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Donor−π–Acceptor-Type Configured, Dimethylamino-Based Organic Push–Pull Chromophores for Effective Reduction of Mild Steel Corrosion Loss in 1 M HCl
[Image: see text] In this work, donor−π–acceptor-type four crystalline compounds have been tested for the first time to restrict the corrosion of mild steel in 1 M HCl. The details of the compounds are: C1, 4-N,N-dimethylamino-β-nitrostyrene; C2, 2-(4-(dimethylamino) benzylidene)malononitrile; C3, e...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641366/ https://www.ncbi.nlm.nih.gov/pubmed/31458644 http://dx.doi.org/10.1021/acsomega.8b00083 |
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author | Tiwari, Madhu Gupta, Vinod Kumar Singh, Ram Adhar Ji, Gopal Prakash, Rajiv |
author_facet | Tiwari, Madhu Gupta, Vinod Kumar Singh, Ram Adhar Ji, Gopal Prakash, Rajiv |
author_sort | Tiwari, Madhu |
collection | PubMed |
description | [Image: see text] In this work, donor−π–acceptor-type four crystalline compounds have been tested for the first time to restrict the corrosion of mild steel in 1 M HCl. The details of the compounds are: C1, 4-N,N-dimethylamino-β-nitrostyrene; C2, 2-(4-(dimethylamino) benzylidene)malononitrile; C3, ethyl 2-cyano-3-(4-(dimethylamino) phenyl)acrylate; and C4, methyl 2-cyano-3-(4-(dimethylamino)phenyl)acrylate. The corrosion inhibition potentials of the compounds have been primarily investigated by electrochemical techniques, such as linear polarization resistance, Tafel polarization curves, and electrochemical impedance spectroscopy. The secondary investigation is performed by scanning electron microscopy, fluorescence surface imaging, spectroscopic techniques (UV–visible and Fourier transform infrared spectroscopy), and X-ray diffraction patterns. The results disclosed that 50 mg L(–1) of the compounds (1–4) in 1 M HCl provided the maximum inhibition efficiency as 93% (1), 88% (2), 82% (3), and 86% (4). The function of the compounds as corrosion inhibitors is explained with equilibrium corrosion potential, adsorption isotherms, and the frontier molecular orbital energies of the compounds (E(HOMO) and E(LUMO)) estimated by cyclic voltammetry curves and UV–visible spectra. |
format | Online Article Text |
id | pubmed-6641366 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66413662019-08-27 Donor−π–Acceptor-Type Configured, Dimethylamino-Based Organic Push–Pull Chromophores for Effective Reduction of Mild Steel Corrosion Loss in 1 M HCl Tiwari, Madhu Gupta, Vinod Kumar Singh, Ram Adhar Ji, Gopal Prakash, Rajiv ACS Omega [Image: see text] In this work, donor−π–acceptor-type four crystalline compounds have been tested for the first time to restrict the corrosion of mild steel in 1 M HCl. The details of the compounds are: C1, 4-N,N-dimethylamino-β-nitrostyrene; C2, 2-(4-(dimethylamino) benzylidene)malononitrile; C3, ethyl 2-cyano-3-(4-(dimethylamino) phenyl)acrylate; and C4, methyl 2-cyano-3-(4-(dimethylamino)phenyl)acrylate. The corrosion inhibition potentials of the compounds have been primarily investigated by electrochemical techniques, such as linear polarization resistance, Tafel polarization curves, and electrochemical impedance spectroscopy. The secondary investigation is performed by scanning electron microscopy, fluorescence surface imaging, spectroscopic techniques (UV–visible and Fourier transform infrared spectroscopy), and X-ray diffraction patterns. The results disclosed that 50 mg L(–1) of the compounds (1–4) in 1 M HCl provided the maximum inhibition efficiency as 93% (1), 88% (2), 82% (3), and 86% (4). The function of the compounds as corrosion inhibitors is explained with equilibrium corrosion potential, adsorption isotherms, and the frontier molecular orbital energies of the compounds (E(HOMO) and E(LUMO)) estimated by cyclic voltammetry curves and UV–visible spectra. American Chemical Society 2018-04-11 /pmc/articles/PMC6641366/ /pubmed/31458644 http://dx.doi.org/10.1021/acsomega.8b00083 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Tiwari, Madhu Gupta, Vinod Kumar Singh, Ram Adhar Ji, Gopal Prakash, Rajiv Donor−π–Acceptor-Type Configured, Dimethylamino-Based Organic Push–Pull Chromophores for Effective Reduction of Mild Steel Corrosion Loss in 1 M HCl |
title | Donor−π–Acceptor-Type Configured,
Dimethylamino-Based Organic Push–Pull Chromophores for Effective
Reduction of Mild Steel Corrosion Loss in 1 M HCl |
title_full | Donor−π–Acceptor-Type Configured,
Dimethylamino-Based Organic Push–Pull Chromophores for Effective
Reduction of Mild Steel Corrosion Loss in 1 M HCl |
title_fullStr | Donor−π–Acceptor-Type Configured,
Dimethylamino-Based Organic Push–Pull Chromophores for Effective
Reduction of Mild Steel Corrosion Loss in 1 M HCl |
title_full_unstemmed | Donor−π–Acceptor-Type Configured,
Dimethylamino-Based Organic Push–Pull Chromophores for Effective
Reduction of Mild Steel Corrosion Loss in 1 M HCl |
title_short | Donor−π–Acceptor-Type Configured,
Dimethylamino-Based Organic Push–Pull Chromophores for Effective
Reduction of Mild Steel Corrosion Loss in 1 M HCl |
title_sort | donor−π–acceptor-type configured,
dimethylamino-based organic push–pull chromophores for effective
reduction of mild steel corrosion loss in 1 m hcl |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641366/ https://www.ncbi.nlm.nih.gov/pubmed/31458644 http://dx.doi.org/10.1021/acsomega.8b00083 |
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