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首页> 外文期刊>Science of the total environment >In-situ formation and self-immobilization of biogenic Fe oxides in anaerobic granular sludge for enhanced performance of acidogenesis and methanogenesis
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In-situ formation and self-immobilization of biogenic Fe oxides in anaerobic granular sludge for enhanced performance of acidogenesis and methanogenesis

机译:厌氧颗粒污泥中生物二氧化碳的原位形成和自固定,提高酸性生成和甲烷的性能

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摘要

Addition of ferric oxides into flocculent anaerobic sludge was reported to enhance methanogenesis due to accelerated direct interspecies electron transfer (DIET) between syntrophic microbial communities. However, it is generally hard to incorporate Fe oxides into already matured anaerobic granular sludge (AGS) due to its special aggregated structure. In this study, a novel method was attempted to fast incorporate Fe oxides into AGS through in-situ microbial formation and immobilization of biogenic Fe oxides. Factors influencing the formation of Fe oxides were investigated and effects of Fe oxides on the acidogenic and methanogenic performance of AGS were assessed. Results showed that AGS could form Fe oxides mainly in the form of magnetite and hematite through biological reduction of Fe( Ⅲ) oxyhydroxide. A maximum loading amount of 83.9 mg Fe/g MLVSS was obtained at pH 7 after contacting with 60 mM Fe(Ⅲ) oxyhydroxide. The efficiency of electron donors which supported Fe( Ⅲ) reduction followed the order of pyruvate > propionate > glucose > acetate > lactate > formate. Addition of electron transfer mediators (ETMs) promoted the formation of Fe oxides and their performance followed the order of AQDS > AQC > humics > FMN > riboflavin. Presence of Fe oxides in AGS (134.6 Fe/g VSS) increased the production of volatile fatty acids (VFAs) and methane by 16.28% and 41.94% respectively, comparing to the control. The enhancement may be attributed to increased conductivity and stimulated growth of exoelectrogens (Clostridium and Anaerolinea) and methanogenic endoelectrogens Methanosaeta in granular sludge which may strengthen direct interspecies electron transfer between syntrophic microbial communities. Overall, this study provides an alternative strategy to improve the digestion performance of AGS through in-situ formation and immobilization of biogenic Fe oxides.
机译:据报道,向絮凝剂中添加氧化铁进入絮凝厌氧污泥,以提高甲烷,由于同步微生物群落之间的直接散列电子转移(饮食)增强了甲烷。然而,由于其特殊的聚集结构,通常很难将Fe氧化物掺入已经成熟的厌氧颗粒污泥(AGS)中。在这项研究中,通过原位微生物形成和生物氧化物固定,尝试将Fe氧化物快速将Fe氧化物掺入AGS中。研究了影响Fe氧化物形成的因素,并评估了Fe氧化物对AGS的酸性和甲状腺化合物的影响。结果表明,AGS可以通过Fe(Ⅲ)羟基氧化物的生物学还原成主要以磁铁矿和赤铁矿形式形成Fe氧化物。在与60mM FE(Ⅲ)羟基氧化物接触后,在pH7下获得最大加载量为83.9mg Fe / g mLVS。支持Fe(Ⅲ)还原的电子供体的效率遵循丙酮酸>丙酸盐>醋酸甘露糖>乳酸盐>甲酸盐。添加电子转移介质(ETM)促进了Fe氧化物的形成及其性能,然后遵循AQDS> AQC>蜂窝> FMN>核苷酸的顺序。 AGS中的Fe氧化物(134.6 Fe / g VSS)的存在将挥发性脂肪酸(VFA)和甲烷的产生分别与对照相比,分别将挥发性脂肪酸(VFA)和41.94%的产生。增强可归因于增加粒状污泥中的导电性和促进exoeLoColecencens(Clostridium和Anaerolinea)和甲状腺内电酶甲蛋白酶甲蛋白酶的粒状污泥,其可以加强语言微生物群落之间的直接间隙电子转移。总体而言,本研究提供了通过原位形成和生物二氧化碳的原位形成和固定来改善AGS的消化性能的替代策略。

著录项

  • 来源
    《Science of the total environment》 |2021年第15期|147400.1-147400.9|共9页
  • 作者单位

    Key Laboratory of Water and Sediment Sciences of Ministry of Education State Key Laboratory of Water Environment Simulation School of Environment. Beijing Normal University Beijing 100875 China;

    Key Laboratory of Water and Sediment Sciences of Ministry of Education State Key Laboratory of Water Environment Simulation School of Environment. Beijing Normal University Beijing 100875 China;

    Key Laboratory of Water and Sediment Sciences of Ministry of Education State Key Laboratory of Water Environment Simulation School of Environment. Beijing Normal University Beijing 100875 China;

    Key Laboratory of Water and Sediment Sciences of Ministry of Education State Key Laboratory of Water Environment Simulation School of Environment. Beijing Normal University Beijing 100875 China;

    School of Chemistry Beijing Normal University Beijing 100875 China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Anaerobic granular sludge; Ferric oxides; Magnetite; Methane; Direct interspecies electron transfer;

    机译:厌氧颗粒污泥;氧化铁;磁铁矿;甲烷;直接散列电子转移;

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