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Microbial Reduction of U(Ⅵ) under Alkaline Conditions: Implications for Radioactive Waste Geodisposal

机译:碱性条件下U(Ⅵ)的微生物还原:对放射性废物地球处置的意义

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摘要

Although there is consensus that microorganisms significantly influence uranium speciation and mobility in the subsurface under circumneutral conditions, microbiologically mediated U(Ⅵ) redox cycling under alkaline conditions relevant to the geological disposal of cementitious intermediate level radioactive waste, remains unexplored. Here, we describe microcosm experiments that investigate the biogeochemical fate of U(Ⅵ) at pH 10-10.5, using sediments from a legacy lime working site, stimulated with an added electron donor, and incubated in the presence and absence of added Fe(Ⅲ) as ferrihydrite. In systems without added Fe(Ⅲ), partial U(Ⅵ) reduction occurred, forming a U(Ⅳ)-bearing non-uraninite phase which underwent reoxidation in the presence of air (O_2) and to some extent nitrate. By contrast, in the presence of added Fe(Ⅲ), U(Ⅵ) was first removed from solution by sorption to the Fe(Ⅲ) mineral, followed by bioreduction and (bio)magnetite formation coupled to formation of a complex U(Ⅳ)-bearing phase with uraninite present, which also underwent air (O_2) and partial nitrate reoxidation. 16S rRNA gene pyrosequencing showed that Gram-positive bacteria affiliated with the Firmicutes and Bacteroidetes dominated in the post-reduction sediments. These data provide the first insights into uranium biogeochemistry at high pH and have significant implications for the long-term fate of uranium in geological disposal in both engineered barrier systems and the alkaline, chemically disturbed geosphere.
机译:尽管人们普遍认为微生物会在周围环境条件下显着影响地下铀的形态和迁移率,但仍未探索在与胶结性中等水平放射性废物地质处置有关的碱性条件下微生物介导的U(Ⅵ)氧化还原循环。在这里,我们描述了微观实验,该实验研究了使用传统石灰工作现场的沉淀物,用添加的电子供体刺激并在有无添加Fe(Ⅲ)的条件下孵育的pH为10-10.5的U(Ⅵ)的生物地球化学命运。 )作为水铁矿。在未添加Fe(Ⅲ)的体系中,部分U(Ⅵ)被还原,形成了一个含U(Ⅳ)的非铀矿相,该相在空气(O_2)和一定程度的硝酸盐存在下进行了再氧化。相比之下,在添加的Fe(Ⅲ)存在下,首先通过吸附到Fe(Ⅲ)矿物上而从溶液中除去U(Ⅵ),然后进行生物还原和(生物)磁铁矿形成,再形成复杂的U(Ⅳ)。含铀的矿物相,也经历了空气(O_2)和部分硝酸盐再氧化。 16S rRNA基因焦磷酸测序表明,革兰氏阳性菌和拟杆菌和拟杆菌属在还原后的沉积物中占主导地位。这些数据提供了对高pH下铀生物地球化学的初步见解,并且对铀在工程屏障系统和碱性,化学扰动地球圈中的地质处置中的长期命运具有重要意义。

著录项

  • 来源
    《Environmental Science & Technology》 |2014年第22期|13549-13556|共8页
  • 作者单位

    Research Centre for Radwaste Disposal and Williamson Research Centre for Molecular Environmental Science, School of Earth, Atmospheric and Environmental Sciences, The University of Manchester, Manchester, M13 9PL, United Kingdom;

    Research Centre for Radwaste Disposal and Williamson Research Centre for Molecular Environmental Science, School of Earth, Atmospheric and Environmental Sciences, The University of Manchester, Manchester, M13 9PL, United Kingdom;

    Centre for Radiochemistry Research and Research Centre for Radwaste Disposal, School of Chemistry, The University of Manchester, Manchester, M13 9PL, United Kingdom;

    Research Centre for Radwaste Disposal and Williamson Research Centre for Molecular Environmental Science, School of Earth, Atmospheric and Environmental Sciences, The University of Manchester, Manchester, M13 9PL, United Kingdom;

    Research Centre for Radwaste Disposal and Williamson Research Centre for Molecular Environmental Science, School of Earth, Atmospheric and Environmental Sciences, The University of Manchester, Manchester, M13 9PL, United Kingdom;

    Research Centre for Radwaste Disposal and Williamson Research Centre for Molecular Environmental Science, School of Earth, Atmospheric and Environmental Sciences, The University of Manchester, Manchester, M13 9PL, United Kingdom;

  • 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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