Ionic liquid modified bar code carbon strip back coating and preparation method thereof
A technology of ionic liquid and back coating, which is used in replication/marking methods, coatings, fire-resistant coatings, etc., can solve the problems of difficult product quality control, damage to the insulation of the print head, low system viscosity, etc., and saves batching equipment. and manpower input, maintain cleanliness and insulation, and achieve uniform coating and film formation.
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[0031] A preparation method of ionic liquid modified type bar code carbon tape back coating coating includes the following steps:
[0032] Step 1. Take 0.5-2 parts of silane coupling agent monomer, 15-30 parts of organosilicon and 13-30 parts of organic solvent into the double-layer reactor according to parts by weight, and control the temperature in the reactor under stirring conditions Raise it to 80-90℃, and carry out reflux reaction at this temperature for 1-3h, and then control the temperature in the reactor to decrease to 70-80℃;
[0033] Step 2. Take 10-50 parts of acrylic monomers and 0.5-3 parts of ionic liquid containing double bonds according to parts by weight. After mixing them evenly, add 0.5-2 parts of catalyst AIBN and 0-43.5 parts of organic solvent to them , After mixing thoroughly, the mixed additives are obtained for use;
[0034] Step 3. Keep the temperature of the reaction kettle at 70-80°C and start dripping. Add the mixed additives prepared in step 2 to the r...
Embodiment 1
[0037] Step 1. Take 200 g of acrylic triethoxy silane, 6 kg of dihydroxy polysiloxane with 1% hydroxyl content, 20 kg of butyl acetate (w): methyl ethyl ketone (w) = 3:1 mixed solvent , After mixing uniformly, heat up to 90 ℃, keep for 1 hour, and cool down to 80 ℃;
[0038] Step two, 400 g styrene, 1.2 kg cyclohexyl methacrylate, 2.2 kg methyl methacrylate, 400 g isobornyl methacrylate, 200 g 1-allyl-3-methylimidazole benzene Formate, 9.4 kg mixed solvent (the same ratio as above), 200 g AIBN, after mixing evenly, take 4 kg directly into the reaction kettle of step 1, the remaining material is added dropwise to the reaction kettle within 3 hours, continue to react for 4 hours, wait The solid content is higher than 95% of the theoretical value.
Embodiment 2
[0040] Step 1. Take 200 g of acrylic triethoxysilane, 5 kg of dihydroxy polysiloxane with 1% hydroxyl content, and 5 kg of butyl acetate (w): methyl ethyl ketone (w) = 1:1 mixed solvent , After mixing uniformly, heat up to 90 ℃, keep for 1 h, and cool down to 80 ℃;
[0041] Step two, 400 g styrene, 2.8 kg cyclohexyl methacrylate, 4.0 kg methyl methacrylate, 800 g isobornyl methacrylate, 400 g 1-allyl-3-methylimidazole ethyl Acidic acid salt, 1.2 kg mixed solvent (the same ratio as above), 200 g AIBN, after mixing evenly, take 6 kg directly into the reaction kettle of step 1, the remaining material is added dropwise to the reaction kettle within 3.5 hours, continue to react for 5 hours, wait for solidification The finished product is obtained when the content is higher than 95% of the theoretical value.
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