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Conference Spotlight
2025 ANS Winter Conference & Expo
November 9–12, 2025
Washington, DC|Washington Hilton
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Latest News
IAEA again raises global nuclear power projections
Noting recent momentum behind nuclear power, the International Atomic Energy Agency has revised up its projections for the expansion of nuclear power, estimating that global nuclear operational capacity will more than double by 2050—reaching 2.6 times the 2024 level—with small modular reactors expected to play a pivotal role in this high-case scenario.
IAEA director general Rafael Mariano Grossi announced the new projections, contained in the annual report Energy, Electricity, and Nuclear Power Estimates for the Period up to 2050 at the 69th IAEA General Conference in Vienna.
In the report’s high-case scenario, nuclear electrical generating capacity is projected to increase to from 377 GW at the end of 2024 to 992 GW by 2050. In a low-case scenario, capacity rises 50 percent, compared with 2024, to 561 GW. SMRs are projected to account for 24 percent of the new capacity added in the high case and for 5 percent in the low case.
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.