Preparation method of ultraviolet cured silica sol modified aqueous urethane acrylate dispersoid
A polyurethane acrylate and acrylate technology, applied in polyurea/polyurethane coatings, coatings, etc., can solve the problems of insignificant improvement of coating surface mechanical properties, lack of interaction, cumbersome modification process, etc., to achieve easy reaction The effect of control, simple process, and large range of emulsion particle size
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Embodiment 1
[0030] This example is a control example without silica sol modification.
[0031] Add 38.0 g of isophorone diisocyanate (IPDI) into a 250 mL four-necked flask equipped with a stirrer, a thermometer, and a reflux condenser, and add 46.7 g of polyethylene glycol that has been dehydrated through molecular sieves dropwise with a dropping funnel while stirring at room temperature. For the mixed solution of diol PEG400 and 0.05g catalyst dibutyltin dilaurate (DBTDL), the dropping speed is controlled within 1.5h. After the dropwise addition, react at 45±5°C for 1-2h, then raise the temperature to 60°C until the measured NCO group reaches the theoretical value (measured by di-n-butylamine back titration), and NCO-terminated polyurethane prepolymer I is obtained.
[0032] Add 5.16 g of pre-dried dimethylol propionic acid (DMPA) powder into polyurethane prepolymer I in three batches, and react at 65±5° C. During the reaction, add an appropriate amount of acetone to adjust the viscosity...
Embodiment 2
[0036] Add 25.7g of isophorone diisocyanate (IPDI) into a 250mL four-necked flask equipped with a stirrer, a thermometer and a reflux condenser, and add molten 59.1g of PEG1000 and 0.05g of catalyst dropwise with a dropping funnel while stirring at room temperature For the mixed solution of stannous octoate, the dropping speed is controlled within 1.5h. After the dropwise addition, react at 45±5°C for 1-2h, then raise the temperature to 60°C until the measured NCO group reaches the theoretical value (measured by di-n-butylamine back titration), and NCO-terminated polyurethane prepolymer I is obtained.
[0037]Add 5.69g of dried dimethylolbutyric acid (DMBA) into the polyurethane prepolymer I in three batches, react at 65±5°C, and add an appropriate amount of acetone during the reaction to adjust the viscosity of the system. The degree of reaction was measured by di-n-butylamine back titration method, and the prepolymer II containing hydrophilic groups was obtained after reachi...
Embodiment 3
[0041] Add 32.2g of 2,4-toluene diisocyanate (TDI) into a 250mL four-necked flask equipped with a stirrer, a thermometer and a reflux condenser, and add 52.5g of polystyrene dehydrated through molecular sieves dropwise with a dropping funnel while stirring at room temperature. For the mixed solution of propylene glycol PPG400 and 0.05g catalyst triethylamine, the dropping rate is controlled within 1.5h. After the dropwise addition, react at 45±5°C for 1-2h, then raise the temperature to 60°C until the measured NCO group reaches the theoretical value (measured by di-n-butylamine back titration), and NCO-terminated polyurethane prepolymer I is obtained.
[0042] Add 5.16 g of dried dimethylol propionic acid (DMPA) powder into polyurethane prepolymer I in three batches, and react at 65±5° C. During the reaction, add an appropriate amount of acetone to adjust the viscosity of the system. The degree of reaction was measured by di-n-butylamine back titration method, and the prepolym...
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