Spatial distribution of crystalline corrosion products formed during corrosion of stainless steel in concrete |
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| Affiliation: | 1. Department of Materials, Faculty of Civil Engineering, University of Zagreb, 10000 Zagreb, Croatia;2. Middle East Technical University, Department of Civil Engineering, Ankara, Turkey;3. Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, CA 94720, United States;4. Department of Earth and Planetary Science, University of California, Berkeley, CA 94720, United States;5. Department of Civil and Environmental Engineering, University of California, Berkeley, CA 94720, United States;1. Univ Grenoble Alpes, CNRS, LEPMI, F-38000 Grenoble, France;2. LafargeHolcim Research Center, 38291 Saint Quentin Fallavier, France;3. Gas Research Center, Khalifa University of Science and Technology, Abu Dhabi, United Arab Emirates |
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| Abstract: | The mineralogy and spatial distribution of nano-crystalline corrosion products that form in the steel/concrete interface were characterized using synchrotron X-ray micro-diffraction (μ-XRD). Two types of low-nickel high-chromium reinforcing steels embedded into mortar and exposed to NaCl solution were investigated. Corrosion in the samples was confirmed by electrochemical impedance spectroscopy (EIS). μ-XRD revealed that goethite (α-FeOOH) and akaganeite (β-FeOOH) are the main iron oxide–hydroxides formed during the chloride-induced corrosion of stainless steel in concrete. Goethite is formed closer to the surface of the steel due to the presence of chromium in the steel, while akaganeite is formed further away from the surface due to the presence of chloride ions. Detailed microstructural analysis is shown and discussed on one sample of each type of steel. |
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