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November 8–12, 2025
Washington, DC|Washington Hilton
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Nuclear News 40 Under 40—2025
Last year, we proudly launched the inaugural Nuclear News 40 Under 40 list to shine a spotlight on the exceptional young professionals driving the nuclear sector forward as the nuclear community faces a dramatic generational shift. We weren’t sure how a second list would go over, but once again, our members resoundingly answered the call, confirming what we already knew: The nuclear community is bursting with vision, talent, and extraordinary dedication.
J. E. Klein
Fusion Science and Technology | Volume 60 | Number 4 | November 2011 | Pages 1371-1374
Detritiation and Isotope Separation | Proceedings of the Ninth International Conference on Tritium Science and Technology (Part 2) | doi.org/10.13182/FST11-A12685
Articles are hosted by Taylor and Francis Online.
Titanium is used as a low pressure tritium storage material. The absorption/desorption rates and temperature rise during air passivation have been reported previously for a 4400 gram prototype titanium hydride storage vessel (HSV). A desorption limit of roughly 0.25 Q/M was obtained when heating to 700°C which represents a significant residual tritium process vessel inventory. To prepare an HSV for disposal, batch-wise isotopic exchange has been proposed to reduce the tritium content to acceptable levels.A prototype HSV was loaded with deuterium and exchanged with protium to determine the effectiveness of a batch-wise isotopic exchange process. A total of seven exchange cycles were performed. Gas samples were taken nominally at the beginning, middle, and end of each desorption cycle. Sample analyses showed the isotopic exchange process does not follow the standard dilution model commonly reported. Samples taken at the start of the desorption process were lower in deuterium (the gas to be removed) than those taken later in the desorption cycle. The results are explained in terms of incomplete mixing of the exchange gas in the low pressure hydride.