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在化学吸收-生物还原一体化 NOx 去除系统中,氧对 Fe(III)EDTA 还原的生物化学相互作用。

Biological and chemical interaction of oxygen on the reduction of Fe(III)EDTA in a chemical absorption-biological reduction integrated NOx removal system.

机构信息

Institute of Environmental Engineering, Zhejiang University (Zijingang Campus), Hangzhou, China.

出版信息

Appl Microbiol Biotechnol. 2012 Mar;93(6):2653-9. doi: 10.1007/s00253-011-3573-z. Epub 2011 Sep 20.

Abstract

A promising chemical absorption-biological reduction integrated process has been proposed. A major problem of the process is oxidation of the active absorbent, ferrous ethylenediaminetetraacetate (Fe(II)EDTA), to the ferric species, leading to a significant decrease in NO removal efficiency. Thus the biological reduction of Fe(III)EDTA is vitally important for the continuous NO removal. Oxygen, an oxidizing agent and biological inhibitor, is typically present in the flue gas. It can significantly retard the application of the integrated process. This study investigated the influence mechanism of oxygen on the regeneration of Fe(II)EDTA in order to provide insight on how to eliminate or decrease the oxygen influence. The experimental results revealed that the dissolved oxygen and Fe(III)EDTA simultaneously served as electron acceptor for the microorganism. The Fe(III)EDTA reduction activity were directly inhibited by the dissolved oxygen. When the bioreactor was supplied with 3% and 8% oxygen in the gas phase, the concentration of initial dissolved oxygen in the liquid phase was 0.28 and 0.68 mg l(-1). Correspondingly, the instinct Fe(III)EDTA reduction activity of the microorganism determined under anoxic condition in a rotation shaker decreased from 1.09 to 0.84 and 0.49 mM h(-1). The oxidation of Fe(II)EDTA with dissolved oxygen prevented more dissolved oxygen access to the microorganism and eased the inhibition of dissolved oxygen on the microorganisms.

摘要

一种有前景的化学吸收-生物还原集成工艺已经被提出。该工艺的一个主要问题是活性吸收剂(乙二胺四乙酸亚铁(Fe(II)EDTA))被氧化为铁(III)物种,导致 NO 去除效率显著降低。因此,Fe(III)EDTA 的生物还原对于连续去除 NO 至关重要。氧气是一种氧化剂和生物抑制剂,通常存在于烟道气中。它会显著阻碍集成工艺的应用。本研究考察了氧气对 Fe(II)EDTA 再生的影响机制,以期深入了解如何消除或减少氧气的影响。实验结果表明,溶解氧和 Fe(III)EDTA 同时作为微生物的电子受体。溶解氧直接抑制 Fe(III)EDTA 的还原活性。当生物反应器气相中分别通入 3%和 8%的氧气时,液相中初始溶解氧的浓度分别为 0.28 和 0.68mg l(-1)。相应地,在旋转摇床中无氧条件下确定的微生物初始 Fe(III)EDTA 还原活性从 1.09 降低至 0.84 和 0.49mM h(-1)。溶解氧对 Fe(II)EDTA 的氧化作用阻止了更多的溶解氧进入微生物,并缓解了溶解氧对微生物的抑制作用。

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