Affiliations 

  • 1 Production Engineering and Metallurgy, University of Technology-Iraq, Baghdad 10001, Iraq
  • 2 The Supreme National Authority for Accountability and Justice, Baghdad 10001, Iraq
  • 3 Department of Medical Instruments Engineering Techniques, Al-Farahidi University, Baghdad 10001, Iraq
  • 4 College of Industrial Management of Oil and Gas, Basrah University of Oil and Gas, Basrah 61001, Iraq
  • 5 Department of Chemical and Process Engineering, Faculty of Engineering and Built Environment, Universiti Kebangsaan Malaysia (UKM), Bangi P.O. Box 43000, Malaysia
  • 6 Faculty of Medicine, University of Al-Ameed, Karbala 56001, Iraq
  • 7 Chemical and Water Desalination Engineering Program, Department of Mechanical & Nuclear Engineering, College of Engineering, University of Sharjah, Sharjah 26666, United Arab Emirates
Molecules, 2022 Jul 29;27(15).
PMID: 35956814 DOI: 10.3390/molecules27154857

Abstract

Using traditional weight-loss tests, as well as different electrochemical techniques (potentiodynamic polarization and electrochemical impedance spectroscopy), we investigated the corrosion-inhibition performance of 2,2′-(1,4-phenylenebis(methanylylidene)) bis(N-(3-methoxyphenyl) hydrazinecarbothioamide) (PMBMH) as an inhibitor for mild steel in a 1 M hydrochloric acid solution. The maximum protection efficacy of 0.0005 M of PMBMH was 95%. Due to the creation of a protective adsorption layer instead of the adsorbed H2O molecules and acidic chloride ions, the existence of the investigated inhibitor reduced the corrosion rate and increased the inhibitory efficacy. The inhibition efficiency increased as the inhibitor concentration increased, but it decreased as the temperature increased. The PMBMH adsorption mode followed the Langmuir adsorption isotherm, with high adsorption-inhibition activity. Furthermore, the value of the ∆Gadso indicated that PMBMH contributed to the physical and chemical adsorption onto the mild-steel surface. Moreover, density functional theory (DFT) helped in the calculation of the quantum chemical parameters for finding the correlation between the inhibition activity and the molecular structure. The experimental and theoretical findings in this investigation are in good agreement.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.