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首页> 外文期刊>Geochimica et Cosmochimica Acta: Journal of the Geochemical Society and the Meteoritical Society >Microscale controls on the fate of contaminant uranium in the vadose zone, Hanford Site, Washington
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Microscale controls on the fate of contaminant uranium in the vadose zone, Hanford Site, Washington

机译:华盛顿汉福德基地渗流带中铀污染命运的微观控制

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An alkaline brine containing uranyl (UO22+) leaked to the thick unsaturated zone at the Hanford Site. We examined samples from this zone at microscopic scale to determine the mode of uranium occurrence-microprecipitates of uranyl (UO22+) silicate within lithic-clast microfractures-and constructed a conceptual model for its emplacement, which we tested using a model of reactive diffusion at that scale. The study was driven by the need to understand the heterogeneous distribution of uranium and the chemical processes that controlled it. X-ray and electron microprobe imaging showed that the uranium was associated with a minority of clasts, specifically granitic clasts occupying less than four percent of the sediment volume. XANES analysis at micron resolution showed the uranium to be hexavalent. The uranium was precipitated in microfractures as radiating clusters of uranyl silicates, and sorbed uranium was not observed on other surfaces. Compositional determinations of the 1-3 mu m precipitates were difficult, but indicated a uranyl silicate. These observations suggested that uranyl was removed from pore waters by diffusion and precipitation in microfractures, where dissolved silica within the granite-equilibrated solution would cause supersaturation with respect to sodium boltwoodite. This hypothesis was tested using a reactive diffusion model operating at microscale. Conditions favoring precipitation were simulated to be transient, and driven by the compositional contrast between pore and fracture space. Pore-space conditions, including alkaline pH, were eventually imposed on the microfracture environment. However, conditions favoring precipitation were prolonged within the microfracture by reaction at the silicate mineral surface to buffer pH in a solubility limiting acidic state, and to replenish dissolved silica. During this time, uranyl was additionally removed to the fracture space by diffusion from pore space. Uranyl is effectively immobilized within the microfracture environment within the presently unsaturated Vadose Zone. (c) 2006 Elsevier Inc. All rights reserved.
机译:含铀酰(UO22 +)的碱性盐水泄漏到汉福德工地的较厚不饱和区。我们在微观尺度上检查了该区域的样品,以确定铀的发生方式-碎屑岩微裂缝中铀酰(UO22 +)硅酸盐的微沉淀-并为其定位建立了概念模型,我们在该模型中使用反应扩散模型进行了测试规模。该研究的驱动是需要了解铀的非均质分布和控制铀的化学过程。 X射线和电子探针成像表明,铀与少数碎屑有关,特别是花岗岩碎屑,其含量不到沉积物体积的4%。微米分辨率的XANES分析表明铀是六价的。铀以硅酸铀酰的辐射团簇形式在微裂缝中沉淀,在其他表面未观察到吸附的铀。 1-3μm沉淀物的组成测定很困难,但表明是铀酰硅酸盐。这些观察结果表明,在微裂缝中通过扩散和沉淀从孔水中除去了铀酰,在花岗岩均衡溶液中溶解的二氧化硅相对于螺栓木酸钠会引起过饱和。使用在微尺度下运行的反应扩散模型测试了该假设。模拟有利于降水的条件是瞬态的,并且受孔隙和裂缝空间之间成分对比的驱动。孔隙空间条件,包括碱性pH值,最终施加在微裂缝环境上。然而,通过在硅酸盐矿物表面上反应以限制溶解度为酸性的pH值缓冲pH,并补充溶解的二氧化硅,在微裂缝内延长了有利于沉淀的条件。在此期间,通过从孔空间扩散将铀酰另外除去至裂缝空间。铀酰有效地固定在目前不饱和渗流区内的微裂缝环境中。 (c)2006 Elsevier Inc.保留所有权利。

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