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Management of Commercially Generated Radioactive Waste - U.S. ...

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4.25<br />

inventory remains essentially constant. The calcine is collected in canisters and residual<br />

water and nitrate are removed by heating to 700°C before the canisters are sealed shut. The<br />

output <strong>of</strong> the example process amounts to about 0.9 m 3 <strong>of</strong> calcine per GWe-yr. A smaller<br />

diameter canister may be required for waste calcine than for waste glass to prevent over-<br />

heating at the centerline <strong>of</strong> the canister, because <strong>of</strong> the lower thermal conductivity <strong>of</strong><br />

calcine.<br />

4.3.2.1 Chemical Partitioning<br />

The partitioning or separation <strong>of</strong> certain elements from nuclear fuel cycle wastes has<br />

been viewed as a potential means for improving waste management (ERDA 1976, Campbell 1976,<br />

Schneider and Platt 1974, Cooperstein 1976). The perceived benefits result from removal <strong>of</strong><br />

certain radionuclides and, hence, improvements in the management <strong>of</strong> the resulting parti-<br />

tioned radionuclide fraction compared to the management options for the unpartitioned<br />

wastes. Three subsequent options for disposal <strong>of</strong> partitioned radionuclides are discussed<br />

in this document: 1)_transmutation as discussed in Section 6.1.7, 2) chemical resynthesis<br />

as discussed in Section 4.3.2.3, and 3) space disposal as discussed in Section 6.1.8.<br />

In general, to partition simply means to separate elements, or groups <strong>of</strong> elements, from<br />

some mixture <strong>of</strong> chemical species. In a nuclear fuel cycle, partitioning would occur mainly<br />

during the reprocessing <strong>of</strong> spent fuel (ERDA 1976). There are many chemical elements in<br />

spent nuclear fuels (see Section 2.1), and many combinations in which these elements may be<br />

chemically separated. Consequently, there are also numerous partitioning alternatives that<br />

may facilitate useful waste treatment alternatives or disposal options. For all the speci-<br />

fic partitioning candidates described here, one must realize that: 1) no partitioning<br />

processes have been demonstrated for waste disposal on a commercial scale; 2) historically<br />

most recovery processes leave several percent, or more, <strong>of</strong> the desired elements in the waste<br />

streams; and 3) partitioning for waste management purposes requires substantially higher<br />

recoveries than have been achieved to date. Partitioning itself is not an option for final<br />

disposal <strong>of</strong> radioactive wastes, although some waste partitioning may be required as a<br />

pretreatment to permit the final disposal <strong>of</strong> the resulting waste fraction (e.g., the parti-<br />

tioning <strong>of</strong> fission product iodine for space disposal).<br />

With respect to waste management, partitioning may lead to improved waste characteris-<br />

tics for either the short term (less than 1000 years) or the long term (greater than<br />

1000 years). The partitioning <strong>of</strong> strontium and cesium, for example, may be a useful option<br />

to reduce the self-heating (Buckingham 1967) characteristics <strong>of</strong> high-level wastes over the<br />

short term and thereby permit the storage <strong>of</strong> salt cakes that are not overly self-heating.<br />

In addition, the partitioning <strong>of</strong> actinides as well as some fission products may be useful to<br />

reduce the long-term radiotoxicity <strong>of</strong> wastes (Bond and Leuze 1975, Cr<strong>of</strong>f et al. 1977) and,<br />

therefore, reduce the exposure <strong>of</strong> future populations to radioactivity should the wastes ever<br />

be reintroduced into man's environment in the distant future (say after 100,000 years <strong>of</strong><br />

storage).

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