Preparation method of three-dimensional skeleton of heat-conducting filler, three-dimensional skeleton and polymer composite material
A technology of thermally conductive filler and three-dimensional skeleton, which is applied in the direction of heat exchange materials, chemical instruments and methods, etc., can solve the problems of thermal conductivity anisotropy, complex process, etc., and achieve the effects of enhanced heat transfer, simple operation, and improved thermal conductivity
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Embodiment 1
[0047] 500ml concentration is 2mg / ml graphene oxide water dispersion liquid and 50g hexagonal boron nitride flakes are stirred in the beaker or ultrasonically mix uniformly, then add 1 gram of ascorbic acid, 2 grams of alkyl glycoside water dispersion liquid (50%wt) with stirring Continue stirring at low paddle speed (below 600 rpm) until homogeneous. Increase the rotation speed to 1500 rpm, stir and foam for about 5 minutes, pour the foaming solution obtained at this time into a container, seal it, and place it in a blast oven at 65°C for 6 hours for reduction. The foamed hydrogel taken out was further dried in a blast oven at 60°C. The dried gel was further heat-treated in a blast oven at 200° C. for 5 hours. Submerge the obtained gel in the liquid silicone rubber that has been evenly mixed with the curing agent, put it in a vacuum oven at room temperature to vacuum and degas for 2 hours, take out the airgel impregnated with the silicone rubber, and vulcanize it at 100°C A...
Embodiment 2
[0049] Stir or ultrasonically mix 50ml of graphene oxide aqueous dispersion with a concentration of 20mg / ml and 5g of graphene nanosheets in a beaker, then add 2g of ethylenediamine and 2.5g of sodium dodecylsulfonate with a stirring paddle at low speed (below 600 rpm) and continue to stir until even. Increase the rotation speed to 1500 rpm, stir and foam for about 5 minutes, pour the foaming solution obtained at this time into a container, seal it, and place it in a blast oven at 90°C for 15 minutes for reduction. The foamed hydrogel taken out was further dried in a blast oven at 60°C. The dried gel was further heat-treated in a blast oven at 2000°C for 1 min. Immerse the obtained gel in the liquid epoxy resin monomer that has been evenly mixed with the curing agent, put it in a vacuum oven at room temperature and degas it for 2 hours, take out the airgel impregnated with epoxy resin, and put it on the After curing for 1 hour at 100° C., a composite material containing 17.6...
Embodiment 3
[0051] 100ml concentration is that 10mg / ml graphene oxide aqueous dispersion and 30g aluminum oxide are stirred in the beaker or ultrasonically mixed, then add 3 grams of pyrrole, 1 gram of alkylphenol polyoxyethylene ether with stirring paddle at low speed (600 rpm Minutes below) continue to stir until uniform. Increase the rotation speed to 1500 rpm, stir and foam for about 5 minutes, pour the foaming solution obtained at this time into a container, seal it, and place it in a blast oven at 80°C for 2 hours for reduction. The foamed hydrogel taken out was further dried in a blast oven at 60°C. The dried gel was further heat-treated in a blast oven at 1000° C. for 2 hours. Submerge the obtained gel in the liquid polyurethane that has been evenly mixed with the curing agent, put it in a vacuum oven at room temperature to vacuum and degas for 2 hours, take out the airgel impregnated with polyurethane, and vulcanize it at 100°C for 1 hour , that is, a composite material contain...
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