Polyethyleneglycol-containing fluorinated polysiloxane modification acrylic acid antifouling paint and preparing method thereof
A polyethylene glycol, fluorosilicon modification technology, applied in antifouling/underwater coatings, polyether coatings, paints containing biocides, etc., can solve the problems of quaternary ammonium salt toxicity, easy adsorption of active anions, etc. Easy to use, good anti-bioadhesion, long-term use effect
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Embodiment 1
[0036] The present embodiment provides the synthetic method that contains PEG prepolymer A: 20 g dimethylbenzene and 20 g butyl acetate are joined in the there-necked flask that stirrer, constant pressure separatory funnel, reflux condenser are equipped with, be heated up to 85 °C. Weigh 20 g of xylene, 20 g of butyl acetate, 1.6 g of AIBN, 50 g of butyl acrylate, 40 g of methyl methacrylate, and 10 g of allyl polyethylene glycol, mix and dissolve them, and drop them slowly within 1.5 h. Put it into a three-necked flask, and continue to keep warm for 2 h after the dropwise addition. After the temperature was raised to 110 °C, 0.4 g of AIBN, 20 g of xylene, and 20 g of butyl acetate were mixed and dissolved, and then slowly dropped into a three-necked flask within 0.5 h. After the dropwise addition, the temperature was continued for 2 h. Cooling and discharging, the hydroxyacrylic acid prepolymer A containing PEG was obtained in a white emulsion state.
Embodiment 2
[0038] This embodiment provides the synthesis method of polydimethoxysilane oligomer B: 15.1870 g tetrahydrofuran and 15.0000 g hydroxyl silicone oil are added to a three-necked flask equipped with a stirrer, a constant pressure dropping funnel, and a reflux condenser. The heating bath was heated to 65 °C. Weigh again 5.1870 g of 3-isocyanatopropyltriethoxysilane and 0.0063 g of dibutyltin dilaurate, mix and dissolve, slowly drop them into a three-necked flask under vigorous stirring, continue to keep warm for 5 h after the dropwise addition, and cool down The α,ω-triethoxysilane-terminated polydimethylsilane oligomer B was obtained in the form of a colorless transparent oil.
Embodiment 3
[0040] This example provides the synthesis method of perfluoropolyether oligomer C: 12.6870 g tetrahydrofuran and 7.5000 g bishydroxypropyl perfluoropolyether are added to the three ports equipped with agitator, constant pressure dropping funnel and reflux condenser In the flask, the oil bath was heated to 65°C. Then take by weighing 5.1870 g 3-isocyanatopropyltriethoxysilane, 0.0063 g dibutyltin dilaurate, mix and dissolve, slowly drop into the three-necked flask under vigorous stirring within 10 minutes, continue to insulate for 2 hours after the dropwise addition is completed. h, the temperature was lowered and the material was discharged to obtain a -triethoxysilane-terminated perfluoropolyether oligomer, which was denoted as PFU, and was in the form of light yellow transparent oil.
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