Abstract
Fe0 is a promising electron donor for autotrophic denitrification in the simultaneous removal of nitrate and phosphorus in low C/N wastewater. However, P removal may inevitably inhibit bio-denitrification. It has not been well recognized and led to an overdose of iron materials. This study employed carbon-coated zerovalent iron (Fe0@C) to support autotrophic denitrification to mitigate the inhibition effects of P removal and enhance both N and P removal. The critical role of the carbon shell in Fe0@C was to block the direct contact between Fe0 and P and NO3-N, to maintain the Fe0 activity. Besides, P inhibited the chemical reduction of NO3-N by competing for Fe0 active sites. This indirectly boosted H2 generation and promoted bio-denitrification. P removal displayed negligible effects on microbial species but indirectly enhanced the nitrogen metabolic activities because of promoted H2 in Fe0@C-based autotrophic denitrification. Bio-denitrification, in turn, strengthened Fe-P co-precipitation by promoting the formation of ferric hydroxide as a secondary adsorbent for P removal. This study demonstrated an efficient method for simultaneous N and P removal in autotrophic denitrification and revealed the synergistic interactions among N and P removal processes.
Original language | English |
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Pages (from-to) | 13314-13326 |
Number of pages | 13 |
Journal | Environmental Science and Technology |
Volume | 56 |
Issue number | 18 |
DOIs | |
Publication status | Published - Sept 20 2022 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2022 American Chemical Society.
ASJC Scopus Subject Areas
- General Chemistry
- Environmental Chemistry
Keywords
- autotrophic denitrification
- carbon-coated zerovalent iron
- NO-N removal
- nZVI
- P removal