Insights on the corrosion thermodynamics of chromium in molten LiF-NaF-KF eutectic salts

Abstract The thermodynamic stability of chromium in the Cr0, Cr2+, and Cr3+ oxidation states considering various F− ion coordination compounds was investigated in molten LiF–NaF-KF (FLiNaK) eutectic salt. Potential fluoride ion activity (F− and CrF3 −) diagrams were constructed to predict the most s...

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Main Authors: Ho Lun Chan, Elena Romanovskaia, Jie Qiu, Peter Hosemann, John R. Scully
Format: Article
Language:English
Published: Nature Portfolio 2022-06-01
Series:npj Materials Degradation
Online Access:https://doi.org/10.1038/s41529-022-00251-3
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author Ho Lun Chan
Elena Romanovskaia
Jie Qiu
Peter Hosemann
John R. Scully
author_facet Ho Lun Chan
Elena Romanovskaia
Jie Qiu
Peter Hosemann
John R. Scully
author_sort Ho Lun Chan
collection DOAJ
description Abstract The thermodynamic stability of chromium in the Cr0, Cr2+, and Cr3+ oxidation states considering various F− ion coordination compounds was investigated in molten LiF–NaF-KF (FLiNaK) eutectic salt. Potential fluoride ion activity (F− and CrF3 −) diagrams were constructed to predict the most stable Cr oxidation states as a function of anion activity, solvation state of chromium ions and potential at 600 °C. The Gibbs free energies of these compounds were estimated by utilizing a combined cyclic voltammetry – Nernst theory analysis approach in FLiNaK salt. To verify the constructed diagrams, X-ray diffraction was utilized after exposure of Cr at various applied potentials to determine whether compounds detected in solidified FLiNaK salts agreed with thermodynamic calculations. This work aims to identify key thermodynamic factors that are significant to chromium corrosion for molten salt nuclear reactor applications. The F− stability region spans the entire region where spontaneous corrosion of Cr occurs. Cr may be oxidized to Cr2+ and Cr3+ in the presence HF (due to moisture as an impurity) spontaneously except some conditions of p1/2H2/aHF etc. This situation is not changed qualitatively for various states of solvation between oxidized Cr solute in F− solvent and this aspect is substantially similar for the two cases (pair 1: Cr0/CrF3 −/ CrF6 3−; pair 2: Cr0/CrF4 2−/CrF5 2−) considered in this work.
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spelling doaj.art-3d82c582df404e67ad6b83c1fb8863012022-12-22T03:26:56ZengNature Portfolionpj Materials Degradation2397-21062022-06-016111010.1038/s41529-022-00251-3Insights on the corrosion thermodynamics of chromium in molten LiF-NaF-KF eutectic saltsHo Lun Chan0Elena Romanovskaia1Jie Qiu2Peter Hosemann3John R. Scully4Center of Electrochemical Science and Engineering, University of VirginiaCenter of Electrochemical Science and Engineering, University of VirginiaDepartment of Nuclear Science and Engineering, University of California, BerkeleyDepartment of Nuclear Science and Engineering, University of California, BerkeleyCenter of Electrochemical Science and Engineering, University of VirginiaAbstract The thermodynamic stability of chromium in the Cr0, Cr2+, and Cr3+ oxidation states considering various F− ion coordination compounds was investigated in molten LiF–NaF-KF (FLiNaK) eutectic salt. Potential fluoride ion activity (F− and CrF3 −) diagrams were constructed to predict the most stable Cr oxidation states as a function of anion activity, solvation state of chromium ions and potential at 600 °C. The Gibbs free energies of these compounds were estimated by utilizing a combined cyclic voltammetry – Nernst theory analysis approach in FLiNaK salt. To verify the constructed diagrams, X-ray diffraction was utilized after exposure of Cr at various applied potentials to determine whether compounds detected in solidified FLiNaK salts agreed with thermodynamic calculations. This work aims to identify key thermodynamic factors that are significant to chromium corrosion for molten salt nuclear reactor applications. The F− stability region spans the entire region where spontaneous corrosion of Cr occurs. Cr may be oxidized to Cr2+ and Cr3+ in the presence HF (due to moisture as an impurity) spontaneously except some conditions of p1/2H2/aHF etc. This situation is not changed qualitatively for various states of solvation between oxidized Cr solute in F− solvent and this aspect is substantially similar for the two cases (pair 1: Cr0/CrF3 −/ CrF6 3−; pair 2: Cr0/CrF4 2−/CrF5 2−) considered in this work.https://doi.org/10.1038/s41529-022-00251-3
spellingShingle Ho Lun Chan
Elena Romanovskaia
Jie Qiu
Peter Hosemann
John R. Scully
Insights on the corrosion thermodynamics of chromium in molten LiF-NaF-KF eutectic salts
npj Materials Degradation
title Insights on the corrosion thermodynamics of chromium in molten LiF-NaF-KF eutectic salts
title_full Insights on the corrosion thermodynamics of chromium in molten LiF-NaF-KF eutectic salts
title_fullStr Insights on the corrosion thermodynamics of chromium in molten LiF-NaF-KF eutectic salts
title_full_unstemmed Insights on the corrosion thermodynamics of chromium in molten LiF-NaF-KF eutectic salts
title_short Insights on the corrosion thermodynamics of chromium in molten LiF-NaF-KF eutectic salts
title_sort insights on the corrosion thermodynamics of chromium in molten lif naf kf eutectic salts
url https://doi.org/10.1038/s41529-022-00251-3
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