Method for preparing polytetrafluoroethylene fiber by wet spinning
A polytetrafluoroethylene and polytetrafluoroethylene spinning technology, applied in wet spinning, fiber treatment, fiber chemical characteristics, etc., to achieve the effect of not easy to break, avoid sticking, and continuous spinning
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Embodiment 1
[0052] This embodiment provides a method for preparing polytetrafluoroethylene fibers by wet spinning.
[0053] (1) Dissolve 6g of sodium alginate with M:G ratio of 1:2 in 194g of deionized water at 70°C, cool to room temperature and add 0.1g of non-ionic silicone defoamer and polytetrafluoroethylene dispersion ( The massfraction of polytetrafluoroethylene dispersion liquid is 60%, promptly contains polytetrafluoroethylene (72g) 120g mixes in 120g, prepares the spinning solution that polytetrafluoroethylene mass concentration is 22.5%;
[0054] (2) The spinning solution is wet-spun with a spinning temperature of 25°C and a spinneret hole diameter of 70 μm, and then molded in a calcium chloride coagulation bath with a mass fraction of 1% ethanol at a temperature of 25°C to obtain a primary fiber;
[0055] (3) After washing the as-spun fiber, disperse it with an aluminum sulfate solution with a concentration of 2%, then wash it with ethanol, dry it at 100°C, and sinter it at 36...
Embodiment 2
[0058] This embodiment provides a method for preparing polytetrafluoroethylene fibers by wet spinning.
[0059] The difference from Example 1 is that in this example, the dispersion is carried out with white oil.
[0060] figure 2 This is the metallographic optical microscope image of the polytetrafluoroethylene fiber obtained in this example. It can be seen from the figure that the diameter of the polytetrafluoroethylene fiber obtained in this example is 36.88 μm.
Embodiment 3
[0062] This embodiment provides a method for preparing polytetrafluoroethylene fibers by wet spinning.
[0063] The difference from Example 1 is that in this example, ethanol is not added to the coagulation bath.
[0064] In this example, when ethanol is not added to the coagulation bath, there will be a phenomenon of uneven sintering on the fiber surface. From the comparison of Example 1 and Example 3, it can be seen that adding ethanol to the coagulation bath can regulate the interfiber ions The exchange rate makes the exchange rate tend to be moderate, and the surface of the sintered fiber is more uniform.
[0065] image 3 This is the metallographic optical microscope image of the polytetrafluoroethylene fiber obtained in this example. It can be seen from the figure that the diameter of the polytetrafluoroethylene fiber finally obtained in this example is 35.33 μm.
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