Hitzemann Moritz, Kirk Ansgar T, Lippmann Martin, Bohnhorst Alexander, Zimmermann Stefan
Department of Sensors and Measurement Technology, Institute of Electrical Engineering and Measurement Technology, Leibniz Universität Hannover, 30167 Hannover, Germany.
Anal Chem. 2022 Jan 18;94(2):777-786. doi: 10.1021/acs.analchem.1c03268. Epub 2022 Jan 5.
Ion mobility spectrometers (IMS) are well suited for detecting trace gases down to levels at ppb and even ppt within 1 s of analysis time when using chemical ionization. The measuring principle is based on the separation and detection of the ionized constituents of a sample. Depending on the sample composition, certain ionization sources create both positive and negative analyte ions, but the simultaneous detection of both ion polarities usually requires two drift tubes. Contained within this effort, we present an alternative approach for detecting both ion polarities using one single drift tube that can switch the polarity of the drift tube within 12 ms. This technique allows for generating one positive and one negative ion mobility spectrum, each with a drift time range of 13 ms (minimum reduced ion mobility of = 0.72 cm V s), within a total experiment time of 50 ms. Additionally, ions are continuously generated in the ionization region during both the polarity switching and the analysis of one of the polarities, which allows for an effective ionization/reaction time of 25 ms. Comparable to the performance of similar instrument designs we reported previously, the presented device has a high resolving power of = 70 with a drift length of 51 mm. The limits of detection are for the monomers between 70 and 370 ppt and for the dimers between 450 and 800 ppt for 1 s of averaging for various ketones, methyl salicylate, and chlorinated hydrocarbons. Although this work focuses on applying ultra-fast polarity switching to an existing IMS, the techniques shown here may be applied to other IMS implementations for different applications.
离子迁移谱仪(IMS)非常适合在使用化学电离的情况下,在1秒的分析时间内检测低至ppb甚至ppt水平的痕量气体。其测量原理基于对样品中离子化成分的分离和检测。根据样品组成,某些电离源会产生正、负两种分析物离子,但同时检测两种离子极性通常需要两个漂移管。在这项工作中,我们提出了一种使用单个漂移管检测两种离子极性的替代方法,该漂移管可在12毫秒内切换极性。这项技术能够在50毫秒的总实验时间内,生成一个正离子迁移谱和一个负离子迁移谱,每个谱的漂移时间范围为13毫秒(最小折合离子迁移率为 = 0.72 cm V s)。此外,在极性切换和其中一种极性的分析过程中,离子在电离区域持续产生,这使得有效电离/反应时间达到25毫秒。与我们之前报道的类似仪器设计的性能相当,该设备在漂移长度为51毫米时具有70的高分辨率。对于各种酮类、水杨酸甲酯和氯代烃,1秒平均时间下,单体的检测限在70至370 ppt之间,二聚体的检测限在450至800 ppt之间。尽管这项工作侧重于将超快速极性切换应用于现有的离子迁移谱仪,但这里展示的技术可能适用于其他不同应用的离子迁移谱仪实现方式。