Mechanistic insights into nitrogen removal performance and electron competition with mixed electron donor supply in a biofilm electrode reactor

生物膜 电子 电极 竞赛(生物学) 氮气 化学 材料科学 光电子学 生物 生态学 物理 细菌 遗传学 物理化学 核物理学 有机化学
作者
Xin Yuan,Chunfang Chao,Jiaojiao Niu,Jinxin Song,Yiwen Liu,Siyuan Zhai,Yingxin Zhao
出处
期刊:Eco-environment & health [Elsevier BV]
卷期号:4 (2): 100153-100153 被引量:1
标识
DOI:10.1016/j.eehl.2025.100153
摘要

In this study, a unique electrode configuration in the form of an "inverted T" was developed in the biofilm electrode reactor (BER), enabling superior nitrogen removal via the synergistic effect of hydrogen autotrophic denitrification and heterotrophic denitrification. In contrast to the sole heterotrophic denitrification in the biofilm reactor (BR), weak electric stimulation in the BER system promoted in situ hydrogen production as well as electron transport and utilization, resulting in a notable 20% improvement in NO3- removal efficiency for both influent COD/N ratios. Conversely, notable NO2- accumulation occurred under both COD/N ratios, with concentrations ranging from 6.0 to 8.0 ​mg/L. The enrichment of non-heterotrophic denitrifiers, such as Thermomonas, Pelomonas, and Hydrogenophaga, was observed in the BER with a relative abundance exceeding 1.0%, contributing to the hydrogen autotrophic denitrification pathway. Based on the outcomes of the multiple electron donor utilization in the coexistence of different electron acceptor combinations, despite H2 serving as an additional electron donor in the BER, electron competition was still detectable. Notably, nitrite reductase (Nir) emerged as the weakest competitor, resulting in a constrained NO2- reduction capacity. Based on the analysis of the electron competition characteristic, the potential NO3- metabolic pathway in the BER system was primarily driven by heterotrophic denitrification processes. The introduced electricity in the BER system was favorable for facilitating nitrogen removal through in situ production of hydrogen, direct supply of electrons from the electrode, improvement of functional microbial activity, and enhancement of enzymatic activity.
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