Preparation method capable of controlling oriented growth of bismuth oxybromide photocatalysts
A technology of photocatalyst and bismuth oxybromide, applied in the field of photocatalysis, can solve the problems of easy recombination and low photocatalytic efficiency, and achieve the effects of simple process, low cost and easy operation
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Embodiment example 1
[0020] Embodiment example 1: a kind of preparation method of controlling bismuth oxybromide photocatalyst orientation growth of the present invention, concrete preparation process is:
[0021] Dissolve 2mmol of bismuth nitrate in 5mL of glacial acetic acid to form a transparent solution A; dissolve 2mmol of potassium bromide in 10mL of deionized water, slowly add to solution A, continue to stir for 0.5h, and then transfer to 50mL of polytetrafluoroethylene In a lined stainless steel autoclave, react at 160°C for 12h, centrifuge the obtained product, and dry it in vacuum at 50°C to obtain bismuth oxybromide photocatalyst BiOBr-1.
Embodiment 2
[0022]Implementation example 2: a kind of preparation method of controlling bismuth oxybromide photocatalyst orientation growth of the present invention, concrete preparation process is:
[0023] Dissolve 2mmol of bismuth nitrate in 5mL of glacial acetic acid to form a transparent solution A; dissolve 0.1g of PVP in 20mL of deionized water, and slowly add it to solution A, stir for 0.5h, and record the formed solution as solution B; Dissolve potassium bromide in 10mL deionized water, slowly add it into solution B, continue to stir for 0.5h, then transfer it to a 50mL stainless steel autoclave lined with polytetrafluoroethylene, react at 160°C for 12h, and centrifuge the obtained product , and dried under vacuum at 50°C to obtain bismuth oxybromide photocatalyst BiOBr-2.
Embodiment 3
[0024] Implementation example 3: a kind of preparation method of controlling bismuth oxybromide photocatalyst orientation growth of the present invention, concrete preparation process is:
[0025] Dissolve 2mmol of bismuth nitrate in 5mL of glacial acetic acid to form a transparent solution A; dissolve 0.5g of PVP in 20mL of deionized water, slowly add it to solution A, stir for 0.5h, and record the formed solution as solution B; Dissolve potassium bromide in 10mL deionized water, slowly add it into solution B, continue to stir for 0.5h, then transfer it to a 50mL stainless steel autoclave lined with polytetrafluoroethylene, react at 160°C for 12h, and centrifuge the obtained product , and dried under vacuum at 50°C to obtain bismuth oxybromide photocatalyst BiOBr-3.
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