Method of removing pollutant from cadmium-containing sewage
A technology for pollutants and sewage, applied in the fields of water pollutants, chemical instruments and methods, water/sewage multi-stage treatment, etc., can solve problems such as ecological environment pollution, human physical and mental health hazards, and complexity, and achieve good application prospects.
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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 concentrations of the above-mentioned raw material bacteria were all controlled at 1×10 8 pieces / ml.
[0028] Sewage pretreatment: First, the sewage (NH3-N is 300mg / L, su...
Embodiment 2
[0031] Use DNAMAN software to design primers, add BamHI and SalI restriction sites respectively, synthesize the nucleotide sequence HP gene according to the amino acid sequence NP_744955.1 whole gene, obtain the target fragment by amplification, and obtain the target gene by PCR amplification HP (the corresponding mutation sites 71S / T, 89T / Y, 121T / A, 143D / S, 184S / Q, 239W / G, 246V / P, 269K / N, 304P / S, 353K / E, 369G / D, 372C / S, 422D / R, and 448G / I were introduced into the gene sequence, thus 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 cloning expression vector PWB980 was connected, and the successfully verified recombinant plasmid was transformed into the Phanerochaetechrysosporium (Phanerochaetechrysosporium) ATCC24725 to obtain a cadmium-degrading genetically engineered bacterium.
Embodiment 3
[0032] Example 3 Verification of the sewage treatment effect of Phanerochaete chrysosporium 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 of different mutation sites obtained in Example 2 were used to carry out the reaction of removing cadmium, and it was found through experiments that 71S / T, 89T / Y, 121T / A, 143D / S, 184S / Q, 239W / G, 246V / P, 269K / N, 304P / S, 353K / E, 369G / D, 372C / S, 422D / R, 448G / 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 sa...
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