Preparation method of biodegradable high oil absorption material
A technology of biodegradation and high oil absorption, applied in the direction of microorganism-based methods, biochemical equipment and methods, microorganisms, etc., can solve the problems of low oil absorption ratio, lower cellulose crystallinity, secondary pollution, etc., achieve short oil absorption time, The effect of high oil absorption ratio and fast oil absorption speed
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example 1
[0017] First weigh 15g of caprolactone, 5g of peptone, 8g of yeast extract, 3g of agar and 800mL of water, add them to a petri dish, stir and mix for 1min, then add a 5% hydrochloric acid solution to adjust the pH to 6.3 to form a culture medium , and put it in a sterilizing tank, and sterilize it at 90°C for 5 minutes to obtain the Acetobacter xylinum culture medium; Bacteria were inoculated into the fermenter and fermented at 30°C for 5 days. After the fermentation was over, the gelatinous bacterial cellulose on the surface of the fermented liquid was taken out with tweezers, washed twice with water, placed in a beaker, and then added with a mass fraction of Immerse it in 10% sodium hydroxide solution, heat the beaker to 70°C, keep it warm for 30 minutes, remove the residual bacteria, and then wash it with water to neutral to obtain grafted bacterial cellulose; add the above-mentioned grafted bacterial cellulose to After pulverizing in the pulverizer for 30 minutes, pass thr...
example 2
[0020] First weigh 18g of caprolactone, 6g of peptone, 10g of yeast extract, 4g of agar and 900mL of water, add them to a petri dish, stir and mix for 2 minutes, then add a 5% hydrochloric acid solution to adjust the pH to 6.4 to form a culture medium , and put it in a sterilizing tank, and sterilize it at 92°C for 8 minutes to obtain Acetobacter xylinum culture medium; Bacteria were inoculated into the fermenter and fermented at 35°C for 5 days. After the fermentation was over, the gelatinous bacterial cellulose on the surface of the fermented liquid was taken out with tweezers, washed twice with water, placed in a beaker, and then added with a mass fraction of Immerse it in 10% sodium hydroxide solution, heat the beaker to 75°C, keep it warm for 35 minutes, remove the residual bacteria, and then wash it with water until neutral to obtain grafted bacterial cellulose; add the above-mentioned grafted bacterial cellulose to After crushing in the pulverizer for 35 minutes, pass t...
example 3
[0023] First weigh 20g of caprolactone, 8g of peptone, 12g of yeast extract, 5g of agar and 1000mL of water, add them to a petri dish, stir and mix for 3 minutes, then add a 5% hydrochloric acid solution to adjust the pH to 6.5 to form a culture medium , and put it in a sterilizing tank, and sterilize it at 95°C for 10 minutes to obtain the Acetobacter xylinum culture medium; Bacteria were inoculated into the fermenter and fermented at 40°C for 6 days. After the fermentation was over, the gelatinous bacterial cellulose on the surface of the fermented liquid was taken out with tweezers, washed with water for 3 times, placed in a beaker, and then added with a mass fraction of Immerse it in 10% sodium hydroxide solution, heat the beaker to 80°C, keep it warm for 40 minutes, remove the residual bacteria, and then wash it with water to neutral to obtain grafted bacterial cellulose; add the above-mentioned grafted bacterial cellulose to After pulverizing in the pulverizer for 40 min...
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