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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.
Yun Mi Kim, Ronald Baney, Kevin Powers, Ben Koopman, James Tulenko
Nuclear Technology | Volume 149 | Number 3 | March 2005 | Pages 337-342
Technical Note | Nuclear Plant Operations and Control | doi.org/10.13182/NT05-A3600
Articles are hosted by Taylor and Francis Online.
Screening experiments for low levels of tritiated water (HTO) remediation based upon selective adsorption/desorption mechanisms utilizing equilibrium isotope effects have been carried out. Several organic and inorganic high surface area materials were investigated to assess their ability to selectively adsorb low concentrations of HTO. Ion-exchange resins with cation functionalities, chitosan, sodium alginate, and several inorganic media modified with metal cations exhibited promising results. Biomaterials, for example, chitosan and modified alginate, demonstrated positive results. Based on the literature and our preliminary testing, we postulate four possible mechanisms for selected tritium adsorption: hydrogen ion exchange, HTO coordination with surface cation sites, hydrogen bonding to surface basic sites, and secondary hydrogen bonding (structural water) in fine pores.