A high flame-retardant composite material for new energy vehicles and its preparation method
A technology for new energy vehicles and composite materials, which is applied in the field of high flame-retardant composite materials for new energy vehicles and its preparation. Stability of material properties and small effect on environment
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Embodiment 1
[0030] A method for preparing a high flame-retardant composite material for new energy vehicles, comprising the steps of:
[0031] Ⅰ Preparation of matrix material: Add 10g of bisphenol A bischloroformate and 3g of 4-dimethylaminopyridine into a reaction kettle containing 30g of dimethyl sulfoxide, and add dissolved bis(2-aminopyridine) while stirring. Ethyl) hydrogen phosphate 19.2g dichloromethane 60g, stirred and reacted at 30°C for 24 hours, then precipitated in acetone, and the precipitated polymer was washed 3 times with acetone, and then placed in a vacuum oven at 80°C Dry for 18 hours to obtain the base material;
[0032] Ⅱ Surface modification of glass fiber: disperse 30g of glass fiber in 100g of N-methylpyrrolidone to form a dispersion, then add 12g of vinyltriethoxysilane, 2,4-diamino-6-vinyl to the dispersion -S-triazine 5g, azobisisobutyronitrile 0.3g, stirred and reacted at 65°C under nitrogen atmosphere for 4 hours, then precipitated in water, washed the preci...
Embodiment 2
[0036] A method for preparing a high flame-retardant composite material for new energy vehicles, comprising the steps of:
[0037] Ⅰ Preparation of matrix material: Add 10g of bisphenol A bischloroformate and 3g of anhydrous pyridine into a reaction kettle containing 35g of N,N-dimethylformamide, and add di(2 -Aminoethyl) hydrogen phosphate 19.2g of 1,2-dichloroethane 70g, stirred and reacted at 35°C for 26 hours, then precipitated in acetone, and the precipitated polymer was washed 4 times with acetone, and then placed Dry in a vacuum oven at 83°C for 20 hours to obtain a matrix material;
[0038]Ⅱ Surface modification of glass fiber: disperse 35g of glass fiber in 115g of N-methylpyrrolidone to form a dispersion liquid, then add 12g of vinyltriethoxysilane, 2,4-diamino-6-vinyl -S-triazine 5g, azobisisoheptanonitrile 0.35g, stirred and reacted at 68°C for 4.5 hours under a helium atmosphere, then precipitated in water, washed the precipitated product with ethanol 4 times, an...
Embodiment 3
[0042] A method for preparing a high flame-retardant composite material for new energy vehicles, comprising the steps of:
[0043] Ⅰ Preparation of matrix material: Add 10g of bisphenol A bischloroformate and 3g of triethylamine into a reaction kettle containing 40g of N-methylpyrrolidone, and add dissolved bis(2-aminoethyl) while stirring. ) Hydrogen phosphate 19.2g THF 75g, stirred and reacted at 41°C for 28 hours, then precipitated in acetone, and washed the precipitated polymer with acetone 5 times, and then dried in a vacuum oven at 86°C for 21 hours, Get the base material;
[0044] Ⅱ Surface modification of glass fiber: disperse 40g of glass fiber in 135g of N-methylpyrrolidone to form a dispersion liquid, then add 12g of vinyltriethoxysilane, 2,4-diamino-6-vinyl -S-triazine 5g, azobisisobutyronitrile 0.4g, stirred and reacted at 70°C for 5 hours under a neon atmosphere, then precipitated in water, washed the precipitated product with ethanol 5 times, and placed in a va...
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