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

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4.31<br />

enough to prevent access <strong>of</strong> water to the interior <strong>of</strong> the composite. A barrier can be<br />

formed, however, as is done in the PAMELA process, by suspending the waste-containing par-<br />

ticles in a basket in the canister and filling the annulus between the basket and the can-<br />

ister wall with pure matrix metal.<br />

Coated Particles<br />

Coated particle composite waste forms are being developed, partially based on the tech-<br />

nology developed for the manufacture <strong>of</strong> high temperature gas-cooled reactor (HTGR) fuels<br />

(Rusin et al 1978, 1979a and 1979b). These fuels consist <strong>of</strong> ceramic pellets that are coated<br />

with pyrolytic graphite and silicon carbide, and embedded in a graphite matrix. The core<br />

material that has been most studied for coated particle composite waste forms is the synthe-<br />

tic mineral calcine described in Section 4.3.2.3; however, the concept can utilize other<br />

core materials. Calcine pellets are formed in,a disk pelletizer and coated with pyrolytic<br />

graphite and silicon carbide in a fluidized bed. Laboratory tests have shown that an outer<br />

coating <strong>of</strong> durable A1 20 3 can be added. The coated particles would be surrounded by a<br />

metal matrix in canisters before emplacement in a geologic repository.<br />

Coated particles are a way <strong>of</strong> adapting the multiple barrier concept to the waste form<br />

itself. Tests have shown that the particles can have very good chemical durability. How-<br />

ever, the processing would be very complex and require a large amount <strong>of</strong> development before<br />

it could be done remotely.<br />

Cermet<br />

This waste form concept, under development at Oak Ridge National Laboratory, produces<br />

a uniform dispersion <strong>of</strong> waste oxide particles within a metal matrix (Quinby 1978). The<br />

waste and specific additives required to form the desired ceramic oxide phases and metal<br />

alloy matrix are dissolved together in molten urea. The urea solution is precipitated and<br />

calcined and the fine powders produced in this step are compacted by extrusion or pressing<br />

into desired shapes. In the final processing step the reducible metal oxides, such as<br />

oxides <strong>of</strong> Cr, Ni, Fe, and Co, are reduced in a H 2 or CO atmosphere to form an alloy that<br />

encapsulates the unreduced ceramic oxides. After the 800 0 C reduction the composite is mixed<br />

with an organic binder, extruded to form rods and sintered in a nonoxidizing atmosphere at<br />

1200 0 C to form a dense

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