High performance epoxy resins composite material and preparation thereof
A technology of epoxy resin and composite materials, which is applied in chemical instruments and methods, fibrous fillers, inorganic pigment treatment, etc., can solve the problems of uneven dispersion of carbon nanotubes, weak interface between carbon nanotubes and matrix materials, etc. Achieve the effects of reduced volume resistivity, convenient preparation, and simple process
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Embodiment 1
[0031] Step 1: Mix 500 mg of multi-walled carbon nanotubes with an average diameter of 8 to 15 nm and a length of 50 μm with 150 ml of H 2 SO 4 with HNO 3 mixed solution (98%H 2 SO 4 : 68% HNO 3 = 3:1) mixed, and reflux reaction for 4 hours at 35-40° C. and ultrasonic vibration. Then filter with a metafluoride membrane with a pore size of 0.45 μm, and wash with water until the pH is neutral. The product was placed in a vacuum oven and dried under vacuum at 40°C for 24h. Then the above-mentioned one-step acidified and washed product was placed in H 2 SO 4 with H 2 o 2 mixed solution (98%H 2 SO 4 : 30%H 2 o 2 =4:1) at 70°C for 2h. Then filter with a metafluoride membrane with a pore size of 0.45 μm, and wash with water until the pH is neutral. The product was placed in a vacuum oven and dried under vacuum at 40°C for 24h.
[0032] Step 2: Take 400 mg of the above-mentioned acidified carbon nanotubes and place them in a reaction flask, add 20 ml of SOCl 2 and 1ml...
Embodiment 2
[0036] The first and second steps are to prepare acyl chloride carbon nanotubes according to the method described in Example 1.
[0037] Step 3: Mix 0.2 g of carbonyl chloride carbon nanotubes and 30 g of ethylene glycol evenly, and heat and reflux in an oil bath at 96° C. for 36 hours. After the reaction is completed, filter with a microporous membrane (0.45 μm in diameter) and dry in vacuum to obtain carbon nanotubes with hydroxyl groups on the surface. Dissolve 400 mg of hydroxyl carbon nanotubes in dimethyl sulfoxide, oscillate ultrasonically for 30 minutes, add 4 g of benzophenone tetraacid dianhydride, add 1 ml of concentrated sulfuric acid as a catalyst, and stir well. Under nitrogen protection at 90 ° C, magnetic stirring, the reaction time is 48 Hours, carbon nanotubes with acid anhydride groups on the surface were obtained.
[0038] Step 4: Take 30g E-51 epoxy resin and preheat it at 60°C. According to 1 wt% of the total amount, 0.3 g of carbon nanotubes modified w...
Embodiment 3
[0040] In the first to third steps, the carbon nanotubes modified with pyromellitic dianhydride were prepared according to the method described in Example 1.
[0041] Step 4: Take 30g E-51 epoxy resin and preheat it at 60°C. According to 1% of the total amount, 0.3 g of carbon nanotubes modified with pyromellitic dianhydride was taken, added to the preheated epoxy resin, vigorously stirred for 8 hours, ultrasonically dispersed for 4 hours, and mixed uniformly. Add 16g of curing agent diphenyl ether tetra-acid dianhydride, mechanically stir evenly; place in a vacuum oven to remove air bubbles, pour, cure at 200°C for 1 hour, and demould to obtain an epoxy resin composite material.
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