This review provides a comprehensive evaluation of the state-of-knowledge of radiation effects in crystalline ceramics that may be used for the immobilization of high-level nuclear waste and plutonium. The current understanding of radiation damage processes, defect generation, microstructure development, theoretical methods, and experimental methods are reviewed. Fundamental scientific and technological issues that offer opportunities for research are identified. The most important issue is the need for an understanding of the radiation-induced structural changes at the atomic, microscopic, and macroscopic levels, and the effect of these changes on the release rates of radionuclides during corrosion.
This paper is a comprehensive review of the state-of-knowledge in the field of radiation effects in glasses that are to be used for the immobilization of high-level nuclear waste and plutonium disposition. The current status and issues in the area of radiation damage processes, defect generation, microstructure development, theoretical methods and experimental methods are reviewed. Questions of fundamental and technological interest that offer opportunities for research are identified.
We report the results from a study of europium-doped fluorochlorozirconate glasses that have been thermally processed to induce nucleation and crystallization of BaCl2 crystallites. The resulting glass ceramics show a photostimulated luminescence (PSL) effect with a conversion efficiency which is up to 80% of that found in the commercial crystalline x-ray storage phosphor material BaFBr:Eu2+. Thermal processing for 20 min in the range 240–260 °C produces small (∼6–11nm) hexagonal BaCl2 crystallites, while temperatures in the range 270–290 °C lead to the formation and growth of larger (∼15–100nm) orthorhombic BaCl2 crystallites, as well as additional unidentified phases. We observe only weak PSL from glass ceramics containing hexagonal BaCl2 (∼0.1% conversion efficiency compared to BaFBr:Eu2+ at room temperature), but orthorhombic phase crystallites give rise to a much larger relative efficiency that increases with particle size, and reaches ∼80% for 100 nm diameter particles. The PSL is attributed to the excitation of electrons trapped as F centers in the BaCl2 crystallites, while the dependence on crystallite size is consistent with a PSL-inert surface shell of thickness ∼7nm surrounding the BaCl2 crystallites.
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