Culture method of petroleum degrading bacteria
A technology of petroleum-degrading bacteria and culturing method, which is applied in the field of culturing petroleum-degrading bacteria, can solve problems such as shortage, and achieve the effects of good low temperature resistance and good salt resistance.
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Embodiment 1
[0023] Take 100mL of simulated oily sewage with a salinity of 6500mg / L, a pH of 6.0, and an oil content of 200mg / L in four 150mL Erlenmeyer flasks, numbered A, B, C, and D, and pour them into three flasks A, B, and C. Insert 0.2mL of purified oil-removing bacteria solution into the Erlenmeyer flask, D as a blank control, 25, cultured for 24h respectively, based on the D blank, measure the content with a UV spectrophotometer, and calculate the oily degradation rate, the result As shown in the following table:
[0024] Numbering Culture temperature / (℃) Oil degradation rate / (%) A 15 81.2 B 25 89.5 C 35 86.8
Embodiment 2
[0026] Take 100mL of simulated oily sewage with a salinity of 6500mg / L, an oil content of 200mg / L, and a pH configured according to the table below, and place them in five 150mL conical flasks, numbered A, B, C, D, E, and pour them into A and B Insert 0.2mL of purified oil-removing bacteria solution into three Erlenmeyer flasks, C, D, and E as a blank control. Under the condition of 25°C, culture them for 24 hours respectively. Based on the blank of E, measure with an ultraviolet spectrophotometer With content, calculate the oil-containing degradation rate, the results are as follows:
[0027] Numbering pH Oil degradation rate / (%) A 5.0 77.6 B 6.0 81.8 C 7.0 82.9 D 8.0 79.5
Embodiment 3
[0029] Take 100mL of oily sewage with an oil content of 200mg / L, pH7.0, and salinity set as shown in the table below, and place them in four 150mL conical flasks, numbered A, B, C, and D, and pour them into three flasks A, B, and C. Insert 0.2mL of the bacteria solution of high-efficiency oil-removing bacteria into the Erlenmeyer flask, and D was used as a blank control. Under the condition of 25°C, cultured for 24 hours respectively. Based on the blank of D, the content was measured with a UV spectrophotometer, and the oil-containing degradation rate was calculated. The results are as follows:
[0030] Numbering Salinity / (mg / L) Oil degradation rate / (%) A 6000 88.6 B 7000 82.9 C 8000 80.8
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