A Rapid Synthesis of Block-shaped Ag4V2O7 Photocatalyst
A photocatalyst, block-shaped technology, applied in chemical instruments and methods, catalyst activation/preparation, physical/chemical process catalysts, etc., can solve the problems of high preparation temperature and uneven product size, and achieve stable chemical properties and product Consistent quality and mild conditions
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Embodiment 1
[0028] (1) Add 0.04g of citric acid to 20mL of 0.1mol / L vanadium pentoxide (V 2 o 5 ) aqueous solution, magnetically stirred at 90° C. for 2 h, cooled to room temperature, and mixed solution A was obtained.
[0029] (2) Mix 60mL of 0.3mol / L silver nitrate (AgNO 3 ) solution was added dropwise into the mixed solution A, and magnetically stirred for 2 h to obtain the mixed solution B.
[0030] (3) Use 0.1mol / L ammonia water to adjust the pH value of the mixed solution B to 12, then stir it magnetically for 4 hours, and conduct a microwave hydrothermal reaction at 80°C and 600W for 120 minutes. After the reaction, filter the reaction solution to obtain a precipitate. After the precipitate was filtered, it was centrifuged and washed with distilled water and ethanol, and dried in an oven at 70 °C to obtain a square Ag 4 V 2 o 7 catalyst of light.
Embodiment 2
[0032] (1) Add 0.03g of citric acid to 20mL of 0.1mol / L vanadium pentoxide (V 2 o 5 ) aqueous solution, magnetically stirred at 80° C. for 2 h, cooled to room temperature, and mixed solution A was obtained.
[0033] (2) Mix 60mL of 0.3mol / L silver nitrate (AgNO 3 ) solution was added dropwise into the mixed solution A, and magnetically stirred for 2 h to obtain the mixed solution B.
[0034] (3) Use 0.2 mol / L ammonia water to adjust the pH value of the mixed solution B to 9, then magnetically stir for 4 hours, microwave hydrothermal reaction at 95°C and 500W for 90 minutes, after the reaction, filter the reaction solution to obtain a precipitate, and the obtained After the precipitate was filtered, it was centrifuged and washed with distilled water and ethanol, and dried in an oven at 70 °C to obtain a square Ag 4 V 2 o 7 catalyst of light.
[0035] see figure 1 , through the XRD diffraction pattern, it can be clearly seen that the present invention prepares pure phase ...
Embodiment 3
[0039] (1) Add 0.02g of citric acid to 20mL of 0.1mol / L vanadium pentoxide (V 2 o 5 ) aqueous solution, magnetically stirred at 70° C. for 2 h, cooled to room temperature, and mixed solution A was obtained.
[0040] (2) Mix 60mL of 0.3mol / L silver nitrate (AgNO 3 ) solution was added dropwise into the mixed solution A, and magnetically stirred for 2 h to obtain the mixed solution B.
[0041] (3) Use 0.3 mol / L ammonia water to adjust the pH value of the mixed solution B to 6, then magnetically stir for 4 hours, microwave hydrothermal reaction at 105°C and 400W for 60 minutes, after the reaction, filter the reaction solution to obtain a precipitate, and the obtained After the precipitate was filtered, it was centrifuged and washed with distilled water and ethanol, and dried in an oven at 70 °C to obtain a square Ag 4 V 2 o 7 catalyst of light.
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