Oxide composite material and preparation method and application thereof
A composite material and oxide technology, applied in the field of wave absorbing materials, can solve the problems of limited use, insufficient effective absorption frequency band, etc., and achieve the effects of increasing electrical conductivity, good wave absorbing effect, and convenient operation.
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Embodiment 1
[0029] Preparation of oxide composites:
[0030] (1) Dissolve 0.39g of samarium nitrate, 2.95g of calcium acetate, 3.56g of iron nitrate and 3.16g of manganese nitrate in 45mL of deionized water, then add 11.13g of citric acid as an organic complexing agent, and form a brownish brown under the action of a mechanical stirrer. Yellow solution to obtain metal-citric acid solution;
[0031] (2) aging the metal-citric acid solution in a constant temperature water bath at 80°C and stirring for 3 hours under the action of a magnetic stirrer to obtain a precursor gel;
[0032] (3) putting the precursor gel into a blast drying oven and drying at 80°C for 10 hours to obtain a dry gel;
[0033] (4) pre-calcining the xerogel at 200° C. for 10 minutes to obtain a black precursor powder;
[0034](5) Put the black precursor powder into a muffle furnace for a second calcination at 750°C for 10h to obtain the oxide composite material Sm 0.05 Ca 0.95 Fe 0.5 Mn 0.5 O 3-x .
Embodiment 2
[0036] Preparation of oxide composites:
[0037] (1) Dissolve 0.76g of samarium nitrate, 3.02g of calcium acetate, 2.77g of iron nitrate and 3.07g of manganese nitrate in 45mL of deionized water, then add 10.82g of citric acid as a complexing agent, and form a brownish yellow under the action of a mechanical stirrer solution to obtain a metal-citric acid solution;
[0038] (2) aging the metal-citric acid solution in a constant temperature water bath at 80°C and stirring for 3 hours under the action of a magnetic stirrer to obtain a precursor gel;
[0039] (3) putting the precursor gel into a blast drying oven and drying at 80°C for 10 hours to obtain a dry gel;
[0040] (4) pre-calcining the xerogel at 200° C. for 10 minutes to obtain a black precursor powder;
[0041] (5) Put the black precursor powder into a muffle furnace for a second calcination at 750°C for 10h to obtain the oxide composite material Sm 0.1 Ca 0.9 Fe 0.5 Mn 0.5 O 3-x .
Embodiment 3
[0043] Preparation of oxide composites:
[0044] (1) Dissolve 1.09g of samarium nitrate, 2.45g of calcium acetate, 3.31g of iron nitrate and 2.93g of manganese nitrate in 45mL of deionized water, then add 10.32g of citric acid as a complexing agent, and form a brownish yellow under the action of a mechanical stirrer solution to obtain a metal-citric acid solution;
[0045] (2) aging the metal-citric acid solution in a constant temperature water bath at 80°C and stirring for 3 hours under the action of a magnetic stirrer to obtain a precursor gel;
[0046] (3) putting the precursor gel into a blast drying oven and drying at 80°C for 10 hours to obtain a dry gel;
[0047] (4) pre-calcining the xerogel at 200° C. for 10 minutes to obtain a black precursor powder;
[0048] (5) Put the black precursor powder into a muffle furnace for a second calcination at 750°C for 10h to obtain the oxide composite material Sm 0.15 Ca 0.85 Fe 0.5 Mn 0.5 O 3-x .
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