Peng Yuxiang, Bawane Kaustubh K, Liu Xiaoyang, Zheng Xiaoyin, Ge Mingyuan, Xiao Xianghui, Kim Ellie M, Halstenberg Phillip W, Dai Sheng, Wishart James F, Chen-Wiegart Yu-Chen Karen
Department of Materials Science and Chemical Engineering, Stony Brook University, Stony Brook, New York 11790, United States.
Advanced Characterization Department, Idaho National Laboratory, Idaho Falls, Idaho 83415, United States.
ACS Appl Mater Interfaces. 2025 May 14;17(19):28764-28776. doi: 10.1021/acsami.4c23034. Epub 2025 Apr 29.
Understanding the interfacial evolution of alloys in molten salt with different amounts of water (HO) and oxygen (O) impurities is significant for applications in many fields, including concentrated solar power, molten salt reactors, and applications in pyrochemical reprocessing and electrorefining. Additionally, the impurity-driven corrosion mechanisms that lead to various morphological and chemical evolution characteristics at the interfaces of structural alloys and molten salts are not fully understood. In the present work, the three-dimensional (3D) morphological evolution of Ni-20Cr microwires in LiCl-KCl was studied at 500 °C under different moisture and oxygen conditions using in situ synchrotron transmission X-ray microscopy (TXM) and scanning transmission electron microscopy (STEM) techniques. No significant morphological changes were observed in Ni-20Cr microwires under vacuum conditions. However, the wires exhibited distinct morphological evolutions when exposed to molten salt containing HO alone, as well as when both HO and O were present. Furthermore, CrO precipitates were observed in the molten salt during corrosion with only HO present, while Cr species were identified in the salt when O was added. These findings are crucial for understanding the corrosion mechanisms of molten salt with different amounts of HO and O contamination, providing insights for developing corrosion mitigation methods and improving the stability of containment alloys in molten salt applications.
了解不同含水量(HO)和含氧量(O)杂质的熔盐中合金的界面演变对于许多领域的应用具有重要意义,这些领域包括聚光太阳能发电、熔盐反应堆以及热化学后处理和电精炼中的应用。此外,导致结构合金与熔盐界面出现各种形态和化学演变特征的杂质驱动腐蚀机制尚未完全了解。在本工作中,使用原位同步辐射透射X射线显微镜(TXM)和扫描透射电子显微镜(STEM)技术,研究了500℃下不同湿度和氧气条件下LiCl-KCl中Ni-20Cr微丝的三维(3D)形态演变。在真空条件下,Ni-20Cr微丝未观察到明显的形态变化。然而,当暴露于仅含HO的熔盐中以及同时存在HO和O时,微丝呈现出明显的形态演变。此外,仅存在HO时,在腐蚀过程中熔盐中观察到CrO沉淀,而添加O时在盐中鉴定出Cr物种。这些发现对于理解不同HO和O污染量的熔盐的腐蚀机制至关重要,为开发腐蚀缓解方法和提高熔盐应用中包容合金的稳定性提供了见解。