Preparation method of porous nano material yttrium vanadate
A nanomaterial, yttrium vanadate technology, applied in the field of materials science, can solve the problems of poor catalytic effect of photocatalyst, achieve the effect of improving reaction rate and efficiency, high sample purity and simple equipment
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Embodiment 1
[0020] (1) Dissolve 5g of glucose in 40ml of deionized water to form a clear aqueous solution, then put the above aqueous solution in a 50ml hydrothermal reaction kettle, and conduct a hydrothermal reaction at 150°C for 4 hours. Then cool down to room temperature naturally, and separate the carbon spheres with a centrifuge. Wash three times with deionized water and absolute ethanol, and dry at 70°C.
[0021] (2) Weigh 0.2258g (1mmol) of Y 2 o 3 and 0.2340 g (2 mmol) of NH 4 VO 3 Dissolve in dilute nitric acid with a mass fraction of 15% to 20%. After complete dissolution, add 2.52g of citric acid (12mmol) as a chelating agent. After stirring for 1.5h, a uniform gel is formed.
[0022] (3) Take 0.05 g of the charcoal powder prepared in step (1) and add it to the gel, stir for another 3 hours, and then put it in an oven and dry it at 90°C for 12 hours. Finally, the obtained product was calcined at 350°C for 2h in a muffle furnace, and then calcined at 800°C for 3h. The fin...
Embodiment 2
[0025] 1) take by weighing the YVO of gained in 0.02g embodiment 1 4 The photocatalyst was dispersed in 100mL (10mg / L) rhodamine B (RhB) solution, and magnetically stirred for 20min in the dark.
[0026] 2) A UV lamp with a dominant wavelength of 320nm was placed 10cm directly above the glass reactor, and 2~3mL of the solution was taken every 10min after the photocatalysis started.
[0027] 3) After the collected samples were centrifuged at 10000 r / min for 10 min by a centrifuge, the RhB concentration was measured by a spectrophotometer.
[0028] 4) Weigh 0.02g of pure bismuth vanadate and repeat the first three steps of experiment.
[0029] figure 2 For the results obtained in the implementation of case 2 experiment, it can be seen from the figure that the photocatalyst prepared by the method of the present invention has a RhB degradation efficiency of 86.7% after 80min of light irradiation
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