Bacterial strain capable of rapidly degrading nitrogen in sewage, and applications of bacterial strain
A bacterial strain and sewage treatment technology, applied in the field of environmental engineering, can solve problems such as difficult nitrogen treatment, achieve broad application prospects, and shorten the start-up time
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Embodiment 1
[0039] Embodiment 1: the screening of bacterial strain
[0040] The bacterial strain of the present invention adopts the plate dilution separation method to isolate and screen the bacterial strain capable of degrading nitrogen under aerobic conditions from sludge flora.
[0041]The isolation screening method is as follows:
[0042] 1. Dilution of mixed strains: Take the bottom sludge from Boshan Sewage Treatment Plant in Zibo City, dissolve the sludge in deionized water (1g of sludge is dissolved in 200ml of deionized water), and perform gradient dilution of the strains .
[0043] 2. Preparation of industrial sewage samples: Take industrial sewage (total nitrogen content is about 100 mg / L) from Boshan sewage treatment plant in Zibo City, filter impurities and adjust its pH to about 7. Put in 150ml of Erlenmeyer flask (specification: 250ml), add 0.48g of glucose (molar ratio of carbon to nitrogen: 10), and sterilize at 115°C for 30min.
[0044] 3. Preliminary screening of st...
Embodiment 2
[0050] Example 2: Detection of the aerobic denitrification performance of Paracoccus denitrificans DYTN-1
[0051] Prepare simulated sewage (glucose 5.3g, NaNO 3 1.5g, NaCl 3g, KH 2 PO 4 1.0g, FeCl 2 ·H 2 O 0.5g, CaCl 2 ·H 2 O 0.2g, MgSO 4 1.0g, H 2 O 1.0L, pH7.0~7.5), the initial concentration of nitrate nitrogen is 247mg / L, and the molar ratio of carbon to nitrogen is 10. Pick 1 ring of denitrifying Paracoccus DYTN-1 from the slope and inoculate it in 50ml of nutrient gravy liquid medium (peptone 10.0g, beef extract 3.0g, sodium chloride 5.0g, agar 15.0g, distilled water 1L, pH = 7.0) in a 250ml Erlenmeyer flask, 30°C, 200rpm shaking culture for 36h, 5000rpm centrifugation for 10min, discard the supernatant, and collect the bacteria. Resuspend the bacteria with sterilized simulated sewage, put them into a 250ml Erlenmeyer flask containing 150ml simulated sewage, and ferment for 36 hours under the conditions of 30°C and 200rpm shaking culture, the removal rates of ni...
Embodiment 3
[0052] Example 3: Detection of heterotrophic nitrification-aerobic denitrification performance of Paracoccus denitrificans DYTN-1
[0053] Prepare simulated wastewater 1 (glucose 5.9g, (NH 4 ) 2 SO 4 1.25g, NaCl 3g, KH 2 PO 4 1.0g, FeCl 2 ·H 2 O0.5g, CaCl 2 ·H 2 O 0.2g, MgSO 4 1.0g, H 2 O 1.0L, pH7.0~7.5), the initial concentration of nitrate nitrogen is 265mg / L, and the molar ratio of carbon to nitrogen is 10. Pick 1 ring of denitrifying Paracoccus DYTN-1 from the slope and inoculate it in 50ml of nutrient gravy liquid medium (peptone 10.0g, beef extract 3.0g, sodium chloride 5.0g, agar 15.0g, distilled water 1L, pH = 7.0) in a 250ml Erlenmeyer flask, 30°C, 200rpm shaking culture for 36h, 5000rpm centrifugation for 10min, discard the supernatant, and collect the bacteria. The bacterium was resuspended with sterilized simulated sewage 1, and inserted into a 250ml Erlenmeyer flask containing 150ml simulated sewage 1, and fermented for 36 hours at a temperature of 30°...
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