Method for preparing oil absorbing and degrading material by waste keratins
A keratin and lysate technology, applied in microorganism-based methods, biochemical equipment and methods, chemical instruments and methods, etc., can solve the problems of slow growth, short survival period, limited application, etc., to improve growth efficiency and cost. low effect
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Embodiment 1
[0021] Take 0.5kg of hair, wash it with detergent, crush it, put it into 2.5kg of solution (8M urea, 0.1M sodium metabisulfite and 0.5M sodium dodecylsulfate (SDS)), 80°C, 70r / The speed of min was shaken to dissolve for 40 min. The protein solution was placed at room temperature for cross-linking, and then filtered and dried. Take 100 grams of the cross-linked sample and add 1000 mL of bacterial (Escherichia coli1098-3, CGMCC No.8696) culture solution, put it in a shaker, 20 ° C, 120 r / min immobilization for 24 hours, filter to obtain the finished product of oil-absorbing sponge immobilized bacteria, 20 ° C Protect from light and dry. Put the dried sample into 100 kg of water with 100 g of kerosene on the surface, and after 24 hours, the residual oil basically disappears.
Embodiment 2
[0023] Take 0.5 kg of feathers, wash them with detergent, crush them, put them into 5 kg of solution (4M urea, 0.5M sodium metabisulfite and 0.3M sodium dodecylsulfate (SDS)), 90°C, 120r / min Shake at a high speed to dissolve for 30 minutes. The protein solution was placed at room temperature for cross-linking, and then filtered and dried. Take 100 grams of cross-linked samples and add 1000 mL of bacteria (Pseudomonas mendocina Palleroni, CGMCC No.1.871) culture solution, place in a shaker, 30 ° C, 150 r / min immobilization for 20 h, filter to obtain the finished product of oil-absorbing sponge immobilized bacteria, 30 ° C to avoid Light dry. Put the dried sample into 100kg of water with 100g of diesel oil on the surface. After 48 hours, the residual oil basically disappeared.
Embodiment 3
[0025] Take 0.5 kg of wool, wash it with detergent, crush it, put it into 10 kg of solution (0.5M urea, 0.01M sodium metabisulfite and 0.05M sodium dodecylsulfate (SDS)), 100°C, 200r / The speed of min was oscillated to dissolve for 30 min. The protein solution was placed at room temperature for cross-linking, and then filtered and dried. Take 100 grams of the cross-linked sample and add 1000 mL of bacterial (Escherichia coli1098-3, CGMCC No.8696) culture solution, place in a shaker, 20 ° C, 120 r / min immobilization for 24 hours, filter to obtain the finished product of oil-absorbing sponge immobilized bacteria, 30 ° C Protect from light and dry. Put the dry sample into 100kg of water with 100g of kerosene and kerosene mixed on the surface. After 50 hours, the residual oil basically disappears.
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