Method for preparing microbial fuel cell anode electrodes from agricultural wastes
A technology of agricultural waste and fuel cells, which is applied in the direction of battery electrodes, circuits, electrical components, etc., can solve the problems that the specific surface area is difficult to further increase and the steps are complicated, and achieve strong functionality, high raw material utilization, and high specific surface area. Effect
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Embodiment 1
[0040] Dry the sample, and react for 30 minutes in a nitrogen atmosphere with a heating rate of 10°C / min and 400°C, and control the nitrogen flow rate at 600Ml / min to carbonize the sample, then take it out and grind it to 60 mesh, and soak it in 5wt% HCl for 6h , wash to neutral. Soak in 3wt% HF for 6h, wash until neutral, and dry; mix and grind the sample with KOH to 100 mesh, move it to a nickel crucible, and set the activation conditions as follows: temperature setting 700°C, temperature 1h, ratio 1:4, the obtained activated porous carbon material is marked as D-700-4-1.
Embodiment 2
[0042] Dry the sample, and react for 30 minutes in a nitrogen atmosphere with a heating rate of 10°C / min and 400°C, and control the nitrogen flow rate at 600Ml / min to carbonize the sample, then take it out and grind it to 60 mesh, and soak it in 5wt% HCl for 6h , wash to neutral. Soak in 3wt% HF for 6h, wash until neutral, and dry; mix and grind the sample with KOH to 100 mesh, move to a nickel crucible, and set the activation conditions as follows: temperature setting 800°C, temperature 1h, ratio 1:2, the activated porous carbon material was obtained, marked as D-800-2-1.
Embodiment 3
[0044] Dry the sample, and react for 30 minutes in a nitrogen atmosphere with a heating rate of 10°C / min and 400°C, and control the nitrogen flow rate at 600Ml / min to carbonize the sample, then take it out and grind it to 60 mesh, and soak it in 5wt% HCl for 6h , wash to neutral. Soak in 3wt% HF for 6h, wash until neutral, and dry. Mix and grind the sample with KOH to 100 mesh, move it to a nickel crucible, and set the activation conditions as follows: temperature setting 800°C, temperature 1h, ratio 1:3, and the activated porous carbon material is obtained, marked as D -800-3-1.
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