Floatable photocatalyst for inhibiting blue algae in water as well as preparation method and application of photocatalyst
A photocatalyst and water suppression technology, applied in catalyst activation/preparation, chemical instruments and methods, physical/chemical process catalysts, etc., can solve problems such as unfavorable reuse, difficult catalyst recovery, insufficient light utilization rate, etc., and achieve excellent photoelectricity. Conversion efficiency, excellent visible light photocatalytic activity, and the effect of improving photocatalytic performance
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[0031] The present invention also provides a preparation method of the photocatalyst described in the above technical solution, comprising the following steps:
[0032] Bismuth nitrate is mixed with ethylene glycol methyl ether to obtain a bismuth nitrate solution;
[0033] Mixing thiourea, potassium bromide, ethylene glycol methyl ether and expanded perlite to obtain a mixed material liquid;
[0034] Adding the bismuth nitrate solution dropwise to the mixture liquid to obtain a suspension;
[0035] The suspension undergoes solvothermal reaction to obtain a floating photocatalyst that inhibits cyanobacteria in water.
[0036] The invention mixes bismuth nitrate and ethylene glycol methyl ether to obtain a bismuth nitrate solution. In the present invention, the concentration of the bismuth nitrate solution is preferably 0.1-0.3 mol / L, more preferably 0.2-0.25 mol / L. In the present invention, the mixing is preferably ultrasonic, and the present invention has no special limita...
Embodiment 1
[0051] Weigh 1mmol Bi(NO 3 ) 3 ·5H 2 O was dissolved in 10 mL of ethylene glycol methyl ether, and ultrasonicated for 15 minutes to obtain a colorless bismuth nitrate solution; 2.4 mmol of thiourea and 0.7 mmol of KBr were dissolved in 30 mL of ethylene glycol methyl ether, ultrasonicated for 15 min, and stirred until a colorless and transparent solution was obtained. Weigh 1 g of EP and add it to the colorless transparent solution, and stir mechanically for 30 minutes to obtain the mixture. Under mechanical stirring, add the bismuth nitrate solution dropwise to the mixture, mix well to obtain a yellow EP suspension, and then let it stand for 30 minutes. Transfer to a high-pressure reactor and react at 120°C for 12 hours. After natural cooling, filter the sample with suction and wash with a large amount of deionized water, and dry it at 60°C to obtain a brown EP-Bi 2 S 3 / BiOBr.
Embodiment 2
[0053] Weigh 1.5mmol Bi(NO 3 ) 3 ·5H 2 O was dissolved in 10 mL of ethylene glycol methyl ether, and ultrasonicated for 15 minutes to obtain a colorless bismuth nitrate solution; 2.4 mmol of thiourea and 0.7 mmol of KBr were dissolved in 30 mL of ethylene glycol methyl ether, ultrasonicated for 15 min, and stirred until a colorless and transparent solution was obtained. Weigh 1 g of EP and add it to the colorless transparent solution, and stir mechanically for 30 minutes to obtain the mixture. Under mechanical stirring, add the bismuth nitrate solution dropwise to the mixture, mix well to obtain a yellow EP suspension, and then let it stand for 30 minutes. Transfer to a high-pressure reactor and react at 130°C for 18 hours. After natural cooling, filter the sample with suction and wash with a large amount of deionized water, and dry it at 60°C to obtain a brown EP-Bi 2 S 3 / BiOBr.
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