TY - JOUR
T1 - Experimental and computational studies on hydroxamic acids as environmental friendly chelating corrosion inhibitors for mild steel in aqueous acidic medium
AU - Verma, Dakeshwar Kumar
AU - Al Fantazi, Akram
AU - Verma, Chandrabhan
AU - Khan, Fahmida
AU - Asatkar, Ashish
AU - Hussain, Chaudhery Mustansar
AU - Ebenso, Eno E.
N1 - Publisher Copyright:
© 2020 Elsevier B.V.
PY - 2020/9/15
Y1 - 2020/9/15
N2 - In the present study, three hydroxamic acids (HAs) namely acetohydroxamic acid (AHA), benzohydroxamic acid (BHA) and oxalohydroxamic acid (OHA) were synthesized, characterized and used as inhibitors for mild steel corrosion in1 M HCl using chemical, electrochemical, surface and computational methods. Results of the studies show that the HAs act as effective corrosion inhibitors and their inhibition efficiencies follow the order: OHA (96.37%) > BHA (95.69%) > AHA (93.29%). EIS study showed that studied HAs act as interface type inhibitors. Polarization study revealed that HAs demonstrate mixed-type corrosion inhibitors characteristics and adsorb on the active sites of metallic surface. Adsorption of HAs on metal-1 M HCl interfaces followed the Langmuir adsorption isotherm model. Surface morphological analyses of inhibited and uninhibited metallic surface were carried out using SEM-EDX and XRD methods. DFT analyses showed that studied compounds act as chelating type of ligands. Effect of Keto-enol tautomerism and different possible conformational isomers on metallic corrosion inhibition was demonstrated. The conformational isomers in which >C=O and –OH (hydroxyl) groups present in same side behave as chelating ligands and form relatively more stable complex than that of conformational isomers in which >C=O and –OH groups present in opposite side. Experimental and DFT studies complimented each other well.
AB - In the present study, three hydroxamic acids (HAs) namely acetohydroxamic acid (AHA), benzohydroxamic acid (BHA) and oxalohydroxamic acid (OHA) were synthesized, characterized and used as inhibitors for mild steel corrosion in1 M HCl using chemical, electrochemical, surface and computational methods. Results of the studies show that the HAs act as effective corrosion inhibitors and their inhibition efficiencies follow the order: OHA (96.37%) > BHA (95.69%) > AHA (93.29%). EIS study showed that studied HAs act as interface type inhibitors. Polarization study revealed that HAs demonstrate mixed-type corrosion inhibitors characteristics and adsorb on the active sites of metallic surface. Adsorption of HAs on metal-1 M HCl interfaces followed the Langmuir adsorption isotherm model. Surface morphological analyses of inhibited and uninhibited metallic surface were carried out using SEM-EDX and XRD methods. DFT analyses showed that studied compounds act as chelating type of ligands. Effect of Keto-enol tautomerism and different possible conformational isomers on metallic corrosion inhibition was demonstrated. The conformational isomers in which >C=O and –OH (hydroxyl) groups present in same side behave as chelating ligands and form relatively more stable complex than that of conformational isomers in which >C=O and –OH groups present in opposite side. Experimental and DFT studies complimented each other well.
KW - Chelating corrosion inhibitors
KW - Conformational isomers
KW - Hydroxamic acid
KW - Langmuir adsorption isotherm
KW - Tautomers as corrosion inhibitors
UR - http://www.scopus.com/inward/record.url?scp=85087337020&partnerID=8YFLogxK
U2 - 10.1016/j.molliq.2020.113651
DO - 10.1016/j.molliq.2020.113651
M3 - Article
AN - SCOPUS:85087337020
SN - 0167-7322
VL - 314
JO - Journal of Molecular Liquids
JF - Journal of Molecular Liquids
M1 - 113651
ER -