Bu Wenting, Zheng Jian, Ketterer Michael E, Hu Sheng, Uchida Shigeo, Wang Xiaolin
Institute of Nuclear Physics and Chemistry, China Academy of Engineering Physics, Mianyang 621900, China.
Biospheric Assessment for Waste Disposal Team & Fukushima Project Headquarters, National Institute of Radiological Sciences, National Institutes for Quantum and Radiological Science and Technology, Chiba 263-8555, Japan.
Anal Chim Acta. 2017 Dec 1;995:1-20. doi: 10.1016/j.aca.2017.09.029. Epub 2017 Sep 28.
Measurements of the long-lived radionuclide U are an important endeavor, not only in nuclear safeguards work, but also in terms of using this emerging nuclide as a tracer in chemical oceanography, hydrology, and actinide sourcing. Depending on the properties of a sample and its neutron irradiation history, U/U ratios from different sources vary significantly. Therefore, this ratio can be treated as an important fingerprint for radioactive source identification, and in particular, affords a definitive means of discriminating between naturally occurring U and specific types of anthropogenic U. The development of mass spectrometric techniques makes it possible to determine ultra-trace levels of U in environmental samples. In this paper, we review the current status of mass spectrometric approaches for determination of U in environmental samples. Various sample preparation methods are summarized and compared. The mass spectrometric techniques emphasized herein are thermal ionization mass spectrometry (TIMS), inductively coupled plasma mass spectrometry (ICP-MS) and accelerator mass spectrometry (AMS). The strategies or principles used by each technique for the analysis of U are described. The performances of these techniques in terms of abundance sensitivity and detection limit are discussed in detail. To date, AMS exhibits the best capability for ultra-trace determinations of U. The levels and behaviors of U in various environmental media are summarized and discussed as well. Results suggest that U has an important, emerging role as a tracer for geochemical studies.
对长寿命放射性核素铀的测量是一项重要工作,不仅在核保障工作中如此,而且在将这种新兴核素用作化学海洋学、水文学和锕系元素溯源中的示踪剂方面也是如此。根据样品的性质及其中子辐照历史,不同来源的铀/铀比率差异很大。因此,该比率可被视为放射性源识别的重要指纹,特别是提供了区分天然存在的铀和特定类型人为铀的明确方法。质谱技术的发展使得测定环境样品中痕量铀成为可能。在本文中,我们综述了测定环境样品中铀的质谱方法的现状。总结并比较了各种样品制备方法。本文重点介绍的质谱技术是热电离质谱(TIMS)、电感耦合等离子体质谱(ICP-MS)和加速器质谱(AMS)。描述了每种技术用于分析铀的策略或原理。详细讨论了这些技术在丰度灵敏度和检测限方面的性能。迄今为止,AMS在超痕量铀测定方面表现出最佳能力。还总结并讨论了各种环境介质中铀的含量和行为。结果表明,铀作为地球化学研究的示踪剂具有重要的新兴作用。