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首页> 外文期刊>Journal of Environmental Radioactivity >The Workshop on Signatures of Medical and Industrial Isotope Production - WOSMIP; Strassoldo, Italy, 1-3 July 2009
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The Workshop on Signatures of Medical and Industrial Isotope Production - WOSMIP; Strassoldo, Italy, 1-3 July 2009

机译:医学和工业同位素生产特征研讨会-WOSMIP; 2009年7月1-3日,意大利斯特拉索尔多

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Radiopharmaceuticals make contributions of inestimable value to medical practice. With growing demand new technologies are being developed and applied worldwide. Most diagnostic procedures rely on ~(99)Tc and the use of uranium targets in reactors is currently the favored method of production, with 95% of the necessary ~(99)Mo parent currently being produced by four major global suppliers. Coinciden-tally there are growing concerns for nuclear security and proliferation. New disarmament treaties such as the Comprehensive Nuclear-Test-Ban Treaty (CTBT) are coming into effect and treaty compliance-verification monitoring is gaining momentum. Radioxenon emissions (isotopes Xe-131, 133, 133m and 135) from radiopharmaceutical production facilities are of concern in this context because radioxenon is a highly sensitive tracer for detecting nuclear explosions. There exists, therefore, a potential for confusing source attribution, with emissions from radiopharmaceutical-production facilities regularly being detected in treaty compliance-verification networks. The CTBT radioxenon network currently under installation is highly sensitive with detection limits approaching 0.1 mBq/m~3 and, depending on transport conditions and background, able to detect industrial release signatures from sites thousands of kilometers away. The method currently employed to distinguish between industrial and military radioxenon sources involves plots of isotope ratios ~(133m)Xe/~(131m)Xe versus ~(135)Xe/~(133)Xe, but source attribution can be ambiguous. Through the WOSMIP Workshop the environmental monitoring community is gaining a better understanding of the complexities of the processes at production facilities, and the production community is recognizing the impact their operations have on monitoring systems and their goal of nuclear non-proliferation. Further collaboration and discussion are needed, together with advances in Xe trapping technology and monitoring systems. Such initiatives will help in addressing the dichotomy which exists between expanding production and improving monitoring sensitivity, with the ultimate aim of enabling unambiguous distinction between different nuclide signatures.
机译:放射性药物对医学实践的贡献不可估量。随着需求的增长,新技术正在全球范围内开发和应用。大多数诊断程序都依赖于〜(99)Tc,目前在反应堆中使用铀靶标是当前的首选生产方法,目前有95%的必要〜(99)Mo母体由四家主要的全球供应商生产。巧合的是,人们越来越关注核安全和核扩散。新的裁军条约,如《全面禁止核试验条约》(《全面禁试条约》)正在生效,并且条约遵守情况核查监督正在获得发展。在这种情况下,放射性药物生产设施的放射性氙排放(同位素Xe-131、133、133m和135)值得关注,因为放射性氙是检测核爆炸的高度敏感的示踪剂。因此,存在混淆来源归属的可能性,在条约合规性验证网络中定期检测到放射性药物生产设施的排放。目前正在安装的CTBT氙气网络非常敏感,检测极限接近0.1 mBq / m〜3,并且根据运输条件和背景,能够检测数千公里外站点的工业释放特征。当前用来区分工业和军事放射性氙源的方法涉及同位素比〜(133m)Xe /〜(131m)Xe与〜(135)Xe /〜(133)Xe的关系图,但是源归属可能不明确。通过WOSMIP讲习班,环境监测界可以更好地了解生产设施中流程的复杂性,生产界也可以认识到其运营对监测系统及其核不扩散目标的影响。需要进一步的合作和讨论,以及Xe捕获技术和监视系统的进步。这些举措将有助于解决扩大生产与提高监测灵敏度之间的二分法,其最终目的是能够在不同核素特征之间进行明确区分。

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