Anaerobic complex microbial inoculant for degrading COD (Chemical Oxygen Demand) in wastewater and application of anaerobic complex microbial inoculant
A compound bacterial agent and oxygen compound technology, applied in the field of environmental microorganisms, can solve the problems of the original process cost of secondary pollution, low COD degradation efficiency, substandard effluent COD, etc., achieving good COD degradation effect, improving processing capacity and impact resistance. capacity, the effect of improving the settling performance
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Embodiment 1
[0039] Example 1: Screening and isolation of Brevundimonas mediterranei COD-Y-1
[0040] (1) Screening and isolation of bacterial strains
[0041] The sewage from the anaerobic pool of the biochemical section of an industrial sewage treatment station in Feixian County, Linyi City was collected, and the sewage was diluted to 10 by gradient dilution method. -2 、10 -3 and 10 -4 100 μl of each dilution was drawn into the separation medium (peptone 10g, beef powder 3g, sodium chloride 5g, agar powder 15g, tap water 1000mL), coated evenly and then inverted in an anaerobic tank, cultured at 30°C, About 72h to grow a single colony. Single colonies with different shapes were selected and transferred to the test tube slant separation medium, placed in an anaerobic tank at 30°C for about 72 hours, and then transferred to a 4°C refrigerator for storage for later use.
[0042] A total of 4 strains were obtained according to the above isolation method, numbered respectively: COD-Y-1, CO...
Embodiment 2
[0051] Example 2: Detection and identification of Brevundimonas mediterranei COD-Y-1
[0052] 1. Experimental method
[0053] 1.1 Extraction of bacterial genomic DNA
[0054] (1) Use a 2ml centrifuge tube to collect 1.0×10 9 (1ml bacterial solution OD600 is 1-1.5) bacterial culture, centrifuge at 12,000×g for 30s, and discard the supernatant. Suspend the pellet with 150 μl Buffer S to which RNase A has been added.
[0055] (2) Add 20 μl of lysozyme stock solution, mix well, and let stand at room temperature for 5 minutes.
[0056] (3) Add 30 μl of 0.25mol / L EDTA (pH 8.0), mix well, and ice-bath for 5 minutes.
[0057] (4) Add 450 μl Buffer G-A, vortex for 15 seconds, and bathe in water at 65° C. for 10 minutes.
[0058] (5) Add 400μl Buffer G-B and 1ml Buffer DV (pre-cooled at 4°C), mix vigorously, and centrifuge at 12,000×g for 2min.
[0059] (6) Discard the upper phase as much as possible, and keep the interphase precipitate and the lower phase. Add 1ml of 4°C pre-coo...
Embodiment 3
[0096] Embodiment 3: the effect evaluation of the different proportions of each strain in the bacterial agent formula
[0097] 3.1 Degradation COD evaluation experiment:
[0098]Each bacterial powder in the bacterial agent formula was evaluated according to different proportions (mass ratio), and the live bacteria amount of Bacillus cereus bacterial powder was (100-120)×10 8 CFU / g, the amount of live bacteria of Brevundimonas mediterranea powder is (70-90)×10 8 CFU / g;
[0099] Separately pack 100mL of biochemical papermaking wastewater into 100mL anaerobic bottles, sterilize at 115°C for 30 minutes, and then cool to room temperature. Under aseptic conditions, 200 ppm of solid bacterial agents compounded by Bacillus cereus and Brevundimonas mediterranei in different proportions were added to it, and then placed at 30°C for static culture, and the waste water was detected every 2 days. COD content. Three parallel experiments were set up for each experimental group, and a bla...
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