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DOE fast tracks test reactor projects: What to know
The Department of Energy today named 10 companies that want to get a test reactor critical within the next year using the DOE’s offer to authorize test reactors outside of national laboratories. As first outlined in one of the four executive orders on nuclear energy released by President Trump on May 23 and in the request for applications for the Reactor Pilot Program released June 18, the companies must use their own money and sites—and DOE authorization—to get reactors operating. What they won’t need is a Nuclear Regulatory Commission license.
K. Isobe et al.
Fusion Science and Technology | Volume 48 | Number 1 | July-August 2005 | Pages 302-305
Technical Paper | Tritium Science and Technology - Tritium Handling Facilities | doi.org/10.13182/FST05-A932
Articles are hosted by Taylor and Francis Online.
The behavior of tritium release from the vacuum vessel of JT-60U during air exposure phase at controlled water vapor concentration and gas purging in the wall conditioning phase has been investigated. For the air exposure with varying water vapor concentrations of 40ppm, 300ppm, 680ppm and 3400ppm, tritium concentration in the vacuum vessel of JT-60U was measured. At each water vapor concentration, tritium concentration initially increased with time and then became steady finally. The steady tritium concentration increased with water vapor concentration. The total amount of tritium released from the vacuum vessel was 13MBq for 3400ppm. This amount is almost the same as that removed by 5 hours' H2-GDC, which has been the most effective method for tritium removal from JT-60U. This suggests that tritium in the vacuum vessel of JT-60U can be easily removed by water vapor. Tritium released into exhaust gas during gas purging was also measured for varying gases (H2, He and Ar), at different pressures and temperatures of the vacuum vessel. Tritium concentration of the exhaust gas was about 0.1Bq/cm3 at room temperature and was independent of gas species within the pressure from 0.05 to 0.3 Pa. This result indicates that isotope exchange of tritium with hydrogen molecules was not so active under these purge conditions.