a flake 2 w 3 o 12 synthesis method
A technology of Y2W3O12 and synthesis method, applied in the field of material chemistry, to achieve the effects of simple process, compensation of thermal expansion, and stable shape control
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Embodiment 1
[0010] Dissolve 0.225mol / L ammonium tungstate and 0.1-0.15mol / L yttrium nitrate in N,N-dimethylformamide, add 3 mol / L oxalic acid and 0.2mol / L α-naphthalenesulfonic acid, stir well, Move the solution into a hydrothermal reaction kettle with a polytetrafluoroethylene liner, tighten the seal, and put it in a constant temperature oven at 220°C for 8 hours; after the reaction, filter the precipitate and wash it repeatedly with deionized water until the pH value is 7 ~8; Use centrifuge sedimentation or suction filtration equipment to filter and separate the sediment, put it in an oven at 70 ° C to dry to obtain figure 1 The final product shown is flake Y 2 W 3 o 12 .
Embodiment 2
[0012] Dissolve 0.225mol / L ammonium metatungstate and 0.15mol / L yttrium nitrate in N,N-dimethylformamide, add 2mol / L oxalic acid and 0.15mol / L β-naphthalenesulfonic acid, stir well, and transfer the solution into In a hydrothermal reaction kettle with a polytetrafluoroethylene liner, tighten the seal, put it in a constant temperature oven at 200°C and let it stand for 12 hours to react; after the reaction, filter the precipitate and wash it repeatedly with deionized water until the pH value is 7-8; Use centrifuge sedimentation or suction filtration equipment to filter and separate the precipitate, and put it in an oven at 70 ° C to dry to obtain the final product sheet Y 2 W 3 o 12 .
Embodiment 3
[0014] Dissolve 0.15mol / L sodium tungstate and 0.1mol / L yttrium chloride in N,N-dimethylformamide, add 1.5mol / L oxalic acid and 0.15mol / L 1,5-dinaphthalenesulfonic acid, stir Evenly, move the solution into a hydrothermal reaction kettle with a polytetrafluoroethylene liner, tighten the seal, and put it in a constant temperature oven at 220°C for 10 hours; after the reaction, filter the precipitate and wash it repeatedly with deionized water until the pH The value is 7~8; use centrifuge sedimentation or suction filtration equipment to filter and separate the precipitate, put it in an oven at 60°C and dry it to get the final product sheet Y 2 W 3 o 12 .
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