Atmospheric concentrations, dry deposition and air-soil exchange of polycyclic aromatic hydrocarbons (PAHs) in an industrial region in Turkey

Concurrent ambient air and dry deposition samples were collected during two sampling periods at the Aliaga industrial region in Izmir, Turkey. Sigma 15-PAH (particulate+gas) concentrations ranged between 7.3 and 44.8 ng m(-3) (average+/-S.D., 25.2+/-8.8 ng m(-3)) and 10.2-71.9 ng m(-3) (44.1+/-16.6 ng m(-3)) in summer and winter, respectively. Winter/summer individual ambient PAH concentration ratios ranged between 0.8 (acenaphthene) and 6.6 (benz[a]anthracene) indicating that wintertime concentrations were affected by residential heating emissions. In contrast to the ambient concentrations, summation operator(15)-PAH particle dry deposition fluxes were higher in summer (5792+/-3516 ng m(-2)day(-1), average+/-S.D.) than in winter (2650+/-1829 ng m(-2)day(-1)), probably due to large particles from enhanced re-suspension of polluted soil particles and road dust. Average overall dry deposition velocity of PAHs calculated using the dry deposition fluxes and particle-phase concentrations was 2.9+/-3.5 cm s(-1). summation operator(15)-PAH concentrations in soils taken from 50 points in the area ranged between 11 and 4628 microg kg(-1) in dry weight. The spatial distribution of these concentrations indicated that the urban Aliaga, steel plants, the petroleum refinery, and the petrochemical plant are the major Sigma 15-PAH sources in the area. Fugacity calculations in air and soil showed that the soil acts as a secondary source to the atmosphere for low molecular weight PAHs in summer and as a sink for the higher molecular weight ones in summer and winter.     

色谱-质谱联机测定厦门港和员当湖表层沉积物中的石油烃和多环芳香烃的含量

2002年4月厦门港沿岸设九个站,员当湖设两个站采集表层积物,用有机溶剂萃取,硅胶柱色层分离,气相色谱-质谱联机带SIM数据采集系统对样品的石油烃类(M/Z=55),多环芳香烃类(15个典型的多环芳香烃,9个甲基化多环芳香烃作外标)进行分析,结果显示员当湖石油烃和多环芳香浓度分别高达1397微克/克(干)和1376.5纳克/克(干)。厦门港沉积物石油烃和多环芳香浓度范围为:石油烃133.3～943.3微克/克(干)多环芳香烃97.6～308.5纳克/克(干)。厦门港船只活动,厦门港四周工业废水、车辆燃油滴漏是石油烃污染的主要来源。厦门工业用煤、用油、生活用煤及船只、车辆燃料泄漏是沉积物多环芳香烃的主要来源,其工业排废、生活废水排放,市区雨水冲刷和大气灰尘沉降是多环芳香烃进入海湾的主要途径。     

Degradation of polycyclic aromatic hydrocarbons by the Chilean white-rot fungus Anthracophyllum discolor

The degradation of three- and four-ring polycyclic aromatic hydrocarbons (PAHs) in Kirk medium by Anthracophyllum discolor, a white-rot fungus isolated from the forest of southern Chile, was evaluated. In addition, the removal efficiency of three-, four- and five-ring PAHs in contaminated soil bioaugmented with A. discolor in the absence and presence of indigenous soil microorganisms was investigated. Production of lignin-degrading enzymes and PAH mineralization in the soil were also determined. A. discolor was able to degrade PAHs in Kirk medium with the highest removal occurring in a PAH mixture, suggesting synergistic effects between PAHs or possible cometabolism. A high removal capability for phenanthrene (62%), anthracene (73%), fluoranthene (54%), pyrene (60%) and benzo(a)pyrene (75%) was observed in autoclaved soil inoculated with A. discolor in the absence of indigenous microorganisms, associated with the production of manganese peroxidase (MnP). The metabolites found in the PAH degradation were anthraquinone, phthalic acid, 4-hydroxy-9-fluorenone, 9-fluorenone and 4,5-dihydropyrene. A. discolor was able to mineralize 9% of the phenanthrene. In non-autoclaved soil, the inoculation with A. discolor did not improve the removal efficiency of PAHs. Suitable conditions must be found to promote a successful fungal bioaugmentation in non-autoclaved soils.     

Characterization of PM10 fraction of road dust for polycyclic aromatic hydrocarbons (PAHs) from Anshan, China

Nineteen road dust samples were collected during 2005 in different parts of the urban area of Anshan, Liaoning Province, China, and 11 polycyclic aromatic hydrocarbons (PAHs) species were quantitatively analyzed using GC–MS. The results indicated that the total average concentration of PAHs over the investigated sites ranged from 48.73 to 638.26 μg/g, with a mean value of 144.25 μg/g, higher than the concentrations measured in previous studies. PAHs concentrations were higher with high molecular weight homologues (4–6 rings PAHs), accounting for 83.24–96.98%, showing combustion of petroleum fuels was a potential source. Organic carbon in road dust was considered one of the important factors that influenced the concentrations of PAHs in this study, and it was found that concentrations of total PAHs were correlated with those of organic carbon in road dust. The results of diagnostic ratios analysis showed traffic emission (gasoline or diesel) was one of the most important sources of road dust PAHs. Principal component analysis (PCA) indicated that the major sources of road dust PAHs might be emission from traffic, steel industry, cooking and coal combustion.     

A wintertime study of polycyclic aromatic hydrocarbons in PM(2.5) and PM(2.5-10) in Beijing: assessment of energy structure conversion

Sixteen priority polycyclic aromatic (PAHs) in PM(2.5) and PM(2.5-10) samples collected from 20 sites in Beijing, China in December 2005 and January 2006 were analyzed to determine the composition, spatial distribution and sources. Total PAHs of PM(2.5) and PM(2.5-10) ranged from 5.2 to 1062.2 ng m(-3) and 7.6 to 759.7 ng m(-3), respectively, categorized as heavier pollution. Among five kind of functional zones involved, industrial center, commercial area and village were heavily polluted. The mean concentration of PAHs in PM(2.5) of 407 ng m(-3) was 1.67-fold of that in PM(2.5-10), which was relatively high compared to the previous studies (winter in 2001 and 2002). The most evident change was the increase of Flu, BbkF and InP, which are believed to be less harmful and related to the increasing use of clean energy. However, pollution distribution was spatially heterogeneous inside the city. The most polluted sites located in the southeast of the city. Unlike previous studies, fluoranthene was the most abundant component quantified, which could be associated with increasing use of natural gas as clean energy. Compositional analysis and principal component analysis (PCA) suggested that different kinds of combustion were the main source of the PAHs in PM, though contribution of coal was still evident.     

Multivariate analysis of a biologically activated carbon (BAC) system and its efficiency for removing PAHs and aliphatic hydrocarbons from wastewater polluted with petroleum products

The efficiency of a biologically activated carbon system for treating wastewater polluted with petroleum products was examined and the effects of process parameters on its efficacy were evaluated. In each experiment 17 alkylated and 19 non-alkylated polycyclic aromatic hydrocarbons (PAHs) and total petroleum hydrocarbons (TPHs, C₁₀–C₄₀) were extracted using semipermeable membrane devices from wastewater before and after treatment. The acquired data during experiments were analyzed using principal component analysis (PCA). The treatment system robustly removed dissolved PAHs across the studied ranges of the process parameters, providing overall removal efficiencies of 96.9–99.7% for the sum of 36 PAHs. However, the major contributor to their removal was sorption rather than biodegradation, and despite the general efficiency of the process there was up to a 9-fold range in the sums of quantified PAHs in the effluents between experiments. Combinations of long process contact time (24 h) with high temperature (24 °C) and moderate oxygen concentration (6–7 mg O₂ L⁻¹) resulted in good removal of bioavailable PAHs. The removal of TPHs was more dependent on biological activities during the wastewater treatment, and consequently more dependent on the process parameters. In addition, small but significant proportions of PAHs were volatilized and released during the wastewater treatment.     

Pollution patterns of polycyclic aromatic hydrocarbons in tobacco smoke

Concentrations of polycyclic aromatic hydrocarbons (PAHs) in tobacco smoke of 12 commercial brand cigarettes were determined in a simulated chamber of 20.25 m3 in size. The total concentrations of 17 PAHs (summation operatorPAHs) in the chamber were 3500 and 1152 ng/m3 in vapor phase and particulate phase, respectively. In vapor phase, the yield of naphthalene (NA) appeared to be the most abundant (2462 ng/cig) followed by fluorene (FLUOR) and acenaphthylene (ACY), while the yield of benzo[ghi]perylene (BP) was the most abundant (259.7 ng/cig) in particulate phase followed by phenanthrene (PHEN) and FLUOR. The proportion of PAHs in particulate phase increased with increasing molecular weight. PAHs with two to six rings accounted for 40.2%, 35.3%, 11.7%, 7.6%, 5.2% of summation operatorPAHs, respectively. There was no obvious correlation between PAHs, benzo[a]pyrene (BaP) concentrations in tobacco smoke and smoking tar contents, nicotine contents. With the source fingerprint of PAHs in tobacco smoke, NA could be regarded as the marker of tobacco smoke source because of its largest contribution to summation operatorPAHs (40.2%), followed by FLUOR (12.7%) and ACY (9.8%). Further study indicated that more than 80% of BaP in indoor air of resident homes in Hangzhou was from tobacco smoke.     

The influence of baking fuel on residues of polycyclic aromatic hydrocarbons and heavy metals in bread

The influence of fuel type used to bake bread on the spectrum and concentrations of some polycyclic aromatic hydrocarbons and heavy metals in baked bread was assessed. Bread samples were collected from different bakeries operated by either electricity, solar, mazot or solid waste and their residue content of PAHs and heavy metals was assessed. The total concentration of PAHs detected in mazot, solar, solid waste and electricity operated bakeries had an average of 320.6, 158.4, 317.3 and 25.5 μg kg⁻¹, respectively. Samples collected from mazot, solar and solid waste operated bakeries have had a wide spectrum of PAHs, in comparison to that detected in bread samples collected from electricity operated bakeries. Lead had the highest concentrations in the four group of bread samples, followed by nickel, while the concentrations of zinc and cadmium were the least. The concentration of lead detected in bread samples produced from mazot, solar, solid waste and electricity fueled bakeries were 1375.5, 1114, 1234, and 257.3 μg kg⁻¹, respectively. Estimated daily intake of PAHs based on bread consumption were 48.2, 28.5, 80.1, and 4.8 μg per person per day for bread produced in bakeries using mazot, solar, solid waste and electricity, respectively. Meanwhile, the estimated daily intake of benzo (a) pyrene were 3.69, 2.65, 8.1, and 0.81 μg per person per day for bread sample baked with mazot, solar, solid waste and electricity, respectively. The daily intake of lead, based on bread consumption was 291, 200.5, 222, and 46.31 μg per person per day for bread sample baked with mazot, solar, solid waste and electricity, respectively. The present work has indicated the comparatively high level of daily intake of benzo (a) pyrene and lead in comparison to levels reported from many other countries and those recommended by international regulatory bodies. It is probable that residues detected in bread samples are partially cereal-borne but there is strong evidence that the process of baking and the gases emitted are responsible for most of the contamination load.     

Direct photolysis of polycyclic aromatic hydrocarbons in drinking water sources

The widely used low pressure lamps were tested in terms of their efficiency to degrade polycyclic aromatic hydrocarbons listed as priority pollutants by the European Water Framework Directive and the U.S. Environmental Protection Agency, in water matrices with very different compositions (laboratory grade water, groundwater, and surface water). Using a UV fluence of 1500 mJ/cm², anthracene and benzo(a)pyrene were efficiently degraded, with much higher percent removals obtained when present in groundwater (83-93%) compared to surface water (36-48%). The removal percentages obtained for fluoranthene were lower and ranged from 13 to 54% in the different water matrices tested. Several parameters that influence the direct photolysis of polycyclic aromatic hydrocarbons were determined and their photolysis by-products were identified by mass spectrometry. The formation of photolysis by-products was found to be highly dependent on the source waters tested.     

Removal of PAHs from highly contaminated soils found at prior manufactured gas operations

Removal of PAHs from highly contaminated soil found at a manufactured gas site was evaluated using solvent washing with mixed solvents. The following solvents were considered as water miscible co-solvents in mixed solvents: ethanol, 2-propanol, acetone, and 1-pentanol. In batch solvent extraction of soil, ethanol and 2-propanol were selected as primary components of mixed solvents in addition to 1-pentanol. Using ternary solutions containing either ethanol or 2-propanol with a volume fraction of 1-pentanol ranging from 5 to 25% and a water volume fraction ranging from 5 to 30%, ethanol was more effective than 2-propanol in extracting PAHs from soil. A solvent mixture of 5% 1-pentanol, 10% water and 85% ethanol was selected as the extraction solvent. Using a 1 g:4 ml soil:solvent extraction ratio, extraction kinetics showed that from 65 to 90% of the extractable PAHs were removed within an hour of contact between soil and solvent. Using this 1 g:4 ml extraction ratio, PAHs were removed in a three-stage cross-current solvent washing process where the same batch of soil was extracted with clean solvent for 1 h in each stage. PAH removals in three-stage cross-current solvent washing were comparable to PAH removals obtained with Soxhlet extraction.     

塑料食品包装制品中多环芳烃的分析及检测

通过模拟向聚酯(PET)、聚碳酸酯(PC)两类包装材料中添加回收塑料,探索了塑料食品包装中多环芳烃(PAHs)的来源,并对样品中的PAHs进行分析检测.由新料加工制成的样品中不含PAHs;添加回收料的样品中出现了PAHs的累积与放大;添加回收料并引入氯源(PVC)的样品,经反复加工,其有害物质的含量增加,组分更趋复杂.结果表明,添加回收塑料的包装制品中含有大量有害物质,如萘、苊烯、苊等2～3环的多环芳烃.     

Source identification and health risk of polycyclic aromatic hydrocarbons associated with electronic dismantling in Guiyu town, South China

In this study the concentrations and distribution of sixteen polycyclic aromatic hydrocarbons (PAHs) were investigated in gas and total suspended particle (TSP) samples collected during daytime and night time. The sampling locations included an electronic waste dismantling workshop (EW), a plastic recycling workshop (PW) and a waste incineration field (WF) in Guiyu, China. A large residential area (RA) in this region was used as a control site. In the daytime, the highest concentration was found at WF (1041 ng m⁻³); while in the night time the highest concentration was found outside of EW (744 ng m⁻³). Comparison between work hours (daytime) and rest hours (night time) displayed that the total PAHs (gas + particulate phase) concentrations and the percentages of PAHs associated with TSP were higher at night than those in the daytime in all sampling workshops except WF. Source diagnostic-ratio analysis revealed that unwanted materials and smoldering honeycomb coals were the main sources of PAHs in EW, WF and PW. Benzo[a]pyrene equivalent [BaPeq] concentrations calculated by using the toxic equivalent factors [TEFs] suggested that the occupational exposure levels were not significantly high when compared with other occupational exposure. Additionally, our study suggested that the smoldering of unwanted materials could produce much more toxic PAHs compounds.     

Biodegradation of aged polycyclic aromatic hydrocarbons (PAHs) by microbial consortia in soil and slurry phases

Microbial consortia isolated from aged oil-contaminated soil were used to degrade 16 polycyclic aromatic hydrocarbons (15.72 mgkg(-1)) in soil and slurry phases. The three microbial consortia (bacteria, fungi and bacteria-fungi complex) could degrade polycyclic aromatic hydrocarbons (PAHs), and the highest PAH removals were found in soil and slurry inoculated with fungi (50.1% and 55.4%, respectively). PAHs biodegradation in slurry was lower than in soil for bacteria and bacteria-fungi complex inoculation treatments. Degradation of three- to five-ring PAHs treated by consortia was observed in soil and slurry, and the highest degradation of individual PAHs (anthracene, fluoranthene, and benz(a)anthracene) appeared in soil (45.9-75.5%, 62-83.7% and 64.5-84.5%, respectively) and slurry (46.0-75.8%, 50.2-86.1% and 54.3-85.7%, respectively). Therefore, inoculation of microbial consortia (bacteria, fungi and bacteria-fungi complex) isolated from in situ contaminated soil to degrade PAHs could be considered as a successful method.     

Accumulation of polycyclic aromatic hydrocarbons and heavy metals in lettuce grown in the soils contaminated with long-term wastewater irrigation

Accumulation of polycyclic aromatic hydrocarbons (PAHs) and heavy metals (HMs) by crop plants from contaminated soils may pose health risks. A greenhouse pot experiment using lettuce (Lactuca satuva L.) as a representative vegetable was conducted to assess the concentrations of PAHs and HMs in vegetables grown in wastewater-contaminated soils. The concentrations of total PAHs were ranged from 1.5 to 3.4 mg kg(-1) in the contaminated soils, while 1.2 mg kg(-1) in the reference soil. Linear regression analyses showed that the relationships between soil and shoot PAH concentrations were stronger for LMW-PAHs (R(2) between 0.51 and 0.92) than for HMW-PAHs (R(2) 0.02 and 0.60), suggesting that translocation for LMW-PAHs is faster than HMW-PAHs. Furthermore, the data imply that root uptake was the main pathway for HMW-PAHs accumulation. The plant shoots were also highly contaminated with HMs, particularly Cd (0.4-0.9 mg kg(-1)), Cr (3.4-4.1 mg kg(-1)), Ni (11.7-15.1 mg kg(-1)) and Pb (2.3-5.3 mg kg(-1)), and exceed the guidance limits set by State Environmental Protection Administration (SEPA), China and the World Health Organization (WHO). This study highlights the potential health risks associated with cultivation and consumption of leafy vegetables on wastewater-contaminated soils.     

Organic/inorganic hybrid nanospheres based on hyperbranched poly(ethylene imine) encapsulated into silica for the sorption of toxic metal ions and polycyclic aromatic hydrocarbons from water

Organic–inorganic hybrid silica nanospheres were prepared through a biomimetic silicification process in water at ambient conditions by the interaction of low cost poly(ethylene imine) hyperbranched polymer with silicic acid. The characterization of these nanoparticles by FTIR spectroscopy, scanning electron microscopy (SEM), zeta-potential and dynamic light scattering (DLS) experiments confirmed that the dendritic polymer was incorporated into the silica network. Preliminary experiments show that these hybrid nanoparticles can be employed for the removal of toxic water contaminants. Hybrid nanospheres’ sorption of two completely different categories of pollutants, i.e. metal ions such as Pb²⁺, Cd²⁺, Hg²⁺, Cr₂O₇²⁻, and polycyclic aromatic hydrocarbons such as pyrene and phenanthrene, was largely enhanced in comparison with the corresponding polymer-free silica nanospheres. This was attributed to the to the formation of conventional metal-ligand and charge-transfer complexes proving that although integrated into the silica network poly(ethylene imine) retains its chemical properties.     

高温热解析在多环芳烃污染土修复中的应用

多环芳烃(PAHs)是一类重毒污染物,其污染土壤对人类的健康造成了严重危害,所以对污染土壤进行修复势在必行.首先讨论了处理多环芳烃(PAHs)污染土壤的多种可行技术;然后详细介绍了回转窑高温热解析在北京某焦化厂多环芳烃污染土壤修复中的应用及效果,研究发现回转窑高温热解析技术不仅能有效去除污染土中的有机污染物,而且还能抑制二噁英等剧毒物的产生.     

Gas-particle concentrations of atmospheric polycyclic aromatic hydrocarbons at an urban and a residential site in Osaka, Japan: effect of the formation of atmospherically stable layer on their temporal change

A comparative study on atmospheric polycyclic aromatic hydrocarbons (PAHs) in particulate matter and the gaseous phase was performed at an urban and a residential site in Osaka, Japan, during 2005-2006. PAH concentrations at the urban site were found to be approximately twice higher than those at the residential site. At both sites, particulate PAH concentrations increased mainly in winter while the trends of temporal change in gaseous PAH concentrations were not clearly observed. The main sources of PAHs were estimated to be local traffic, e.g., diesel engines with catalytic converter. PAH concentrations did not significantly negatively correlate with ozone concentrations and meteorological parameters. Gas-particle partitioning coefficients of representative PAHs with low molecular weight (LMW) significantly negatively correlated with ambient temperature, showing that temporal change in the LMW PAH concentrations in PM could be attributable to the shift of their gas-particle distribution caused by the change in ambient temperature. For the first time, we studied the effect of the formation of atmospherically stable layer following an increase in PAH concentrations in Japan. At the urban site, PAHs showed a significant positive correlation with potential temperature gradients, indicating that temporal variability in PAH concentrations would be dominantly controlled by the formation of atmospherically stable layer in Osaka area.     

Levels, fingerprint and daily intake of polycyclic aromatic hydrocarbons (PAHs) in bread baked using wood as fuel

Concentrations, fingerprint and daily intake of 16 PAHs in 15 bread samples baked using wood as fuel are examined in this work. Analysis was performed by GC/MS after saponification of the samples and clean up of the extract. The total concentration of the 16 analytes varies from 6 to 230 microg/kg on dry weight (d.w.). The better extraction procedure was estimated by analyzing test-samples and using different extraction methods. Additionally, for every analyzed sample, the extraction yield has been determined by the use of surrogate standards. Extraction yields were never less than 77% and in most cases almost 100%. The profiles of PAHs (percentage) are similar for all the analyzed samples but are different from those reported when other types of fuels are taken in consideration. The daily intake of PAHs was found to range between 1.6 and 68 microg day(-1), while the intake of B[a]P ranges from 0.33 to 8.0 microg day(-1). These results are considerably lower than the slope factor for 14 of the 15 analyzed samples.     

Risk assessment of polycyclic aromatic hydrocarbons in a Mediterranean semi-enclosed basin affected by human activities (Abu Qir Bay, Egypt)

The contamination of sediments and mussels sampled from Abu Qir Bay by polycyclic aromatic hydrocarbons (PAHs) was investigated. Concentrations of PAHs recorded in the bay sediments ranged from <MDL to 2660 μg/kg dw. In general, concentrations of PAHs in mussels were higher than their corresponding sediment concentrations reflecting their great bioavailability (242–3880 μg/kg dw). The highest concentration was observed in the western part of the bay, a location affected by intensive shipping activities. The distribution pattern of PAHs was similar for mussels and sediments, particularly for sediments characterized by high contamination level, and they were dominated by the high molecular weight PAHs (4–6-rings). Applying different PAHs ratios, it was found that PAHs originated predominantly from the pyrogenic source either from the combustion of grass, wood and coal (majority of the samples) or from petroleum combustion (harbour area). The output of a Screening Level Ecological Risk Assessment (SLERA) on the bay sediments revealed that adverse ecological effects to benthic organisms are expected to occur in only one sample, and thus PAHs are not considered as contaminants of concern in Abu Qir Bay. Also adverse health effects are not expected to occur from the consumption of the investigated mussels with respect to PAHs in Abu Qir Bay.