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Isotopic investigation of the transport of oxygen species in Y-stabilized zirconia
KTH, Skolan för industriell teknik och management (ITM), Materialvetenskap.
(engelsk)Inngår i: Journal of Chemical Physics, ISSN 0021-9606, E-ISSN 1089-7690Artikkel i tidsskrift (Annet vitenskapelig) Submitted
HSV kategori
Identifikatorer
URN: urn:nbn:se:kth:diva-6094OAI: oai:DiVA.org:kth-6094DiVA, id: diva2:10705
Merknad
QC 20100629Tilgjengelig fra: 2006-09-08 Laget: 2006-09-08 Sist oppdatert: 2017-12-14bibliografisk kontrollert
Inngår i avhandling
1. Modified oxygen and hydrogen transport in Zr-based oxides
Åpne denne publikasjonen i ny fane eller vindu >>Modified oxygen and hydrogen transport in Zr-based oxides
2006 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

Most metals and alloys in the presence of oxygen and moisture will instantaneously react and form a thin (2-5 nm) surface oxide layer. For further reaction to occur, oxygen ions and/or metal cations often diffuse through the already formed oxide layer. The corrosion resistance of a metal in aggressive environments at high temperatures depends on the properties of the surface oxide scale.

Zirconium-based alloys represent the main structural materials used in water-cooled nuclear reactors. For these materials, the formation of a thin, adherent oxide scale with long-term stability in high temperature water/steam under irradiation conditions, is crucial. In this thesis, the transport of oxygen and hydrogen through Zr-based oxide scales at relevant temperatures for the nuclear industry is investigated using isotopic gas mixtures and isotope-monitoring techniques such as Gas Phase Analysis and Secondary Ion Mass Spectrometry.

Porosity development in the oxide scales generates easy diffusion pathways for molecules across the oxide layer during oxidation. A considerable contribution of molecular oxygen to total oxygen transport in zirconia has been observed at temperatures up to 800°C. A novel method for evaluation of the gas diffusion, gas concentration and effective pore size of oxide scales is presented in this thesis. Effective pore sizes in the nanometer range were found for pretransition oxides on Zircaloy-2. A mechanism for densification of oxide scales by obtaining a better balance between inward oxygen and outward metal transport is suggested. Outward Zr transport can be influenced by the presence of hydrogen in the oxide and/or metal substrate. Inward oxygen transport can be promoted by oxygen dissociating elements such as Fe-containing second phase particles. The results suggest furthermore that a proper choice of the second-phase particles composition and size distribution can lead to the formation of dense oxides, which are characterized by low oxygen and hydrogen uptake rates during oxidation.

Hydrogen uptake in Zr-based materials during oxidation in high temperature water/steam can generate degradation due to the formation of brittle hydrides in the metal substrate. A promising method for the suppression of hydrogen uptake has been developed and is presented in this thesis.

sted, utgiver, år, opplag, sider
Stockholm: KTH, 2006. s. 48
Emneord
Zirconia, Zirconium, Zircaloy, hydrogen and oxygen diffusion, SPP, oxygen dissociating elements, oxidation, dissociation, hydration, CO adsorption, molecular transport, porosity.
HSV kategori
Identifikatorer
urn:nbn:se:kth:diva-4095 (URN)91-7178-429-2 (ISBN)
Disputas
2006-09-22, F3, Lindstedtsvägen 26, Stockholm, 10:00
Opponent
Veileder
Merknad
QC 20100629Tilgjengelig fra: 2006-09-08 Laget: 2006-09-08 Sist oppdatert: 2011-10-05bibliografisk kontrollert

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