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Electrochemical and Surface Characterization Study on the Corrosion Inhibition of Mild Steel 1030 by the Cationic Surfactant Cetrimonium Trans-4-hydroxy-cinnamate
[Image: see text] Effective corrosion inhibition of mild steel 1030 at 0.01 M NaCl concentration was achieved by the use of the nontoxic surfactant salt cetrimonium trans-4-hydroxy-cinnamate (CTA-4OHcinn). Polarization analysis on the steel samples immersed for 24 h in the control and CTA-4OHcinn-co...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7841790/ https://www.ncbi.nlm.nih.gov/pubmed/33521434 http://dx.doi.org/10.1021/acsomega.0c04733 |
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author | Soto Puelles, Jhonatan Ghorbani, Mahdi Yunis, Ruhamah Machuca, Laura L. Terryn, Herman Forsyth, Maria Somers, Anthony E. |
author_facet | Soto Puelles, Jhonatan Ghorbani, Mahdi Yunis, Ruhamah Machuca, Laura L. Terryn, Herman Forsyth, Maria Somers, Anthony E. |
author_sort | Soto Puelles, Jhonatan |
collection | PubMed |
description | [Image: see text] Effective corrosion inhibition of mild steel 1030 at 0.01 M NaCl concentration was achieved by the use of the nontoxic surfactant salt cetrimonium trans-4-hydroxy-cinnamate (CTA-4OHcinn). Polarization analysis on the steel samples immersed for 24 h in the control and CTA-4OHcinn-containing solutions shows the development of a passivation potential that is more obvious at higher inhibitor concentrations along with a maximum inhibition efficiency of 97.8%. Electrochemical impedance spectroscopy (EIS) pinpoints the effect of the inhibitor on the corroding regions of the metal surface, showing an increase in the local electric resistance and conversely a decrease in the local capacitance, which indicates that the charge transfer in the corroding regions is being hindered by a deposition process. This is consistent with scanning electron microscopy (SEM) images, showing the presence of a porous oxide matrix that fills localized corrosion sites on the metal surface after 24 h of immersion in a 0.01 M NaCl + 10 mM inhibitor solution. Additionally, SEM analysis also shows the formation of an organic film surrounding the defects that is able to shield chloride attack. As a result of diffusion of chloride from the defects below the protective film, filiform corrosion can be seen. Time-resolved impedance analysis over the first 120 min of immersion in the control and inhibitor solution shows that significant inhibitor protection does not take place immediately and there is a lag phase in the first 50 min of immersion, suggesting that early localized corrosion drives further adsorption of inhibitor micelles on the metal surface. This is in agreement with X-ray photoelectron spectroscopy (XPS) analysis, which indicates a complete surface coverage over the first 2 h of immersion in a concentrated inhibitor solution. XPS also shows the heterogeneity of the film, where some parts are poorly covered, revealing the underlying surface containing iron. |
format | Online Article Text |
id | pubmed-7841790 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-78417902021-01-29 Electrochemical and Surface Characterization Study on the Corrosion Inhibition of Mild Steel 1030 by the Cationic Surfactant Cetrimonium Trans-4-hydroxy-cinnamate Soto Puelles, Jhonatan Ghorbani, Mahdi Yunis, Ruhamah Machuca, Laura L. Terryn, Herman Forsyth, Maria Somers, Anthony E. ACS Omega [Image: see text] Effective corrosion inhibition of mild steel 1030 at 0.01 M NaCl concentration was achieved by the use of the nontoxic surfactant salt cetrimonium trans-4-hydroxy-cinnamate (CTA-4OHcinn). Polarization analysis on the steel samples immersed for 24 h in the control and CTA-4OHcinn-containing solutions shows the development of a passivation potential that is more obvious at higher inhibitor concentrations along with a maximum inhibition efficiency of 97.8%. Electrochemical impedance spectroscopy (EIS) pinpoints the effect of the inhibitor on the corroding regions of the metal surface, showing an increase in the local electric resistance and conversely a decrease in the local capacitance, which indicates that the charge transfer in the corroding regions is being hindered by a deposition process. This is consistent with scanning electron microscopy (SEM) images, showing the presence of a porous oxide matrix that fills localized corrosion sites on the metal surface after 24 h of immersion in a 0.01 M NaCl + 10 mM inhibitor solution. Additionally, SEM analysis also shows the formation of an organic film surrounding the defects that is able to shield chloride attack. As a result of diffusion of chloride from the defects below the protective film, filiform corrosion can be seen. Time-resolved impedance analysis over the first 120 min of immersion in the control and inhibitor solution shows that significant inhibitor protection does not take place immediately and there is a lag phase in the first 50 min of immersion, suggesting that early localized corrosion drives further adsorption of inhibitor micelles on the metal surface. This is in agreement with X-ray photoelectron spectroscopy (XPS) analysis, which indicates a complete surface coverage over the first 2 h of immersion in a concentrated inhibitor solution. XPS also shows the heterogeneity of the film, where some parts are poorly covered, revealing the underlying surface containing iron. American Chemical Society 2021-01-08 /pmc/articles/PMC7841790/ /pubmed/33521434 http://dx.doi.org/10.1021/acsomega.0c04733 Text en © 2021 The Authors. Published by American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Soto Puelles, Jhonatan Ghorbani, Mahdi Yunis, Ruhamah Machuca, Laura L. Terryn, Herman Forsyth, Maria Somers, Anthony E. Electrochemical and Surface Characterization Study on the Corrosion Inhibition of Mild Steel 1030 by the Cationic Surfactant Cetrimonium Trans-4-hydroxy-cinnamate |
title | Electrochemical and Surface Characterization Study
on the Corrosion Inhibition of Mild Steel 1030 by the Cationic Surfactant
Cetrimonium Trans-4-hydroxy-cinnamate |
title_full | Electrochemical and Surface Characterization Study
on the Corrosion Inhibition of Mild Steel 1030 by the Cationic Surfactant
Cetrimonium Trans-4-hydroxy-cinnamate |
title_fullStr | Electrochemical and Surface Characterization Study
on the Corrosion Inhibition of Mild Steel 1030 by the Cationic Surfactant
Cetrimonium Trans-4-hydroxy-cinnamate |
title_full_unstemmed | Electrochemical and Surface Characterization Study
on the Corrosion Inhibition of Mild Steel 1030 by the Cationic Surfactant
Cetrimonium Trans-4-hydroxy-cinnamate |
title_short | Electrochemical and Surface Characterization Study
on the Corrosion Inhibition of Mild Steel 1030 by the Cationic Surfactant
Cetrimonium Trans-4-hydroxy-cinnamate |
title_sort | electrochemical and surface characterization study
on the corrosion inhibition of mild steel 1030 by the cationic surfactant
cetrimonium trans-4-hydroxy-cinnamate |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7841790/ https://www.ncbi.nlm.nih.gov/pubmed/33521434 http://dx.doi.org/10.1021/acsomega.0c04733 |
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