Preparation method of one-dimensional porous carbon nanotube
A technology of porous carbon and nanotubes, applied in the direction of carbon nanotubes, nanocarbons, chemical instruments and methods, etc., can solve the problem of reducing the number of mesopores, and achieve the effect of an environmentally friendly preparation process
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Embodiment 1
[0043] (1) Take 80.0 mg of ZnO nanowires and add them to an Erlenmeyer flask filled with a mixed solvent of DMF and water (64 mL, volume ratio 3:1), ultrasonicate for 20 min at room temperature to fully diffuse, and then add 0.41 g of 2-methyl For imidazole, after ultrasonication for 2-3min, add 18.0mg of cobalt salt and mix evenly, pour the solution in the conical flask into a hydrothermal kettle, and place it in a 50°C oven to react for 4h. After the reaction, centrifuge, wash and dry , to obtain the ZnO@Zn / Co-ZIF precursor.
[0044] (2) The ZnO@Zn / Co-ZIF precursor obtained in step 1) was placed in a high-temperature tube furnace, and the temperature was raised to 800 °C at a rate of 5 °C / min in a nitrogen atmosphere with an inert gas flow rate of 50 mL / min. After carbonization at 900° C. for 3 h, it was naturally cooled to room temperature to obtain the nitrogen-cobalt co-doped one-dimensional porous carbon nanotube (Co / NCNT) of the present invention.
[0045] from figure...
Embodiment 2
[0047] (1) Take 80.0 mg of ZnO nanowires and add them to an Erlenmeyer flask filled with a mixed solvent of DMF and water (64 mL, volume ratio 2:1), ultrasonicate for 20 min at room temperature to fully diffuse, and then add 1.6 g of 2-methyl For imidazole, after ultrasonication for 2-3min, add 12.0mg of cobalt salt and mix evenly, pour the solution in the conical flask into a hydrothermal kettle, and place it in an oven at 60°C for 3h. After the reaction, centrifuge, wash and dry , to obtain the ZnO@Zn / Co-ZIF precursor.
[0048] (2) The ZnO@Zn / Co-ZIF precursor obtained in step 1) was placed in a high-temperature tube furnace, and the temperature was raised to 800 °C at a rate of 5 °C / min in a nitrogen atmosphere with an inert gas flow rate of 50 mL / min. After carbonization at 800° C. for 3 h, it was naturally cooled to room temperature to obtain the nitrogen-cobalt co-doped one-dimensional porous carbon nanotube (Co / NCNT) of the present invention.
Embodiment 3
[0050] (1) Take 80.0 mg of ZnO nanowires and add them to an Erlenmeyer flask filled with a mixed solvent of DMF and water (64 mL, volume ratio 3:1). For imidazole, after ultrasonication for 2-3min, add 8.0mg of cobalt salt and mix evenly, pour the solution in the conical flask into a hydrothermal kettle, and place it in an oven at 70°C for 2h. After the reaction, centrifuge, wash and dry , to obtain the ZnO@Zn / Co-ZIF precursor.
[0051] (2) The ZnO@Zn / Co-ZIF precursor obtained in step 1) was placed in a high-temperature tube furnace, and the temperature was raised to 900 °C at a rate of 5 °C / min in a nitrogen atmosphere with an inert gas flow rate of 50 mL / min. After carbonization at 900° C. for 2 h, it was naturally cooled to room temperature to obtain the nitrogen-cobalt co-doped one-dimensional porous carbon nanotube (Co / NCNT) of the present invention.
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