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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.
Mahmoud Bakr, Kai Masuda, Masaya Yoshida
Fusion Science and Technology | Volume 75 | Number 6 | August 2019 | Pages 479-486
Technical Paper | doi.org/10.1080/15361055.2019.1609821
Articles are hosted by Taylor and Francis Online.
Neutrons are generated in the inertial electrostatic confinement (IEC) device through different types of fusion reactions of the fuel gas such as deuterium (D) and tritium (T). Fusion in the IEC device takes place via various kinds of collisions like beam-beam collision, beam–background gas collision, and beam-target collision on the electrode surfaces. Two identical anodes for the IEC chamber made from titanium (Ti) and SUS-316L stainless steel (SS) are used to study the effect of the anode material on the neutron production rate (NPR). The NPRs from the chambers are measured at different applied powers. The achieved NPRs, so far, for Ti and SS are 8.9 × 107 n/s at 5.25 kW (75 kV, 70 mA) and 2.8 × 107 n/s at 10.5 kW (70 kV, 150 mA), respectively. The normalized NPR (NPR rated to the cathode current) from the Ti chamber is three to four times higher than that from the SS chamber. We observed a better NPR for the Ti chamber compared with the SS chamber. This is explained by the fusion reaction occurring between the neutrals and D atoms adsorbed/embedded on the inner surface of the anode. Moreover, the Ti chamber shows an improvement of the NPR as a function of the operating time ranging from 1.5 to 1.75 after 25 h from the first discharge.
