Microstructure change and deuterium permeation behavior of ceramic-metal multi-layer coatings after immersion in liquid lithium-lead alloy

For the establishment of liquid tritium breeding concepts, static lithium-lead corrosion tests for single-layer erbium oxide coatings and erbium oxide-metal multi-layer coatings were carried out, followed by deuterium permeation measurements. Grain boundary corrosion of erbium oxide coatings was confirmed by the static immersion tests at 550 and 600 °C. An erbium oxide-iron two-layer coating sustained its structure after lithium-lead immersion at 600 °C for up to 3000 h. The results of gas-driven deuterium permeation measurements for multi-layer coatings immersed at 550 and 600 °C indicated that crystallization and grain growth of erbium oxide would sufficiently occur during the immersion at 600 °C, and then the sample showed lower permeabilities in the first measurements at lower temperature. On the other hand, permeation reduction factors of the sample immersed at 550 °C were estimated to be 100‒200 in the temperature range of 400‒550 °C. A corrosion layer formed on the coating surface might work as an additional diffusion barrier after the permeation test at 600 °C. Keywords: Lithium-lead, Tritium permeation barrier, Corrosion, Erbium oxid

Deuterium permeation through multi-layer ceramic coatings under liquid lithium-lead exposure condition

autho

The effect of γ-ray irradiation on deuterium permeation through reduced activation ferritic steel and erbium oxide coating

Deuterium permeation through a fusion-relevant ferritic steel F82H with and without erbium oxide coatings under γ-ray irradiation has been investigated in a temperature range from 300 to 700 °C. The deuterium permeation flux through F82H sample increased by γ-ray irradiation at lower temperatures below 450 °C. The irradiation effect increased with dose rate, and the percentage of the permeation flux gain might be several percent under the dose rate of a few Gy s‒1. Temperature of the F82H sample surface rose by about 0.5 °C depending on the dose rate, and so the γ-ray irradiation effect is mainly attributed to γ-heating. On the other hand, at higher temperature above 500 °C, no appreciable change of the deuterium permeation was observed. Similarly, the deuterium permeation flux through erbium oxide coated samples increased under γ-ray irradiation at lower temperatures (350‒450 °C), but no appreciable change of permeation flux through coatings was observed at higher temperatures (600‒700 °C). The coating surface temperature increased at lower sample temperatures by γ-heating. Keywords: Tritium, Permeation, γ-ray, Irradiation, F82H, Erbium oxid

Surface oxidation effect on deuterium permeation in reduced activation ferritic/martensitic steel F82H for DEMO application

Fuel loss and environmental contamination by tritium permeation through structural materials are critical issuesfor the establishment of a fusion DEMO reactor. In this study, the effectivity of a chromium oxide layer formedon reduced activation ferritic/martensitic steel F82H as a tritium permeation barrier and its stability undersimulated solid/liquid breeder blanket conditions have been investigated. A uniform 100-nm-thick chromiumoxide layer was formed by heat treatment at 710 °C for 5 min in 50% argon-50% hydrogen mixed gas with theflow rate of 200 standard cubic centimeter per minute. After exposure to simulated solid breeder blanket con-ditions, an iron oxide layer and a spinel-type iron-chromium oxide layer formed. In the case of a liquid breederblanket condition, the chromium oxide layer partly lost at 500 °C for 100 h. The chromium oxide-formed sampledecreased deuterium permeationflux by a factor of up to 150. The permeation reduction efficiency deterioratedafter exposure to a solid breeder blanket condition due to a change of the chromium oxide layer. However, thechromium oxide formation would play a role to reduce hydrogen isotope permeation even after reduction of theoxide layer

Oxide layer formation in reduced activation ferritic steel F82H under DEMOreactor blanket condition

Tritium permeation through structure materials in fusion blanket systems is a critical issue from the perspectives of fuel loss and radiological hazard. In the previous studies, detailed hydrogen isotope permeation behaviors in reduced activation ferritic/martensitic steels have been investigated; however, oxidation of the steel surface is expected under an actual DEMO reactor condition, and then the tritium permeation behavior will be changed. In this study, deuterium permeation through the steels heat-treated under simulated environment conditions has been investigated for more precise predictions of tritium loss at DEMO reactor blankets. Reduced activation ferritic/martensitic steel F82H substrates were heat-treated in helium gas flow containing 1 vol% hydrogen at 300, 400 and 500 °C for 100 and 200 h to simulate a solid breeder DEMO reactor blanket condition. After surface observation and analysis for the heat-treated samples, gas-driven deuterium permeation measurements were performed. An iron oxide layer was formed on the sample surface, and the thickness of the layer was 50 nm‒12 μm. The oxide layer on the sample surface heat-treated at 500 °C for 100 h decreased deuterium permeation by a factor of 5. After the permeation tests, dissipation of the oxide layers was confirmed

Deuterium permeation behavior and its iron-ion irradiation effect in yttrium oxide coating deposited by magnetron sputtering

Tritium permeation through structural materials is a critical issue in fusion reactors from the viewpoints of sufficient fuel balance and radiological hazard. Ceramic coatings have been investigated as tritium permeation barrier for several decades; however, irradiation effects of the coatings on permeation are not elucidated. In this work, yttrium oxide coatings were fabricated on reduced activation ferritic/martensitic steels by radio frequency magnetron sputtering, and their microstructures and deuterium permeation behaviors were investigated before and after iron-ion irradiation at different temperatures. An as-deposited coating had a columnar structure and transformed into a granular one after annealing. An amorphous layer formed near the coating-substrate interface of irradiated coatings, and its thickness became thinner with increasing irradiation temperature. Voids of approximately 20 nm in diameter also formed in the irradiated coatings. Deuterium permeation flux of the sample irradiated to 1 dpa at room temperature was the lowest among the unirradiated and irradiated samples, and a permeation reduction factor indicated up to 390. The amorphous layer disappeared after deuterium permeation measurements due to damage recovery, while the voids remained and aggregated. The irradiation damage would accelerate nucleation of the crystal, resulting in a decrease of the permeation flux