Method for preparing high-efficiency Bi-containing photocatalyst and Bi-containing photocatalyst prepared by method
A photocatalyst and high-efficiency technology, applied in chemical instruments and methods, physical/chemical process catalysts, chemical/physical processes, etc., can solve the problems of low utilization rate of NaOH, large amount of NaOH, difficult sewage treatment, etc., to improve photocatalysis Oxidation activity, improving photocatalytic oxidation ability, and increasing the effect of application range
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[0028] (1) Preparation of titanium source solution: configure nitric acid solution, and dissolve titanium dioxide in the nitric acid solution;
[0029] (2) Preparation of bismuth source solution: Bi(NO 3 ) 3 ·5H 2 O is a bismuth source, which is dissolved in nitric acid solution;
[0030] (3) Reaction: Quantitatively measure the titanium source solution and the bismuth source solution, continue to stir vigorously after mixing, and leave to settle after the reaction;
[0031] (4) Filtration and collection: wash and filter the above precipitate, dry in an oven, cool to room temperature and collect for later use;
[0032] (5) Roasting: The intermediate product collected above is roasted in a muffle furnace to obtain the final product BTO.
[0033] Wherein, the concentration of the nitric acid solution in the steps (1) and (2) is 0.1-3 mol / L.
[0034] Wherein, the titanium dioxide in the step (1) is P25 titanium dioxide or industrial titanium dioxide.
[0035] Wherein, in th...
Embodiment 1
[0049] First prepare HNO according to the molar concentration of 2mol / L 3 solution. Add 60mL of the above nitric acid solution into a 250mL beaker, then accurately weigh 2.0g of P25 or titanium dioxide and add it into it, and disperse it evenly under ultrasonic conditions, and record it as solution A, that is, the titanium source solution. In another 250mL beaker, add 3.03g Bi(NO 3 ) 3 ·5H 2 O and 2mol / L HNO 3 Solution, after the bismuth nitrate is completely dissolved under ultrasonic conditions, keep it for later use, and record it as solution B, that is, the bismuth source solution. Then follow R Bi =Bi / (Bi+Ti)=0.2 Add solution B to solution A. At this time, solution B is added dropwise. The resulting suspension is stirred vigorously by magnetic force for 24 hours, and then left to stand for 24 hours. Then the resulting precipitate was filtered, dried in an oven at 70°C for 8h, and finally the dried sample was calcined in a muffle furnace at 600°C for 6h to obtain a l...
Embodiment 2
[0051] First prepare HNO according to the molar concentration of 2mol / L 3 solution. Add 60mL of the above-mentioned nitric acid solution into a 250mL beaker, then accurately weigh 2.0g of P25 into it, and disperse it evenly under ultrasonic conditions, which is recorded as solution A. In another 250mL beaker, add 12.13g Bi(NO 3 ) 3 ·5H 2 O and 2mol / L HNO 3 Solution, after the bismuth oxide is completely dissolved under ultrasonic conditions, keep it for future use, and record it as solution B. Then follow R Bi =Bi / (Bi+Ti)=0.5 ratio Add B solution to the above A solution. At this time, B solution is added dropwise. The resulting suspension is stirred vigorously by magnetic force for 24 hours, and then left to stand for 24 hours. Then the resulting precipitate was washed and filtered, dried in an oven at 110°C for 3h, and finally the dried sample was calcined in a muffle furnace at 600°C for 6h to obtain a light yellow powder, which is the Bi-containing photocatalyst Bi 2...
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