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DOE announces NEPA exclusion for advanced reactors
The Department of Energy has announced that it is establishing a categorical exclusion for the application of National Environmental Policy Act (NEPA) procedures to the authorization, siting, construction, operation, reauthorization, and decommissioning of advanced nuclear reactors.
According to the DOE, this significant change, which goes into effect today, “is based on the experience of DOE and other federal agencies, current technologies, regulatory requirements, and accepted industry practice.”
Yung Sung Cheng, Yue Zhou, Charles A. Gentile, Charles H. Skinner
Fusion Science and Technology | Volume 41 | Number 3 | May 2002 | Pages 867-871
Material Interaction and Permeation | Proceedings of the Sixth International Conference on Tritium Science and Technology Tsukuba, Japan November 12-16, 2001 | doi.org/10.13182/FST02-A22708
Articles are hosted by Taylor and Francis Online.
Amorphous tritiated carbon films are formed through co-deposition of the radioactive isotope tritium (3H or T) with carbon onto plasma facing surfaces in fusion plasmas. The Tokamak Fusion Test Reactor (TFTR), operated by the Princeton Plasma Physics Laboratory, was fueled by tritium and deuterium neutral beam injection and gas puffing. Tritium was co-deposited as amorphous hydrogenated carbon onto graphite tiles and stainless steel surfaces inside the reactor. Since termination of plasma operations, carbon tritide particles have remained in the air in the vessel. Dosimetric limits for occupational exposure to carbon tritide particles need to be established. The purpose of this study was to characterize carbon tritide particle samples inside the TFTR in terms of size, self-absorption of tritium beta, and dissolution rate in simulated lung fluid. Dose estimates of the inhaled carbon tritide particles can be calculated based on the dissolution rate, particle size, and self-absorption factor. The count median diameter and geometric standard deviation were 1.23 µm and 1.72, respectively, indicating that they are respirable particles and can stay suspended in the air for a longer time. The dissolution rate in the lung-simulated fluid was determined in a static system. The dissolution rate ranged from 10−1–10−3 per day in the first few hours, then it decreased to between 10−3 and 10−4. The retention curve of tritium in carbon indicated that >90% of the tritium remained in the particles after 110 d in the simulated lung fluid. This information is being used to support the establishment of respiratory protection requirements.