An annealing study has been completed on two compositionally identical Pu-s
ubstituted zircons (Zr0.92Pu0.08SiO4) prepared 18 yr ago with different Pu-
238/Pu-239 isotopic ratios. The activity and accumulated dose for each mate
rial varies greatly due to the very different half-lives of Pu-238 (87.7 yr
) and Pu-239 (24100 yr). The predominantly Pu-238-substituted zircon is in
a highly amorphous state after accumulating a dose of 2.8 x 10(19) alpha-de
cays/g, which is a factor of two higher than the dose previously determined
necessary to amorphize this material. The Pu-239-substituted zircon has re
mained highly crystalline after an accumulated dose of 1.2 x 10(17) alpha-d
ecays/g. The Pu in both samples is trivalent due to sintering under reducin
g conditions. The short-range and long-range structures of each sample have
been characterized by detailed X-ray absorption spectroscopy and X-ray dif
fraction (XRD) methods. The oxidation of Pu3+ to Pu4+ the crystalline Pu-23
9-substituted zircon during annealing in air resulted in a decrease in latt
ice distortion due to the decrease in ionic radius of Pu3+ to Pu4+ On the Z
r4+ site. A significant amount of PuO2 exsolved from the zircon structure a
fter annealing at 1200 degrees C in air. Detailed characterization of the a
morphous Pu-238-substituted zircon demonstrated that while devoid of long-r
ange order it still retained a distorted zircon structure and composition o
ver a length scale of 0.5 nm. The recrystallization of the amorphous Pu-238
-substituted zircon could be achieved directly at temperatures as low as 12
00 degrees C when annealed for 12 h in air; however, annealing at 1000 degr
ees C resulted in decomposition into constituent oxides. (C) 2000 Elsevier
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