Dominant microbial agent for water pollution control and preparation method thereof
A microbial inoculum, water pollution technology, applied in the methods of using microorganisms, water pollutants, water/sludge/sewage treatment, etc., can solve the problem of high professional cost, achieve high universality, low cost, professional low-level effects
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[0035] The present invention provides a kind of preparation method of the dominant microbial bacterial agent of water pollution control, comprises the following steps:
[0036] (1) Get the activated sludge of the aerobic tank of the sewage treatment plant, mix the activated sludge of the aerobic tank with the stock solution of EM bacteria according to the ratio of mass ratio 100:5~15, and obtain the mixed sludge;
[0037] (2) Take the sewage to be treated, sterilize it and concentrate it to 5-10% of the original volume, and adjust the pH value to 8-10 to obtain concentrated sewage;
[0038] (3) Mix the mixed sludge with the concentrated sewage, and culture them under the conditions of dissolved oxygen 3.0-3.5 mg / L, 1.5-2.0 mg / L and 0.5-1.0 mg / L successively for 5-7 days to obtain cultures;
[0039] (4) separating the solid and liquid of the culture to obtain a solid part and a liquid part;
[0040] (5) Filter the liquid part through a 0.45 μm microporous membrane to obtain Pr...
Embodiment 1
[0063] (1) Take the activated sludge from the aerobic tank of a sewage treatment plant in a certain place, mix the activated sludge from the aerobic tank with the stock solution of EM bacteria according to the ratio of 100:10 in mass ratio, and obtain the mixed sludge;
[0064] (2) Take the waste water of a paper mill, after high-pressure steam sterilization, concentrate the sterilized waste water to 10% of the original volume, and adjust the pH value to 8 to obtain concentrated sewage;
[0065] (3) Mix the mixed sludge and concentrated sewage according to the ratio of 1g: 200ml, and cultivate them under the conditions of dissolved oxygen 3.0-3.5mg / L, 1.5-2.0mg / L and 0.5-1.0mg / L successively for 5 days. Stir at a speed of 200rpm, and the culture temperature is 20°C; obtain the culture;
[0066] (4) centrifuging the culture to obtain a solid part and a liquid part;
[0067] (5) Filter the liquid part through a 0.45 μm microporous membrane to obtain Precipitate 1;
[0068] (6)...
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