Published August 2024, Pg. 45-52

Section: Еcology and industrial safety

UOT: 621.7-4

DOI: 10.37474/0365-8554/2024-08-45-52

Hydrogen diffusion and hydrogen embrittlement in iron (steel)

M.M. Asadov Dr. in Ch. Sc. - Institute of Catalysis and Inorganic Chemistry

This article examines the diffusion of hydrogen (H-diffusion) and the temperature dependences of the diffusion coefficient of hydrogen (DH) in the metal (M)-hydrogen system. The metal used was iron and low-alloy steel. Taking into account experimental data on hydrogen diffusion in the Fe-H and steel-H systems, the main diffusion parameters were calculated and compared. It is shown that the temperature dependences of the hydrogen diffusion coefficient in metal samples in a one-stage reaction under isothermal conditions are described by the Arrhenius equation. For some M-H systems, experimental data show a deviation of the diffusion coefficient from the ideal one calculated using the Arrhenius equation. This discrepancy can be eliminated using the statistical theory of absolute reaction rates. For the temperature range 25–1250 oС, the pre-exponential coefficient and activation energy of hydrogen diffusion in a body-centered cubic (bcc) lattice of iron (α–Fe) were calculated using the Arrhenius equation. These parameters make it possible to describe the dependence of the rate of hydrogen diffusion in a metal on temperature and to predict the behavior of hydrogen diffusion when changing the conditions of the kinetic process (concentration of substances, pressure, structure, composition, etc.). Tabular values of the calculated pre-exponential factor and activation energy of hydrogen diffusion in previously studied iron-based samples are presented. The temperature dependences of the hydrogen diffusion coefficient in a lattice of iron α–Fe can be divided into low-temperature and high-temperature regions. The calculated diffusion parameters of hydrogen in the metal lattice for the low-temperature 25–
800 oC and high-temperature 800–1250 oC regions differ markedly from each other. In addition, these calculated values are significantly influenced by the structure and composition of the metal. We also studied the diffusion of hydrogen in α-iron using ab initio density functional calculations. Molecular dynamics calculations using transition state theory were used. The calculated diffusion coefficient of hydrogen in α-Fe is consistent with previously obtained experimental data. Hydrogen embrittlement (HE) is considered using internal pressure, hydrogen enhanced localized plasticity (HELP) and hydrogen enhanced decohesion embrittlement (HEDE) theories.

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