Immobilized microbial preparation and method of treating meat product processing waste water by utilizing same
A technology for immobilizing microorganisms and processing wastewater, applied in biological water/sewage treatment, chemical instruments and methods, fixed on/in organic carriers, etc. High concentration of pollutants and other problems, to achieve high-purity and high-efficiency strains, strong ability to adapt to water quality and pH changes, and high treatment efficiency
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Embodiment 1
[0022] An immobilized microbial preparation prepared by the following steps:
[0023] S1. Fermentation culture of strains, inoculate Bacillus subtilis (Bacillus subtilis ATCC 14579), Bacillus megaterium ATCC 13578, Nitrobacter ATCC 14123 and Nitrosomonas europaea ATCC 25978, respectively Into the enrichment medium, cultured at 30°C and 160rpm for 24h, centrifuged at 5000rpm for 10min to obtain the logarithmic growth phase cells of each bacteria;
[0024] S2, the mixing of thalline, after the cells in step S1 are washed 2 times with phosphate buffer saline, by volume percentage, get 40% Bacillus subtilis, 30% Bacillus megaterium, 15% Nitrobacter, 15% subtilis Nitrobacteria are mixed and suspended in physiological saline to obtain a bacterial cell mixture;
[0025] The immobilization of S3, PVA-sodium alginate, it comprises the following substeps:
[0026] S31. Preparation of PVA gel: Take PVA and add it to water, dissolve it completely at 80°C, the weight / volume ratio of PVA ...
Embodiment 2
[0033] Immobilized microbial preparations, immobilized microbial preparations, are prepared by the following steps:
[0034] S1. Fermentation culture of strains, inoculate Bacillus subtilis (Bacillus subtilis ATCC 14579), Bacillus megaterium ATCC 13578, Nitrobacter ATCC 14123 and Nitrosomonas europaea ATCC 25978, respectively In the enrichment medium, cultured at 28°C and 170rpm for 26h, centrifuged at 5000rpm for 10min to obtain the logarithmic growth phase cells of each bacteria;
[0035] S2, the mixing of thalli, after the cells in step S1 are washed 3 times with phosphate buffer saline, by volume percentage, get 60% Bacillus subtilis, 25% Bacillus megaterium, 10% Nitrobacter, 5% subtilis Nitrobacteria are mixed and suspended in physiological saline to obtain a bacterial cell mixture;
[0036] The immobilization of S3, PVA-sodium alginate, it comprises the following substeps:
[0037] S31. Preparation of PVA gel: Take PVA and add it to water, dissolve it completely at 80°...
Embodiment 3
[0044] Immobilized microbial preparations, immobilized microbial preparations, are prepared by the following steps:
[0045] S1. Fermentation culture of strains, inoculate Bacillus subtilis (Bacillus subtilis ATCC 14579), Bacillus megaterium ATCC 13578, Nitrobacter ATCC 14123 and Nitrosomonas europaea ATCC 25978, respectively Into the enrichment medium, cultured at 32°C and 150rpm for 22h, centrifuged at 5000rpm for 10min to obtain the logarithmic growth phase cells of each bacteria;
[0046] S2, the mixing of thalline, after the cells in step S1 are washed 2 times with phosphate buffer saline, by volume percentage, get respectively 55% Bacillus subtilis, 20% Bacillus megaterium, 12% Nitrobacter, 13% subtilis Nitrobacteria are mixed and suspended in physiological saline to obtain a bacterial cell mixture;
[0047] The immobilization of S3, PVA-sodium alginate, it comprises the following substeps:
[0048] S31. Preparation of PVA gel: Take PVA and add it to water, dissolve it...
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