Plutonium Isotopes Research in the Marine Environment: A synthesis

Jinlong Wang, Jinzhou Du, Z. Jian
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引用次数: 7

Abstract

Plutonium (Pu), mainly derived from thermonuclear bomb testing, nuclear accidents, nuclear reprocessing facilities and nuclear power plants since the 1950s, entered the ocean by global fallout and by direct release and was then transported by ocean current, exchanged, transformed and eventually buried in the ocean. Pu in the marine environment consists mainly of four isotopes, namely,Pu (T1/2 = 87.7 a), Pu (T1/2 = 24100 a), Pu (T1/2 = 6561 a) and Pu (T1/2 = 14.3 a), in which a very small fraction of Pu originates from uranium mineral and most Pu comes f rom anth ropogenic act iv it y. Additionally, Pu has two isotopes with extremely low concentrations namely, Pu (T1/2 = 376000 a) and Pu (T1/2 = 8.7 ×10 a). The distribution of Pu concentration in the marine environment is influenced by ocean current distribution and biogeochemical cycles, and therefore, Pu isotopes are typically utilized to trace water mass exchange, particle scavenging and biogeochemical cycles. Compared to Sr (Kd: 10-10 L kg) and Cs (Kd: 10-10 L kg), Pu has a much stronger particle affinity in marine environments (Kd: 10-10 L kg) and thus can serve as a better tracer for indicating transport, scavenging and particle deposition. To use Pu as a tracer for environmental process, the geochemical behavior of Pu should be understood and the analytical method for Pu need to be improved. With the development of analytical methods for Pu, the detection limit of Pu in seawater and sediments has continuously decreased, which allows increasing numbers of researchers (Figure 1) to focus on the sources, geochemical behaviors, distribution and environmental implications. Pu fr om different sources or incidents has unique atom (or activity) ratios, e.g., Pu/Pu, Pu/Pu and Pu/Pu, and these ratios can be used to quantitatively evaluate the source of Pu and to study different marine processes along with Pu activity concentration. Therefore, this study aims to synthesize the application of Pu to marine processes based on a summary of its sources, geochemical behaviors, distribution and analytical methods.
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海洋环境中钚同位素研究综述
钚(Pu)主要来源于20世纪50年代以来的热核炸弹试验、核事故、核后处理设施和核电站,通过全球沉降和直接释放进入海洋,然后被洋流运输、交换、转化,最终埋在海洋中。海洋环境中的Pu主要由4种同位素组成,分别为Pu (T1/2 = 87.7 a)、Pu (T1/2 = 24100 a)、Pu (T1/2 = 6561 a)和Pu (T1/2 = 14.3 a),其中极小部分Pu来源于铀矿物,大部分来自于人工活动。另外,Pu还有2种浓度极低的同位素,分别为:Pu (T1/2 = 376000 a)和Pu (T1/2 = 8.7 ×10 a)。海洋环境中Pu浓度的分布受洋流分布和生物地球化学循环的影响,因此通常利用Pu同位素来追踪水质交换、颗粒清除和生物地球化学循环。与Sr (Kd: 10-10 L kg)和Cs (Kd: 10-10 L kg)相比,Pu在海洋环境中具有更强的颗粒亲和力(Kd: 10-10 L kg),因此可以作为更好的示踪剂来指示运输、清除和颗粒沉积。要将蒲公英作为环境过程的示踪剂,必须了解蒲公英的地球化学行为,改进蒲公英的分析方法。随着分析方法的发展,海水和沉积物中Pu的检出限不断降低,使得越来越多的研究人员(图1)开始关注Pu的来源、地球化学行为、分布和环境影响。不同来源或事件的Pu具有独特的原子(或活度)比,如Pu/Pu、Pu/Pu和Pu/Pu,这些比可用于定量评价Pu的来源,并研究不同海洋过程随Pu活度浓度的变化。因此,本文拟在总结其来源、地球化学行为、分布及分析方法的基础上,综合探讨其在海洋过程中的应用。
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