Low-surface-energy polyurethane photocureable coating and preparation method thereof
A light-curing coating, low surface energy technology, applied in the coating and other directions, can solve the problems of poor compatibility between fluorine-containing small molecules and resins, the performance of the coating film cannot be effectively improved, and the coating is easy to mix unevenly. Separation, not easy to precipitate crystals, low energy consumption
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Embodiment 1
[0037] Preparation of hydroxy (meth)acrylate single-terminated polyurethane oligomer: polyether PEG400 (molecular weight: 400) was vacuum-dried in a vacuum oven at 120° C. to remove water for 4 hours. According to the weight ratio, heat up 100 parts of dehydrated polyether PEG400 to 65°C, then add 25 parts of isophorone diisocyanate, mix evenly under the condition of stirring, heat up to 70°C, and react for 6 hours to obtain the end group as - NCO-polyurethane prepolymer; then add 8 parts of hydroxyethyl methacrylate to block part of the -NCO-group, and react at 80°C for 4h to obtain hydroxyethyl methacrylate single-blocked polyurethane oligomer object PU1.
[0038] The preparation of the fluorine-containing (meth) polyacrylate prepolymer solution of mercaptoethanol single end-capping: by weight, with 100 parts of trifluoroethyl methacrylate, 2 parts by weight of mercaptoethanol, 100 parts of dioxane ring, 2 parts of azobisisoheptanonitrile were stirred and mixed evenly, and ...
Embodiment 2
[0043] Preparation of hydroxy (meth)acrylate single-terminated polyurethane oligomer: polyether N210 (molecular weight: 1000) was vacuum-dried in a vacuum oven at 120° C. to remove water for 4 hours. According to the weight ratio, heat up 100 parts of dehydrated polyether N210 to 60°C, then add 25 parts of toluene diisocyanate, mix evenly under stirring, heat up to 70°C, and react for 6 hours to get the terminal group -NCO- The polyurethane prepolymer; then add 26 parts of hydroxyethyl acrylate to block part of the -NCO-group, and react at 70°C for 5h to obtain the polyurethane oligomer PU2 which is mono-blocked by hydroxyethyl acrylate.
[0044] The preparation of the fluorine-containing (meth) polyacrylate prepolymer solution of mercaptoethanol single-termination: by weight, with 100 parts of dodecafluoroheptyl methacrylate, 10 parts by weight of mercaptoethanol, 100 parts of xylene, Stir and mix 3 parts of azobisisovaleronitrile evenly, heat up to 100° C. and react for 10 h...
Embodiment 3
[0049] Preparation of hydroxy (meth)acrylate single-terminated polyurethane oligomer: polyether PEG300 (molecular weight: 300) was vacuum-dried in a vacuum oven at 120° C. to remove water for 4 hours. According to the weight ratio, heat up 100 parts of dehydrated polyether PEG300 to 58°C, then add 20 parts of diphenylmethane diisocyanate, mix evenly under stirring, raise the temperature to 75°C, and react for 5 hours to obtain the end group as - NCO-polyurethane prepolymer; then add 10 parts of hydroxypropyl methacrylate to block part of the -NCO-group, and react at 90°C for 3 hours to obtain a single-capped polyurethane oligomer of hydroxypropyl methacrylate object PU3.
[0050] The preparation of the fluorine-containing (meth) polyacrylate prepolymer solution of mercaptoethanol mono-capping: by weight, with 100 parts of hexafluorobutyl methacrylate, 5 parts by weight of mercaptoethanol, 100 parts of ethylene glycol mono Methyl ether and 2.5 parts of azobisisobutyronitrile w...
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