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Aerospace Nuclear Science & Technology
Organized to promote the advancement of knowledge in the use of nuclear science and technologies in the aerospace application. Specialized nuclear-based technologies and applications are needed to advance the state-of-the-art in aerospace design, engineering and operations to explore planetary bodies in our solar system and beyond, plus enhance the safety of air travel, especially high speed air travel. Areas of interest will include but are not limited to the creation of nuclear-based power and propulsion systems, multifunctional materials to protect humans and electronic components from atmospheric, space, and nuclear power system radiation, human factor strategies for the safety and reliable operation of nuclear power and propulsion plants by non-specialized personnel and more.
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2027 ANS Winter Conference and Expo
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Disney World should have gone nuclear
There is extra significance to the American Nuclear Society holding its annual meeting in Orlando, Florida, this past week. That’s because in 1967, the state of Florida passed a law allowing Disney World to build a nuclear power plant.
Takayuki Terai, Akihiro Suzuki, Satoru Tanaka
Fusion Science and Technology | Volume 30 | Number 3 | December 1996 | Pages 911-915
Fuel Cycle and Tritium Technology | doi.org/10.13182/FST96-A11963054
Articles are hosted by Taylor and Francis Online.
The 2:1 mixture of LiF and BeF2 (Flibe) is a potential liquid tritium breeding material for fusion reactors, because of low electric conductivity, high chemical stability in air, etc. We have been studying tritium release behavior from Flibe by in-pile tritium release experiment in the fast neutron source reactor “YAYOI” of the University of Tokyo. About 100g of Flibe was utilized for neutron irradiation to produce tritium, and the tritium released from the specimen was swept by making purge gas flowing over the specimen. Tritium release rate increased with elapsed time after the start of irradiation and a steady state was attained in about four hours at 873K in case of H2 purge gas. Released chemical forms of tritium were HT and TF, and their proportions depended not on the kind of container and tubing materials, but on the chemical composition of purge gas and the dehumidification time of specimen at high temperatures. Tritium generated as T+ in Flibe was released by way of two routes; (1) direct release to purge gas as TF and (2) release to purge gas after converted to HT by the isotopic exchange reaction with H2. The reaction rate was controlled by the H2 concentration and F+ potential in the system. In case of high hydrogen concentration and low F+ potential in the system, tritium was released as HT with a relatively high rate. In case of high F+ potential in the system, on the other hand, tritium was released as TF with a low rate.
