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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.”
Bernd Sohnius, Rudolf Anton, Erwin Wehner, Frank-Dietrich Heidt, Rudolf Rabenstein
Nuclear Technology | Volume 99 | Number 2 | August 1992 | Pages 213-221
Technical Paper | Nuclear Fuel Cycle | doi.org/10.13182/NT92-A34691
Articles are hosted by Taylor and Francis Online.
A method to determine the release of low activities through natural air exchange from a decommissioned fuel fabrication plant is described. The method has been applied to the buildings of the NUKEM-A plant and was important in obtaining governmental authorization for the plant decommissioning. The air exchange rate in the NUKEM-A plant was measured by using a tracer gas method. For that purpose, N2O as inert gas was injected into representative rooms, and the decrease of concentration caused by exfiltration processes was measured by an infrared gas analyzer as a function of time. The knowledge of this decay curve allows the calculation of low activities, which may be released into the environment by the natural air exchange. The activity is determined according to the German radiation protection regulation. From this, an air exchange rate of ∼25 h−1 would be equivalent to 10% of the tolerable activity emission. The measured exchange rates are less than ∼0.5 h−1. This results—at least for the meteorological conditions during the measurement period—in a significantly lower activity release than that permitted. The measuring method was successfully performed and can be recommended for similar investigations.