Document Type

Article

Publication Date

2-2022

Publisher

Royal Society of Chemistry

Source Publication

Environmental Science: Water Research & Technology

Source ISSN

2053-1419

Original Item ID

DOI: 10.1039/d1ew00700a

Abstract

Denitratation, the selective reduction of nitrate to nitrite, is a novel process and when coupled with anaerobic ammonium oxidation (anammox) could achieve resource-efficient biological nitrogen removal of ammonium- and nitrate-laden waste streams. Using a fundamentally-based, first principles approach, this study optimized a stoichiometrically-limited, glycerol-driven denitratation process and characterized mechanisms supporting nitrite accumulation with results that aligned with expectations. At the optimal influent chemical oxygen demand to nitrate ratio of 3.0 : 1 identified, glycerol supported selective nitrate reduction to nitrite (nitrite accumulation ratio, NAR = 62%) and near-complete nitrate conversion (nitrate reduction ratio, NRR = 96%), indicating its viability in a denitratation system. Specific rates of nitrate reduction (135.3 mg N per g VSS h−1) were at least one order of magnitude greater than specific rates of nitrite reduction (14.9 mg N per g VSS h−1), potentially resulting in transient nitrite accumulation and indicating glycerol's superiority over other organic carbon sources in denitratation systems. Optimal stoichiometric limitation pH and ORP inflection points in nitrogen transformation assays corresponded to maximum nitrite accumulation, indicating operational setpoints to prevent further nitrite reduction. Denitratation conditions supported enrichment of Thauera sp. as the dominant genus. Stoichiometric limitation of influent organic carbon, coupled with differential nitrate and nitrite reduction kinetics, optimized operational controls, and a distinctively enriched microbial ecology was identified as causal in glycerol-driven denitratation.

Comments

Published version. Environmental Science: Water Research & Technology, Vol. 8, No. 2 (February 2022): 729-741. DOI. © 2022 Royal Society of Chemistry. Used with permission.

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