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Synthesis and characterization of Schiff bases NBBA, MNBA and CNBA

Three Schiff base compounds, N(1),N(2)-bis(3-nitrobenzylidene)phenylene diamine (NBBA), 2-methyl-N-(3-nitrobenzylidene)aniline (MNBA) and N-(2-chlorobenzylidene)-4-nitroaniline (CBNA) were synthesized, characterised and applied for the first time as potential mild steel (MS) corrosion inhibitors in...

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Autores principales: Elemike, Elias E., Nwankwo, Henry U., Onwudiwe, Damian C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031242/
https://www.ncbi.nlm.nih.gov/pubmed/29984329
http://dx.doi.org/10.1016/j.heliyon.2018.e00670
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author Elemike, Elias E.
Nwankwo, Henry U.
Onwudiwe, Damian C.
author_facet Elemike, Elias E.
Nwankwo, Henry U.
Onwudiwe, Damian C.
author_sort Elemike, Elias E.
collection PubMed
description Three Schiff base compounds, N(1),N(2)-bis(3-nitrobenzylidene)phenylene diamine (NBBA), 2-methyl-N-(3-nitrobenzylidene)aniline (MNBA) and N-(2-chlorobenzylidene)-4-nitroaniline (CBNA) were synthesized, characterised and applied for the first time as potential mild steel (MS) corrosion inhibitors in 1 M HCl at 30 °C. Fourier transform infra-red (FTIR), (1)H, (13)C Nuclear magnetic resonance (NMR) and Mass spectrometry (MS) were used for the characterisation of the compounds. The electrochemical studies and evaluation of corrosion inhibition potency were achieved using potentiodynamic polarization (PDP) and electrochemical impedance spectroscopy (EIS) techniques. Density functional theory (DFT) calculations were further employed to describe the electronic distribution on the molecules and potential sites that aided corrosion inhibition. The results of the employed characterisation techniques confirmed the proposed structures of the compounds with the MS revealing the exact molecular mass of the compounds. Electrochemical results showed that the trend in inhibition efficiency of the three compounds was in the order: MNBA > NBBA > CBNA. MNBA recorded the highest inhibition efficiency at 100 ppm. Corrosion kinetics of the set of inhibitors was found to prefer the Langmuir adsorption isotherm with both physisorption and chemisorption mechanisms as revealed by ΔG values. In an effort to develop efficient corrosion inhibitors with non-toxic effect, low cost and multiple adsorption centres, these Schiff bases are presented.
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spelling pubmed-60312422018-07-06 Synthesis and characterization of Schiff bases NBBA, MNBA and CNBA Elemike, Elias E. Nwankwo, Henry U. Onwudiwe, Damian C. Heliyon Article Three Schiff base compounds, N(1),N(2)-bis(3-nitrobenzylidene)phenylene diamine (NBBA), 2-methyl-N-(3-nitrobenzylidene)aniline (MNBA) and N-(2-chlorobenzylidene)-4-nitroaniline (CBNA) were synthesized, characterised and applied for the first time as potential mild steel (MS) corrosion inhibitors in 1 M HCl at 30 °C. Fourier transform infra-red (FTIR), (1)H, (13)C Nuclear magnetic resonance (NMR) and Mass spectrometry (MS) were used for the characterisation of the compounds. The electrochemical studies and evaluation of corrosion inhibition potency were achieved using potentiodynamic polarization (PDP) and electrochemical impedance spectroscopy (EIS) techniques. Density functional theory (DFT) calculations were further employed to describe the electronic distribution on the molecules and potential sites that aided corrosion inhibition. The results of the employed characterisation techniques confirmed the proposed structures of the compounds with the MS revealing the exact molecular mass of the compounds. Electrochemical results showed that the trend in inhibition efficiency of the three compounds was in the order: MNBA > NBBA > CBNA. MNBA recorded the highest inhibition efficiency at 100 ppm. Corrosion kinetics of the set of inhibitors was found to prefer the Langmuir adsorption isotherm with both physisorption and chemisorption mechanisms as revealed by ΔG values. In an effort to develop efficient corrosion inhibitors with non-toxic effect, low cost and multiple adsorption centres, these Schiff bases are presented. Elsevier 2018-07-02 /pmc/articles/PMC6031242/ /pubmed/29984329 http://dx.doi.org/10.1016/j.heliyon.2018.e00670 Text en © 2018 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Elemike, Elias E.
Nwankwo, Henry U.
Onwudiwe, Damian C.
Synthesis and characterization of Schiff bases NBBA, MNBA and CNBA
title Synthesis and characterization of Schiff bases NBBA, MNBA and CNBA
title_full Synthesis and characterization of Schiff bases NBBA, MNBA and CNBA
title_fullStr Synthesis and characterization of Schiff bases NBBA, MNBA and CNBA
title_full_unstemmed Synthesis and characterization of Schiff bases NBBA, MNBA and CNBA
title_short Synthesis and characterization of Schiff bases NBBA, MNBA and CNBA
title_sort synthesis and characterization of schiff bases nbba, mnba and cnba
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031242/
https://www.ncbi.nlm.nih.gov/pubmed/29984329
http://dx.doi.org/10.1016/j.heliyon.2018.e00670
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