A kind of decolorization bacterium and application
A technology for bacteria and decolorization, which is applied in the direction of bacteria, process wastewater treatment, water/sludge/sewage treatment, etc. It can solve the problems of difficult application and microbial coordination, and achieves wide application prospects, fast growth, and is not easy to lose and die. Effect
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Embodiment 1
[0031] Screening and Identification of Acinetobacter YH-02 (Acinetobacter sp.).
[0032] The experimental materials come from the silt on the banks of the Yi River in Linyi City, Shandong Province.
[0033] Take 0.1ml of the sludge dilution, spread it on the screening medium plate, cultivate it in a 30°C incubator, pick a single colony and repeat the streak purification 2-3 times to obtain the purified strain. After 16S rDNA identification, it belongs to Acinetobacter sp., the phylogenetic tree is shown in the appendix of the manual figure 1 , having the sequence shown in 1 in the sequence table.
Embodiment 2
[0035] Decolorization experiment 1 of Acinetobacter sp. YH-02.
[0036] The object of treatment is papermaking wastewater, and the operation mode is shaking culture in shake flasks.
[0037] The specific implementation steps are as follows: the strains are inoculated into LB medium, and cultured with shaking at 30°C until the bacterial concentration is O.D. 600 ≈2.0, inoculated in papermaking wastewater with 8% inoculation amount, cultured at 35°C for 5 days, and maintained dissolved oxygen above 3.0mg / L; centrifuged to take supernatant, and measured according to "Determination of Water Quality Chromaticity (GB11903-89)" Chromaticity, measure COD according to "Dichromate Method (GB11914-89)". The results are shown in Table 1 below.
[0038] Table 1
[0039] Chroma (degrees) COD (mg / L) flooded 560 2800 out of water 40 274 Removal rate (%) 92.9 90.2
Embodiment 3
[0041] Decolorization experiment 2 of Acinetobacter sp. YH-02.
[0042] The treatment object is papermaking wastewater, and the operation mode is aeration cultivation in a 3L SBR (sequencing batch bioreactor) system.
[0043] The specific implementation steps are as follows: the strains are inoculated into LB medium, and cultured with shaking at 30°C until the bacterial concentration is O.D. 600 ≈2.0, inoculated in papermaking wastewater with 5% inoculation amount, cultured at 30°C for 3 days, and maintained dissolved oxygen above 3.0mg / L; centrifuged to take supernatant, and measured according to "Determination of Color of Water Quality (GB11903-89)" Chromaticity, measure COD according to "Dichromate Method (GB11914-89)". The results are shown in Table 2 below.
[0044] Table 2
[0045] Chroma (degrees) COD (mg / L)
[0046] flooded 560 2800 out of water 60 397.6 Removal rate (%) 89.3 85.8
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