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Sökning: WFRF:(Svensson Jesper) > Persdotter Amanda 1987

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1.
  • Eklund, Johan, 1991, et al. (författare)
  • The influence of silicon on the corrosion properties of FeCrAl model alloys in oxidizing environments at 600 °C
  • 2018
  • Ingår i: Corrosion Science. - : Elsevier BV. - 0010-938X. ; 144, s. 266-276
  • Tidskriftsartikel (refereegranskat)abstract
    • The present study investigates the influence of Si on the high temperature corrosion behaviour of FeCrAl model alloys in O2, O2+H2O and O2+H2O + KCl at 600 °C for up to 168 h. The investigation by SEM/EDX showed that all alloys displayed a protective behaviour in dry O2. In the more corrosive environments (O2+H2O and O2+H2O + KCl) the addition of Si affected the oxidation properties in two ways; Alloys containing Si resisted breakaway oxidation caused by Cr-evaporation (O2+H2O) and the thickness of the oxide formed after breakaway oxidation decreased with increasing amount of Si (O2+H2O + KCl).
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2.
  • Larsson, Erik, 1983, et al. (författare)
  • The Influence of KCl and HCl on the High-Temperature Oxidation of a Fe-2.25Cr-1Mo Steel at 400 °C
  • 2020
  • Ingår i: Oxidation of Metals. - : Springer Science and Business Media LLC. - 1573-4889 .- 0030-770X. ; 93:1-2, s. 29-52
  • Tidskriftsartikel (refereegranskat)abstract
    • The influence of alkali- and chlorine-containing compounds on the corrosion of superheater alloys has been studied extensively. The current paper instead investigates the corrosive effects of KCl and HCl under conditions relevant to waterwall conditions. A low-alloy (Fe-2.25Cr-1Mo) steel was exposed to KCl(s), 500 vppm HCl(g) and (KCl + HCl) in the presence of 5%O2 and 20% H2O at 400 °C. The results indicate that alloy chlorination by KCl occurs by an electrochemical process, involving cathodic formation of chemisorbed KOH on the scale surface and anodic formation of solid FeCl2 at the bottom of the scale. The process is accompanied by extensive cracking and delamination of the iron oxide scale, resulting in a complex, convoluted scale morphology. Adding 500 vppm HCl to the experimental environment (KCl + HCl) initially greatly accelerated the formation of FeCl2 at the scale/alloy interface. The accelerated alloy chlorination is attributed to HCl reacting with KOH at the scale surface, causing the cathodic process to be depolarized. A rapid slowing down of the rate of chlorination and corrosion in KCl + HCl environment was observed which was attributed to the electronically insulating nature of the FeCl2 layer which forms at the bottom of the scale, disconnecting the anodic and cathodic regions.
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3.
  • Olivas Ogaz, Mercedes Andrea, 1985, et al. (författare)
  • The Influence of Oxide-Scale Microstructure on KCl(s)-Induced Corrosion of Low-Alloyed Steel at 400 °C
  • 2019
  • Ingår i: Oxidation of Metals. - : Springer Science and Business Media LLC. - 1573-4889 .- 0030-770X. ; 91:3-4, s. 291-310
  • Tidskriftsartikel (refereegranskat)abstract
    • The high-temperature corrosion of low-alloyed steels and stainless steels in the presence of KCl(s) has been studied extensively in the last decades by several authors. The effect of KCl(s) on the initial corrosion attack has retained extra focus. However, the mechanisms behind the long-term behavior, e.g., when an oxide scale has already formed, in the presence of KCl(s) are still unclear. The aim of this study was to investigate the effect of the microstructure of a pre-formed oxide scale on low-alloyed steel (Fe–2.25Cr–1Mo) when exposed to small amounts of KCl(s). The pre-oxidation exposures were performed at different temperatures and durations in order to create oxide scales with different microstructures but with similar thicknesses. After detailed characterization, the pre-oxidized samples were exposed to 5%O2 + 20%H2O + 75%N2 (+KCl(s)) at 400 °C for 24, 48, and 168 h and analyzed with scanning electron microscopy, energy-dispersive X-ray spectroscopy, X-ray diffraction, and focused ion beam. The microstructural investigation indicated that Cl-induced corrosion is a combination of oxide thickness and microstructure, and the breakaway mechanism in the presence of KCl(s) is diffusion-controlled as porosity changes prior to breakaway oxidation were observed.
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