Corrosion Inhibition of Carbon Steel in 0.5 M H2SO4 by New Reduced Schiff Base Ligand

The effect of new reduced Schiff base ligand, named 2,2′-(((2,2-dimethylpropane-1,3-diyl)bis(azanediyl)bis(methylene)disphenol (RSH2), on the corrosion inhibiting of carbon steel in 0.5 M H 2 SO 4 has been studied. The inhibitor effects on the corrosion behavior of the samples were determined at thr...

Full description

Saved in:
Bibliographic Details
Published inJournal of bio- and tribo-corrosion Vol. 8; no. 3
Main Authors Jafari, Hojat, Rezaeivala, Majid, Mokhtarian, Nader, Berisha, Avni, Ameri, Elham
Format Journal Article
LanguageEnglish
Published Cham Springer International Publishing 01.09.2022
Springer Nature B.V
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:The effect of new reduced Schiff base ligand, named 2,2′-(((2,2-dimethylpropane-1,3-diyl)bis(azanediyl)bis(methylene)disphenol (RSH2), on the corrosion inhibiting of carbon steel in 0.5 M H 2 SO 4 has been studied. The inhibitor effects on the corrosion behavior of the samples were determined at three different concentrations, 1.0, 1.5, and 2.0 mg L −1 . Weight loss, potentiodynamic polarization curves, AC impedance measurements, and atomic force microscopy were utilized to study the corrosion behavior of carbon steel in corrosive environment in the presence and absence of new ligand. Results showed that the inhibition occurs through adsorption of the inhibitors molecules on the metal surface. The inhibition efficiency was found to increase with increasing inhibitor’s concentration. Potentiodynamic polarization data indicated that this compounds act as mixed-type inhibitors. The corrosion efficiency of RSH2 at an optimal concentration of 2 mg L −1 was 81. The adsorption of inhibitors followed the Langmuir isotherm. The value of free energy of adsorption in the presence of the corrosion inhibitor was around − 32 kJ mol −1 , which indicated chemisorption of the molecules. Powerful microscopy was used for the surface morphology studies. The DFT calculations have been demonstrated that the inhibitor is relatively flat-adsorbed on both sides of the phenyl rings.
ISSN:2198-4220
2198-4239
DOI:10.1007/s40735-022-00679-9