A kind of preparation method of organosilicon modified polyurethane
A technology of organosilicon and polyurethane, applied in the field of preparation of organosilicon modified polyurethane, can solve the problems of poor heat resistance of hyperbranched polyurethane, limited application, low content, etc., and achieve excellent alkali resistance and salt resistance, good mechanical and mechanical properties. , the effect of good thermal stability
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preparation example 1
[0040] 1. Preparation of hydroxy -based seal -end overpowered fatty polyether polyethylene polymond metropolitan silicone
[0041] (1) Preparation of hydroxy -based seal -end hypertrophic aliphed polyether
[0042] Take a clean and dry three-mouth bottle, and under the protection of nitrogen, add 134.2g (1.0mol) trimethyl methyl propionane, 73.5ml of methanol potassium-methanol solution (1.36 mol / L). G shrinks gly glycerin (21.0mol), and after about 6h dripping, continue to react for 6h. At the end of the reaction, add methanol dissolving products, add 36.5 % hydrochloric acid neutralization, and pour peltone precipitation. After repeating the twice, the transparent viscous liquid is obtained after the vacuum is 24h at 70 ° C, that is, the hydroxyl seal -end hypertrophic alipher polyether.
[0043] FT-IR spectrum of hydroxyl sealing end hyperpolitic aliphed polyether, such as figure 1 Show, the 1HNMR spectrum of hydroxy -based sealing end of the aliphed polyether is figure 2 Show....
Embodiment 1
[0048] (1) Obtaining hydroxyl seal in the preparation for preparation example 1 The hydroxygenic chip ether-organic silicon embedded cluster 5g, end hydroxyl seal polyether-organic silicon-polyether triangular cluster 10g, molecular weight 2000 polymer Tetrahydrofurate 38.0g, 1,4-butyl binary alcohol 0.530g and HDI 11.0g. In the reactive solvent acetone 76.2g, under the catalysis of the two-dicotya February cinnamon sour tin / 130mmHg remove the solvents and obtain a hyper silicon -mitated polyurethane compound of the beesein -based sealing end, as a component A;
[0049] (2) Obtaining hydroxyl seal in the preparation for preparation example 1 The hydroxygenic chip ether-organic silicon embedded cluster 3g, end hydroxyl seal polyether-organic silicon-polyether triangular cluster 20g, molecular weight 2000 polymer四氢呋喃72g、1,4-丁二元醇1.778g和HDI 4.0g,在反应溶剂丙酮73.2g中,在二丁基二月桂酸锡0.508g催化下,40℃反应4h,减压到60℃ / 130mmHg remove the solvents and obtain a hyper silicon -mitated polyurethane compounds at t...
Embodiment 2
[0053] (1) Obtaining hydroxyl seal in the preparation for preparation example 1 The hydroxygenic chip ether-organic silicon embedded cluster 6g, end hydroxyl seal polyether-organic silicon-polyether triangular cluster 20g, molecular weight 2000 polymer Tetrahydrocarfu 55g, 1,4-butin binaryol 1.5g and TDI 25.0g, in the reactive solvent N-methylpylpylene 37.2g, under the catalysis of the 2-butyl February cinnamonic acid tin 0.93g, the 90 ° C reaction is 1h, the decompression is decompressed To 120 ° C / 130mmHg remove the solvents, obtain a hyper silicon -mitated polyurethane compounds at the beekeehyl sealing end, as a group A;
[0054] (2) Obtaining the hydroxyl seal of the hydroxyl seal of the hydroxyl section of the hydroxyl seal-organic polyether-organic silicon embedded cluster 5g, end hydroxyl seal polyether-organic silicon-polyether triangular section 20g of cluster, molecular weight 2000 polythexia fuuu 43.6G, 1,4-butyl glycol 1.778g and TDI 6.0g. In the reactive solvent N-me...
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