Recovery of Strategic Metals from Tungsten Carbide-Cobalt Bonded Waste by Electrochemical Processing

Detalhes bibliográficos
Autor(a) principal: Katiyar,Prvan Kumar
Data de Publicação: 2023
Outros Autores: Randhawa,Navneet Singh
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-19042023000200103
Resumo: Abstract Scraped or end-of-life WC-Co bonded makes it an attractive resource. The conventional technologies to recover these metals entail energy-intensive pre-treatment steps, followed by their dissolution in a high volume of concentrated acids/alkali reagents. Recently, much attention has been given to the development of energy-efficient and environmentally friendly routes based on WC-Co direct electrochemical dissolution as anodes. However, the metals have a retarded dissolution, in NaOH alkali media, due to the formation of passive oxide layers, in the acidic electrolytes, and of hydroxides, on the anodic surface. The present study investigated WC and Co dissolution fundamentals in aqueous NH3, in order to develop a greener process, by the suitable addition of (NH4)2CO3, (NH4)2SO4 and NH4Cl Preliminary PDP studies revealed the necessary concentration of NH3 and additives, and their effect on the metals passivation tendency, for obtaining the best anodic dissolution parameters. The electrodissolution experiments in a specially designed cell achieved the maximum values, by adjusting those parameters. The highest dissolution of W and Co occurred under optimum conditions (10 V, 150 g/L NH3 and 15% w/v NH4Cl). Co was deposited at the cathode, while H8N2O4W remained in the electrolyte and was recovered as H2WO4 or YTO. Topographical analysis of the polarized surface by AFM has confirmed the pitting corrosion mechanism responsible for W and Co dissolution. A process flow chart for the newly developed single-step direct recycling methods of WC scraps has also been proposed. This process has produced pure saleable WO3 powder and Co.
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spelling Recovery of Strategic Metals from Tungsten Carbide-Cobalt Bonded Waste by Electrochemical ProcessingWC-Co scraprecyclingNH3 electrolytePDPelectrodissolutionWO3 and CoAbstract Scraped or end-of-life WC-Co bonded makes it an attractive resource. The conventional technologies to recover these metals entail energy-intensive pre-treatment steps, followed by their dissolution in a high volume of concentrated acids/alkali reagents. Recently, much attention has been given to the development of energy-efficient and environmentally friendly routes based on WC-Co direct electrochemical dissolution as anodes. However, the metals have a retarded dissolution, in NaOH alkali media, due to the formation of passive oxide layers, in the acidic electrolytes, and of hydroxides, on the anodic surface. The present study investigated WC and Co dissolution fundamentals in aqueous NH3, in order to develop a greener process, by the suitable addition of (NH4)2CO3, (NH4)2SO4 and NH4Cl Preliminary PDP studies revealed the necessary concentration of NH3 and additives, and their effect on the metals passivation tendency, for obtaining the best anodic dissolution parameters. The electrodissolution experiments in a specially designed cell achieved the maximum values, by adjusting those parameters. The highest dissolution of W and Co occurred under optimum conditions (10 V, 150 g/L NH3 and 15% w/v NH4Cl). Co was deposited at the cathode, while H8N2O4W remained in the electrolyte and was recovered as H2WO4 or YTO. Topographical analysis of the polarized surface by AFM has confirmed the pitting corrosion mechanism responsible for W and Co dissolution. A process flow chart for the newly developed single-step direct recycling methods of WC scraps has also been proposed. This process has produced pure saleable WO3 powder and Co.Sociedade Portuguesa de Electroquímica2023-04-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articletext/htmlhttp://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-19042023000200103Portugaliae Electrochimica Acta v.41 n.2 2023reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPenghttp://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-19042023000200103Katiyar,Prvan KumarRandhawa,Navneet Singhinfo:eu-repo/semantics/openAccess2024-02-06T17:07:39Zoai:scielo:S0872-19042023000200103Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T02:20:30.250643Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Recovery of Strategic Metals from Tungsten Carbide-Cobalt Bonded Waste by Electrochemical Processing
title Recovery of Strategic Metals from Tungsten Carbide-Cobalt Bonded Waste by Electrochemical Processing
spellingShingle Recovery of Strategic Metals from Tungsten Carbide-Cobalt Bonded Waste by Electrochemical Processing
Katiyar,Prvan Kumar
WC-Co scrap
recycling
NH3 electrolyte
PDP
electrodissolution
WO3 and Co
title_short Recovery of Strategic Metals from Tungsten Carbide-Cobalt Bonded Waste by Electrochemical Processing
title_full Recovery of Strategic Metals from Tungsten Carbide-Cobalt Bonded Waste by Electrochemical Processing
title_fullStr Recovery of Strategic Metals from Tungsten Carbide-Cobalt Bonded Waste by Electrochemical Processing
title_full_unstemmed Recovery of Strategic Metals from Tungsten Carbide-Cobalt Bonded Waste by Electrochemical Processing
title_sort Recovery of Strategic Metals from Tungsten Carbide-Cobalt Bonded Waste by Electrochemical Processing
author Katiyar,Prvan Kumar
author_facet Katiyar,Prvan Kumar
Randhawa,Navneet Singh
author_role author
author2 Randhawa,Navneet Singh
author2_role author
dc.contributor.author.fl_str_mv Katiyar,Prvan Kumar
Randhawa,Navneet Singh
dc.subject.por.fl_str_mv WC-Co scrap
recycling
NH3 electrolyte
PDP
electrodissolution
WO3 and Co
topic WC-Co scrap
recycling
NH3 electrolyte
PDP
electrodissolution
WO3 and Co
description Abstract Scraped or end-of-life WC-Co bonded makes it an attractive resource. The conventional technologies to recover these metals entail energy-intensive pre-treatment steps, followed by their dissolution in a high volume of concentrated acids/alkali reagents. Recently, much attention has been given to the development of energy-efficient and environmentally friendly routes based on WC-Co direct electrochemical dissolution as anodes. However, the metals have a retarded dissolution, in NaOH alkali media, due to the formation of passive oxide layers, in the acidic electrolytes, and of hydroxides, on the anodic surface. The present study investigated WC and Co dissolution fundamentals in aqueous NH3, in order to develop a greener process, by the suitable addition of (NH4)2CO3, (NH4)2SO4 and NH4Cl Preliminary PDP studies revealed the necessary concentration of NH3 and additives, and their effect on the metals passivation tendency, for obtaining the best anodic dissolution parameters. The electrodissolution experiments in a specially designed cell achieved the maximum values, by adjusting those parameters. The highest dissolution of W and Co occurred under optimum conditions (10 V, 150 g/L NH3 and 15% w/v NH4Cl). Co was deposited at the cathode, while H8N2O4W remained in the electrolyte and was recovered as H2WO4 or YTO. Topographical analysis of the polarized surface by AFM has confirmed the pitting corrosion mechanism responsible for W and Co dissolution. A process flow chart for the newly developed single-step direct recycling methods of WC scraps has also been proposed. This process has produced pure saleable WO3 powder and Co.
publishDate 2023
dc.date.none.fl_str_mv 2023-04-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-19042023000200103
url http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-19042023000200103
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-19042023000200103
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Portuguesa de Electroquímica
publisher.none.fl_str_mv Sociedade Portuguesa de Electroquímica
dc.source.none.fl_str_mv Portugaliae Electrochimica Acta v.41 n.2 2023
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv
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