Abstract
The evolution of hydrogen from 347 stainless steel has been studied by using a real time dynamic technique under ultrahigh vacuum conditions. Auger electron spectroscopy was used to determine the surface composition as a function of time and temperature. The surface film on the electropolished samples was found to be approximately 15 Å thick and consisted of a carbon-oxygen complex and a metal oxide(Fe x0y . Upon heating to 400 °C, the carbon-oxygen complex desorbed as CO and the remaining oxygen and carbon began to incorporate. Also at this temperature sulfur began to diffuse out of the bulk to the surface and at approximately 800 °C formed a complete monolayer. At 900 °C, carbon and oxygen virtually disappeared, leaving the monolayer of sulfur as the only surface contaminant. The hydrogen diffusivity was found to follow closely the equationD = 7.01 × 10-7 exp[-48.0/RT] m2 per second over the entire temperature range studied, thus indicating that hydrogen evolution is not significantly affected by the changing surface composition. The somewhat higher value of the diffusivity obtained in this work compared to past measurements in austenitic stainless steels may indicate the importance of sample preprocessing and ultrahigh vacuum conditions in minimizing the effects of surface layers.
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Outlaw, R.A., Peterson, D.T. The diffusivity of hydrogen in Nb stabilized stainless steel. Metall Trans A 14, 1869–1874 (1983). https://doi.org/10.1007/BF02645557
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DOI: https://doi.org/10.1007/BF02645557