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采用单柱色谱法与三重四极杆电感耦合等离子体质谱联用技术快速测定环境样品中的¹³⁵Cs 并精确测定 ¹³⁵Cs/¹³⁷Cs 原子比。

Rapid determination of ¹³⁵Cs and precise ¹³⁵Cs/¹³⁷Cs atomic ratio in environmental samples by single-column chromatography coupled to triple-quadrupole inductively coupled plasma-mass spectrometry.

机构信息

Department of Radiation Chemistry, Institute of Radiation Emergency Medicine, Hirosaki University, 66-1 Hon-cho, Hirosaki, Aomori 036-8564, Japan; Division of Nuclear Technology and Applications, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049, China; Beijing Engineering Research Center of Radiographic Techniques and Equipment, Beijing 100049, China.

Department of Radiation Chemistry, Institute of Radiation Emergency Medicine, Hirosaki University, 66-1 Hon-cho, Hirosaki, Aomori 036-8564, Japan.

出版信息

Anal Chim Acta. 2016 Feb 18;908:177-84. doi: 10.1016/j.aca.2015.12.041. Epub 2016 Jan 7.

Abstract

For source identification, measurement of (135)Cs/(137)Cs atomic ratio not only provides information apart from the detection of (134)Cs and (137)Cs, but it can also overcome the application limit that measurement of the (134)Cs/(137)Cs ratio has due to the short half-life of (134)Cs (2.06 y). With the recent advancement of ICP-MS, it is necessary to improve the corresponding separation method for rapid and precise (135)Cs/(137)Cs atomic ratio analysis. A novel separation and purification technique was developed for the new generation of triple-quadrupole inductively coupled plasma-mass spectrometry (ICP-MS/MS). The simple chemical separation, incorporating ammonium molybdophosphate selective adsorption of Cs and subsequent single cation-exchange chromatography, removes the majority of isobaric and polyatomic interference elements. Subsequently, the ICP-MS/MS removes residual interference elements and eliminates the peak tailing effect of stable (133)Cs, at m/z 134, 135, and 137. The developed analytical method was successfully applied to measure (135)Cs/(137)Cs atomic ratios and (135)Cs activities in environmental samples (soil and sediment) for radiocesium source identification.

摘要

为了进行源识别,测量 (135)Cs/(137)Cs 原子比不仅提供了除检测 (134)Cs 和 (137)Cs 之外的信息,而且还可以克服由于 (134)Cs 半衰期短(2.06 年)而导致 (134)Cs/(137)Cs 比测量的应用限制。随着 ICP-MS 的最新进展,有必要改进相应的分离方法,以实现快速、精确的 (135)Cs/(137)Cs 原子比分析。一种新的分离和纯化技术已被开发用于新一代三重四极杆电感耦合等离子体质谱仪 (ICP-MS/MS)。简单的化学分离,包括磷钼酸铵对 Cs 的选择性吸附,以及随后的单阳离子交换色谱,去除了大部分同量异位素和多原子干扰元素。随后,ICP-MS/MS 去除了残余的干扰元素,并消除了稳定 (133)Cs(m/z 134、135 和 137)的峰拖尾效应。所开发的分析方法成功地应用于测量环境样品(土壤和沉积物)中的 (135)Cs/(137)Cs 原子比和 (135)Cs 活度,以进行放射性铯源识别。

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