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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.”
A. Fessler, A. J. M. Plompen, D. L. Smith, J. W. Meadows, Y. Ikeda
Nuclear Science and Engineering | Volume 134 | Number 2 | February 2000 | Pages 171-200
Technical Paper | doi.org/10.13182/NSE99-14
Articles are hosted by Taylor and Francis Online.
Cross sections have been measured with the activation technique at various neutron energies in the range of 16.0 to 20.5 MeV for the following 22 reactions: 19F(n,p)19O, 23Na(n,p)23Ne, 23Na(n,)20F, 25Mg(n,p)25Na, 27Al(n,p)27Mg, 28Si(n,p)28Al, 29Si(n,p)29Al, 29Si(n, np + pn + d)28Al, 31P(n,)28Al, 35Cl(n,2n)34mCl, 37Cl(n,p)37S, 46Ti(n,p)46mSc, 50Ti(n,p)50g+mSc, 51V(n,p)51Ti, 55Mn(n,)52V, 56Fe(n,p)56Mn, 57Fe(n, np + pn + d)56Mn, 57Fe(n,p)57Mn, 93Nb(n,)90mY, 93Nb(n,2n)92mNb, 119Sn(n,p)119gIn, and 138Ba(n,2n)137mBa. The half-lives for the reaction products range from 11 s to 10.15 days. Quasi-monoenergetic neutrons were produced via the 3H(d, n)4He reaction. In some cases isotopically enriched materials were used to enhance the reaction yield or to facilitate correction for interfering reactions leading to the same product. The gamma rays emitted from the irradiated samples were measured with a high-purity germanium detector. A pneumatic sample transport system was used to limit the decay of the radioactive products between neutron irradiation and gamma-ray counting. All cross sections were obtained as ratios to the standard reaction 27Al(n,)24Na, using as secondary neutron fluence references the 27Al(n,p)27Mg reaction as well as a calibrated Bonner sphere. Corrections have been applied for sample-irradiation and counting environment geometric effects, neutron absorption and multiple scattering, time variation of neutron-source strength, neutron-source angular distributions, secondary neutrons from the target, gamma-ray absorption, and gamma-ray sum coincidences. A detailed analysis of the uncertainty sources was performed. The present results are compared with other measurements and evaluated data. For seven reactions, measured cross sections have been obtained for the first time beyond 15 MeV. These new data help appreciably to resolve discrepancies in evaluated data files.
