Wave absorption material and preparation method thereof
A microwave-absorbing material, carbonyl iron powder technology, applied in the field of microwave-absorbing materials, can solve the problems of large fluctuations in dielectric constant and magnetic permeability, unstable metal powder, poor thermal stability, etc., to improve high-temperature microwave absorption The performance and preparation method are simple and feasible, and the effect of excellent high temperature resistance
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[0023] The preparation method of the wave absorbing material provided in the present application includes the following steps: in the presence of grams of ammonium molybdate, a phthalocyanine precursor and carbonyl iron powder are made into a carbonyl iron powder composite with phthalocyanine molecules on the surface in a solvent. Specifically, a phthalocyanine precursor, gram ammonium molybdate, N-methylpyrrolidone, and carbonyl iron powder are mixed.
[0024] The first heat treatment is performed on the carbonyl iron powder composite coated with phthalocyanine molecules to form a first coating layer on the surface of the carbonyl iron powder.
[0025] The surface modification treatment of the carbonyl iron powder with the first coating layer (also called graphene-coated carbonyl iron powder) is carried out with the silane coupling agent solution, (drying), and then the second heat treatment is performed. A second coating layer is formed on the surface of the carbonyl iron powder ...
Example Embodiment
[0052] Example 1
[0053] A high-energy planetary ball mill was used to ball mill the carbonyl iron for 5 hours, and the inside of the ball mill was protected by nitrogen gas. After the ball milling, it was taken out and sieved with a 300-mesh screen to obtain flake carbonyl iron powder.
[0054] Add biphenol, 4-nitrophthalonitrile and anhydrous potassium carbonate to N,N-dimethylformamide in a mass ratio of 1:2:1.5 to dissolve them, and then dissolve them at 60℃. Stir in a water bath for 11.5 hours. After stirring, put it into 30% mass fraction of hydrochloric acid and stir for 4 hours, then suction and filter, rinse with deionized water repeatedly, and place the filter in a vacuum oven at a drying temperature of 60°C and vacuum The phthalocyanine precursor was obtained by drying for 6 hours under the condition of pressure less than -0.1MPa.
[0055] After stirring the phthalocyanine precursor, grams of ammonium molybdate and N-methylpyrrolidone for 1.5 hours at 180°C, the solution...
Example Embodiment
[0060] Example 2
[0061] A high-energy planetary ball mill was used to ball mill the carbonyl iron for 10 hours. The inside of the ball mill was protected by nitrogen gas. After the ball milling, it was taken out and sieved with a 300 mesh screen to obtain flake carbonyl iron powder.
[0062] Add biphenol, 4-nitrophthalonitrile and anhydrous potassium carbonate to N,N-dimethylformamide in a mass ratio of 1:2.5:2 to dissolve them, and then dissolve them at 55°C Stir in a water bath for 13 hours. After stirring, put it in 30% mass fraction of hydrochloric acid and stir for 3 hours, then suction and filter, rinse with deionized water repeatedly, and place the filter in a vacuum oven at a drying temperature of 70°C and a vacuum pressure The phthalocyanine precursor was obtained by drying for 4.5 hours under the condition of less than -0.1MPa.
[0063] After stirring the phthalocyanine precursor, grams of ammonium molybdate and N-methylpyrrolidone for 2 hours at 175℃, the solution turne...
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