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Characterization of a Membrane Interface for Analysis of Air Samples Using Time-of-flight Mass Spectrometry

机译:使用飞行时间质谱分析空气样品的膜界面特性

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摘要

In the present study, we constructed a membrane inlet assembly for selective permeation of volatile airborne organic compounds for subsequent analysis by time-of-flight mass spectrometry. The time-dependent diffusion of analytes through a 75 μm thick polydimethylsiloxane membrane was measured by monitoring the ion signal after a step change in the sample concentration. The results fit well to a non-steady-state permeation equation. The diffusion coefficient, response time, and sensitivity were determined experimentally for a range of polar (halogenated) and nonpolar (aromatic) compounds. We found that the response times for several volatile organic compounds were greatly influenced by the alkyl chain length as well as the size of the substituted halogen atoms. The detection limits for benzene, ethylbenzene, and 2-propanol were 0.2 ppm, 0.1 ppm, and 3.0 ppm by volume, respectively, with a linear dynamic range greater than three orders of magnitude. These results indicate that the membrane inlet/time-of-flight mass spectrometry technique will be useful for a wide range of applications, particularly for in situ environmental monitoring.
机译:在本研究中,我们构建了一种膜入口组件,用于选择性渗透挥发性空气传播的有机化合物,以便随后通过飞行时间质谱进行分析。通过监测样品浓度的阶跃变化后的离子信号,可以测量分析物在75μm厚的聚二甲基硅氧烷膜上的时间依赖性扩散。结果非常适合非稳态渗透方程。通过实验确定了一系列极性(卤化)和非极性(芳香族)化合物的扩散系数,响应时间和灵敏度。我们发现,几种挥发性有机化合物的响应时间受烷基链长以及取代卤素原子的大小影响很大。苯,乙苯和2-丙醇的检出限分别为0.2 ppm,0.1 ppm和3.0 ppm(体积),线性动态范围大于三个数量级。这些结果表明,膜入口/飞行时间质谱技术将在广泛的应用中有用,尤其是在现场环境监测中。

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