Deuterium retention in tungsten based materials for fusion applications

•Tungsten alloys were investigated for their deuterium retention at an implantation temperature of 100°C.•The “heavy alloy” HPM 1850 retains similar amounts as pure tungsten.•The self-passivating alloy W10Cr0.5Y retains 10 times more. The tungsten “heavy alloy” HPM 1850, a liquid-phase sintered comp...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Nuclear materials and energy 2019-01, Vol.18, p.245-249
Hauptverfasser: Maier, H., Schwarz-Selinger, T., Neu, R., Garcia-Rosales, C., Balden, M., Calvo, A., Dürbeck, T., Manhard, A., Ordás, N., Silva, T.F.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:•Tungsten alloys were investigated for their deuterium retention at an implantation temperature of 100°C.•The “heavy alloy” HPM 1850 retains similar amounts as pure tungsten.•The self-passivating alloy W10Cr0.5Y retains 10 times more. The tungsten “heavy alloy” HPM 1850, a liquid-phase sintered composite material with two weight percent Ni and one weight percent Fe, as well as the self-passivating tungsten alloy W-10Cr-0.5Y, a high temperature oxidation resistant alloy with 10 weight percent of Cr and 0.5 weight percent of Y, were investigated with respect to their deuterium retention. The samples were deuterium loaded in an electron cyclotron resonance plasma up to a fluence of 1025m−2. The deuterium retention was then investigated by Nuclear Reaction Analysis and by Thermal Desorption. In HPM 1850 the observed deuterium amount was similar to pure tungsten, however the outgassing behaviour during thermal desorption was considerably faster. In W-10Cr-0.5Y the released deuterium amount during thermal desorption was about one order of magnitude higher; by comparison of nuclear reaction analysis and thermal desorption this was attributed to deeper diffusion of deuterium into the bulk of the material.
ISSN:2352-1791
2352-1791
DOI:10.1016/j.nme.2018.12.032