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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.
Jacopo Buongiorno, Eric P. Loewen, Kenneth Czerwinski, Christopher Larson
Nuclear Technology | Volume 147 | Number 3 | September 2004 | Pages 406-417
Technical Paper | Medium-Power Lead-Alloy Reactors | doi.org/10.13182/NT04-A3539
Articles are hosted by Taylor and Francis Online.
The isotope 210Po is the main product of neutron activation in fast reactors cooled by molten lead-bismuth eutectic (LBE). The isotope 210Po is a pure alpha emitter with a half-life of 138.38 days. For typical values of the neutron flux the 210Po concentration in the coolant can reach 1-10 Ci/kg. While exposure of plant personnel to Po is prevented under normal operating conditions because the primary system is sealed, Po does pose a radiological hazard during maintenance activities for which access to submerged structures is required as well as during accidents resulting in breach of the primary-system barrier. Obviously, continuous removal of Po from the LBE reduces this hazard. Therefore, it is important to understand the mechanisms by which Po is formed in and released from the LBE. We summarize research performed at the Idaho National Engineering and Environmental Laboratory and the Massachusetts Institute of Technology to investigate the basic chemistry of four mechanisms of Po release, which could serve as the basis for a coolant cleanup system in LBE-cooled reactors. The mechanisms explored are lead polonide evaporation, formation of polonium hydride, rare-earth filtering, and alkaline extraction. For the key chemical species involved expressions are given for useful quantities such as formation energy, release, and deposition rates. It is concluded that the most promising removal mechanism is alkaline extraction, although a more systematic investigation of this mechanism is needed.