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General Kenneth Nichols and the Manhattan Project
Nichols
The Oak Ridger has published the latest in a series of articles about General Kenneth D. Nichols, the Manhattan Project, and the 1954 Atomic Energy Act. The series has been produced by Nichols’ grandniece Barbara Rogers Scollin and Oak Ridge (Tenn.) city historian David Ray Smith. Gen. Nichols (1907–2000) was the district engineer for the Manhattan Engineer District during the Manhattan Project.
As Smith and Scollin explain, Nichols “had supervision of the research and development connected with, and the design, construction, and operation of, all plants required to produce plutonium-239 and uranium-235, including the construction of the towns of Oak Ridge, Tennessee, and Richland, Washington. The responsibility of his position was massive as he oversaw a workforce of both military and civilian personnel of approximately 125,000; his Oak Ridge office became the center of the wartime atomic energy’s activities.”
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.