生物技术通报 ›› 2026, Vol. 42 ›› Issue (5): 248-256.doi: 10.13560/j.cnki.biotech.bull.1985.2025-1399

• 微生物组学专题 • 上一篇    

零价铁对厌氧氨氧化系统的影响及累积作用机制

陈仔龙1(), 张超1,2(), 郝宛婷1, 宋贤威1, 陈雨婷1, 陈欣怡1, 高明原1, 朱易春1,2   

  1. 1.江西理工大学环境工程学院,赣州 341000
    2.河流源头水生态保护江西省重点实验室,赣州 341000
  • 收稿日期:2025-12-22 出版日期:2026-05-26 发布日期:2026-06-10
  • 通讯作者: 张超,博士,讲师,研究方向 :生物脱氮新技术;E-mail: 1403916177@qq.com
  • 作者简介:陈仔龙,男,硕士研究生,研究方向 :生物脱氮新技术;E-mail: 2546739685@qq.com
  • 基金资助:
    国家自然科学基金项目(52260004);江西理工大学高层次人才科研启动项目(205200100642);江西理工大学研究生创新专项资金项目(YC2025-S579);江西理工大学大学生创新创业训练资助项目(S202510407027);江西理工大学教育基金会限定性捐赠项目(JXUST-XJ2026001)

Influence and Cumulative Effect Mechanism of Zero-valent Iron on Anaerobic Ammonia Oxidation System

CHEN Zai-long1(), ZHANG Chao1,2(), HAO Wan-ting1, SONG Xian-wei1, CHEN Yu-ting1, CHEN Xin-yi1, GAO Ming-yuan1, ZHU Yi-chun1,2   

  1. 1.School of Environmental Engineering, Jiangxi University of Science and Technology, Ganzhou 341000
    2.Jiangxi Provincial Key Laboratory of Water Ecological Conservation at Headwater Regions, Ganzhou 341000
  • Received:2025-12-22 Published:2026-05-26 Online:2026-06-10

摘要:

目的 探究零价铁对厌氧氨氧化系统的影响,并揭示其累积作用机制。 方法 设定3组零价铁投加量L0(0 g/L)、L1(2 g/L)和L2(4 g/L),测定不同零价铁投加量时厌氧氨氧化系统脱氮除磷性能、污泥特性、菌群结构和氮代谢相关功能基因。 结果 适量的零价铁(L1)短期内(第3-22天)可通过腐蚀作用促进反硝化过程,并为厌氧氨氧化提供更多的亚硝酸盐底物,同时生成Fe-P沉淀实现同步除磷,使L1平均亚硝态氮、总氮和总磷去除率较L0分别提高17.64%、10.52%和84.33%。然而,零价铁过量累积(L2)会产生显著的负面效应,过量铁腐蚀产物在污泥表面积累并阻碍传质,Fe²⁺竞争性还原亚硝酸盐导致厌氧氨氧化底物失衡,使L2第23-32天的平均氨氮、亚硝态氮和总氮去除率较L0分别降低31.16%、15.56%和13.94%。同时,零价铁的累积导致Candidatus KueneniaCandidatus BrocadiaSM1A02的相对丰度降低,而DenitratisomaLimnobacter的相对丰度提高。L1和L2中氮代谢相关功能基因norBhao等的上调,是由零价铁引发厌氧氨氧化系统物理和化学环境改变所导致的。 结论 适量的零价铁可有效提高厌氧氨氧化系统脱氮除磷性能,但存在累积抑制效应,其作用机制是从化学还原、物理覆盖到微生物生态与代谢功能改变的链式过程。

关键词: 零价铁, 厌氧氨氧化, 脱氮除磷, 菌群结构, 功能基因, 作用机制

Abstract:

Objective To explore the effect of zero-valent iron on anaerobic ammonium oxidation system and reveal its cumulative effect mechanism. Method We established three groups of zero-valent iron dosage—L0 (0 g/L), L1 (2 g/L), and L2 (4 g/L), and then determined the nitrogen and phosphorus removal performance, sludge characteristics, microbial community structure and nitrogen metabolism-related functional genes of the anaerobic ammonia oxidation system at different zero-valent iron dosages. Result An appropriate amount of zero-valent iron (L1) can promote the denitrification process through corrosion in the short term (3–22 days), provide more nitrite substrates for anaerobic ammonia oxidation, and generate Fe-P precipitation to achieve synchronous phosphorus removal. This increases the average removal rates of nitrite nitrogen, total nitrogen, and total phosphorus in L1 by 17.64%, 10.52%, and 84.33%, respectively, compared to L0. However, excessive accumulation of zero-valent iron (L2) leads to significant negative effects: the corrosion products of excess iron accumulate on the surface of sludge and hinder mass transfer, and the competitive reduction of nitrite by Fe²⁺ leads to an imbalance of anaerobic ammonia oxidation substrates, resulting in a decrease of 31.16%, 15.56%, and 13.94% in the average removal rates of ammonia nitrogen, nitrite nitrogen, and total nitrogen in L2 on days 23 to 32 compared to L0, respectively. Meanwhile, the accumulation of zero-valent iron leads to a decrease in the relative abundance of Candidatus Kuenenia, Candidatus Brocadia, and SM1A02, while the relative abundance of Denitratisoma and Limnobacter increases. The upregulation of nitrogen metabolism-related functional genes norB and hao in both L1 and L2 is caused by changes in the physical and chemical environment of the anaerobic ammonia oxidation system triggered by zero-valent iron. Conclusion Moderate zero-valent iron can effectively improve the nitrogen and phosphorus removal performance of anaerobic ammonia oxidation systems, but there is a cumulative inhibitory effect. Its mechanism of action is a chain-like process containing chemical reduction, physical coverage, and changes in microbial ecology and metabolic functions.

Key words: zero-valent iron, anammox, nitrogen and phosphorus removal, microbial community structure, functional gene, mechanism of action