锆石
锕系元素
材料科学
溶解
耐久性
水溶液
相(物质)
核化学
化学
物理化学
有机化学
复合材料
焦绿石
作者
Lewis R. Blackburn,Daniel J. Bailey,Shi‐Kuan Sun,Laura J. Gardner,Martin C. Stennett,Claire L. Corkhill,Neil C. Hyatt
标识
DOI:10.1080/17436753.2021.1877596
摘要
Zirconolite (CaZrTi2O7) has been identified as a candidate ceramic wasteform for the immobilisation and disposal of Pu inventories, for which there is no foreseen future use. Here, we provide an overview of relevant zirconolite solid solution chemistry with respect to Ce, U and Pu incorporation, alongside a summary of the available literature on zirconolite aqueous durability. The zirconolite phase may accommodate a wide variety of tri- and tetravalent actinide and rare-earth dopants through isovalent and heterovalent solid solution, e.g. CaZr1–xPuxTi2O7 or Ca1–xPuxZrTi2–2xFe2xO7. The progressive incorporation of actinides within the zirconolite-2M parent structure is accommodated through the formation of zirconolite polytypoids, such as zirconolite-4M or 3T, depending on the choice of substitution regime and processing route. A variety of standardised durability tests have demonstrated that the zirconolite phase exhibits exceptional chemical durability, with release rates of constituent elements typically <10−5 gm−2·d−1. Further work is required to understand the extent to which polytype formation and surrogate choice influence the dissolution behaviour of zirconolite wasteforms.
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