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Isotopic and Geochemical Tracers for U(Ⅵ) Reduction and U Mobility at an in Situ Recovery U Mine

机译:同位素和地球化学示踪剂,用于原位回收U矿中的U(Ⅵ)还原和U迁移

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摘要

In situ recovery (ISR) uranium (U) mining mobilizes U in its oxidized hexavalent form (U(Ⅵ)) by oxidative dissolution of U from the roll-front U deposits. Postmining natural attenuation of residual U(Ⅵ) at ISR mines is a potential remediation strategy. Detection and monitoring of naturally occurring reducing subsurface environments are important for successful implementation of this remediation scheme. We used the isotopic tracers ~(238)U/~235U (δ~(238)U), ~(234)U/~(238)U activity ratio, and ~(34)S/~(32)S (δ~(34)S), and geochemical measurements of U ore and groundwater collected from 32 wells located within, upgradient, and downgradient of a roll-front U deposit to detect U(Ⅵ) reduction and U mobility at an ISR mining site at Rosita, TX, USA. The δ~(238)U in Rosita groundwater varies from +0.61‰ to -2.49‰, with a trend toward lower δ~(238)U in downgradient wells. The concurrent decrease in U(Ⅵ) concentration and δ~(238)U with an ε of 0.48‰ ± 0.08‰ is indicative of naturally occurring reducing environments conducive to U(Ⅵ) reduction. Additionally, characteristic ~(234)U/~(238)U activity ratio and δ~(34)S values may also be used to trace the mobility of the ore zone groundwater after mining has ended. These results support the use of U isotope-based detection of natural attenuation of U(Ⅵ) at Rosita and other similar ISR mining sites.
机译:原位回收(ISR)铀(U)通过从卷前铀矿床中氧化溶解铀来动员以氧化六价形式(U(Ⅵ))的铀。在ISR矿山中对残留U(Ⅵ)的自然衰减进行后期开采是一种潜在的补救策略。自然发生的还原性地下环境的检测和监视对于成功实施此修复方案很重要。我们使用了同位素示踪剂〜(238)U /〜235U(δ〜(238)U),〜(234)U /〜(238)U活度比和〜(34)S /〜(32)S(δ 〜(34)S)以及从位于前滚轧铀矿床内,上坡度和下坡度的32口井中收集的铀矿石和地下水的地球化学测量,以检测Rosita ISR采矿场的U(Ⅵ)还原和U迁移率,美国得克萨斯州。 Rosita地下水中的δ〜(238)U在+ 0.61‰至-2.49‰之间变化,并具有下降井中δ〜(238)U较低的趋势。 U(Ⅵ)浓度和δ〜(238)U的同时降低,ε为0.48‰±0.08‰,表明自然存在的还原环境有利于U(Ⅵ)的还原。另外,特征(〜234)U /〜(238)U活度比和δ〜(34)S值也可用于追踪采矿结束后矿区地下水的迁移率。这些结果支持在Rosita和其他类似的ISR采矿场使用基于U同位素的U(Ⅵ)自然衰减检测方法。

著录项

  • 来源
    《Environmental Science & Technology》 |2015年第10期|5939-5947|共9页
  • 作者单位

    Department of Earth and Planetary Science, University of California, Berkeley, 307 McCone Hall, Berkeley, California 94720, United States,Department of Earth and Planetary Science, 483 McCone Hall, University of California, Berkeley, Berkeley, CA 94720, USA;

    Department of Earth and Planetary Science, University of California, Berkeley, 307 McCone Hall, Berkeley, California 94720, United States,Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, California 94720, United States;

    Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, California 94720, United States;

    Department of Earth and Planetary Science, University of California, Berkeley, 307 McCone Hall, Berkeley, California 94720, United States,Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, California 94720, United States;

    Earth and Environmental Sciences Division, Los Alamos National Laboratory, Los Alamos, New Mexico 87545, United States;

    Earth and Environmental Sciences Division, Los Alamos National Laboratory, Los Alamos, New Mexico 87545, United States;

    Earth and Environmental Sciences Division, Los Alamos National Laboratory, Los Alamos, New Mexico 87545, United States;

    Earth and Environmental Sciences Division, Los Alamos National Laboratory, Los Alamos, New Mexico 87545, United States;

    Earth and Environmental Sciences Division, Los Alamos National Laboratory, Los Alamos, New Mexico 87545, United States,Scripps Institution of Oceanography, University of California, San Diego, La Jolla, California 92093, United States;

    Uranium Resources, Inc., 6950 S. Potomac Street, Suite 300, Centennial, Colorado 80112, United States;

    Department of Geological and Environmental Sciences, Stanford University, Stanford, California 94305, United States;

  • 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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