Rapid Analysis of Trace Gases in Complex Mixtures Using Selected Ion Flow Tube–Mass Spectrometry

2002 ◽  
Vol 55 (8) ◽  
pp. 491 ◽  
Author(s):  
C. G. Freeman ◽  
M. J. McEwan

Although the human nose is an extremely sensitive olfactory organ, detecting some odoriferous compounds at concentrations as low as a few ppt (parts per trillion by volume) it is not quantitative. Furthermore, it cannot identify some volatile species at quite high concentrations, and neither can it recognize the individual components of many mixtures of trace volatile organic compounds (VOCs). For some considerable time the scientific community has experimented with a number of different types of olfactory devices with varying degrees of success. The advent of selected ion flow tube–mass spectrometry (SIFT-MS) has revolutionized thinking in trace gas monitoring due to the simplicity of operation together with the rapidity and sensitivity of detection that this technique provides.

2006 ◽  
Vol 20 (4) ◽  
pp. 563-567 ◽  
Author(s):  
Jiří Kubišta ◽  
Patrik Španěl ◽  
Kseniya Dryahina ◽  
Clive Workman ◽  
David Smith

2019 ◽  
Author(s):  
Michal Lacko ◽  
Nijing Wang ◽  
Kristýna Sovová ◽  
Pavel Pásztor ◽  
Patrik Španěl

Abstract. Soft chemical ionization mass spectrometry (SCI-MS) techniques can be used to accurately quantify volatile organic compounds (VOCs) in air in real time; however, differentiation of isomers still represents a challenge. A suitable pre-separation technique is thus needed, ideally capable of analyses in a few tens of seconds. To this end, a bespoke fast GC with an electrically heated 5 m long metallic capillary column was coupled to a selected ion flow tube mass spectrometry (SIFT-MS) instrument. To assess the performance of this combination a case study of monoterpene isomer (C10H16) analyses was carried out. The monoterpenes were quantified by SIFT-MS using H3O+ reagent ions (analyte ions C10H17+, m/z 137, and C6H9+, m/z 81) and NO+ reagent ions (analyte ions C10H16+, m/z 136, and C7H9+, m/z 93). The combinations of the fragment ion relative intensities obtained using H3O+ and NO+ were shown to be characteristic of the individual monoterpenes. Two non-polar GC columns (Restek Inc.) were tested: the advantage of MXT-1 was shorter retention times whilst the advantage of MXT-Volatiles was better temporal separation. Thus, it is possible to quantify components of a monoterpene mixture in less than 45 s by the MXT-1 column and to separate them in less 180 s by the MXT-Volatiles column. As an illustrative example, the headspace of three conifer needle samples was analysed by both reagent ions with both columns showing that mainly α-pinene, β-pinene and 3-carene were present.


2007 ◽  
Vol 77 (1-2) ◽  
pp. 20-23 ◽  
Author(s):  
Andrew R. Moot ◽  
Katherine M. Ledingham ◽  
Paul F. Wilson ◽  
Senti T. Senthilmohan ◽  
David R. Lewis ◽  
...  

2021 ◽  
Author(s):  
Ilaria Belluomo ◽  
Piers R. Boshier ◽  
Antonis Myridakis ◽  
Bhamini Vadhwana ◽  
Sheraz R. Markar ◽  
...  

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