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用于空气和呼吸中选定离子流漂移管质谱分析的 HO、NO 和 O 试剂离子的静电切换和选择

Electrostatic Switching and Selection of HO, NO, and O Reagent Ions for Selected Ion Flow-Drift Tube Mass Spectrometric Analyses of Air and Breath.

机构信息

J. Heyrovský Institute of Physical Chemistry of the Czech Academy of Sciences , Dolejškova 3 , 18223 Prague 8 , Czech Republic.

出版信息

Anal Chem. 2019 Apr 16;91(8):5380-5388. doi: 10.1021/acs.analchem.9b00530. Epub 2019 Mar 27.

DOI:10.1021/acs.analchem.9b00530
PMID:30869870
Abstract

Soft chemical ionization mass spectrometry techniques, particularly the well-established proton transfer reaction mass spectrometry, PTR-MS, and selected ion flow tube mass spectrometry, SIFT-MS, are widely used for real-time quantification of volatile organic compounds in ambient air and exhaled breath with applications ranging from environmental science to medicine. The most common reagent ions HO, NO, or O can be selected either by quadrupole mass filtering from a discharge ion source, which is relatively inefficient, or by switching the gas/vapor in the ion source, which is relatively slow. The chosen reagent ions are introduced into a flow tube or flow-drift tube reactor where they react with analyte molecules in sample gas. This article describes a new electrostatic reagent ion switching, ERIS, technique by which HO, NO, and O reagent ions, produced simultaneously in three separate gas discharges, can be purified in post-discharge source drift tubes, switched rapidly, and selected for transport into a flow-drift tube reactor. The construction of the device and the ion-molecule chemistry exploited to purify the individual reagent ions are described. The speed and sensitivity of ERIS coupled to a selected ion flow-drift tube mass spectrometry, SIFDT-MS, is demonstrated by the simultaneous quantification of methanol with HO, acetone with NO, and dimethyl sulfide with O reagent ions in single breath exhalations. The present ERIS approach is shown to be preferable to the previously used quadrupole filtering, as it increases analytical sensitivity of the SIFDT-MS instrument while reducing its size and the required number of vacuum pumps.

摘要

软化学电离质谱技术,特别是成熟的质子转移反应质谱(PTR-MS)和选择离子流管质谱(SIFT-MS),广泛用于实时定量环境空气中和呼气中的挥发性有机化合物,应用范围从环境科学到医学。最常见的试剂离子 HO、NO 或 O 可以通过从放电离子源中进行四极质量过滤(相对低效)或通过切换离子源中的气体/蒸汽(相对较慢)来选择。选择的试剂离子被引入流管或流动漂移管反应器中,在那里它们与样品气体中的分析物分子反应。本文描述了一种新的静电试剂离子切换(ERIS)技术,通过该技术,可以在三个单独的气体放电中同时产生的 HO、NO 和 O 试剂离子,在放电后源漂移管中进行纯化,快速切换,并选择输送到流动漂移管反应器中。描述了该装置的结构和用于纯化各个试剂离子的离子-分子化学。通过在单次呼气中同时用 HO 定量甲醇、用 NO 定量丙酮和用 O 试剂离子定量二甲硫醚,展示了 ERIS 与选择离子流-漂移管质谱(SIFDT-MS)结合的速度和灵敏度。所提出的 ERIS 方法被证明优于先前使用的四极过滤,因为它提高了 SIFDT-MS 仪器的分析灵敏度,同时减小了仪器的尺寸和所需的真空泵数量。

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