首页> 外文期刊>Spectrochimica Acta, Part B. Atomic Spectroscopy >Optimization of collision/reaction gases for determination of Sr-90 in atmospheric particulate matter by inductively coupled plasma tandem mass spectrometry after direct introduction of air via a gas-exchange device
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Optimization of collision/reaction gases for determination of Sr-90 in atmospheric particulate matter by inductively coupled plasma tandem mass spectrometry after direct introduction of air via a gas-exchange device

机译:通过气体交换装置直接引入空气后电感耦合等离子体串联质谱法测定大气颗粒物质中SR-90的碰撞/反应气体的优化

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Nuclear power plant accidents release radioactive strontium 90 (Sr-90) into the environment. Monitoring of 90Sr, although important, is difficult and time consuming because it emits only beta radiation. We have developed a new analytical system that enables real-time analysis of Sr-90 in atmospheric particulate matter with an analytical run time of only 10 min. Briefly, after passage of an air sample through an impactor, a small fraction of the sample is introduced into a gas-exchange device, where the air is replaced by Ar. Then the sample is directly introduced into an inductively coupled plasma tandem mass spectrometry (ICP-MS/MS) system equipped with a collision/reaction cell to eliminate isobaric interferences on Sr-90 from Zr-90(+), (YH+)-Y-89-H-1, and Y-90(+). Experiments with various reaction gas conditions revealed that these interferences could be minimized under the following optimized conditions: 1.0 mL min(-1) O-2,10.0 mL min(-1) H-2, and 1.0 mL min(-1) NH3. The estimated background equivalent concentration and estimated detection limit of the system were 9.7 x 10(-4) and 3.6 x 10(-4) ng m(-3), respectively, which are equivalent to 4.9 x 10(-6) and 1.8 x 10(-6) Bq cm(-3). Recoveries of Sr in PM2.5 measured by real-time analysis compared to those obtained by simultaneously collection on filter was 53 +/- 23%, and using this recovery, the detection limit as PM2.5 was estimated to be 3.4 +/- 1.5 x 10(-6) Bq cm(-3). That is, this system enabled detection of Sr-90 at concentrations 5 x 10(-6) Bq cm(-3) even considering the insufficient fusion/vaporization/ionization efficiency of Sr in PM2.5. (C) 2017 Elsevier B.V. All rights reserved.
机译:核电站事故将放射性锶90(SR-90)释放到环境中。监控90SR,虽然重要性,难以耗时,因为它仅发射β辐射。我们开发了一种新的分析系统,可以在大气颗粒物质中实时分析SR-90,分析运行仅为10分钟。简而言之,在通过冲击器通过空气样品之后,将小部分样品引入到气体交换装置中,其中空气被AR取代。然后将样品直接引入配备有碰撞/反应细胞的电感耦合等离子体串联质谱(ICP-MS / MS)系统中,从Zr-90(+),(yh +) - y上消除SR-90上的异常干扰-89-H-1和Y-90(+)。各种反应气体条件的实验表明,在以下优化条件下可以最小化这些干扰:1.0mL min(-1)o-2,10.0mL min(-1)H-2,和1.0mL min(-1)NH 3 。该系统的估计背景等效浓度和估计的检测极限分别为9.7×10(-4)和3.6×10(-4)Ng m(-3),相当于4.9×10(-6)和1.8 X 10(-6)BQ cm(-3)。 PM2.5中Sr的回收率通过实时分析测量,与通过在过滤器上同时收集的那些进行实时分析,使用该恢复,估计PM2.5的检测限估计为3.4 +/- 1.5×10( - 6)BQ cm(-3)。也就是说,该系统能够在浓度下检测SR-90。甚至考虑PM2.5中SR的不足/蒸发/电离效率,5×10(-6)BQ CM(-3)。 (c)2017 Elsevier B.v.保留所有权利。

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