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Effect of reducing groundwater on the retardation of redox-sensitive radionuclides

机译:减少地下水对氧化还原敏感性放射性核素阻滞的影响

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Laboratory batch sorption experiments were used to investigate variations in the retardation behavior of redox-sensitive radionuclides. Water-rock compositions were designed to simulate subsurface conditions at the Nevada Test Site (NTS), where a suite of radionuclides were deposited as a result of underground nuclear testing. Experimental redox conditions were controlled by varying the oxygen content inside an enclosed glove box and by adding reductants into the testing solutions.Under atmospheric (oxidizing) conditions, radionuclide distribution coefficients varied with the mineralogic composition of the sorbent and the water chemistry. Under reducing conditions, distribution coefficients showed marked increases for ~(99)Tc (from 1.22 at oxidizing to 378 mL/g at mildly reducing conditions) and ~(237)Np (an increase from 4.6 to 930 mL/g) in devitrified tuff, but much smaller variations in alluvium, carbonate rock, and zeolitic tuff. This effect was particularly important for ~(99)Tc, which tends to be mobile under oxidizing conditions. A review of the literature suggests that iodine sorption should decrease under reducing conditions when I- is the predominant species; this was not consistently observed in batch tests. Overall, sorption of U to alluvium, devitrified tuff, and zeolitic tuff under atmospheric conditions was less than in the glove-box tests. However, the mildly reducing conditions achieved here were not likely to result in substantial U(VI) reduction to U(IV). Sorption of Pu was not affected by the decreasing Eh conditions achieved in this study, as the predominant sorbed Pu species in all conditions was expected to be the low-solubility and strongly sorbing Pu(OH)_4.Depending on the aquifer lithology, the occurrence of reducing conditions along a groundwater flowpath could potentially contribute to the retardation of redox-sensitive radionuclides ~(99)Tc and ~(237)Np, which are commonly identified as long-term dose contributors in the risk assessment in various radionuclide environmental contamination scenarios. The implications for increased sorption of ~(99)Tc and ~(237)Np to devitrified tuff under reducing conditions are significant as the fractured devitrified tuff serves as important water flow path at the NTS and the horizon for a proposed repository to store high-level nuclear waste at Yucca Mountain.
机译:实验室分批吸附实验用于研究氧化还原敏感放射性核素的延迟行为变化。水岩组合物被设计为模拟内华达试验场(NTS)的地下条件,该试验场是地下核试验的结果,沉积了一系列放射性核素。通过改变密闭手套箱内的氧气含量并向测试溶液中添加还原剂来控制实验氧化还原条件。在大气(氧化)条件下,放射性核素的分布系数随吸附剂的矿物组成和水化学性质而变化。在还原条件下,失透凝灰岩的〜(99)Tc(从氧化时的1.22升高至轻度还原条件下的378 mL / g)和〜(237)Np(从4.6升高至930 mL / g)显着增加,但冲积层,碳酸盐岩和沸石凝灰岩中的变化要小得多。对于〜(99)Tc而言,这种效应尤为重要,后者在氧化条件下易于移动。文献综述表明,当I-为主要种类时,在还原条件下碘的吸附量应减少。在批处理测试中未始终观察到这一点。总体而言,在大气条件下,U对冲积层,失透凝灰岩和沸石凝灰岩的吸附量小于手套箱试验中的吸附量。但是,此处达到的轻度还原条件不太可能导致U(VI)大量还原为U(IV)。由于在所有条件下吸附的主要Pu物种均为低溶解度和强吸附性Pu(OH)_4,因此在本研究中实现的Eh条件降低不会影响Pu的吸附。地下水流径的减少条件的改变可能潜在地导致氧化还原敏感性放射性核素〜(99)Tc和〜(237)Np的延迟,在各种放射性核素环境污染情景中,它们通常被认为是风险评估中的长期剂量贡献者。在还原条件下,〜(99)Tc和〜(237)Np对失透凝灰岩的吸附增加的意义是显着的,因为断裂的失凝凝灰岩在NTS上是重要的水流路径,也是拟议中的储存高浓度水的储层的视线。丝卡山的核废料。

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