Preparation method of thermotropic liquid crystal polyarylester fiber
A technology of polyarylate fiber and thermotropic liquid crystal, which is applied in the field of preparation of thermotropic liquid crystal polyarylate, can solve the problems of complex method of thermotropic liquid crystal polyarylate, low tensile strength of polyarylate fiber and the like, and achieves reaction conditions Easy to control, simple to operate, and solve the effect of complicated preparation steps
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specific Embodiment approach 1
[0011] Specific embodiment one: the preparation method of the thermotropic liquid crystal polyarylate fiber of this embodiment is implemented according to the following steps:
[0012] One, the p-hydroxybenzoic acid and 2-(4-hydroxyphenyl)-5-carboxybenzimidazole, acetic anhydride, 4-diethylaminopyridine and anti- The oxidizing agent is added to the Hastelloy polymerization kettle, kept at 120-160°C for 5-8 hours, then raised to 310°C, kept warm for 2 hours, then filled with nitrogen into the Hastelloy polymerization kettle, and discharged through the Hastelloy polymerization kettle. After crushing and drying, a prepolymer is obtained;
[0013] 2. Place the prepolymer obtained in step 1 under nitrogen protection conditions, and carry out solid-state polycondensation reaction in a rotary kiln at 190-205 ° C to obtain high molecular weight polymer powder;
[0014] 3. The high-molecular-weight polymer powder obtained in step 2 is mixed by a single-screw extruder at 320-350°C, exh...
specific Embodiment approach 2
[0018] Embodiment 2: This embodiment differs from Embodiment 1 in that the purity of the polymerized monomer p-hydroxybenzoic acid and 2-(4-hydroxyphenyl)-5-carboxybenzimidazole in step 1 is greater than 99.5%. Other steps and parameters are the same as those in Embodiment 1.
specific Embodiment approach 3
[0019] Specific embodiment three: the difference between this embodiment and specific embodiment one or two is that the molar weight of acetic anhydride in step one is the polymerized monomer p-hydroxybenzoic acid and 2-(4-hydroxyphenyl)-5-carboxybenzo 2 to 2.5 times the total number of moles of hydroxyl groups in imidazole. Other steps and parameters are the same as those in Embodiment 1 or Embodiment 2.
[0020] The acetic anhydride described in this embodiment is used as an acylating agent.
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