DPB strain and application of DPB strain to domestic sewage treatment
A technology for denitrifying phosphorus accumulating bacteria and domestic sewage is applied in the field of environmental biology, which can solve the problem of low denitrification and phosphorus removal efficiency, and achieve the effects of improving treatment efficiency and stability, strong phosphorus accumulation ability, and good decontamination ability.
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Embodiment 1
[0020] Embodiment 1: Isolation, screening and identification of bacterial strains
[0021] (1) Material preparation:
[0022] 1. From a well-run A 2 Activated sludge is collected from the aeration tank of the / O process as a source for screening denitrifying phosphorus-accumulating bacteria, and inoculated on-site into a sterilized high-concentration nitrogen-phosphorus medium.
[0023] 2. Medium:
[0024] High concentration nitrogen and phosphorus medium: glucose 10g / L, CaCl 2 0.2g / L, MgSO 4 0.5g / L, (NH4) 2 SO 4 2g / L, KH 2 PO 4 0.25g / L, KNO 3 1g / L, adjust the pH to 7.0.
[0025] LB liquid medium is: peptone 10.0g, yeast extract 5.0g, NaCl 10.0g, distilled water 1000mL, pH 7.0.
[0026] LB solid medium is: peptone 10.0g, yeast extract 5.0g, NaCl 10.0g, agar powder 15g, distilled water 1000mL, pH7.0.
[0027] 3. Experimental instruments and equipment:
[0028] Jerell SHZ-82A air bath constant temperature oscillator,
[0029] Heated Incubators,
[0030] Sanyo autom...
Embodiment 2
[0044] Application of Example 2 Pseudomonas aeruginosa LLHD-1 in domestic sewage treatment
[0045] The ability of Pseudomonas aeruginosa LLHD-1 to treat simulated domestic sewage was investigated, and the degradation ability of Pseudomonas aeruginosa LLHD-1 to COD, total nitrogen and total phosphorus in simulated wastewater was studied. The components of simulated domestic sewage are: KNO 3 0.6g / L; KH 2 PO 4 1g / L; MgSO 4 ·7H 2 O1g / L; sodium succinate 2.4g / L; pH 7.2; high temperature and high pressure sterilization at 121.5°C for 20 minutes. Take 600mL of simulated domestic sewage and add it to a 1L Erlenmeyer flask, add 6mL of Pseudomonas aeruginosa LLHD-1 bacterial suspension, culture on a shaker at 30°C and 120 rpm for 2 days, take samples every 12 hours, and measure the CODcr in the solution, Total nitrogen, total phosphorus content, calculation of the removal rate of each index, the removal rate of the three indicators like Figure 4 shown. The results showed tha...
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