离子迁移光谱法
化学
极性(国际关系)
离子
分析化学(期刊)
漂移管,漂移管
探测器
光圈(计算机存储器)
质谱法
电压
占空比
电离
光电子学
光学
材料科学
色谱法
电气工程
物理
生物化学
有机化学
声学
细胞
工程类
作者
Moritz Hitzemann,Ansgar T. Kirk,Martin Lippmann,Alexander Nitschke,Olaf Burckhardt,Jonas Winkelholz,Stefan Zimmermann
标识
DOI:10.1021/acs.analchem.4c03296
摘要
Besides safety and security applications, ion mobility spectrometry (IMS) is increasingly used in other fields such as medicine, environmental monitoring and food quality analysis. However, some applications require gas chromatographic separation before analysis by IMS. Furthermore, different compounds in the sample may form positive or negative ions during ionization and therefore simultaneous detection of both ion polarities is highly beneficial to avoid two chromatographic runs of the same sample. This can be achieved by ultra-fast polarity switching of a single drift tube IMS, allowing for quasi-simultaneous detection of both ion polarities. By using a ramped aperture voltage during the switching process, we overcome the issue of excessive displacement currents at the detector during polarity switching, which usually lead to overdriving the output signal of the high-gain transimpedance amplifier. Furthermore, mechanical aperture grid oscillations caused by polarity switching were also reduced through the ramped aperture voltage. This enables a polarity switching time of only 7 ms at a drift voltage of 8 kV and a drift length of 103 mm, leading to a high resolving power of RP = 117. Requiring 50 ms to acquire a pair of positive and negative spectrum, the IMS achieves an acquisition rate of 20 Hz. It reaches limits of detection of 20 pptv for dimethyl methylphosphonate and 40 pptv for methyl salicylate. For demonstration, different hop varieties were investigated and could be clearly differentiated by considering both, the positive and negative spectra.
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