Long-Term Modeling of Plutonium Solubility at a Desert Disposal Site, Including CO2 Diffusion, Cellulose Decay, and Chelation

H. Stockman
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引用次数: 3

Abstract

The solubility of plutonium was estimated for waste buried at the Greater Confinement Disposal site in Nevada. The EQ3/6 thermochemical database was modified to include recent data on Pu complex formation, and the solubilities of two critical phases (probertite (CaNaB5O9·5H2O), added as a backfill material; and Ca sac-charate) were determined by experiment. Reaction path runs were used to model effects of cellulose degradation, including complexation of actinides by organic acids and carbonate, decay of the complexing agents, and the buildup and diffusive loss of CO2 through the permeable alluvium. For most waste interaction scenarios, long-term (≈103 years) concentrations of Pu in pore waters are ≤10−7 molal and are dominated by carbonate complexes, although organic complexes could dominate in the first ≈103 years. In unusual circumstances, carbonation of buried lithium could produce very high Pu solubilities; however, even in such a system, a slight lowering of the effective redox potential dramatically...
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长期模拟钚溶解度在沙漠处置地点,包括二氧化碳扩散,纤维素衰变,和螯合
钚的溶解度被估计为埋在内华达州大约束处置场址的废物。对EQ3/6热化学数据库进行了修改,以包括Pu络合物形成的最新数据,以及作为充填材料添加的两种关键相(铜辉石(CaNaB5O9·5H2O))的溶解度;和糖化钙)通过实验测定。反应路径运行用于模拟纤维素降解的影响,包括有机酸和碳酸盐对锕系元素的络合作用,络合剂的衰变,以及二氧化碳在可渗透冲积层中的积累和扩散损失。对于大多数废物相互作用情景,孔隙水中长期(≈103年)的Pu浓度≤10−7摩尔,并且以碳酸盐配合物为主,尽管有机配合物可能在最初≈103年占主导地位。在特殊情况下,埋藏锂的碳酸化可以产生非常高的Pu溶解度;然而,即使在这样的系统中,有效氧化还原电位的轻微降低也会显着…
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