A kind of nickel-zinc ferrite/polyacrylic acid nanocomposite material and preparation method thereof
A nano-composite material, nickel-zinc ferrite technology, applied in the magnetic field of inorganic materials, organic materials/organic magnetic materials, etc., can solve the problems of easy demagnetization, easy magnetization, low saturation magnetization, etc. The effect of simplicity, low preparation cost, and high soft magnetic properties
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[0023] The preparation method of nickel-zinc ferrite / polyacrylic acid nanocomposite of the present invention comprises the steps:
[0024] (1) According to Ni 0.1~1 Zn 0.1~1 Fe 1~3 o 2~6 The stoichiometric ratio is 0.1~1:0.1~1:1~3, respectively weigh nickel sulfate, zinc sulfate, and ferrous sulfate to prepare metal salt solution, configure ammonium oxalate solution with a concentration of 0.5~1.5mol / L, and the ammonium oxalate After the solution is heated to 30-50°C, a metal salt solution is added thereto, wherein the volume ratio of the ammonium oxalate solution to the metal salt solution is 2:1, and then the mixed solution is kept warm and stirred, preferably, Ni 0.1~1 Zn 0.1~1 Fe 1~3 o 2~6 The stoichiometric ratio is 0.5~1:0.5~1:2~3.
[0025] (2) Regulating the pH of the mixed solution with 6-8mol / L NaOH solution is 9-12;
[0026] (3) After the mixed solution is centrifuged to obtain the precipitate, use deionized water and absolute ethanol to clean the precipitate...
Embodiment 1
[0031] (1) According to Ni 0.5 Zn 0.5 Fe 2 o 4 The stoichiometric ratio is 0.5:0.5:2, respectively weigh nickel sulfate, zinc sulfate, and ferrous sulfate to prepare metal salt solution, configure ammonium oxalate solution with a concentration of 1.0mol / L, heat the ammonium oxalate solution to 40°C, and It adds a metal salt solution, wherein the volume ratio of the ammonium oxalate solution to the metal salt solution is 2:1, and then heats and stirs the mixed solution.
[0032] (2) Regulating the pH of the mixed solution with the NaOH solution of 7mol / L is 10;
[0033] (3) Centrifuge the mixed solution at a speed of 5000r / min and a time interval of 10min. After obtaining the precipitate, wash the precipitate twice with deionized water and absolute ethanol respectively.
[0034] (4) Dry the washed precipitate under vacuum condition at 60° C. for 24 hours to obtain a ferrite precursor.
[0035] (5) calcining the ferrite precursor at 200°C for 10 hours, then calcining at 800...
Embodiment 2
[0047] The steps are basically the same as in Example 1, except that the mass ratio of nickel zinc ferrite, acrylic acid, initiator, dispersant and crosslinking agent is 0.1:40:0.01:0.5:8.
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