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首页> 外文期刊>Analytical and bioanalytical chemistry >Speciation of Np(V) uptake byOpalinus Clay using synchrotron microbeam techniques
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Speciation of Np(V) uptake byOpalinus Clay using synchrotron microbeam techniques

机译:利用同步加速器微束技术测定Opalinus粘土吸收Np(V)的形态

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摘要

Synchrotron-based X-ray absorption spectroscopy has been used to determine the chemical speciation of Np sorbed on Opalinus Clay (OPA, Mont Terri, Switzerland), a natural argillaceous rock revealing a micro-scale heterogeneity. Different sorption and diffusion samples with Np(V) were prepared for spatially resolved molecular-level investigations. Thin sections of OPA contacted with Np(V) solution under aerobic and anaerobic conditions as well as a diffusion sample were analysed spatially resolved. Micro-X-ray fluorescence (μ-XRF) mapping has been used to determine the elemental distributions of Np, Fe and Ca. Regions of high Np concentration were subsequently investigated by micro-X-ray absorption fine structure spectroscopy to determine the oxidation state of Np. Further, micro-X-ray diffraction (μ-XRD) was employed to gain knowledge about reactive crystalline mineral phases in the vicinity of Np enrichments. One thin sectionwas also analysed by electron microprobe to determine the elemental distributions of the lighter elements (especially Si and Al), which represent the main elements of OPA. The results show that in most samples, Np spots with considerable amounts ofNp(IV) could be found evenwhen the experiments were carried out in air. In some cases, almost pure Np(IV) L_(III)-edge X-ray absorption near-edge structure spectra were recorded. In the case of the anaerobic sample, the μ-XRF mapping showed a clear correlation between Np and Fe, indicating that the reduction of Np(V) is caused by an iron(II)- containing mineral which could be identified by μ-XRD as pyrite. These spatially resolved investigations were complemented by extended X-ray absorption fine structure measurements of powder samples from batch experiments under aerobic and anaerobic conditions to determine the structural parameters of the near-neighbour environment of sorbed Np.
机译:基于同步加速器的X射线吸收光谱法已被用于测定吸附在蛋白石粘土(OPA,瑞士蒙特特里)上的Np的化学形态,蛋白石是一种天然的泥质岩石,具有微观尺度的异质性。准备了具有Np(V)的不同吸附和扩散样品,用于空间分辨的分子水平研究。在空间上分析了在有氧和无氧条件下与Np(V)溶液接触的OPA的薄片以及扩散样品。微X射线荧光(μ-XRF)映射已用于确定Np,Fe和Ca的元素分布。随后通过微X射线吸收精细结构光谱研究高Np浓度的区域,以确定Np的氧化态。此外,采用微X射线衍射(μ-XRD)来获得有关Np富集附近的反应性晶体矿物相的知识。还通过电子探针分析了一个薄片,以确定较轻元素(尤其是Si和Al)的元素分布,这些元素代表了OPA的主要元素。结果表明,即使在空气中进行实验,在大多数样品中也可以发现含有大量Np(IV)的Np斑点。在某些情况下,记录了几乎纯的Np(IV)L_(III)边缘X射线吸收近边缘结构光谱。在厌氧样品的情况下,μ-XRF谱图显示Np和Fe之间有明显的相关性,表明Np(V)的减少是由含铁(II)的矿物引起的,可以通过μ-XRD进行鉴定作为黄铁矿。这些空间分辨的研究得到了有氧和无氧条件下批次实验中粉末样品扩展X射线吸收精细结构测量的补充,以确定吸附Np的近邻环境的结构参数。

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