Anti-corrosive and anti-microbial activity of MTMI on CRCA metal

被引:8
|
作者
Suhas, R. [1 ]
Rao, Srilatha [2 ]
Mahadevaswamy, M. [1 ]
Sowmyashree, A. S. [2 ]
Rao, Padmalatha [2 ]
Kumar, C. B. Pradeep [3 ]
Rekha, N. D. [4 ]
Nadigar, S. [4 ]
Shwetha, K. [2 ]
机构
[1] Univ Mysore, JSS Coll Arts Commerce & Sci, Dept Chem, Recognized Res Ctr, Ooty Rd, Mysuru, India
[2] Nitte Meenakshi Inst Technol, Dept Chem, Bangalore 560064, India
[3] Malnad Coll Engn, Dept Chem, Hassan, India
[4] Univ Mysore, JSS Coll Arts Commerce & Sci, Dept Chem & Biochem, Recognized Res Ctr, Ooty Rd, Mysuru, India
关键词
CRCA steel; Electrochemical studies; Surface morphology; Molecular docking; Biological activity; MILD-STEEL; CORROSION-INHIBITORS; CARBON-STEEL; TRIAZOLE DERIVATIVES; ADSORPTION; SURFACE;
D O I
10.1016/j.molstruc.2023.136106
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The present study was intended to demonstrate the synthesis, and characterization of 1-(3-methoxyphenyl)-N(4H-1,2,4-triazol-4-yl)methan-imine(MTMI) as an inhibitor for the corrosion on CRCA in 1 M HCl. In addition to this, molecular docking, and biological activity was carried out. MTMI formation was confirmed by FTIR and NMR spectroscopic studies. The corrosion inhibition effect was studied by weight loss, potentiodynamic polarization (PDP) measurements, and electrochemical impedance spectroscopy (EIS) techniques. The conditions for optimum inhibition efficiency were established by varying the concentration of the inhibitor and temperature by weight loss method. Kinetic and thermodynamic parameters were calculated and discussed. Results were fitted into various adsorption isotherm models. The adsorption of MTMI on CRCA was confirmed by scanning electron microscopy (SEM). Adsorption obeyed the Langmuir isotherm model and followed physical adsorption. Increasing inhibitor concentration led to a significant reduction in the corrosion rate of mild steel, with an inhibitor efficiency value above 93%. A molecular docking study showed the binding capacity of the protein endopolygalacturonase (1HG8) and the activity of polygalacturonase enzyme on MTMI was measured.
引用
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页数:10
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