Polyuria-acrylate emulsion and aqueous gravure ink prepared from same
A technology of acrylate and polyurea, applied in the field of water-based gravure ink, can solve problems such as difficulty in achieving good results, and achieve the effects of improved performance, excellent flexibility and good water resistance
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Embodiment 1
[0044] 1. Preparation of polyurea-acrylate emulsion:
[0045] Add 26.1g of hexamethylene diisocyanate into the reaction kettle, raise the temperature to 60°C, add dropwise a mixture of 5.0g of polyether triamine T-5000, 49.9g of polyether diamine D-1000 and 10.0g of acetone, 1.2 After hours of dripping, keep warm for 1.5 hours until the residual -NCO reaches the theoretical value; heat up to 80°C, add 7.0g dimethylolpropionic acid, and react for 2.0 hours; add 12.0g hydroxyethyl acrylate, and react for 0.8 hours to obtain poly For urea prepolymer, cool down to room temperature, and use acetone to control the viscosity during the reaction to avoid rod climbing.
[0046] Stir 72.0g of methyl methacrylate, 23.0g of butyl acrylate, and 0.5g of vinyltrimethoxysilane to obtain a mixed monomer, take 14.3g of the above mixed monomer and put it into the polyurea prepolymer and stir evenly, add 5.3g Stir and neutralize triethylamine for 10 minutes, add 175g of deionized water and emuls...
Embodiment 2
[0054] One, the preparation of described polyurea-acrylate emulsion is as follows:
[0055] Add 19.6g of diphenylmethane diisocyanate into the reaction kettle, raise the temperature to 80°C, add dropwise a mixture of 4.6g of polyether diamine D-230, 70.8g of polyether diamine D-2000 and 15.0g of acetone, for 1.0 hour After dropping, keep warm for 2.0 hours until the residual -NCO reaches the theoretical value; raise the temperature to 90°C, add 3.0 g of sodium ethylenediaminoethanesulfonate, and react for 1.5 hours; add 2.0 g of hydroxybutyl acrylate, and react for 1.0 hour to obtain Polyurea prepolymer, cooled to room temperature, controlled with acetone during the reaction to avoid rod climbing.
[0056] Stir 165g methyl methacrylate, 35g butyl methacrylate, 13g methyl acrylate, 6.5g acrylic acid, and 3.5g vinyl tri-tert-butoxysilane to obtain a mixed monomer, take 21.3g of the above mixed monomer and put it into the polymer Stir in the urea prepolymer for 10 minutes, add 1...
Embodiment 3
[0064] One, the preparation of described polyurea-acrylate emulsion is as follows:
[0065] Add 18.0g of isophorone diisocyanate into the reaction kettle, raise the temperature to 75°C, add dropwise a mixture of 73.4g of polyether diamine D-2000 and 12.0g of acetone, drop it in 0.8 hours, keep it warm for 2.0 hours until the residual - NCO reaches the theoretical value; heat up to 85°C, add 3.0g dimethylol butyric acid and 2.0g 1,4-butanediol-2-sodium sulfonate, react for 2.5 hours; add 3.6g hydroxyethyl methacrylate, react After 1.2 hours, the polyurea prepolymer was prepared, and the temperature was lowered to room temperature. During the reaction, acetone was used to control the reaction to avoid rod climbing.
[0066] Stir 190g of methyl methacrylate, 35g of butyl acrylate, 75g of ethyl acrylate, and 6.0g of vinyltrimethoxysilane to obtain a mixed monomer. Take 18.4g of the above mixed monomer and put it into the polyurea prepolymer and stir evenly. Add 0.8g of sodium hyd...
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