A method for degrading benzopyrene in soil
A benzopyrene and soil technology, applied in the field of combined application of Phomopsis and reeds to degrade benzopyrene in soil, degrading benzopyrene in soil, can solve the problem of incomplete restoration, harsh process requirements, and easy to be affected by the environment and other problems, to achieve the effect of remarkable repair effect, simple process, and environmental friendliness
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[0023] Preparation of bran koji medium: Sieve non-mildew bran to remove fine powder, weigh 8g bran, add it to a 250mL Erlenmeyer flask, add 8mL deionized water, mix well, sterilize at 121°C for 30min, and set aside.
[0024] 2) In the following examples, the Phomopsis sp. used was isolated from the root of reed and identified as Phomopsis sp.
[0025] 3) Determination method of benzopyrene content in soil:
[0026] Take 10g of soil before treatment, remove residues such as sand and stones, dry it naturally in the dark, grind it, sieve it through a fine sieve, and store it at 4°C.
[0027] Put the soil sample into a Soxhlet extractor, heat and reflux with chloroform to extract for 30 minutes, recover the solvent, and use HPLC to measure the content of benzopyrene in it. The measuring method is as follows: C18 chromatographic column, specification 4.6×150mm, 10 μm); The phase is: methanol: water = 90:10, the excitation wavelength of the fluorescent agent detector is 365nm, the ...
Embodiment 1
[0030] A method for degrading benzopyrene in soil, comprising the steps of:
[0031] (1) Select healthy, disease-free reeds, remove the upper and lower parts, segment the reed stalks, and each section has 2-3 sections to obtain reed segments, and then soak the reed segments in 5% rhamnose of benzopyrene In the fat solution, after soaking for 8 days (the germination rate is 85.16%), the reed section is taken out, rinsed with sterile water, and blotted the moisture on the surface with sterile filter paper;
[0032] (2) The reed section is transferred to aseptic water to accelerate germination and cultivate until the buds are 3-5cm long, and set aside;
[0033] (3) Activate Phomopsis, insert it into bran yeast culture medium, culture at 28°C for 5 days, filter, add skim milk powder to the obtained bacteria, the weight ratio of bacteria to skim milk powder is 1:3 , after mixing evenly, freeze-drying, obtains the Phomopsis inoculum (recovering the recovery rate of Phomopsis in the...
Embodiment 2
[0036] In step (1), the concentration of the rhamnolipid solution of benzopyrene is 10%, and the germination rate is 87.45% after soaking for 8 days.
[0037] In step (3), the weight ratio of the thallus to skimmed milk powder is 1:2, and after freeze-drying, the recovery rate of Phomopsis in the Phomopsis inoculum is measured to be 85.33%.
[0038] All the other are identical with embodiment 1.
[0039] The soil benzopyrene degradation rate was measured to be 70.62%.
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