Preparation method of reduced graphene oxide/manganese ferrite nano-composite wave absorbing material
A nano-composite material, manganese ferrite technology, applied in chemical instruments and methods, other chemical processes, magnetic/electric field shielding, etc. Excellent, improve the effect of interface polarization relaxation
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Embodiment 1
[0027] 1. Take a 150mL beaker, add 30mL deionized water and 10mL GO water dispersion with a concentration of 2mg / mL. Vigorously stir for 2h, ultrasonic for 30min.
[0028] 2. Add 0.4mmol ferric nitrate nonahydrate (Fe(NO 3 ) 3 9H 2 O) and 0.2 mmol manganous chloride tetrahydrate (MnCl 2 4H 2 O), vigorously stirred for 90min.
[0029] 3. Add ammonia water drop by drop to adjust the pH of the mixed dispersion to 11, and then vigorously stir for 10 minutes.
[0030] 4. Pour the mixed dispersion into a 50mL reactor, and conduct a hydrothermal reaction at 180°C for 24 hours.
[0031] 5. After the reaction, cool to room temperature, repeat centrifugation and wash with water for several times to make the pH of the product reach neutral.
[0032] 6. Put it into a vacuum drying oven, dry at 40°C for 24 hours, and grind to obtain the final product, which is designated as S1.
[0033] The XRD spectrogram of embodiment 1 product sees figure 1 . The powder product and paraffin in...
Embodiment 2
[0035] 1. Take a 150mL beaker, add 30mL deionized water and 10mL GO water dispersion with a concentration of 2mg / mL. Vigorously stir for 2h, ultrasonic for 30min.
[0036] 2. Add 0.8mmol ferric nitrate nonahydrate (Fe(NO 3 ) 3 9H 2 O) and 0.4 mmol manganous chloride tetrahydrate (MnCl 2 4H 2 O), vigorously stirred for 90min.
[0037] 3. Add ammonia water drop by drop to adjust the pH of the mixed dispersion to 11, and then vigorously stir for 10 minutes.
[0038] 4. Pour the mixed dispersion into a 50mL reactor, and conduct a hydrothermal reaction at 180°C for 24 hours.
[0039] 5. After the reaction, cool to room temperature, repeat centrifugation and wash with water for several times to make the pH of the product reach neutral.
[0040] 6. Put it into a vacuum drying oven, dry at 40°C for 24 hours, and grind to obtain the final product, which is designated as S2.
[0041] The XRD spectrum pattern of embodiment 2 product sees figure 1 . The powder product and paraff...
Embodiment 3
[0043]1. Take a 150mL beaker, add 30mL deionized water and 10mL GO water dispersion with a concentration of 2mg / mL. Vigorously stir for 2h, ultrasonic for 30min.
[0044] 2. Add 1.2mmol ferric nitrate nonahydrate (Fe(NO 3 ) 3 9H 2 O) and 0.6 mmol manganous chloride tetrahydrate (MnCl 2 4H 2 O), vigorously stirred for 90min.
[0045] 3. Add ammonia water drop by drop to adjust the pH of the mixed dispersion to 11, and then vigorously stir for 10 minutes.
[0046] 4. Pour the mixed dispersion into a 50mL reactor, and conduct a hydrothermal reaction at 180°C for 24 hours.
[0047] 5. After the reaction, cool to room temperature, repeat centrifugation and wash with water for several times to make the pH of the product reach neutral.
[0048] 6. Put it into a vacuum drying oven, dry at 40°C for 24 hours, and grind to obtain the final product, which is designated as S3.
[0049] The XRD spectrum pattern of embodiment 3 product sees figure 1 . The powder product and paraffi...
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