A kind of polyamide and its production method and application
A technology of polyamide and products, applied in the field of low-cost polyamide and its production, can solve the problem of high cost of raw materials
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Embodiment 1
[0119] The preparation of embodiment 1, nylon 5612
[0120] Under a nitrogen atmosphere, add 30kg of pure water to the reactor, then add 10.56kg (103mol) of pentamethylenediamine (comprising organic carbon from renewable sources meeting the ASTM D6866 standard), stir, add 7.55kg (51mol) of adipic acid and 11.89 kg (51 mol) of dicarbon dibasic acid, and then add 3 g of antioxidant H10 to prepare a nylon salt solution.
[0121] Under a nitrogen environment, the temperature of the oil bath was raised to 230°C. After the pressure in the polymerization kettle rose to 1.73Mpa, the exhaust gas was started. When the temperature in the kettle reached 265°C, the vacuum was pumped to -0.06Mpa, and the vacuum degree was maintained for 20 minutes to obtain Nylon 5612.
[0122] Fill the polymerization kettle with nitrogen to a pressure of 0.5Mpa, start melting and discharging, and use a pelletizer to granulate. After vacuum drying at 80°C for 8 hours, various performance tests were perfor...
Embodiment 2
[0126] Embodiment 2, the preparation of nylon 5612
[0127] In addition to adjusting the addition of pentamethylenediamine in Example 1 to be 9.46kg (92mol), the addition of adipic acid to be 1.35kg (9mol) and the addition of dodecanedioic acid to be 19.18kg (83mol), the same as in Example 1 in the same way. According to embodiment 1, using 1 Characterized by H-NMR, it was confirmed that the target product was obtained. Various performance tests were carried out on the obtained polyamide resin, and the results are shown in Table 1.
Embodiment 3
[0128] Embodiment 3, the preparation of nylon 5612
[0129] In addition to adjusting the addition of pentamethylenediamine in Example 1 to be 11.94kg (117mol), the addition of adipic acid to be 15.36kg (105mol) and the addition of dodecanedibasic acid to be 2.69kg (11mol), the same as in Example 1 in the same way. According to embodiment 1, using 1 Characterized by H-NMR, it was confirmed that the target product was obtained. Various performance tests were carried out on the obtained polyamide resin, and the results are shown in Table 1.
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