Microscale chemical imaging to characterize and quantify corrosion processes at the metal-electrolyte interface

We introduce an experimental setup to chemically image corrosion processes at metal-electrolyte interfaces under stagnant, confined conditions-relevant in a wide range of situations. The setup is based on a glass capillary, in which precipitation of corrosion products in the interfacial aqueous phase can be monitored over time with optical microscopy, and chemically and structurally characterized with microscopic synchrotron-based techniques (X-ray fluorescence, X-ray diffraction, and X-ray absorption spectroscopy). Moreover, quantification of precipitates through X-ray transmission measurements provides in-situ corrosion rates. We illustrate this setup for iron corrosion in a pH 8 electrolyte, revealing the critical role of O<sub>2</sub> and iron diffusion in governing the precipitation of ferrihydrite and its transformation to goethite. Corrosion and coupled reactive transport processes can thus be monitored and fundamentally investigated at the metal-electrolyte interface, with micrometer-scale resolution. This capillary setup has potential applications for in-situ corrosion studies of various metals and environments.

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Publication Details

Journal
npj Materials Degradation
Published
2024-11-06
DOI
https://doi.org/10.1038/s41529-024-00534-x
Citations
5
Primary Topic
Corrosion Behavior and Inhibition
Type
article
Field-Weighted Citation Impact
0.59

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Microscale chemical imaging to characterize and quantify corrosion processes at the metal-electrolyte interface

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npj Materials Degradation
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article

Microscale chemical imaging to characterize and quantify corrosion processes at the metal-electrolyte interface

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article en
5 citations

Abstract

We introduce an experimental setup to chemically image corrosion processes at metal-electrolyte interfaces under stagnant, confined conditions-relevant in a wide range of situations. The setup is based on a glass capillary, in which precipitation of corrosion products in the interfacial aqueous phase can be monitored over time with optical microscopy, and chemically and structurally characterized with microscopic synchrotron-based techniques (X-ray fluorescence, X-ray diffraction, and X-ray absorption spectroscopy). Moreover, quantification of precipitates through X-ray transmission measurements provides in-situ corrosion rates. We illustrate this setup for iron corrosion in a pH 8 electrolyte, revealing the critical role of O<sub>2</sub> and iron diffusion in governing the precipitation of ferrihydrite and its transformation to goethite. Corrosion and coupled reactive transport processes can thus be monitored and fundamentally investigated at the metal-electrolyte interface, with micrometer-scale resolution. This capillary setup has potential applications for in-situ corrosion studies of various metals and environments.

npj Materials DegradationVol. 8(1)
Oregon State University (US), Paul Scherrer Institute (CH), ETH Zurich (CH)
European Commission, Paul Scherrer Institut, H2020 European Research Council, HORIZON EUROPE European Research Council
Clean water and sanitation
Openalex Percentile: Top 33%
Corrosion Behavior and Inhibition
0.59
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