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Nathan D. Smith
Researcher at Pennsylvania State University
Publications - 15
Citations - 118
Nathan D. Smith is an academic researcher from Pennsylvania State University. The author has contributed to research in topics: Electromotive force & Differential scanning calorimetry. The author has an hindex of 4, co-authored 15 publications receiving 76 citations. Previous affiliations of Nathan D. Smith include Argonne National Laboratory.
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Electrochemical Separation of Barium into Liquid Bismuth by Controlling Deposition Potentials
TL;DR: In this paper, a liquid bismuth electrode was used to demonstrate the separation of barium from a multi-component molten salt electrolyte (BaCl2LiCl-CaCl2-NaCl) at 500-700°C, where the electrode potentials at various current densities and electrochemical impedance spectra indicate charge transfer as the most significant overpotential mechanism.
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Thermodynamic Properties of Strontium-Bismuth Alloys Determined by Electromotive Force Measurements
TL;DR: In this article, the thermodynamic properties of Sr-Bi alloys were determined by electromotive force (emf) measurements to evaluate the viability of liquid bismuth metal as a medium for separating alkali/alkaline-earth fission products from molten salt electrolyte.
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Electrochemical deposition of alkaline-earth elements (Sr and Ba) from LiCl-KCl-SrCl2-BaCl2 solution using a liquid bismuth electrode
TL;DR: In this paper, the results of electrochemical deposition of alkaline-earth fission products accumulated in molten salts (Sr2+ and Ba2+) into liquid Bi by electrochemical separation were investigated.
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Electrochemical studies of molten sulfates in LiCl-KCl-Na2SO4 at 700 °C
TL;DR: In this article, the electrochemical reduction behavior of molten Na2SO4 was investigated at 700 °C in LiCl-KCl-Na2SO 4 (5-15 mol%) electrolyte under two different gaseous atmospheres of inert argon and oxidizing O2-0.1% SO2.
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Influence of gaseous atmosphere on electrochemical behavior of nickel alloys in LiCl-KCl-Na2SO4 at 700 °C
TL;DR: In this article, LiCl-KCl-Na 2 SO 4 electrolyte at 700 °C under three gaseous atmospheres (Ar, O 2, O 2 -0.1%SO 2 ).