| 1. |
- Bexell, Ulf, et al.
(författare)
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Chromium evaporation from plastically deformed pre-coated Sandvik Sanergy HT 22% Cr ferritic interconnect steel
- 2010
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Ingår i: 2010 Conference Memory Stick 9th European SOFC Forum. - Lucerne.
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Konferensbidrag (övrigt vetenskapligt/konstnärligt)abstract
- Ferritic stainless steel has attracted a great deal of attention for its use as an interconnector in solid oxide fuel cells (SOFCs). The ferritic Sandvik Sanergy HT chromium steel is specially developed for interconnectors in SOFC with a unique chemical composition, which gives the alloy a good high temperature corrosion resistance as well as good surface conductivity in the formed chromium oxide scale. However, chromium evaporation from metallic interconnectors in SOFC fuel cells tends to poison the cathode of the fuel cell. Furthermore, the evaporation of chromium species from the oxide surface tends to increase the oxidation rate resulting in increased contact resistance. It is nowadays well known that thin coatings of e.g. cobalt can substantially reduce the chromium evaporation from the interconnectors. In this study, a 22% Cr ferritic steel, Sandvik Sanergy HT has been coated with a thin metallic cobalt film. The coated material was plastically deformed and the effect of chromium evaporation was studied as a function of the degree of deformation. Coated samples are also compared to uncoated material. The results show that the metallic cobalt film cracks when the steel sheet is formed but the chromium evaporation is more or less unaffected.
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| 2. |
- Canovic, Sead, et al.
(författare)
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Microstructural investigation of the initial oxidation of the FeCrAlRE alloy Kanthal AF in dry and wet O2 at 600 and 800°C
- 2010
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Ingår i: Journal of the Electrochemical Society. - : The electrochemical society. - 0013-4651 .- 1945-7111. ; 157:6, s. C223-C230
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Tidskriftsartikel (refereegranskat)abstract
- The FeCrAlRE (where RE is reactive element) alloy Kanthal AF was exposed isothermally at 600 and 800°C for 72 h in dry O2 and in O2 with 10 vol % H2O. The mass gains were 3–5 times higher at the higher temperature. The presence of water vapor increased the oxidation rate at 800°C, while no significant effect was observed at 600°C. A thin two-layered oxide formed at 600°C: an outer (Fe,Cr)2O3 corundum-type oxide, containing some Al, and an inner, probably amorphous, Al-rich oxide. At 800°C a two-layered oxide formed in both environments. The inner layer consisted of inward grown a-Al2O3. In dry O2 the originally formed outward grown g-Al2O3 had transformed to a-Al2O3 after 72 h. Water vapor stabilized the outward grown g-Al2O3 and hence no transformation occurred after 72 h in humid environment. RE-rich oxide particles with varying composition (Y, Zr, and Ti) were distributed in the base oxide at both temperatures and in both environments. The RE-rich particles were separated from the alloy substrate by a layer of Al-rich oxide. At 800°C the Y-rich RE particles were surrounded by thick oxide patches in both dry and humid O2.
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| 3. |
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| 4. |
- Engkvist, Josefin, 1972, et al.
(författare)
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Alumina scale formation on a powder metallurgical FeCrAl alloy (Kanthal APMT) at 900-1100°C in dry O2 and in O2 + H2O
- 2010
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Ingår i: Oxidation of Metals. - : Springer Science and Business Media LLC. - 1573-4889 .- 0030-770X. ; 73:1, s. 233-253
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Tidskriftsartikel (refereegranskat)abstract
- A Rapidly Solidified Powder (RSP) metallurgical FeCrAl alloy, Kanthal APMT, was exposed in dry and humid O-2 for 72 h at 900-1,100 A degrees C. The formed oxide scales were characterized using gravimetry in combination with advanced analysis techniques (SEM, EDX, TEM, XRD, AES and SIMS). The oxide scales were at all exposures composed of two-layered alpha-Al2O3 scales exhibiting a top layer of equiaxed grains and a bottom layer containing elongated grains. A Cr-rich zone, originating in the native oxide present before exposure, separated these two layers. The top alpha-Al2O3 layer is suggested to have formed by transformation of outwardly grown metastable alumina, while the inward-grown bottom alpha-Al2O3 layer had incorporated small Zr-, Hf- and Ti-rich oxide particles present in the alloy matrix. The scale also contained larger Y-rich oxide particles. Furthermore, in the temperature range studied, the presence of water vapour accelerated alloy oxidation somewhat and affected scale morphology.
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| 5. |
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| 6. |
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| 7. |
- Engkvist, Josefin, 1972, et al.
(författare)
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Oxidation of FeCrAl foils at 500-900 degrees C in dry O-2 and O-2 with 40% H2O
- 2009
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Ingår i: Materials at High Temperatures. - 0960-3409 .- 1878-6413. ; 26:2, s. 199-210
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Tidskriftsartikel (refereegranskat)abstract
- High temperature resistant FeCrAl alloys are frequently used in high temperature applications Such as heating elements and metal based catalytic converter bodies. When exposed to high temperatures an adherent, slowly growing, dense aluminium oxide layer forms on the surface, which protects the underlying alloy from severe degradation. The composition, structure and properties of the formed oxide layer are strongly dependent on the alloy composition, temperature and oxidation environment. In this study, the Sandvik 0C404 FeCrAl alloy, in the form of 50 mu m thick foils, was exposed isothermally in the temperature range 500-900 degrees C for 168 hours in dry O-2 and in O-2 with 40 vol.% H2O. The surface morphology, composition and microstructure of the grown oxide scales were characterized by using scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDX), grazing incidence X-ray diffraction (GI-XRD), Auger electron spectroscopy (AES), and time of flight secondary ion mass spectrometry (TOF-SIMS). The oxidation process was faster at 900 degrees C than at 500 and 700 degrees C. At 500 degrees C a thin (10-20 nm) mixed oxide of Fe, Cr and Al was formed. Exposure at 700 degrees C resulted ill a similar (40-50 nm) duplex oxide, in both dry O-2 and in O-2 With 40 vol.% H2O. These oxide scales consisted of all inner and an outer relatively pure alumina separated by a Cr-rich band. This type of duplex oxide scale also formed at 900 degrees C with a thin inward growing alpha-Al2O3 at the oxide/metal interface and an outward growing layer outside a Cr-rich band. However, at 900 degrees C the Outward growing layer showed two types of oxide morphologies; a thin smooth base oxide and a much thicker nodular oxide grown on top of substrate ridges. In dry O-2 atmosphere, the main part of this outward growing layer had transformed to alpha-Al2O3. Only in the outer part of the thick oxide nodules, metastable alumina was found. When exposed in the presence of water vapour the main pall of the metastable alumina remained untransformed.
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| 8. |
- Hoseini Hooshyar, Hamed, 1986, et al.
(författare)
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The Effect of H-2 and H2O on the Oxidation of 304L-Stainless Steel at 600 A degrees C: General Behaviour (Part I)
- 2016
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Ingår i: Oxidation of Metals. - : Springer Science and Business Media LLC. - 1573-4889 .- 0030-770X. ; 85:3-4, s. 321-342
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Tidskriftsartikel (refereegranskat)abstract
- The effect of p(H2O) and p(H-2) on the oxidation of 304L stainless steel at 600 A degrees C has been investigated in the present study. The samples were analysed by means of X-ray diffraction, Auger spectroscopy, and scanning electron microscopy equipped with energy dispersive spectroscopy. The results showed that at fixed p(H-2), the corrosion rate increased considerably with increasing p(H2O). At fixed p(H2O), the corrosion rate decreased slightly with increasing p(H-2). Duplex oxide scales formed during the exposure in all environments. The outer and inner layer consisted of Fe3O4 and (Fe, Cr)(3)O-4, respectively. The latter was mainly in the form of internal oxidation. The Cr-rich oxide formation was observed at the initial oxidation process before oxide breakdown. The Auger analysis also suggested the presence of Cr-rich oxide layer just after the breakaway oxidation. The results indicated that the rate-determining step in the corrosion attack is surface controlled or diffusion controlled through an oxide layer with fixed thickness over time.
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| 9. |
- Huang, Biying, et al.
(författare)
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Effects of cigarette smoking on cardiovascular-related protein profiles in two community-based cohort studies
- 2016
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Ingår i: Atherosclerosis. - : Elsevier BV. - 0021-9150 .- 1879-1484. ; 254, s. 52-58
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Tidskriftsartikel (refereegranskat)abstract
- Background and aims: Cardiovascular diseases account for the largest fraction of smoking-induced deaths. Studies of smoking in relation to cardiovascular-related protein markers can provide novel insights into the biological effects of smoking. We investigated the associations between cigarette smoking and 80 protein markers known to be related to cardiovascular diseases in two community-based cohorts, the Prospective Study of the Vasculature in Uppsala Seniors (PIVUS, n = 969, 50% women, all aged 70 years) and the Uppsala Longitudinal Study of Adult Men (ULSAM, n = 717, all men aged 77 years). Methods: Smoking status was self-reported and defined as current smoker, former smoker or never-smoker. Levels of the 80 proteins were measured using the proximity extension assay, a novel PCR-based proteomics technique. Results: We found 30 proteins to be significantly associated with current cigarette smoking in PIVUS (FDR<5%); and ten were replicated in ULSAM (p<0.05). Matrix metalloproteinase-12 (MMP-12), growth/differentiation factor 15 (GDF-15), urokinase plasminogen activator surface receptor (uPAR), TNF-related apoptosis-inducing ligand receptor 2 (TRAIL-R2), lectin-like oxidized LDL receptor 1 (LOX-1), hepatocyte growth factor (HGF), matrix metalloproteinase-10 (MMP-10) and matrix metalloproteinase-1 (MMP-1) were positively associated, while endothelial cell-specific molecule 1 (ESM-1) and interleukin-27 subunit alpha (IL27-A) showed inverse associations. All of them remained significant in a subset of individuals without manifest cardiovascular disease. Conclusions: The findings of the present study suggest that cigarette smoking may interfere with several essential parts of the atherosclerosis process, as evidenced by associations with protein markers representing endothelial dysfunction, inflammation, neointimal formation, foam cell formation and plaque instability. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
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| 10. |
- Ingemarsson, Linda, 1972, et al.
(författare)
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Oxidation behavior of a Mo (Si, Al)(2)-based composite at 300-1000 degrees C
- 2010
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Ingår i: Intermetallics. - : Elsevier BV. - 0966-9795 .- 1879-0216. ; 18:4, s. 633-640
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Tidskriftsartikel (refereegranskat)abstract
- The oxidation behavior of a Mo (Si,Al)(2)-based composite of Mo(Si,Al)(2), Al2O3 and Mo-5(Si,Al)(3) (Kanthal Super ER) in synthetic air was investigated. The samples were oxidized isothermally for up to 72 h at 300-1000 degrees C using a thermobalance. The microstructure was analyzed by X-ray diffraction (XRD), Scanning Electron Microscopy (SEM) and Auger Electron Spectroscopy (AES) depth profiling. Broad ion beam milling (BIB) was used to prepare cross-sections. Oxidation behavior depended strongly on the composition of the substrate which consisted of a Mo(Si,Al)(2) matrix and the minority phases Mo-5(Si,Al)(3) and Al2O3. At 300-500 degrees C the mass gains were small with parabolic kinetics, oxidation resulting in a mixture of oxides that reflects the substrate composition. At 600 and 700 degrees C the oxide scale is thin and protective and depleted in molybdenum, a mass loss occurring due to MoO3 vaporization. At 1000 degrees C a protective alpha-alumina scale forms.
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