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Isotopes & Radiation
Members are devoted to applying nuclear science and engineering technologies involving isotopes, radiation applications, and associated equipment in scientific research, development, and industrial processes. Their interests lie primarily in education, industrial uses, biology, medicine, and health physics. Division committees include Analytical Applications of Isotopes and Radiation, Biology and Medicine, Radiation Applications, Radiation Sources and Detection, and Thermal Power Sources.
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April 8–10, 2021
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Nuclear Science and Engineering
Fusion Science and Technology
NC State celebrates 70 years of nuclear engineering education
An early picture of the research reactor building on the North Carolina State University campus. The Department of Nuclear Engineering is celebrating the 70th anniversary of its nuclear engineering curriculum in 2020–2021. Photo: North Carolina State University
The Department of Nuclear Engineering at North Carolina State University has spent the 2020–2021 academic year celebrating the 70th anniversary of its becoming the first U.S. university to establish a nuclear engineering curriculum. It started in 1950, when Clifford Beck, then of Oak Ridge, Tenn., obtained support from NC State’s dean of engineering, Harold Lampe, to build the nation’s first university nuclear reactor and, in conjunction, establish an educational curriculum dedicated to nuclear engineering.
The department, host to the 2021 ANS Virtual Student Conference, scheduled for April 8–10, now features 23 tenure/tenure-track faculty and three research faculty members. “What a journey for the first nuclear engineering curriculum in the nation,” said Kostadin Ivanov, professor and department head.
Yuji Torikai, Ralf-Dieter Penzhorn, Masao Matsuyama, Kuniaki Watanabe
Fusion Science and Technology | Volume 48 | Number 1 | July-August 2005 | Pages 177-181
Technical Paper | Tritium Science and Technology - Decontamination and Waste | dx.doi.org/10.13182/FST05-4
Articles are hosted by Taylor and Francis Online.
One conceivable option for the disposal of tritium-contaminated stainless steel consists in its storage at ambient temperature in a purged containment. To assess this option several stainless steel 316 specimens, previously loaded at elevated temperatures with 0.8-8.5 MBq of tritium, were flushed continuously with dry argon (water partial pressure 0.073 Pa) for extended periods of time. The released tritium (more than 99 % in the form of tritiated water (HTO)) was collected in bubblers and monitored periodically by liquid scintillation counting. After an initial fast liberation a fairly constant rate of the order of 0.2 % per day established. Tritium depth profile in the SS specimens could be simulated by a diffusion limited desorption model. The rate determining step for tritium release appears to be bulk diffusion.