ABSTRACTCubic pyrochlore structure types, A2-mB2O6(O, OH, F) i-n*pH2O, and their derivatives (e.g., monoclinic zirconolite) are important actinide-bearing phases in polyphase, ceramic waste forms (e.g., SYNROC). These waste form phases may typically accumulate alpha-decay doses of 1025 alpha-events/m3 in 1, 000 years or 1026alpha-events/m3 in one million years (i.e., for SYNROC with 20 wt. % HLW). Natural pyrochlores have calculated doses ranging from 1024 to 1027 alpha-events/m3 (= 0.02 to 50 dpa) which have accumulated over ten to a thousand million years. Actinide doping experiments typically reach doses of 1025 alpha-events/m3over periods of several years. Detailed x-ray diffraction analysis of natural samples reveals that the alpha-decay dose at which there is an initial loss of crystallinity (i.e., transition from crystalline to the aperiodic, metamict state as a result of alpha-decay damage) increases as a function of the geologic age of the sample. The increase in the calculated alpha-decay dose which is associated with a specific degree of damage (e.g., loss of x-ray diffraction intensity) is attributed to annealing of isolated alpha-recoil tracks back to the original, crystalline structure. Based on a model of gradual track fading, the alpha-recoil tracks in natural pyrochlores have mean lives on the order of 108 years. In contrast, minerals which remain crystalline (e.g., uraninite, UO2) despite doses of over 1027 alpha-events/m3 have mean alpha-recoil track lives of approximately 104 years. This demonstrates that the microstructure of alpha-decay damaged materials depends not only on the total alpha-event dose, but also on the annealing kinetics of alpha-recoil track fading. Therefore, the prediction of the long-term performance and final state of crystalline phases in ceramic nuclear waste forms requires the determination of alpha-recoil damage annealing as a function of time and temperature.
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