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Bioreduction of Chromate in a Methane-Based Membrane Biofilm Reactor

机译:甲烷基膜生物膜反应器中铬酸盐的生物还原

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摘要

For the first time, we demonstrate chromate (Cr(Ⅵ)) bioreduction using methane (CH_4) as the sole electron donor in a membrane biofilm reactor (MBfR). The experiments were divided into five stages lasting a total of 90 days, and each stage achieved a steady state for at least 15 days. Due to continued acclimation of the microbial community, the Cr(Ⅵ)-redudng capacity of the biofilm kept increasing. Cr(Ⅵ) removal at the end of the 90-day test reached 95% at an influent Cr(Ⅵ) concentration of 3 mg Cr/L and a surface loading of 0.37g of Cr m~(-2) day~(-1). Meiothermus (Deinococci), a potential Cr(Ⅵ)-reducing bacterium, was negligible in the inoculum but dominated the MBfR biofilm after Cr(Ⅵ) was added to the reactor, while Methylosinus, a type Ⅱ methanotrophs, represented 1196-21% of the total bacterial DNA in the biofilm. Synergy within a microbial consortia likely was responsible for Cr(Ⅵ) reduction based on CH_4 oxidation. In the synergy, methanotrophs fermented CH_4 to produce metabolic intermediates that were used by the Cr(Ⅵ)-reducing bacteria as electron donors. Solid Cr(Ⅲ) was the main product, accounting for more than 88% of the reduced Cr in most cases. Transmission electron microscope (TEM) and energy dispersive X-ray (EDS) analysis showed that Cr(Ⅲ) accumulated inside and outside of some bacterial cells, implying that different Cr(Ⅵ)-reducing mechanisms were involved.
机译:首次,我们证明了在膜生物膜反应器(MBfR)中使用甲烷(CH_4)作为唯一电子供体的铬酸盐(Cr(Ⅵ))生物还原。实验分为五个阶段,总共持续90天,每个阶段都达到稳定状态至少15天。由于微生物群落的不断适应,生物膜的Cr(Ⅵ)-还原能力不断增加。在进水Cr(Ⅵ)浓度为3 mg Cr / L和表面负载为0.37g Cr m〜(-2)day〜(-)的90天试验结束时,去除Cr(Ⅵ)达到95%。 1)。潜在的Cr(Ⅵ)还原菌Meiothermus(Deinococci)在接种物中可忽略不计,但在将Cr(Ⅵ)添加到反应器后,MBfR生物膜占主导地位,而Ⅱ型甲基异养菌甲基肌酐占1196-21%。生物膜中的总细菌DNA。微生物群落中的协同作用可能是基于CH_4氧化作用导致Cr(Ⅵ)还原的原因。在协同作用下,甲烷氧化菌发酵CH_4以产生代谢中间体,该中间体被Cr(Ⅵ)还原菌用作电子供体。固态铬(Ⅲ)是主要产物,在大多数情况下占还原态铬的88%以上。透射电子显微镜(TEM)和能量色散X射线(EDS)分析表明,Cr(Ⅲ)在某些细菌细胞的内部和外部积累,暗示了不同的Cr(Ⅵ)还原机理。

著录项

  • 来源
    《Environmental Science & Technology》 |2016年第11期|5832-5839|共8页
  • 作者单位

    Department of Environmental Engineering, College of Environmental and Resource Science, Zhejiang University, Hangzhou, China;

    Department of Environmental Engineering, College of Environmental and Resource Science, Zhejiang University, Hangzhou, China;

    Department of Environmental Engineering, College of Environmental and Resource Science, Zhejiang University, Hangzhou, China;

    Department of Environmental Engineering, College of Environmental and Resource Science, Zhejiang University, Hangzhou, China;

    Department of Environmental Engineering, College of Environmental and Resource Science, Zhejiang University, Hangzhou, China;

    Department of Environmental Engineering, College of Environmental and Resource Science, Zhejiang University, Hangzhou, China;

    Department of Environmental Engineering, College of Environmental and Resource Science, Zhejiang University, Hangzhou, China;

    State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin 150090, China;

    Swette Center for Environmental Biotechnology, Biodesign Institute at Arizona State University, P.O. Box 875701, Tempe, Arizona 85287-5701, United States;

    Swette Center for Environmental Biotechnology, Biodesign Institute at Arizona State University, P.O. Box 875701, Tempe, Arizona 85287-5701, United States;

    Department of Civil and Environmental Engineering, FAMU-FSU College of Engineering, Florida State University, Tallahassee, Florida 32310-6046, United States;

    Department of Environmental Engineering, College of Environmental and Resource Science, Zhejiang University, Hangzhou, China;

    Department of Environmental Engineering, College of Environmental and Resource Science, Zhejiang University, Hangzhou, China,State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin 150090, China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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  • 入库时间 2022-08-17 13:58:47

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