 160 g of 2,4-toluene diisocyanate was added dropwise at a rate of 10 mL / min. After the addition, the reaction was performed for 2.5 hours to obtain the first intermediate.
[0059] Add 380g of hydroxy silicone oil (n=30), 58g of 4,4'-dihydroxydiphenyl sulfide, 0.32g of dibutyltin dilaurate and 0.61g of p-hydroxyanisole to the first intermediate, and react The temperature of the system was lowered to 80°C, and 165 g of hydroxyethyl acrylate was added dropwise at a rate of 10 mL / min. After the addition was completed, the reaction was carried out for 1.5 hours to obtain an ultraviolet curable resin.
[0060] The NMR analysis of the ultraviolet curable resin prepar...
Example Embodiment
[0064] Example 2
[0065] 320g of poly-1,4-butanediol adipate diol with a number average molecular weight of 3500 Daltons and 145g of trimethylolpropane were mixed in a three-neck flask, heated to 110°C, and reduced pressure for 1.5 hours; Under the protection of nitrogen, the reaction system was cooled to 75° C., and 226 g of diphenylmethane-4,4′-diisocyanate was added dropwise at a rate of 13 mL / min. After the addition, the reaction was carried out for 4 hours to obtain the first intermediate.
[0066] Add 448g of hydroxy silicone oil (n=50), 92g of 3,3'-dihydroxydiphenyl disulfide, 0.55g of dibutyltin dilaurate and 1.15g of p-hydroxyanisole to the first intermediate. The temperature of the reaction system was lowered to 80° C., and 284 g of dipentaerythritol pentaacrylate was added dropwise at a rate of 13 mL / min. After the dropwise addition, the reaction system was reacted for 2 hours to obtain an ultraviolet curable resin.
[0067] Nuclear magnetic resonance analysis was perfor...
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