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Access anywhere, anytime: Nuclear power, Ice Camp, and Rickover’s enduring standard of excellence
Admiral William Houston
As U.S. Navy submarines surface through Arctic ice during Ice Camp 2026, they demonstrate more than operational proficiency in one of the harshest environments on Earth. They reaffirm a technological truth first proven in August 1958, when the USS Nautilus completed its submerged transit of the North Pole: nuclear power enables access anywhere, anytime.
The Arctic is unforgiving, with vast distances, extreme cold, shifting ice, and no logistical infrastructure. Conventional propulsion is constrained by fuel, air, and endurance. Nuclear propulsion removes those constraints. Only a nuclear-powered submarine can operate anywhere in the world’s oceans, including under the polar ice, undetected and at maximum capability for extended periods. Nuclear power provides sustained high speed and the endurance to reposition across the globe without refueling.
Yuezhou Wei, Tsuyoshi Arai, Harutaka Hoshi, Mikio Kumagai, Aimé Bruggeman, Patrick Goethals
Nuclear Technology | Volume 149 | Number 2 | February 2005 | Pages 217-231
Technical Paper | Reprocessing | doi.org/10.13182/NT05-A3591
Articles are hosted by Taylor and Francis Online.
We have studied a new aqueous reprocessing system that consists of anion exchange as the main separation method, electrolytic reduction for reducing U(VI) to U(IV), and extraction chromatography for minor actinide partitioning. In this work, hot tests were carried out on the main flow sheet (U and Pu recovery) using a nitric acid solution of a spent commercial boiling water reactor fuel with burnup of 55 000 MWd/t HM. First, a separation experiment was conducted using a column packed with AR-01 anion exchanger, and the separation behavior of about 20 elements was examined. Then electrolytic reduction was performed for the U(VI) eluate from the first column using a flow-type electrolysis cell. Subsequently, the reduced U solution was applied to the second AR-01 column to separate the U(IV) from contaminated fission products. Most amounts of Pu(IV)-Np(IV), were successfully separated and recovered in the first column. In the electrolysis, U(VI), Np(V,VI), and a trace amount of Pu(VI) were reduced to U(IV), Np(IV), and Pu(IV), respectively. In the second column, the U(IV) with small amounts of Np(IV) and Pu(IV) was completely separated from the fission products. These results demonstrated that the proposed U and Pu recovery process is essentially feasible, though more effective elution methods for Pd and Tc need to be investigated further.