Polyamide copolymer and molded article
A polyamide copolymer and copolymer technology, applied in the field of polyamide copolymers and molded products, can solve the problems of large changes and insufficient rigidity improvement, and achieve the effect of excellent rigidity
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Embodiment 1
[0147] [Example 1] Production of polyamide copolymer (a1)
[0148] 517.0 g (3.54 moles) of adipic acid, 55.1 g (0.33 moles) of isophthalic acid, 285.5 g (1.66 mol) and 642.3 g (5.53 mol) of hexamethylenediamine were dissolved in 1500 g of distilled water to prepare an equimolar 50% by mass homogeneous aqueous solution of the raw material monomers. This aqueous solution was charged into an autoclave with an internal volume of 5.4 L, and nitrogen substitution was performed. Water vapor was slowly removed while stirring at a temperature of 110 to 150° C., and concentrated to a solution concentration of 70% by mass. Then, the internal temperature was raised to 218°C. At this time, the pressure of the autoclave was increased to 1.8 MPa. Then, the reaction was carried out for 1 hour while gradually removing water vapor while maintaining a pressure of 1.8 MPa until the internal temperature reached 270°C. Then, the pressure was lowered to 1 MPa over 1 hour, and polymerization was ...
Embodiment 2
[0149] [Example 2] Production of polyamide copolymer (a2)
[0150] In addition to using 440.9 g (3.02 moles) of adipic acid, 91.1 g (0.55 moles) of isophthalic acid, and 330.6 g (330.6 g) of 1,4-cyclohexanedicarboxylic acid ( 1.92 mol) and 637.4 g (5.49 mol) of hexamethylenediamine were polymerized by the method described in Example 1 to obtain a polyamide copolymer. At this time, the final internal temperature of the polymerization was 291°C. The trans isomer ratio of the 1,4-cyclohexanedicarboxylic acid component contained in the obtained polyamide copolymer was 71.4 mol%. Table 1 shows the composition of the obtained polyamide copolymer (a2). The proportions of the constituent units of the polyamide copolymers shown in Table 1 were obtained by carrying out 1 H-NMR analysis to obtain. The water absorption rigidity, thermal rigidity, and molded appearance of the obtained polyamide copolymer (a2) were evaluated by the methods described above. The evaluation results are sh...
Embodiment 3
[0151] [Example 3] Production of polyamide copolymer (a3)
[0152] In addition to using 509.4 g (3.49 moles) of adipic acid, 128.7 g (0.77 moles) of isophthalic acid, and 219.1 g (219.1 g) of 1,4-cyclohexanedicarboxylic acid ( 1.27 mol) and 642.9 g (5.53 mol) of hexamethylenediamine were polymerized by the method described in Example 1 to obtain a polyamide copolymer. At this time, the final internal temperature of the polymerization was 292°C. The trans isomer ratio of the 1,4-cyclohexanedicarboxylic acid component contained in the obtained polyamide copolymer was 71.8 mol%. Table 1 shows the composition of the obtained polyamide copolymer (a3). The proportions of the constituent units of the polyamide copolymers shown in Table 1 were obtained by carrying out 1 H-NMR analysis to obtain. The water absorption rigidity, thermal rigidity, and molded appearance of the obtained polyamide copolymer (a3) were evaluated by the methods described above. The evaluation results are...
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