Electrochemical behavior of copper in drinking water: evaluation of dissolution process at low anodic overpotential
Autor(a) principal: | |
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Data de Publicação: | 2011 |
Outros Autores: | , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Journal of the Brazilian Chemical Society (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532011000700023 |
Resumo: | The electrochemical behavior of copper in near-neutral aerated tap water was studied by potentiodynamic polarization and electrochemical impedance spectroscopy up to four days of immersion under different hydrodynamic conditions. The impedance results were interpreted by equivalent circuit that showed an increasing film thickness with time that hinders the diffusion of copper species across the oxide layer, which is larger in stagnating condition. At low anodic overpotential, copper impedance presents at least four time constants that could be explained by faradaic processes, adsorption/desorption of intermediate species, diffusion controlled process and oxide layer formation on copper surface. In the anodic region, the overall corrosion resistance decreases possibly due to the dissolution of copper species and the increase of diffusion across the oxide layer, mainly under hydrodynamic condition. |
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Journal of the Brazilian Chemical Society (Online) |
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Electrochemical behavior of copper in drinking water: evaluation of dissolution process at low anodic overpotentialcoppercorrosiondrinking waterEISpolarizationThe electrochemical behavior of copper in near-neutral aerated tap water was studied by potentiodynamic polarization and electrochemical impedance spectroscopy up to four days of immersion under different hydrodynamic conditions. The impedance results were interpreted by equivalent circuit that showed an increasing film thickness with time that hinders the diffusion of copper species across the oxide layer, which is larger in stagnating condition. At low anodic overpotential, copper impedance presents at least four time constants that could be explained by faradaic processes, adsorption/desorption of intermediate species, diffusion controlled process and oxide layer formation on copper surface. In the anodic region, the overall corrosion resistance decreases possibly due to the dissolution of copper species and the increase of diffusion across the oxide layer, mainly under hydrodynamic condition.Sociedade Brasileira de Química2011-07-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532011000700023Journal of the Brazilian Chemical Society v.22 n.7 2011reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532011000700023info:eu-repo/semantics/openAccessRios,J. FCalderón,J. ANogueira,R. Peng2011-07-22T00:00:00Zoai:scielo:S0103-50532011000700023Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2011-07-22T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
Electrochemical behavior of copper in drinking water: evaluation of dissolution process at low anodic overpotential |
title |
Electrochemical behavior of copper in drinking water: evaluation of dissolution process at low anodic overpotential |
spellingShingle |
Electrochemical behavior of copper in drinking water: evaluation of dissolution process at low anodic overpotential Rios,J. F copper corrosion drinking water EIS polarization |
title_short |
Electrochemical behavior of copper in drinking water: evaluation of dissolution process at low anodic overpotential |
title_full |
Electrochemical behavior of copper in drinking water: evaluation of dissolution process at low anodic overpotential |
title_fullStr |
Electrochemical behavior of copper in drinking water: evaluation of dissolution process at low anodic overpotential |
title_full_unstemmed |
Electrochemical behavior of copper in drinking water: evaluation of dissolution process at low anodic overpotential |
title_sort |
Electrochemical behavior of copper in drinking water: evaluation of dissolution process at low anodic overpotential |
author |
Rios,J. F |
author_facet |
Rios,J. F Calderón,J. A Nogueira,R. P |
author_role |
author |
author2 |
Calderón,J. A Nogueira,R. P |
author2_role |
author author |
dc.contributor.author.fl_str_mv |
Rios,J. F Calderón,J. A Nogueira,R. P |
dc.subject.por.fl_str_mv |
copper corrosion drinking water EIS polarization |
topic |
copper corrosion drinking water EIS polarization |
description |
The electrochemical behavior of copper in near-neutral aerated tap water was studied by potentiodynamic polarization and electrochemical impedance spectroscopy up to four days of immersion under different hydrodynamic conditions. The impedance results were interpreted by equivalent circuit that showed an increasing film thickness with time that hinders the diffusion of copper species across the oxide layer, which is larger in stagnating condition. At low anodic overpotential, copper impedance presents at least four time constants that could be explained by faradaic processes, adsorption/desorption of intermediate species, diffusion controlled process and oxide layer formation on copper surface. In the anodic region, the overall corrosion resistance decreases possibly due to the dissolution of copper species and the increase of diffusion across the oxide layer, mainly under hydrodynamic condition. |
publishDate |
2011 |
dc.date.none.fl_str_mv |
2011-07-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532011000700023 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532011000700023 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S0103-50532011000700023 |
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 Brasileira de Química |
publisher.none.fl_str_mv |
Sociedade Brasileira de Química |
dc.source.none.fl_str_mv |
Journal of the Brazilian Chemical Society v.22 n.7 2011 reponame:Journal of the Brazilian Chemical Society (Online) instname:Sociedade Brasileira de Química (SBQ) instacron:SBQ |
instname_str |
Sociedade Brasileira de Química (SBQ) |
instacron_str |
SBQ |
institution |
SBQ |
reponame_str |
Journal of the Brazilian Chemical Society (Online) |
collection |
Journal of the Brazilian Chemical Society (Online) |
repository.name.fl_str_mv |
Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ) |
repository.mail.fl_str_mv |
||office@jbcs.sbq.org.br |
_version_ |
1750318172344418304 |