Effect of phosphonate functional group on corrosion inhibition of imidazoline derivatives in acidic environment

In the present study, ({2-[2-(7-Isopropyl-1,4-dimethyl-9,10-octahydro-phenanthren-1-yl)-4,5-dihydro-1-yl]-ethylamino}-methyl)-phosphonicimidazole (GSIM) was synthesized by introducing phosphonate (-PH2O3) group into imidazoline derivatives and its corrosion inhibition performance was studied for Q345 steel in acidic medium along with SIM using potentiodynamic polarization, EIS and SECM analysis. Surface analysis of steel samples was also performed by optical microscopy and SEM-EDS analysis after polarization tests. XPS was used to detect chemical composition of the surface passive films. It was observed that introducing -PH2O3 group not only improved the adsorption capacity on the metal surface by coordinating with iron ions, but also inhibited the interference of hydrogen bond formed by -NH2 group and water molecules on the adsorption. GSIM not only inhibited intercrystalline corrosion and pitting corrosion, but also reduced uniform corrosion. Thermodynamics studies demonstrated that GSIM followed the Langmuir adsorption isotherm and had a larger adsorption equilibrium constant than SIM, which indicated that it had a stronger adsorption capacity. XPS and UV confirmed that the coordination between GSIM and Fe3+ and hydrogen bonding between SIM and water molecules. The quantum chemical study further clarified that the site and strength of hydrogen bond between SIM and H2O and the dominant configuration and coordination stability of GSIM with Fe3+. (C) 2021 Elsevier Inc. All rights reserved.

Automated summary

GSIM, with phosphonate group, showed improved adsorption capacity by coordinating with iron ions on the metal surface, inhibiting interference from hydrogen bonds formed by -NH2 group and water molecules. It exhibited stronger adsorption capacity and better corrosion inhibition performance than SIM, suppressing various forms of corrosion.