The evolution of H from the stainless steel was studied by using a real-time dynamic technique under ultra-high vacuum conditions. Auger electron spectroscopy was used to determine the surface composition as a function of time and temperature. It was found that the surface film on the electropolished samples was approximately 1.5nm thick, and consisted of a C-O complex and FexOy. Upon heating to 400C, the C-O complexes desorbed as CO and the remaining O and C began to be incorporated. At this temperature, S also began to diffuse out of the bulk and towards the surface. At about 800C, it formed a complete monolayer. At 900C, the C and O almost disappeared; leaving a S monolayer as the only surface contaminant. The H diffusivity was found to be described by the expression:
D (m2/s) = 7.01 x 10-7 exp[-48.0/RT]
over the entire temperature range which was studied (figure 10). This suggested that H evolution was not appreciably affected by the changing surface composition.
The Diffusivity of Hydrogen in Nb Stabilized Stainless Steel. R.A.Outlaw, D.T.Peterson: Metallurgical Transactions A, 1983, 14[9], 1869-74
Table 68
Permeation of H in Deformed A508 Steel
Domain | Stress (MPa) | Strain (%) | Permeation | Permeabilitya |
elastic | 0 | - | first | 6.3 x 10-5 |
elastic | 0 | - | second | 8.5 x 10-5 |
elastic | 200 | - | first | 5.5 x 10-5 |
elastic | 200 | - | second | 7.3 x 10-5 |
elastic | 400 | - | first | 6.8 x 10-5 |
elastic | 400 | - | second | 8.9 x 10-5 |
plastic | - | 1 | first | 6.9 x 10-5 |
plastic | - | 1 | second | 1.1 x 10-4 |
plastic | - | 2 | first | 5.6 x 10-5 |
plastic | - | 2 | second | 9.8 x 10-5 |
a: ppm mm2/s