A kind of preparation method of carbon-based wave absorbing material
A wave-absorbing material and carbon-based technology, applied in chemical instruments and methods, rayon manufacturing, and other chemical processes, to achieve the effects of strong repeatability, improved magnetic permeability, and simple process
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Embodiment 1
[0017] A method for preparing a carbon-based wave-absorbing material, the technical scheme of which is as follows according to the mass g:
[0018] Add 45g of acrylonitrile, 25g of styrene, 6g of itaconic acid, 0.03g of benzotriazole-1-carboxythioacid allylamide, 0.04g of (R, R)-ethylene di( 4,5,6,7-tetrahydroxy-1-indenyl)]difluorotitanium, 0.5g 2-(chloromethyl)-3,5-dioxa-1-hexene, 0.75g of initiator peroxidation Benzoyl and 175g of DMSO were polymerized at a constant temperature of 60~65°C for 26h; then 8g of a mixture of ferrous oxalate, zinc nitrate and nickel nitrate powder (molar ratio 43:12:12) was added to the reaction system, After high-speed dispersion for 35 minutes, wet spinning technology is used to solidify the composite liquid into silk, and the silk is carbonized and ground under the condition of protective gas to obtain a carbon-based wave-absorbing material.
[0019] The sample number is AS-1.
Embodiment 2
[0021] A method for preparing a carbon-based wave-absorbing material, the technical scheme of which is as follows according to the mass g:
[0022] Add 40g of acrylonitrile, 20g of styrene, 4g of itaconic acid, 0.01g of benzotriazole-1-carboxythioacid allylamide, 0.01g of (R, R)-ethylene di( 4,5,6,7-Tetrahydroxy-1-indenyl)]difluorotitanium, 0.1 g of 2-(chloromethyl)-3,5-dioxa-1-hexene, 0.5 g of the initiator azo Diisobutyronitrile and 150g of DMSO were polymerized at a constant temperature of 60-65°C for 24 hours; then a mixture of 6g of ferrous oxalate, zinc nitrate and nickel nitrate powder was added to the reaction system (the molar ratio was 40:10:10), After 30 minutes of high dispersion, wet spinning technology is used to solidify the composite liquid into silk, and the silk is carbonized and ground under the condition of high-purity nitrogen to obtain a carbon-based wave-absorbing material.
[0023] Sample number AS-2.
Embodiment 3
[0025] A method for preparing a carbon-based wave-absorbing material, the technical scheme of which is as follows according to the mass g:
[0026] Add 55g of acrylonitrile, 30g of styrene, 8g of itaconic acid, 0.2g of benzotriazole-1-carboxythioacid allylamide, 0.2g of (R, R)-ethylene di( 4,5,6,7-tetrahydroxy-1-indenyl)]difluorotitanium, 0.8 g of 2-(chloromethyl)-3,5-dioxa-1-hexene, 1 g of initiator cumene Hydrogen peroxide and 200g of DMSO were polymerized at a constant temperature of 60~65°C for 28h; then 10g of a mixture of ferrous oxalate, zinc nitrate and nickel nitrate powder (molar ratio 45:13:13) was added to the reaction system, After high-speed dispersion for 40 minutes, wet spinning technology was used to solidify the composite liquid into silk, and the silk was carbonized and ground under the condition of protective gas to obtain a carbon-based wave-absorbing material.
[0027] Sample number AS-3.
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