摘要：Nitrification is the rate limiting step in the nitrogen removal processes since nitrifiers have high oxygen demand, but poorly compete with aerobic heterotrophs. In a laboratory-scaled system, we investigated a process of ammonium oxidation under ferric-iron reducing condition (feammox) in the presence of organic carbon using influents with high NH4 and COD contents, and ferrihydrite as the only electron acceptor. Batch incubations testing influents with different NH4 and COD concentrations revealed that the [COD]/[NH4 ] ratio of 1.4 and the influent redox potential ranging from − 20 to 20 mV led to the highest removal efficiencies, i.e. 98.3% for NH4 and 58.8% for COD. N2 was detected as the only product of NH4 conversion, whereas NO2− and NO3− were not detected. While operating continuously with influent having a [COD]/[NH4 ] ratio of 1.4, the system efficiently removed NH4 (> 91%) and COD (> 54%) within 6 day retention time. Fluorescence in situ hybridization analyses using Cy3-labeled 16S rRNA oligonucleotide probes revealed that gamma-proteobacteria dominated in the microbial community attaching to the matrix bed of the system. The iron-reduction dependent NH4 and COD co-removal with a thorough conversion of NH4 to N2 demonstrated in this study would be a novel approach for nitrogen treatment.
