Bismuth tungstate/bismuth sulfide/molybdenum disulfide heterojunction ternary composite material and preparation method and application thereof
A technology of molybdenum disulfide and composite materials, applied in chemical instruments and methods, physical/chemical process catalysts, water treatment of special compounds, etc., can solve problems such as low photocatalytic efficiency and weak surface adsorption capacity
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Embodiment 1
[0037] (1) Spherical Bi 2 WO 6 preparation of
[0038] In spherical Bi 2 WO 6 In the synthesis of the precursor, solution A and solution B were prepared. Solution A, 2mmol Bi(NO 3 ) 3 ·5H 2 O and 4g of PVP K30 were added to a mixed solution of 50mL of water, absolute ethanol, and glacial acetic acid (3:1:1 by volume), and stirred at room temperature until the solution was clear. Solution B, in 20mL H 2 Add 1mmol Na to O 2 WO 4 2H 2 O, ultrasound for 30 minutes. Then add solution B dropwise to solution A, stir for 60 minutes to obtain a uniform suspension, transfer it to a 100mL polytetrafluoroethylene-lined autoclave, react with solvent heat at 180°C for 18 hours, and cool to room temperature naturally , through centrifugation, washing, drying, and grinding, the pale yellow Bi 2 WO 6 powder.
[0039] (2) Spherical Bi 2 WO 6 / Bi 2 S 3 / MoS 2 Preparation of heterojunction ternary composites
[0040] 200mg Bi 2 WO 6 Disperse the powder into 40mL water, add ...
Embodiment 2
[0042] (1) Spherical Bi 2 WO 6 preparation of
[0043] In spherical Bi 2 WO 6 In the synthesis of the precursor, solution A and solution B were prepared. Solution A, 2mmol Bi(NO 3 ) 3 ·5H 2 O and 4g of PVP K30 were added to a mixed solution of 50mL of water, absolute ethanol, and glacial acetic acid (3:1:1 by volume), and stirred at room temperature until the solution was clear. Solution B, in 20mL H 2 Add 1mmol Na to O 2 WO 4 2H 2 O, ultrasound for 30 minutes. Then add solution B dropwise to solution A, stir for 60 minutes to obtain a uniform suspension, transfer it to a 100mL polytetrafluoroethylene-lined autoclave, react with solvent heat at 180°C for 18 hours, and cool to room temperature naturally , through centrifugation, washing, drying, and grinding, the pale yellow Bi 2 WO 6 powder.
[0044] (2) Spherical Bi 2 WO 6 / Bi 2 S 3 / MoS 2 Preparation of heterojunction ternary composites
[0045] 200mg Bi 2 WO 6 Disperse the powder into 40mL water, add ...
Embodiment 3
[0047] (1) Spherical Bi 2 WO 6 preparation of
[0048] In spherical Bi 2 WO 6 In the synthesis of the precursor, solution A and solution B were prepared. Solution A, 2mmol Bi(NO 3 ) 3 ·5H 2 O and 4g of PVP K30 were added to a mixed solution of 50mL of water, absolute ethanol, and glacial acetic acid (3:1:1 by volume), and stirred at room temperature until the solution was clear. Solution B, in 20mL H 2 Add 1mmol Na to O 2 WO 4 2H 2 O, ultrasound for 30 minutes. Then add solution B dropwise to solution A, stir for 60 minutes to obtain a uniform suspension, transfer it to a 100mL polytetrafluoroethylene-lined autoclave, react with solvent heat at 180°C for 18 hours, and cool to room temperature naturally , through centrifugation, washing, drying, and grinding, the pale yellow Bi 2 WO 6 powder.
[0049] (2) Spherical Bi 2 WO 6 / Bi 2 S 3 / MoS 2 Preparation of heterojunction ternary composites
[0050] 200mg Bi 2 WO 6 Disperse the powder into 40mL water, add ...
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