A low-cost simple preparing method for nitrogen-doped porous charcoal with a high specific surface area
A high specific surface area, nitrogen doping technology, applied in chemical instruments and methods, inorganic chemistry, non-metallic elements, etc., can solve the problems of complex preparation, increased nitrogen loading process links, difficult to achieve nitrogen loading, etc. Simple, good wettability, stable effect
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Publication Date
- 2017-03-22
- Estimated Expiration
- Not applicable · inactive patent
Abstract
Description
technical field
[0001] The invention relates to a low-cost and simple preparation method of nitrogen-doped porous carbon with high specific surface area, which is especially suitable for high specific capacitance and high specific power supercapacitors with a specific surface area of 600-2100m 2 / g of carbonaceous electrode materials. Background technique
[0002] Porous carbon materials are widely used in the fields of electric double layer supercapacitor electrode materials and adsorption materials due to their excellent stability, electrical conductivity, high specific surface area, and low cost. In electric double layer capacitors, the specific capacitance is mainly related to the pore structure, specific surface area and heteroatoms contained in the electrode material. The larger the effective adsorption specific surface area of the electrode material, the more reasonable the pore structure is, which is the basis for the adsorption of electrons in the electric doubl...
Examples
Embodiment 1
[0015] a. Dry the commercially available soybean meal to remove its own moisture. Mix the dried soybean meal with KOH at a mass ratio of 4:1. KOH is prepared into a solution with a concentration of 50% before mixing, and soaked for 1 hour until the solution is fully absorbed by the soybean meal. can;
[0016] b. Place the mixture obtained in step a in a KOH activation kettle, raise the temperature to 100°C at a heating rate of 10°C / min under nitrogen protection, dehydrate at a constant temperature for 0.5h, then continue to heat up to the activation temperature to 600°C, keep it warm for 1h, and Cool directly to room temperature under room temperature environment;
[0017] c. Wash the substance obtained in step b with 5mol / L HCl and deionized water successively to remove the residual metal K and its compounds (that is, wash to neutrality), and dry it at 110°C to obtain activated carbon with a super high specific surface area .
[0018] The BET specific surface area of the ...
Embodiment 2
[0020] a. Dry the commercially available soybean meal and soybean meal to remove its own moisture. Mix the dried soybean meal with KOH at a mass ratio of 4:1. KOH is prepared into a solution with a concentration of 50% before mixing, and soaked for 1 hour until the solution is fully covered by soybean meal. Just absorb;
[0021] b. Put the mixture obtained in step a in a KOH activation kettle, raise the temperature to 100°C at a heating rate of 10°C / min under nitrogen protection, dehydrate at a constant temperature for 0.5h, then continue to heat up to the activation temperature to 700°C, keep it warm for 1h, and Cool directly to room temperature under room temperature environment;
[0022] c. Wash the substance obtained in step b with 5mol / L HCl and deionized water successively to remove the residual metal K and its compounds (that is, wash to neutrality), and dry it at 110°C to obtain activated carbon with a super high specific surface area .
[0023] The BET specific surf...
Embodiment 3
[0025] a. Dry the commercially available soybean meal and soybean meal to remove its own moisture. Mix the dried soybean meal with KOH at a mass ratio of 4:1. KOH is prepared into a solution with a concentration of 50% before mixing, and soaked for 1 hour until the solution is fully covered by soybean meal. Just absorb;
[0026] b. Place the mixture obtained in step a in a KOH activation kettle, raise the temperature to 100°C at a heating rate of 10°C / min under nitrogen protection, dehydrate at a constant temperature for 0.5h, then continue to heat up to the activation temperature to 800°C, keep it warm for 1h, and Cool directly to room temperature under room temperature environment;
[0027] c. Wash the substance obtained in step b with 5mol / L HCl and deionized water successively to remove the residual metal K and its compounds (that is, wash to neutrality), and dry it at 110°C to obtain activated carbon with a super high specific surface area .
[0028] The BET specific su...