RESUMO
The corrosion behavior of the dissimilar metal welded joint (DMWJ) is highly dependent on its heterogeneous microstructures. However, directly measuring the electrochemical properties of microstructures in different heat-affected zones (HAZs) is a formidable challenge, because traditional bulk electrochemistry can only offer an average signal. Herein, the microelectrochemical properties of an SA508-309L/308L DMWJ were measured in 3.5 wt % NaCl solution using lithography and capillary techniques. Specifically, high-throughput microelectrochemical tests, including open circuit potential (OCP), electrochemical impedance spectroscopy (EIS), and potentiodynamic polarization (PDP), were conducted on 168 spots (Φ 12 µm). Results revealed five typical EIS responses and seven varieties of PDP curves (different magnitudes of the current density). The maps of thermodynamic and kinetic metrics, such as polarization resistance derived from EIS, corrosion potentials, and corrosion currents extracted from potentiodynamic polarization curves, demonstrated good consistency. The uniform corrosion tendency of the SA508 HAZ subregions during the immersion tests is basically consistent with its Ecorr_avg order of subcritical HAZ (C5, -371 mV) < intercritical HAZ (C4, -546 mV) < fine-grained HAZ2 (C3, -579 mV) < fine-grained HAZ1 (C2, -593 mV). The random presence of inclusions leads to highly heterogeneous microelectrochemical properties of the DMWJ, thereby causing localized corrosion to occur preferentially. Moreover, the macroscopic corrosion behavior is affected by the corrosion products, which display a protective effect that modifies the local electrochemical activity of the SA508 HAZ. The combination of microelectrochemical properties allows for a more comprehensive understanding of the macroscopic corrosion behavior of metals and the galvanic effect between the heterogeneous microstructures.
RESUMO
Scanning electrochemical cell microscopy (SECCM) allows for electrochemical imaging at the micro- or nanoscale by confining the electrochemical reaction cell in a small meniscus formed at the end of a micro- or nanopipette. This technique has gained popularity in electrochemical imaging due to its high-throughput nature. Although it shows considerable application potential in corrosion science, there are still formidable and exciting challenges to be faced, particularly relating to the high-throughput characterization and analysis of microelectrochemical big data. The objective of this perspective is to arouse attention and provide opinions on the challenges, recent progress, and future prospects of the SECCM technique to the electrochemical society, particularly from the viewpoint of corrosion scientists. Specifically, four main topics are systematically reviewed and discussed: (1) the development of SECCM; (2) the applications of SECCM for corrosion studies; (3) the challenges of SECCM in corrosion studies; and (4) the opportunities of SECCM for corrosion science.
RESUMO
The localized corrosion behavior of stainless steel (SS) induced by typical inclusion such as MnS and oxy-sulfide in NaCl solution was investigated by immersion tests and microelectrochemical tests. Oxy-sulfide consists of an internal polygonal oxide part and an external sulfide part. The surface Volta potential of the sulfide part is always lower than that of the surrounding matrix, as in the case of individual MnS, while the potential of the oxide part is indistinguishable from that of the surrounding matrix. Sulfides are soluble, while oxides are almost insoluble. Oxy-sulfide exhibits a complex electrochemical behavior in the passive region, which can be attributed to its complex composition and multi-interface coupling effects. It was found that both MnS and oxy-sulfide increase the susceptibility of the local area to pitting corrosion.
