Abstract

The role of hydrogen in the formation behavior of various lattice defects induced by plastic strain in pure iron specimens has been investigated using low-temperature thermal desorption spectroscopy (L-TDS), which can start measurement from −200 °C. Specimens were subjected to various plastic strains within a uniform elongation range in the absence and presence of hydrogen. Strain-induced lattice defects were quantitatively evaluated using L-TDS for specimens saturated with hydrogen as a probe for detecting lattice defects, not only vacancies but also dislocation cores. The L-TDS spectra contained two hydrogen desorption peaks: a low-temperature peak associated with dislocations and a high-temperature peak associated with vacancies. The tracer hydrogen content corresponding to each peak increased with plastic strain. However, when compared at the same plastic strain of 25%, the low-temperature peak, i.e., dislocations, was not enhanced by hydrogen, whereas the high-temperature peak, i.e., vacancies, was enhanced by hydrogen, increasing by about six times at 25% plastic strain and by seven times at 40% plastic strain. Analyses conducted by electron channeling contrast imaging (ECCI) and electron backscattered diffraction (EBSD) revealed that strain was localized along the vicinity of the ferrite grain boundaries at 25% plastic strain in the presence of hydrogen. Hence, the role of hydrogen in the formation behavior of plastic strain-induced lattice defects is presumably to enhance vacancy formation and the localization of the dislocation configuration near the grain boundaries without affecting the amount of dislocations formed.

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