Quantification of actinide α-radiation damage in minerals and ceramics

There are large amounts of heavy alpha-emitters in nuclear waste and nuclear materials inventories stored in various sites around the world(1). These include plutonium and minor actinides such as americium and curium. In preparation for geological disposal there is consensus(2) that actinides that have been separated from spent nuclear fuel should be immobilized within mineral-based ceramics rather than glass(2-4) because of their superior aqueous durability and lower risk of accidental criticality. However, in the long term, the alpha-decay taking place in these ceramics will severely disrupt their crystalline structure(2-4) and reduce their durability(5,6). A fundamental property in predicting cumulative radiation damage is the number of atoms permanently displaced per alpha-decay. At present, this number is estimated to be 1,000 - 2,000 atoms/alpha in zircon(4). Here we report nuclear magnetic resonance, spin-counting experiments that measure close to 5,000 atoms/alpha in radiation-damaged natural zircons. New radiological nuclear magnetic resonance measurements on highly radioactive, Pu-239 zircon show damage similar to that caused by U-238 and Th-232 in mineral zircons at the same dose, indicating no significant effect of half-life or loading levels ( dose rate). On the basis of these measurements, the initially crystalline structure of a 10 weight per cent Pu-239 zircon would be amorphous after only 1,400 years in a geological repository ( desired immobilization timescales are of the order of 250,000 years). These measurements establish a basis for assessing the long-term structural durability of actinide-containing ceramics in terms of an atomistic understanding of the fundamental damage event.