Polycyclic aromatic hydrocarbons in diesel exhaust emissions

Samples of diesel exhaust emissions were analysed for eleven polycyclic aromatic hydrocarbons (PAHs) by high performance liquid chromatography (HPLC) with flourescence detection. The PAHs present in the diesel extracts were then represented by a PAH profile with reference to the concentration of benzo(a)pyrene.     

Polycyclic aromatic hydrocarbons in remote mountain lake waters

Polycyclic aromatic hydrocarbons (PAH), including alkylated and sulfur derivatives, were identified and measured in the waters from three European remote mountain lakes during both ice-free and ice covered periods. The measured concentrations were in the same order in all three lakes (700-1100 pg/l). The PAH patterns in both dissolved and particulate water phases were dominated by the low molecular weight compounds (i.e. phenanthrene, fluoranthene and pyrene) in Lakes Redó (Pyrenees) and Gossenk?lle (Alps). In contrast, the high molecular weight (HMW) compounds (i.e. chrysene+triphenylene, benzofluoranthenes, benzo[e]pyrene) were very significant in lake Ovre Ne?dalsvatn (Caledonian). These HMW PAH correspond to mixtures originating from high temperature combustion processes which have been photodegraded during long range atmospheric transport and parallel the PAH mixtures encountered in the underlying lake sediments. In contrast, dissolved PAH exhibit temperature dependence with higher concentrations found at water temperatures below 6-7 degrees C reflecting higher condensation from the atmospheric gas phase reservoir.     

Polycyclic aromatic hydrocarbons in dustfall in Tianjin, China

Atmospheric dustfall samples from 23 locations in Tianjin, China, were collected and analyzed for 16 polycyclic aromatic hydrocarbons (PAHs) classified by the Environmental Protection Agency as priority pollutants from March 2002 to March 2003. SigmaPAH16 (sum of 16 PAH compounds) concentrations in the dustfall collected during heating season ranged from 2.5 to 85.5 mug/g, while that during the non-heating season varied from 1.0 to 48.2 microg/g dry weight. The dominant components in the heating season included naphthalene, phenanthrene, fluoranthene, and chrysene, while naphthalene, fluorene, phenanthrene, and fluoranthene were dominant during the non-heating season. Compared with the non-heating season, the heating season was characterized by a higher fraction of high-molecular-weight PAHs with four to six rings with exception of the samples from the east industrial area. The east industrial area had more significant correlations between individual PAH compounds, and more discrete triangular components of three-, four-, five- and six-ring PAHs. No significant correlations were observed between the PAHs concentrations and total organic carbon (TOC) in the dustfall samples. The deposition fluxes of sigmaPAH15 (sum of 15 PAHs except naphthalene), sigmaPAH6 (sum of 6 carcinogenic PAHs recommended by IARC) and benzo[a]pyrene (BaP) from atmospheric deposition to the whole area were estimated as 1911, 196, and 53 microg/m2/year, respectively. The deposition rates for PAH compounds in the east industrial area were higher than those in the urban and rural areas. Furthermore, the deposition contribution of PAHs during domestic heating season in winter was not significant relative to the annual inputs.     

Polycyclic aromatic hydrocarbons in nearshore marine sediments of Australia.

The occurrence and fate of polycyclic aromatic hydrocarbons (PAH) in nearshore marine sediments of Australia is discussed. Available information indicates that PAH are accumulating in the sediments and organisms of estuaries and harbours with both highly urbanized/industrialized and non-urban catchments. PAH levels in polluted sediments are similar to those of grossly polluted areas of Japan, North America and Europe, however PAH sources cannot be identified from the information available. PAH appear to persist in reducing environments, while in relatively pristine environments that have been previously exposed to PAH, conditions are probably favourable for the aerobic degradation of PAH by microorganisms.     

Polycyclic aromatic hydrocarbons in air samples of meat smokehouses.

In a screening programme nine Danish meat smokehouses were randomly selected for measurements on concentration of airborne polycyclic aromatic hydrocarbons (PAH). A total of 23 stationary air samples were collected during the entire working period of the kiln either above the kiln doors or approximately 2 m in front of the kiln doors (i.e. total exposure on the day of sampling). Three of these samples had a PAH content below the detection limit of the highly sensitive assay employed. Furthermore, eight personal air samples were collected during the periods of tending the kiln (i.e. peak exposure measurement). Three of these samples were below the detection limit. Total airborne PAH concentration of the stationary air samples calculated as the sum of the concentration of 16 selected PAH compounds, was in general far lower than the total airborne PAH concentration measured in the same manner in smokehouses curing fish (Nordholm et al., 1986). In contrast to the study on PAH exposure in smokehouses curing fish, the present study revealed no significant difference between total PAH content in air samples collected above the kilns compared with samples collected approximately 2 m in front of the kiln doors. Calculation of the relative content of the individual PAH compounds in the stationary air samples collected in meat smokehouses showed naphthalene to be the major compound in (70% +/- 26% of total PAH), whereas the relative content of carcinogenic PAH compounds in average represented 4.0% of the total PAH content. However, only approximately 15% of the stationary air samples with detectable content of total PAH contained detectable amounts of carcinogenic PAH compounds. Hence it was concluded that PAH exposure during cold meat curing might be considered a limited health hazard compared with PAH exposure during hot fish curing.     

Polycyclic aromatic hydrocarbons: levels and phase distributions in preschool microenvironment

This work aims to characterize levels and phase distribution of polycyclic aromatic hydrocarbons (PAHs) in indoor air of preschool environment and to assess the impact of outdoor PAH emissions to indoor environment. Gaseous and particulate (PM₁ and PM_2.5) PAHs (16 USEPA priority pollutants, plus dibenzo[a,l]pyrene, and benzo[j]fluoranthene) were concurrently sampled indoors and outdoors in one urban preschool located in north of Portugal for 35 days. The total concentration of 18 PAHs (ΣPAHs) in indoor air ranged from 19.5 to 82.0 ng/m³; gaseous compounds (range of 14.1–66.1 ng/m³) accounted for 85% ΣPAHs. Particulate PAHs (range 0.7–15.9 ng/m³) were predominantly associated with PM₁ (76% particulate ΣPAHs) with 5‐ring PAHs being the most abundant. Mean indoor/outdoor ratios (I/O) of individual PAHs indicated that outdoor emissions significantly contributed to PAH indoors; emissions from motor vehicles and fuel burning were the major sources.     

Polycyclic aromatic hydrocarbons in storm runoff from urban and coastal South Carolina

Stormwater runoff was collected in urbanized areas of South Carolina to investigate the levels and sources of polycyclic aromatic hydrocarbons (PAHs). Mean concentrations of total PAHs in runoff (sum(PAHs), 14 compounds), determined by gas chromatography-mass spectrometry, were 5590 ng/l in the city of Columbia and 282 ng/l in the coastal community of Murrells Inlet. Lower concentrations were found in estuarine water at Murrells Inlet (mean = 35 ng/l) and at undeveloped North Inlet estuary (13 ng/l). The PAH profiles in Columbia and Murrells Inlet runoff were similar to those of atmospheric particulate matter and unlike those in used crankcase oil. Examination of the aliphatic fraction of Columbia runoff samples by gas chromatography with flame ionization detection showed patterns that were more similar to used crankcase oil than to urban aerosols.     

Polycyclic aromatic hydrocarbons inside and outside of apartments in an urban area

In the context of environmental monitoring in Berlin polycyclic aromatic hydrocarbon (PAH) concentrations in air and household dust were measured inside 123 residences (and simultaneously in a sub group in the air outside the windows). The aim of this study was to determine exposure to PAHs in the environment influencing by several factors, for instance, motor vehicle traffic in a populous urban area. Indoor air samplings were carried out in two periods (winter and spring/summer) in smokers and non-smokers apartments. Benzo(a)pyrene (BaP) median values were 0.65 ng m(-3) (winter) and 0.27 ng m(-3) (spring/summer) in smokers' apartments and 0.25 ng m(-3) (winter) and 0.09 ng m(-3) (spring/summer) in the apartments of non-smokers. The median BaP content in ambient air was 0.10 ng m(-3) (maximum: 1.1 ng/m(-3)) with an indoor-outdoor mean concentration ratio of 0.9 in non-smoker households and 5.4 in smoker apartments. In household dust we obtained median values of 0.3 mg kg(-1) (range: 0.1-1.4 mg kg(-1)). We found a significant relation between indoor and outdoor values. Approximately 75% of the variance of indoor air values was caused by the corresponding BaP concentrations in the air outside the apartment windows. Otherwise a significant correlation between indoor air and household dust values cannot be found. Therefore, according to our results, it is suggested that the indoor PAH concentration in non-smoker apartments could be attributed mainly to vehicular emissions.     

Polycyclic aromatic hydrocarbons, elemental and organic carbon emissions from tire-wear

Tire-wear is an important source of PAHs, elemental carbon (EC) and organic carbon (OC). The emissions of these pollutants have been studied in an experimental set-up, simulating a realistic road-tire interaction (summer tire-concrete road). The large particle non-exhaust emissions (LPNE; diameter greater than 10 μm) have been evaluated over 14,500 km run of the tire. An increasing linear trend with cumulative km run was observed for emissions of PAHs and carbon. Amongst PAHs in LPNE, pyrene has been observed to be the highest (30 ± 4 mg kg^− 1) followed by benzo[ghi]perylene (17 ± 2 mg kg^− 1). Different fractions of EC-OC for tire-wear have been analyzed, and unlike exhaust emissions, EC1 was observed to be 99% of EC whereas more than 70% of the OC was the high temperature carbon (OC3 and OC4). The overall emission factors (mass tire^− 1 km^− 1) for PAHs, EC and OC from tire-wear are 378 ng tire^− 1 km^− 1, 1.46 mg tire^− 1 km^− 1 and 2.37 mg tire^− 1 km^− 1 for small cars.     

Polycyclic aromatic hydrocarbons (PAHs) in agricultural soil and vegetables from Tianjin

Several types of vegetables were collected from two contaminated sites in Tianjin, China. The bulk soil and the rhizosphere soil samples were also collected from the same plots. Sixteen PAHs in the samples were measured. The total concentrations of PAH16 in the bulk soil from the two sites were 1.08 and 6.25 microg/g, respectively, with similar pattern. The concentrations of PAH16 and individual compounds in the rhizosphere were significantly higher than those in the bulk soil with mean values of 2.25 and 7.82 microg/g for the two sites, respectively. The contents of both total and dissolved organic matter in the rhizosphere were also higher than those in the bulk soil. Almost all PAH compounds studied were detected in both roots and aerial parts of the vegetables studied. Abundance of higher molecular weight PAHs in vegetable, however, was lower than that in soil. Concentrations of PAH16 in vegetable were higher than those reported in the literature for other areas. It appears that agricultural soils and vegetables in Tianjin, especially those from the site located immediately next to an urban district and irrigated with wastewater for several decades, are severely contaminated by PAHs. Among the eight types of vegetable studied, the highest concentration of PAHs was found in cauliflower. By average, the concentration of PAH16 in the aerial part of vegetables was 6.5 times higher as that in vegetable root, suggesting that foliar uptake is the primary transfer pathway of PAHs from environment to vegetables.     

Polycyclic aromatic hydrocarbons associated with particles in ambient air from urban and industrial areas

This study takes into consideration an analysis of the chemical polycyclic aromatic hydrocarbon (PAH) profile and its distribution in inhalable and respirable particulate matter in urban and industrial areas in La Plata, Argentina, and Leipzig, Germany. Representative samples from three locations in La Plata (industrial, traffic influenced and control area) and two locations in Leipzig (traffic influenced and control area) were obtained in summer and winter. The sampling of particulate matter was carried out with high volume collectors using cascade impactors to separate six size fractions. PAHs were extracted with hexane through a solid-liquid equilibrium extraction and analysed by HPLC/UV/fluorescence detection. The results showed a PAH seasonal behaviour in both regions, with lower contents in summer and higher ones in winter. Highest concentrations of total PAHs were found in the industrial area in La Plata. The size distribution of particles demonstrates the greater relevance of smaller particles. More than 50% of PAHs were associated with particles of less than 0.49 microm. Moreover, this particle size fraction was associated with traffic, whereas other sources of combustion were related also to particles between 0.49 and 0.95 microm. Considering the ratio of benzo(ghi)perylene (BgP)/benzo(a)pyrene (BaP) as an indicator for traffic influence, it was observed that La Plata City was more affected than Leipzig by the same proportion in summer and in winter. The BgP/InP (indeno(123-cd)pyrene) ratio was lower in winter than in summer in both places and indicates the presence of domestic combustion sources. It is important to point out the significance of using fingerprint compound ratios to identify possible sources of pollution with PAHs bound to particles.     

Polycyclic aromatic hydrocarbons in petroleum products for medicinal and cosmetic uses — analytical procedure

Two methods for extraction and determination of benzo[a]pyrene and other PAH in liquid and white soft paraffins, widely used for medicinal and cosmetic purposes, are compared. A method based on extraction by frontal elution chromatography, column and thin-layer chromatography and final spectrophotofluorometric determination gave the best results in the determination of the very low levels (ng/g) of PAH present in these fully refined samples. The complete analytical procedure showed an acceptable percentage of recoveries and good applicability to routine analysis of the PAH content in these petroleum products for the proper evaluation of their potential hazards to human health.     

Polycyclic aromatic hydrocarbons in fish from remote and high mountain lakes in Europe and Greenland

Polycyclic aromatic hydrocarbons (PAHs) were analysed in liver of fifty-seven individual trout distributed among seven high mountain lakes in Europe and one remote lake in Greenland. In all cases, very similar distributions were observed in which phenanthrene largely predominated and fluoranthene and pyrene were the second major compounds. These distributions were similar to those observed in the dissolved fraction of the waters studied in three of these lakes. The range of concentrations of PAH in fish liver show only a five-fold variation, which is considerably smaller than the range more than two orders of magnitude of sedimentary PAH concentrations of these lakes. No correlation between PAH content in sediments and fish liver has been found both at the level of total and individual compounds. However, lake site is the main statistically significant factor of variability between PAH concentrations in fish liver. Changes in fish species explain significant differences in liver content of some PAHs. Within lake, condition factor and liver concentration are inversely correlated. Female fish display lower average concentrations than male in all lakes but the differences are not statistically significant. No correspondence between fish age and PAH content has been observed.     

Polycyclic aromatic hydrocarbons in soil and plant samples from the vicinity of an oil refinery

Soil samples, and samples of leaves of Plantago major (great plantain) and grass (mixed species) were collected from the vicinity of an oil refinery in Zelzate, Belgium, and analysed for seven polycyclic aromatic hydrocarbons (PAHs). The samples from the site adjacent to the refinery (site 1) contained very high total PAH-concentrations: namely 300, 8 and 2 microg/g dry wt. for soil, P. major and grass, respectively. Concentrations in samples from more remote sites (up to 4 km from the refinery) were a factor of 10-30 lower than those from site 1, but between them the differences were small. The PAH-profiles of the plant samples, in contrast with those of the soil samples, appeared to shift to higher contributions of gaseous PAHs with increasing distance from the refinery. This can be explained by particle-bound PAHs being deposited closer to the source than gaseous PAHs. It is suggested that particle-bound deposition is relatively more important for deposition to soil than to plants, due to blow-off and wash-off of the compounds from the leaves. The total PAH-concentrations in the leaves of P. major were higher than those measured in the grass samples, probably due to differences in aerodynamic surface roughness, leaf orientation and/or leaf age. However, the concentration ratios of P. major/grass were not constant for the different sites, varying from 1.2 to 8.8. Therefore, it appears that a precise prediction of PAH-concentrations for one plant species from known concentrations of another species is not possible. When errors in predicted concentrations need to be smaller than a factor of approximately 10, the sampling strategy has to be focussed on all species of interest.     

Polycyclic aromatic hydrocarbons (PAH) in some algae and invertebrates from moderately polluted parts of the coast of Norway

Analysis of PAH in mussels, snails, other invertebrates and algae demonstrated that PAH often were present even in areas far from any specific sources. In samples with distinct PAH profiles, 20–30 compounds were identified and quantitated by means of glass capillary gas chromatography. Total PAH concentrations were mostly in the range 0.3–3 mg kg⁻¹ dry weight, in a few cases up to 12 mg kg⁻¹. Supposedly cancerogenic species usually constituted less than 5% of the total, benzo(a)pyrene rarely more than 0.5–1%. In most, but not all cases, the variation in PAH levels were explainable in terms of difference in general diffuse loading at the localities investigated. The results agree fairly well with previous investigations in moderately polluted or pristine areas in other parts of the world. PAH profiles were somewhat differing from one species to another at the same locality. Thus the use of more than one indicator species often is recommendable. The potential conflict between mariculture and elevated PAH levels is briefly discussed.     

Polycyclic aromatic hydrocarbons, nickel and vanadium in air particulate matter in Bahrain during the burning of oil fields in Kuwait.

Inhalable air particulate matter (APM) was collected in Bahrain from July 31, 1991 to August 4, 1991, during the burning of the oil fields in Kuwait. The filters collected were black and the levels of APM ranged from 139 to 673 micrograms m-3 with an average value of 199 micrograms m-3. APM were analysed for their contents of PAHs, Ni and V. Analysis was carried out for 32 PAHs and total PAHs ranged from 3.1 to 9.1 ng m-3 and averaged 5.3 ng m-3. The highest individual PAH levels were benzo[ghi]perylene, benzo[b]fluoranthene, benzo[a]pyrene and indeno[1,2,3-cd]pyrene. The concentration of Ni and V ranged from 7 to 42 and 11 to 42 ng m-3, with an average value of 22 and 26 ng m-3, respectively. A strong correlation was found between Ni and V (r = 0.98, P less than 0.01). The results show that the smoke from burning oil wells in Kuwait has contributed to the concentrations of particulate matter, PAHs, Ni and V in APM in Bahrain.     

Polycyclic aromatic hydrocarbons (PAHs) in bottom sediments of the Kara Sea shelf,Gulf of Ob and Yenisei Bay

PAH concentration and distribution has been examined in surface sediments samples from the Kara Sea, Russia. The study includes 13 samples from the South-eastern Kara Sea shelf, one sample from the south-western part of the sea, 4 samples from the Baydaratskaya Bay, 5 samples from the Gulf of Ob and 4 samples from the Yenisei Bay, collected in August-September 1993-1994. Cluster analysis and principal component analysis (PCA) were used to identify common patterns and possible sources of PAHs. The total PAH concentration (sum of two- to six-ring aromatic hydrocarbons) in the Kara Sea sediments was generally lower than in the Barents Sea sediments and comparable to the levels in the Pechora and White seas. Two- and three-ring aromatic hydrocarbons predominated in Kara Sea sediments, which indicate a relatively stronger petrogenic origin than that in the adjacent seas. The highest total PAH concentrations within the Kara Sea were found in sediments from the Yenisei Bay and in the South-western part of the Kara Sea in the Eastern Novaya Zemlya Trough. The PAHs of the Yenisei Bay sediments were dominated by perylene and PAHs of petrogenic origin, but had also a strong indication of PAHs of pyrogenic origin. The dominating PAH group in the South-western part of the Kara Sea were four- to six-ring aromatic hydrocarbons, indicating pyrogenic origin. Perylene levels were high in all the Kara Sea samples, and highest levels were found in areas of strong terrigenous influence. The most probable source is decaying peat products being transported to the Kara Sea by both large and small rivers.     

Photolysis of polycyclic aromatic hydrocarbons in water

The decomposition of benzo[a]pyrene (BAP), chrysene (CHR) and fluorene (FLU) in an aqueous solution by means of photolysis has been studied. The influence of initial polycyclic aromatic hydrocarbons' (PAHs) concentration, pH of the reaction mixture, temperature, presence of oxygen and tert-butyl alcohol (t-BuOH) on the degradation rate has been observed. BAP and CHR are decomposed by a mechanism different than FLU. Quantum yields of the photolytic decomposition of BAP, CHR and FLU were determined and equal 0.014, 0.0031 and 0.0038, respectively.     

Polycyclic aromatic hydrocarbons in soil and surface marine sediment near Jubany Station (Antarctica). Role of permafrost as a low-permeability barrier

Although Antarctica is still considered as one of the most pristine areas of the world, the growing tourist and fisheries activities as well as scientific operations and their related logistic support are responsible for an increasing level of pollutants in this fragile environment. Soils and coastal sediments are significantly affected near scientific stations particularly by polycyclic aromatic hydrocarbons (PAHs). In this work sediment and soil were sampled in two consecutive summer Antarctic expeditions at Potter Cove and peninsula, in the vicinity of Jubany Station (South Shetland Islands). Two- and 3-ring PAHs (methylnaphthalene, fluorene, phenanthrene and anthracene) were the main compounds found in most sites, although total PAH concentrations showed relatively low levels compared with other human-impacted areas in Antarctica. Pattern distribution of PAHs observed in samples suggested that low-temperature combustion processes such as diesel motor combustion and open-field garbage burning are the main sources of these compounds. An increase in PAH concentrations was observed from surface to depth into the active soil layer except for a unique sampling site where a fuel spill had been recently reported and where an inverted PAH concentration gradient was observed. The highest level was detected in the upper layer of permafrost followed by a sharp decrease in depth, showing this layer is acting as a barrier for downward PAH migration. When PAH levels in soil from both sampling programs were compared a significant decrease (p<0.01) was observed in summer 2005 (range at 75-cm depth: 12+/-1-153+/-22 ng/g) compared to summer 2004 (range at 75-cm depth: 162+/-15-1182+/-113 ng/g) whereas concentrations in surface sediment collected nearby the station PAHs increased drastically in 2005 (range: 36+/-3-1908+/-114 ng/g) compared to 2004 (range: 28+/-3-312+/-24 ng/g). Precipitation regime and water run off suggest that an important wash out of soil-PAHs occurred during the interval time between samplings. Results showed that the present PAH contamination level of Jubany Station is relatively low compared to other reported cases in Antarctica but also suggests that an increase in rain and in thawing processes caused by the global warming could result in an important soil-associated PAH mobilization with unpredictable consequences for the biota of Potter Cove.     

Polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs) in sediments from the Mersey Estuary, U.K

Sediments from the Mersey Estuary were analysed for polycylic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs). Total PAH concentrations ranged from 626 to 3766 microg/kg and total PCB concentrations ranged from 36 to 1409 microg/kg. These concentrations are intermediate in comparison to other U.K estuaries with similar histories of industrialisation and urbanisation. The distribution of individual PAHs were consistent throughout the Mersey Estuary, this together with molecular indices suggests mainly pyrolitic inputs, augmented by a variety of industrial petrogenic sources. Comparison of tri-to-hepta PCB congeners revealed multiple sources and inputs throughout the estuary. A sediment core collected in close proximity to Garston Docks revealed the take-off, peak pollutant input and recent decline of PCB pollution. However, a second depth profile of sediments at Ellesmere Port showed little change in total or individual PCB concentrations due to extensive sediment reworking and mixing.