H-grade low-temp. beading polyurethane paint wire-covering paint
A technology of polyurethane paint and enameled wire paint, applied in the direction of polyurea/polyurethane coatings, coatings, etc., can solve the problems of poor thermal shock performance, poor product performance stability, excessive breakdown voltage drop, etc., to improve heat resistance. and hot stamping performance, reducing production costs, and the effect of stable polyester quality
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Embodiment 1
[0070] The preparation of embodiment 1 terephthalic acid dihydric alcohol
[0071] React 17 kg of terephthalic acid, 21 kg of neopentyl glycol, and 0.11 kg of stannous octoate catalyst at 130-200°C for about 3 hours to generate terephthalic acid diol, and the reaction mixture is colorless and transparent above the melting point solution. After analysis, the melting point range of terephthalic acid diol is 40-50°C, the hydroxyl value is 310, and the acid value is 2.8. Preparation of the hydroxyl component
[0072] 30 kg of phthalic anhydride, 22 kg of adipic acid, 34 kg of terephthalic diol mixture, 17 kg of neopentyl glycol, 4 kg of glycerin, tris (α-hydroxyethyl) isocyanurate 22 kg, 10 kg of xylene and 1.5 kg of catalyst stannous octoate were added to the reaction kettle in sequence. The reaction kettle is equipped with a water separation device with a short fractionation column. Start the heating device, react at 140°C to 180°C for 5 hours; ...
Embodiment 2
[0076] The preparation of embodiment 2 amidoimide glycols
[0077] React 35 kg of toluene diisocyanate, 19 kg of trimellitic anhydride, and 40 kg of DMF at 120-130°C for 3 hours, then add 21 kg of neopentyl glycol and react at 140-150°C for about 4 hours to obtain the target product amide imide di Alcohols. The product has good miscibility with the above polyester raw materials. After analysis, the hydroxyl value of the amidoimide diol is 178, and the acid value is 4.8. Preparation of the hydroxyl component
[0078] 30 kg of phthalic anhydride, 22 kg of adipic acid, 96 kg of amidoimide diol mixture, 17 kg of neopentyl glycol, 4 kg of glycerin, tris (α-hydroxyethyl) isocyanurate 22 kg, 8 kg of xylene and 1.6 kg of catalyst stannous octoate were added to the reaction kettle in turn. The reaction kettle is equipped with a water separation device with a short fractionation column. Start the heating device, react at 140°C to 180°C for 5 hours; the...
Embodiment 3
[0082] The preparation of embodiment 3 terephthalic acid dihydric alcohols
[0083] 3 kg of terephthalic acid, 9 kg of 2-methyl-1, 3-propanediol, and 0.15 kg of stannous octoate catalyst are reacted at 130-200°C for about 3 hours to generate terephthalic acid diol, which is above the melting point. The reaction mixture was a colorless transparent solution. After analysis, the melting point range of the modified diol is 40-50°C, the hydroxyl value is 69, and the acid value is 2.8. Preparation of the hydroxyl component
[0084] 15 kg of phthalic anhydride, 3 kg of adipic acid, 2.7 kg of terephthalic acid diol mixture, 2.4 kg of 2-methyl-1, 3-propanediol, 2.7 kg of glycerin, three (α-hydroxyethyl ) 15 kilograms of isocyanurate, 3.8 kilograms of TMP, 10 kilograms of xylene and 0.43 kilogram of catalyst stannous octoate are added in the reactor successively. The reaction kettle is equipped with a water separation device with a short fractionation c...
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