scholarly journals Dual Electrospray Ion Source for Electron-Transfer Dissociation on a Hybrid Linear Ion Trap−Orbitrap Mass Spectrometer

2007 ◽  
Vol 79 (20) ◽  
pp. 7916-7919 ◽  
Author(s):  
D. Keith Williams, ◽  
Graeme C. McAlister ◽  
David M. Good ◽  
Joshua J. Coon ◽  
David C. Muddiman
2007 ◽  
Vol 79 (10) ◽  
pp. 3525-3534 ◽  
Author(s):  
Graeme C. McAlister ◽  
Doug Phanstiel ◽  
David M. Good ◽  
W. Travis Berggren ◽  
Joshua J. Coon

2008 ◽  
Vol 7 (8) ◽  
pp. 3127-3136 ◽  
Author(s):  
Graeme C. McAlister ◽  
W. Travis Berggren ◽  
Jens Griep-Raming ◽  
Stevan Horning ◽  
Alexander Makarov ◽  
...  

2009 ◽  
Vol 2 (4) ◽  
pp. 1837-1861 ◽  
Author(s):  
M. Müller ◽  
L. H. Mielke ◽  
M. Breitenlechner ◽  
S. A. McLuckey ◽  
P. B. Shepson ◽  
...  

Abstract. We performed MS/MS investigations of biogenic volatile organic compounds (BVOC) using a triple quadrupole tandem mass spectrometer (QqQ-MS) equipped with a Townsend Discharge ion source and a Proton Transfer Reaction Linear Ion Trap (PTR-LIT) mass spectrometer. Both instruments use H2O chemical ionization to produce protonated molecular ions. Here we report a study of the application of these instruments to determine methyl vinyl ketone (MVK) and methacrolein (MACR) and a series of monoterpenes (α-pinene, β-pinene, 3-carene, limonene, myrcene, ocimene) and sesquiterpenes (humulene and farnesene). Both instruments achieved sub-ppb detection limits in the single MS mode and in the MS/MS mode for differentiating MVK and MACR. Collision induced dissociation (CID) of protonated monoterpenes and sesquiterpenes was studied under the high-energy, single-to-few collision conditions of the QqQ-MS instrument and under the low-energy, multiple collision conditions of the PTR-LIT. Differences and similarities in the breakdown curves obtained are discussed. In addition, we performed MS4 of protonated limonene to illustrate the analytical power of the PTR-LIT. In spite of the progress we have made, the selective on-line mass-spectrometric detection of individual monoterpenes or sesquiterpenes in complex mixtures currently does not yet seem to be possible.


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