Analysis of partially pulsating fatigue process on carbon steel with microstructural observation

• Published in: Materials science & engineering. A, Structural materials : properties, microstructure and processing Structural materials : properties, microstructure and processing, 2016-01, Vol.651, p.83-88
• Main Authors: Shimano, Hiroyuki, Faiz, M. Khairi, Hara, Asato, Yoshizumi, Kyoko, Yoshida, Makoto, Horibe, Susumu
• Format: Article
• Language: English
• Subjects: Carbon steel; Carbon steels; Dislocations; Fatigue; Fatigue (materials); Fatigue failure; Medium carbon steels; Plastic deformation; Plastic strain amplitude; Ratcheting; Ratcheting strain rate; Serrated yielding; Strain rate; TEM
• ISSN: 0921-5093; 1873-4936
• DOI: 10.1016/j.msea.2015.10.103

Pulsating low-cycle fatigue processes, up to the present, have been divided into three states: the transient state, steady state, and accelerating state of ratcheting. In our previous work, we suggested that fatigue behavior of pulsating fatigue process should be classified into five stages in which the plastic strain amplitude and the ratcheting strain rate are plotted on the X and Y axis, respectively. In this study, at the condition of R=−0.3 (partially pulsating fatigue), the change in the plastic strain amplitude and ratcheting strain rate for each cycle to failure was examined on AISI 1025 carbon steel. The dislocation substructure was examined using transmission electron microscopy (TEM) for each stage, except for stage I. It was also demonstrated that the fatigue process can be divided into five stages: stage I corresponds to the un-pinning of dislocations from the Cottrell atmosphere and propagation of the Luders band. Stage II corresponds to the restriction of dislocation movement by dislocation tangles. Stage III corresponds to the formation of dislocation cells. Stage IV corresponds to the promotion of the to-and-fro (back-and-forth) motion of dislocations by a re-arrangement of the dislocations in the cells. Stage V corresponds to the release of dislocation movement by the collapse of dislocation cells.