Collection of gas and particle semi-volatile organic compounds: use of an oxidant denuder to minimize polycyclic aromatic hydrocarbons degradation during high-volume air sampling

被引:112
作者
Tsapakis, M [1 ]
Stephanou, EG [1 ]
机构
[1] Univ Crete, Dept Chem, Environm Chem Proc Lab, Iraklion 71409, Greece
关键词
polycyclic aromatic hydrocarbons degradation; high-volume sampling; sampling artifacts; ozone denuder; reactivity classification;
D O I
10.1016/j.atmosenv.2003.08.026
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The decomposition of polycyclic aromatic hydrocarbons (PAHs) by ozone in gas and particles, under high-volume sampling, was studied by using in parallel a conventional device and a device protected with an oxidant denuder. Three different sampling regimes-short and long sampling under high-ozone concentration and long sampling under low-ozone concentration-were selected at three representative sampling sites-a boreal forest, an urban site and a background marine station. The results of our study suggest that most PAHs are susceptible to ozone degradation under high ozone atmospheric concentrations (> 50 ppbv) and long sampling times (> 24 h). The highest concentration ratio of total PAHs between the two sampling systems was observed under collection conditions of long sampling and high ozone concentration, especially for the gaseous PAHs (up to 2.10). Conversely, long sampling time under low ozone concentration did not affect the concentration of collected PAHs in the gas or particle phase. The most reactive PAHs collected on filters and polyurethane foam were cyclopentane[cd]pyrene and pyrene, respectively. The use of an oxidant denuder did not affect the PAH gas-particle distribution study. The slopes m, and the intercepts b(r) of the regression between the log K-p and log P-L(0) did not substantially deviate between the two sampling devices. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4935 / 4944
页数:10
相关论文
共 35 条
[1]   HETEROGENEOUS POLYCYCLIC AROMATIC HYDROCARBON DEGRADATION WITH OZONE ON SILICA-GEL CARRIER [J].
ALEBICJURETIC, A ;
CVITAS, T ;
KLASINC, L .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1990, 24 (01) :62-66
[2]   FORMATION OF NITROARENES DURING AMBIENT HIGH-VOLUME SAMPLING [J].
AREY, J ;
ZIELINSKA, B ;
ATKINSON, R ;
WINER, AM .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1988, 22 (04) :457-462
[3]   THE EFFECT OF NITROGEN-DIOXIDE AND OZONE ON THE DECOMPOSITION OF PARTICLE-ASSOCIATED POLYCYCLIC AROMATIC-HYDROCARBONS DURING SAMPLING FROM THE ATMOSPHERE [J].
BRORSTROM, E ;
GRENNFELT, P ;
LINDSKOG, A .
ATMOSPHERIC ENVIRONMENT, 1983, 17 (03) :601-605
[4]   REACTION-RATES OF POLYNUCLEAR AROMATIC-HYDROCARBONS WITH OZONE IN WATER [J].
BUTKOVIC, V ;
KLASINC, L ;
ORHANOVIC, M ;
TURK, J ;
GUSTEN, H .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1983, 17 (09) :546-548
[5]   EXPERIMENTS ON DISTRIBUTION OF ORGANIC POLLUTANTS BETWEEN AIRBORNE PARTICULATE MATTER AND CORRESPONDING GAS-PHASE [J].
CAUTREELS, W ;
VANCAUWENBERGHE, K .
ATMOSPHERIC ENVIRONMENT, 1978, 12 (05) :1133-1141
[6]   LABORATORY INVESTIGATIONS OF THE PARTITIONING OF ORGANOCHLORINE COMPOUNDS BETWEEN THE GAS-PHASE AND ATMOSPHERIC AEROSOLS ON GLASS-FIBER FILTERS [J].
COTHAM, WE ;
BIDLEMAN, TF .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1992, 26 (03) :469-478
[7]   A MULTIPLE-SYSTEM, MULTICHANNEL DIFFUSION DENUDER SAMPLER FOR THE DETERMINATION OF FINE-PARTICULATE ORGANIC MATERIAL IN THE ATMOSPHERE [J].
EATOUGH, DJ ;
WADSWORTH, A ;
EATOUGH, DA ;
CRAWFORD, JW ;
HANSEN, LD ;
LEWIS, EA .
ATMOSPHERIC ENVIRONMENT PART A-GENERAL TOPICS, 1993, 27 (08) :1213-1219
[8]  
*EMEP, 1998, TRANSB PHOT AIR POLL
[9]  
EPA, 1999, EPA/625/R-96/010b
[10]   Air quality model evaluation data for organics.: 5.: C6-C22 nonpolar and semipolar aromatic compounds [J].
Fraser, MP ;
Cass, GR ;
Simoneit, BRT ;
Rasmussen, RA .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1998, 32 (12) :1760-1770