Microbiological oil sludge treatment process
A microbial treatment and biological treatment technology, applied in the direction of biological sludge treatment, sludge treatment, etc., can solve the problems of oil sludge pollution, high operating costs, secondary pollution, etc., and achieve the effect of low cost and low power consumption
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Embodiment 1
[0020] The sewage sludge near the hotel in Yixing City was selected to be screened by the following methods:
[0021] 1.1 Strain enrichment
[0022] Add a certain amount of oil sludge (2%) to the glucose medium in the Erlenmeyer flask, put it in a shaker, and cultivate it at 30° C. for 3 days to obtain a strain enrichment solution. The formula of glucose medium is: sodium chloride 1g, calcium chloride 0.5g, dipotassium hydrogen phosphate 0.5g, potassium dihydrogen phosphate 0.5g, ferric chloride 0.02g, ammonium nitrate 1g, magnesium sulfate heptahydrate, 1g yeast extract , 2g glucose, 1L water, pH 7.0-7.2; sterilize at 110°C for 20min.
[0023] 1.2 strain screening
[0024] After diluting the enrichment solution, streak and separate on the glucose solid medium plate (2% agar is added to the glucose medium), culture at 30°C for 24 hours, pick a single colony that grows well on the plate and streak Inoculate on an alkane plate, culture at 30°C for 48 hours, pick out the two l...
Embodiment 2
[0026] Biological and biochemical tests were carried out on the Y-57 strain. The yeast YPD agar was cultured on the plate (30°C) for 3 days, and the colony could grow to 1-2 mm, and the color was white to cream. The initial colony was smooth, and after prolonged culture, the colony appeared wrinkled. When growing on solid or liquid medium, the cell shape is round or oval, and sometimes the cells are elongated and grow like false filaments, and the cell size is about 4-6×6-8 microns.
[0027] The yeast was identified as Candida lipolytica with the Biolog Microorganism Automatic Analyzer produced by Biolog Company of the United States.
[0028] Biological and biochemical tests were carried out on the P-101 strain. The bacterium was cultured aerobically on a nutrient agar plate for 24 hours. The bacteria grew vigorously, and the colonies were smooth, moist, translucent and light yellow colonies, and produced a strong smell. The Gram staining was negative bacillus , extremely man...
Embodiment 3
[0032] Candida lipolytica Y-57 (CGMCC NO.5790) and Pseudomonas putida P-10 (CGMCC NO.5801) were cultured in LB medium at 30°C, 200rpm shaker for 24 hours, and then according to 5 % of the inoculum was inoculated into the fermentation medium, stirred at 30°C, 200rpm, air volume 1:0.4-0.5, and tank pressure 0.05mpa for 36 hours to obtain Candida lipolytica Y-57 and CGMCC No.5790. Pseudomonas putida P-101 mixed culture solution with preservation number CGMCC No.5801.
[0033] Fermentation medium (g / L): glucose 10, liquid paraffin 15, yeast extract 3.0, magnesium sulfate 0.2, potassium chloride 0.2, potassium dihydrogen phosphate 2.0, urea 1.0, ammonium nitrate 1.5, Tween-80 0.5ml, trace Saline solution 1.0ml. pH natural.
[0034] Among them: every liter of trace salt solution contains 11.0 grams of zinc sulfate, 6.0 grams of manganese sulfate, 1.0 grams of ferrous sulfate, EDTA-Na 2 7.3 grams, 0.3 grams of cobalt sulfate, 40 mg of copper sulfate, 60 mg of boric acid, 1 mg of p...
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