A method of using apg06 to promote acid production by anaerobic fermentation of excess sludge
A technology for anaerobic fermentation and excess sludge, applied in the field of solid waste resource utilization, can solve the problems of poor biodegradability, environmental impact, and insufficient improvement of the effect of anaerobic fermentation of excess sludge to produce acid, and achieve easy Biodegradation, human and environmental safety, the effect of shortening the time of fermentation and acid production
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Embodiment 1
[0029] Embodiment 1: APG promotes the determination of the best type of sludge anaerobic fermentation acid production
[0030] (1) Six kinds of APG (APG06, APG08, APG0810, APG0812, APG10, APG1214) were selected for batch sludge fermentation experiments.
[0031] (2) Each reactor (500mL anaerobic bottle, sealed with a rubber cap) contains 300mL activated sludge, and the 6 kinds of APG are added at the doses of 0.1g / gTSS, 0.15g / gTSS, and 0.2g / gTSS respectively In each reactor, another group without adding APG was set up as a control group.
[0032] (3) Before fermentation, each reactor was fed with nitrogen for 5 minutes to remove oxygen, and then sealed and anaerobically fermented at 35±1° C. and 200 rpm for 12 days. During the fermentation process, samples were taken for each group at 60min, 6h, 12h and 1, 2, 3, 4, 5, 6, 8, 10, 12d, including liquid and gas samples.
[0033] 4) performing solid-liquid separation by centrifuging the fermented liquid to obtain a supernatant co...
Embodiment 2
[0039] Embodiment 2: APG promotes the determination of the optimal type and concentration of sludge anaerobic fermentation acid production
[0040] (1) Two kinds of APG (APG06, APG1214) were selected for batch sludge fermentation experiments.
[0041] (2) Each reactor (500mL anaerobic bottle, sealed with a rubber cap) contained 300mL activated sludge, and the two APGs were added to each reactor at the dose of 0.1, 0.2, 0.3, 0.4, 0.5g / gTSS In the reactor, another group without adding APG was set as the control group.
[0042] (3) Before fermentation, each reactor was fed with nitrogen for 5 minutes to remove oxygen, then sealed and cultivated at 35±1° C., 200 rpm for 12 days. During the fermentation process, samples were taken for each group at 60min, 6h, 12h and 1, 2, 3, 4, 5, 6, 8, 10, 12d, including liquid and gas samples.
[0043] (4) performing solid-liquid separation by centrifuging the fermented liquid to obtain a supernatant liquid containing volatile fatty acids.
...
Embodiment 3
[0047] (1) Two kinds of APG (APG06, APG1214) were selected for batch sludge fermentation experiments.
[0048] (2) Each reactor (500mL anaerobic bottle, sealed with a rubber cap) contained 300mL activated sludge, and the two APGs were added to each reactor at the dose of 0.1, 0.2, 0.3, 0.4, 0.5g / gTSS In the reactor, another group without adding APG was set as the control group, and the composition of VFAs in each experimental group was measured when the concentration of VFAs reached the maximum value.
[0049] (3) Before fermentation, each reactor was fed with nitrogen for 5 minutes to remove oxygen, then sealed and cultivated at 35±1° C., 200 rpm for 12 days.
[0050] Through the implementation of this example, the composition of VFAs gradually remained stable after the third day of fermentation, and the composition of VFAs in each experimental group when the concentration of VFAs reached the maximum value was as follows: Figure 5 shown. It can be seen that the composition...
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