Method for increasing yield of short chain fatty acid produced with excess sludge through enzyme and alkali combined pretreatment
A short-chain fatty acid and excess sludge technology, applied in the direction of microorganism-based methods, biochemical equipment and methods, microorganisms, etc., can solve the problems of unstable acid production system and low efficiency of short-chain fatty acid production, and achieve resource reduction , sludge reduction, microbial system stabilization effect
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Embodiment 1
[0029] Add 13.2 liters of concentrated residual sludge to 11 identical 2-liter reactors (the material of the reactor is plexiglass, the working volume is 1.5L, the inner diameter is 100mm, the height is 260mm, and it is cylindrical), and the reactor is added Protease K to a concentration of 0-0.04U / g VSS, hydrolyzed at a temperature of 35-37°C and a stirring rate of 120rpm for 2-28h, the best enzyme concentration was measured to be 0.018-0.022U / g VSS, and the time was At 22-26h, the maximum soluble COD obtained was 250.97 mg COD / g VSS. The following examples 2-8 all select better hydrolysis conditions: the concentration of proteinase K is 0.018-0.022U / g VSS, the time is 22-26h, the temperature is 35-37°C, and the stirring rate is 120rpm.
Embodiment 2
[0031] Add 1.2 liters of excess sludge into a 2-liter reactor (the material of the reactor is plexiglass, the working volume is 1.5 L, the inner diameter is 100 mm, the height is 260 mm, and it is cylindrical), and proteinase K is added to the reactor to a concentration of 0.018- 0.022U / g VSS, hydrolyzed for 22-26h at a temperature of 35-37°C and a stirring rate of 120rpm, adding anaerobic granular sludge with a volume percentage of 10%, adjusting the initial pH value to 8.5-9.5, anaerobic fermentation In 1-3 days, the production of short-chain fatty acids was 250.47 mg COD / g VSS, as determined by fluorescence in situ hybridization with 16S rRNA oligonucleotide probes, and the proportion of Clostridium was 28%.
Embodiment 3
[0033] Add 1.2 liters of excess sludge into a 2-liter reactor (the material of the reactor is plexiglass, the working volume is 1.5 L, the inner diameter is 100 mm, the height is 260 mm, and it is cylindrical), and proteinase K is added to the reactor to a concentration of 0.018- 0.022U / g VSS, hydrolyzed for 22-26h at a temperature of 35-37°C and a stirring rate of 120rpm, adding anaerobic granular sludge with a volume percentage of 10%, adjusting the initial pH value to 9.5-10.5, anaerobic fermentation On 1-3 days, the production of short-chain fatty acids was 292.49 mg COD / g VSS, as determined by fluorescence in situ hybridization with 16S rRNA oligonucleotide probes, and the proportion of Clostridium was 32%.
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