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60 Years of U: Perspectives on resources, demand, and the evolving role of nuclear energy
Recent years have seen growing global interest in nuclear energy and rising confidence in the sector. For the first time since the early 2000s, there is renewed optimism about the industry’s future. This change is driven by several major factors: geopolitical developments that highlight the need for secure energy supplies, a stronger focus on resilient energy systems, national commitments to decarbonization, and rising demand for clean and reliable electricity.
Suddhasattwa Ghosh, Krishan Kumar, Aligati Venkatesh, P. Venkatesh, Bandi Prabhakara Reddy
Nuclear Technology | Volume 195 | Number 3 | September 2016 | Pages 253-272
Technical Paper | doi.org/10.13182/NT16-37
Articles are hosted by Taylor and Francis Online.
The DIFAC (DIFfusion of Actinides in EleCtrorefiner) computer code for pyroprocessing, developed earlier by the authors, is modified in the present work to model electrorefining at the liquid cadmium electrode. The modeling of electrorefining of metal fuels requires accurate knowledge of two important kinetic parameters: exchange current density io and diffusion layer thickness δ. These are estimated in the present work by polarization methods and employing Tafel and Allen-Hickling analysis for Gd3+/Gd, U3+/U, and Zr2+/Zr couples in LiCl-KCl eutectic at 773 K for an inert cathode and compared with literature data, wherever possible. The equilibrium potentials for these couples at an inert electrode are found to be −1.94, −1.52, and −1.22 V, respectively, at 773 K. Electrochemical studies are also carried out in LiCl-KCl eutectic to estimate io and δ for the anodic dissolution of Na-bonded U-Zr and Gd-U-Zr alloy and are compared with the anodic dissolution of U-Pu-Zr alloy. The equilibrium potential of Na-bonded U-Zr alloy in LiCl-KCl-UCl3 was found to be −1.46 V, and those for Gd-U-Zr alloy in blank LiCl-KCl and LiCl-KCl-UCl3 were −1.56 and −1.34 V, respectively, at 773 K. The exchange current densities of Na-bonded U-Zr and Gd-U-Zr alloy were found to be in the range of 40.1 to 46.5 mA · cm−2 and 16.8 to 27.3 mA · cm−2 at 773 K, respectively.
A preliminary design of the liquid cadmium electrode suitable for laboratory-scale experiments on uranium- and plutonium-based systems is also reported in the present work. The io and δ of gadolinium, uranium, and zirconium are subsequently estimated at the liquid cadmium electrode at 773 K. The equilibrium potentials for Gd3+/Cd6Gd, U3+/[U]Cd, and Zr2+/Cd3Zr couples in LiCl-KCl eutectic at 773 K for the liquid cadmium electrode are found to be −1.35, −1.13, and−1.12 V, respectively. Finally, a few algorithms are proposed for modeling electrorefining data at the liquid cadmium electrode for multicomponent systems.