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Scientific Articles - PTR-MS Bibliography

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Publications

Found 3 results
Title [ Year(Desc)]
Filters: Author is Klüpfel, Thomas  [Clear All Filters]
2004
[Gouw2004] de Gouw, J., C. Warneke, R. Holzinger, T. Klüpfel, and J. Williams, "Inter-comparison between airborne measurements of methanol, acetonitrile and acetone using two differently configured PTR-MS instruments", International Journal of Mass Spectrometry, vol. 239, no. 2: Elsevier, pp. 129–137, 2004.
Link: http://www.sciencedirect.com/science/article/pii/S1387380604003513
Abstract
Proton-transfer-reaction mass spectrometry (PTR-MS) has emerged as a useful tool to study the atmospheric chemistry of volatile organic compounds (VOCs). The technique combines a fast response time with a low detection limit, and allows atmospheric measurements of many important VOCs and their oxidation products. Here, we inter-compare the results obtained with two differently configured PTR-MS instruments operated onboard a Falcon aircraft during the Mediterranean Intensive Oxidants Study (MINOS) campaign in the Mediterranean region. One PTR-MS was operated at a drift tube pressure of 2.3 mbar and an electric field divided by gas number density value (E/N) of 120 Td for the detection of VOCs and aromatic hydrocarbons. The other PTR-MS was operated at an increased pressure of 2.8 mbar and a reduced E/N of 97 Td for the detection of peroxyacetyl nitrate (PAN). As a consequence, more H3O+(H2O)n cluster ions were present in the drift tube, which undergo proton-transfer reactions with VOCs similar to H3O+ ions. The results for methanol (CH3OH), acetonitrile (CH3CN) and acetone (CH3COCH3) obtained with the instruments compared very well. The agreement between the two results was relatively independent of the ambient mixing ratio of water, which influences the H3O+(H2O)n cluster ion distribution, and of ozone, which has been implicated in the artificial formation of aldehydes and ketones.
2006
[Colomb2006] Colomb, A., J. Williams, J. Crowley, V. Gros, R. Hofmann, G. Salisbury, T. Klüpfel, R. Kormann, A. Stickler, C. Forster, et al., "Airborne measurements of trace organic species in the upper troposphere over Europe: the impact of deep convection", Environmental Chemistry, vol. 3, no. 4: CSIRO, pp. 244–259, 2006.
Link: http://www.publish.csiro.au/?paper=EN06020
Abstract
The volume mixing ratios of several organic trace gases and ozone (O3) were measured in the upper troposphere over Europe during the UTOPIHAN-ACT aircraft campaign in July 2003. The organic trace gases included alkanes, isoprene, aromatics, iodomethane, and trichloroethylene, oxygenates such as acetone, methanol, formaldehyde, carbon monoxide, and longer-lived tracer species such as chlorofluorocarbons and halochloroflurocarbons. The aim of the UTOPIHAN-ACT project was to study the chemical impact of deep convection on the continental upper troposphere. A Lear Jet aircraft, based in Germany, was flown at heights between 6 and 13 km in the region 59°N–42°N to 7°W–13°E during July 2003. Overall, the convectively influenced measurements presented here show a weaker variability lifetime dependence of trace gases than similar measurements collected over the Mediterranean region under more stable high-pressure conditions. Several cases of convective outflow are identified by the elevated mixing ratios of organic species relative to quiescent background conditions, with both biogenic and anthropogenic influences detectable in the upper troposphere. Enhancement at higher altitudes, notably of species with relatively short chemical lifetimes such as benzene, toluene, and even isoprene indicates deep convection over short timescales during summertime. The impact of deep convection on the local upper tropospheric formaldehyde and HOx budgets is assessed.
2009
[Colomb2009] Colomb, A., V. Gros, S. Alvain, R. Sarda-Esteve, B. Bonsang, C. Moulin, T. Klüpfel, and J. Williams, "Variation of atmospheric volatile organic compounds over the Southern Indian Ocean (30–49 S)", Environmental Chemistry, vol. 6, no. 1: CSIRO, pp. 70–82, 2009.
Link: http://www.publish.csiro.au/?paper=EN08072
Abstract
Considering its size and potential importance, the ocean is poorly characterised in terms of volatile organic compounds (VOC) that play important roles in global atmospheric chemistry. In order to better understand their potential sources and sinks over the Southern Indian Austral Ocean, shipborne measurements of selected species were made during the MANCHOT campaign during December 2004, on board the research vessel Marion Dufresne. Along the transect La Réunion to Kerguelen Island, air measurements of selected VOC (including dimethylsulfide (DMS) isoprene, carbonyls and organohalogens), carbon monoxide and ozone were performed, crossing subtropical, temperate and sub-Antarctic waters as well as pronounced subtropical and sub-Antarctic oceanic fronts. The remote marine boundary layer was characterised at latitudes 45–50°S. Oceanic fronts were associated with enhanced chlorophyll and biological activity in the seawater and elevated DMS and organohalogens in the atmosphere. These were compared with a satellite-derived phytoplankton distribution (PHYSAT). Diurnal variation for isoprene, terpenes, acetone and acetaldehyde was observed, analogously to recent results observed in mesocosm experiments.

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Selected PTR-MS related Reviews

F. Biasioli, C. Yeretzian, F. Gasperi, T. D. Märk: PTR-MS monitoring of VOCs and BVOCs in food science and technology, Trends in Analytical Chemistry 30 (7) (2011).
Link

J. de Gouw, C. Warneke, T. Karl, G. Eerdekens, C. van der Veen, R. Fall: Measurement of Volatile Organic Compounds in the Earth's Atmosphere using Proton-Transfer-Reaction Mass Spectrometry. Mass Spectrometry Reviews, 26 (2007), 223-257.
Link

W. Lindinger, A. Hansel, A. Jordan: Proton-transfer-reaction mass spectrometry (PTR–MS): on-line monitoring of volatile organic compounds at pptv levels, Chem. Soc. Rev. 27 (1998), 347-375.
Link

 

Lists with PTR-MS relevant publications of the University of Innsbruck can be found here: Atmospheric and indoor air chemistry, IMR, Environmental Physics and Nano-Bio-Physics

 

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