z-logo
open-access-imgOpen Access
Electrochemical, surface and computational studies on the inhibition performance of some newly synthesized 8-hydroxyquinoline derivatives containing benzimidazole moiety against the corrosion of carbon steel in phosphoric acid environment
Author(s) -
M. El Faydy,
B. Lakhrissi,
Charafeddine Jama,
A. Zarrouk,
Lukman O. Olasunkanmi,
Eno E. Ebenso,
Fouad Bentiss
Publication year - 2019
Publication title -
journal of materials research and technology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.832
H-Index - 44
eISSN - 2214-0697
pISSN - 2238-7854
DOI - 10.1016/j.jmrt.2019.11.014
Subject(s) - adsorption , benzimidazole , 8 hydroxyquinoline , electrochemistry , moiety , chemistry , langmuir adsorption model , quinoline , molecule , corrosion , inorganic chemistry , nuclear chemistry , organic chemistry , electrode
Four new 8-hydroxyquinoline derivatives, namely 5-((1H-benzimidazol-2-yl)methyl)quinolin-8-ol (BIMQ), 5-((5-methyl-1H-benzimidazol-2-yl)methyl)quinolin-8-ol (MBMQ), 5-((5-chloro-1H-benzimidazol-2-yl)methyl)quinolin-8-ol (CBMQ) and 5-((5,6-dichloro-1H-benzimidazol-2-yl)methyl)quinolin-8-ol (DCBMQ) were prepared in moderate to good yields through the condensation of 5-(carboxymethyl)-8-hydroxyquinoline and substituted o-phenylenediamine. 1H, 13C NMR and elemental analysis confirm the formation of the desired compounds. The anti-corrosive potential of these heterocyclic compounds has been studied on carbon steel in 2 M phosphoric acid (H3PO4) electrolyte by means of electrochemical measurements. The inhibition efficiency of these heterocyclic compounds was strongly linked to the concentration and the structure of the molecules; reached a maximum of 94.7% for DCBMQ at 10−3 M. Data generated from potentiodynamic revealed that the investigated 8-hydroxyquinoline derivatives are mixed type inhibitors. The influence of temperature on the corrosion behaviour was assessed. The four quinoline derivatives adsorbed according to the Langmuir's adsorption isotherm. Surface analysis (SEM and XPS) confirmed the formation of a protective layer adsorbed on the steel surface. DFT calculations suggested that 8-hydroxyquinoline derivatives adsorb on the metal via the 8-hydroxyquinoline ring and their corrosion inhibition potential have some linear correlation with the degree of co-planarity of the benzimidazole and hydroxyquinoline rings. Monte Carlo simulations showed that the molecules adsorbed on Fe(1 1 0) surface through the 8-hydroxyquinoline in a near-flat mode and the adsorption energies both in the absence and presence of aqueous phosphate ions agree with the observed trends of inhibition efficiencies.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom