Corrosion and Passivation Behaviours of Iron in Molten Alkali Carbonates

Detalhes bibliográficos
Autor(a) principal: Mahmoud,S.S.
Data de Publicação: 2005
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=S0872-19042005000400001
Resumo: The corrosion and passivation behaviours of iron in ternary molten Li2CO3-Na2CO3-K2CO3 mixture at different temperatures (475- 550 ºC) were studied. The techniques of measurements were: open- circuit potential, galvanostatic anodic polarization, and cyclic voltammetry. The amounts of iron dissolved in the melt were determined by atomic absorption spectroscopy after each experiment. Iron undergoes spontaneous passivation upon its immersion in the melt and the thickness of the oxide scales increases with the increase of temperature. During the passivation potential range different oxides and spinals are formed. These include a cubic solid solution of FeO and a-LiFeO2, a-LiFe5O8 and a-Fe2O3. At high anodic potentials the decomposition of carbonate takes place leading to passivity break down and CO2 and O2 gases evolution. Also, the spoliation of oxide scales in the carbonate melt occurs at the passivity breakdown. The values of corrosion parameters (Rp, i o, i corr, i p) were calculated. The different values of activation energy of corrosion process were calculated. The results of cyclic voltammetric investigation indicate the formation of different oxides and spinals, and the cathodic and anodic decomposition of carbonate. The corrosion tests in 0.05 M HCl solution indicate that the oxide scales formed on iron are multilayered. The outer layer is less protective than the inner one.
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spelling Corrosion and Passivation Behaviours of Iron in Molten Alkali Carbonatesmolten alkali carbonatecorrosionpassivationironThe corrosion and passivation behaviours of iron in ternary molten Li2CO3-Na2CO3-K2CO3 mixture at different temperatures (475- 550 ºC) were studied. The techniques of measurements were: open- circuit potential, galvanostatic anodic polarization, and cyclic voltammetry. The amounts of iron dissolved in the melt were determined by atomic absorption spectroscopy after each experiment. Iron undergoes spontaneous passivation upon its immersion in the melt and the thickness of the oxide scales increases with the increase of temperature. During the passivation potential range different oxides and spinals are formed. These include a cubic solid solution of FeO and a-LiFeO2, a-LiFe5O8 and a-Fe2O3. At high anodic potentials the decomposition of carbonate takes place leading to passivity break down and CO2 and O2 gases evolution. Also, the spoliation of oxide scales in the carbonate melt occurs at the passivity breakdown. The values of corrosion parameters (Rp, i o, i corr, i p) were calculated. The different values of activation energy of corrosion process were calculated. The results of cyclic voltammetric investigation indicate the formation of different oxides and spinals, and the cathodic and anodic decomposition of carbonate. The corrosion tests in 0.05 M HCl solution indicate that the oxide scales formed on iron are multilayered. The outer layer is less protective than the inner one.Sociedade Portuguesa de Electroquímica2005-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articletext/htmlhttp://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-19042005000400001Portugaliae Electrochimica Acta v.23 n.4 2005reponame: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=S0872-19042005000400001Mahmoud,S.S.info:eu-repo/semantics/openAccess2024-02-06T17:06:47Zoai:scielo:S0872-19042005000400001Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T02:19:59.753533Repositório 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 Corrosion and Passivation Behaviours of Iron in Molten Alkali Carbonates
title Corrosion and Passivation Behaviours of Iron in Molten Alkali Carbonates
spellingShingle Corrosion and Passivation Behaviours of Iron in Molten Alkali Carbonates
Mahmoud,S.S.
molten alkali carbonate
corrosion
passivation
iron
title_short Corrosion and Passivation Behaviours of Iron in Molten Alkali Carbonates
title_full Corrosion and Passivation Behaviours of Iron in Molten Alkali Carbonates
title_fullStr Corrosion and Passivation Behaviours of Iron in Molten Alkali Carbonates
title_full_unstemmed Corrosion and Passivation Behaviours of Iron in Molten Alkali Carbonates
title_sort Corrosion and Passivation Behaviours of Iron in Molten Alkali Carbonates
author Mahmoud,S.S.
author_facet Mahmoud,S.S.
author_role author
dc.contributor.author.fl_str_mv Mahmoud,S.S.
dc.subject.por.fl_str_mv molten alkali carbonate
corrosion
passivation
iron
topic molten alkali carbonate
corrosion
passivation
iron
description The corrosion and passivation behaviours of iron in ternary molten Li2CO3-Na2CO3-K2CO3 mixture at different temperatures (475- 550 ºC) were studied. The techniques of measurements were: open- circuit potential, galvanostatic anodic polarization, and cyclic voltammetry. The amounts of iron dissolved in the melt were determined by atomic absorption spectroscopy after each experiment. Iron undergoes spontaneous passivation upon its immersion in the melt and the thickness of the oxide scales increases with the increase of temperature. During the passivation potential range different oxides and spinals are formed. These include a cubic solid solution of FeO and a-LiFeO2, a-LiFe5O8 and a-Fe2O3. At high anodic potentials the decomposition of carbonate takes place leading to passivity break down and CO2 and O2 gases evolution. Also, the spoliation of oxide scales in the carbonate melt occurs at the passivity breakdown. The values of corrosion parameters (Rp, i o, i corr, i p) were calculated. The different values of activation energy of corrosion process were calculated. The results of cyclic voltammetric investigation indicate the formation of different oxides and spinals, and the cathodic and anodic decomposition of carbonate. The corrosion tests in 0.05 M HCl solution indicate that the oxide scales formed on iron are multilayered. The outer layer is less protective than the inner one.
publishDate 2005
dc.date.none.fl_str_mv 2005-01-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-19042005000400001
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dc.language.iso.fl_str_mv eng
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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.23 n.4 2005
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
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reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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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
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