Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (5/5 displayed)

  • 2020Effect of zirconium-based conversion treatments of zinc, aluminium and magnesium on the chemisorption of ester-functionalized molecules20citations
  • 2020ATR-FTIR in Kretschmann configuration integrated with electrochemical cell as in situ interfacial sensitive tool to study corrosion inhibitors for magnesium substratescitations
  • 2020ATR-FTIR in Kretschmann configuration integrated with electrochemical cell as in situ interfacial sensitive tool to study corrosion inhibitors for magnesium substrates50citations
  • 2020The effect of time evolution and timing of the electrochemical data recording of corrosion inhibitor protection of hot-dip galvanized steel34citations
  • 2019A complementary electrochemical approach for time-resolved evaluation of corrosion inhibitor performance16citations

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Terryn, Herman
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Fockaert, L. I.
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Mol, J. M. C.
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Hauffman, Tom
1 / 59 shared
Pletincx, S.
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Lamaka, Sviatlana
1 / 8 shared
Unbehau, Reneé
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Zheludkevich, Mikhail
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Fockaert, Laura Lynn
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Würger, Tim
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Meißner, Robert
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Mol, Arjan
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Lamaka, S. V.
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Unbehau, R.
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Würger, T.
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Zheludkevich, M. L.
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Meißner, R. H.
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Andreatta, F.
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Zardet, L.
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Lekka, M.
2 / 5 shared
Meeusen, Mats
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Fedrizzi, L.
2 / 11 shared
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2019

Co-Authors (by relevance)

  • Terryn, Herman
  • Fockaert, L. I.
  • Mol, J. M. C.
  • Hauffman, Tom
  • Pletincx, S.
  • Lamaka, Sviatlana
  • Unbehau, Reneé
  • Zheludkevich, Mikhail
  • Fockaert, Laura Lynn
  • Würger, Tim
  • Meißner, Robert
  • Mol, Arjan
  • Lamaka, S. V.
  • Unbehau, R.
  • Würger, T.
  • Zheludkevich, M. L.
  • Meißner, R. H.
  • Andreatta, F.
  • Zardet, L.
  • Lekka, M.
  • Meeusen, Mats
  • Fedrizzi, L.
OrganizationsLocationPeople

document

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

  • Lamaka, Sviatlana
  • Boelen, B.
  • Terryn, Herman
  • Unbehau, Reneé
  • Zheludkevich, Mikhail
  • Fockaert, Laura Lynn
  • Mol, J. M. C.
  • Würger, Tim
  • Meißner, Robert
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...

Topics
  • surface
  • compound
  • corrosion
  • Magnesium
  • Magnesium
  • Sodium
  • density functional theory
  • forming
  • electrochemical-induced impedance spectroscopy
  • Fourier transform infrared spectroscopy
  • molecular structure
  • aligned