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Experimental and Theoretical Studies of α-Linolenic Acid as Green Corrosion Inhibitor for Carbon Steel in 0.5 M Sulfuric Acid
A component of Salvia hispanica, α-linolenic acid, has been evaluated as a green corrosion inhibitor for 1018 carbon steel in 0.5 M sulfuric acid using weight loss tests, potentiodynamic polarization curves and electrochemical impedance spectroscopy (EIS) measurements. Theoretical calculations using...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8540272/ https://www.ncbi.nlm.nih.gov/pubmed/34684751 http://dx.doi.org/10.3390/molecules26206169 |
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author | Hermoso-Diaz, I.A. Lopez-Cecenes, R. Rios, J.P. Flores-De los Landeros-Martínez, L.L. Sarmiento-Bustos, E. Uruchurtu-Chavarin, J. Gonzalez-Rodriguez, J.G. |
author_facet | Hermoso-Diaz, I.A. Lopez-Cecenes, R. Rios, J.P. Flores-De los Landeros-Martínez, L.L. Sarmiento-Bustos, E. Uruchurtu-Chavarin, J. Gonzalez-Rodriguez, J.G. |
author_sort | Hermoso-Diaz, I.A. |
collection | PubMed |
description | A component of Salvia hispanica, α-linolenic acid, has been evaluated as a green corrosion inhibitor for 1018 carbon steel in 0.5 M sulfuric acid using weight loss tests, potentiodynamic polarization curves and electrochemical impedance spectroscopy (EIS) measurements. Theoretical calculations using Density Functional Theory (DFT) were used also. The results have shown that this compound is a good corrosion inhibitor, with an efficiency which increased with an increase in its concentration up to 600 ppm, but it decreased with a further increase in the concentration. α-linolenic acid formed protective corrosion products layer because it was chemically adsorbed onto the steel surface according to a Langmuir type of adsorption isotherms. Polarization curves have shown that α-linolenic acid is a good, mixed type of inhibitor with a predominant effect on the cathodic hydrogen evolution reactions. EIS measurements indicated a charge transfer-controlled corrosion process. DFT calculations indicated that α-linolenic acid was more efficient in an acidic environment than in a neutral one because has a high tendency to donate electrons and can be easily protonated. In addition to this, it had the highest E(HUMO) value, the best chemical reactivity, the greatest tendency to transfer electrons and a greater facility of modifying its electronic configuration in the presence of carbon steel specimens according to its chemical hardness value. |
format | Online Article Text |
id | pubmed-8540272 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-85402722021-10-24 Experimental and Theoretical Studies of α-Linolenic Acid as Green Corrosion Inhibitor for Carbon Steel in 0.5 M Sulfuric Acid Hermoso-Diaz, I.A. Lopez-Cecenes, R. Rios, J.P. Flores-De los Landeros-Martínez, L.L. Sarmiento-Bustos, E. Uruchurtu-Chavarin, J. Gonzalez-Rodriguez, J.G. Molecules Article A component of Salvia hispanica, α-linolenic acid, has been evaluated as a green corrosion inhibitor for 1018 carbon steel in 0.5 M sulfuric acid using weight loss tests, potentiodynamic polarization curves and electrochemical impedance spectroscopy (EIS) measurements. Theoretical calculations using Density Functional Theory (DFT) were used also. The results have shown that this compound is a good corrosion inhibitor, with an efficiency which increased with an increase in its concentration up to 600 ppm, but it decreased with a further increase in the concentration. α-linolenic acid formed protective corrosion products layer because it was chemically adsorbed onto the steel surface according to a Langmuir type of adsorption isotherms. Polarization curves have shown that α-linolenic acid is a good, mixed type of inhibitor with a predominant effect on the cathodic hydrogen evolution reactions. EIS measurements indicated a charge transfer-controlled corrosion process. DFT calculations indicated that α-linolenic acid was more efficient in an acidic environment than in a neutral one because has a high tendency to donate electrons and can be easily protonated. In addition to this, it had the highest E(HUMO) value, the best chemical reactivity, the greatest tendency to transfer electrons and a greater facility of modifying its electronic configuration in the presence of carbon steel specimens according to its chemical hardness value. MDPI 2021-10-13 /pmc/articles/PMC8540272/ /pubmed/34684751 http://dx.doi.org/10.3390/molecules26206169 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Hermoso-Diaz, I.A. Lopez-Cecenes, R. Rios, J.P. Flores-De los Landeros-Martínez, L.L. Sarmiento-Bustos, E. Uruchurtu-Chavarin, J. Gonzalez-Rodriguez, J.G. Experimental and Theoretical Studies of α-Linolenic Acid as Green Corrosion Inhibitor for Carbon Steel in 0.5 M Sulfuric Acid |
title | Experimental and Theoretical Studies of α-Linolenic Acid as Green Corrosion Inhibitor for Carbon Steel in 0.5 M Sulfuric Acid |
title_full | Experimental and Theoretical Studies of α-Linolenic Acid as Green Corrosion Inhibitor for Carbon Steel in 0.5 M Sulfuric Acid |
title_fullStr | Experimental and Theoretical Studies of α-Linolenic Acid as Green Corrosion Inhibitor for Carbon Steel in 0.5 M Sulfuric Acid |
title_full_unstemmed | Experimental and Theoretical Studies of α-Linolenic Acid as Green Corrosion Inhibitor for Carbon Steel in 0.5 M Sulfuric Acid |
title_short | Experimental and Theoretical Studies of α-Linolenic Acid as Green Corrosion Inhibitor for Carbon Steel in 0.5 M Sulfuric Acid |
title_sort | experimental and theoretical studies of α-linolenic acid as green corrosion inhibitor for carbon steel in 0.5 m sulfuric acid |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8540272/ https://www.ncbi.nlm.nih.gov/pubmed/34684751 http://dx.doi.org/10.3390/molecules26206169 |
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