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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.”
Karl G. E. Brenner, Leslie W. Graham
Nuclear Technology | Volume 66 | Number 2 | August 1984 | Pages 404-414
D.Gas/Metal Reaction | Status of Metallic Materials Development for Application in Advanced High-Temperature Gas-Cooled Reactor / Material | doi.org/10.13182/NT84-A33443
Articles are hosted by Taylor and Francis Online.
The main processes of metallic corrosion in primary circuits of advanced high-temperature gas-cooled reactors (HTGRs) at temperatures above 800 °C are oxidation, carburization, and decarburization. These are caused by helium impurity traces of H2O (causing oxidation and decarburization), CO (causing oxidation and carburization), and CH4 (causing carburization). At the very low partial pressures of these impurities, the three processes happen independently, leading to a multitude of corrosion effects, which can be classified in terms of active and passive regimes. In an active regime internal corrosion proceeds rapidly— usually linear with exposure time—thereby severely affecting the structural integrity of the alloy. Passive regimes are characterized by stable oxide layers, which either completely inhibit internal corrosion or limit it to a parabolic dependence with exposure time. These passive and active regimes can be related to absolute partial pressures and partial pressure ratios of the main gaseous impurities, H2O, CO, and CH4. This relationship is illustrated in the form of ternary corrosion maps termed Ternary Environmental Attack diagrams. For each temperature and alloy, such a diagram can be constructed from existing results and used for outlining the likely shape of the passive area for the given temperature. A set of diagrams defines a common passive area for a given alloy over a temperature range, which can be compared with the range of gas compositions expected in the HTGR primary circuit. If it is found that the area representing the expected primary circuit environment is not fully enclosed in the passive corrosion area for commercially available candidate alloys, it will either be necessary to control the primary circuit impurity concentration to such levels that the gas composition is completely shifted into the passive corrosion area, or it will be necessary to develop new alloys with passive corrosion areas big enough to engulf any given primary circuit environment.