Abstract

Integrated attenuated total reflection – Fourier transform infrared spectroscopy (ATR-FTIR) – Electrochemical impedance spectroscopy (EIS) measurements were used to simultaneously follow chemisorption mechanisms of organic inhibitors as well as their corrosion inhibition efficiency towards magnesium based substrates. Four carboxylic compounds, i.e. 2,5-pyridinedicarboxylic acid (PDC), 3-methylsalicylic acid (MSA), sodium salicylate (SS) and fumaric acid (FA), were selected based on their promising inhibiting capacities and were all shown to chemisorb at the MgO/Mg(OH)2 surface by carboxylate bond formation. Orientation analysis using polarized infrared light showed that carboxylate bonds established using aliphatic carboxylate compound aligned perpendicular to the magnesium surface, whereas carboxylate bonds with aromatic compounds were oriented in plane with the magnesium surface. This different orientation is associated to the involvement of π-interactions in the MgO/Mg(OH)2 – aromatic carboxylate adsorption. Additionally, DFT calculations revealed that the addition of hetero-atoms (i.e. N or OH) in the molecular structure contributes to increased adsorption energies, indicating that next to carboxylate groups also these hetero-atoms are involved in interfacial interactions. Integrating the ATR-FTIR setup with an electrochemical cell allowing for simultaneous EIS measurements lead to two surface phenomena determining the inhibition efficiency. Surface hydroxylation processes on one hand forming a MgO/Mg(OH)2 layer on one hand, and the chemisorption of carboxylate compounds on the other hand. The inhibition efficiency was found to increase in following order: FA < PDC < MSA and was mainly associated to the formation of a MgO/Mg(OH)2 layer. SS was shown to act as a corrosion accelerator rather than a corrosion inhibitor. Despite its high sensitivity for water, both surface processes could be followed in situ by means of ATR-FTIR. Simultaneously, protective properties of the formed films could be quantified by means of EIS. Consequently, integrated ATR-FTIR – EIS methodology has shown to be highly valuable for gaining in-situ insights in the inhibition mechanism, while quantifying the inhibition efficiency. This was even possible for highly active metal substrate as magnesium, although further developments are suggested if one aims to quantify electrochemical constants related to corrosion and other surface processes measured at the low frequencies (i.e. < 1 Hz).

Highlights

  • Surface phenomena, including both hydration and dissolution, as well as inhibitor chemisorption mechanisms were followed in situ using the integrated attenuated total reflection (ATR)-Fourier transform infrared spectroscopy (FTIR) e Electrochemical impedance spectroscopy (EIS) setup

  • Orientation analysis using polarized IR-light showed the transition dipoles of carboxylate bonds established with aromatic compounds are in plane with the surface, whereas those observed for aliphatic fumaric acid (FA) are oriented perpendicular to the surface

  • Further development of the proposed in situ screening methodology is recommended

Read more

Summary

Introduction

The accessibility of metalelectrolyte interfaces from the metal side allows for the integration of an electrochemical cell in the ATR-FTIR setup, creating the opportunity to monitor molecular phenomena at the surface, while simultaneously probing electrochemical properties such as oxide resistance and barrier properties [28e30]. Such an integrated setup could be very useful to gain fundamental in situ insights in inhibiting mechanism of corrosion inhibitors [7]

Objectives
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call