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Fusion Science and Technology
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Glass strategy: Hanford’s enhanced waste glass program
The mission of the Department of Energy’s Office of River Protection (ORP) is to complete the safe cleanup of waste resulting from decades of nuclear weapons development. One of the most technologically challenging responsibilities is the safe disposition of approximately 56 million gallons of radioactive waste historically stored in 177 tanks at the Hanford Site in Washington state.
ORP has a clear incentive to reduce the overall mission duration and cost. One pathway is to develop and deploy innovative technical solutions that can advance baseline flow sheets toward higher efficiency operations while reducing identified risks without compromising safety. Vitrification is the baseline process that will convert both high-level and low-level radioactive waste at Hanford into a stable glass waste form for long-term storage and disposal.
Although vitrification is a mature technology, there are key areas where technology can further reduce operational risks, advance baseline processes to maximize waste throughput, and provide the underpinning to enhance operational flexibility; all steps in reducing mission duration and cost.
M. Saito, Y. Torikai, R.-D. Penzhorn, K. Akaishi, M. Matsuyama
Fusion Science and Technology | Volume 60 | Number 4 | November 2011 | Pages 1459-1462
Interaction with Materials | Proceedings of the Ninth International Conference on Tritium Science and Technology (Part 2) | doi.org/10.13182/FST11-A12706
Articles are hosted by Taylor and Francis Online.
Uptake, distribution, and release behavior of tritium in Ni was investigated by chemical etching and thermal release rate measurements. Liberated tritium was found to consist almost exclusively of tritiated water. The chronic release rate of tritium from Ni was significantly larger than that from type 316 stainless steel. Depth profiles in specimens that partially lost tritium due to its chronic release into vacuum, air or a stream of argon could be reproduced by a one-dimensional diffusion model using best fit diffusion coefficients. Values of the best-fit diffusion coefficients at 298 K were found to be independent from the ambient into which tritium was released. The average diffusion coefficient from all measurements at 298 K, i.e. (2.7 ± 1.3) × 10-10 [cm2/s] was in line with diffusion coefficients calculated from literature data at the same temperature. Hence, the diffusion model constitutes a useful tool for the prediction of tritium bulk depth profiles in Ni during chronic release (CR).