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

IF 6.6 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY
Cristhiana C. Albert, Shishir Mundra, Dario Ferreira Sanchez, Fabio E. Furcas, Ashish D. Rajyaguru, O. Burkan Isgor, Daniel Grolimund, Ueli M. Angst
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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 O2 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.

Abstract Image

利用微尺度化学成像技术表征和量化金属-电解质界面的腐蚀过程。
我们介绍了一种实验装置,用于在停滞、密闭条件下对金属电解质界面的腐蚀过程进行化学成像,适用于多种情况。该装置以玻璃毛细管为基础,其中界面水相中腐蚀产物的沉淀可通过光学显微镜进行长期监测,并通过微观同步加速器技术(X 射线荧光、X 射线衍射和 X 射线吸收光谱)进行化学和结构表征。此外,通过 X 射线透射测量对沉淀物进行定量,可提供原位腐蚀率。我们以 pH 值为 8 的电解质中的铁腐蚀为例,说明了氧气和铁的扩散在控制铁水物的沉淀及其转化为高铁的过程中所起的关键作用。因此,可以在金属-电解质界面上以微米级的分辨率对腐蚀和耦合反应传输过程进行监测和基本研究。这种毛细管装置可用于各种金属和环境的原位腐蚀研究。
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来源期刊
npj Materials Degradation
npj Materials Degradation MATERIALS SCIENCE, MULTIDISCIPLINARY-
CiteScore
7.80
自引率
7.80%
发文量
86
审稿时长
6 weeks
期刊介绍: npj Materials Degradation considers basic and applied research that explores all aspects of the degradation of metallic and non-metallic materials. The journal broadly defines ‘materials degradation’ as a reduction in the ability of a material to perform its task in-service as a result of environmental exposure. The journal covers a broad range of topics including but not limited to: -Degradation of metals, glasses, minerals, polymers, ceramics, cements and composites in natural and engineered environments, as a result of various stimuli -Computational and experimental studies of degradation mechanisms and kinetics -Characterization of degradation by traditional and emerging techniques -New approaches and technologies for enhancing resistance to degradation -Inspection and monitoring techniques for materials in-service, such as sensing technologies
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