Porous dual-metal hydroxide catalyst for electric catalysis of alcohol selective oxidation and preparation method and application thereof
A hydroxide and catalyst technology, applied in the direction of metal/metal oxide/metal hydroxide catalyst, catalyst activation/preparation, physical/chemical process catalyst, etc., can solve the problem of insufficient electrode specific surface area and low electrocatalytic oxidation performance , limited effective catalytic area, etc., to achieve the effect of improving catalytic activity and stability, broad application prospects, and low cost
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Embodiment 1
[0030] Example 1: Porous Ni 0.75 Fe 0.75 (OH) x Synthesis of / CF
[0031] 1) The carbon cloth (4cm×2cm) was ultrasonicated for 30 min in acetone, absolute ethanol, deionized water, and aqueous nitric acid solution (4mol / L nitric acid concentration) in order to remove impurities on the surface of the carbon cloth substrate. Then take out the carbon cloth and rinse the nitric acid on the carbon cloth with deionized water, and finally dry it in vacuum at 60°C to obtain the pretreated carbon cloth for subsequent use;
[0032] 2) Weigh 218.25mg of nickel nitrate, 303.01mg of ferric nitrate and 450mg of urea into 40mL of distilled water, and ultrasonically disperse them evenly for 30 minutes to obtain a precursor solution;
[0033] 3) Add the precursor solution obtained in step 2) and the pretreated carbon cloth (4cm×2cm) obtained in step 1) into the hydrothermal kettle, and raise the temperature to 120°C under microwave radiation (put the hydrothermal kettle in the microwave de...
Embodiment 2
[0036] Example 2: Porous Ni 0.75 Cu 0.75 (OH) x Synthesis of / CF
[0037] 1) Sonicate the carbon cloth (4cm×2cm) in acetone, absolute ethanol, deionized water, and nitric acid aqueous solution (nitric acid concentration is 4mol / L) for 30min in order to remove impurities on the surface of the carbon cloth substrate. Then take out the carbon cloth and rinse the nitric acid on the carbon cloth with deionized water, and finally dry it in vacuum at 60°C to obtain the pretreated carbon cloth for subsequent use;
[0038] 2) Weigh 218.25 mg of nickel nitrate, 181.2 mg of copper nitrate and 450 mg of urea into 40 mL of distilled water, and ultrasonically disperse them evenly for 30 minutes to obtain a precursor solution;
[0039] 3) Add the precursor solution obtained in step 2) and the pretreated carbon cloth (4cm×2cm) obtained in step 1) into the hydrothermal kettle, and raise the temperature to 120°C under microwave radiation (put the hydrothermal kettle in the microwave device)...
Embodiment 3
[0042] Embodiment 3: Porous Ni 0.75 co 0.75 (OH) x Synthesis of / CF
[0043] 1) Sonicate the carbon cloth (4cm×2cm) in acetone, absolute ethanol, deionized water, and nitric acid aqueous solution (nitric acid concentration is 4mol / L) for 30min in order to remove impurities on the surface of the carbon cloth substrate. Then take out the carbon cloth and rinse the nitric acid on the carbon cloth with deionized water, and finally dry it in vacuum at 60°C to obtain the pretreated carbon cloth for subsequent use;
[0044] 2) Weigh 218.25 mg of nickel nitrate, 218.25 mg of cobalt nitrate and 450 mg of urea into 40 mL of distilled water, and ultrasonically disperse them evenly for 30 minutes to obtain a precursor solution;
[0045] 3) Add the precursor solution obtained in step 2) and the pretreated carbon cloth (4cm×2cm) obtained in step 1) into the hydrothermal kettle, and raise the temperature to 120°C under microwave radiation (put the hydrothermal kettle in the microwave dev...
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