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Front-end nuclear fuel supply cooperation: Turning allied interdependence into strategic advantage
The global nuclear revival, which is fueled by unprecedented demand for firm, affordable, dispatchable power for artificial intelligence and data center build-out, energy security imperatives, and climate commitments, has exposed a structural reality of the Western fuel cycle: No single allied nation currently possesses the full suite of front-end capabilities. From mining through conversion, enrichment, fabrication, and the emerging deconversion and metallization steps required for reactor fuels, capability is distributed across Canada, France, Japan, the United Kingdom, and the United States (collectively, the “Sapporo Five”), as well as a small group of close partners.
Motomasa Fuse, Makoto Nagase, Naoshi Usui, Yoshiteru Sato, Motohiro Aizawa, Tsuyoshi Ito, Hideyuki Hosokawa, Yoichi Wada, Kazushige Ishida
Nuclear Science and Engineering | Volume 181 | Number 2 | October 2015 | Pages 175-190
Technical Paper | doi.org/10.13182/NSE14-101
Articles are hosted by Taylor and Francis Online.
While under normal water chemistry without any specific metal ions in reactor coolant a high electrochemical corrosion potential caused by highly oxidizing species such as hydrogen peroxide promotes the formation of hematite film on piping surfaces with a densely packed film structure, the presence of a certain amount of nickel ions prevents the magnetite film from changing to hematite by forming a nickel ferrite. This formation of nickel ferrite instead of hematite accelerates cobalt buildup, and this is especially notable for carbon steel. The observed reduction of radioactivity concentration in reactor water by zinc injection or by nickel/iron ratio control can be explained by the role of zinc or nickel in preventing the film on the fuel rod surfaces from changing to hematite, thereby stabilizing the cobalt activity on this surface. A thermodynamic evaluation suggests that zinc ferrite is more stable than cobalt ferrite only when the ratio of cobalt to zinc divalent ions, [Co2+]/[Zn2+], is <0.011 in molar units. This ratio is consistent with the ratio of 60Co activity to zinc concentration commonly used in industry to control reactor water zinc levels for a dose rate reduction under the hydrogen water chemistry condition. Based on the present understanding of radioactivity behaviors, the actual radiation dose reduction methods are classified into the several groups and summarized from the viewpoint of the interaction between the oxide and various metal ions.