Carbon nitride quantum dot/tungsten trioxide composite photocatalytic material and preparation method thereof
A technology of composite photocatalysis and tungsten trioxide, which is applied in the direction of catalyst activation/preparation, metal/metal oxide/metal hydroxide catalysts, chemical instruments and methods, etc., can solve complex preparation methods, easy aggregation of quantum dots, and problems that have not yet been solved. See the problems of tungsten trioxide composite photocatalytic materials, etc., to achieve the effect of expanding the photoresponse range, improving the separation efficiency, and reducing the probability of recombination
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[0029]The invention provides a carbon nitride quantum dot / tungsten trioxide composite photocatalytic material and a preparation method thereof. The carbon nitride quantum dot / tungsten trioxide composite photocatalytic material is formed by loading carbon nitride quantum dots on the surface of tungsten trioxide The preparation method of the dense heterojunction structure includes the following steps:
[0030](1) Preparation of carbon nitride quantum dots: Weigh sodium citrate and urea in a certain molar ratio, dissolve in deionized water after grinding, disperse ultrasonically, and transfer to a hydrothermal kettle for reaction. The reaction temperature is 160-200℃. The time is 0.5-4h, then it is cooled and filtered through a 0.22μm microfiltration membrane, dialyzed for 12-48h, and lyophilized to obtain carbon nitride quantum dots;
[0031]Among them, the molar ratio of sodium citrate and urea is 2-8:1.
[0032](2) Preparation of tungsten trioxide nanorods: Weigh a certain amount of ammonium...
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[0039]Example 1
[0040]Weigh 1.01g sodium citrate and 0.81g urea, grind for 30 minutes, dissolve in 60mL deionized water, disperse ultrasonically, transfer to a hydrothermal kettle, react at 180°C for 2h, filter through 0.22μm microfiltration membrane after cooling, and dialyze for 24h , After freeze-drying, carbon nitride quantum dots are obtained.
[0041]Weigh 3.5g of ammonium metatungstate and dissolve it in 50mL of deionized water after grinding. After ultrasonic dispersion, add a certain amount of acid to adjust the pH of the solution to 2, then transfer it to a hydrothermal kettle to react at 180°C for 24h. After cooling, wash with water and alcohol Wash each 3 times, and dry at 60°C to obtain tungsten trioxide nanorods.
[0042]Weigh 0.05g carbon nitride quantum dots into 100mL deionized water, add 1g tungsten trioxide nanorods, stir for 30min, ultrasonically disperse, put in a hydrothermal kettle for reaction at 120℃ for 2h, cool, and freeze-dry the sample at 50℃ After vacuum dryin...
Example Embodiment
[0044]Example 2
[0045]Weigh 1.01g sodium citrate and 0.81g urea, grind for 30 minutes, dissolve in 60mL deionized water, disperse ultrasonically, transfer to a hydrothermal kettle, react at 180°C for 2h, filter through 0.22μm microfiltration membrane after cooling, and dialyze for 24h , After freeze-drying, carbon nitride quantum dots are obtained.
[0046]Weigh 3.5g of ammonium metatungstate and dissolve it in 50mL of deionized water after grinding. After ultrasonic dispersion, add a certain amount of acid to adjust the pH of the solution to 2, then transfer it to a hydrothermal kettle to react at 180°C for 24h. After cooling, wash with water and alcohol Wash each 3 times, and dry at 60°C to obtain tungsten trioxide nanorods.
[0047]Weigh 0.05g carbon nitride quantum dots into 100mL deionized water, add 1g tungsten trioxide nanorods, stir for 30min, ultrasonically disperse, put in a hydrothermal kettle for reaction at 120℃ for 2h, cool, and freeze-dry the sample at 50℃ After vacuum dryin...
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