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September 8–11, 2025
Atlanta, GA|Atlanta Marriott Marquis
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Fusion Science and Technology
Latest News
Take steps on SNF and HLW disposal
Matt Bowen
With a new administration and Congress, it is time once again to ponder what will happen—if anything—on U.S. spent nuclear fuel and high-level waste management policy over the next few years. One element of the forthcoming discussion seems clear: The executive and legislative branches are eager to talk about recycling commercial SNF. Whatever the merits of doing so, it does not obviate the need for one or more facilities for disposal of remaining long-lived radionuclides. For that reason, making progress on U.S. disposal capabilities remains urgent, lest the associated radionuclide inventories simply be left for future generations to deal with.
In March, Rick Perry, who was secretary of energy during President Trump’s first administration, observed that during his tenure at the Department of Energy it became clear to him that any plan to move SNF “required some practical consent of the receiving state and local community.”1
H. Huang, A. Nikroo, R. B. Stephens, S. A. Eddinger, D. R. Wall, K. A. Moreno, H. W. Xu
Fusion Science and Technology | Volume 55 | Number 4 | May 2009 | Pages 356-366
Technical Paper | Eighteenth Target Fabrication Specialists' Meeting | doi.org/10.13182/FST55-356
Articles are hosted by Taylor and Francis Online.
National Ignition Facility (NIF) specifications require nondestructive, independent profiling of copper, argon, and oxygen in a delivered beryllium capsule. We use a combination of two methods to accomplish this goal: (a) model-enhanced energy dispersive spectroscopy (EDS) of witness shell fragments for destructive profiling of all three elements in a select sample within a batch and (b) differential radiography (DR) to profile copper and argon on multiple shells to nondestructively prove the sample-to-sample consistency within a batch. This combination fully qualifies the delivered shells. For EDS, we developed a physics model and fabricated standards to quantify low concentrations of relatively light elements in a very low-Z matrix. For model validation, we produced sputtered beryllium capsules containing a single dopant in each shell and used contact radiography (CR) to characterize the dopant profiles to 5 to 10% accuracy. The copper calibration was also checked against bulk Cu-Be standards with known composition, and the argon and oxygen calibrations were also checked against the X-ray absorption edge spectroscopy (Edge method) and the weight gain methods. Together, the EDS method gives ±0.1, ±0.05, and ±0.2 at.% accuracy for copper, argon, and oxygen, respectively, in NIF specification capsules. For DR, we conduct two CR measurements with the X-ray tube running at 9 and 30 kVp, respectively. The differential response between copper and argon enables elemental separation. The dopant profiles can be measured to ±0.1 at.% for NIF specification capsules. The oxygen profile in DR must be inferred from the EDS measurement. In the production work flow, we use EDS to obtain the oxygen profile and use it as input to the DR measurement. We then check that the copper and argon profiles obtained from DR and those from EDS are consistent. The average argon and copper contents from either method can also be checked against the results from the Edge method. These two levels of cross-checks offer critical assurances to the data integrity in production metrology.