Data underlying the publication: Nitrous Oxide as a Major Product of Anoxic Bioanode Ammonium Oxidation: Pathway Insights and Implications
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https://data.4tu.nl/datasets/4b6b112f-d2ce-4f8c-867f-70bb651f27b5/1
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资源简介:
Anoxic ammonium (NH<sub>4</sub><sup>+</sup>) oxidation at bioanodes offers a feasible alternative to conventional biological nitrogen removal (BNR), eliminating the need for aeration and enabling direct nitrogen gas (N<sub>2</sub>) production. However, the extent of nitrous oxide (N<sub>2</sub>O) emissions in this process remains unclear. This study examines N<sub>2</sub>O emissions during anoxic NH<sub>4</sub><sup>+</sup> oxidation at a polarized bioanode (+0.55 V vs Ag/AgCl), focusing on the roles of key intermediates—hydroxylamine (NH<sub>2</sub>OH) and nitrite (NO<sub>2</sub><sup>-</sup>)—in N<sub>2</sub>O formation, and microbial functional groups involved in N<sub>2</sub>O production, aiming to elucidate the underlying N<sub>2</sub>O production pathways during bioanodic NH<sub>4</sub><sup>+</sup> oxidation. Results show that up to 40% of oxidized NH<sub>4</sub><sup>+</sup> was converted to N<sub>2</sub>O, while NO<sub>2</sub><sup>-</sup> and NO<sub>3</sub><sup>-</sup> remained at relatively low levels (2.1%–11.1%). NH<sub>2</sub>OH oxidation was identified as the dominant N<sub>2</sub>O production pathway, likely involving nitric oxide (NO) as an intermediate. NO<sub>2</sub><sup>-</sup> reduction also contributed to N<sub>2</sub>O formation, albeit to a minor extent, while in situ N<sub>2</sub>O reduction—considered to be mediated by denitrifiers—offers potential for mitigating its emissions. In parallel, an electro-anammox-like pathway, which does not involve nitrifiers, facilitated direct NH<sub>4</sub><sup>+</sup> conversion to N<sub>2</sub> without N<sub>2</sub>O formation. These findings highlight the potential for substantial N<sub>2</sub>O emissions from bioanode-based systems and underscore the importance of pathway control to mitigate greenhouse gas release.
生物阳极(bioanode)上的缺氧氨(NH₄⁺)氧化为传统生物脱氮(BNR)提供了可行替代方案,无需曝气即可直接生成氮气(N₂)。然而,该过程中一氧化二氮(N₂O)的排放水平仍未明确。
本研究考察了极化生物阳极(相对于Ag/AgCl参比电极为+0.55 V)上的缺氧氨氧化过程中的N₂O排放,重点关注关键中间体——羟胺(NH₂OH)与亚硝酸盐(NO₂⁻)在N₂O生成中的作用,以及参与N₂O产生的微生物功能菌群,旨在阐明生物阳极氨氧化过程中N₂O生成的潜在途径。
研究结果显示,高达40%的被氧化氨会转化为N₂O,而亚硝酸盐(NO₂⁻)与硝酸盐(NO₃⁻)的残留水平相对较低(2.1%~11.1%)。研究证实羟胺氧化是N₂O生成的主要途径,该过程可能以一氧化氮(NO)作为中间体。亚硝酸盐还原同样对N₂O生成有贡献,但占比极小;而由反硝化菌(denitrifiers)介导的原位N₂O还原则为缓解其排放提供了潜在可能。
与此同时,一条无需硝化菌(nitrifiers)参与的类电厌氧氨氧化途径,可直接将氨转化为氮气(N₂)且不会产生N₂O。
上述研究结果凸显了基于生物阳极的系统存在显著N₂O排放的潜力,并强调了调控反应途径以缓解温室气体释放的重要性。
提供机构:
Buisman, Cees; Liu, Dandan; Yang, Zhenqiu
创建时间:
2025-07-08



