Deuterium retention in tungsten irradiated by high-dose neutrons at high temperature
Creators
- 1. Faculty of Engineering Sciences, Kyushu University, Kasuga 8168580 (Japan)
- 2. Fusion Safety Program, Idaho National Laboratory, Idaho Falls ID83415 (United States)
- 3. National Institute for Fusion Science, Toki 5095202 (Japan)
- 4. Graduate School of Engineering, Hokkaido University, Sapporo 0600808 (Japan)
- 5. College of Science, Academic Institute, Shizuoka University, Shizuoka 422-8529 (Japan)
- 6. Graduate School of Engineering, Osaka University, 2-1 Suita, Osaka 565-0871 (Japan)
- 7. Hydrogen Isotope Research Center, University of Toyama, Toyama 9308555 (Japan)
Description
Highlights: • D retention in W irradiated by high-dose neutrons at high temp. were investigated. • Neutron irradiation temperature affected D retentions; 894 > 1074 ≈ 1379 K. • TDS and D implantation simulation were performed to estimate retention properties. • Detrapping energy, depth and D/W were estimated. We investigated deuterium (D) retention in three W samples irradiated with MeV neutrons at high damage level of 0.39 ~ 0.74 displacements per atom (dpa) at high temperatures, 894 K, 1074 K and 1379 K. The W specimens were exposed to high-flux (~1 × 1022 m−2 s−1) and high-fluence (~5 × 1025 m−2) D plasma at 873 K in the Tritium Plasma Experiment. Broad desorption peaks extended from 900 K to 1200 K were observed for the neutron-irradiated W by thermal desorption spectroscopy (TDS). The retention in neutron-irradiated specimens was much larger than for an un-irradiated specimen. The highest D retention was obtained for a specimen irradiated at 894 K. With increasing neutron irradiation temperature, the retention was reduced about by half at 1074 K and further increase of the temperature (1379 K) resulted in comparable retention. In addition, one-dimensional diffusion calculations (D desorption in TDS and D depth distribution in plasma exposure) were performed to derive retention parameters (the detrapping energy, the depth occupied by D atoms and D/W ratio) from experimental D retention properties of neutron-irradiated W. By TDS simulation calculation, simple dependences of the peak temperature, height and width of TDS peaks on the retention parameters were obtained with total retention in the orders of 1019 ~ 1022 m−2. The calculation of the depth distribution of trapped D atoms made a relationship between the D/W ratio and the depth occupied by D atoms after plasma exposure at relevant conditions. By comparing the relationship (the D/W and the depth) with that obtained from the experimental results, we estimate each retention parameters for the specimens irradiated by high-dose neutrons at the high temperatures. And, we discussed the neutron-irradiation temperature dependence of D retentions.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.nme.2021.100980Additional details
Identifiers
- DOI
- 10.1016/j.nme.2021.100980;
- PII
- S2352179121000636;
Publishing Information
- Journal Title
- Nuclear Materials and Energy
- Journal Volume
- 27
- Journal Page Range
- vp.
- ISSN
- 2352-1791
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 54013063
- Subject category
- S73: NUCLEAR PHYSICS AND RADIATION PHYSICS; S36: MATERIALS SCIENCE;
- Descriptors DEI
- ATOMIC DISPLACEMENTS; ATOMS; COMPUTERIZED SIMULATION; DESORPTION; DEUTERIUM; IRRADIATION; NEUTRONS; ONE-DIMENSIONAL CALCULATIONS; PLASMA; RADIATION DOSES; SPATIAL DISTRIBUTION; TEMPERATURE DEPENDENCE; THERMAL DESORPTION SPECTROSCOPY; TRITIUM; TUNGSTEN
- Descriptors DEC
- BARYONS; BETA DECAY RADIOISOTOPES; BETA-MINUS DECAY RADIOISOTOPES; DISTRIBUTION; DOSES; ELEMENTARY PARTICLES; ELEMENTS; FERMIONS; HADRONS; HYDROGEN ISOTOPES; ISOTOPES; LIGHT NUCLEI; METALS; NUCLEI; NUCLEONS; ODD-EVEN NUCLEI; ODD-ODD NUCLEI; PHYSICAL RADIATION EFFECTS; RADIATION EFFECTS; RADIOISOTOPES; REFRACTORY METALS; SIMULATION; SORPTION; SPECTROSCOPY; STABLE ISOTOPES; TRANSITION ELEMENTS; YEARS LIVING RADIOISOTOPES
Optional Information
- Copyright
- Copyright (c) 2021 The Authors. Published by Elsevier Ltd.