Corrosion-resistant strong-adhesion FEVE water-based fluorocarbon color paste and preparation method thereof
A water-based fluorocarbon and water-based fluorocarbon emulsion technology, applied in the direction of pigment paste, etc., can solve the problems of reduced adhesion of FEVE water-based fluorocarbon paste and reduced corrosion resistance of coatings, so as to improve adhesion performance and improve dispersion effect. , the effect of improving the bonding strength
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preparation example 1
[0046] A modified material 1:
[0047] 8 kg of trimethylolpropane three (3-mercaptopropyl ester) and 6 kg of 3-aminopropyltriethoxysilane were mixed with 6 kg of tetrahydrofuran, and the reaction was heated at 50 ° C for 12 h, and the reaction liquid was collected and the solvent was removed. Collect reactants;
[0048] Nano-hydroxyapatite with 0.5 kg of 2 to 10 μm was stirred with 2 kg of reactants and were placed in 200 W under ultrasonic dispersion. After the dispersion treatment, the reaction was heated at 50 ° C for 12 h, and the dried and dried can be prepared. .
preparation example 2
[0050] Modified material 2:
[0051] 8 kg of trimethylolpropane three (3-mercaptopropyl ester) and 6 kg of 3-aminopropyltriethoxysilane were mixed with 6 kg of tetrahydrofuran, and the reaction was heated at 50 ° C for 12 h, and the reaction liquid was collected and the solvent was removed. Collect reactants;
[0052] Nano-hydroxyapatite with 0.5 kg of 11 to 80 μm was mixed with 2 kg of reactants and was stirred in 200 W. After the dispersion treatment, the reaction was heated at 50 ° C for 12 h, and the dried and dried can prepare the modified material 2. .
preparation example 3
[0054] Modified material 3:
[0055] 8 kg of trimethylolpropane three (3-mercaptopropyl ester) and 6 kg of 3-aminopropyltriethoxysilane were mixed with 6 kg of tetrahydrofuran, and the reaction was heated at 50 ° C for 12 h, and the reaction liquid was collected and the solvent was removed. Collect reactants;
[0056] Nano-hydroxyapatite with 0.5 kg of 81 to 100 μm was stirred with 2 kg of reactants and were placed at 200 W under ultrasonic dispersion. After dispersion treatment, the reaction was heated at 50 ° C for 12 h, and the modified material 3 was prepared. .
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