Creep-resistant polyester and its preparation method
A technology of creep resistance and polyester, applied in the direction of single-component copolyester rayon, conjugated synthetic polymer rayon, etc., to improve hydrolysis resistance, increase relative molecular weight, and expand application range Effect
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Embodiment 1
[0050] Preparation of 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylene]diphenol diglycidyl ether:
[0051] In a nitrogen atmosphere, mix epichlorohydrin and 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]diphenol at a molar ratio of 4:1 , add 1.5% of 15mol / L sodium hydroxide solution of 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl) ethylene] diphenol mass, at room temperature Stir the reaction for 16 hours; then cool to room temperature, then add 5mol / L of 30% of the mass of 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylene]diphenol Sodium hydroxide solution, the sodium hydroxide solution is a solution saturated with anhydrous sodium carbonate, stirred and reacted at room temperature for 10 h; then extracted with chloroform, and the resulting organic phase was obtained by distilling off chloroform and excess epichlorohydrin to obtain a thick like liquid, which was added to absolute ethanol for recrystallization to obtain 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylene]dip...
Embodiment 2
[0056] Preparation of 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylene]diphenol diglycidyl ether:
[0057] In a nitrogen atmosphere, mix epichlorohydrin and 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]diphenol at a molar ratio of 4:1 , add 2.0% 10mol / L sodium hydroxide solution of 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylene]diphenol mass, at room temperature Stir the reaction for 18 hours; cool to room temperature, then add 40% of the mass of 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylene]diphenol of 3mol / L Sodium hydroxide solution, sodium hydroxide solution is a solution saturated with anhydrous sodium carbonate, stirred and reacted at room temperature for 15 hours; then extracted with chloroform, and the resulting organic phase was obtained by distilling off chloroform and excess epichlorohydrin to obtain a thick liquid, add it to absolute ethanol for recrystallization, and obtain 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylene]diphenol diglycidyl Crys...
Embodiment 3
[0062] Preparation of 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylene]diphenol diglycidyl ether:
[0063] In a nitrogen atmosphere, mix epichlorohydrin and 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]diphenol at a molar ratio of 4:1 , add 1.8% of 12mol / L sodium hydroxide solution of 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylene]diphenol mass, at room temperature Stir the reaction for 17h; cool to room temperature, then add 35% of the mass of 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylene]diphenol of 4mol / L Sodium hydroxide solution, sodium hydroxide solution is a solution saturated with anhydrous sodium carbonate, stirred and reacted at room temperature for 13h; then extracted with chloroform, and the resulting organic phase was obtained by distilling off chloroform and excess epichlorohydrin to obtain a thick liquid, add it to absolute ethanol for recrystallization, and obtain 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylene]diphenol diglycidyl Crystals of...
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