Surface-modified aramid fiber and preparation method thereof
An aramid fiber and surface modification technology, applied in the field of organic fibers and their preparation, can solve the problems of large surface inertness and poor UV resistance, and achieve the effects of improving UV resistance, low cost, and improving flame retardant properties
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[0026] Example one
[0027] 1. Preparation of surface modified aramid fiber
[0028] (1) Take 0.5g of para-aramid fiber (Kevlar-49, diameter 12um, density 1.43g / cm 3 , Produced by DuPont in the United States) were successively immersed in acetone, petroleum ether, and deionized water, and cleaned at reflux for 3 hours; after cleaning, the fiber was taken out and dried at 80°C for 12 hours to obtain clean aramid fiber, denoted as KF . See attached for its infrared spectrum figure 1 , The surface contact angle and free energy are shown in Table 1.
[0029] (2) Dissolve 10.5 g of sodium hydroxide in 120 mL of ethanol with stirring to obtain an ethanol solution of sodium hydroxide; immerse 0.1 g of the KF fiber obtained in step (1) in the ethanol solution of sodium hydroxide, and react under reflux for 5 hours; After the reaction, the fiber was washed with water and dried to obtain a fiber with amino groups on the surface.
[0030] (3) Under the protection of nitrogen atmosphere, tak...
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[0040] Example two
[0041] 1. Preparation of surface modified aramid fiber
[0042] (1) 10.5g of sodium hydroxide was stirred and dissolved in 120mL of ethanol to obtain an ethanol solution of sodium hydroxide; 0.1g of the clean fiber KF obtained in step (1) of Example 1 was immersed in the ethanol solution of sodium hydroxide, Reflux the reaction for 5 hours; after the reaction, wash with water and dry to obtain fibers with amino groups on the surface.
[0043] (2) Under the protection of nitrogen atmosphere, take 0.1g of aramid fiber with amino groups, 30mL of γ-glycidoxypropyltrimethoxysilane, 150mL of absolute ethanol, and add it to a 250mL three-necked flask at 70℃. Reflux and react for 12 hours to obtain aramid fiber with methoxy group on the surface.
[0044] (3) Add 14.9g of cerium chloride and 1.11g of calcium chloride to 150mL of deionized water to dissolve to obtain a mixed solution of cerium chloride and calcium chloride; add 6g of sodium hydroxide to the mixed solution ...
Example Embodiment
[0050] Example three
[0051] 1. Preparation of surface modified aramid fiber
[0052] (1) 10.5g of sodium hydroxide was stirred and dissolved in 120mL of ethanol to obtain an ethanol solution of sodium hydroxide; 0.1g of the clean fiber KF obtained in step (1) of Example 1 was immersed in the ethanol solution of sodium hydroxide, Reflux the reaction for 5 hours; after the reaction, wash with water and dry to obtain fibers with amino groups on the surface.
[0053] (2) Under the protection of nitrogen atmosphere, take 0.1g of aramid fiber with amino groups, 30mL of γ-glycidoxypropyltrimethoxysilane, 150mL of absolute ethanol, and add it to a 250mL three-necked flask at 70℃. Reflux and react for 12 hours to obtain aramid fiber with methoxy group on the surface.
[0054] (3) Add 14.9g of cerium chloride and 1.11g of calcium chloride to 150mL of deionized water to dissolve to obtain a mixed solution of cerium chloride and calcium chloride; add 6g of sodium hydroxide to the mixed solutio...
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