A zirconium-titanium co-doped barium ferrite wave-absorbing powder material and preparation method thereof
A barium ferrite and powder material technology is applied in the field of zirconium-titanium co-doped barium ferrite wave absorbing powder material and its preparation, which can solve the problems of low matching layer thickness and difficulty in achieving, and achieves reduced matching Thickness, energy saving, effect of increasing dielectric loss
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Embodiment 1
[0025] 1) Mix barium nitrate, ferric nitrate, zirconium nitrate and citric acid in a molar ratio of 1:11.6:0.2:18.6, add deionized water and stir for 3 hours to dissolve to obtain metal salt solution A, wherein the total of barium nitrate, ferric nitrate and zirconium nitrate The molar concentration is 1.5mol / L;
[0026] 2) Tetrabutyl titanate and citric acid were mixed and dissolved in absolute ethanol at a molar ratio of 1:2 to obtain solution B; the molar concentration of tetrabutyl titanate was 0.05mol / L.
[0027] 3) Slowly add solution B to solution A and stir for 1 h, adjust the pH value of the solution to 6 to obtain solution C; wherein the molar ratio of tetrabutyl titanate to barium nitrate in solution C is 0.2:1.
[0028] 4) Move the solution C to a clean stainless steel vessel, place it on an electronic universal furnace, adjust the power to 600W, and perform self-propagating combustion to obtain the precursor powder;
[0029] 5) Add the precursor powder in step 4)...
Embodiment 2
[0034] 1) Mix barium nitrate, ferric nitrate, zirconium nitrate and citric acid in a molar ratio of 1:11.4:0.3:18.7, add deionized water and stir for 4 hours to dissolve to obtain metal salt solution A, wherein the total of barium nitrate, ferric nitrate and zirconium nitrate The molar concentration is 2.0mol / L;
[0035] 2) Tetrabutyl titanate and citric acid were mixed and dissolved in absolute ethanol at a molar ratio of 1:2 to obtain solution B; the molar concentration of tetrabutyl titanate was 0.1mol / L.
[0036] 3) Solution B was slowly added to solution A and stirred for 2 hours, and the pH value of the solution was adjusted to 7 to obtain solution C; wherein the molar ratio of tetrabutyl titanate to barium nitrate in solution C was 0.3:1.
[0037] 4) Move the solution C to a clean stainless steel container, place it on an electronic universal furnace, adjust the power to 700W, and perform self-propagating combustion to obtain the precursor powder;
[0038] 5) Add the p...
Embodiment 3
[0043] 1) Mix barium nitrate, ferric nitrate, zirconium nitrate and citric acid in a molar ratio of 1:11.2:0.4:18.8, add deionized water and stir for 5 hours to dissolve to obtain metal salt solution A, wherein the total of barium nitrate, ferric nitrate and zirconium nitrate The molar concentration is 2.5mol / L;
[0044] 2) Tetrabutyl titanate and citric acid were mixed and dissolved in absolute ethanol at a molar ratio of 1:2 to obtain solution B; the molar concentration of tetrabutyl titanate was 0.15mol / L.
[0045] 3) Slowly add solution B to solution A and stir for 3 hours to adjust the pH value of the solution to 8 to obtain solution C; wherein the molar ratio of tetrabutyl titanate to barium nitrate in solution C is 0.4:1.
[0046] 4) Move the solution C to a clean stainless steel container, place it on an electronic universal furnace, adjust the power to 800W, and perform self-propagating combustion to obtain the precursor powder;
[0047] 5) Add the precursor powder i...
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