A method for promoting reduction of chromium by dissimilating iron reducing bacteria by taking pyrite as electron shuttle carrier
A technology of shuttle carrier and dissimilatory iron, applied in the field of biological treatment of pollutants, can solve problems such as inability to exert effects, and achieve the effects of easy promotion, high efficiency and low cost
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Embodiment 1
[0032] The method described in this example mainly includes the following steps:
[0033] (1) Insert Shewanella oneidensis MR-1 into LB liquid medium for enrichment culture, the initial pH of the culture is 7, the temperature is 30°C, and the shaker speed is 170rpm. After culturing for 12 hours to the logarithmic growth phase, the collected culture solution was collected by centrifugation at 6000 rpm, 8 minutes, and 20°C. Wash the collected thalline twice with bicarbonate buffer, then suspend the thalline in the buffer to obtain a bacterial suspension;
[0034] (2) Add the bacterial suspension in step (1) to 100mL basal medium in the anaerobic operation box, and the final concentration of the bacterial strains in the system is 4×108 / mL. And add 20mM sodium lactate, 0.01g pyrite to the system in the anaerobic operation box, and add different concentrations of Cr(Ⅵ) solutions (15.6, 25, 36, 50 mg / L) respectively. At the same time, set blank control group: basal medium + Cr(Ⅵ) ...
Embodiment 2
[0038] The method described in this example mainly includes the following steps:
[0039] (1) Insert Shewanella oneidensis MR-1 into LB liquid medium for enrichment culture, the initial pH of the culture is 7, the temperature is 30°C, and the shaker speed is 170rpm. After culturing for 12 hours to the logarithmic growth phase, the collected culture fluid was collected by centrifugation at 6000 rpm, 8 minutes, and 20°C. Wash the collected bacteria twice with bicarbonate buffer, and then suspend the bacteria in the buffer to obtain a bacterial suspension;
[0040](2) Add the bacterial suspension in step (1) to 100mL basal medium in the anaerobic operation box, and the final concentration of the bacterial strains in the system is 4×108 / mL. And in the anaerobic operation box, 20mM sodium lactate, 25 mg / L Cr(VI) solution, and different concentrations of pyrite (0.1g / L, 1g / L) were added to the system. At the same time, set blank control group: basal medium + Cr(Ⅵ) solution; biolog...
Embodiment 3
[0044] The method described in this example mainly includes the following steps:
[0045] (1) Insert Shewanella oneidensis MR-1 into LB liquid medium for enrichment culture, the initial culture pH is 7, the temperature is 30°C, and the shaker speed is 170rpm. After culturing for 12 hours to the logarithmic growth phase, the collected culture fluid was collected by centrifugation at 6000 rpm, 8 minutes, and 20°C. The collected bacterial cells were washed twice with bicarbonate buffer solution, and then the bacterial cells were suspended in the buffer solution to obtain a bacterial suspension. Air-dry the chromium residue soil with a chromium content of 530 mg / kg, grind it finely, and pass a 0.25 mm soil sieve;
[0046] (2) Add the bacterial suspension in step (1) to 100mL basal medium in the anaerobic operation box, and the final concentration of the bacterial strains in the system is 4×108 / mL. And add 20mM sodium lactate, 6g of chromium slag soil and 0.01g of pyrite to the s...
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