Synthesis, characterization and corrosion inhibition studies of N-phenyl-benzamides on the acidic corrosion of mild steel: Experimental and computational studies
-
Add time:09/03/2019 Source:sciencedirect.com
Present study aims to demonstrate the effect of electron withdrawing nitro (NO2) and electron releasing methoxy (OCH3) substituents on the inhibition behavior of N-Phenyl-benzamide derivatives (BNAs), namely N-(4-nitrophenyl) benzamide (BNA-1; NO2), N-phenylbenzamide (BNA-2; H) and N-(4-methoxyphenyl)benzamide (BNA-3; OCH3) for mild steel acidic (1 M HCl) corrosion. Results of the computational and experimental studies showed that methoxy (OCH3) substituent enhances the inhibition efficiency whereas nitro (NO2) decreases the inhibition efficiency. Electrochemical impedance spectroscope (EIS) study showed that BNAs acted as interface corrosion inhibitors and polarization study shows they acted as cathodic type corrosion inhibitors. They showed maximum efficiencies of 89.56%, 93.91% and 96.52% for BNA-1, BNA-2 and BNA-3, respectively. The BNAs strongly (high Kads values) and spontaneously (negative ∆ G0 values) adsorbed at metal/electrolyte interfaces and their mode of adsorption obeyed the Langmuir adsorption isotherm. Surface investigation of the mild steel surfaces using AFM and SEM analyses revealed that BNAs adsorb on the surface and increase the energy barrier for corrosive dissolution which is also supported by the higher values of Ea (activation energy). DFT study carried out using 3-21G, 6-31G and 6-311G basis sets provides significant support to the experimental efficiency order. DFT indices like EHOMO, ELUMO, electronegativity (χ), softness (σ), hardness (η), dipole moment (μ), energy band gap (∆ E) and fraction of electron transfer (∆ N) were derived for all basis sets. Experimental and DFT study was further supported by molecular dynamic (MD) simulations study.
We also recommend Trading Suppliers and Manufacturers of N-(2-methyl-3-nitrophenyl)benzamide (cas 133053-84-6). Pls Click Website Link as below: cas 133053-84-6 suppliers
Prev:Facile synthesis of new quinazolinone benzamides as potent tyrosinase inhibitors: Comparative spectroscopic and molecular docking studies
Next:Design, synthesis and anti-inflammatory activity of pyrimidine scaffold benzamide derivatives as epidermal growth factor receptor tyrosine kinase inhibitors) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Montmorillonite K10: An efficient organo heterogeneous catalyst for one-pot synthesis of new N,N′-alkylidene bisamide derivatives under solvent free condition09/07/2019
- Biological evaluation and molecular docking studies of nitro benzamide derivatives with respect to in vitro anti-inflammatory activity09/06/2019
- Synthesis, structural, optical and thermal properties of N-methyl–N-aryl benzamide organic single crystals grown by a slow evaporation technique09/05/2019
- Design, synthesis and anti-inflammatory activity of pyrimidine scaffold benzamide derivatives as epidermal growth factor receptor tyrosine kinase inhibitors09/04/2019
- Facile synthesis of new quinazolinone benzamides as potent tyrosinase inhibitors: Comparative spectroscopic and molecular docking studies09/02/2019


