Preparation method for ordered mesoporous non-noble metal-nitrogen-graphitized carbon material
A non-precious metal and graphitized carbon technology, applied in chemical instruments and methods, chemical/physical processes, physical/chemical process catalysts, etc., can solve the problem of reducing the optimal amount of metal used, reducing the overall nitrogen density of materials, and accessing active sites Reduce other problems, achieve superior catalytic stability and methanol resistance, high nitrogen density, and good electrical conductivity
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Embodiment 1
[0031] a. Synthesis of filling materials
[0032] Add 5g of o-phenanthroline into 60ml of ethanol, add 1.57g of cobalt acetate under stirring, stir and dissolve, add 1g of mesoporous silica SBA-15, and continue stirring at room temperature until dry. Then, it was dried at a constant temperature of 60°C.
[0033] b. High temperature roasting of filling materials
[0034] The dry filling material is placed in a quartz tube, heated in a high-purity nitrogen (40ml / min) atmosphere at 500°C, and kept for 6 hours. The black powder is the carbonized filling material.
[0035] c. Removal of the mesoporous silica template
[0036] The carbonized filling material was stirred with 50 mL of 25% hydrofluoric acid solution for 10 h, washed with deionized water, and dried to obtain an ordered mesoporous non-noble metal-nitrogen-graphitized carbon material.
Embodiment 2
[0038] a. Synthesis of filling materials
[0039] Add 0.5g of o-phenanthroline to 30ml of ethanol, add 0.196g of cobalt acetate under stirring, stir to dissolve, add 1g of mesoporous silica SBA-15, and continue stirring at room temperature until dry. Then, it was dried at a constant temperature of 60°C.
[0040] b. High temperature roasting of filling materials
[0041] The dry filling material is placed in a quartz tube, heated in a high-purity nitrogen (40ml / min) atmosphere at 700°C, and kept for 2 hours. The black powder is the carbonized filling material.
[0042] c. Removal of the mesoporous silica template
[0043] The carbonized filling material was stirred with 30 mL of 25% hydrofluoric acid solution for a certain period of time for 20 h, washed with deionized water, and dried to obtain an ordered mesoporous non-noble metal-nitrogen-graphitized carbon material.
Embodiment 3
[0045] a. Synthesis of filling materials
[0046] Add 1g of o-phenanthroline into 60ml of ethanol, add 1.26g of cobalt acetate under stirring, stir and dissolve, add 1g of mesoporous silica SBA-15, and continue stirring at room temperature until dry. Then, it was dried at a constant temperature of 60°C.
[0047] b. High temperature roasting of filling materials
[0048] The dry filling material is placed in a quartz tube, heated in a high-purity nitrogen (40ml / min) atmosphere at 550°C, and kept for 5 hours. The black powder is the carbonized filling material.
[0049] c. Removal of the mesoporous silica template
[0050] The carbonized filling material was stirred with 40 mL of 25% hydrofluoric acid solution for 24 hours, washed with deionized water, and dried to obtain an ordered mesoporous non-noble metal-nitrogen-graphitized carbon material.
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