High-modulus low-shrinkage creep-resistant activated polyester industrial yarn and preparation method thereof
A technology of high modulus, low shrinkage and creep resistance, applied in the direction of single-component copolyester rayon, conjugated synthetic polymer rayon, melt spinning, etc., to improve hydrolysis resistance and increase relative molecular weight Quality, effect of extending application range
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Embodiment 1
[0059] Preparation of 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylene]diphenol diglycidyl ether:
[0060] 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% 15mol / L sodium hydroxide solution of 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylene]diphenol mass, at room temperature Stir the reaction for 16h; then cool to room temperature, then add 30% of the mass of 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylene]diphenol with anhydrous carbonic acid Sodium-saturated 5mol / L sodium hydroxide solution, stirred and reacted at room temperature for 10h; then extracted with chloroform, and the resulting organic phase was evaporated to remove chloroform and excess epichlorohydrin to obtain a thick liquid, which was added to anhydrous Recrystallization in ethanol to obtain crystals of 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylene]diphenol diglycidyl ether;
[0061] Preparation of fluor...
Embodiment 2
[0069] Preparation of 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylene]diphenol diglycidyl ether:
[0070] 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 with anhydrous sodium carbonate Saturated 3mol / L sodium hydroxide solution, stirred and reacted at room temperature for 15h; then extracted with chloroform, the resulting organic phase was evaporated to remove chloroform and excess epichlorohydrin to obtain a thick liquid, which was added to absolute ethanol Medium recrystallization, namely obtain the crystal of 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylene]diphenol diglycidyl ether;
[0071] Preparation of fl...
Embodiment 3
[0079] Preparation of 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylene]diphenol diglycidyl ether:
[0080] 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% 12mol / L sodium hydroxide solution of 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylene]diphenol mass, at room temperature Stir the reaction for 17 hours; cool to room temperature, then add 35% of the mass of 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylene]diphenol with anhydrous sodium carbonate Saturated 4mol / L sodium hydroxide solution, stirred and reacted at room temperature for 13h; then extracted with chloroform, the resulting organic phase was evaporated to remove chloroform and excess epichlorohydrin to obtain a thick liquid, which was added to absolute ethanol Medium recrystallization, namely obtain the crystal of 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylene]diphenol diglycidyl ether;
[0081] Preparation of fl...
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