Volatile and intermediate volatility organic compounds in suburban Paris: variability, origin and importance for SOA formation

被引:89
|
作者
Ait-Helal, W. [1 ,2 ,3 ]
Borbon, A. [3 ]
Sauvage, S. [1 ,2 ]
de Gouw, J. A. [4 ,5 ]
Colomb, A. [6 ]
Gros, V. [7 ]
Freutel, F. [8 ]
Crippa, M. [9 ]
Afif, C. [3 ,10 ]
Baltensperger, U. [9 ]
Beekmann, M. [3 ]
Doussin, J-F [3 ]
Durand-Jolibois, R. [3 ]
Fronval, I. [1 ,2 ]
Grand, N. [3 ]
Leonardis, T. [1 ,2 ]
Lopez, M. [7 ]
Michoud, V. [3 ]
Miet, K. [3 ]
Perrier, S. [3 ]
Prevot, A. S. H. [9 ]
Schneider, J. [8 ]
Siour, G. [3 ]
Zapf, P. [3 ]
Locoge, N. [1 ,2 ]
机构
[1] Univ Lille Nord France, F-59000 Lille, France
[2] Ecole Mines Douai, Dept Chim & Environm, F-59508 Douai, France
[3] UPD, LISA, UMR CNRS 7583, UPEC,IPSL, Creteil, France
[4] NOAA, Div Chem Sci, Earth Syst Res Lab, Boulder, CO USA
[5] Univ Colorado, Cooperat Inst Res Environm Sci, Boulder, CO 80309 USA
[6] Univ Blaise Pascal, Clermont Univ, LaMP, UMR CNRS 6016, Aubiere, France
[7] Univ Versailles St Quentin Yvelines, LSCE, CNRS 8212, CEA, Gif Sur Yvette, France
[8] Max Planck Inst Chem, D-55128 Mainz, Germany
[9] Paul Scherrer Inst, Lab Atmospher Chem, Villigen, Switzerland
[10] Univ St Joseph, Fac Sci, Ctr Anal & Rech, Beirut, Lebanon
基金
欧盟第七框架计划;
关键词
AIR-POLLUTION SOURCES; POLYCYCLIC AROMATIC-HYDROCARBONS; RADICAL-INITIATED REACTIONS; AEROSOL MASS-SPECTROMETRY; URBAN BACKGROUND SITE; ON-ROAD EMISSIONS; NONMETHANE HYDROCARBONS; GAS-PHASE; CHEMICAL-COMPOSITION; HIGH-RESOLUTION;
D O I
10.5194/acp-14-10439-2014
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Measurements of gaseous and particulate organic carbon were performed during the MEGAPOLI experiments, in July 2009 and January-February 2010, at the SIRTA observatory in suburban Paris. Measurements comprise primary and secondary volatile organic compounds (VOCs), of both anthropogenic and biogenic origins, including C-12-C-16 n-alkanes of intermediate volatility (IVOCs), suspected to be efficient precursors of secondary organic aerosol (SOA). The time series of gaseous carbon are generally consistent with times series of particulate organic carbon at regional scale, and are clearly affected by meteorology and air mass origin. Concentration levels of anthropogenic VOCs in urban and suburban Paris were surprisingly low (2-963 ppt) compared to other megacities worldwide and to rural continental sites. Urban enhancement ratios of anthropogenic VOC pairs agree well between the urban and suburban Paris sites, showing the regional extent of anthropogenic sources of similar composition. Contrary to other primary anthropogenic VOCs (aromatics and alkanes), IVOCs showed lower concentrations in winter (< 5 ppt) compared to summer (13-27 ppt), which cannot be explained by the gas-particle partitioning theory. Higher concentrations of most oxygenated VOCs in winter (18-5984 ppt) suggest their dominant primary anthropogenic origin. The respective role of primary anthropogenic gaseous compounds in regional SOA formation was investigated by estimating the SOA mass concentration expected from the anthropogenic VOCs and IVOCs (I/VOCs) measured at SIRTA. From an integrated approach based on emission ratios and SOA yields, 38% of the SOA measured at SIRTA is explained by the measured concentrations of I/VOCs, with a 2% contribution by C-12-C-16 n-alkane IVOCs. From the results of an alternative time-resolved approach, the average IVOC contribution to SOA formation is estimated to be 7 %, which is half of the average contribution of the traditional aromatic compounds (15 %). Both approaches, which are based on in situ observations of particular I/VOCs, emphasize the importance of the intermediate volatility compounds in the SOA formation, and support previous results from chamber experiments and modeling studies. They also support the need to make systematic the IVOCs' speciated measurement during field campaigns.
引用
收藏
页码:10439 / 10464
页数:26
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