Abstract

Constituents of syngas, such as water, carbon monoxide and sulfides, can cause the degradation of the steel pipes they move through, leading to carbon dusting and corrosion. In spite of considerable attention to this process, many questions remain about its origin. We conduct reactive molecular dynamics simulations of multi-grain iron systems exposed to carburizing gas mixtures to investigate the effect of water content on metal dusting corrosion. To simulate carbon monoxide (CO) dissociation followed by carbon diffusion, we employ an extended-ReaxFF potential that allows accounting for both the high C atoms coordination in bulk iron as well as the lower C coordination at the iron surface and interfaces. The reactions happening in the sample at different water concentrations and at different time frames are explored. We demonstrate that the presence of water on a clean Fe surface promotes different catalytic reactions at the beginning of the simulations that boost the C, H, O diffusion into the sample. At later stage, the formation of oxide scale leads to an elevated concentration of H2O/OH molecules on the surface due to the decrease in Fe affinity to dissociate water. This results into blocking the Fe catalytic sites leading to lower C and O diffusion to the bulk of the sample.

Highlights

  • Water and varying amounts of carbon monoxide and sulfides are among the constituents of syngas that affect the integrity of mild steel pipes as it flows through them [1]

  • We examine the effect of varying water concentration at the early stages of iron corrosion by analyzing the molecular dynamics (MD) results

  • How­ ever, we observe weak effect of concentration on carbon diffusion: the MD fluctuations associated with each run are larger than the difference of the C having diffused for water concentration of 3%, 9% and 15%

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Summary

Introduction

Water and varying amounts of carbon monoxide and sulfides are among the constituents of syngas that affect the integrity of mild steel pipes as it flows through them [1]. Shaoli et al studied the coverage dependent of H2O, OH, O, and H adsorption and dissociation and showed that the H2O dissociation bar­ rier can go as low as 0.32 eV for the Fe(1 1 1) surface with 4O + H2O(s) + 4H2(g) + 4H2O(g) system for example, proving that the practically complex chemical reactions could drastically change the barriers on Fe surface [9] Despite these insights from DFT simulations, especially regarding the very early stages reactions leading to metal dusting corrosion, their high computational costs have limited their application to the more relevant time and length scales. These limitations make it difficult to observe the effect of competing dissociation mechanisms due to mutually adsorbed syngas molecules on iron surface at high tem­ perature. An effect that has not and could not be treated correctly by ReaxFF due to the limitations of the earlier versions [14]

Computational details
Results and discussion
Atom diffusion
Charge map
Full Text
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