A kind of preparation method of non-precious metal catalyst for hydroelectric desorption of oxygen
A non-precious metal and catalyst technology, which is applied in the field of preparation of non-precious metal catalysts, can solve the problems of cumbersome preparation methods, high oxygen evolution overpotential, and high cost, and achieve the effects of simple preparation methods, many surface defects, and high specific surface area
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Embodiment 1
[0033] A method for preparing a non-noble metal catalyst for electrolysis of water, the operation steps are as follows:
[0034] (1) Weigh 1.3g of 2,6-diacetylpyridine into a flat-bottomed flask, add 50ml of absolute ethanol, stir until 2,6-diacetylpyridine is completely dissolved, then add 0.9g of 1,8-diacetylpyridine Aminonaphthalene, stir until 1,8-diaminonaphthalene is completely dissolved, add 0.1g oxalic acid as a catalyst, transfer to an oil bath and raise the temperature to 60°C for synthesis, keep stirring at this temperature for 12 hours, and naturally cool to room temperature;
[0035] (2) Add 2.15 g of ferric chloride hexahydrate while stirring in the solution obtained after cooling in step (1), and stir at room temperature for complexation for 12 hours;
[0036] (3) The solution obtained after the complexation in step (2) is removed by rotary evaporation to remove the solvent, and the remaining solid matter is placed in a blast drying oven and dried at 80° C. for ...
Embodiment 2
[0041] A method for preparing a non-noble metal catalyst for electrolysis of water, the operation steps are as follows:
[0042] (1) Weigh 1.0g of 1,3-diacetylbenzene into a single-necked flask, add 125ml of absolute ethanol, stir until 1,3-diacetylbenzene is completely dissolved, then add 0.9g of 2,6-diacetylbenzene Aminopyridine, stir until 2,6-diaminopyridine is completely dissolved, add 0.08g oxalic acid as a catalyst, transfer to an oil bath and raise the temperature to 25°C for synthesis, keep stirring at this temperature for 24 hours, then cool naturally to room temperature;
[0043] (2) Add 1.29 g of ferric chloride hexahydrate while stirring in the solution obtained after cooling in step (1), and stir at room temperature for complexation for 24 hours;
[0044] (3) The solution obtained after the complexation in step (2) is removed by rotary evaporation to remove the solvent, and the remaining solid matter is placed in a blast drying oven and dried at 90 ° C for 24 hou...
Embodiment 3
[0048] A method for preparing a non-noble metal catalyst for electrolysis of water, the operation steps are as follows:
[0049] (1) Weigh 1.0g of 4,4-diacetylbiphenyl into a single-necked flask, add 200ml of absolute ethanol, stir until 1,3-diacetylbiphenyl is completely dissolved, then add 0.78g of 2,3 -Diaminopyridine, stir until the 2,3-diaminopyridine is completely dissolved, add 0.05g oxalic acid as a catalyst, transfer to an oil bath and raise the temperature to 150°C for synthesis, keep stirring at this temperature for 6 hours, then cool naturally to room temperature ;
[0050] (2) Add 1.12 g of cobalt trichloride hexahydrate while stirring in the solution obtained after cooling in step (1), and stir at room temperature for complexation for 8 hours;
[0051] (3) The solution obtained after the complexation in step (2) is removed by rotary evaporation to remove the solvent, and the remaining solid matter is placed in a blast drying oven and dried at 100 ° C for 8 hours...
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