Electrochemical and Surface Characterization Study on the Corrosion Inhibition of Mild Steel 1030 by the Cationic Surfactant Cetrimonium Trans-4-hydroxy-cinnamate.


Journal

ACS omega
ISSN: 2470-1343
Titre abrégé: ACS Omega
Pays: United States
ID NLM: 101691658

Informations de publication

Date de publication:
26 Jan 2021
Historique:
received: 27 09 2020
accepted: 16 11 2020
entrez: 1 2 2021
pubmed: 2 2 2021
medline: 2 2 2021
Statut: epublish

Résumé

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.

Identifiants

pubmed: 33521434
doi: 10.1021/acsomega.0c04733
pmc: PMC7841790
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1941-1952

Informations de copyright

© 2021 The Authors. Published by American Chemical Society.

Déclaration de conflit d'intérêts

The authors declare no competing financial interest.

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Auteurs

Jhonatan Soto Puelles (J)

Institute for Frontier Materials, Deakin University, Burwood, Victoria 3125, Australia.

Mahdi Ghorbani (M)

Institute for Frontier Materials, Deakin University, Burwood, Victoria 3125, Australia.

Ruhamah Yunis (R)

Institute for Frontier Materials, Deakin University, Burwood, Victoria 3125, Australia.

Laura L Machuca (LL)

Curtin Corrosion Centre, Curtin University, Bentley, Western Australia 6102, Australia.

Herman Terryn (H)

Research Group of Electrochemical and Surface Engineering (SURF), Department of Materials and Chemistry, Vrije Universiteit Brussel, 1050 Brussels, Belgium.

Maria Forsyth (M)

Institute for Frontier Materials, Deakin University, Burwood, Victoria 3125, Australia.

Anthony E Somers (AE)

Institute for Frontier Materials, Deakin University, Burwood, Victoria 3125, Australia.

Classifications MeSH