一种基于选择性光聚合物 (PS) 的新方法,用于分析光
I Giménez1, J Rotger1, E Apellániz1
1Departament d'Enginyeria Química i Química Analítica, Universitat de Barcelona, Marti i Franqués, 1-11, ES, 08028, Barcelona, Spain.
概括
一种使用酸盐沉和PS树脂的新方法有效地测量核样本中的-90 (90Sr). 与传统的液晶闪光计数 (LSC) 相比,这种方法可以减少危险废物和分析时间.
科学领域:
- 环境科学 环境科学
- 分析化学 分析化学
- 核化学 核化学 核化学
背景情况:
- -90 (90Sr) 是一个重要的放射性裂变产物,与有化学相似之处,对环境和安全存在担忧.
- 目前90Sr的检测方法通常依赖于液体闪计数 (LSC),这需要化学分离,但产生混合危险和放射性废物.
- -210 (210Pb) 的干扰是基于PS的替代90Sr分析方法的挑战.
研究的目的:
- 开发一种改进的分析方法来检测90 (90Sr).
- 解决与传统的LSC方法相关的废物产生问题.
- 在基于PS树脂的分析中克服-210 (210Pb) 的干扰.
主要方法:
- 开发了一种涉及酸盐沉的新方法,以将与分离.
- 然后,使用PS树脂分析分离的.
- 这种新方法通过将其结果与已建立的基于LSC的技术进行比较来验证.
主要成果:
- 开发的方法有效地将与分离出来,减轻了PS分析中的干扰.
- 这种新方法的结果与传统的LSC方法得到的结果相当.
- 酸盐沉和PSresin方法表明,分析时间缩短,废物产生显著减少.
结论:
- 开发的酸盐沉与PS树脂分离相结合,为90Sr分析提供了一种高效和更环保的替代方案.
- 这种方法提供了与LSC相等的分析准确性,同时最大限度地减少了危险废物产量.
- 这种新技术适用于涉及90Sr监测的应急和环境控制计划.
相关概念视频
Super-resolution Fluorescence Microscopy
7.1K
Super-resolution fluorescence microscopy (SRFM) provides a better resolution than conventional fluorescence microscopy by reducing the point spread function (PSF). PSF is the light intensity distribution from a point that causes it to appear blurred. Due to PSF, each fluorescing point appears bigger than its actual size, and it is the PSF interference of nearby fluorophores that causes the blurred image. Various approaches to achieving higher resolution through SRFM have recently been...
7.1K
Protein Dynamics in Living Cells
2.2K
Different fluorescence-based techniques are used to study the protein dynamics in living cells. These techniques include FRAP, FRET, and PET.
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...
2.2K


