Water-soluble organic compounds (WSOC) from atmospheric aerosols in Bou-Ismail (Algeria).

In this contribution, we report the study of nuclear resonance magnetic spectroscopy techniques (1H-NMR, 13C-NMR, and 2D-NMR) efficiency in the characterisation of the functional composition of water-soluble organic compounds (WSOC) from atmospheric aerosols. The chosen site was our scientific and technical center of research (CRAPC) situated in Algerian Bou-Ismail city. where the concentrations of PM10 were found to be between 15.66 and 142.19 µg.m-3. As results, 1H-NMR analysis showed the coexistence of biological material and emissions from urban and biomass burning. The dominant source was identified by quantitative integration of each 1H NMR spectral region. By using the HSQC technique, many peaks are revealed in biogenic samples including biomass burning. On the other hand, the identification of the source of various organic compounds and their functional composition is possible through specific NMR spectra, which can also be used to adjust the surrounding organic aerosol sources.

Sources of PM10 ionic species in the South-West Mediterranean (Algeria).

The contents of water-soluble major's ions (MSA, Cl-, NO3-, SO42-, Na+, NH4+, K+, Mg2+, and Ca2+) in the PM10 particle fraction were investigated thanks to detailed measurements of the main chemical constituents of PM10 in remote coastal areas in Bou-Ismail; in the South-West of the Mediterranean Sea (Algeria), during a 2-year period; from July 2011 to August 2013, under the framework of the ChArMEx project (Chemistry-Aerosol Mediterranean Experiment, http://charmex.lsce.ipsl.fr ). The total water-soluble ion concentrations in PM10 at the Bou-Ismail measurement station varied from 3.3 µg/m3 (July 2011) to 49.6 µg/m3 (March 2012). The annual mean mass concentrations of ions in the PM10 particulate fraction were Cl- > Na+ > SO42- > Mg2+ > NO3- > Ca2+ > K+ > NH4+ > Oxalate. The change in potassium nss-K + concentrations in PM10 over the course of a year reveals that biomass burning (BB) has an effect on three separate seasons: the beginning of winter (February and March), the end of summer (August), and the autumn (September and October). The origin periods of biomass burning BB identified employing the mapping of hotspots and fires during periods of August and September 2011, 2012, and 2013 underlined the important fires in the surrounding areas of the Mediterranean Sea (Sardinia Islands from Italy, Corsica from France).

Chemical characterization of fine particles (PM2.5) at a coastal site in the South Western Mediterranean during the ChArMex experiment.

As part of the ChArMEx project (Chemistry-Aerosol Mediterranean Experiment, http://charmex.lsce.ipsl.fr), one year of continuous filter sampling was conducted from August 2012 to August 2013 at a rural (coastal) site in Algeria aiming to better document fine aerosol seasonal variability and chemical composition in the Southern part of the Mediterranean. Over 350 filters have been collected, weighted, and analyzed for the main ions and organic and elemental carbon. The obtained mass concentrations varied between 2.5 and 50.6 µg/m3 for PM2.5. The annual modulations of PM2.5 showed higher concentrations in the end summer 2012 and the early summer 2013 (28.50 µg/m3 in August 2012, 20.23 µg/m3 in September 2012, 20.19 µg/m3 in July 2013, and 17.88 µg/m3in August 2013). The particulate organic matter (POM) presented the greatest contribution (50%), followed by the secondary inorganic aerosols (SIA, 27%). The average organic carbon OC concentrations ranged from 1.66 to 6.05 µgC/m3. The average elemental carbon EC concentrations ranged from 0.92 to 3.49 µgC/m3 and contributed 7% of the PM2.5 mass to Bou-Ismail. The average value of the OC /EC ratio was close to 5.1 in Bou-Ismail, and was close to that found in Finokalia 4 (Greece 2004, 2006) but was lower than that of Montseny 11 (Spain 2002-2007) Western Mediterranean Basin (WMB). The concentrations of water-soluble organic carbon WSOC in the PM2.5 ranging from 0.66 to 3.70 µg/m3 recorded the minimum level in March 2013, and the maximum level in August 2012, with an average of 2.02 µg/m3.

Polycyclic aromatic hydrocarbons, phthalates, parabens and other environmental contaminants in dust and suspended particulates of Algiers, Algeria.

Chemicals such as polycyclic aromatic hydrocarbons (PAHs), phthalateesters, parabens, siloxanes and squalene, all of them classified as endocrine-disrupting chemicals (EDCs), have been reported to occur in all environmental compartments. The effects of EDCs on development, reproduction, growth, metabolism and obesity constitute a real public health issue. A list of EDCs (> 40 compounds) were characterised in total suspended particulates (outdoor soot: 92 samples) collected in July-September 2016 in an Algiers urban area; besides, settled indoor dusts (36 samples) were collected between November and December 2016 in schools, homes, manufacture and hospital of the same province. The analytical procedure consisted of ultrasonic bath extraction, column chromatography separation into fractions of different polarity and gas chromatographic-mass spectrometric processing. The total loads of phthalates ranging from 6.0 to 347 ng/m2 (median, 26 ng/m2) were determined in indoor dust and 4.6 to 11.6 ng/m3 (median, 7.9 ng/m3) in outdoor soot; meanwhile, PAHs ranged from 12.1 to 108 ng/m2 (median, 36 ng/m2) in indoor dust and ranged from 5.6 to 7.7 ng/m3 (median 5.7 ng/m3) in outdoor soot. Finally, illicit substances such as cocaine, cannabinol and Δ9-tetrahydrocannabinol were found to range from 0.5 to 11 pg/m3, 4.6 to 9.2 pg/m3 and 11 to 81 pg/m3, respectively, in outdoor soot.

Assessment of dioxin-like activity in PM10 air samples from an industrial location in Algeria, using the DRE-CALUX bioassay.

When compared to the European guidelines, PM10 (particulate matter up to 10-µm size) concentrations in Algeria are often exceeding the maximum limits, and in general, no information exists on the compounds bound on its surface. The objective of this study was to measure the dioxin-like activity of polychlorinated dibenzodioxines and dibenzofurans (PCDD/Fs) and dioxin-like polychlorinated biphenyls (PCBs) in the PM10 fraction at the Sour El Ghozlane cement plant in Algeria. PM10 samples (n = 23) were taken between 24 March and 15 April 2013, using a medium volume sampler and 47-mm PTFE filters. The 24-h samples were dried to determine the PM10 content and afterward extracted, cleaned up, and analyzed with the dioxin-responsive element-chemical-activated luciferase gene expression (DRE-CALUX) bioassay. Our results showed that the measured bioanalytical equivalents (BEQs) were similar to those in other international industrial sites worldwide. The PCDD/Fs and dioxin-like PCBs (dl-PCBs) were positively correlated (rho = 0.6, p = 0.002), indicating that they have similar sources. Furthermore, samples from March showed higher PCDD/F and dl-PCB BEQs and humidity but lower temperatures compared to samples from April, while there was no difference in the PM10 concentrations between the two months. These results reveal that PM10 alone is not a good proxy and that meteorological conditions are an important factor in assessing dioxin-like pollution in the atmosphere. It seems that, at present, there is no health hazard through direct airborne human exposure to dioxin-like pollutants in PM10 from this site. However, it is important to monitor these POPs for a longer period of time and also to gain more insight in their distribution between the particulate and gas phase in relation to meteorological conditions.

Biogenic and anthropogenic organic components of Saharan sands.

Till now, the Sahara desert sands have scarcely characterized for their organic contents, despite they are known to heavily affect Europe and America when transported by winds. In this study, the composition of sands collected in ten oasis lying in two regions of the Algerian Sahara during 2011 was investigated with regards to organic fraction. Attention was paid to anthropogenic and biogenic sources of organics associated to sands, through the characterization of n-alkanes, n-alkanoic and n-alkanedioic acids, n-alkanols, sterols, PAHs and caffeine. The organic fraction load on sands associable to natural sources was higher in the Region of Biskra than in that of Ouargla. The biogenic contribution to the total amount of organics in sands exceeded that of the anthropogenic sources. The composition of sands from Hassi Messaoud, compared to that observed there in 2006, showed that the anthropic impact over the region was not changed.

A wintertime study of polycyclic aromatic hydrocarbons (PAHs) in indoor and outdoor air in a big student residence in Algiers, Algeria.

The wintertime concentrations and diel cycles of n-alkanes and polycyclic aromatic hydrocarbons (PAHs) associated to atmospheric particulate matter with aerodynamic diameter lesser than 10 µm were determined at the biggest student residence in Algeria located in Bab-Ezzouar, 15 km southeast from Algiers city area. Samplings were carried out from December 2009 to March 2010, and organic compounds were characterized using gas chromatography coupled with mass spectrometric detection. Volatile PAHs were also monitored inside some student residence rooms in order to evaluate the impact of indoor air pollution to student health. For the sake of comparison, aerial concentrations of n-alkanes and PAHs were determined in parallel in the Oued Smar industrial zone and two suburban areas, all located in Algiers. Total concentrations recorded in CUB1 student residence ranged from 101 to 204 ng m(-3) for n-alkanes and from 8 to 87 ng m(-3) for PAHs. Diel cycles have shown that, while concentrations of n-alkanes peaked at morning and afternoon-evening and dropped at night, those of PAHs exhibited higher levels at morning and night and lower levels at afternoon-evening, likely due to the reactivity of some PAHs. As expected, the indoor levels of PAHs were larger than in the outdoor of the student residence and were of serious health concern. Overall, the concentrations of n-alkanes and PAHs were as high as those observed in the industrial zone and higher than the two suburban sites.

Organic components of Algerian desert dusts.

The organic fraction associated to sands of five localities of Algerian Sahara Desert was characterized with regards to n-alkanes, polynuclear aromatic hydrocarbons (PAH) and mono/dicarboxylic acids. Huge differences were observed among total contents of the three groups in the sands and, within each group, with regard to percent distribution patterns of congeners. Mutagenic nitro-PAH were virtually absent. Organic acids were identified as the most abundant compounds in all samples (up to 4800 ng g(-1) vs. less than 700 of n-alkanes and 22 ng g(-1) of PAH); their presence was overall related to biogenic sources except for the Hassi Messaoud petroleum area, where an important contribution of anthropogenic emission was present. The sand composition at Hassi Messaoud (and, at lesser extent, Tougguort) seemed to indicate that environmental conditions promote there the oxidative decomposition of organics; by contrast, at Laghouat, Hassi Bahbah and Gardaïa oases the deposition involved fresh (non-reacted) air pollutants. The sand composition at the Hassi Messaoud was compared to that of airborne particulates of the industrial district and city. Airborne n-alkanes (≈500 ng m(-3)) and fatty acids (≈15000 ng m(-3)) were very high compared to Algiers city, whilst PAH contents (10-60 ng m(-3)) were typical of polluted areas in winter; similarly, the sands were reach of the two aliphatic groups and relatively poor of PAH.

Distribution of the solvent-extractable organic compounds in fine (PM1) and coarse (PM1-10) particles in urban, industrial and forest atmospheres of Northern Algeria.

The distribution of the solvent-extractable organic components in the fine (PM(1)) and coarse (PM(1-10)) fractions of airborne particulate was studied for the first time in Algeria. That was done during October 2006 concurrently in a big industrial district, a busy urban area, and a forest national park located in Algiers, Boumerdes, Blida, respectively, which are the three biggest provinces of Northern Algeria. Most of the organic matter identified in both particle size ranges consisted of n-alkanes and n-alkanoic acids, with minor contributions coming from polycyclic aromatic hydrocarbons (PAHs), nitrated polycyclic aromatic hydrocarbons (NPAHs), oxygenated PAHs, and other polar compounds (e.g., caffeine and nicotine). The potential emission sources of airborne contaminants were reconciled by combining the values of n-alkane carbon preference index (CPI) and selected diagnostic ratios of PAHs, calculated in both size ranges. The mean cumulative concentrations of PAHs reached 3.032 ng m(-3) at the Boumerdes site, urban, 80% of which (i.e. 2.246 ng m(-3)) in the PM(1) fraction, 6.462 ng m(-3) at Rouiba-Réghaia, industrial district, (5.135 ng m(-3) or 80% in PM(1)), and 0.512 ng m(-3) at Chréa, forested mountains (0.370 ng m(-3) or 72% in PM(1)). Similar patterns were shown by all organic groups, which resulted overall enriched in the fine particles at the three sites. Carcinogenic and mutagenic potencies associated to PAHs were evaluated by multiplying the concentrations of "toxic" compounds times the corresponding potency factors normalized vs. benzo(a)pyrene (BaP), and were found to be both acceptable.