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1.
The concentration of polycyclic aromatic hydrocarbons (PAHs) was determined in seawater, sediment, and Rock oyster Saccostrea cucullata collected from four sampling sites in the inter-tidal areas of Bushehr province. The total concentrations of 14 PAHs varied from 1.5 to 3.6 ng/L in seawater, 41.7 to 227.5 ng/g dry weight in surface sediment, and 126 to 226.1 ng/g dry weight in oyster tissue. In comparing PAH concentrations among the three matrices in Bushehr province, data showed that the pattern of individual PAHs in seawater, oyster, and sediment were different. The oysters tended to accumulate the lower molecular weight and the more water-soluble PAHs. Sediment samples were distinguished from the sea water and oyster samples by the presence of high molecular weight PAHs, especially six-ring PAHs. Three- and four-ring PAHs were the most abundant compounds among the 14 PAHs investigated in surface seawater, sediment, and oyster samples. As expected, differences in octanol/water partition coefficient among individual PAHs and the greater persistence of the higher molecular weight PAHs contributed to the accumulation patterns in oyster and sediment. The results of the study suggested that the main sources of PAHs in the seawater and sediment in the region were mixed pyrolitic and petrogenic inputs.  相似文献   

2.
Examination of the risk of contamination by polycyclic aromatic hydrocarbons in the harvested crops of carrots and fungi after the application of composted municipal waste Investigations were conducted to determine if the often high, naturally-occuring concentrations of polycyclic aromatic hydrocarbon (PAHs) present in municipal waste composts could cause hazardous contamination of plants when the composts are used as soil conditioners in agriculture and gardening. Carrots (Daucus carota) and mushrooms (Agaricus bisporus), used as representatives of higher and lower plants, respectively, were cultivated on compost-free or compost-amended substrates. To determine concentrations of PAHs in soils and plants a gas-chromatographic method was employed which allowed benzo(a)pyrene and 12 other PAHs to be determined singly or as isomeric mixtures. In the experiments with Agaricus it was found that fruiting bodies, even though grown in a substrate with very high concentrations of PAHs (i- e., 1000 ppb benzo(a)pyrene), contained no detectible quantities of these compounds. In contrast to this, experiments with carrots showed that there was a direct correlation between PAH concentrations in the substrate and PAH concentrations in both below- and above-ground portions of the plants. The 25 to 40 fold increase of the PAH concentration in the substrate containing waste compost caused an increase of these compounds in the carrot roots by the same factor. The only 2 to 4 fold increment of the PAHs in the corresponding foliage was thought to be mainly due to a relatively great portion of air contamination by which the increase of the PAH quantities entering from below ground to the foliage was not so evident. The concentrations of benzo(a)pyrene used in the present series of experiments with composted waste are 7 to 10 times higher than those found in soil to which compost has been added as in practical agricultural application. Relating the result of the described experiments to actual practice, it could be suggested that the normally very low concentrations of PAHs in below ground plant parts would increase with the use of composted municipal waste, but they would not become greater than the concentrations in above ground plant as caused by contamination from naturally occuring PAHs in the air.  相似文献   

3.
Aim and Background  Little data are available on the levels of polycyclic aromatic hydrocarbons (PAHs) in the sediments of the Mediterranean Sea Coast of Egypt in general and the Alexandria coastal zone in particular. It was therefore deemed necessary to set up a monitoring programme to determine the current concentrations of PAHs in bottom sediments, and to identify any area where high concentrations of these potential hazardous contaminants were present in the Western Harbour of Alexandria. Methods  The composition, distribution and the source of PAHs in surficial sediments of the harbour were investigated. To document the spatial PAH input, surficial sediment samples from 23 locations throughout the harbour were analysed. as]Results and Discussion The total PAH load determined in the surficial sediment samples ranged from 8 to 131150 ng g1 dry wt, generally with most of the samples having total concentrations of PAHs greater than 5000 ng g1 dry weight. The highest concentration of total PAHs was recorded in sediments of the inner harbour. Ratio values of specific compounds such as phenanthrene to anthracene, fluoranthrene to pyrene, methyl-phen-anthrene to phenanthrene, methyl-dibenzothiophenes to dibenzothiophenes, alkylated to non-alkylated and high molecular weight to low molecular weight PAH, were calculated to evaluate the possible source of PAH contamination in the harbour sediments. Conclusions  Two main sources of PAH in the study area have been found: pyrolytic and petrogenic. Interferences of rather petrogenic and pyrolytic PAH contaminations were noticed for most samples. The dominant sources of PAH appear to be the combustion processes through run-off, industrial and sewage discharges, and atmospheric input. The concentrations of PAHs were generally above levels expected to cause adverse biological effects. Recommendations and outlook  Information from this study and any other relevant studies should be useful in designing future strategies for environmental protection and management of the harbour.  相似文献   

4.
Background, Aim and Scope   Polycyclic aromatic hydrocarbons (PAHs) are formed as a result of incomplete combustion and are among the most frequently occurring contaminants in soils and sediments. PAHs are of great environmental concern due to their ubiquitous nature and toxicological properties. Consequently, extensive research has been conducted into the development of methods to remediate soils contaminated with PAHs. Fenton's reagent or ozone is the most commonly studied chemical oxidation methods. However, the majority of remediation studies use soils that have been artificially contaminated with either one or a limited number of PAH compounds in the laboratory. Hence, it is essential to extend such studies to soils contaminated with multiple PAHs under field conditions. Objectives   The objective of this study is to investigate the capacity of Fenton's reagent and ozone to degrade PAHs in soils. The soils have been collected from a number of different industrial sites and, therefore, will have been exposed to different PAH compounds in varying concentrations over a range of time periods. The capacity of Fenton's reagent and ozone to degrade PAHs in industrially contaminated soils is compared to results obtained in studies using soils artificially contaminated with PAHs in the laboratory. Materials and Methods: Nine soil samples, contaminated with PAHs, were collected from five different industrial sites in Sweden. For the Fenton's reagent procedure, the pH of the soil slurry samples was adjusted to pH 3 and they were kept at a constant temperature of 70oC whilst H2O2 was added. For the ozone procedure, soil samples were mixed with 50% water and 50% ethanol and kept at a constant temperature of 45 oC. Ozone was then continually introduced to each soil sample over a period of four hours. Following the Fenton's reagent and ozone oxidation procedures, the samples were filtered to isolate the solid phase, which was then extracted using pressurized liquid extraction (PLE). The sample extracts were cleaned up using open columns and then analysed by gas chromatography-mass spectrometry (GC-MS). Results: The relative abundance of the detected PAHs varied between soils, associated with different industries. For example, low molecular weight (LMW) PAHs were more abundant in soil samples collected from wood impregnation sites and high overall PAH degradation efficiencies were observed in soils originating from these sites. In the contaminated soils studied, PAHs were more effectively degraded using Fenton's reagent (PAH degradation efficiency of 40-86%) as opposed to ozone (PAH degradation efficiency of 10-70%). LMW PAHs were more efficiently degraded, using ozone as the oxidizing agent, whereas the use of Fenton's reagent resulted in a more even degradation pattern for PAHs with two through six fused aromatic rings. Discussion: The degradation efficiency for both methods was largely dependent on the initial PAH concentration in the soil sample, with higher degradation observed in highly polluted soils. LMW PAHs are more susceptible to degradation than high molecular weight (HMW) PAHs. As a result of this the relative abundance of large (often carcinogenic) PAHs increased after chemical oxidation treatment, particularly after ozone treatment. Repeated Fenton's reagent treatment did not result in any further degradation of soil PAHs, indicating that residual soil PAHs are strongly sorbed. The effectiveness of the two oxidation treatment approaches differed between industrial sites, thus highlighting the importance of further research into the influence of soil properties on the sorption capacity of PAHs. Conclusions: This study demonstrates that the degree to which chemical oxidation techniques can degrade soil bound PAHs chemical degradation is highly dependent on both the concentration of PAHs in the soils and the compounds present, i.e. the various PAH profiles. Therefore, similarities in the PAH degradation efficiencies in the nine soil samples studied were observed with the two chemical oxidation methods used. However, the degradation performance of Fenton's reagent and ozone differed between the two methods. Overall, Fenton's reagent achieved the highest total PAH degradation due to stronger oxidation conditions. LMW PAHs showed higher susceptibility to oxidation, whereas high molecular weight (HMW) PAHs appear to be strongly sorbed to the soils and therefore less chemically available for oxidation. This study highlights the importance of including soils collected from a range of contaminated sites in remediation studies. Such soil samples will contain PAH contaminants of varying concentrations, chemical and physical properties, and have been aged under field conditions. In addition to the chemical and physical properties of the soils, these factors will all influence the chemical availability of PAHs to oxidation. Recommendations and Perspectives: We recommend including aged contaminated soils in chemical degradation studies. In future chemical remediation work, we intend to investigate the potential influence of the chemical and physical properties of PAHs and soil parameters potential influence on the chemical oxidation efficiency in aged contaminated soils. Due to the vast number of contaminated sites there is a great need of efficient remediation methods throughout the world. This study shows the difficulties which may be experienced when applying remediation methods to a variation of contaminated sites.  相似文献   

5.
From 1990 to 1994, a total of 21 sediment cores and 37 grab sediment samples were collected from the Milwaukee Harbor Estuary. Each sediment core was sectioned and dated using 210Pb and137 Cs radioisotope techniques. A total of 305 samples were analyzed for sixteen polycyclic aromatic compounds (PAHs). Grain size distribution, porosity, and total organic carbon content as measured by loss on ignition were also determined. The results provide a historical overview of the impact of industrialization in the Milwaukee area. Although highly variable, the concentration profile of PAHs show, in general, peaks in the 1950's through 1980's. The PAH concentrations have declined since then for most sediment cores. The current levels of total PAHs in most surface sediment samples range from 25 to 200 ppm. A few cores, some of which were collected in 1994, have an elevated PAH concentration at the surface. Toxicity of the surface sediments was evaluated by comparing with the benchmark values developed by the United States National Oceanic and Atmospheric Administration (NOAA). The most heavily contaminated area was found in the Kinnickinnic River between the Becher Street Bridge and the Wisconsin Wrecking Company Wharf. The highest total PAH concentration determined from seven vibra cores collected in this area ranges from 380 to 1000 ppm. The former Wisconsin Solvay Coke Company may have been a major point source of PAHs until the 1970's. Highway traffic and various industrial discharges also contribute to the sediment PAHs in this area.  相似文献   

6.
The presence of polycyclic aromatic hydrocarbons (PAHs) in five commercial liquid smoke flavorings, used in the European food industry, was studied. The samples were subjected to an alkaline treatment, extracted with cyclohexane, cleaned up by means of solid-phase extraction tubes, and analyzed by gas chromatography-mass spectrometry. Three different procedures for the cleanup were tested. The results revealed the presence of 34 PAHs, some of them with methyl substituents. In all cases, the concentrations of compounds of low molecular weight were much higher than those of high molecular weight. Relationships between smoke flavoring compositions and PAH levels were also studied. Three of the samples contained high levels of both total and carcinogenic PAHs. Benzo[a]pyrene was also detected in these three samples, but its concentration did not exceed the 10 microg/kg level fixed by the FAO/WHO. Finally, a relation was found, first between the concentrations of total carcinogenic PAHs and benzo[a]pyrene and also between the concentrations of pyrene and benzo[a]pyrene. The latter ratio reveals that pyrene concentration could be very useful in predicting the level of benzo[a]pyrene and, consequently, in estimating the carcinogenicity arising from the presence of benzo[a]pyrene and other carcinogenic PAHs.  相似文献   

7.
Thirteen polycyclic aromatic hydrocarbon (PAH) compounds were identified in organic horizons of tundra surface-gleyed soils ( Histic Stagnosols (Gelistagnic) and plants. The total content of PAHs in contaminated soils exceeded the background values by three times. Concentrations of low-molecular weight hydrocarbons in soils at different distances from the coalmines were relatively stable. Concentrations of highmolecular weight hydrocarbons had a distinct maximum at a distance of about 0.5 km from the source of emission. The increased values of correlation coefficients were found between PAH concentrations in organic soil horizons, plants, and coal of the Vorkutinskaya mine. Mostly low-molecular weight structures predominated in the organic soil horizons and in the studied plant species. The maximum capacity for the biological accumulation of PAHs was displayed by Pleurozium schreberi and the minimum capacity was displayed by Vaccinium myrtillus. Mosses and lichens actively absorbed polyarenes from the surface; most of the PAHs were transported into the plants. This phenomenon was not observed for Vaccinium myrtillus Concentrations of PAHs on the surface and in plant tissues decreased with an increase in the distance from the mine. Distribution of polyarenes in plant organs was nonuniform. Insignificant excess of concentration of polyarenes was found in dead part of Pleurozium schreberi in comparison with its living part. The accumulation of polyarenes in the leaves of Vaccinium myrtillus was higher than that in its stems and roots.  相似文献   

8.
Dissolved concentrations of polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs) in the influents and effluents of two municipal sewage treatment plants (STPs) were monitored over 16- (Umeå, Sweden) and 22- (?iauliai, Lithuania) day sampling periods. Sampling was performed using a passive sampling technique (semipermeable membrane devices; SPMDs) for sequestration of the dissolved (readily bioavailable) fraction of persistent organic pollutants (POPs). Removal efficiencies for individual low molecular weight (LMW) PAH compounds varied from 84% to levels at which the compounds were not detected in effluents from Umeå. The corresponding efficiencies of the ?iauliai plant were 33–95%. Measurements revealed that dissolved concentrations of most of the PCBs and some of the high molecular weight (HMW) PAHs increased during the conventional wastewater treatment at both plants. The release of dissolved PAHs and PCBs in the effluents from municipal wastewater treatment plants might increase the environmental contamination by readily bioavailable pollutants in the recipient waters; the rivers Umeälven and Kulpè. SPMDs were found to be suitable sampling tools for long-term (weeks-month) integrative monitoring of trace concentrations of the dissolved fraction of hydrophobic pollutants in the wastewater process, since the sampling and clean-up steps were easy to perform.  相似文献   

9.
The rate at which creosote-treated pilings release polycyclic aromatic hydrocarbons (PAHs) into the environment should diminish with structure age and weathering, and so, it may be assumed that PAH concentrations in the vicinity of old structures (>30 years) may approach background levels. However, this may not be true in cold environments where PAH release and degradation rates are slow and where pilings continue to experience significant physical damage. Moreover, PAHs will remain high in the vicinity of pilings if current and wave action is insufficient to disperse and dilute PAHs over a wider area and/or where PAHs do not become diluted and buried by uncontaminated sediments. This is demonstrated in our investigation of the sediments of the Grey Owl Marina, located in Prince Albert National Park, in central Saskatchewan, Canada. The marina, constructed in the early 1960s, consists of six piers and is protected from strong wave action by a breakwater. PAH concentrations were high in sediments collected under the piers and inside the boat slips, exceeding probable effect levels for several compounds. Various lines of physical and chemical evidence pointed to creosote as being the primary PAH source with a mixture of relatively undegraded and weathered PAHs being present. PAH concentrations decreased rapidly 2 m and further away from the pilings as a result of dilution with increasing dispersal over a broadening area. There was evidence of benthic community impairment, with total abundances negatively correlated with PAH concentrations. According to the Methods for Ranking Contaminated Aquatic Sites on Canadian Federal Properties, areas with the highest hazard scores were under the piers and inside the boat slips, while areas with the lowest hazard scores were >10 m from the pilings. Therefore, remedial actions based on piling and contaminated sediment removal may need to be conducted over only a small area, i.e., within 2 m of the pilings.  相似文献   

10.
Forests of the Northern Czech mountains decline due to industrial emissions. To examine the state of soil contamination with PAHs we analyzed the concentrations of 20 PAHs in the O and A horizons of 4 lower and 4 upper slope sites under beech (Fagus sylvatica L.) in the Western (WE) and the Eastern Erzgebirge (EE, Kru?né Hory), the Isergebirge (IS, Jizerské Hory), and the Riesengebirge (RI, Krkono?e) at microsites affected and not affected by stem flow. Average PAH sum concentrations in the organic layers ranged between 2000 and 30000 μg kg?1 increasing in the line WE <RI<EE<IS. PAH concentrations were significantly higher at upper than at lower slope sites indicating long-distance transport. Microsites affected by stem flow had significantly higher PAH concentrations but lower percentages of lower molecular PAHs than microsites not affected by stem flow. This was due to the water collecting effect of the beech bark. Lower molecular PAHs preferentially were sorbed to the bark or leached from the organic layers. PAH concentrations increased from Oi to Oa horizons but decreased in the mineral soil. This was the more pronounced the higher the molecular weight was. The slope of the regression line between the enrichment factors (concentration of a single PAH in the Oa divided by that in the Oi horizon) and the octanol-water partition coefficient decreased as the PAH concentration of the soils increased. This indicates that the microbial activity of organic layers may be reduced by soil contamination. Cluster analysis suggested that the sources of the PAH contamination in the WE were different from the other sites.  相似文献   

11.
Actual information on the level of accumulation of PAHs in soils, their inputs/outputs and fate is still unsatisfactory. The regional scale of data collection is important from practical point of view, since decisions regarding environment protection often require proper assessment of soil information aggregated on this level. The objective of the study was to define the regional levels of PAHs in soils and to examine the relationship with the parameters related to their inputs (emission factors) and to natural conditions (soil properties, geographical localisation). The territory of Poland, comprising 16 regions, was chosen as a model area representing the Central/East European countries. The concentrations of 16 PAH compounds were determined in 266 soil samples collected from 0 to 30-cm upper soil layer from agricultural lands. The data were supplemented with basic soil properties. The regional concentrations of Σ16PAHs were within the limits of 125–756 μg kg?1 (geometric means) and did not exceed the limit values specified in Polish regulations. They complied also with European soil screening values for intermediate or negligible risk. The key variable affecting the accumulation of PAHs in soils was the regional emission of those contaminants, which described soil concentrations of PAHs in at least 50%; the results suggest time-dependent (delayed) reaction of soil environment to the emission changes. The effect was sensitive to PAH compositions in soils and was most pronounced in the case of higher molecular weight compounds (≥4 rings) transported predominantly with atmospheric particles. The regression models, comprising actual regional emission data, did not indicated on the increasing risk of PAHs accumulation in soils. The evaluations based on the regional content of benzo(a)pyrene in soils implied significant discrepancies between Polish and other internationally accepted criteria in soil contamination. The natural factors (soil characteristics and climate) affected the regional PAH concentrations in very small extent.  相似文献   

12.
Intention, Goal and Background  Contaminated sediments represent a significant, worldwide environmental problem since they contain a mixture of different xenobiotics and heavy metals. The presence of mixed contamination presents a unique set of obstacles for remediation efforts. Often sediment remediation occurs as an ex-situ application (i.e., after dredging) in an attempt to minimize some of the problems. However, dredging poses it’s own issues. It does not address contaminated water and often material is not completely removed thereby leaving a long-term residual contamination source in the waterway. Objective  The potential of bio remediation to treat sediments contaminated with polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls, and heavy metals was addressed. The primary objective was to assess two delivery mechanisms for microbial inoculation to facilitate in-situ remediation of PAH contaminated sediments. Methods  Simulated river beds were constructed to mimic the Mahoning River. Contaminated sediment from the river was added to each reactor at a uniform depth, followed by the addition of river water. Fifteen inoculation points were used in each simulated river bed to ensure adequate microbial populations. One tank was inoculated with an acclimated bacteria solution as a free suspension. The other tank was inoculated with an attached growth biofilm system. Sediment samples were taken throughout the experiment and the percent PAH degradation determined. Water characteristics (DO, pH, bacterial activity, etc.) were also tracked as corroborating evidence. Results and Discussion  The monitoring sites indicated that an attached growth system was more effective, and achieved a 99% PAH degradation efficiency at some of the sampling sites. Tracking individual PAH compounds also indicated a higher overall microbial activity with the attached growth system. This activity was evident by the formation and subsequent biodegradation of lower molecular weight degradation byproducts. However, more of the sediment area was treated by the free suspension inoculum due to the ease of microbial migration. Conclusions  The applicability of using an aerobic microbial consortium composed ofMycobacterium sp., Pseudomonas aeruginosa, andPseudomonas flourescens to treat contaminated sediment was demonstrated. In addition, it was found that introducing the consortium as an attached growth was more effective than when delivered as a free suspension. Recommendation and Outlook  The results demonstrated that the consortium was effective at treating the PAHs present in the contaminated soil. An additional study to evaluate the consortium’s effectiveness at remediating the PCB present in the sediment is warranted. Optimization of the consortium-nutrient combination could enable a treatment approach to effective for all the organic contaminants present. Although this would not address the heavy metals present in the sediment, it would afford a great opportunity at remediating a severely contaminated sediment system.  相似文献   

13.
The purpose of this study was to determine the degree of PAH contamination and the association of PAHs with metals in urban soil samples from Sevilla (Spain). Fifteen polycyclic aromatic hydrocarbons-PAHs (naphthalene, acenaphthene, fluorene, phenanthrene, anthracene, fluoranthene, pyrene, benzo[a]anthracene, chrysene, benzo[b]fluoranthene, benzo[k]fluoranthene, benzo[a]pyrene, dibenzo[a,h]anthracene, benzo[g,h,i]perylene, indeno[1,2,3-c,d]pyrene) and seven metals (Cd, Cr, Cu, Mn, Ni, Pb, Zn) have been evaluated in representative urban soil samples. Forty-one top soils (0–10 cm) under different land use (garden, roadside, riverbank and agricultural allotment) were selected. PAHs from soil samples were extracted by sonication using dichloromethane. The simultaneous quantification of 15 different PAH compounds were carried out by HPLC using multiple wavelength shift in the fluorescence detector. For qualitative analysis a photo diode-array detector was used. Metal (pseudo-total) analysis was carried out by digestion of the soils with aqua regia in microwave oven. The mean concentration of each PAH in urban soils of Sevilla showed a wide range, they are not considered highly contaminated. The results of the sum of 15 PAHs in Sevilla soils are in the range 89.5–4004.2 μg kg?1, but there seems not to be a correlation between the concentration of PAHs and the land use. Of the 15 PAHs examined, phenanthrene, fluoranthene and pyrene were present at the highest concentrations, being the sum of these PAHs about 40% of the total content. Although metal content were not especially high in most soils, there are significant hints of moderate pollution in some particular spots. Such spots are mainly related with some gardens within the historic quarters of the city. The associations among metals and PAHs content in the soil samples was checked by principal components analysis (PCA). The largest values both for ‘urban’ metals (Pb, Cu and Zn) and for PAHs were mainly found in sites close to the historic quarters of the city in which a heavy traffic of motor vehicles is suffered from years.  相似文献   

14.

Purpose

The purpose of this study was to elucidate historical trends, spatial variations, and the sources of polycyclic aromatic hydrocarbons (PAHs) pollution in several Japanese lakes.

Materials and methods

The vertical distributions of PAHs in the core samples of sediments taken at several points in lakes Kasumigaura, Suwa, Kizaki, and Shinji were determined using a gas chromatograph equipped with a mass selective detector and combined with chronological information and the physical/elemental properties of the sediment.

Results and discussion

Seventeen related compounds (congeners) typically had concentration peaks at sediment depths corresponding to the 1960s to 1970s. In Lake Shinji and one bay of Lake Kasumigaura, there was a tendency for PAH concentrations to increase downstream; in contrast, another bay of Lake Kasumigaura showed the reverse trend. During big flood events, the fluxes of PAHs increased due to large inputs of particulate matter, although PAH concentrations were reduced. For the four study lakes and other similar lakes, PAH concentrations of surface sediments were approximately proportional to population densities in the respective watersheds, while the total input of PAHs to the lakes were correlated with their population and watershed area. The source apportionment analysis using isomer ratios for the congener profiles indicated that the principal sources of the PAHs in the lake sediments were gasoline and/or diesel engine exhausts and biomass burning.

Conclusions

The observed concentration peaks showed a deterioration of the chemical quality of atmospheric conditions around 1960?C1970 and a recent tendency for their amelioration. Between-lake differences suggest that the influence of human activity in the watersheds influences sediment PAH concentrations. The PAH sources were identified to be of pyrogenic origin.  相似文献   

15.

Purpose

Sediment contamination in US waterways is an expensive and complicated issue, and as acceptance of nontraditional sediment remediation strategies broadens, novel and efficient methods to assess and monitor the bioavailability of hydrophobic organic contaminants (HOCs) in contaminated sediments will play an important role.

Materials and methods

In this project, solid phase microextraction (SPME) fibers inside perforated steel tubes were used as in situ passive samplers to measure polycyclic aromatic hydrocarbon (PAH) concentrations in sediment before and after treatment with activated carbon (AC). Two modes of waterjet amendment injection were used to apply the AC. In the first treatment, a single 2-min injection was shot into the center of a test vessel, and in the second treatment, multiple 7-s injections in a grid were placed in sediment.

Results and discussion

In the single injection, no treatment was observed 5 cm away from the injection, while at 2.5 cm, >90 % decrease of PAH pore water concentration was observed, indicating a similar bioavailability decrease. In the multiple injection experiment, >90 % PAH pore water level reductions were observed throughout the test vessel. Highly contaminated and less contaminated sediments were mixed with 0–5 % AC by weight to develop AC treatment curves. Over 99 % reduction in PAH pore water concentrations and bioavailability was observed in the less contaminated sediment at 3 % AC, while 99 % reduction was never reached even at 5 % AC addition in the highly contaminated sediment. Different treatment curves were observed for the different contaminated sediments. In situ equilibration times were 120, 215, and 250 h for phenanthrene, pyrene, and benzo(a)anthracene, respectively.

Conclusions

The results show that in situ SPME is a viable method to observe AC treatment and evaluate reductions in pore water concentrations and bioavailability.  相似文献   

16.
Polycyclic aromatic hydrocarbons (PAHs) are considered to be atmospheric pollutants and well-known human carcinogens. This study analyzes the pollution scenarios of PAHs in the aerosol of Higashi Hiroshima, Japan. We examined the characteristics, the influences of meteorological conditions, the distribution and seasonal variation of PAHs in aerosol samples collected from June 2000 to May 2001. The concentration of PAHs in the aerosol of Higashi Hiroshima was ranging from 11.8 to 157.5 μg/g with a mean concentration of 63.4 μg/g. Results showed that there is positive correlation between aerosol PAH concentrations and ambient temperature but a relatively little correlation with solar radiation. Seasonal variation was observed with a higher concentration during winter and lower concentration during summer. Apart from that, principal component analysis and molecular diagnostic ratios were also used to characterize and identify possible PAHs emission sources. Results obtained strongly suggested that vehicular emissions appeared to be the major source of aerosol PAHs in this study although other sources do have some degree of influence.  相似文献   

17.
To assess PAH contamination pastures, grass and soil samples have been collected from 10 m (d1), 50 m (d2), and 150 m (d3) perpendicular to a French highway (70,000 vehicles per day) and at a control site in a rural area away from nearby contaminating sources. Total PAH concentration ranges from 767 ng/g dry weight to 3989 ng/g dry weight, according to the matrix and the distance from the highway. Distance is not a significant factor for PAH deposition on grass, while in soil it has an effect between d1 and d2 or d3. The total PAH concentration in highway samples is 8 times higher than in control site samples for grass and 7 to 4 times higher for soil. Fluoranthene, pyrene, and phenanthrene are the major PAHs in grass samples at the control site and the highway, but the concentrations are about 5 times higher near the highway. In soil samples collected near the highway, the values of concentrations between all compounds are not statistically different. PAH deposition on grass is linked to the physicochemical properties of the compounds, which lead to a specific distribution of each molecule (according to their volatility and the number of aromatic rings) while no specific behavior is revealed in soil.  相似文献   

18.
PAHs are mainly produced by combustion processes and consist of a number of toxic compounds. While the concentrations of individual PAHs in soil produced by natural processes (e.g., vegetation fires, volcanic exhalations) are estimated to be around 1—10 μg kg−1, recently measured lowest concentrations are frequently 10 times higher. Organic horizons of forest soils and urban soils may even reach individual PAH concentrations of several 100 μg kg−1. The PAH mixture in temperate soils is often dominated by benzofluoranthenes, chrysene, and fluoranthene. The few existing studies on tropical soils indicate that the PAH concentrations are relatively lower than in temperate soils for most compounds except for naphthalene, phenanthrene, and perylene suggesting the presence of unidentified PAH sources. PAHs accumulate in C‐rich topsoils, in the stemfoot area, at aggregate surfaces, and in the fine‐textured particle fractions, particularly the silt fraction. PAHs are mainly associated with soil organic matter (SOM) and soot‐like C. Although the water‐solubility of PAHs is low, they are encountered in the subsoil suggesting that they are transported in association with dissolved organic matter (DOM). The uptake of PAHs by plants is small. Most PAHs detected in plant tissue are from atmospheric deposition. However, earthworms bioaccumulate considerable amounts of PAHs in short periods. The reviewed work illustrates that there is a paucity of data on the global distribution of PAHs, particularly with respect to tropical and southern hemispheric regions. Reliable methods to characterize bioavailable PAH pools in soil still need to be developed.  相似文献   

19.
Polycyclic aromatic hydrocarbons and heavy metal (Pb, Cd, Cu, Zn, Hg, Fe, Co, Cr, Mo) contents were established in soil and plant samples collected in different areas of the railway junction I?awa G?ówna, Poland. Soil and plant samples were collected in four functional parts of the junction, i.e. the loading ramp, main track within platform area, rolling stock cleaning bay and the railway siding. It was found that all the investigated areas were strongly contaminated with polycyclic aromatic hydrocarbons (PAHs). The PAH contamination of the soil was the highest in the railway siding and in the platform area (59,508 and 49,670?μg?kg(-1), respectively). In the loading ramp and cleaning bay, the PAH concentration in soil was lower but still relatively very high (17,948 and 15,376?μg?kg(-1), respectively). The contamination in the railway siding exceeded the average control level up to about 80 times. In the soil of all the investigated areas, four- and five-ring PAHs prevailed. The concentrations of PAHs were determined in four dominating species of plants found at the junction. The highest concentration was found in the aerial parts of Taraxacum officinale (22,492?μg?kg(-1)) growing in the cleaning bay. The comparison of the soil contamination with PAHs in the investigated railway junction showed a very significant increase of the PAHs level since 1995. It was found that the heavy metal contamination was also very high. Pb, Zn, Hg and Cd were established at the highest levels in the railway siding area, whereas Fe concentration was the highest in the platform area. A significant increase in mercury content was observed in the cleaning bay area. The investigations proved very significant increase of contamination with PAHs and similar heavy metals contamination in comparison with the concentration determined in the same areas 13?years ago.  相似文献   

20.
Surface and core sediments from Lake Maryut, Egypt, one of the most polluted lakes in Egypt, were analyzed for polycyclic aromatic hydrocarbons (PAHs) using gas chromatography?Cmass spectrometry. This investigation represents the first extensive study of the distribution and sources of PAHs in sediments from Lake Maryut. The total PAHs concentrations (sum of 39 PAH compounds) in surface sediments varied greatly depending on the sampling location and ranged from 106 to 57,800 ng/g dry weight with a mean concentration of 6,950 ng/g. The most polluted areas are distributed in areas which are mainly influenced by municipal sewage and industrial effluent discharges, suggesting a direct influence of these sources on the pollutant distribution patterns. PAH concentrations were one to two orders of magnitude higher in comparison with those reported for riverine/estuaries systems around the world. Molecular indices, such as pyrogenic index (PI), methylphenanthrenes to phenanthrene ratio, HMWPAH/LMWPAH, A-PAHs/P-PAHs, FL/FL?+?PY, BaP/BaP?+?C, IP/IP?+?BgP, and Per/??(penta-aromatics) were calculated to evaluate different hydrocarbon origins and their relative importance. In general, sediments from the main basin and northwest basin of Lake Maryut showed the highest PAH concentrations with petrogenic signatures, indicating major sources of petrogenic PAHs in the city. On the other hand, lower levels of PAHs with a pyrogenic signature were widely recorded in areas that are distant from anthropogenic sources. At other locations, both petrogenic and pyrogenic inputs were significant. The concentrations of perylene relative to the penta-aromatic isomers are dominant especially in locations associated with terrestrial inputs and in the deepest core sediments, indicating diagenetic origin for the presence of perylene. Temporal trends of PAH concentrations in both cores sediments were influenced by input pathways and followed the economic development and the environmental policies of the Egyptian Government in the last 15 years. Finally, PAH levels in sediments were compared with Sediments Quality Guidelines (effects range median?Ceffects range low) for evaluation probable toxic effects on organism. Results suggest an ecotoxicological risk for benthic organisms mainly in the main basin area, where high concentrations of PAHs were found in sediments influenced by anthropogenic activities.  相似文献   

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