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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.
Wallace Davis, Jr.
Nuclear Science and Engineering | Volume 14 | Number 2 | October 1962 | Pages 174-178
Technical Paper | doi.org/10.13182/NSE62-A28117
Articles are hosted by Taylor and Francis Online.
Some of the published data on the extraction of nitric acid from aqueous solutions, containing ≦5 M acid, by tributyl phosphate-hydrocarbon diluent solutions were tested for their agreement with a mathematical description presented in Part 1. In all cases the agreement of the literature data with this description ranged from adequate to very good, thereby adding support to the interpretation of the parameters of the equation in terms of the equilibrium constant, , for the extraction reaction and the two activity coefficients y′T and . The form of the mathematics suggests that TBP and TBP·H2O are indistinguishable in their reaction with HNO3 and that y′T is an approximate mean molar activity coefficient of these two in the water-saturated system; similarly, is an approximate mean molar activity coefficient of the two species TBP·HNO3 and TBP·HNO3H2O. The quantity has a value of ∼1.5 in molar units for diluent-free TBP; its extrapolated value in the pure diluent Amsco 125-82, or odorless kerosene, is ∼0.23, while its value in n-hexane is ∼0.27.