2000
DOI: 10.1002/(sici)1521-4176(200005)51:5<329::aid-maco329>3.0.co;2-k
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Compositions at Al2O3/FeCrAl interfaces after high temperature oxidation

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Cited by 35 publications
(17 citation statements)
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References 23 publications
(41 reference statements)
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“…Although sulfur was found to be the major segregant at these scale/alloy interfaces, the segregation behavior, in terms of rate and amount, varied significantly with different alloys and differed from surface segregation. For example, at the Ah03/FeCrAI interface, cosegregation of Cr with S took place, which gave rise to greater than one monolayer of S. The amount saturated as early as 12 minutes at 1000°C, where the rate was determined by S diffusion in the alloy [5,7,8]. For the iron aluminides, S was the sole segregant at these scale/alloy interfaces, but its steady state level was slowly reached only after a complete a-…”
Section: Introductionmentioning
confidence: 57%
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“…Although sulfur was found to be the major segregant at these scale/alloy interfaces, the segregation behavior, in terms of rate and amount, varied significantly with different alloys and differed from surface segregation. For example, at the Ah03/FeCrAI interface, cosegregation of Cr with S took place, which gave rise to greater than one monolayer of S. The amount saturated as early as 12 minutes at 1000°C, where the rate was determined by S diffusion in the alloy [5,7,8]. For the iron aluminides, S was the sole segregant at these scale/alloy interfaces, but its steady state level was slowly reached only after a complete a-…”
Section: Introductionmentioning
confidence: 57%
“…The segregation of indigenous sulfur impurity from an alloy to the Ah03 scale/alloy interface during high temperature oxidation is often considered the major cause that weakens the interface [1][2][3][4]' Systematic studies of the chemical changes at Ah03/alloy interfaces as a function of oxidation time have in recent years been carried out for FeCrAI [5], Fe3AI and FeAI [6,7], where the alloys normally contain about 20 ppm of sulfur. Although sulfur was found to be the major segregant at these scale/alloy interfaces, the segregation behavior, in terms of rate and amount, varied significantly with different alloys and differed from surface segregation.…”
Section: Introductionmentioning
confidence: 99%
“…The segregation of sulfur to growing oxide/metal interfaces has been studied using conventional Auger electron microscopy (AES) with a typical probe size of about 1µm 15,16,61,62 , and with field emission AES of probe sizes ~30nm 63 . The chemical composition of the alloy surface was examined after spalling the oxide scale in ultra high vacuum (UHV) by scratching an oxidized specimen surface 61,64 .…”
Section: Sulfurmentioning
confidence: 99%
“…Other than sulfur, there were also excess carbon and chromium at the interface. The carbon segregated during cooling and the Cr co-segregated with sulfur 15,65 . This co-segregation caused excess sulfur to be present at the interface, giving rise to the high concentration that amounts to ~2 monolayers, where a monolayer is defined as one physical layer on the alloy surface.…”
Section: Sulfurmentioning
confidence: 99%
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