The initiation and evolution of the localized corrosion in carbon steel were investigated in a simulated marine environment of Xisha Island in the South China Sea. In the initial stage, localized corrosion occurred in the form of corrosion spot. The localized corrosion morphology and electrochemical information during corrosion process were tracked by field emission scanning electron microscopy energy dispersive spectrometry (FE-SEM-EDS), scanning vibrating electrode technique (SVET) and scanning Kelvin probe force microscopy (SKPFM). Localized corrosion was induced by the microcrevices around Al₂O₃ inclusions. The occluded cells and oxygen concentration cell formed in the pits could accelerate the localized corrosion. Pearlite accelerated the dissolution of the inside and surrounding ferrite via the galvanic effect between Fe₃C and ferrite. Overall, the localized corrosion was initiated and evaluated under a synergistic effect of crevice corrosion, occluded cells, oxygen concentration cell and the galvanic couple between FeC₃ and ferrite.

The present work systematically investigated the initiation mechanism of localized corrosion induced by Al₂O₃-MnS composite inclusion in E690 steel under a simulated marine environment. The results showed that a micro-gap exists between the Al₂O₃-MnS inclusion and the matrix, and electron backscattered diffraction (EBSD) analysis revealed significant lattice dislocation zones around the Al₂O₃-MnS composite inclusion. The presence of the micro-gap and the lattice dislocation both promoted the localized corrosion initiation. The Volta potential of Al₂O₃ detected by scanning Kelvin probe force microscopy (SKPFM) was approximately 149.33 mV higher than that of the steel matrix, and the Volta potential of MnS was 10 mV lower than that of the steel matrix. The current-sensing atomic force microscopy (CSAFM) results showed that the Al₂O₃ was not conductive, while the MnS had good conductive properties. Therefore, it was not possible for a galvanic couple to be formed between Al₂O₃ and the adjacent steel matrix. A galvanic couple effect between the MnS and the adjacent steel matrix was directly demonstrated for the first time. The MnS acted as the anode phase for preferential dissolution in the corrosion process. The in situ immersion experiments and the Pourbaix diagram results confirmed that the dissolution of MnS was an electrochemical reaction process and the dissolution of Al₂O₃ was a chemical reaction.

Ductile iron is a high-strength cast iron material. The spherical graphite obtained by inoculation treatment effectively improves the mechanical properties of cast iron, resulting in higher strength than carbon steel. However, severe corrosion may occur under specific circumstances, especially in thermal water pipelines. In this paper, the corrosion mechanisms at the main defective points of ductile iron were investigated using microscopic morphological characterization after accelerated tests combined with numerical simulations. The influence law of each environmental factor on the corrosion kinetics of ductile iron in a complex water quality environment was studied using dynamic potential polarization tests. The results showed that the main causative factors leading to the increased corrosion of ductile iron were the presence of tail-like gaps on its surface, and the crescent-shaped shrinkage and loosening organization around the graphite spheres. After mechanical treatment was applied to eliminate the obvious defects, the number of corrosion pits was reduced by 41.6%, and the depth of the pits was slowed down by 40% after five days. By comparison, after ten days, the number of pits was reduced by 51%, and the depth of the pits was slowed down by 50%. The dynamic potential polarization test results show that the dissolved oxygen concentration has the greatest influence on the corrosion of ductile iron in the simulated water environment; meanwhile, the water hardness can slow down the corrosion of ductile iron. The relative influence of each environmental factor is as follows: dissolved oxygen concentration > temperature > immersion time > water hardness > pH > Cl⁻.

The corrosion resistance of the HRB400 steel rebar alloyed with Cr and rare earths (RE) was systematically studied from two aspects, including the properties of the passive film and the protectiveness of the rust layer. The results presented that Cr increased the corrosion resistance of the steel rebar through stabilizing the passive film and was not involved in the formation of corrosion pits, while the pitting corrosion was initiated by the dissolution of (RE)₂O₂S inclusion, resulting in the local acidification at the bottom of the corrosion pits, which decreased the stability of the passive film. As for the long-term corrosion process, both Cr and RE decreased the corrosion rate of the steel rebar, which was related to the promotion effect on the formation of α-FeOOH in the rust layer from Cr and RE.