Denitrification method by sewage short-cut simultaneous nitrification and denitrification
A technology of simultaneous nitrification and denitrification, applied in chemical instruments and methods, biological water/sewage treatment, water/sludge/sewage treatment, etc., can solve the problems of microbial function restriction, unstable denitrification effect, etc., and reach the scope of application Wide, improved effect, strong impact resistance effect
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[0017] A kind of specific preparation method of the nitrous acid type denitrification microbial bacterial agent that the inventive method uses comprises the following content:
[0018] 1. Arthrobacter FDN-1, Flavobacterium waterii FDN-2, Paracoccus nitrogenus DN-3 and Methylobacterium SDN-3 of the present invention are respectively inoculated on a solid medium for activation;
[0019] 2. Use the inoculation loop to inoculate the colonies on the plate into the corresponding liquid culture solution, and culture them under aerobic conditions at a temperature of 25-35°C and 150-240 rpm for 1-3 days until the logarithmic growth phase, and obtain liquid bacteria agent seed liquid;
[0020] 3. After amplifying and culturing the above-mentioned seed liquid, the bacteria are collected, filtered and concentrated, and then mixed according to the required ratio to obtain the nitrous acid denitrification microbial bacterial agent of the present invention. The seed solution of each bacteri...
Embodiment 1
[0026] The preparation of embodiment 1 microbial bacterial agent
[0027] 1. Bacteria activation: The activation medium formula of Arthrobacter FDN-1 and Flavobacterium waterii FDN-2 is: beef extract: 5g / L, peptone: 10g / L, NaNO 2 : 1g / L, add 2.0% agar; the activation medium formula of Paracoccus nitrogen DN-3 is: KNO 3 : 1g / L, sodium succinate: 8g / L, KH 2 PO 4 : 1g / L, FeCL 2 : 0.5g / L, add 2.0% agar; the activation medium formula of Methylobacterium SDN-3 is: ammonium sulfate: 0.5g / L, methanol: 0.75mL / L, KH 2 PO 4 : 1g / L, FeCL 2 : 0.5g / L,; add 2% agar. After spreading evenly on the plate, place it in a constant temperature incubator at a temperature of 30°C for activation.
[0028] 2. Use the inoculation loop to scrape the bacteria on the plate and inoculate them in the corresponding liquid culture solution respectively, and culture them with shaking under aerobic conditions of 25-35°C and 150-240rpm for 1-3 days until the logarithmic growth phase, and obtain Liquid bac...
Embodiment 2
[0031] Get the bacterium suspension A that a certain amount of embodiment 1 obtains and inoculate in two aeration reactors according to the inoculum size of 5% (volume), at 30 ℃ of temperature, pH 7.7, DO (dissolved oxygen) is 0.9~2.9mg. L -1 Under the conditions, the treatment of ammonia-containing wastewater generated in the urea production process, NH 3 -The average concentration of N is 450mg / L, the average concentration of total nitrogen (TN) is 500mg / L, COD Cr The average concentration is 150mg / L. During the treatment process, methanol is supplemented in No. 1 reactor as a carbon source, and no carbon source is supplemented in No. 2 reactor. After 18 hours of reaction, the ammonia nitrogen removal rate of the two reactors was greater than 90%, and the total nitrogen removal rate of No. 1 reactor with sufficient carbon source was 90%. During the reaction, the molar ratio of nitrite to nitrate was greater than 9:1, Simultaneous short-range nitrification and denitrificati...
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