Method for repairing arsenic pollution soil by nano zero-valent iron and bacteria
A nano-zero-valent iron and arsenic pollution technology, applied in the restoration of contaminated soil, etc., can solve the problems of reducing activity, soil biological toxicity, increasing costs, etc., and achieve the effect of avoiding damage and reducing dosage
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment example 1
[0027] 1) Enrichment culture of bacterial strains
[0028] Pseudomonas putida P. putida strain MnB1, strain MnB1 from the American Type Bacteria Collection Center, accession number ATCC 23483, inoculate the bacteria into Pseudomonas putida enrichment medium A at a volume ratio of 5%, and then shake at 30℃. (150 rpm), aerobic enrichment culture for 3 days; the composition of medium A is peptone 5g, beef powder 2, sodium chloride 3, pH 7.2, deionized water 1 liter;
[0029] 2) Preparation of active metabolites
[0030] Add the Pseudomonas putida bacteria solution obtained in step 1) to the inoculum of 5% by volume with the initial concentration of divalent manganese of 20 mg / L (dosing amount is calculated as Mn), and the odor of 6.8 Monosporium culture medium B, then cultured at 30 degrees Celsius under aerobic conditions for 2 days, brown-black flocs appear in the culture medium, that is, bacterial metabolites are produced; the composition of medium B is ferrous ammonium sulfate 0.3g...
Embodiment example 2
[0037] 1) Enrichment culture of bacterial strains
[0038] The selected bacterial strain is Pseudomonas putida P. putida strain MnB1, strain MnB1 from the American Type Bacteria Collection Center, deposit number ATCC 23483, inoculate the bacteria in Pseudomonas putida enrichment medium A at a volume ratio of 10%, and then shake at 25℃. (150 rpm), aerobic enrichment culture for 5 days; the medium A component is peptone 5g, beef powder 5, sodium chloride 3, pH 7.4, deionized water 1 liter;
[0039] 2) Preparation of active metabolites
[0040] Add the Pseudomonas putida bacteria solution obtained in step 1) to the inoculum of 10% by volume, with the initial concentration of divalent manganese of 5mg / L (dosing amount is calculated as Mn) and the foul-smelling pseudomonas with a pH of 7.4 Cell culture medium B, and then cultured for 7 days under aerobic conditions at 25 degrees Celsius, brown-black flocs appear in the medium, that is, bacterial metabolites are prepared; the composition ...
Embodiment example 3
[0047] 1) Enrichment culture of bacterial strains
[0048] Pseudomonas putida P. putida Strain MnB1 was inoculated into Pseudomonas putida enrichment medium A at a volume ratio of 7%, and then aerobic enrichment culture was carried out for 3 days under 30°C horizontal shaking (120 rpm); the medium A The ingredients are peptone 4g, beef powder 2, sodium chloride 2, pH 7.2, and 1 liter of deionized water. The selected bacterial strains are from the American Type Bacteria Collection Center and the deposit number is ATCC 23483;
[0049] 2) Preparation of active metabolites
[0050] Add the Pseudomonas putida bacteria solution obtained in step 1) to the inoculum of 8% by volume with the initial concentration of divalent manganese of 15 mg / L (dosing amount is calculated as Mn) and the malodorous phlegm with pH 7.0 Monosporium culture medium B, then cultured at 25 degrees Celsius under aerobic conditions for 3 days, brown-black flocs appear in the culture medium, that is, bacterial metabol...
PUM
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