Ultraviolet (UV) curing ink and preparation method thereof
A technology of ink and nano-silica, which is applied in ink, household utensils, applications, etc., can solve the problems of less research on UV-curable inks, and achieve the effects of rapid light-curing, excellent adhesion, and good gloss
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Embodiment 1
[0027] The UV curing ink of this embodiment includes the following components in mass percentage: 40% of non-isocyanate urethane acrylate oligomer, 18% of epoxy acrylate oligomer, 24% of reactive diluent, 4% of photoinitiator, nano Silica 3%, additives 2%, pigment 9%.
[0028] The non-isocyanate urethane acrylate oligomer is prepared by the following method: 51.4g ethylene carbonate, 1.73g 1,6-hexamethylenediamine, 0.5g catalyst zinc acetate are added to the container, at a temperature of 180°C, the speed React under 200r / min stirring for 6 hours. During this period, decompression and vacuuming are carried out every 2 hours to remove small molecules. After the reaction is completed, cool to obtain product A, which is a polyurethane oligomer with hydroxyl groups at the end;
[0029] The product A was reacted with 13.2 g of acrylic anhydride at 110° C. for 5 h, and the final product, non-isocyanate urethane acrylate oligomer, was obtained after cooling. The weight average molecu...
Embodiment 2
[0049] The UV curing ink of this embodiment includes the following components in mass percentage: 36% of non-isocyanate urethane acrylate oligomer, 23% of epoxy acrylate oligomer, 20% of reactive diluent, 6% of photoinitiator, nano Silica 4%, additives 2%, pigment 9%.
[0050] The non-isocyanate urethane acrylate oligomer is prepared by the following method: 43.4g ethylene carbonate, 1.86g 1,6-hexamethylenediamine, 0.4g catalyst zinc acetate are added to the container, at a temperature of 180°C, the rotation speed Stirring and reacting at 200r / min for 6h, during which the small molecules were removed by decompression and vacuuming every 2h, and cooled after the reaction to obtain product A, that is, a polyurethane oligomer with a hydroxyl group at the end;
[0051] The product A was reacted with 9.4 g of acrylic anhydride at 110° C. for 5 h, and the final product, non-isocyanate urethane acrylate oligomer, was obtained after cooling. The weight average molecular weight of the ...
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