UV moisture dual-curing type acrylate pressure-sensitive adhesive and preparation method thereof
A technology of acrylate and ester acrylate, which is used in the field of synthesis and preparation of acrylate pressure-sensitive adhesives. It can solve the problems of low initial adhesion and peel strength, poor mechanical properties, and weak cohesion, and achieve less volatile matter and comprehensive performance. Well-balanced, low-cost effect
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Embodiment 1
[0045] Mix hydroquinone monomethyl ether and diglycidyl phthalate evenly, heat to dissolve, raise the temperature to 85°C, add acrylic acid containing tetraethylammonium bromide dropwise, keep warm, and react until the acid value is less than 3mgKOH / g stops, and the epoxy acrylate monoester containing hydroxyl is obtained after the reaction is completed. N 2 Under a protective atmosphere, after dehydrating hexanediol, add isophorone diisocyanate containing dibutyltin dilaurate dropwise to it while stirring, heat to 60°C for 4 hours after the dropwise addition, and cool to room temperature after the reaction is completed. Obtain an isocyanate-terminated oligomer; then continue to add dropwise the prepared hydroxyl-containing epoxy acrylate monoester, after the dropwise addition, heat to 85°C for 3 hours, stop heating and lower the temperature; then carry out low-pressure distillation on the obtained product, After removing low-molecular substances, the desired epoxy-modified ...
Embodiment 2
[0051] After mixing 5 parts by weight of 2-ethylhexyl acrylate monomer and 0.05 parts by weight of azobisisobutyronitrile, the temperature was raised to 65 ° C, stirred at a speed of 120 rad / min and nitrogen was introduced, and then 10 parts by weight of acrylic acid was added dropwise A mixture of 2-ethylhexyl ester monomer and 0.05 parts by weight of azobisisobutyronitrile, after the dropwise addition, 0.05 parts by weight of azobisisobutyronitrile is added, the reaction is continued for 2 to 4 hours, cooled to room temperature and discharged to obtain The viscosity of the first prepolymer is (25° C.) 7000-8000 mPa·s.
[0052] 10 parts by weight of butyl methacrylate monomer, 10 parts by weight of hexyl acrylate monomer, 1 part by weight of urethane acrylate (25°C viscosity 7cps), 5 parts by weight of 2-ethylhexyl acrylate monomer and After mixing 0.2 parts by weight of azobisisobutyronitrile, the temperature was raised to 65° C., stirred at a speed of 120 rad / min and nitrog...
Embodiment 3
[0056] Mix 30 parts by weight of 2-ethylhexyl acrylate monomer and 0.005 parts by weight of benzoin butyl ether, heat to 75°C, use a maximum wavelength of 250-400nm, and an intensity of 1-2mW / cm 2 When the viscosity of the mixture reaches 3500-4500mPa·s, add 7 parts by weight of hydrogenated rosin resin and stir, continue mixing for 2-4 hours, and then stand at room temperature for 20-30 hours to obtain the first prepolymer. It is (25°C) 6000-6500mPa·s.
[0057]10 parts by weight of butyl methacrylate monomer, 18.5 parts by weight of hexyl acrylate monomer, 1.5 parts by weight of urethane acrylate (25°C viscosity 9cps), 10 parts by weight of 2-ethylhexyl acrylate monomer and Mix 0.005 parts by weight of benzoin butyl ether, heat to 75°C, use a maximum wavelength of 250-400nm, and an intensity of 1-2mW / cm 2 The ultraviolet light source is irradiated to carry out the polymerization reaction for 2-4 hours, and then it is left to stand at room temperature for 20-30 hours to obtai...
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