Corrosion inhibition of carbon steel in 1 M H2SO4 using new Azo Schiff compound: Electrochemical, gravimetric, adsorption, surface and DFT studies
Ali Ahmed Abdulridha
1
,
Mahmood A Albo Hay Allah
2
,
Sajjad Q Makki
3
,
Yusuf Sert
4
,
Hamida Edan Salman
5
,
Asim A. Balakit
6
1
Department of Education and Higher Education in The Abbas Holy Shrine, Al-Ameed Educational Group, Karbala, Iraq
|
2
Ministry of Education, Educational Directorate of Karbala, Iraq
|
3
Department of Pharmacy, AlSafwa University College, Karbala, Iraq
|
Publication type: Journal Article
Publication date: 2020-10-01
scimago Q1
wos Q1
SJR: 0.935
CiteScore: 10.5
Impact factor: 5.2
ISSN: 01677322, 18733166
Materials Chemistry
Electronic, Optical and Magnetic Materials
Physical and Theoretical Chemistry
Spectroscopy
Atomic and Molecular Physics, and Optics
Condensed Matter Physics
Abstract
New Azo Schiff compound namely 4-((4-hydroxy-3-((pyridine-2-ylimino)methyl)phenyl)diazenyl)benzonitrile (5) which is denoted as AS was synthesized and characterized using FT-IR, 13C NMR and 1H NMR spectroscopy. The new compound was evaluated as corrosion inhibitor for carbon steel in 1 M H2SO4, using electrochemical and gravimetric techniques. Tween-80 surfactant was added to enhance the solubility of AS in the acidic medium. The inhibition efficiency was found to be dependent on the concentration of AS and temperature, the highest inhibition efficiency values (91.32% and 90.30% by potentiodynamic and weight loss measurements respectively) were recorded in the presence of relatively low concentration of AS (0.08 mM) at 303 K, and it acts as anodic inhibitor. To understand the mechanism of the corrosion inhibition, the adsorption of AS onto carbon steel surface was studied, the results indicated that the adsorption process obeys Langmuir adsorption isotherm, the calculated ΔGads values were found to be around −37 kJ mol−1 which indicates that AS is adsorbed on the carbon steel surface by chemical and physical interactions. For further investigations DFT studies were employed to explain the nature of interaction between the AS molecules (neutral and protonated) and metal surface. Finally, the morphology of both corroded and inhibited surfaces were studies by scanning electron microscopy (SEM) and atomic force microscopy (AFM) techniques which confirmed the high inhibition efficiency of AS at the optimum conditions, a significant reduction in the distortion and roughness of the surface were observed (the surface roughness was reduced from 17.10 nm to 2.15 nm as measured by AFM).
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Abdulridha A. A. et al. Corrosion inhibition of carbon steel in 1 M H2SO4 using new Azo Schiff compound: Electrochemical, gravimetric, adsorption, surface and DFT studies // Journal of Molecular Liquids. 2020. Vol. 315. p. 113690.
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Abdulridha A. A., Albo Hay Allah M. A., Makki S. Q., Sert Y., Salman H. E., Balakit A. A. Corrosion inhibition of carbon steel in 1 M H2SO4 using new Azo Schiff compound: Electrochemical, gravimetric, adsorption, surface and DFT studies // Journal of Molecular Liquids. 2020. Vol. 315. p. 113690.
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TY - JOUR
DO - 10.1016/j.molliq.2020.113690
UR - https://doi.org/10.1016/j.molliq.2020.113690
TI - Corrosion inhibition of carbon steel in 1 M H2SO4 using new Azo Schiff compound: Electrochemical, gravimetric, adsorption, surface and DFT studies
T2 - Journal of Molecular Liquids
AU - Abdulridha, Ali Ahmed
AU - Albo Hay Allah, Mahmood A
AU - Makki, Sajjad Q
AU - Sert, Yusuf
AU - Salman, Hamida Edan
AU - Balakit, Asim A.
PY - 2020
DA - 2020/10/01
PB - Elsevier
SP - 113690
VL - 315
SN - 0167-7322
SN - 1873-3166
ER -
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@article{2020_Abdulridha,
author = {Ali Ahmed Abdulridha and Mahmood A Albo Hay Allah and Sajjad Q Makki and Yusuf Sert and Hamida Edan Salman and Asim A. Balakit},
title = {Corrosion inhibition of carbon steel in 1 M H2SO4 using new Azo Schiff compound: Electrochemical, gravimetric, adsorption, surface and DFT studies},
journal = {Journal of Molecular Liquids},
year = {2020},
volume = {315},
publisher = {Elsevier},
month = {oct},
url = {https://doi.org/10.1016/j.molliq.2020.113690},
pages = {113690},
doi = {10.1016/j.molliq.2020.113690}
}