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不同浓度 Mn(II) 下生物锰氧化物 (BioMnOx) 促进的生物脱氮除磷的特性和机制。

Characteristic and mechanism of biological nitrogen and phosphorus removal facilitated by biogenic manganese oxides (BioMnOx) at various concentrations of Mn(II).

机构信息

College of Resources and Environment, Anhui Agricultural University, Anhui Provincial Key Laboratory of Hazardous Factors and Risk Control of Agri-Food Quality Safety, Hefei, 230036, China.

College of Resources and Environment, Anhui Agricultural University, Anhui Provincial Key Laboratory of Hazardous Factors and Risk Control of Agri-Food Quality Safety, Hefei, 230036, China.

出版信息

Environ Res. 2024 Jul 1;252(Pt 2):118943. doi: 10.1016/j.envres.2024.118943. Epub 2024 Apr 16.

DOI:10.1016/j.envres.2024.118943
PMID:38631471
Abstract

Biogenic manganese oxides (BioMnOx) have attracted considerable attention as active oxidants, adsorbents, and catalysts. However, characteristics and mechanisms of nitrification-denitrification in biological redox reactions mediated by different concentrations of BioMnOx are still unclear. Fate of nutrients (e.g., NH-N, TP, NO-N) and COD were investigated through different concentrations of BioMnOx produced by Mn(II) in the moving bed biofilm reactor (MBBR). 34% and 89.2%, 37.8% and 89.8%, 57.3% and 88.9%, and 62.1% and 90.4% of TN and COD by MBBR were synchronously removed in four phases, respectively. The result suggested that Mn(II) significantly improved the performance of simultaneous nitrification and denitrification (SND) and TP removal based on manganese (Mn) redox cycling. Characteristics of glutathione peroxidase (GSH-Px), reactive oxygen species (ROS), and electron transfer system activity (ETSA) were discussed, demonstrating that ROS accumulation reduced the ETSA and GSH-Px activities when Mn(II) concentration increased. Extracellular polymeric substance (EPS) function and metabolic pathway of Mn(II) were explored. Furthermore, effect of cellular components on denitrification was evaluated including BioMnOx performances, indicating that Mn(II) promoted the non-enzymatic action of cell fragments. Finally, mechanism of nitrification and denitrification, denitrifying phosphorus and Mn removal was further elucidated through X-ray photoelectron spectroscopy (XPS), high throughput sequencing, and fourier transform infrared reflection (FTIR). This results can bringing new vision for controlling nutrient pollution in redox process of Mn(II).

摘要

生物成因的锰氧化物 (BioMnOx) 作为活性氧化剂、吸附剂和催化剂引起了广泛关注。然而,不同浓度的 BioMnOx 介导的生物氧化还原反应中的硝化-反硝化特性和机制仍不清楚。通过移动床生物膜反应器 (MBBR) 中 Mn(II) 产生的不同浓度的 BioMnOx 研究了营养物质(例如 NH-N、TP、NO-N)和 COD 的命运。在四个阶段中,MBBR 分别同步去除了 34%和 89.2%、37.8%和 89.8%、57.3%和 88.9%和 62.1%和 90.4%的 TN 和 COD。结果表明,Mn(II) 显著提高了基于锰(Mn)氧化还原循环的同步硝化反硝化(SND)和 TP 去除性能。讨论了谷胱甘肽过氧化物酶 (GSH-Px)、活性氧 (ROS) 和电子传递系统活性 (ETSA) 的特性,表明 ROS 积累会降低 ETSA 和 GSH-Px 活性当 Mn(II)浓度增加时。探索了胞外聚合物 (EPS) 的功能和 Mn(II)的代谢途径。此外,还评估了细胞成分对反硝化的影响,包括 BioMnOx 的性能,表明 Mn(II)促进了细胞碎片的非酶作用。最后,通过 X 射线光电子能谱 (XPS)、高通量测序和傅里叶变换红外反射 (FTIR) 进一步阐明了硝化和反硝化、反硝化除磷和 Mn 去除的机制。这些结果可以为控制 Mn(II) 氧化还原过程中的营养污染带来新的视角。

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