核燃料后处理应用的微罗曼测量

Amanda Casella , Amanda Lines , Gilbert Nelson , Job Bello , Samuel Bryan
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引用次数: 8

摘要

乏燃料的处理和再使用是关闭核燃料循环的关键组成部分。已开发的溶剂萃取后处理方法包含适合分离特定放射性核素的各种步骤,这些步骤高度依赖于溶液性质。用于监控这些过程的仪器必须坚固耐用,几乎不需要维护,并且能够承受恶劣的环境,如高辐射场和腐蚀性化学基质。我们的小组一直在研究使用光谱学在线监测锕系元素、镧系元素和燃料后处理流中的酸强度。本文主要研究了一种新型微型罗曼探针的研制与应用,用于对乏燃料后处理相关溶液中的U(VI)/硝酸盐离子/硝酸进行在线实时监测。先前的研究已经成功地证明了在宏观尺度上的适用性,使用需要更大溶液体积的样品探针。为了尽量减少浪费和减少对人员的剂量,我们修改了这项技术,允许使用拉曼微探针在微流控尺度上进行测量。在目前的采样环境下,拉曼样品通常需要10ml以上或更大。使用新的采样系统,我们可以在10 μL或更小的范围内采样,这是样本大小的1000倍以上的规模缩小。本文将总结我们目前在这一领域的工作,包括:比较宏观和微观探针的检测限,优化通道聚焦,以及在不同水平HNO3和UO2(NO3)2的流动池中的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MicroRaman Measurements for Nuclear Fuel Reprocessing Applications

Treatment and reuse of used nuclear fuel is a key component in closing the nuclear fuel cycle. Solvent extraction reprocessing methods that have been developed contain various steps tailored to the separation of specific radionuclides, which are highly dependent upon solution properties. The instrumentation used to monitor these processes must be robust, require little or no maintenance, and be able to withstand harsh environments such as high radiation fields and aggressive chemical matrices.

Our group has been investigating the use of optical spectroscopy for the on-line monitoring of actinides, lanthanides, and acid strength within fuel reprocessing streams. This paper will focus on the development and application of a new MicroRaman probe for on-line real-time monitoring of the U(VI)/nitrate ion/nitric acid in solutions relevant to used nuclear fuel reprocessing. Previous research has successfully demonstrated the applicability on the macroscopic scale, using sample probes requiring larger solution volumes. In an effort to minimize waste and reduce dose to personnel, we have modified this technique to allow measurement at the microfluidic scale using a Raman microprobe. Under the current sampling environment, Raman samples typically require upwards of 10 mL and larger. Using the new sampling system, we can sample volumes at 10 μL or less, which is a scale reduction of over 1,000 fold in sample size.

This paper will summarize our current work in this area including: comparisons between the macroscopic and microscopic probes for detection limits, optimized channel focusing, and application in a flow cell with varying levels of HNO3, and UO2(NO3)2.

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