Key Laboratory of Groundwater Resources and Environment of Ministry of Education, College of New Energy and Environment, Jilin University, Changchun 130021, China; National and Local Joint Engineering Laboratory for Petrochemical Contaminated Site Control and Remediation Technology, Jilin University, Changchun 130021, China; Jilin Provincial Key Laboratory of Water Resources and Environment, College of New Energy and Environment, Jilin University, Changchun 130021, China.
Sinopec Research Institute of Petroleum Processing Co., LTD, Beijing 100083, China.
Sci Total Environ. 2024 Dec 10;955:177021. doi: 10.1016/j.scitotenv.2024.177021. Epub 2024 Oct 22.
Sulfate-reducing bacteria (SRB) and iron minerals are widespread in subsurface environments, where their mediated Fe and S transformations are crucial for contaminant immobilization. However, the mechanism mediated by SRB to transform natural iron minerals into reduced iron-sulfur compounds and the contaminant removal capacity of the transformation products remain unclear. Herein, the mechanism of native SRB-mediated transformation of iron-minerals from natural aquifer media into biogenic ferrous sulfide (FeS) was revealed and the Cr(VI) removal performance of the transformation product was evaluated. The results showed that Fe production, sulfate reduction, and sulfide production occurred sequentially (rather than simultaneously) in the liquid phase. This suggests new processes and mechanisms for iron-mineral transformation: first, iron minerals dissolve to produce Fe under enzymatic action rather than sulfide reduction; then, the generated Fe accelerates sulfate reduction by SRB, producing sulfide in large amounts; finally, sulfide combines rapidly with Fe to produce FeS. Elevated temperatures markedly shortened the required transformation time to start: maximum Fe production occurred at 18-24 days, 6-12 days, and 0-6 days at 10 °C, 20 °C, and 35 °C, respectively. Ambient temperature strongly affected SRB community composition, with Desulfosporosinus dominant at 10 °C and 20 °C and Desulfotomaculales prevalent at 35 °C. Sequential extraction, scanning electron microscopy, X-ray photoelectron spectroscopy, and X-ray diffraction analyses confirmed FeS as the main transformation product, which exhibited a highly efficient Cr(VI) removal capacity. Extending transformation time or increasing transformation temperature enhanced the Cr(VI) removal capacity of the transformation product. In column experiments, in-situ stimulation of SRB growth in aquifer media is able to form FeS, the Cr(VI) removal capacity of FeS reached up to 90.1 mg(Cr(VI))/kg(media). These findings suggest that biostimulation of SRB to mediate the in-situ transformation of iron-minerals to FeS has great potential for remediation of contaminated groundwater.
硫酸盐还原菌(SRB)和铁矿物广泛存在于地下环境中,它们介导的铁和硫转化对于污染物的固定化至关重要。然而,SRB 介导的将天然铁矿物转化为还原态铁-硫化合物的机制以及转化产物的污染物去除能力仍不清楚。本文揭示了天然 SRB 介导的从天然含水层介质中转化铁矿物为生物亚铁硫化物(FeS)的机制,并评估了转化产物对六价铬(Cr(VI))的去除性能。结果表明,铁的产生、硫酸盐的还原和硫化物的产生在液相中依次发生(而不是同时发生)。这为铁矿物的转化提出了新的过程和机制:首先,在酶的作用下,铁矿物溶解产生 Fe,而不是硫化物还原;然后,生成的 Fe 加速了 SRB 对硫酸盐的还原,大量产生硫化物;最后,硫化物与 Fe 快速结合生成 FeS。升高温度显著缩短了开始转化所需的时间:在 10℃、20℃和 35℃下,最大铁产量分别出现在 18-24 天、6-12 天和 0-6 天。环境温度强烈影响 SRB 群落组成,在 10℃和 20℃时以脱硫菌属(Desulfosporosinus)为主,在 35℃时脱硫杆菌目(Desulfotomaculales)占优势。顺序提取、扫描电子显微镜、X 射线光电子能谱和 X 射线衍射分析证实了 FeS 是主要的转化产物,其对 Cr(VI)具有高效的去除能力。延长转化时间或提高转化温度可提高转化产物的 Cr(VI)去除能力。在柱实验中,原位刺激含水层介质中 SRB 的生长能够形成 FeS,FeS 对 Cr(VI)的去除能力高达 90.1mg(Cr(VI))/kg(介质)。这些发现表明,通过 SRB 的生物刺激来介导铁矿物的原位转化为 FeS,对于受污染地下水的修复具有巨大的潜力。