Plant-bacterium-fungus-rhamnolipid combined remediation method for petroleum-contaminated soil
A technology of rhamnolipid and oil pollution, applied in the restoration of contaminated soil, etc., can solve the problems of destroying soil structure and components, high price, secondary pollution, etc., and achieve easy biodegradation, fast spreading, and strong vitality Effect
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[0037] (2) the preparation method of composite microbial bacterial agent comprises the steps:
[0038] 1) Cultivate Bacillus subtilis in LB medium until the number of colonies is greater than 1×10 10 cfu mL -1 ;
[0039] The composition of the LB medium is: 10 g of peptone, 5 g of yeast extract, 10 g of sodium chloride, 1 L of distilled water, pH=7.5, and sterilized at 121° C. for 20 min.
[0040] 2) Cultivate Pseudomonas fluorescens in beef extract peptone medium until the number of colonies is greater than 1×10 10 cfu mL -1 ;
[0041] The composition of the beef extract-peptone medium is: 5 g of beef extract, 10 g of peptone, 5 g of sodium chloride, 1 L of distilled water, pH=7.2-7.4, and sterilized at 121° C. for 20 minutes.
[0042] 3) Cultivate Streptococcus faecalis in MRS medium until the number of colonies is greater than 1×10 10 cfu mL -1 ;
[0043]The composition of the MRS medium is: casein 10g, beef extract 10g, yeast extract juice 5g, glucose 5g, sodium ac...
Embodiment 1
[0059] Taking the site of Xinkai village tire cracking oil refinery, Jiguanshan Town, Fengcheng City, Dandong as the test site, 7 test areas are set as table 1, and each test area is divided into 2 pieces, wherein one test area adopts the method of the present invention, and the other test area as a control experiment.
[0060] One, adopt the method of the present invention
[0061] A method for plant-bacteria-fungi-rhamnolipid joint restoration of oil-contaminated soil, comprising the steps of:
[0062] 1. Remove impurities on the surface of oil-contaminated soil;
[0063] 2, the preparation method of composite microbial bacterial agent comprises the steps:
[0064] 1) Put Bacillus subtilis in LB medium, at 30°C, 200r·min -1 Cultivate until the number of colonies is greater than 1×10 10 cfu mL -1 ;
[0065] The composition of the LB medium is: 10 g of peptone, 5 g of yeast extract, 10 g of sodium chloride, 1 L of distilled water, pH=7.5, and sterilized at 121° C. for 20...
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