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采矿后环境条件下铁氢氧化物对铀的滞留。

Uranium retention on iron oxyhydroxides in post-mining environmental conditions.

机构信息

Sorbonne Université, CNRS UMR7590, MNHN, IRD, Institut de minéralogie, de physique des matériaux et de cosmochimie (IMPMC), 4 place Jussieu, F-75005, Paris, France.

Sorbonne Université, CNRS UMR7590, MNHN, IRD, Institut de minéralogie, de physique des matériaux et de cosmochimie (IMPMC), 4 place Jussieu, F-75005, Paris, France.

出版信息

Chemosphere. 2021 Feb;264(Pt 1):128473. doi: 10.1016/j.chemosphere.2020.128473. Epub 2020 Oct 1.

Abstract

Investigating uranium migration mechanisms related to the weathering of waste rocks is essential for developing strategies that can address the potential environmental issues caused by uranium mining. This work is based on environmental samples containing 2 L ferrihydrite, lepidocrocite and goethite collected in the technosols from granitic waste rock piles, mine drainage conduits and mine waters. The results show the important role of iron oxyhydroxide in U immobilization and re-concentration. EXAFS spectroscopy combined with mineralogical and geochemical studies (Scanning electronic microscopy, Wavelength-dispersive X-ray spectroscopy microprobe, inductively coupled plasma - optical emission spectrometry/mass spectrometry and X-ray diffraction) allowed for the identification of uranyl ternary surface complexes at the ferrihydrite surface that were either composed of phosphate groups or organic matter. Moreover, goethite and lepidocrocite were also identified as a secondary trap for U immobilization. U(VI) is known to be mobile in oxidizing conditions. This study highlights the control of the uranyl mobility by various iron oxyhydroxides in supergene conditions.

摘要

研究与风化废石有关的铀迁移机制对于制定策略至关重要,这些策略可以解决铀矿开采所引发的潜在环境问题。这项工作基于从花岗质废石堆、矿坑排水管道和矿水中采集的含有 2L 水铁矿、纤铁矿和针铁矿的环境样本。结果表明,铁氢氧化物在 U 固定和再浓缩中起着重要作用。扩展 X 射线吸收精细结构(EXAFS)光谱学结合矿物学和地球化学研究(扫描电子显微镜、波长分散 X 射线光谱微探针、电感耦合等离子体 - 发射光谱/质谱和 X 射线衍射),鉴定出水铁矿表面上由磷酸基团或有机物组成的铀酰三元表面配合物。此外,针铁矿和纤铁矿也被确定为 U 固定的二次捕获剂。U(VI)在氧化条件下是可移动的。本研究强调了各种铁氢氧化物在表生条件下对铀酰迁移性的控制。

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