High-elasticity composite fiber and preparation method thereof
A composite fiber, high elasticity technology, applied in fiber processing, melt spinning, stretch spinning, etc., can solve the problems of poor elasticity, low crimp shrinkage of composite fibers, poor softness, etc., to reduce crystalline properties, excellent fluffy Sex, good shrinkage effect
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Embodiment 1
[0053] In this embodiment, the composite fiber is prepared by the following method:
[0054] (1) Blend terephthalic acid, ethylene glycol and isophthalic acid into a mixed slurry, wherein the molar ratio of isophthalic acid to terephthalic acid is 0.1:1, and the molar ratio of terephthalic acid to ethylene glycol The ratio is 1:1.2;
[0055] (2) Transport the mixed slurry in step (1) to the reactor for esterification reaction, the reaction temperature is 265°C, and the reaction is terminated when the esterification rate reaches 97%, to obtain a polyester pre-reaction melt;
[0056] (3) in the polyester pre-reaction melt of step (2), add the polyamide 6 that is equivalent to the relative viscosity of 10wt% of terephthalic acid weight in step (1) and be 2.4 to carry out polycondensation reaction, reaction temperature is 270 ℃, The reaction time is 3 hours. After the reaction is completed, the material is discharged and pelletized to obtain polyamide ester slices. The intrinsic ...
Embodiment 2
[0059] In this embodiment, the composite fiber is prepared by the following method:
[0060] (1) Terephthalic acid, ethylene glycol and 2-methyl-1,3-propanediol are formulated into a mixed slurry, wherein the molar ratio of 2-methyl-1,3-propanediol to terephthalic acid is 0.2: 1. The molar ratio of terephthalic acid to ethylene glycol is 1:1.05;
[0061] (2) transporting the mixed slurry in step (1) to the reactor for esterification reaction, the reaction temperature is 260° C., and when the esterification rate reaches 98%, the reaction is terminated to obtain a polyester pre-reaction melt;
[0062] (3) In the polyester pre-reaction melt in step (2), adding polyamide 56 with a relative viscosity equivalent to 20 wt % of terephthalic acid weight in step (1) is 2.8 for polycondensation reaction, and the reaction temperature is 275 ° C. The reaction time is 4 hours. After the reaction is completed, the material is discharged and pelletized to obtain polyamide ester slices. The i...
Embodiment 3
[0065] In this embodiment, the composite fiber is prepared by the following method:
[0066] (1) Blend terephthalic acid, ethylene glycol and 1,2-propanediol into a mixed slurry, wherein the molar ratio of 1,2-propanediol to terephthalic acid is 0.05:1, and terephthalic acid and ethylene glycol The molar ratio is 1:1.1;
[0067] (2) Transport the mixed slurry in step (1) to the reactor for esterification reaction, the reaction temperature is 270°C, and when the esterification rate reaches 92%, the reaction is terminated to obtain a polyester pre-reaction melt;
[0068] (3) in the polyester pre-reaction melt of step (2), adding the polyamide 66 corresponding to the relative viscosity of 5wt% terephthalic acid weight in the step (1) is 4.0 to carry out polycondensation reaction, and the reaction temperature is 280 ℃, The reaction time is 4 hours. After the reaction is completed, the material is discharged and pelletized to obtain polyamide ester slices. The intrinsic viscosity ...
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