Preparation of Z-type BiVO4-Au/g-C3N4 photocatalytic material and application of material to photocatalytic reduction of CO2
A photocatalytic material and photocatalytic technology, applied in the field of composite materials and photocatalysis, can solve the problems of small specific surface area, easy and fast recombination of photogenerated electron-holes, low visible light utilization efficiency, etc., to optimize the reduction performance and increase the yield.
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Embodiment 1
[0026] 1. Preparation of photocatalytic materials
[0027] (1) Weigh 0.005mol of Bi(NO 3 )·5H 2 O and 0.005mol of NH 4 VO 3 respectively dissolved in 2mol / L HNO 3 and 2mol / L NaOH solution to obtain solutions A and B, then add B solution dropwise to A to form a yellow suspension, then adjust the pH of the solution to 7 with NaOH solution, stir for 30min, and then transfer the suspension to a high-pressure hydrothermal kettle In the reaction at 180°C for 10h. After it was cooled to room temperature, it was taken out and centrifuged, washed three times with deionized water and ethanol solution, and dried in vacuum at 60 °C for 8 h to obtain BiVO 4 catalyst.
[0028] (2) Weigh 5g of urea into a covered crucible, transfer it to a temperature-programmed muffle furnace, raise the temperature to 550°C at a heating rate of 4°C / min, and calcine at a constant temperature for 4h. After cooling, grind to obtain g-C 3 N 4 Powder; in g-C 3 N 4 Quality score W (Au) = 0.5% chloroaur...
Embodiment 2
[0033] 1. Preparation of photocatalytic materials
[0034] (1) Weigh 0.005mol of Bi(NO 3 )·5H 2 O and 0.005mol of NH 4 VO 3 respectively dissolved in 2mol / L HNO 3 and 2mol / L NaOH solution to obtain solutions A and B, then add B solution dropwise to A to form a yellow suspension, then adjust the pH of the solution to 8 with NaOH solution, stir for 30min, and then transfer the suspension to a high-pressure hydrothermal kettle In the reaction at 180°C for 12h. After it was cooled to room temperature, it was taken out and centrifuged, washed three times with deionized water and ethanol solution, and dried in vacuum at 60 °C for 8 h to obtain BiVO 4 catalyst.
[0035] (2) Weigh 3g of urea into a covered crucible, transfer it to a temperature-programmed muffle furnace, raise the temperature to 550°C at a heating rate of 4°C / min, and calcine at a constant temperature for 4h. After cooling, grind to obtain g-C 3 N 4 Powder; in g-C 3 N 4 Quality score W (Au) = 1% chloroauric...
Embodiment 3
[0040] 1. Preparation of photocatalytic materials
[0041] (1) Weigh 0.005mol of Bi(NO 3 )·5H 2 O and 0.005mol of NH 4 VO 3 respectively dissolved in 2mol / L HNO 3 and 2mol / L NaOH solution to obtain solutions A and B, then add B solution dropwise to A to form a yellow suspension, then adjust the pH of the solution to 9 with NaOH solution, stir for 30min, and then transfer the suspension to a high-pressure hydrothermal kettle In the reaction at 180°C for 12h. After it was cooled to room temperature, it was taken out and centrifuged, washed 4 times with deionized water and ethanol solution, and dried in vacuum at 60 °C for 9 h to obtain BiVO 4 catalyst.
[0042] (2) Weigh 7g of urea into a covered crucible, transfer it to a temperature-programmed muffle furnace, raise the temperature to 550°C at a heating rate of 4°C / min, and calcine at a constant temperature for 4h. After cooling, grind to obtain g-C 3 N 4 Powder; in g-C 3 N 4 Quality score W (Au) =1.5% chloroauric ac...
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