The electrodissolution and passivation of mild steel in alkaline sulphide solutions
- Autores
- Salvarezza, Roberto Carlos; Videla, Héctor A.; Arvia, Alejandro Jorge
- Año de publicación
- 1981
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- The electrodissolution and passivation of mild steel in alkaline sulphide solutions at 25°C is investigated by the use of steady state and transient electrochemical techniques and by scanning electron microscopy and energy dispersive X-ray analysis. The electrodissolution and passivation processes are explained by the initial competitive adsorption of OH−, HS− and H2O and the subsequent charge transfer and proton transfer processes involving the OH and HS adsorbed species. The former is responsible for the passivation of the metal by an oxide metal layer while the second species undergoes two different reactions yielding in one case a precipitated mackinawite film on the metal, which is a poorly protective layer, and in the other a soluble Fe(II) species which can be detected by chemical analysis. The contribution of the reactions starting from each adsorbed species depends on the HS−/OH− concentration ratio in the solution. The initiation of pitting on iron is also explained through the postulated reaction pattern.
Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas
Facultad de Ciencias Exactas - Materia
-
Ciencias Exactas
Química
Acero
Sulfuros
Metales Alcalinos
Hierro
Técnicas Electroquímicas
scanning electron microscopy - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by-nc-sa/4.0/
- Repositorio
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/82558
Ver los metadatos del registro completo
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The electrodissolution and passivation of mild steel in alkaline sulphide solutionsSalvarezza, Roberto CarlosVidela, Héctor A.Arvia, Alejandro JorgeCiencias ExactasQuímicaAceroSulfurosMetales AlcalinosHierroTécnicas Electroquímicasscanning electron microscopyThe electrodissolution and passivation of mild steel in alkaline sulphide solutions at 25°C is investigated by the use of steady state and transient electrochemical techniques and by scanning electron microscopy and energy dispersive X-ray analysis. The electrodissolution and passivation processes are explained by the initial competitive adsorption of OH−, HS− and H2O and the subsequent charge transfer and proton transfer processes involving the OH and HS adsorbed species. The former is responsible for the passivation of the metal by an oxide metal layer while the second species undergoes two different reactions yielding in one case a precipitated mackinawite film on the metal, which is a poorly protective layer, and in the other a soluble Fe(II) species which can be detected by chemical analysis. The contribution of the reactions starting from each adsorbed species depends on the HS−/OH− concentration ratio in the solution. The initiation of pitting on iron is also explained through the postulated reaction pattern.Instituto de Investigaciones Fisicoquímicas Teóricas y AplicadasFacultad de Ciencias Exactas1981-11-15info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf815-829http://sedici.unlp.edu.ar/handle/10915/82558enginfo:eu-repo/semantics/altIdentifier/issn/0010-938Xinfo:eu-repo/semantics/altIdentifier/doi/10.1016/0010-938X(82)90078-6info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/4.0/Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-29T11:15:31Zoai:sedici.unlp.edu.ar:10915/82558Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-29 11:15:32.24SEDICI (UNLP) - Universidad Nacional de La Platafalse |
dc.title.none.fl_str_mv |
The electrodissolution and passivation of mild steel in alkaline sulphide solutions |
title |
The electrodissolution and passivation of mild steel in alkaline sulphide solutions |
spellingShingle |
The electrodissolution and passivation of mild steel in alkaline sulphide solutions Salvarezza, Roberto Carlos Ciencias Exactas Química Acero Sulfuros Metales Alcalinos Hierro Técnicas Electroquímicas scanning electron microscopy |
title_short |
The electrodissolution and passivation of mild steel in alkaline sulphide solutions |
title_full |
The electrodissolution and passivation of mild steel in alkaline sulphide solutions |
title_fullStr |
The electrodissolution and passivation of mild steel in alkaline sulphide solutions |
title_full_unstemmed |
The electrodissolution and passivation of mild steel in alkaline sulphide solutions |
title_sort |
The electrodissolution and passivation of mild steel in alkaline sulphide solutions |
dc.creator.none.fl_str_mv |
Salvarezza, Roberto Carlos Videla, Héctor A. Arvia, Alejandro Jorge |
author |
Salvarezza, Roberto Carlos |
author_facet |
Salvarezza, Roberto Carlos Videla, Héctor A. Arvia, Alejandro Jorge |
author_role |
author |
author2 |
Videla, Héctor A. Arvia, Alejandro Jorge |
author2_role |
author author |
dc.subject.none.fl_str_mv |
Ciencias Exactas Química Acero Sulfuros Metales Alcalinos Hierro Técnicas Electroquímicas scanning electron microscopy |
topic |
Ciencias Exactas Química Acero Sulfuros Metales Alcalinos Hierro Técnicas Electroquímicas scanning electron microscopy |
dc.description.none.fl_txt_mv |
The electrodissolution and passivation of mild steel in alkaline sulphide solutions at 25°C is investigated by the use of steady state and transient electrochemical techniques and by scanning electron microscopy and energy dispersive X-ray analysis. The electrodissolution and passivation processes are explained by the initial competitive adsorption of OH−, HS− and H2O and the subsequent charge transfer and proton transfer processes involving the OH and HS adsorbed species. The former is responsible for the passivation of the metal by an oxide metal layer while the second species undergoes two different reactions yielding in one case a precipitated mackinawite film on the metal, which is a poorly protective layer, and in the other a soluble Fe(II) species which can be detected by chemical analysis. The contribution of the reactions starting from each adsorbed species depends on the HS−/OH− concentration ratio in the solution. The initiation of pitting on iron is also explained through the postulated reaction pattern. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas Facultad de Ciencias Exactas |
description |
The electrodissolution and passivation of mild steel in alkaline sulphide solutions at 25°C is investigated by the use of steady state and transient electrochemical techniques and by scanning electron microscopy and energy dispersive X-ray analysis. The electrodissolution and passivation processes are explained by the initial competitive adsorption of OH−, HS− and H2O and the subsequent charge transfer and proton transfer processes involving the OH and HS adsorbed species. The former is responsible for the passivation of the metal by an oxide metal layer while the second species undergoes two different reactions yielding in one case a precipitated mackinawite film on the metal, which is a poorly protective layer, and in the other a soluble Fe(II) species which can be detected by chemical analysis. The contribution of the reactions starting from each adsorbed species depends on the HS−/OH− concentration ratio in the solution. The initiation of pitting on iron is also explained through the postulated reaction pattern. |
publishDate |
1981 |
dc.date.none.fl_str_mv |
1981-11-15 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Articulo http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://sedici.unlp.edu.ar/handle/10915/82558 |
url |
http://sedici.unlp.edu.ar/handle/10915/82558 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/issn/0010-938X info:eu-repo/semantics/altIdentifier/doi/10.1016/0010-938X(82)90078-6 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by-nc-sa/4.0/ Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://creativecommons.org/licenses/by-nc-sa/4.0/ Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) |
dc.format.none.fl_str_mv |
application/pdf 815-829 |
dc.source.none.fl_str_mv |
reponame:SEDICI (UNLP) instname:Universidad Nacional de La Plata instacron:UNLP |
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Universidad Nacional de La Plata |
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UNLP |
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SEDICI (UNLP) - Universidad Nacional de La Plata |
repository.mail.fl_str_mv |
alira@sedici.unlp.edu.ar |
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score |
13.070432 |