Construction method of indium oxide photocatalysis composite material
A technology of indium trioxide and composite materials is applied in the field of construction of indium trioxide photocatalytic composite materials, which can solve problems such as energy bandwidth, and achieve the effects of low equipment requirements, high specific surface area and excellent catalytic effect.
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Embodiment 1
[0024] Weigh 1.6g of indium nitrate and 1.5g of spherical urea, dissolve in 40ml, and stir for 30min. Afterwards, the mixed solution was transferred to a hydrothermal reaction kettle, and reacted at 120° C. for 12 h. After cooling, wash and centrifuge, and dry at 60°C for 12 hours to obtain the precursor of diindium trioxide. The obtained diindium trioxide precursor was put into a tube furnace, and calcined at 550° C. for 0.5 h with a heating rate of 2° C. / min to obtain diindium trioxide. Weigh 5g of citric acid, dissolve in 40ml of deionized water, and stir for 30min. Afterwards, the mixed solution was transferred to a hydrothermal reaction kettle and reacted at 160° C. for 6 h. After cooling, 10 ml of the obtained solution was taken, and 10 mg of the prepared indium trioxide was added, and stirred for 30 minutes to obtain a photocatalytic composite material of indium trioxide.
Embodiment 2
[0026] Weigh 1.7g of indium nitrate and 1.52g of spherical urea, dissolve in 40ml, and stir for 30min. Afterwards, the mixed solution was transferred to a hydrothermal reaction kettle, and reacted at 130° C. for 13 h. After cooling, wash and centrifuge, and dry at 60°C for 12 hours to obtain the precursor of diindium trioxide. The obtained diindium trioxide precursor was put into a tube furnace, and calcined at 580° C. for 1 hour with a heating rate of 2° C. / min to obtain diindium trioxide. Weigh 5.5g of citric acid and 8g of urea in 40ml of deionized water and stir for 30min. Afterwards, the mixed solution was transferred to a hydrothermal reactor, and reacted at 170° C. for 6 h. After cooling, 10 ml of the obtained solution was taken, and 12 mg of the obtained indium trioxide was added, and stirred for 30 minutes to obtain a photocatalytic composite material of indium trioxide.
Embodiment 3
[0028] Weigh 1.8g of indium nitrate and 1.54g of spherical urea, dissolve in 40ml, and stir for 30min. Afterwards, the mixed solution was transferred to a hydrothermal reactor, and reacted at 140° C. for 14 h. After cooling, wash and centrifuge, and dry at 60°C for 12 hours to obtain the precursor of diindium trioxide. The obtained diindium trioxide precursor was put into a tube furnace, and calcined at 600° C. for 2 hours with a heating rate of 3° C. / min to obtain diindium trioxide. Weigh 6g of citric acid, dissolve 26g of ammonia water in 40ml of deionized water, and stir for 30min. Afterwards, the mixed solution was transferred to a hydrothermal reactor, and reacted at 180° C. for 8 h. After cooling, 10 ml of the obtained solution was taken, and 16 mg of the prepared indium trioxide was added, and stirred for 30 minutes to obtain a photocatalytic composite material of indium trioxide.
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