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Conference Spotlight
Nuclear Energy Conference & Expo (NECX)
September 8–11, 2025
Atlanta, GA|Atlanta Marriott Marquis
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EPA administrator Lee Zeldin talks the future of nuclear
In a recent interview on New York radio station 77 WABC, administrator of the Environmental Protection Agency Lee Zeldin talked with host John Catsimatidis about the near-term future of the domestic nuclear industry and the role the EPA will play in the sector.
Catsimatidis kicked off the interview by asking if the U.S. will be able to reach total energy independence. Zeldin responded by saying that decreasing energy dependence on other countries, especially adversaries, was a top priority for him and the Trump administration.
Michael Epstein, Hans K. Fauske, Charles F. Askonas, Marc A. Vial, Patricia Paviet-Hartmann
Nuclear Technology | Volume 163 | Number 2 | August 2008 | Pages 285-293
Technical Paper | Reprocessing | doi.org/10.13182/NT08-A3988
Articles are hosted by Taylor and Francis Online.
Accurate prediction of the bubble-enhanced mass transport rate of dissolved water from a layer of aqueous nitric acid ("aqueous phase") to an overlying, reactive layer of tri-n-butyl phosphate and nitric acid ("organic phase") is crucial to assessing the conditions for a runaway reaction in the organic phase. This paper presents a rational, predictive model of the concentration profile history of a dissolved species in a vertical column comprising an organic phase overlying an aqueous phase. The model incorporates both interfacial and axial dispersion limitations to species transport. Open-literature correlations on enhanced heat transfer in bubbling pools, after conversion to mass transfer correlations, provide the model's needed interfacial resistance coefficients. The model shows that in laboratory-scale systems interfacial limitations to dissolved species mass transport are controlling while in full-scale columns mass transport is axial dispersion controlled. The model is capable of rationalizing available measurements of dissolved species mass transfer between the organic and aqueous phases. A previous interpretation of the measurements is shown to be incorrect.