Assessing the kinetics of high temperature oxidation of Inconel 617 in a dedicated HTR impure helium facility coupling thermogravimetry and gas phase chromatography
- 1. Ecole Nationale Supérieure des Mines, SMS-EMSE, CNRS: UMR5146, LCG, 158 Cours Fauriel, 42023 Saint Etienne (France)
- 2. AREVA NP, Centre Technique, Département Corrosion-Chimie, 30 Bd de l'industrie, 71200 Le Creusot (France)
- 3. CEA, DEN, DPC, SCCME, Laboratoire d'Etude de la Corrosion Non Aqueuse, 91191 Gif sur Yvette (France)
- 4. ACXCOR, 63, chemin de l'Arnica, 42660 Le Bessat (France)
- 5. Ecole Nationale Supérieure des Mines, SPIN-EMSE, CNRS: UMR5148, LCG, 158 Cours Fauriel, 42023 Saint Etienne (France)
Description
Graphical abstract: Display Omitted -- Highlights: •New facility coupling thermogravimetry (TGA) with gas phase chromatography (GPC). •Dedicated for HT oxidation study in VHTR impure helium containing CO, H2O and H2. •The oxidation kinetics obeys a complete parabolic law due to a mixed kinetic regime. •CO contributes during initial stage of oxidation only for very low H2O partial pressure. •Long-term oxidation of Inconel 617 by H2O is diffusion controlled with constant kp. -- Abstract: A new facility coupling thermogravimetric analysis (TGA) with gas phase chromatography (GPC) has been developed. This facility is dedicated for studying high temperature oxidation of Inconel 617 in impure helium environment containing H2O, H2 and CO at very low partial pressures (in the Pa range), which is representative of the high temperature reactor (HTR) concept developed within the Generation IV Forum. Simultaneous acquisition of mass gain and gas composition has allowed the influence of carbon monoxide and water vapour on the kinetics of oxidation to be studied. GPC measurements of gas consumption have allowed the plotting of individual mass gain curves for oxidation by H2O and CO. During isothermal exposure at 1123 K for 20 h, the oxidation was mainly due to water vapour with a minor contribution of carbon monoxide during the first hours. The contribution of water vapour to the oxidation kinetics was extracted. It was shown to obey a complete parabolic law and to be limited by an interfacial reaction during the first few hours of oxidation and to be controlled by a mixed interfacial and diffusion process, diffusion becoming the rate-determining step for long term oxidation. There was very good agreement between GPC measurements and the experimental TGA results
Availability note (English)
Available from http://dx.doi.org/10.1016/j.jnucmat.2013.06.012Additional details
Identifiers
- DOI
- 10.1016/j.jnucmat.2013.06.012;
- PII
- S0022-3115(13)00835-0;
Publishing Information
- Journal Title
- Journal of Nuclear Materials
- Journal Volume
- 441
- Journal Issue
- 1-3
- Journal Page Range
- p. 293-300
- ISSN
- 0022-3115
- CODEN
- JNUMAM
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 45093831
- Subject category
- S36: MATERIALS SCIENCE;
- Descriptors DEI
- CARBON MONOXIDE; COUPLING; DIFFUSION; HELIUM; INCONEL 617; KINETICS; OXIDATION; PARTIAL PRESSURE; THERMAL GRAVIMETRIC ANALYSIS; WATER VAPOR
- Descriptors DEC
- ALLOY-NI54CR22CO13MO9; ALLOYS; ALUMINIUM ADDITIONS; ALUMINIUM ALLOYS; CARBON COMPOUNDS; CARBON OXIDES; CHALCOGENIDES; CHEMICAL ANALYSIS; CHEMICAL REACTIONS; CHROMIUM ALLOYS; COBALT ALLOYS; CORROSION RESISTANT ALLOYS; ELEMENTS; FLUIDS; GASES; GRAVIMETRIC ANALYSIS; HEAT RESISTANT MATERIALS; HEAT RESISTING ALLOYS; INCONEL ALLOYS; MATERIALS; MOLYBDENUM ALLOYS; NICKEL ALLOYS; NICKEL BASE ALLOYS; NONMETALS; OXIDES; OXYGEN COMPOUNDS; PHYSICAL PROPERTIES; QUANTITATIVE CHEMICAL ANALYSIS; RARE GASES; THERMAL ANALYSIS; THERMODYNAMIC PROPERTIES; TRANSITION ELEMENT ALLOYS; VAPORS
Optional Information
- Copyright
- Copyright (c) 2013 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.