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Hydrazino-methoxy-1,3,5-triazine Derivatives’ Excellent Corrosion Organic Inhibitors of Steel in Acidic Chloride Solution
The corrosion inhibition performance of 2-hydrazino-4,6-dimethoxy-1,3,5-tirazine (DMeHT), 2,4-dihydrazino-6-methoxy-1,3,5-triaizine (DHMeT), and 2,4,6-tridydrazino-1,3,5-triaizne (TH(3)) on steel corrosion in acidic media was examined using electrochemical techniques. The results showed 2,4-Ddihydra...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274460/ https://www.ncbi.nlm.nih.gov/pubmed/27258241 http://dx.doi.org/10.3390/molecules21060714 |
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author | El-Faham, Ayman Osman, Sameh M. Al-Lohedan, Hamad A. El-Mahdy, Gamal A. |
author_facet | El-Faham, Ayman Osman, Sameh M. Al-Lohedan, Hamad A. El-Mahdy, Gamal A. |
author_sort | El-Faham, Ayman |
collection | PubMed |
description | The corrosion inhibition performance of 2-hydrazino-4,6-dimethoxy-1,3,5-tirazine (DMeHT), 2,4-dihydrazino-6-methoxy-1,3,5-triaizine (DHMeT), and 2,4,6-tridydrazino-1,3,5-triaizne (TH(3)) on steel corrosion in acidic media was examined using electrochemical techniques. The results showed 2,4-Ddihydrazino-6-methoxy-1,3,5-triaizine (DHMeT) gave the best corrosion protection performance among the other hydrazino derivatives even at a low concentration of 25 ppm (95%). The number of hydrazino groups play an important role in the corrosion inhibition, where the two hydrazine groups increased the electrostatic interactions between the protonated tested compounds, the negatively charged steel surface resulted from the adsorption of the chloride anions, and the presence of the methoxy group made the compound more reliable for formation of film protection on the surface of steel through the lone pair of oxygen atoms. Electrochemical Impedance Spectroscopy (EIS) measurements suggested that the corrosion process of steel in presence of the hydrazino-s-triazine derivatives (TH(3), DMeHT and DHMeT) were being controlled by the charge transfer reaction. Polarization curves indicated that the examined TH(3), DMeHT and DHMeT behaved as mixed type inhibitors. |
format | Online Article Text |
id | pubmed-6274460 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62744602018-12-28 Hydrazino-methoxy-1,3,5-triazine Derivatives’ Excellent Corrosion Organic Inhibitors of Steel in Acidic Chloride Solution El-Faham, Ayman Osman, Sameh M. Al-Lohedan, Hamad A. El-Mahdy, Gamal A. Molecules Article The corrosion inhibition performance of 2-hydrazino-4,6-dimethoxy-1,3,5-tirazine (DMeHT), 2,4-dihydrazino-6-methoxy-1,3,5-triaizine (DHMeT), and 2,4,6-tridydrazino-1,3,5-triaizne (TH(3)) on steel corrosion in acidic media was examined using electrochemical techniques. The results showed 2,4-Ddihydrazino-6-methoxy-1,3,5-triaizine (DHMeT) gave the best corrosion protection performance among the other hydrazino derivatives even at a low concentration of 25 ppm (95%). The number of hydrazino groups play an important role in the corrosion inhibition, where the two hydrazine groups increased the electrostatic interactions between the protonated tested compounds, the negatively charged steel surface resulted from the adsorption of the chloride anions, and the presence of the methoxy group made the compound more reliable for formation of film protection on the surface of steel through the lone pair of oxygen atoms. Electrochemical Impedance Spectroscopy (EIS) measurements suggested that the corrosion process of steel in presence of the hydrazino-s-triazine derivatives (TH(3), DMeHT and DHMeT) were being controlled by the charge transfer reaction. Polarization curves indicated that the examined TH(3), DMeHT and DHMeT behaved as mixed type inhibitors. MDPI 2016-06-01 /pmc/articles/PMC6274460/ /pubmed/27258241 http://dx.doi.org/10.3390/molecules21060714 Text en © 2016 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article El-Faham, Ayman Osman, Sameh M. Al-Lohedan, Hamad A. El-Mahdy, Gamal A. Hydrazino-methoxy-1,3,5-triazine Derivatives’ Excellent Corrosion Organic Inhibitors of Steel in Acidic Chloride Solution |
title | Hydrazino-methoxy-1,3,5-triazine Derivatives’ Excellent Corrosion Organic Inhibitors of Steel in Acidic Chloride Solution |
title_full | Hydrazino-methoxy-1,3,5-triazine Derivatives’ Excellent Corrosion Organic Inhibitors of Steel in Acidic Chloride Solution |
title_fullStr | Hydrazino-methoxy-1,3,5-triazine Derivatives’ Excellent Corrosion Organic Inhibitors of Steel in Acidic Chloride Solution |
title_full_unstemmed | Hydrazino-methoxy-1,3,5-triazine Derivatives’ Excellent Corrosion Organic Inhibitors of Steel in Acidic Chloride Solution |
title_short | Hydrazino-methoxy-1,3,5-triazine Derivatives’ Excellent Corrosion Organic Inhibitors of Steel in Acidic Chloride Solution |
title_sort | hydrazino-methoxy-1,3,5-triazine derivatives’ excellent corrosion organic inhibitors of steel in acidic chloride solution |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274460/ https://www.ncbi.nlm.nih.gov/pubmed/27258241 http://dx.doi.org/10.3390/molecules21060714 |
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