Construction method and application of immobilized biological bacterium agent for micro-polluted water source
A technology of biological bacterial agent and construction method, which is applied in the construction and application field of immobilized biological bacterial agent in micro-polluted water sources, and can solve the problems of poor treatment effect of algae and algal toxins
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specific Embodiment approach 1
[0031] Specific embodiment one: The construction method of a kind of slightly polluted water source immobilized biological bacterial agent of this embodiment is carried out according to the following steps:
[0032] (1) Re-screening and compounding of multifunctional oligotrophic bacteria: After fermenting high-efficiency COD-degrading bacteria, ammonia-nitrogen bacteria and phosphorus-removing bacteria separately, the concentration of the above three bacteria was maintained at a CFU of 10 6each / mL, and then mixed according to the volume ratio of 2:2:1 to obtain multifunctional oligotrophic bacteria; wherein, the high-efficiency COD degrading bacteria, ammonia nitrogen bacteria and phosphorus removal bacteria are all activated carbon domesticated from oligotrophic After being obtained on the biofilm, it is separated and obtained through starvation resistance experiments and purification effect experiments;
[0033] (2) Screening of high-efficiency algae-dissolving bacteria: un...
specific Embodiment approach 2
[0038] Specific embodiment 2: The difference between this embodiment and specific embodiment 1 is that when high-efficiency COD degrading bacteria are separated by starvation resistance test and purification effect test, the required culture medium is composed of 0.5g / L glucose, 0.5g / L NHCl, 0.5g / L KH 2 PO 4 , 0.5g / L of K 2 HPO 4 , 0.05g / L of CaCl 2 , 0.5g / L of MgSO 4 ·7H 2 O, the trace element solution of 1mL / L, the yeast extract of 2g / L and the water of balance are made up of, and wherein, described trace element solution is the CoCl of 0.2g / L 2 ·6H 2 O, 0.3g / L MnCl 2 4H 2 O, 0.04g / L ZnCl 2 , 0.01g / L NiCl 2 ·6H 2 O, 0.02g / L CuSO 4 ·5H 2 O, 0.01g / L Na 2 MoO 4 2H 2 O, 0.01g / L Na 2 SeO 4 2H 2 O and 0.2g / L FeSO 4 Composition, the pH of the medium is 7.0-7.5. Others are the same as in the first embodiment.
specific Embodiment approach 3
[0039] Specific embodiment three: the difference between this embodiment and specific embodiment one or two is: when ammonia-nitrogen bacteria are separated by starvation resistance test and purification effect test, the required culture medium is composed of 0.5g / L glucose, 1.0g / L NHCl, 1.0g / L NaNO 3 , 0.5g / L of KH 2 PO 4 , 0.5g / L of K 2 HPO 4 , 0.05g / L of CaCl 2 , 0.5g / L of MgSO 4 ·7H 2 O, the trace element solution of 1mL / L, the yeast extract of 2g / L and the water of balance are made up of, and described trace element solution is made of the CoCl of 0.2g / L 2 ·6H 2 O, 0.3g / L MnCl 2 4H 2 O, 0.04g / L ZnCl 2 , 0.01g / L NiCl 2 ·6H 2 O, 0.02g / L CuSO 4 ·5H 2 O, 0.01g / L Na 2 MoO 4 2H 2 O, 0.01g / L Na 2 SeO 4 2H 2 O and 0.2g / L FeSO 4 Composition, the pH of the medium is 7.0-7.5. Others are the same as in the first or second embodiment.
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