Method for preparing nano bismuth oxide by using liquid phase precipitation method
A technology of nano-bismuth oxide and liquid phase precipitation, which is applied in the field of nano-materials, can solve the problems of long reaction cycle and high energy consumption, and achieve the effects of good shape, low preparation cost and easy control of operating conditions
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Embodiment 1
[0023] Take 14g NaOH in a beaker, add 175mL deionized water and stir to dissolve, then add 1.5g sodium lignosulfonate, and magnetically stir to dissolve evenly. Heat in a water bath until the solution temperature reaches 80°C; then add 25mL of 0.2M Bi(III) dropwise to control the formation of drops but not lines. After the solution was reacted in a constant temperature water bath for 1 hour, it was filtered and washed while it was hot, baked in a constant temperature oven at 60°C for 24 hours, and then calcined in a muffle furnace at 500°C for 3 hours. The XRD pattern of the sample is as follows figure 1 a. Scanning electron microscope picture as figure 2 .
Embodiment 2
[0025] Take 14g NaOH in a beaker, add 175mL deionized water and stir to dissolve, then add 1.0g sodium lignosulfonate, and magnetically stir to dissolve evenly. Heat in a water bath until the solution temperature reaches 80°C; then add 25mL of 0.2M Bi(III) dropwise to control the formation of drops but not lines. After the solution was reacted in a constant temperature water bath for 1 hour, it was filtered and washed while it was hot, baked in a constant temperature oven at 60°C for 22 hours, and then calcined in a muffle furnace at 500°C for 3 hours. The XRD pattern of the sample is as follows figure 1 b.
Embodiment 3
[0027] Take 14g NaOH in a beaker, add 175mL deionized water and stir to dissolve, then add 0.5g sodium lignosulfonate, and magnetically stir to dissolve evenly. Heat in a water bath until the solution temperature reaches 75°C; then add 25 mL of 0.2M Bi(III) dropwise to control the formation of drops but not lines. After the solution was reacted in a constant temperature water bath for 1 hour, it was filtered and washed while it was hot, baked in a constant temperature oven at 50°C for 20 hours, and calcined in a muffle furnace at 400°C for 3 hours. The XRD pattern of the sample is as follows figure 1 c.
[0028] figure 1 Among them, a is the XRD spectrum of the sample in Example 1, b in the figure is the XRD spectrum of the sample in Example 2, and c in the figure is the XRD spectrum of the sample in Example 3. figure 1 Among them, the sharper the peak shape, the better the crystallinity. Curve c has the best crystallinity, which shows that the lower the concentration of s...
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