Electrolytic Extraction of Copper, Molybdenum and Rhenium from Molten Sulfide Electrolyte

The validity of the electrochemical series for metal sulfides decomposition in their standard state has been tested experimentally at 1500 K for La₂S₃, Cu₂S, MoS₂, and ReS₂ in a molten electrolyte with the following molar composition: (BaS)₅₄₋(Cu₂S)₃₁₋(La₂S₃)₁₅ (electrolyte B). Voltammetry measureme...

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Main Authors: Sahu, Sulata K., Chmielowiec, Brian John, Allanore, Antoine
Other Authors: Massachusetts Institute of Technology. Department of Materials Science and Engineering
Format: Article
Language:English
Published: Elsevier BV 2021
Online Access:https://hdl.handle.net/1721.1/131165
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author Sahu, Sulata K.
Chmielowiec, Brian John
Allanore, Antoine
author2 Massachusetts Institute of Technology. Department of Materials Science and Engineering
author_facet Massachusetts Institute of Technology. Department of Materials Science and Engineering
Sahu, Sulata K.
Chmielowiec, Brian John
Allanore, Antoine
author_sort Sahu, Sulata K.
collection MIT
description The validity of the electrochemical series for metal sulfides decomposition in their standard state has been tested experimentally at 1500 K for La₂S₃, Cu₂S, MoS₂, and ReS₂ in a molten electrolyte with the following molar composition: (BaS)₅₄₋(Cu₂S)₃₁₋(La₂S₃)₁₅ (electrolyte B). Voltammetry measurements indicated the presence of faradaic reactions in the investigated electrolyte with and without the addition of MoS₂ and/or ReS₂. Electrolysis experiments showed that the addition of La₂S₃ to BaS-Cu₂S increases the faradaic efficiency for liquid copper production with respect to a previously studied (BaS)₅₄₋(Cu₂S)₄₆ electrolyte, and enabled isolation of elemental sulfur as the anodic product. Electrochemical measurements suggested the need to take into account the activity of dissolved Cu₂S in order to explain the observed cell voltage during electrolysis. Electrolysis in the presence and absence of ReS₂ and/or MoS₂ confirmed their relative stability as predicted by assuming decomposition in their standard states. Analysis of the metal products electrowon from an electrolyte containing Cu₂S, MoS₂, and ReS₂ indicated the simultaneous production of solid and liquid phases with nonequilibrium compositions.
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spelling mit-1721.1/1311652022-09-28T18:54:04Z Electrolytic Extraction of Copper, Molybdenum and Rhenium from Molten Sulfide Electrolyte Sahu, Sulata K. Chmielowiec, Brian John Allanore, Antoine Massachusetts Institute of Technology. Department of Materials Science and Engineering MIT Materials Research Laboratory The validity of the electrochemical series for metal sulfides decomposition in their standard state has been tested experimentally at 1500 K for La₂S₃, Cu₂S, MoS₂, and ReS₂ in a molten electrolyte with the following molar composition: (BaS)₅₄₋(Cu₂S)₃₁₋(La₂S₃)₁₅ (electrolyte B). Voltammetry measurements indicated the presence of faradaic reactions in the investigated electrolyte with and without the addition of MoS₂ and/or ReS₂. Electrolysis experiments showed that the addition of La₂S₃ to BaS-Cu₂S increases the faradaic efficiency for liquid copper production with respect to a previously studied (BaS)₅₄₋(Cu₂S)₄₆ electrolyte, and enabled isolation of elemental sulfur as the anodic product. Electrochemical measurements suggested the need to take into account the activity of dissolved Cu₂S in order to explain the observed cell voltage during electrolysis. Electrolysis in the presence and absence of ReS₂ and/or MoS₂ confirmed their relative stability as predicted by assuming decomposition in their standard states. Analysis of the metal products electrowon from an electrolyte containing Cu₂S, MoS₂, and ReS₂ indicated the simultaneous production of solid and liquid phases with nonequilibrium compositions. Office of Naval Research (Contract N00014-12-1-0521) 2021-08-10T20:00:20Z 2021-08-10T20:00:20Z 2017-07 2017-04 2021-08-06T16:32:53Z Article http://purl.org/eprint/type/JournalArticle 0013-4686 https://hdl.handle.net/1721.1/131165 Sahu, Sulata K. et al. "Electrolytic Extraction of Copper, Molybdenum and Rhenium from Molten Sulfide Electrolyte." Electrochimica Acta 243 (July 2017): 382-389. © 2017 Elsevier Ltd en http://dx.doi.org/10.1016/j.electacta.2017.04.071 Electrochimica Acta Creative Commons Attribution-NonCommercial-NoDerivs License http://creativecommons.org/licenses/by-nc-nd/4.0/ application/pdf Elsevier BV Elsevier
spellingShingle Sahu, Sulata K.
Chmielowiec, Brian John
Allanore, Antoine
Electrolytic Extraction of Copper, Molybdenum and Rhenium from Molten Sulfide Electrolyte
title Electrolytic Extraction of Copper, Molybdenum and Rhenium from Molten Sulfide Electrolyte
title_full Electrolytic Extraction of Copper, Molybdenum and Rhenium from Molten Sulfide Electrolyte
title_fullStr Electrolytic Extraction of Copper, Molybdenum and Rhenium from Molten Sulfide Electrolyte
title_full_unstemmed Electrolytic Extraction of Copper, Molybdenum and Rhenium from Molten Sulfide Electrolyte
title_short Electrolytic Extraction of Copper, Molybdenum and Rhenium from Molten Sulfide Electrolyte
title_sort electrolytic extraction of copper molybdenum and rhenium from molten sulfide electrolyte
url https://hdl.handle.net/1721.1/131165
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AT chmielowiecbrianjohn electrolyticextractionofcoppermolybdenumandrheniumfrommoltensulfideelectrolyte
AT allanoreantoine electrolyticextractionofcoppermolybdenumandrheniumfrommoltensulfideelectrolyte