Abstract

While hydrogen pipelines have attracted increased attention, safety of the pipelines has been a concern in terms of hydrogen embrittlement (HE) occurring upon hydrogen atom (H) generation and permeation in the steels. In this work, thermodynamic analyses regarding H generation and adsorption on pipeline steels by two potential mechanisms, i.e., spontaneous dissociation and dissociative adsorption, were conducted through theoretical calculations based on Gibbs free energy change of the H generation reactions. Moreover, H adsorption free energy and configurations were determined based on density functional theory (DFT) calculations. Effects of H adsorption site, H coverage and hydrostatic stress on H adsorption and absorption were discussed. Spontaneous dissociation of hydrogen gas molecules to generate hydrogen atoms is thermodynamically impossible. Dissociative adsorption is thermodynamically feasible at wide temperature and pressure ranges. Particularly, an increased hydrogen gas partial pressure and elevated temperature favor the dissociative adsorption of hydrogen. Hydrogen atoms generated by dissociative adsorption mechanism can adsorb stably at On-Top (OT) and 2-fold (2F) Cross-Bridge sites of Fe (100), while hydrogen adsorption at 2F site is more stable due to a higher electron density and a stronger electronic hybridization between Fe and H. The influence of H atom coverage on dissociative adsorption occurs at low coverages only, i.e., 0.25–1.00 ML as determined in this work. External stresses make dissociative adsorption more difficult to occur compared with a fully relaxed steel. Both tetrahedral sites (TS) and octahedral sites (OS) can potentially host absorbed H atoms at subsurface of the steel. Absorbed H atoms will be predominantly trapped at TS due to a low energy path and exothermic feature. Diffusion of H atoms from steel surface to the subsurface is more difficult compared with the dissociative adsorption.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call