Thermal desorption of CO and H2 from degassed 304 and 347 stainless steel
Author(s) -
Shokrollah Rezaie-Serej,
R. A. Outlaw
Publication year - 1994
Publication title -
journal of vacuum science and technology a vacuum surfaces and films
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.583
H-Index - 112
eISSN - 1520-8559
pISSN - 0734-2101
DOI - 10.1116/1.578949
Subject(s) - desorption , analytical chemistry (journal) , auger electron spectroscopy , thermal desorption , activation energy , thermal desorption spectroscopy , atmospheric temperature range , chemistry , hydrogen , diffusion , auger , spectroscopy , materials science , adsorption , atomic physics , thermodynamics , chromatography , quantum mechanics , physics , organic chemistry , nuclear physics
Thermal desorption spectroscopy (TDS), along with Auger electron spectroscopy, was used to study the desorption of H2 and CO from baked 304 and 347 stainless‐steel samples exposed only to residual gases. Both 347 and 304 samples gave identical TDS spectra. The spectra for CO contained a sharp leading peak centered in the temperature range 410–440 °C and an exponentially increasing part for temperatures higher than 500 °C, with a small peak around 600 °C appearing as a shoulder. The leading peak followed a second‐order desorption behavior with an activation energy of 28±2 kcal/mol, suggesting that the rate‐limiting step for this peak is most likely a surface reaction that produces the CO molecules in the surface layer. The amount of desorbed CO corresponding to this peak was ∼0.5×1014 molecules/cm2. The exponentially rising part of the CO spectrum appeared to originate from a bulk diffusion process. The TDS spectrum for H2 consisted of a main peak centered also in the temperature range 410–440 °C, with two...
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