High-flame-retardancy nylon composite material resistant to high temperature and preparing method thereof
A nylon composite material and high flame retardant technology, which is applied in the field of flame retardant and high temperature resistant nylon synthesis, can solve the problems of high price of carbon nanotubes and ionic liquids, high cost of synergistic flame retardants, deterioration of material properties, etc., and is conducive to industrialization promotion. Implementation, preparation method is simple and efficient, and the effect of good mechanical properties
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Embodiment 1
[0025] Example 1. In this example, under the action of ultrasonic waves, 2.0 g of expanded graphite is uniformly dispersed in 200 ml of mixed acid of perchloric acid and concentrated nitric acid (the Hammett acidity function HO value is less than -10), and then the temperature is raised to Continue ultrasonication at 60°C for 2~3h, and obtain carboxylated expanded graphite after vacuum filtration, multiple washings with a large amount of deionized water and methanol, and vacuum drying.
[0026] Weigh 1.1g of carboxylated expanded graphite and disperse it in 100ml of dry dimethyl sulfoxide solution, add 0.2g of sodium hydride and reflux at 50°C for 1h, then slowly add 50ml of hexachlorocyclotriphosphazene dissolved in 2g After the dropwise addition, the temperature was raised to 80°C to continue the reaction for 12 hours, filtered under reduced pressure, washed with a large amount of deionized water and acetone for many times, and vacuum dried to obtain hexachlorocyclotriphospha...
Embodiment 2
[0029] Example 2, the difference between this example and Example 1 is that the prepared hexachlorocyclotriphosphazene graft modified expanded graphite 25%, PA6T 50%, PA66 20%, stabilizer 1.5%, antioxidant 0.5 %, 1.5% lubricant, 1.5% coupling agent, mixed evenly with a high-speed mixer, and granulated by a twin-screw extruder to obtain a high-flame-resistance high-temperature nylon composite material.
[0030] After testing, the composite material has an oxygen index of 31 and a tensile strength of 92Mpa.
Embodiment 3
[0031] Example 3. In this example, under the action of ultrasonic waves, take 5.0 g of expanded graphite and evenly disperse it in 400 ml of a mixed acid of concentrated sulfuric acid and concentrated nitric acid (the HO value of the Hammett acidity function is less than -9), and then raise the temperature to 60 Continuous ultrasonication at ℃ for 3~4h, after vacuum filtration, multiple washings with a large amount of deionized water and ethanol, and vacuum drying, carboxylated expanded graphite was obtained.
[0032] Weigh 3g of carboxylated expanded graphite and disperse it in 200ml of dry N,N-dimethylformamide solution, add 0.5g of sodium hydride and reflux at 50°C for 1.5h, then slowly add dropwise 150ml of 5g hexachloro The N,N-dimethylformamide solution of cyclotriphosphazene, after the dropwise addition, the temperature was raised to 80°C to continue the reaction for 18 hours, and the cyclotriphosphazene was filtered under reduced pressure, washed with a large amount of ...
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