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Two steps forward for U.K. advanced nuclear
This week, two significant announcements have emerged from the United Kingdom’s advanced reactor sector.
On June 14, Rolls-Royce, the United Kingdom National Nuclear Laboratory, and the Japan Atomic Energy Agency announced that they had signed two trilateral memorandums of cooperation to collaborate on “advanced modular reactor (AMR) technology, specifically high-temperature gas-cooled reactors (HTGR), and the coated particle fuel these reactors will use.”
Separately, on June 16, Bellevue, Wash.–based TerraPower announced that its Natrium reactor design has been formally submitted for U.K. regulatory review. The company also announced the formation of a new subsidiary, TerraPower UK Ltd.
S. Rosanvallon, J.L. Courouau, G. Marbach, W. Gulden
Fusion Science and Technology | Volume 41 | Number 3 | May 2002 | Pages 695-699
Decontamination and Waste | Proceedings of the Sixth International Conference on Tritium Science and Technology Tsukuba, Japan November 12-16, 2001 | doi.org/10.13182/FST41-695
Articles are hosted by Taylor and Francis Online.
The waste management is a challenge for any future fusion facility including ITER. Detritiation could allow easier procedures since the practices in different countries already limit tritium contents and releases for disposal in nuclear waste storage. The experience developed in steel-making processes, for liquid steel degassing by gas injection, has been applied for modeling of tritium removal. A numerical model, initially developed at IRSID (USINOR's Process Research Center) for hydrogen removal, is adapted to determine detritiation efficiency. The hydrogen isotope transfer between liquid metal and injected gas occurs in two elementary steps, liquid phase mass transfer and interfacial reaction driven by Sievert's law for H2 and T2. In the gas phase, H2 and T2 react to give HT, according to the thermodynamic equilibrium and the isotopic exchange. The model takes into account the change in bubbles swarms (sizes and velocities) as they ascent from the bottom of the vessel to the metal free surface. It is thus possible to predict the tritium content evolution during the treatment as a function of process parameters. Duration and inlet gas mixture, which have the major influence on detritiation efficiency, must be set according to the tritium initial concentration and the activity expected in the final waste.