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Post-source decay of alkylated and functionalized polycyclic aromatic compounds
Authors:Frache Gilles  Krier Gabriel  Vernex-Loset Lionel  Muller Jean-François  Manuelli Pascal
Affiliation:1. Laboratoire de Spectrométrie de Masse et de Chimie Laser, Université Paul Verlaine – Metz, 1 Bd Arago, 57078 Metz, Technop?le 2000 Cedex 03, France;2. Laboratoire de Spectrométrie de Masse et de Chimie Laser, Université Paul Verlaine – Metz, 1 Bd Arago, 57078 Metz, Technop?le 2000 Cedex 03, FranceLaboratoire de Spectrométrie de Masse et de Chimie Laser, Université Paul Verlaine – Metz, 1 Bd Arago, 57078 Metz, Technop?le 2000 Cedex 03, France.;3. TOTAL France, Direction Recherche, 51 esplanade du Général de Gaulle, La Défense 10, 92907 Paris La Défense Cedex, France
Abstract:
Post-source decay (PSD) is a valuable tool for providing structural information from large molecules by time-of-flight mass spectrometry (TOFMS). We used PSD to obtain this type of data from small molecules in the laser desorption/ionization (LDI) study of diesel engine exhaust particles. As the original nitrogen laser (lambda = 337 nm, E = 3.5 eV/photon) of our TOF mass spectrometer does not yield sufficient energy to ionize polycyclic aromatic hydrocarbons (PAHs), a second laser with a shorter wavelength has been coupled to the instrument. The fourth harmonic of a Nd:YAG laser (lambda = 266 nm, 4.6 eV/photon) has been chosen to achieve two-photon single-step desorption/ionization of PAHs. The PSD fragmentation of functionalized, alkylated and sulfur PAHs is discussed. Diesel engine exhaust particles are also studied as an example of a real complex sample. This technique is presented herein as a way to identify small molecules in environmental samples. Information provided by LDI-PSD-TOFMS can be a way to distinguish pollutants with very close molecular weights even if the resolving power of a TOF mass spectrometer is not sufficient.
Keywords:
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