University of Oxford, Department of Materials, Oxford, United Kingdom OX1 3PH.
AWE, Aldermaston, Reading, Berkshire, United Kingdom, RG7 4PR.
Sci Rep. 2016 Jul 12;6:25618. doi: 10.1038/srep25618.
Understanding the corrosion of uranium is important for its safe, long-term storage. Uranium metal corrodes rapidly in air, but the exact mechanism remains subject to debate. Atom Probe Tomography was used to investigate the surface microstructure of metallic depleted uranium specimens following polishing and exposure to moist air. A complex, corrugated metal-oxide interface was observed, with approximately 60 at.% oxygen content within the oxide. Interestingly, a very thin (~5 nm) interfacial layer of uranium hydride was observed at the oxide-metal interface. Exposure to deuterated water vapour produced an equivalent deuteride signal at the metal-oxide interface, confirming the hydride as originating via the water vapour oxidation mechanism. Hydroxide ions were detected uniformly throughout the oxide, yet showed reduced prominence at the metal interface. These results support a proposed mechanism for the oxidation of uranium in water vapour environments where the transport of hydroxyl species and the formation of hydride are key to understanding the observed behaviour.
了解铀的腐蚀对于其安全、长期储存非常重要。金属铀在空气中会迅速腐蚀,但确切的机制仍存在争议。原子探针层析技术被用于研究经过抛光和暴露在潮湿空气中的贫铀金属样品的表面微观结构。观察到一个复杂的、波纹状的金属氧化物界面,氧化物中含有约 60 原子%的氧。有趣的是,在氧化物-金属界面处观察到非常薄(约 5nm)的铀氢化物界面层。暴露在重水蒸汽中会在金属-氧化物界面处产生等效的氘化物信号,这证实了氢化物是通过水蒸汽氧化机制产生的。在整个氧化物中均匀检测到氢氧根离子,但在金属界面处的突出程度降低。这些结果支持了一种在水蒸汽环境中氧化铀的机制,其中羟基物种的传输和氢化物的形成是理解观察到的行为的关键。