同位素分离
同位素
材料科学
核素
动力学同位素效应
分离(统计)
扩散
稳定同位素比值
化学物理
分离法
氘
分离过程
机制(生物学)
可扩展性
纳米技术
能量(信号处理)
同位素标记
放射化学
催化作用
离子交换
工艺工程
化学工程
作者
Yuchen Yang,Yuchen Yang,Tye Milazzo,Wenbo Bao,Zhihao Yang,Yihan Li,Ying Zhou,Zhihao Xu,Jinkai Si,Joseph F. Wild,Heng Chen,Tengfei Luo,A. N. Halliday,Yuan Yang,Yuan Yang
标识
DOI:10.1021/acsami.5c13443
摘要
Isotope separation is essential for cutting-edge developments in sustainability, health, and fundamental sciences. Chemical exchange-based isotope separation (CEIS) is a scalable approach that stems from the isotope-dependent free energy of chemicals, which has already been commercialized for H/D and 6/7Li separation. However, existing CEIS processes often involve toxic materials such as H2S and LixHg amalgam. Environmentally benign and low-cost materials and techniques are urgently needed to develop scalable isotope separations. CEIS processes are often between liquids and gases. Solids are attractive due to their high concentration of the nuclide of interest and the wide tunability of free energy at low temperatures. However, isotope diffusion is sluggish in most solids, making the time for isotope exchange impractical. Here we report a new exchange strategy based on accelerated dissolution/precipitation of solids in liquids where the exchange is not limited by solid diffusion. An attractive isotope separation factor of 1.021-1.026 is achieved within 10 min between solid LiCl and LiCl solution in acetone at 2 °C, which aligns with the prediction from the first-principle simulation. These results open new possibilities for scalable isotope separation between solids and liquids.
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