A preparation method of nanometer tungsten trioxide hollow agglomerated sphere powder
A nano-tungsten trioxide, hollow technology, applied in tungsten oxide/tungsten hydroxide, metal processing equipment, transportation and packaging, etc., can solve problems affecting the application of metal tungsten materials, achieve excellent physical and chemical properties, promote valence changes, active effect
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Embodiment 1
[0040] (1) Measure 200ml of a commercially available nitric acid solution with a mass concentration of 63% and a density of 1.4g / ml, put it in a clean beaker, and fill the volume of the solution in the beaker to 400ml with deionized water.
[0041] (2) Weigh 303g of ammonium metatungstate [(NH 4 ) 6 h 2 W 12 o 40 ] White crystalline powder, added to the beaker filled with nitric acid solution in step (1), stirred for 30 minutes to make it evenly mixed.
[0042] (3) Transfer the reaction system mixed in step (2) to a polytetrafluoroethylene-lined hydrothermal reaction kettle within 10 minutes, place it in a vacuum drying oven, and control the heating rate to 3°C / min. The hydrothermal reaction was carried out at 170°C for 15 hours to obtain a hydrothermal product.
[0043] (4) Cool the hydrothermal product obtained in step (3) to room temperature, then take it out from the hydrothermal reaction kettle, and perform repeated stirring and standing treatment twice, wherein each...
Embodiment 2
[0048] (1) Measure 215ml of a commercially available nitric acid solution with a mass concentration of 63% and a density of 1.4g / ml, put it in a clean beaker, and fill the volume of the solution in the beaker to 400ml with deionized water.
[0049] (2) Weigh a certain amount of ammonium metatungstate [(NH 4 ) 6 h 2 W 12 o 40 ] White crystalline powder, added to the beaker filled with nitric acid solution in step (1), stirred for 30 minutes to make it evenly mixed.
[0050] (3) Transfer the reaction system mixed in step (2) to a polytetrafluoroethylene-lined hydrothermal reaction kettle within 10 minutes, place it in a vacuum drying oven, and control the heating rate to 4°C / min. The hydrothermal reaction was carried out at 170°C for 15 hours to obtain a hydrothermal product.
[0051] (4) Cool the hydrothermal product obtained in step (3) to room temperature, then take it out from the hydrothermal reaction kettle, and perform repeated stirring and standing treatment for 3 t...
Embodiment 3
[0056] (1) Measure 250ml of a commercially available nitric acid solution with a mass concentration of 63% and a density of 1.4g / ml, put it in a clean beaker, and fill the volume of the solution in the beaker to 400ml with deionized water.
[0057] (2) Weigh 303g of ammonium metatungstate [(NH 4 ) 6 h 2 W 12 o 40 ] White crystalline powder, added to the beaker filled with nitric acid solution in step (1), stirred for 30 minutes to make it evenly mixed.
[0058] (3) Transfer the reaction system mixed in step (2) to a polytetrafluoroethylene-lined hydrothermal reaction kettle within 10 minutes, place it in a vacuum drying oven, and control the heating rate to 5°C / min. The hydrothermal reaction was carried out at 180°C for 20 hours to obtain a hydrothermal product.
[0059] (4) Cool the hydrothermal product obtained in step (3) to room temperature, then take it out from the hydrothermal reaction kettle, and perform repeated stirring and standing treatment twice, wherein each...
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Abstract
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