The potential of NO+ and O2+• in switchable reagent ion proton transfer reaction time-of-flight mass spectrometry

被引:12
作者
Hegen, Oliver [1 ]
Gomez, Jorge I. Salazar [1 ]
Schloegl, Robert [1 ,2 ]
Ruland, Holger [1 ]
机构
[1] Max Planck Inst Chem Energy Convers, Dept Heterogeneous React, Mulheim, Germany
[2] Fritz Haber Inst Max Planck Soc, Dept Inorgan Chem, Berlin, Germany
关键词
NO+-O-2(+) -H3O+-mass spectrometry; PTR-MS; SIFT-MS; VOLATILE ORGANIC-COMPOUNDS; TRACE GAS-ANALYSIS; PTR-MS CALIBRATION; FLOW TUBE SIFT; NITRIC-OXIDE; DRIFT-TUBE; HUMIDITY DEPENDENCE; STRUCTURAL ISOMERS; ONLINE ANALYSIS; ENGINE EXHAUST;
D O I
10.1002/mas.21770
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Selected ion flow tube mass spectrometry (SIFT-MS) and proton transfer reaction mass spectrometry with switchable reagent ion capability (PTR+SRI-MS) are analytical techniques for real-time qualification and quantification of compounds in gas samples with trace level concentrations. In the detection process, neutral compounds-mainly volatile organic compounds-are ionized via chemical ionization with ionic reagents or primary ions. The most common reagent ions are H3O+, NO+ and O-2(+center dot). While ionization with H3O+ occurs by means of proton transfer, the ionization via NO+ and O-2(+center dot) offers a larger variety on ionization pathways, as charge transfer, hydride abstraction and so on are possible. The distribution of the reactant into various reaction channels depends not only on the usage of either NO+ or O-2(+center dot), but also on the class of analyte compounds. Furthermore, the choice of the reaction conditions as well as the choice of either SIFT-MS or PTR+SRI-MS might have a large impact on the resulting products. Therefore, an overview of both NO+ and O-2(+center dot) as reagent ions is given, showing differences between SIFT-MS and PTR+SRI-MS as used analytical methods revealing the potential how the knowledge obtained with H3O+ for different classes of compounds can be extended with the usage of NO+ and O-2(+center dot).
引用
收藏
页码:1688 / 1726
页数:39
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