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Conference Spotlight
2025 ANS Winter Conference & Expo
November 9–12, 2025
Washington, DC|Washington Hilton
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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.
Keith B. Harvey, Carol A. B. Larocque
Nuclear Technology | Volume 89 | Number 3 | March 1990 | Pages 358-364
Technical Paper | Radioactive Waste Management | doi.org/10.13182/NT90-A34373
Articles are hosted by Taylor and Francis Online.
Waste form glasses that contain substantial quantities of iron, manganese, and aluminum oxides, such as the Savannah River SRL TDS-131 glass, form a thick, hydrated surface layer when placed in contact with water. The dissolution of such a glass has been modeled by Wallace and Wicks, with their “Savannah River Model.” We showed previously that the equations of the Savannah River Model could be fitted to published experimental data if a time-dependent diffusion coefficient was assumed for species diffusing through the surface layer. The Savannah River Model assumes that all of the material dissolved from the glass enters solution, whereas it was observed that substantial quantities of material were retained in the surface layer. An alternative model, presented here, contains a mass balance equation that allows material either to enter solution or to be retained in the surface layer. It is shown that the equations derived using this model can be fitted to the published experimental data assuming a constant diffusion coefficient for species diffusing through the surface layer.