A method for removing lead-containing sewage pollutants
A technology for pollutants and sewage, applied in botany equipment and methods, biochemical equipment and methods, chemical instruments and methods, etc., can solve problems such as ecological environment pollution, human physical and mental health hazards, abnormal operation, etc., and achieve good application foreground effect
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Embodiment 1
[0026] A method for removing pollutants in sewage, comprising the steps of:
[0027] Preparation of composite microbial agent: mix the mixed bacterial liquid and the carrier according to the weight ratio of 1:1, stir evenly, then leave it to stand for 6 hours, and finally put it in 4°C for low-temperature drying, and control the water content at 6% after drying, to obtain final product The carrier is obtained by mixing bamboo charcoal, chitosan and diatomaceous earth according to the mass ratio of 2:2:1; the above-mentioned mixed bacteria liquid is mixed by the raw material bacteria of the following parts by weight: 10 parts of Rhodococcus, 9 parts of Thiobacillus denitrificans , 7 parts of Pseudomonas stutzeri, 6 parts of Sphingomonas, 5 parts of Bacillus pumilus, 2 parts of Phanerochaete chrysosporium; the concentration of the above-mentioned raw material bacteria is controlled at 1X10 8 pcs / ml.
[0028] Sewage pretreatment: First, the sewage NH3-N is 300mg / L, sulfide is 80...
Embodiment 2
[0031] Use DNAMAN software to design primers, add BamHI and SalI restriction sites respectively, synthesize the nucleotide sequence OXR gene according to the amino acid sequence NP_744952.1 whole gene, obtain the target fragment by amplification, and obtain the target gene by PCR amplification OXR (corresponding mutation sites 11D / S, 59K / Q, 77A / D, 99R / G, 133N / Y, 182L / D, 208A / I, 241M / K, 259V / P, 302A / S, 366V / P, 383S / G, 421P / T, 433F / I were introduced into the gene sequence, thereby obtaining different mutant genes), the PCR product was double-digested with BamHI and SalI, and the PCR product was double digested with BamHI and SalI The digested expression vector pBPSE was connected, and the successfully verified recombinant plasmid was transformed into the Pseudomonas stutzeri CCTCC NO: M209107 to obtain a degraded genetically engineered bacterium.
Embodiment 3
[0032] Example 3 Verification of the sewage treatment effect of Pseudomonas stutzeri genetically engineered bacteria and other bacterial agents
[0033] According to the method of Example 1, the corresponding sewage treatment experiment was carried out, and the sewage and the sewage of Example 1 belonged to the same batch and had the same concentration of pollutants. Wherein each component composition of bacterial agent is identical with embodiment 1.
[0034] The genetically engineered bacteria with different mutation sites prepared in Example 2 were respectively used to carry out the reaction of removing lead. It was found through experiments that 11D / S, 59K / Q, 77A / D, 99R / G, 133N / Y, 182L / D, 208A / I, 241M / K, 259V / P, 302A / S, 366V / P, 383S / G, 421P / T, 433F / I mutants all have significantly enhanced effects compared with the original strain. The total treatment time is not more than 4 days, and the result is as follows: the sewage is the same batch of sewage, so as to ensure the same...
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