Prospects for Biological Nitrogen Removal from Anaerobic Effluents during Mainstream Wastewater Treatment

Growing interest in the anaerobic treatment of domestic wastewater requires a parallel focus on developing downstream technologies that address nitrogen pollution, especially for treatment systems located in eutrophication-impacted watersheds. Anaerobic effluents contain sulfide and hydrogen sulfide (a corrosive gas), dissolved methane (a potent greenhouse gas), ammonium, and residual organic carbon predominantly in the form of volatile fatty acids. Conventional approaches to nitrogen removal are energy- and chemical-intensive and are not appropriate for application to anaerobic effluents. Innovative, energy efficient nitrogen removal processes are being developed and involve several novel chemotrophic processes. This review provides information about these processes, identifies how to control and retain the most desirable microorganisms, and considers the impact of reactor configuration on performance. Given the complexity of the technologies under development that remove nitrogen from anaerobically treated domestic wastewater, we conclude that computational models can support their development and that sensor-mediated controls are essential to achieving energy efficiency

Urine Bacterial Community Convergence through Fertilizer Production: Storage, Pasteurization, and Struvite Precipitation

Source-separated human urine was collected from six public events to study the impact of urine processing and storage on bacterial community composition and viability. Illumina 16S rRNA gene sequencing revealed a complex community of bacteria in fresh urine that differed across collection events. Despite the harsh chemical conditions of stored urine (pH > 9 and total ammonia nitrogen > 4000 mg N/L), bacteria consistently grew to 5 ± 2 × 10⁸ cells/mL. Storing hydrolyzed urine for any amount of time significantly reduced the number of operational taxonomic units (OTUs) to 130 ± 70, increased Pielou evenness to 0.60 ± 0.06, and produced communities dominated by <i>Clostridiales</i> and <i>Lactobacillales</i>. After 80 days of storage, all six urine samples from different starting materials converged to these characteristics. Urine pasteurization or struvite precipitation did not change the microbial community, even when pasteurized urine was stored for an additional 70 days. Pasteurization decreased metabolic activity by 50 ± 10% and additional storage after pasteurization did not lead to recovery of metabolic activity. Urine-derived fertilizers consistently contained 16S rRNA genes belonging to Tissierella, Erysipelothrix, Atopostipes, Bacteroides, and many <i>Clostridiales</i> OTUs; additional experiments must determine whether pathogenic species are present, responsible for observed metabolic activity, or regrow when applied