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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.
J. M. Fletcher, C. J. Hardy
Nuclear Science and Engineering | Volume 16 | Number 4 | August 1963 | Pages 421-427
Technical Paper | doi.org/10.13182/NSE63-A26554
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The extraction by TBP of nitrato complexes of metals occurs mainly by the formation of nonconducting complexes in which the oxygen of the PO group is covalently bound to the metal, e.g., P==0 → M. In other TBP complexes, this O atom is bonded to hydrogen, e.g., to a hydrogen atom of water, of an undissociated acid, or of the hydronium ion. Three features in the extraction of metal nitrates at trace concentration from nitric acid concentrations >7M which await interpretation are the second increase in the distribution coefficient, DM; the decrease in the magnitude of this second increase as the fraction of inert diluent increases; and the change in the temperature coefficient of DM from negative to positive. Extraction (i) by bonding of the phosphoryl oxygen to an aquo group (of the aquonitrato metal complex), or (ii) by nitrato acids, do not explain these features. Measurements of the conductivity and viscosity of 100% TBP-HNO3-H2O phases are consistent with the existence of three steps as the ratio HNO3/TBP increases. In the first step, ions, postulated as (TBP·H2O·H)3O+ and (TBP·H)2(H2O·H)O+, are formed. In the second step, the molar conductivity decreases as the predominant species becomes TBP·HNO3. In the third step the molar conductivity and the water content increase by the formation of ions such as (TBP·H)(H2O·H)(HNO3·H)O+, in which a nitric acid molecule is bonded to the hydronium ion: the second increase in DM for certain metals is explained by there being similar bonding, through the oxygen of a nitrato group of the metal complex, in place of the HNO3 in this complex ion when HNO3/TBP is >1. The positive temperature coefficient shown by this form of extraction of metal nitrates is also shown in this region by the extraction of nitric acid, the conductivity, and the water content.
