Allers Maria, Kirk Ansgar T, Eckermann Manuel, Schaefer Christoph, Erdogdu Duygu, Wissdorf Walter, Benter Thorsten, Zimmermann Stefan
Leibniz University Hannover, Institute of Electrical Engineering and Measurement Technology, Appelstraße 9a, 30167 Hannover, Germany.
Department of Physical and Theoretical Chemistry, University of Wuppertal, Gauss Str. 20, 42119 Wuppertal, Germany.
J Am Soc Mass Spectrom. 2020 Jun 3;31(6):1291-1301. doi: 10.1021/jasms.0c00114. Epub 2020 May 19.
In contrast to classical Ion Mobility Spectrometers (IMS) operating at ambient pressure, the High Kinetic Energy Ion Mobility Spectrometer (HiKE-IMS) is operated at reduced pressures of between 10 and 40 mbar and higher reduced electric field strengths of up to 120 Td. Thus, the ion-molecule reactions occurring in the HiKE-IMS can significantly differ from those in classical ambient pressure IMS. In order to predict the ionization pathways of specific analyte molecules, profound knowledge of the reactant ion species generated in HiKE-IMS and their dependence on the ionization conditions is essential. In this work, the formation of positive reactant ions in HiKE-IMS is investigated in detail. On the basis of kinetic and thermodynamic data from the literature, the ion-molecule reactions are kinetically modeled. To verify the model, we present measurements of the reactant ion population and its dependence on the reduced electric field strength, the operating pressure, and the water concentration in the sample gas. All of these parameters significantly affect the reactant ion population formed in HiKE-IMS.
与在常压下运行的经典离子迁移谱仪(IMS)不同,高动能离子迁移谱仪(HiKE - IMS)在10至40毫巴的减压下运行,且具有高达120汤德(Td)的更高折合电场强度。因此,HiKE - IMS中发生的离子 - 分子反应可能与经典常压IMS中的反应有显著差异。为了预测特定分析物分子的电离途径,深入了解HiKE - IMS中产生的反应物离子种类及其对电离条件的依赖性至关重要。在这项工作中,详细研究了HiKE - IMS中正反应物离子的形成。基于文献中的动力学和热力学数据,对离子 - 分子反应进行了动力学建模。为了验证该模型,我们展示了反应物离子丰度的测量结果及其对折合电场强度、工作压力和样品气中水浓度的依赖性。所有这些参数都显著影响HiKE - IMS中形成的反应物离子丰度。