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PLENTIFUL ENERGY

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Figure 1-11. Rendering of the EBR-II Plant and its Fuel Cycle Facility<br />

The downside was the fact that the metal fuel used by EBR-II was not at all<br />

satisfactory. It would not withstand even reasonably lengthy irradiation in the<br />

reactor. A uranium alloy, it swelled substantially under irradiation, and it would<br />

burst its steel cladding if left in the reactor more than a few months. In fact, it was<br />

just this problem that was the pressing reason for providing the reactor with an<br />

onsite processing facility at all. The fact that fuel would have a short life was<br />

accepted and provided for. After its short irradiation time, it was taken out of the<br />

reactor and simply melted. Melting itself partly purified the new fuel. It released the<br />

fission product gases and a chemical reaction with the melt-vessel extracted more of<br />

the fission products, though many were left. It was a crude beginning for<br />

processing, but it did work. Importantly, it introduced the thought that onsite<br />

processing might be simple, feasible and desirable.<br />

Nonetheless, a much longer irradiation life was going to be necessary if there<br />

was to be a successful scale-up to commercial size. This would have been a feature<br />

of EBR-III, the reactor that never was. In the sweeping political changes of the mid<br />

1960s, the most important immediate technical change was to discard metal in favor<br />

of oxide fuel. When problems with metallic fuel burnup became evident in the early<br />

1960s, General Electric led the way in advocating a move to oxide fuel for fast<br />

reactors. The experience with oxide in the thermal reactors that were then starting to<br />

commercialize had been favorable, and it seemed natural to move in that direction.<br />

It was known that oxide would withstand irradiations of considerable length, and, as<br />

a further incentive, the very high melting point was thought to be favorable for<br />

safety.<br />

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