Polyaniline/oxidized graphene/ferriferrous oxide absorbing material and preparation method
A technology of ferroferric oxide and wave-absorbing materials, which is applied in the field of preparation of new polyaniline/graphene oxide/ferric oxide composite materials, can solve the problems of less graphene oxide, reduce the density of absorbents, etc., and achieve surface energy Large, improved magnetic loss, low density effect
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Embodiment 1
[0021] A preparation of absorbing material
[0022] (1) Add 1g of natural flake graphite and 0.5g of sodium nitrate into 50mL of concentrated sulfuric acid, cool in an ice bath to 4°C, slowly add 5g of potassium permanganate, stir for 90min; then raise the temperature to 35°C and stir for 4h; slowly add 100mL Deionized water, stirred at 90°C for 2h, cooled to room temperature, added 10mL of hydrogen peroxide, washed by centrifugation and vacuum dried to obtain graphite oxide.
[0023] (2) 1.99gFeCl 2 4H 2 O and 4.06 g FeCl 3 ·H 2 O was added to 100mL deionized water, stirred to dissolve, 20mL ammonia water (28wt%) was quickly added to the above solution, stirred vigorously, and the water was kept at a constant temperature of 75°C. When the mixed solution changed from orange red to black, continue to stir for 15min. Centrifugal washing and vacuum drying to obtain ferric oxide.
[0024] (3) Weigh 1g of aniline and 0.5g of ferric oxide into 100mL containing 0.25MFeCl 3 and...
Embodiment 2
[0028] A preparation of absorbing material
[0029] (1) Add 1g of natural flake graphite and 0.5g of sodium nitrate into 50mL of concentrated sulfuric acid, cool in an ice bath to 4°C, slowly add 5g of potassium permanganate, stir for 90min; then raise the temperature to 35°C and stir for 4h; slowly add 100mL Deionized water, stirred at 90°C for 2h, cooled to room temperature, added 10mL of hydrogen peroxide, washed by centrifugation and vacuum dried to obtain graphite oxide.
[0030] (2) 1.99gFeCl 2 4H 2 O and 4.06 g FeCl 3 ·H 2 O was added to 100mL deionized water, stirred to dissolve, 20mL ammonia water (28wt%) was quickly added to the above solution, stirred vigorously, and the water was kept at a constant temperature of 75°C. When the mixed solution changed from orange red to black, continue to stir for 15min. Centrifugal washing and vacuum drying to obtain ferric oxide.
[0031] (3) Weigh 1g of aniline and 1g of ferric oxide into 100mL containing 0.25MFeCl 3 and 0....
Embodiment 3
[0035] A preparation of absorbing material
[0036] (1) Add 1g of natural flake graphite and 0.5g of sodium nitrate to 50mL of concentrated sulfuric acid, cool in an ice bath to 4°C, slowly add 5g of potassium permanganate, stir for 90min; then raise the temperature to 35°C and stir for 4h; slowly add 100mL Deionized water, stirred at 90°C for 2h, cooled to room temperature, added 10mL of hydrogen peroxide, washed by centrifugation and vacuum dried to obtain graphite oxide.
[0037] (2) 1.99gFeCl 2 4H 2 O and 4.06 g FeCl 3 ·H 2 O was added to 100mL deionized water, stirred to dissolve it, 20mL ammonia water (28wt%) was quickly added to the above solution, stirred vigorously, and the water was kept at a constant temperature of 75°C. When the mixed solution changed from orange red to black, continue to stir for 15min. Centrifugal washing and vacuum drying to obtain ferric oxide.
[0038] (3) Weigh 1g of aniline and 1.5g of ferric oxide into 100mL containing 0.25MFeCl 3 and...
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