Hexagonal crystal tungsten bronze short rod nanoparticles and preparation method thereof
A technology of tungsten bronze and hexagonal crystal, which is applied in the field of tungsten bronze nano-rod particles and its preparation, can solve the problems of dark color, small shielding range, and reduced transparency of heat-insulating films, and achieve high uniformity, improve uniformity, and reduce The effect of small average size
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Embodiment 1
[0065] Preparation of Cs 0.32 WO 3 Hexagonal cesium tungsten bronze nanorod particles
[0066] ①Weigh 6.3503g of sodium tungstate, add 30ml of deionized water, fully dissolve, and quickly add 5mol / L hydrochloric acid under stirring conditions to make the pH ≤ 1, after stirring for 30min, milky yellow flocculent tungsten Acid colloidal suspension, after suction filtration, to obtain milky yellow solid colloidal tungstic acid with a certain volume; add solid colloidal tungstic acid to 120ml deionized water, stir evenly under the condition of ultrasonic vibration, and make it redisperse into a suspension solution, continue to filter, repeat three times; then use 120ml of absolute ethanol to repeat the above operation, filter three times, take out the obtained massive gel and add an appropriate amount of absolute ethanol to make the total volume 77ml, stir and redisperse under the condition of ultrasonic vibration Suspension, obtain solid colloidal tungstic acid ethanol dispersi...
Embodiment 2
[0071] Preparation of Cs 0.32 WO 3 Hexagonal cesium tungsten bronze nanorod particles
[0072] ①Preparation of solid colloidal tungstic acid ethanol dispersion: same as step ① in Example 1
[0073] ② Preparation of reaction precursor and powder synthesis
[0074] Weigh 0.6g of cesium sulfate, add it to 40ml solid colloidal tungstic acid ethanol dispersion, then measure and add 70ml of acetylacetone, finally add 4.536g of ascorbic acid, 1g of P123 inducer, stir for 2h, and obtain the reaction precursor; The reaction precursor solution was transferred into a 200ml autoclave, and reacted continuously at 190°C for 72 hours. The precipitate after the reaction was washed with water and alcohol for 3 times in sequence, and after centrifugation, it was dried at 60°C for 10 hours to obtain a blue Cs 0.32 WO 3 Hexagonal cesium tungsten bronze powder.
Embodiment 3
[0076] Preparation of Cs 0.32 WO 3 Hexagonal cesium tungsten bronze nanorod particles
[0077] ①Preparation of solid colloidal tungstic acid ethanol dispersion: same as step ① in Example 1
[0078] ② Preparation of reaction precursor and powder synthesis
[0079] Weigh 0.6g of cesium sulfate, add it to 40ml of solid colloidal tungstic acid ethanol dispersion, then measure and add 60ml of acetylacetone, finally add 10ml of acetic acid, 1g of P123 inducer, stir for 2h, and obtain the reaction precursor; The precursor solution was transferred into a 200ml autoclave, and reacted continuously at 190°C for 72 hours. The precipitate after the reaction was washed with water and alcohol for 3 times, and after centrifugation, it was dried at 60°C for 10 hours to obtain blue Cs 0.32 WO 3 Hexagonal cesium tungsten bronze powder.
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