Chemical composition of size-resolved atmospheric aerosols in the eastern Mediterranean during summer and winter

被引:258
作者
Bardouki, H
Liakakou, H
Economou, C
Sciare, J
Smolík, J
Zdímal, V
Eleftheriadis, K
Lazaridis, M
Dye, C
Mihalopoulos, N
机构
[1] Univ Crete, Dept Chem, Environm Chem Proc Lab, Iraklion 71409, Greece
[2] CE Saclay, LSCE, F-91191 Gif Sur Yvette, France
[3] Inst Chem Proc Fundamentals AS CR, Prague, Czech Republic
[4] NCSR Demokritos, Inst Nucl Technol Radiat Protect, Athens, OH USA
[5] Tech Univ Crete, Khania, Greece
[6] NILU, N-2007 Kjeller, Norway
关键词
size resolved aerosol composition; regional pollution; eastern Mediterranean;
D O I
10.1016/S1352-2310(02)00859-2
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The chemical composition of aerosols has been determined in 30 size-resolved samples collected using a Berner low-pressure impactor during two campaigns conducted at a coastal site in the Eastern Mediterranean in July 2000 and in January 2001. Sulfate (SO42-) and ammonium (NH4+) have been identified as the main ionic components of the submicronic aerosol fraction, with SO42- accounting for up to 38% of the total fine mass and up to 65% of the total ionic mass during both seasons. On the other hand, nitrate (NO3-), chloride (Cl-), sodium (Na+) and calcium (Ca2+) were identified as the main components of the super-micron mode. The ionic organic compounds (including carboxylic, dicarboxylic and ketoacids) were distributed both between sub-micron and super-micron mode, indicating origin from both gas-to-particle conversion and heterogeneous reactions on pre-existing particles. The total water-soluble ionic organic fraction although accounting for only up to 1-2% of both coarse (> 1 mum) and fine (< 1 mum) mass fractions, accounts for up to 15% of the organic carbon (OC) mass. NH4+ was found to be significantly correlated to non-sea-salt sulfate (nss-SO42+), with NH4+/nss-SO42- molar ratio ranging from 1.3 to 2, the lower ratio associated with transport from the W sector. Chloride depletion was observed mainly during summer and was significantly correlated with NO3- concentrations, with a molar ratio of 0.80, indicating the reaction of nitric acid with NaCl as the main source of NO3- in the area. Total ionic mass both in the fine and coarse fraction accounted for up to 58% of the total aerosol mass during both seasons. An attempt to perform a mass closure analysis indicates that nss-SO42- and organic carbon are the main components of the fine fraction with relative contributions of 38% and 16%, respectively. In the coarse fraction, the ionic part accounts for 58%, mineral dust for 32% and the remaining non-identified part of 12-30% could be partly attributed to water. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:195 / 208
页数:14
相关论文
共 38 条
[1]   ATMOSPHERIC MEASUREMENTS OF PYRUVIC AND FORMIC-ACID [J].
ANDREAE, MO ;
TALBOT, RW ;
LI, SM .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1987, 92 (D6) :6635-6641
[2]  
Andreae T.W., 2002, J GEOPHYS RES, V107, P252
[3]   Carboxylic acids in gas and particulate phase above the Atlantic Ocean [J].
Baboukas, ED ;
Kanakidou, M ;
Mihalopoulos, N .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2000, 105 (D11) :14459-14471
[4]   Elemental carbon-based method for monitoring occupational exposures to particulate diesel exhaust [J].
Birch, ME ;
Cary, RA .
AEROSOL SCIENCE AND TECHNOLOGY, 1996, 25 (03) :221-241
[5]  
CHARLSON RJ, 1991, TELLUS A, V43, P152, DOI 10.1034/j.1600-0870.1991.00013.x
[6]   Carboxylic acids in the troposphere, occurrence, sources, and sinks: A review [J].
Chebbi, A ;
Carlier, P .
ATMOSPHERIC ENVIRONMENT, 1996, 30 (24) :4233-4249
[7]  
Draxler RR, 1998, AUST METEOROL MAG, V47, P295
[8]   Atmospheric aerosol and gaseous species in Athens, Greece [J].
Eleftheriadis, K ;
Balis, D ;
Ziomas, IC ;
Colbeck, I ;
Manalis, N .
ATMOSPHERIC ENVIRONMENT, 1998, 32 (12) :2183-2191
[9]  
ELEFTHERIADIS K, 1999, P 6 C ENV SCI TECHN, VA, P137
[10]   TRANSPORT OF SAHARAN DUST ACROSS THE EASTERN MEDITERRANEAN [J].
GANOR, E ;
MAMANE, Y .
ATMOSPHERIC ENVIRONMENT, 1982, 16 (03) :581-587