Abstract
Proton transfer reaction mass spectrometry has become increasingly prominent since the 1990s and has a wide range of applications in analytical science. Essentially the technique relies on chemical ionisation via proton transfer from H3O+ to molecules with proton affinities greater than water. Coupling chemical ionisation to time-of-flight mass spectrometers has been demonstrated [Blake et al, Anal.Chem., 76, 3841-3845, 2004] to be a powerful technique for real time multichannel detection of trace species.
In this work, we will explore the use of differing chemi-ionisation reagents, in particular NO+, which depending on the ionisation energy of the analyte will undertake charge transfer, for the ionisation of trace VOC/OVOCs. The ability for real-time speciation of a range of VOC/OVOCs using multi-chemi-ionisation reagents will be assessed.
In this work, we will explore the use of differing chemi-ionisation reagents, in particular NO+, which depending on the ionisation energy of the analyte will undertake charge transfer, for the ionisation of trace VOC/OVOCs. The ability for real-time speciation of a range of VOC/OVOCs using multi-chemi-ionisation reagents will be assessed.
Original language | English |
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Publication status | Published - 24 Apr 2005 |
Event | EGU General Assembly 2005 - Vienna, Austria Duration: 24 Apr 2005 → 29 Apr 2005 |
Conference
Conference | EGU General Assembly 2005 |
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Abbreviated title | EGU 2005 |
Country/Territory | Austria |
City | Vienna |
Period | 24/04/05 → 29/04/05 |
Keywords
- volatile organic compound
- proton transfer reaction mass spectrometry (PTR-MS)
- air quality
- Chemical ionisation reaction time-of-flight mass spectrometry