Source Journal of CSCD
Source Journal for Chinese Scientific and Technical Papers
Core Journal of RCCSE
Included in JST China
Volume 38 Issue 9
Nov.  2020
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JU Hong-hai. CHARACTERICS OF DENITRIFICATION AND N2O EMISSION OF ACCLIMATED GLYCOGEN ACCUMULATING ORGANISMS USING DIFERENT ELECTRON ACCEPTOR[J]. ENVIRONMENTAL ENGINEERING , 2020, 38(9): 113-118. doi: 10.13205/j.hjgc.202009019
Citation: JU Hong-hai. CHARACTERICS OF DENITRIFICATION AND N2O EMISSION OF ACCLIMATED GLYCOGEN ACCUMULATING ORGANISMS USING DIFERENT ELECTRON ACCEPTOR[J]. ENVIRONMENTAL ENGINEERING , 2020, 38(9): 113-118. doi: 10.13205/j.hjgc.202009019

CHARACTERICS OF DENITRIFICATION AND N2O EMISSION OF ACCLIMATED GLYCOGEN ACCUMULATING ORGANISMS USING DIFERENT ELECTRON ACCEPTOR

doi: 10.13205/j.hjgc.202009019
  • Received Date: 2020-04-25
  • Using an anaerobic-aerobic sequencing batch reactor (AO-SBR), the glycogen accumulating organisms (GAOs) had been enriched with sodium acetate as the carbon source and the P/C ratio lower than 2/100. Cultured in anaerobic-anoxic operation mode, the acclimated GAOs could perform endogenous denitrification reaction with NOx--N as electron acceptor and poly-β-hydroxyalkanoate(PHA) as electron donor, where PHB (poly-β-hydro-xybutyrate) accounted for more than 80% of the PHA decomposition and utilization. The higher NO2- concentration inhibited the activity of DGAOs, which led to the decrease of PHA synthesis. More energy from PHA decomposition would be used for glycogen storage. During the reduction process of NO3- and NO2-, the PHA degradation rate was 19.28 mg/(g·h) and 10.02 mg/(g·h) respectively, which resulted in the related endogenous denitrification rates were 3.32 mg/(g·h) and 2.29 mg/(g·h). The TN removal efficiency reached more than 95% in the end. With the increase of NO2-/NOx-, the N2O yield during the endogenous denitrification process increased from 29.1% to 59.0%. The higher NO2- inhibition on the activity of Nos, as well as the electron competition between Nir and Nos, resulted in the higher N2O production during PHA-driven denitrification by DGAOs.
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