Degradation bacterium for oil-base drilling cuttings, and preparation method and application method thereof
A technology for oil-based drilling cuttings and degrading bacteria, which is applied in biochemical equipment and methods, chemical instruments and methods, and microorganism-based methods, etc. The effect of short processing cycle and simple operation
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[0025] The preparation of medium is listed in Table 1:
[0026] Table 1
[0027]
Embodiment 1
[0029] (1) Take petroleum-contaminated soil at the well site, carry out enrichment culture on the bacteria in the soil under the conditions of LB medium, neutral environment, and temperature at 30°C, and isolate, purify and screen the bacteria after enrichment culture, Three strains of degrading monobacteria were obtained, including Pseudomonas aeruginosa, Micrococcus krusei, and Acinetobacter calcoaceticus.
[0030] (2) Mix the three strains of degrading monobacteria obtained in step 1 according to the volume ratio of Pseudomonas aeruginosa: Micrococcus krusei: Acinetobacter calcium acetate 1:0.9:0.9 to obtain a mixed bacterial solution, in which oil-based drilling cuttings The viable count of degrading bacteria is 10 9 ~10 11 pcs / g.
[0031] (3) The mixed bacterial liquid of step (2) is fermented and amplified in the industrial medium P1, and the fermentation process conditions are: 33° C. of fermentation temperature, 10% v / v of inoculum size, 100 rpm of stirring speed, 24...
Embodiment 2
[0034] Oil-contaminated soil was taken at the well site, and the bacteria in the soil were enriched and cultured in LB medium, neutral environment, and temperature at 35°C. The bacteria after enrichment culture were separated, purified and screened to obtain 3 strains Degradative monobacteria, including Pseudomonas aeruginosa, Micrococcus krusei, and Acinetobacter calcoaceticus.
[0035] The same step as in Example 1, the difference is that Pseudomonas aeruginosa: Micrococcus krusei: Acinetobacter calcium acetate is mixed in a volume ratio of 1:1:1; the mixed bacteria solution is carried out in industrial medium P3 Fermentation scale-up cultivation; fermentation process conditions are: fermentation temperature is 35 ℃, inoculum size is 15% v / v, stirring speed is 120rpm, fermentation time is 36h, and the gas-liquid volume ratio of feeding air per minute is 1.2; after fermentation, Filter and separate the degrading bacteria through a plate and frame filter press with a pressure ...
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