A biological cleaning agent for treating oily sludge and its application method
A cleaning agent, biological technology, applied in sludge treatment, chemical instruments and methods, immiscible solvent sludge treatment, etc., can solve the problems of poor biodegradability, high concentration, treatment temperature, toxicity and so on of chemical surfactants
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Embodiment 1
[0020] Embodiment 1: Preparation of single rhamnolipid fermentation broth
[0021] Weigh separately with electronic balance, 30g glucose, 3g NaNO 3 , 1g KH 2 PO 4 , 2g K 2 HPO 4 ·3H 2 O, 0.4gMgSO 4 ·7H 2 O, 1g of yeast powder; add distilled water and mix well, then dilute to 1L with distilled water; add 30% NaOH to adjust the pH of the medium to 7.0; aliquot and sterilize at 121°C for 30min.
[0022] Select the rhamnolipid product to be Pseudomonas stutzeriRhl (for related records of Pseudomonas stutzeri Rhl, refer to Zhao et al.2015Heterologousproduction of Pseudomonas aeruginosa rhamnolipid under anaerobic conditions for microbial enhanced oil recovery) which is completely single rhamnolipid as A strain of monorhamnolipid.
[0023] After the fermentation medium is cooled to room temperature (20-30° C.), inoculate the seed liquid of the bacterium Rh1 that produces monorhamnolipid of 3% of culture medium volume (number of bacteria is 10 5 per ml), cultured for 5 days ...
Embodiment 2
[0026] Embodiment 2: Preparation of monorhamnolipid aqueous solution
[0027] The fermented liquid obtained from the above examples was centrifuged at 10,000 g to remove insoluble matter such as bacteria, and the monorhamnolipid in the fermented liquid was extracted by chloroform / methanol (v / v, 2:1) extraction method.
[0028] Utilize thin-layer chromatography to carry out qualitative analysis to the extracted monorhamnolipid product, get the rhamnolipid product after a small amount of extraction and be dissolved in methylene chloride, prepare the monorhamnolipid sample of 200mg / L, sample Spot on a silica gel plate, develop in a developer of chloroform / methanol / acetic acid=65:15:2 (v / v / v), and develop a color with a developer. Under the phenol-sulfuric acid developer, the product showed yellow color, and its Rf value was calculated. Under the phenol-sulfuric acid developer, the product showed yellow color, and there was only one spot on the thin-layer silica gel plate, and it...
Embodiment 3
[0031] Embodiment 3: application example
[0032] Utilize the biocleaning agent that embodiment 1 and 2 obtain respectively to clean oily sludge of an oil field in Northwest China
[0033] Weigh 10g of oily sludge with an electronic balance, pour it into a conical flask, add 100ml of the biological cleaning agent with a concentration of 300mg / L obtained in Example 1 or Example 2, stir and mix well, and under the conditions of 37°C and 180rpm, Oscillate to clean the sludge for 48 hours. After cleaning, oil, water and mud were separated, and the cleaned upper layer oil was recovered. The final oil recovery rate of the biological cleaning agent obtained in Example 1 was 56.8%; the final oil recovery rate of the biological cleaning agent obtained in Example 2 was 59.1%.
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