We show that the process of local electrochemical dissolution of iron of loaded low-carbon 20 steel (c0. 2 = 270 MPa) in a corrosive medium (3% aqueous NaCI solution, pH 6.9) is multistage. The characteristics of the process depend on the form of the surface interacting with the corrosive medium. The investigated cases are arranged in the following order according to the rate of dissolution of the metal: a smooth surface, a stress concentrator, and a stress concentrator with a short crack-like defect. We propose and detect the corresponding electrochemical reactions and their sequence (stagewise behavior) realized in the course of the process. The electrochemical parameters of local anodic dissolution of the metal at tips of corrosion cracks of various depths and openings are determined, On the basis of these results, we suggest an autocatalytic mechanism of dissolution of the metal in which Fe 2+ ions are autocatalytic particles. We demonstrate agreement between the results calculated by using classical electrochemical equations for the kinetics of electrode processes and experimental data obtained in corrosive media with various concentrations of Fe 2+ ions in the range Cre2~ = 1.0.10~s-2.0 9 10 -1 mole/liter. This means that the indicated mechanism can be realized at the tip of a corrosion crack.The nature of corrosion fracture of structural metals depends on many factors, whose investigation requires the performance of simultaneous experiments in various fields (fracture mechanics, materials science, and the physics and chemistry of materials). Numerous researchers call special attention [1][2][3], in particular, to the dominant role of electrochemical processes in the early stages of corrosion fracture of a metal as compared to mechanical factors. In certain cases, these processes can govern the mechanism and rate of formation of corrosion defects on the surface, which is important for evaluation of the serviceability of structural materials under the action of corrosive media.Up to now, one studied mainly electrochemical dissolution of a smooth unloaded surface of the metal [4] in the case where the rate of dissolution is determined only by diffusion processes in the medium and the electric double layer on the surface is homogeneous. However, in practice, electrochemical processes of dissolution of metal from the surfaces of complicated geometry (technological and structural stress concentrators, cracks, mechanical defects, etc.) are more widespread. It is known [1] that the complicated form of the surface results in the inhomogeneity of the structure of the electric double layer and, hence, heterogeneity of its energy state. This leads to the appearance of localized centers with increased energy on the surface, which significantly decrease the energy barrier of electrochemical dissolution of the metal. As a result, significant acceleration of the process can be observed, which is not typical of a smooth open surface. Here, the type and sequence (stagewise behavior) of the electrochemical reactions that des...