A kind of green preparation method of porous graphene
A porous graphene and graphene technology, applied in the direction of microorganism-based methods, biochemical equipment and methods, microorganisms, etc., can solve the problems of limited application fields, high cost, and inability to be widely promoted, and achieve a green and pollution-free process. Mild conditions, convenient and easy to obtain the effect of fecundity
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0027] Preparation of seed culture solution: Boil 200g of fresh potato pieces with water for 30 minutes, mash them and filter with 8 layers of gauze to obtain the filtrate; then add 20g of glucose, 1.5g of potassium dihydrogen phosphate, and 0.75g of magnesium sulfate for mixing, and finally use deionized water Dilute to 1 L, sterilize at 121°C for 20 min, and cool to room temperature.
[0028] Preparation of liquid nutrient-limited medium: Glucose 10g, ammonium tartrate 0.1g, potassium dihydrogen phosphate 2g, calcium chloride 0.1g, magnesium sulfate 0.25g, ferrous sulfate 0.1g, veratrol 150mg, sodium chloride 1mg, VB with Tween-80 5 mg, manganese sulfate 0.5 mg 1 Mix 5 mg with deionized water to 1 L and adjust the pH to 5.0; finally sterilize at 121°C and cool to room temperature.
Embodiment 1
[0030] A kind of green preparation method of porous graphene of the present invention comprises the following steps:
[0031] (1) Immobilized white rot fungi
[0032] Put 1 L of seed culture solution into 4 Erlenmeyer flasks, add 4 pieces of bacterial cellulose membrane (1.5 cm×1.5 cm×0.5 cm) into each Erlenmeyer flask, sterilize and cool;
[0033] Then inoculate 1×10 in each Erlenmeyer flask 7 CFU of spore suspension of white-rot fungus 5 mL, in which the spore concentration is 2 × 10 5 CFU; then place the flask in a constant temperature shaking incubator at 150 r / min and 30°C for 5 days, so that the hyphae can attach to and completely wrap the bacterial cellulose membrane; finally take it out and wash the surface with sterile water Three times, remove the residual culture medium to obtain immobilized white rot fungi;
[0034] (2) Preparation of porous graphene by biodegradation
[0035] Divide 1 L of liquid nutrient-limited medium into four 1 L Erlenmeyer flasks (250 mL / ...
Embodiment 2
[0040] A kind of green preparation method of porous graphene of the present invention comprises the following steps:
[0041] (1) First divide the seed culture solution into 4 Erlenmeyer flasks, add 2 bacterial cellulose membrane blocks (2.5 cm×2.5 cm×1.5 cm) into each Erlenmeyer flask, sterilize and cool;
[0042] Inoculate 2×10 7 5 mL of spore suspension of CFU white-rot fungi, in which the spore concentration is 4 × 10 5CFU; place the above four Erlenmeyer flasks in a constant temperature shaking incubator at 180 r / min, 30°C and incubate for 4 days, mycelium adheres to and completely wraps the bacterial cellulose membrane block, takes it out and cleans the surface three times with sterile water to remove The remaining culture medium is the immobilized white-rot fungus;
[0043] (2) Divide 1 L of liquid nutrient-limited medium into four 1 L Erlenmeyer flasks (250 mL / bottle), then add 2 pieces of immobilized white-rot fungi to each Erlenmeyer flask, and place in a constant ...
PUM
Property | Measurement | Unit |
---|---|---|
diameter | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com