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1.
The paper presents results of analyses of 7671 groundwater samples collected from 1115 screens in the period 1993 to 2001 for the Danish National Groundwater Monitoring Program. In Denmark groundwater is widely used for drinking water and the objectives of the monitoring program is to describe the present conditions, the development of, and the impacts on the groundwater. The design of the Danish National Groundwater Monitoring Program is described and data are provided. Data originate from monitoring areas and are supplemented with data from the waterworks' control of nearly 6000 water supply wells. In addition to pesticides there is a series of other organic compounds that must be considered in relation to possible groundwater contamination. Sources of these compounds and their importance in relation to groundwater contamination is discussed on the basis of the monitoring data. The organic micropollutants monitored are grouped according to chemical properties: aromatic hydrocarbons, chlorophenols, detergents, halogenated aliphatic hydrocarbons, ethers (MTBE), phenols, and phthalates. The most frequently found compounds were toluene (18.7% ), phenol (14.6%), xylene (10.9), trichloromethane (9.5%), and benzene (in 8.8% of the screens monitored). The five compounds most frequently found at a concentration above the maximum residue limits (MRL) for drinkingwater were: dibuthylphthalate (28%), phenol (14%), 2,4-dichlorophenol (10%), trichloromethane (10%), pentachlorophenol (7% of findings exceeding the MRL for drinkingwater). Overall, one or several compound was observed at least once in 57.8% of the 1115 screens monitored within the period 1993–2001. On a yearly basis the median finding frequency was 19%.  相似文献   

2.
Normative regulations on benzene in fuels and urban management strategies are expected to improve air quality. The present study deals with the application of self-organizing maps (SOMs) in order to explore the spatiotemporal variations of benzene, toluene, ethylbenzene, and xylene levels in an urban atmosphere. Temperature, wind speed, and concentration values of these four volatile organic compounds were measured after passive sampling at 21 different sampling sites located in the city of Trieste (Italy) in the framework of a multi-year long-term monitoring program. SOM helps in defining pollution patterns and changes in the urban context, showing clear improvements for what concerns benzene, toluene, ethylbenzene, and xylene concentrations in air for the 2001–2008 timeframe.  相似文献   

3.
Understanding and controlling air pollution in highly populated areas is very important, although interpreting the levels of gaseous pollutants and airborne particulate matter is complicated by dominant natural and anthropogenic emissions, micro-meteorological processes, and chemical reactions which take place directly in the atmosphere. For this reason, it is very difficult to relate the characteristics of air pollution to one or more specific emission sources. The aim of this paper is to detect associations among elements and organic compounds emitted from specific sources by means of chemical analyses, statistical processing of data, seasonal evolution study, and geochemical considerations to trace their origin. A detailed characterization of air quality during the period September 2000–September 2001 was carried out in three locations of the Venice region: A heavy traffic urban site, a public park, and the island centre of the city of Venice. Twenty-eight inorganic elements, four polycyclic aromatic hydrocarbons, CO and benzene were quantified and processed by a statistical procedure based on factor analysis considering variations on a seasonal basis. Results show the presence of associations between elements and compounds with the same behaviour in all sampling points. This indicates that several pollutants originate from a common source, and are then “diluted” throughout the study area, maintaining the imprint of their origin. Pt, polycyclic aromatic hydrocarbons, CO and benzene originating from the exhaust gas of vehicles are all linked in the traffic factor, whereas Cd is associated with Se, having a common source in industrial processes.  相似文献   

4.
以苏南某焦化厂为研究对象,在对污染区域初步识别的基础上,采集了0～4.5 m深的22个土壤样品和2个地下水样品,利用GC/MS等检测了多环芳烃类、总石油烃、苯系物、重金属,总氰化物、挥发酚、硫化物的含量,并研究了其在不同功能区土壤和地下水中的特征分布。结果表明：（1）该焦化场土壤和地下水受到了不同程度的污染,其中炼焦炉周边、焦油和洗油储罐区、焦油和粗苯加工车间是污染最严重的区域;（2）土壤中主要超标污染物是多环芳烃、总氰化物、总石油烃、单环芳香烃、二苯呋喃、苯胺、硫化物、挥发酚和一些苯酚类化合物;（3）地下水重点污染区域粗苯车间受到总氰化物、苯胺、苯酚类、萘、总石油烃、单环芳香烃的严重污染,污水处理站区域地下水主要污染物包括总氰化物、萘、总石油烃、苯。  相似文献   

5.
Monocyclic Aromatic Hydrocarbons in Kathmandu During the Winter Season   总被引：1，自引：0，他引：1  
Mixing ratios of seven monocyclic aromatic hydrocarbons, as well as NO2, SO2 and O3, were measured by long path differential optical absorption spectroscopy (DOAS) at a suburban site in Kathmandu, Nepal, during Jan.–Feb. 2003. The results showed average benzene (3.9?±?1.8 ppbv), toluene (13.3?±?7.1 ppbv), and sum of xylene isomers (42.2?±?15.7 ppbv) mixing ratios in Kathmandu. The xylenes concentrations were higher than in the large cities that have been studied. The observed ratio of toluene to benzene (2.9?±?1.8) reflected the small fraction of vehicles with catalytic converters in the Kathamndu. Analysis of the late afternoon time series of aromatics, NO x , and wind data indicated that road traffic was one of the main sources of aromatics in the urban air. In addition, the correlations between aromatics, SO2, NO x , and PM10 during the night strongly suggested that fossil and biomass fuel burning made an important contribution to air pollution in the Kathmandu valley. Aromatic pollution was further strengthened by daily recurring stable meteorological conditions and the surrounding topography. The chemical reaction of aromatics with free radicals during the daytime could also be deduced. High ratios of phenol/benzene and para-cresol/toluene could not be explained by chemical processes, and suggested direct emission of phenol and para-cresol in the Kathmandu atmosphere.  相似文献   

6.
The non-steady-state fluxes of aromatic hydrocarbons were measured in the laboratory from the surface of soils contaminated with coal tar. Four soil samples from a former gasworks site were used for the experiments. The fluxes were quantified for 11 selected compounds, 4 mono- and 7 polycyclic aromatic hydrocarbons, for a period of up to 8 or 16 days. The concentrations of the selected compounds in the soils were between 0.2 and 3,100 µg/g. The study included the experimental determination of the distribution coefficient of the aromatic hydrocarbons between the sorbed phase and the water under saturated conditions. The determined distribution coefficients showed that the aromatic hydrocarbons were more strongly sorbed to the total organic carbon including the coal tar pitch — by a factor of 8 to 25 — than expected for natural organic matter. The fluxes were also estimated using an analytical solution of the Fick's diffusion equation and assuming that the compounds diffused independently of each other and that instant equilibrium existed between the air, water and sorbed phases. A relatively good agreement was found between the predicted and the measured flux. The predicted fluxes were between 0.11 and 7.5 time the measured fluxes. The fluxes were overestimated for the monocyclic aromatic hydrocarbons and underestimated for 3-rings-PAHs.  相似文献   

7.
Using an automated gas chromatography system coupled with an online sampling/thermal desorption module, benzene, toluene, and their alkylated derivatives were measured in Las Vegas, Nevada from 3 July to 28 August 2008. The levels of hydrocarbons were comparable to those typically found in urban environments. Statistically significant (at 95?% level) higher concentrations were measured on mid-week days as compared with those measured during weekends. This was correlated to a local traffic pattern rather than traffic on highways. The concentrations of aromatic hydrocarbons also increased during periods when transport of smoke from wildfires in central and north California was identified by remote sensing but these levels were comparable to other days with volatile organic compounds concentrations. The high toluene/benzene ratios and the estimated photochemical age of air masses implied the contribution of other local sources. Fuel evaporation accounted for the vast majority of toluene enhanced concentrations in early July (as compared with those measured in June) for sites within the urban grid, but very little for sites located outside the urban area.  相似文献   

8.
为了控制猪粪好氧发酵中产生的挥发性有机物(volatile organic compounds)及主要致臭物质,开展了猪粪好氧发酵试验,通过连续监测猪粪好氧发酵过程中所排放的挥发性气体,研究猪粪好氧发酵中产生的VOCs组分及其致臭因子。研究表明,在猪粪好氧发酵过程中共产生33种挥发性物质,除氨气和硫化氢外,共有31种VOCs,包括芳香烃12种,醛类8种,硫醇硫醚类4种,卤代烃4种,酮类2种,胺类1种;猪粪好氧发酵中主要致臭物质为:二甲二硫、甲硫醚、二甲三硫、乙醛和硫化氢,并建议将甲硫醚作为猪粪好氧发酵中产生的恶臭污染指示物。该研究可为猪粪堆肥过程中恶臭物质的监测、制定控制策略提供参考。  相似文献   

9.
Samples of soil in dry waste pits and of sediment from waste pits currently in-use for natural gas production in the San Juan Basin of northwest New Mexico were collected for characterization of the presence and concentration of organic compounds. Samples were dried at 25 °C and about 50 g were extracted successively in a Soxhlet apparatus using hexane, benzene, and methanol. Extracts were filtered and condensed to 10 mL. Analyses of hexane extracts of samples using high-resolution gas chromatography showed presence of a complex mixture of 40 to 50 organic compounds in dry soil and in sediment from in-use pits. The range of size for compounds was C10 to C25. Although no compounds were detected in GC analyses of subsequent benzene and methanol extracts of the same soil samples, these extracts were highly colored and contained 5 to 10% of total absorptivity at 254 nm. Total extractable residues in the hexane extracts ranged from 49 to 110 mg g?1 of soil. Polycyclic aromatic hydrocarbons were detected in hexane extracts at concentrations of 270 to 870μg g?1 of dry sample.  相似文献   

10.
All commercial gasoline fuels build up deposits on the spark plugs, injectors, oxygen sensors, catalytic converter, and inside the combustion chamber, which will lower the engine's performance and increase air pollution. As a result, fuel-based detergents have been developed to prevent and remove unwanted deposits. Unfortunately, many of the detergents use high amounts of aromatic solvents, which result in a greater risk of exposure to aromatic compounds like benzene. In this study, car exhaust was analyzed for benzene, toluene, ethylbenzene, and xylenes (BTEX), as well as formaldehyde and acetaldehyde during engine cleaning service using different chemical cleaners. A special device was designed for sampling from car exhaust using solid phase microextraction. The extracted compounds were analyzed using a gas chromatograph with flame ionization detector. The cleaning products were rated with regard to the amount of pollutants produced during the cleaning service.  相似文献   

11.
Time of flight mass spectrometry (TOF-MS) combined with resonant two-photon ionization is applied to detect aromatic hydrocarbons in combustion products. The sample is introduced through a heated capillary into the supersonic jet of a TOF-MS. For ionization, a tunable, frequency-doubled dye-laser is used. The inlet system allows a direct measurement of samples at atmospheric pressure. The resonant ionization can distinguish structural isomers without preceding chromatography. The short response time of the system allows for example on-line monitoring of combustion emissions. This is demonstrated by thermodesorption experiments of anthracene from activated charcoal and from diesel soot. A significant higher desorption temperature from charcoal than from diesel soot is found. In addition, examples showing selective measurements of benzene, toluene and three dimethyl-benzene isomers in the exhaust gas of a gasoline engine are presented.  相似文献   

12.
The non-steady-state fluxes of aromatic hydrocarbons from coal tar contaminated soil, placed below a 5 cm deep layer of uncontaminated soil, were measured in the laboratory over a period of 53 days. The contaminated soil originated from a former gasworks site and contained concentrations of 11 selected aromatic hydrocarbons between 50 to 840 µg/cm3. Where the microbial activity was inhibited, the fluxes stabilized on a semi-steady-state level for the monocyclic aromatic hydrocarbons, naphthalene and 1-methylnaphthalene after a period of 10–20 days. Fluxes of acenaphthene and fluorene were only measurable in an experiment that utilized a cover soil with a low organic content. The fluxes were predicted by a numerical model assuming that the compounds acted independently of each other and that local equilibrium between the air, water, and sorbed phases existed. The model overestimated the fluxes for all the detected aromatic hydrocarbons by a factor of 1.3 to 12. When the cover soil was adapted to degrade naphthalene, the fluxes of naphthalene and 1-methylnaphthalene approached the detection limit after 5 to 8 days. Thereafter the fluxes of these two compounds were less than predicted by the model employing half-life values of 0.5 and 1 day for naphthalene and 1-methylnaphthalene respectively.  相似文献   

13.
Polycyclic aromatic hydrocarbons (PAHs) were measured in two wetland plant species grown outdoors in pots of sediment contaminated with up to 730,000 μg/kg total PAHs. After approximately 3 months, the plants were harvested, cleaned, and analyzed for an expanded suite of PAHs which included both the 16 priority PAHs and 22 alkyl PAH homologs. Sediment and air samples were also collected and analyzed. PAH compounds were detected in all of the samples, with the highest concentrations in the contaminated sediment. The root sample concentrations were generally about one order of magnitude lower than that of the sediment, and were strongly correlated with the concentration in the sediment in which they were grown. The concentrations in foliage were much lower and did not correlate with sediment concentration. Concentrations of low molecular weight PAH compounds detected in the foliage were not significantly lower in plants grown in control sediments, suggesting that the sediment is not the primary source of these PAHs. Several high molecular weight PAHs were detected only in plants grown in contaminated sediment. Plants of both species grown in control sediment were larger than plants grown in contaminated sediment.  相似文献   

14.
It is well known that volatile hydrocarbons such as benzene, toluene, and xylene, which are abundant in many refined oils, affect phytoplankton growth. However, experiments to determine these effects in many cases have been improperly designed resulting in questionable conclusions. Experiments presented in this paper indicate that ambient benzene concentrations reported in the published literature may be lower than stated by an order of 10 to 100. By continuous monitoring the benzene concentration decrease was observed and it was possible to determine whether the loss was due to degassing because of loose closures or biological uptake. Unless tight closures are used benzene is quickly lost to the atmosphere (exponential decay rate ≌ 1.2d -1). Experiments demonstrated that benzene is quickly lost from cotton stoppered bioassay flasks that are typically used. Rubber stoppered flasks with little gaseous headspace showed minimum benzene loss. Biological uptake of benzene can be demonstrated when closures are secure and the effect of certain concentrations on growth can be correctly interpreted. Benzene concentrations above 10 to 20 ppm significantly reduce the growth rate of Skeletonema sp. The benzene concentration decreased quickly in 10 to 20 ppm benzene solutions implying metabolic uptake. These experiments indicate that proper closures and analysis of the volatile pollutant concentration during bioassay experiments increase the likelihood of correct interpretation and may yield additional insights into the causation factors.  相似文献   

15.
Aliphatic and aromatic hydrocarbons, fatty acids and heavy metals (Pb, Cu, Ni, Zn, Fe and Cd) were analyzed in atmospheric particulate matter in the city of Caracas, Venezuela. Samples were taken from 6 stations within the metropolitan area of Caracas, characterized as industrial (one), urban (two), suburban (two) and rural (one). In addition, the concentration and composition of the organic compounds was monitored over a 5 month period at an urban site to determine seasonal and temporal variabilities. In general terms, the concentrations of pollutants decreased from industrial and urban sites to suburban to rural. A similar trend was observed for preliminary toxicity tests carried out on the particulate extracts. The concentration levels of most of the pollutants were high for the industrial and urban sites, and comparable with those of other major cities worldwide.  相似文献   

16.
Polycyclic aromatic hydrocarbons (PAHs); their derivatives nitro, and methyl-PAHs; n-alkanes; and organic acids were investigated in the aerosol samples collected during two field campaigns conducted at three sampling stations in an industrialized city in southern Italy. The main sources affecting the atmosphere and its toxicity were investigated by means of the diagnostic ratios of: specific particulate-phase PAHs, marker compounds among nitro-PAHs, alkanes, and acids, the dominant wind direction, daily and seasonal abundance of carcinogenic organic substances. The potential importance of the non-regulated pollutants to assess the air quality was confirmed; in fact the carcinogenic organic compounds showed to have scarce correlation with particulate matter (PM) concentration. An exceptionally high variability of toxic compounds at a daily scale was due to meteorological condition causing periods of extremely high pollution levels.  相似文献   

17.
The aggregate potential health impact due to ambient volatile organic compounds on the population living in the area nearby the petrochemical industrial complex in Thailand was evaluated using measured air contaminants concentration. Airborne volatile organic compounds were collected using canisters and were analyzed by gas chromatography/mass spectrophotometer following the US.EPA TO 15 procedure. Composite samples taken over a 24-h period were collected monthly. Concentrations of volatile organic compounds (VOCs) were analyzed for a suite of 24 compounds covering both carcinogenic and non-carcinogenic substances. Results were determined and analyzed in order to evaluate their spatial variability and their potential health risk. Comparison of data from each monitoring site indicated that patterns of VOCs across sites were different from their major species and their concentrations which might be influenced by nearest potential emission sources. Carcinogenic VOCs such as benzene, 1,3butadiene, and 1,2 dichloroethane were found to be higher than their annual national standards. A potential cancer risk map was drawn based on benzene concentration in order to illustrate the zone of impact and the number in the population likely to be exposed. Results indicated that 82% of the total area, and 89.6% of the total population were within the impact area. It was suspected that high concentrations of benzene and 1,3 butadiene might be attributed by both the mobile source and the point source of emissions while 1,2 dichloroethane was suspected to be emitted from factories located upwind from the monitoring sites. Hazard quotients and hazard indexes were applied to determine chronic health effects with non-cancer endpoints. Calculated values of hazard indexes for each of the target organ systems were lower than 1, which indicated that the non-cancer chronic risk due to level of volatile organic compounds in the study area was less.  相似文献   

18.
The Food and Drug Administration multi-component regulatory procedure for determining polynuclear aromatic hydrocarbons in foods was recently used to survey 24 foodstuffs for the presence of these compounds. The procedure has a reliable limit of quantitation of 2 ppb. The potent carcinogen benzo(a)pyrene was detected in only one of the 24 products analyzed, at a level of 3 ppb. Pyrene and/or fluoranthene were found in 19 of the 24 samples examined, at levels ranging from less than 1 ppb to about 75 ppb. A comparison of the recent survey data to that obtained approximately 10 years ago reveals that the types and levels of polynuclear aromatic hydrocarbons found are essentially unchanged.  相似文献   

19.

Investigations were carried out to assess air and potable waterpollution with selected highly bioactive organic compounds,including polycyclic aromatic hydrocarbons (PAHs), in theenvironment of the Silesian Rehabilitation Centre, Repty ?l?skie, Poland. The results were compared with those forother towns of the region.Solid phase extraction (SPE) and capillary gas chromatography(CGC) with flame ionization detector (FID) and mass spectrometer(MS) were used for a qualitative-quantitative analysis. Moreover, water concentration of calcium, magnesium ions andnitrite ions were measured by spectrophotometric methods. Thequality of the Centre environment air and water found to besatisfactory and better than that in the other sampling sites which were studied for all the parameters.

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20.
Few analytical methods exist that combine chemical and sensory analysis of odorous compounds in whole air. Volatile organic compounds were collected by sampling air downwind from a small dairy through sorbent tubes of Tenax TA and Carboxen 569. Samples were analyzed by thermal desorption into a cryotrap and subsequent gas chromatographic separation, followed by simultaneous olfactometry and mass spectrometry. Because compounds are concentrated during sampling, sensory analysis encountered compounds at a concentration 40 times that in air, making this a useful method for identifying trace compounds participating in odor. Twenty odorous and nonodorous compounds were identified and quantified, including straight-chain and aromatic hydrocarbons, chlorinated compounds, alcohols, ketones, aldehydes, and organic acids, at air concentrations of 0.55-320.20 microg/m(3). Compound peaks were characterized by odors ranging from offensive to pleasant, demonstrating the integrative nature of olfaction. This method could be useful in studying many kinds of odors in air.  相似文献   

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