Sulejmanovic Dino, Pint Bruce A, Su Yi-Feng, Raiman Stephen, Kurley J Matthew
Enrichment Science and Engineering Division, Oak Ridge National Laboratory, P.O. Box 2008, Oak Ridge, Tennessee 37831-6378, United States.
Materials Science and Technology Division, Oak Ridge National Laboratory (retired), P.O. Box 2008, Oak Ridge, Tennessee 37831-6156, United States.
ACS Appl Eng Mater. 2025 Jun 16;3(6):1657-1663. doi: 10.1021/acsaenm.5c00191. eCollection 2025 Jun 27.
The rising interest in molten salts, both as thermal energy storage media and as high-temperature solvents for fissile materials in advanced nuclear reactors, has spurred significant growth in research on structural and functional salt-facing materials. Impurities, such as water, play a significant role in the degradation of materials in molten salt environments. Other impurities, such as fission products, are expected to accumulate in molten salts during normal reactor operation and can affect the properties of the salt and salt-facing materials. During normal reactor operation, rare-earth element species are expected to form as byproducts of fission reactions, potentially degrading or altering the performance of both structural and functional materials exposed to salts. In this work, fission product surrogates, europium metal and EuCl, were added to the KCl-MgCl salt while exposing pure Cr specimens in the melt at 600 and 700 °C for 1000 h. Low reactivity was observed with the baseline salt, while both the Eu and EuCl additions to the salt resulted in increased mass loss of Cr specimens. A capillary electrophoresis technique was developed to enable the detection of low parts-per-million (ppm) concentrations of europium (Eu) in chloride salt both before and after exposure of Cr metal. This technique provides a sensitive and reliable method for monitoring trace levels of Eu, which is critical for understanding the interactions and potential contamination effects in salt-facing materials during reactor operation. This quantification technique can be applied to other cationic and anionic contaminants in halide salts.
作为热能储存介质以及先进核反应堆中裂变材料的高温溶剂,熔盐越来越受到关注,这推动了面向盐的结构和功能材料研究的显著增长。诸如水之类的杂质在熔盐环境中的材料降解过程中起着重要作用。其他杂质,如裂变产物,预计会在反应堆正常运行期间在熔盐中积累,并可能影响盐和面向盐的材料的性能。在反应堆正常运行期间,稀土元素种类预计会作为裂变反应的副产物形成,可能会降低或改变暴露于盐中的结构材料和功能材料的性能。在这项工作中,将裂变产物替代物铕金属和EuCl添加到KCl-MgCl盐中,同时在600和700°C的熔体中暴露纯Cr试样1000小时。观察到与基线盐的反应性较低,而向盐中添加Eu和EuCl均导致Cr试样的质量损失增加。开发了一种毛细管电泳技术,用于检测Cr金属暴露前后氯化物盐中百万分之几(ppm)浓度的铕(Eu)。该技术为监测痕量水平的Eu提供了一种灵敏且可靠的方法,这对于理解反应堆运行期间面向盐的材料中的相互作用和潜在污染影响至关重要。这种定量技术可应用于卤化物盐中的其他阳离子和阴离子污染物。