Atmospheric concentrations of PCDD/Fs, dl-PCBs and some pesticides in northern Algeria using passive air sampling.

Two monitoring campaigns were conducted in northern Algeria to assess the contamination level of pesticides and persistent organic pollutants (POPs) in ambient air. Six pesticides (alpha- and gamma-hexachlorocyclohexane, fenitrothion, malathion, chlorpyrifos and lambda-cyhalothrin) were monitored at two different sampling locations during the first campaign. The passive sampling was performed at a semi urban/industrial site but also in a rural area between July to September 2008. The pesticides levels, analyzed by GC/MS/MS, ranged from 16pgm(-3) to 11ngm(-3). The second campaign was carried out from May to November 2009. The polychlorodibenzo-p-dioxins, dibenzofurans (PCDD/Fs) and dioxin-like polychlorinated biphenyls (dl-PCBs) concentrations were evaluated at an urban/industrial and at an industrial site. The PCDD/Fs and dl-PCBs, analyzed by HRGC/HRMS, ranged from 249 to 923fg TEQ m(-3). In addition to passive sampling, active sampling using an isokinetic sampler was also performed at an industrial waste incinerator. The PCDD/Fs and dl-PCBs found was 268pg TEQ m(-3). This paper presents the first measurements of PCDD/Fs, dl-PCBs and pesticides in rural, urban and industrial areas of northern Algeria

Exposure levels and health risk of PAHs associated with fine and ultrafine aerosols in an urban site in northern Algeria

Size distribution of toxicants in airborne particulates remains insufficiently investigated in Algeria. A 1-year campaign was performed at Bab Ezzouar, Algiers (Algeria), aimed at characterizing particulates for their physical and chemical features. For this purpose, scanning electronic microscopy (SEM), Raman spectroscopy (RaS), and GC-MS methodologies were applied. The samples were collected on daily basis by means of a high-volume sampling (HVS) system equipped with cascade impactor separating three size fractions, i.e., particles with aerodynamic diameters d < 1.0 μm (PM1), 1.0 μm <d<2.5 μm (PM2.5), and 2.5 μm <d<10 μm (PM10), respectively. The organic fraction was recovered from substrate through solvent extraction in an ultrasonic bath, separated and purified by column chromatography, then analyzed by gas chromatography coupled with mass spectrometry (GC-MS). Investigation was focused on polycyclic aromatic hydrocarbons (PAHs) and the concentration ratios suitable to investigate the source nature. Further information was drawn from SEM and Raman analyses. Total PAH concentrations ranged broadly throughout the study period (namely, from 4.1 to 59.7 ng m-3 for PM1, from 2.72 to 32.3 ngm-3 for PM2.5 and from3.30 to 32.7 ngm-3 for PM10). Both approaches and principal component analysis (PCA) of data revealed that emission from vehicles was the most important PAH source, while tobacco smoke provided an additional contribution

Exposure levels and health risk of PAHs associated with fine and ultrafine aerosols in an urban site in northern Algeria

Size distribution of toxicants in airborne particulates remains insufficiently investigated in Algeria. A 1-year campaign was performed at Bab Ezzouar, Algiers (Algeria), aimed at characterizing particulates for their physical and chemical features. For this purpose, scanning electronic microscopy (SEM), Raman spectroscopy (RaS), and GC-MS methodologies were applied. The samples were collected on daily basis by means of a high-volume sampling (HVS) system equipped with cascade impactor separating three size fractions, i.e., particles with aerodynamic diameters d < 1.0 μm (PM1), 1.0 μm 2.5), and 2.5 μm 10), respectively. The organic fraction was recovered from substrate through solvent extraction in an ultrasonic bath, separated and purified by column chromatography, then analyzed by gas chromatography coupled with mass spectrometry (GC-MS). Investigation was focused on polycyclic aromatic hydrocarbons (PAHs) and the concentration ratios suitable to investigate the source nature. Further information was drawn from SEM and Raman analyses. Total PAH concentrations ranged broadly throughout the study period (namely, from 4.1 to 59.7 ng m-3 for PM1, from 2.72 to 32.3 ng m-3 for PM2.5 and from 3.30 to 32.7 ng m-3 for PM10). Both approaches and principal component analysis (PCA) of data revealed that emission from vehicles was the most important PAH source, while tobacco smoke provided an additional contribution

Spatial and temporal variations of volatile organic compounds using passive air samplers in the multi-industrial city of Ulsan, Korea

The source-receptor relationship of volatile organic compounds (VOCs) is an important environmental concern, particularly in large industrial cities; however, only a few studies have identified VOC sources using high spatial resolution data. In this study, 28 VOCs were monitored in Ulsan, the biggest multi-industrial city in Korea. Passive air samplers were seasonally deployed at eight urban and six industrial sites. The target compounds were detected at all sites. No significant seasonal variations of VOCs were observed probably due to the continuous emissions from major industrial facilities. Benzene, toluene, ethylbenzene, xylenes, and styrene accounted for 66-86% of the concentration of ??28 VOCs. The spatial distribution of the individual VOCs clearly indicated that petrochemical, automobile, non-ferrous, and shipbuilding industries were major VOC sources. Seasonal wind patterns were found to play a role in the spatial distribution of VOCs. Diagnostic ratios also confirmed that the industrial complexes were the dominant VOC sources. The results of principal component analysis and correlation analyses identified the influence of specific compounds from each industrial complex on individual sites. To the best of our knowledge, this is the first comprehensive report on the seasonal distribution of VOCs with high spatial resolution in a metropolitan industrial city in Korea