Method for preparing graphene simultaneously doped with nitrogen and sulfur through biological reduction
A graphene and biological technology, which is applied in the field of graphene reduction based on sulfate-reducing bacteria, and achieves the effects of wide distribution, broad application prospects and low cost.
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Embodiment 1
[0027] The preparation of embodiment 1 graphene oxide
[0028] Mix 1.5g of natural flake graphite powder with 1.5g of sodium nitrate and 69ml of concentrated sulfuric acid in an ice bath. Slowly add 9g of potassium permanganate, and stir the reaction for 1h in a normal temperature water bath. Gradually add 100ml of deionized water, the temperature is gradually increased, stirring at 90 ° C to continue the reaction for 30min, the mixture turns from brown to bright yellow, add 10ml, 30% hydrogen peroxide solution, the mixture turns from brown to bright yellow. Filtrate while hot, and fully wash with hydrochloric acid solution and deionized water until the filtrate is pH=6. The graphene oxide filter cake was fully dried in a vacuum oven at 80°C and stored for future use.
Embodiment 2
[0029] The activation of embodiment 2 SRB bacterial classification
[0030] Take out the SRB strains stored in the refrigerator, place them in a constant temperature incubator at a suitable temperature and incubate them for 2 to 3 hours, pipette an appropriate amount of strains into a sterilized bottle, and fill the entire bottle with the sterilized medium. Close the stopper to ensure that there is no air in the bottle. Place the culture solution inoculated with SRB in a constant temperature incubator and cultivate it for 24 hours. If the solution in the bottle turns black, it means that the cultured SRB has considerable activity. If it does not turn black, follow the above steps to re-inoculate until the solution in the bottle turns black. If the solution in the bottle does not turn black after three inoculations, it means that the strain has been inactivated and needs to be replaced.
Embodiment 3
[0031] Example 3 Graphene modified electrode detects heavy metal ions
[0032] (1) Graphene oxide is prepared by the Hummers method. Graphene oxide was dispersed in water and ultrasonically dispersed to prepare a 0.1 mg / ml dispersion.
[0033] (2) The composition of SRB medium is as follows: sodium lactate 4.0ml; yeast infusion 1.0g; magnesium sulfate heptahydrate 0.2g; dipotassium hydrogen phosphate 0.01g; sodium chloride 10g; distilled water 1000ml. Use sodium hydroxide to adjust the pH to 7.0-7.2, at 0.12×10 5 Under high-pressure steam of Pa, sterilize for 20 minutes, rapidly cool to about 37°C, and store at a constant temperature for later use.
[0034] (3) The SRB strain came from the sewage of Shengli Oilfield in my country. After activation according to the method of Application Example 2, it is ready for use.
[0035] (4) Get 100ml of graphene oxide solution with a concentration of 0.1mg / ml, 20ml of diluted cultured SRB bacterial solution with considerable activity...
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