X-ray Science Division, Argonne National Laboratory, Argonne, IL 60439, USA. Mineral Physics Institute, Stony Brook University, Stony Brook, NY 11794-2100, USA. Materials Development, Inc., 3090 Daniels Court, Arlington Heights, IL 60004, USA.
X-ray Science Division, Argonne National Laboratory, Argonne, IL 60439, USA.
Science. 2014 Nov 21;346(6212):984-7. doi: 10.1126/science.1259709.
Uranium dioxide (UO2) is the major nuclear fuel component of fission power reactors. A key concern during severe accidents is the melting and leakage of radioactive UO2 as it corrodes through its zirconium cladding and steel containment. Yet, the very high temperatures (>3140 kelvin) and chemical reactivity of molten UO2 have prevented structural studies. In this work, we combine laser heating, sample levitation, and synchrotron x-rays to obtain pair distribution function measurements of hot solid and molten UO2. The hot solid shows a substantial increase in oxygen disorder around the lambda transition (2670 K) but negligible U-O coordination change. On melting, the average U-O coordination drops from 8 to 6.7 ± 0.5. Molecular dynamics models refined to this structure predict higher U-U mobility than 8-coordinated melts.
二氧化铀 (UO2) 是裂变动力反应堆的主要核燃料组件。在严重事故中,一个关键问题是放射性 UO2 的熔化和泄漏,因为它会通过锆合金包壳和钢安全壳腐蚀。然而,熔融 UO2 的极高温度(>3140 开尔文)和化学反应性阻止了结构研究。在这项工作中,我们结合激光加热、样品悬浮和同步加速器 X 射线,获得了高温固体和熔融 UO2 的配分函数测量结果。高温固体在 lambda 转变(2670 K)附近显示出氧无序的显著增加,但 U-O 配位变化可以忽略不计。在熔化时,平均 U-O 配位从 8 下降到 6.7±0.5。精修到该结构的分子动力学模型预测,U-U 迁移率高于 8 配位的熔体。