Polyester amide, its preparation method and its product fiber
A polyester amide and fiber technology, applied in the field of polyester amide, can solve problems such as difficult control of molecular weight distribution and influence on spinning, and achieve the effects of improving spinnability, low equipment requirements, and improved dyeability
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[0039] The preparation method of the polyester amide of the present invention comprises the polycondensation of raw material diol, terephthalic acid or its derivative and nylon salt to obtain the polyester amide random copolymer.
[0040] Preferably, the molar ratio of the nylon salt, diol, terephthalic acid and its derivatives is (0.002-99):(1-3):1, preferably (0.005-3):(1.2-2.6 ):1, more preferably (0.01-0.3):(1.5-2.2):1. In the present invention, the diol may be an aliphatic diol containing 2 to 18 carbon atoms, such as ethylene glycol, propylene glycol, butanediol, pentanediol, hexanediol, heptanediol, octanediol Alcohol, Nonanediol, Decanediol, Undecanediol, Dodecanediol, Tridecanediol, Tetradecanediol, Pentadecanediol, Hexadecandiol Alcohol, heptadecanediol, and octadecanediol, among them, ethylene glycol, propylene glycol, and butanediol are preferred.
[0041] In step (1), two or more dihydric alcohols can be added simultaneously to form polyester amides with differe...
Embodiment 1
[0083] Preparation of polyester amide copolymer
[0084] 19.4kg of dimethyl terephthalate, 12.4kg of ethylene glycol and 0.1kg of hexamethylene adipate (commercially available, the same below) were added to the 200L reactor, heated to 205°C to react, and fractionated low For the boiling point components, the reaction was carried out for 80 minutes, and when the fraction reached 98% of the theoretical amount, the esterification and acylation reactions were terminated. Then add 13g of tetrabutyl titanate polycondensation catalyst, heat up to 250°C, evacuate to 50Pa, continue to heat up to 280°C, and the reaction is carried out for 4 hours. When the intrinsic viscosity of the polyester amide in the kettle is 0.78dL / g , into the polymerization kettle filled with 0.4MPa nitrogen, wire drawing and granulation. The resulting polyesteramide had a melting point of 249°C.
Embodiment 2
[0086] Preparation of polyester amide copolymer
[0087] 18.8kg of dimethyl terephthalate, 11.2kg of ethylene glycol and 0.7kg of adipate pentamethylenediamine salt (commercially available, the same below), 3.8g of tetrabutyl titanate were added to the 200L reactor, and the temperature was raised to 198 The reaction is carried out at ℃, and the low boiling point components are fractionated. The reaction is carried out for 80 minutes. When the fraction reaches 99% of the theoretical amount, the esterification and acylation reactions are terminated. Then add 10g of tetrabutyl titanate polycondensation catalyst, heat up to 240°C, evacuate to 50Pa, continue to heat up to 270°C, and the reaction is carried out for 4 hours. When the intrinsic viscosity of the polyester amide in the kettle is 0.84dL / g , charge 0.5MPa nitrogen into the polymerization kettle, and draw and granulate. The resulting polyesteramide had a melting point of 237°C.
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