Dual inhibitory effects of high ammonia and nitrite accumulation on biocathode in three-electrode bio-electrochemical system: Electrochemical activity and microbial succession
Jiaojiao Niu , Naiyu Wang , Yujie Feng , Jia Liu , Yingxin Zhao , Weihua He
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引用次数: 0
Abstract
Applying a constant potential (20 mV vs. saturated calomel electrode) to a three-electrode bio-electrochemical system is considered an effective method to investigate the biocathode's response to high ammonia load without other interferences. In this study, the ammonia nitrogen concentration was gradually increased in steps of 100, 300, 450, and 600 mg L−1. The sharp decrease in the maximum output current, from 26.12 ± 1.51 mA to 11.64 ± 1.35 mA, was partly due to the inhibition caused by free ammonia. Meanwhile, the prolonged duration of nitrite accumulation with increasing ammonia nitrogen correlated with the lag phase of output current, suggesting that nitrite toxicity was another factor limiting the biocathode's output performance. Moreover, the cathodic reduction current was significantly inhibited by higher ammonia concentrations, with a marked decline when ammonia nitrogen levels exceeded 450 mg L−1. However, the increase of conductivity based on high ammonium concentration only slightly reduced the charge transfer resistances (Rct) but could not fully counteract the free ammonia inhibition. Notably, the dual inhibitory effects of high ammonia and nitrite accumulation was also reflected in the reduced richness of microbial community, along with a decrease in the abundance of denitrifying functional bacteria (e.g., Ferruginibacter) and nitrifying bacteria (e.g., Nitrospira). Thus, a comprehensive investigation into the inhibitory effects of different ammonia loads on the biocathode provides theoretical support for understanding the impact of high ammonia shocks on biocathode in microbial electrochemical system (MES) during practical wastewater treatment.
期刊介绍:
The Journal of Water Process Engineering aims to publish refereed, high-quality research papers with significant novelty and impact in all areas of the engineering of water and wastewater processing . Papers on advanced and novel treatment processes and technologies are particularly welcome. The Journal considers papers in areas such as nanotechnology and biotechnology applications in water, novel oxidation and separation processes, membrane processes (except those for desalination) , catalytic processes for the removal of water contaminants, sustainable processes, water reuse and recycling, water use and wastewater minimization, integrated/hybrid technology, process modeling of water treatment and novel treatment processes. Submissions on the subject of adsorbents, including standard measurements of adsorption kinetics and equilibrium will only be considered if there is a genuine case for novelty and contribution, for example highly novel, sustainable adsorbents and their use: papers on activated carbon-type materials derived from natural matter, or surfactant-modified clays and related minerals, would not fulfil this criterion. The Journal particularly welcomes contributions involving environmentally, economically and socially sustainable technology for water treatment, including those which are energy-efficient, with minimal or no chemical consumption, and capable of water recycling and reuse that minimizes the direct disposal of wastewater to the aquatic environment. Papers that describe novel ideas for solving issues related to water quality and availability are also welcome, as are those that show the transfer of techniques from other disciplines. The Journal will consider papers dealing with processes for various water matrices including drinking water (except desalination), domestic, urban and industrial wastewaters, in addition to their residues. It is expected that the journal will be of particular relevance to chemical and process engineers working in the field. The Journal welcomes Full Text papers, Short Communications, State-of-the-Art Reviews and Letters to Editors and Case Studies