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Organized to promote the advancement of knowledge in the use of nuclear science and technologies in the aerospace application. Specialized nuclear-based technologies and applications are needed to advance the state-of-the-art in aerospace design, engineering and operations to explore planetary bodies in our solar system and beyond, plus enhance the safety of air travel, especially high speed air travel. Areas of interest will include but are not limited to the creation of nuclear-based power and propulsion systems, multifunctional materials to protect humans and electronic components from atmospheric, space, and nuclear power system radiation, human factor strategies for the safety and reliable operation of nuclear power and propulsion plants by non-specialized personnel and more.
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September 8–11, 2025
Atlanta, GA|Atlanta Marriott Marquis
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NextGen MURR Working Group established in Missouri
The University of Missouri’s Board of Curators has created the NextGen MURR Working Group to serve as a strategic advisory body for the development of the NextGen MURR (University of Missouri Research Reactor).
C. F. Baes, Jr.
Nuclear Science and Engineering | Volume 16 | Number 4 | August 1963 | Pages 405-412
Technical Paper | doi.org/10.13182/NSE63-A26552
Articles are hosted by Taylor and Francis Online.
Combinations of dialkylphosphoric acids (HA) and neutral organophosphorus reagents (B) have for some time been known to produce enhanced (synergistic) extraction of and other actinide ions. This effect may be attributed to the formation of a mixed complex—either a substitution product MO2A3HB or an addition product MO2A4H2B resulting from the reaction of B with the extraction complex MO2A4H2 normally formed with HA alone. Available extraction data, when analyzed in terms of the competing hydrogen-bonding interactions between HA and B, appear more consistent with an addition product MO2A4H2B. The stability of this mixed complex as a function of the neutral organophosphate used and as a function of the diluent used is consistent with hydrogen bonding or solvation of MO2A4H2 by B. The much stronger and more general synergism found in systems wherein HA is replaced by the β-diketone, Thenoyltrifluoroacetone (HY) may be attributed to the relatively weaker competing interaction between HY and B and to the less coordinatively saturated extraction complexes formed by HY alone.