Preparation method of a three-dimensional network multi-walled carbon nanotube/nickel ferrite composite absorbing material
A technology of multi-walled carbon nanotubes and composite wave absorbing materials, applied in chemical instruments and methods, magnetic/electric field shielding, other chemical processes, etc., can solve the problems of high density, narrow absorption frequency band, limited application, etc. , Enhance attenuation ability, easy operation effect
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Embodiment 1
[0029] 1. Take a 100mL beaker, add 30mL ethylene glycol (EG) and 0mg MWCNTs, and sonicate for 30min;
[0030] 2. Add 0.54g ferric chloride hexahydrate (FeCl 3 ·6H 2 O) and 0.21g nickel chloride hexahydrate (NiCl 2 ·6H 2 O), vigorously stirred for 20min. Among them, Fe 3+ with you 2+ The molar ratio satisfies n Fe3+ :n Ni2+ =2:1;
[0031] 3. Add 2.37g of anhydrous ammonium acetate (NH 4 Ac), vigorously stirred for 30min;
[0032] 4. Pour the mixed dispersion liquid into a 50mL reactor, and react with solvent heat at 200°C for 12 hours;
[0033] 5. After the reaction, cool to room temperature, magnetically separate, and wash with deionized water and absolute ethanol several times to make the pH of the product reach neutral;
[0034] 6. Put it into a vacuum drying oven, dry at 50°C for 24 hours, and grind to obtain the final product, which is recorded as S1.
[0035] The XRD spectrogram of embodiment 1 product sees figure 1 . The powder product and paraffin in Examp...
Embodiment 2
[0037] 1. Take a 100mL beaker, add 30mL ethylene glycol (EG) and 10mg MWCNTs, and sonicate for 30min;
[0038] 2. Add 0.54g ferric chloride hexahydrate (FeCl 3 ·6H 2 O) and 0.21g nickel chloride hexahydrate (NiCl 2 ·6H 2 O), vigorously stirred for 20min. Among them, Fe 3+ with you 2+ The molar ratio satisfies n Fe3+ :n Ni2+ =2:1;
[0039] 3. Add 2.37g of anhydrous ammonium acetate (NH 4 Ac), vigorously stirred for 30min;
[0040] 4. Pour the mixed dispersion liquid into a 50mL reactor, and react with solvent heat at 200°C for 12 hours;
[0041] 5. After the reaction, cool to room temperature, magnetically separate, and wash with deionized water and absolute ethanol several times to make the pH of the product reach neutral;
[0042] 6. Put it into a vacuum drying oven, dry at 50°C for 24 hours, and grind to obtain the final product, which is recorded as S2.
[0043] The XRD spectrum pattern of embodiment 2 product sees figure 1. The powder product and paraffin in ...
Embodiment 3
[0045] 1. Take a 100mL beaker, add 30mL ethylene glycol (EG) and 20mg MWCNTs, and sonicate for 30min;
[0046] 2. Add 0.54g ferric chloride hexahydrate (FeCl 3 ·6H 2 O) and 0.21g nickel chloride hexahydrate (NiCl 2 ·6H 2 O), vigorously stirred for 20min. Among them, Fe 3+ with you 2+ The molar ratio satisfies n Fe3+ :n Ni2+ =2:1;
[0047] 3. Add 2.37g of anhydrous ammonium acetate (NH 4 Ac), vigorously stirred for 30min;
[0048] 4. Pour the mixed dispersion liquid into a 50mL reactor, and react with solvent heat at 200°C for 12 hours;
[0049] 5. After the reaction, cool to room temperature, magnetically separate, and wash with deionized water and absolute ethanol several times to make the pH of the product reach neutral;
[0050] 6. Put it into a vacuum drying oven, dry at 50°C for 24 hours, and grind to obtain the final product, which is recorded as S3.
[0051] The XRD spectrum pattern of embodiment 3 product sees figure 1 . The powder product and paraffin in...
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