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乏燃料弹测试中三元 U(v)氧化物环境稳定性的证据:UFeO 的多模态 X 射线微分析。

Multimodal X-ray microanalysis of a UFeO: evidence for the environmental stability of ternary U(v) oxides from depleted uranium munitions testing.

机构信息

Immobilisation Science Laboratory, Department of Materials Science and Engineering, The University of Sheffield, UK.

出版信息

Environ Sci Process Impacts. 2020 Jul 1;22(7):1577-1585. doi: 10.1039/d0em00243g. Epub 2020 Jul 7.

Abstract

An environmentally aged radioactive particle of UFeO recovered from soil contaminated with munitions depleted uranium (DU) was characterised by microbeam synchrotron X-ray analysis. Imaging of uranium speciation by spatially resolved X-ray diffraction (μ-XRD) and X-ray absorption spectroscopy (μ-XAS) was used to localise UFeO in the particle, which was coincident with a distribution of U(v). The U oxidation state was confirmed using X-ray Absorption Near Edge Structure (μ-XANES) spectroscopy as +4.9 ± 0.15. Le-Bail fitting of the particle powder XRD pattern confirmed the presence of UFeO and a minor alteration product identified as chernikovite (HO)(UO)(PO)·3HO. Refined unit cell parameters for UFeO were in good agreement with previously published values. Uranium-oxygen interatomic distances in the first co-ordination sphere were determined by fitting of Extended X-ray Absorption Fine Structure (μ-EXAFS) spectroscopy. The average first shell U-O distance was 2.148 ± 0.012 Å, corresponding to a U valence of +4.96 ± 0.13 using bond valence sum analysis. Using bond distances from the published structure of UFeO, U and Fe bond valence sums were calculated as +5.00 and +2.83 respectively, supporting the spectroscopic analysis and confirming the presence of a U(v)/Fe(iii) pair. Overall this investigation provides important evidence for the stability of U(v) ternary oxides, in oxic, variably moist surface environment conditions for at least 25 years.

摘要

从受弹药贫铀 (DU) 污染的土壤中回收的环境老化放射性 UFeO 颗粒,通过微束同步加速器 X 射线分析进行了表征。通过空间分辨 X 射线衍射 (μ-XRD) 和 X 射线吸收光谱 (μ-XAS) 对铀形态成像,用于在颗粒中定位 UFeO,其与 U(v) 的分布一致。使用 X 射线吸收近边结构 (μ-XANES) 光谱学确认 U 氧化态为+4.9±0.15。颗粒粉末 XRD 图谱的 Le-Bail 拟合证实了 UFeO 的存在和鉴定为磷铀矿 (HO)(UO)(PO)·3HO 的次要变质产物。UFeO 的 refined 晶胞参数与先前发表的值非常吻合。通过拟合扩展 X 射线吸收精细结构 (μ-EXAFS) 光谱学确定了第一配位球中的铀-氧原子间距离。平均第一壳层 U-O 距离为 2.148±0.012 Å,使用键价和分析,对应于+4.96±0.13 的 U 价。使用 UFeO 发表结构的键距离,计算 U 和 Fe 的键价和分别为+5.00 和+2.83,这支持了光谱分析,并证实了 U(v)/Fe(iii)对的存在。总体而言,这项研究为 U(v) 三元氧化物在至少 25 年的有氧、多变潮湿的表面环境条件下的稳定性提供了重要证据。

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