ATR-FTIR in Kretschmann configuration integrated with electrochemical cell as in situ interfacial sensitive tool to study corrosion inhibitors for magnesium substrates

被引:49
作者
Fockaert, L., I [1 ,2 ]
Wuerger, T. [3 ,4 ]
Unbehau, R. [3 ]
Boelen, B. [5 ]
Meissner, R. H. [3 ,4 ]
Lamaka, S., V [3 ]
Zheludkevich, M. L. [3 ]
Terryn, H. [6 ]
Mol, J. M. C. [2 ]
机构
[1] Netherlands Org Sci Res NWO, Postbus 3021, NL-3502 GA Utrecht, Netherlands
[2] Delft Univ Technol, Dept Mat Sci & Engn Res Grp Corros Technol & Elec, Mekelweg 2, NL-2628 CD Delft, Netherlands
[3] Helmholtz Zentrum, Magnesium Innovat Ctr MagIC, Max Planck Str 1, D-21502 Geesthacht, Germany
[4] Hamburg Univ Technol, Inst Polymer & Composites, Denickestr 15, D-21073 Hamburg, Germany
[5] Tata Steel IJmuiden BV, Res & Dev Surface Engn Coating Dev, NL-1970 CA Ijmuiden, Netherlands
[6] Vrije Univ Brussel, Dept Mat & Chem, Res Grp Electrochem Surface Engn, Pleinlaan 2, B-1050 Brussels, Belgium
关键词
Corrosion inhibitors; Magnesium; Integrated ATR-FTIR; EIS setup; Chemisorption; DFT; ENHANCED CATALYTIC-ACTIVITY; INITIO MOLECULAR-DYNAMICS; TOTAL-ENERGY CALCULATIONS; IMPEDANCE SPECTROSCOPY; COATING PERFORMANCE; TRANSITION-METALS; ADSORPTION; DFT; ALLOY; TIO2;
D O I
10.1016/j.electacta.2020.136166
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
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 pi-interactions in the MgO/Mg(OH)(2) - aromatic carboxylate adsorption. Additionally, DFT calculations revealed that the addition of heteroatoms (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). (C) 2020 The Authors. Published by Elsevier Ltd.
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页数:14
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