The Inhibition Effect of Sodium Glutarate towards Carbon Steel Corrosion in Neutral Aqueous Solutions
The inhibition effect of sodium glutarate towards corrosion of carbon steel in neutral 0.02 M NaCl solution was investigated with potentiodynamic polarization and electrochemical impedance measurements. Results of electrochemical measurements revealed a poor inhibitive action for low concentrations...
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2016-01-01
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Series: | International Journal of Corrosion |
Online Access: | http://dx.doi.org/10.1155/2016/8013706 |
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doaj-f700129ad61c4bbea53d6df2c218062c2020-11-24T21:21:41ZengHindawi LimitedInternational Journal of Corrosion1687-93251687-93332016-01-01201610.1155/2016/80137068013706The Inhibition Effect of Sodium Glutarate towards Carbon Steel Corrosion in Neutral Aqueous SolutionsG. Chan-Rosado0M. A. Pech-Canul1Departamento de Física Aplicada, Cinvestav-Mérida, Km. 6 Ant. Carr. a Progreso, AP73, Cordemex, 97310 Mérida, YUC, MexicoDepartamento de Física Aplicada, Cinvestav-Mérida, Km. 6 Ant. Carr. a Progreso, AP73, Cordemex, 97310 Mérida, YUC, MexicoThe inhibition effect of sodium glutarate towards corrosion of carbon steel in neutral 0.02 M NaCl solution was investigated with potentiodynamic polarization and electrochemical impedance measurements. Results of electrochemical measurements revealed a poor inhibitive action for low concentrations (1 mM and 5 mM) and a significant improvement in efficiency for concentrations of 32 mM or higher. The protective film exhibited excellent stability in the temperature range 22°C–55°C. Full chemical passivation was accomplished and analysis of the impedance spectra for the high concentrations of glutarate was consistent with the inhibition mechanism which assumes that the carboxylates support the passivation of carbon steel in aerated solutions by plugging the defect sites and that the passivation process is enhanced by adsorption of the carboxylates on the oxide-covered surface. Such mechanism was confirmed by the XPS analysis.http://dx.doi.org/10.1155/2016/8013706 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
G. Chan-Rosado M. A. Pech-Canul |
spellingShingle |
G. Chan-Rosado M. A. Pech-Canul The Inhibition Effect of Sodium Glutarate towards Carbon Steel Corrosion in Neutral Aqueous Solutions International Journal of Corrosion |
author_facet |
G. Chan-Rosado M. A. Pech-Canul |
author_sort |
G. Chan-Rosado |
title |
The Inhibition Effect of Sodium Glutarate towards Carbon Steel Corrosion in Neutral Aqueous Solutions |
title_short |
The Inhibition Effect of Sodium Glutarate towards Carbon Steel Corrosion in Neutral Aqueous Solutions |
title_full |
The Inhibition Effect of Sodium Glutarate towards Carbon Steel Corrosion in Neutral Aqueous Solutions |
title_fullStr |
The Inhibition Effect of Sodium Glutarate towards Carbon Steel Corrosion in Neutral Aqueous Solutions |
title_full_unstemmed |
The Inhibition Effect of Sodium Glutarate towards Carbon Steel Corrosion in Neutral Aqueous Solutions |
title_sort |
inhibition effect of sodium glutarate towards carbon steel corrosion in neutral aqueous solutions |
publisher |
Hindawi Limited |
series |
International Journal of Corrosion |
issn |
1687-9325 1687-9333 |
publishDate |
2016-01-01 |
description |
The inhibition effect of sodium glutarate towards corrosion of carbon steel in neutral 0.02 M NaCl solution was investigated with potentiodynamic polarization and electrochemical impedance measurements. Results of electrochemical measurements revealed a poor inhibitive action for low concentrations (1 mM and 5 mM) and a significant improvement in efficiency for concentrations of 32 mM or higher. The protective film exhibited excellent stability in the temperature range 22°C–55°C. Full chemical passivation was accomplished and analysis of the impedance spectra for the high concentrations of glutarate was consistent with the inhibition mechanism which assumes that the carboxylates support the passivation of carbon steel in aerated solutions by plugging the defect sites and that the passivation process is enhanced by adsorption of the carboxylates on the oxide-covered surface. Such mechanism was confirmed by the XPS analysis. |
url |
http://dx.doi.org/10.1155/2016/8013706 |
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