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1.
Spontaneous combustion of oil shale is very common as a result of long-time exposure to the air in the Fushun West Open-Pit Mine and West Dump. The PAHs in the high-grade off shale and its spontaneous combustion product were analyzed semiquantitatively by GC-MS in order to investigate their distribution in different states and their potential negative effects on the environment. Totally 57 and 60 PAHs and their alkyl homologues were identified in the two analyzed samples, among which the alkyl derivatives were predominant, taking up to about 65% in the total PAHs. Those low-molecular mass PAHs (3- or 4-ring) were the main compounds in the two samples. Ten of sixteen USEPA priority pollutant PAHs were detected in two samples, of which phenanthrene was the richest whose contents were 6.93% and 15.03%. Based on comparison of analysis results, the amount and contents of PAHs, except for triaromatic steroid group, were higher in the burning oil shale. So it can be determined that the effects caused by spontaneous combustion of oil shale would be more serious and that the effects of the Fushun oil shale and its spontaneous combustion on the environment should not be ignored in the future work.  相似文献   

2.
《Applied Geochemistry》2001,16(11-12):1429-1445
Polycyclic aromatic hydrocarbons (PAHs) were measured in surface sediments and dated core sediments from the Pearl river and estuary, China, to investigate the spatial and temporal variability of anthropogenic pollutants. The sediments from the sampling stations at the Guangzhou channel have the highest concentrations of PAHs, owing to contributions from the large amount of urban/industrial discharges from the city of Guangzhou. The significant decrease of PAHs concentrations in sediments from the Shiziyang channel is mainly attributed to the increasing degradation and desorption of low molecular weight PAHs and alkyl PAHs, and the dilution by less contaminated water and particles from the East river. The PAH contaminants were concentrated on the western side in the Lingding bay of the Pearl river estuary because of the hydrodynamic and sedimentation conditions. Based on the characteristics of the parent compound distributions (PCDs) and the alkyl homologue distributions (AHDs) of PAHs, the potential source of PAHs in sediments from each sampling station was identified. Results indicated that the pyrogenic (combustion) source, characterized by the abundance of parent PAHs, were predominant in the heavily contaminated station (ZB01) near the aging industrial area, and the petrogenic (petroleum- derived) PAHs were more abundant in the stations (ZB02, ZB03) adjacent to the petrochemical plant and shipping harbor. Sediments from Lingding bay show variable distributions of PAH composition and variety in the proportion of combustion and petrogenic sources for the PAHs in different stations. Perylene, a naturally derived PAH, was found to be highly abundant in less contaminated stations. Analysis of the dated sediments (210Pb) indicates that higher PAH concentrations occurred in the sediments deposited after 1980, and higher fluxes of PAHs discharged to the Pearl river are found after 1990.  相似文献   

3.
Concentrations, spatial distribution and sources of 16 polycyclic aromatic hydrocarbons (PAHs) listed by the United States Environmental Protection Agency as priority pollutants were investigated in surface sediments of Bohai Bay, North China. Total concentrations of PAHs were in the range of 140.6–300.7 ng/g (dry wt), with an average of 188.0 ng/g. The three predominant PAHs were phenanthrene, acenaphthene and naphthalene. Sedimentary PAH concentrations of the north and central Bohai Bay were higher than those of the southern side of this bay. PAHs source analysis suggested that PAHs in most of the sediments were mainly from grass, wood and coal incomplete combustion. At other stations near the estuaries (Luanhe River Estuary and Chaohe River Estuary) or the oil drilling platform, both petrogenic and pyrogenic inputs were significant. The pyrogenic PAHs close to the oil drilling platform were mainly from petroleum combustion.  相似文献   

4.
Black carbon (BC) in soils plays a key role of carrying hydrophobic pollutants like polycyclic aromatic hydrocarbons (PAHs). However, little is known about the spatial distribution, sources of BC and its relationship with PAHs in urban soils. We studied BC, total organic carbon (TOC) and PAHs concurrently in 77 soils collected from downtown area, suburban and rural area and industrial area of Shanghai, China. BC was determined by both chemical oxidation (dichromate oxidation, BCCr) and chemo-thermal oxidation (CTO-375, BCCTO). BC sources were identified qualitatively by BC/TOC concentration ratios and BC-cogenerated high molecular weight (HMW) PAH isomer ratios and quantitatively by principal component analysis followed by multiple linear regression (PCA-MLR). Results showed that BCCr concentration (4.65 g/kg on average) was significantly higher than BCCTO (1.91 g/kg on average) in Shanghai soils. BCCr concentrations in industrial area were significantly higher than those in other two. Stronger correlation was found between PAHs and TOC, BCCr than that between PAHs and BCCTO, which indicates the possibility of PAHs being carried by charcoal and other organic matters thus negating its exclusive dependence on soot. Charcoal was therefore suggested to be taken into account in studies of BC and its sorption of PAHs. BC/TOC ratios showed a mixed source of biomass burning and fossil fuel combustion. PCA scores of BC-cogenerated HMW PAHs isomer ratios in potential sources and soil samples clearly demonstrated that sources of BC in urban soils may fall into two categories: coal and biomass combustion, and traffic (oil combustion and tire wear). PCA-MLR of HMW PAHs concentrations in soil samples indicated that coal and oil combustion had the largest contribution to BC in urban soils while tire wear and biomass combustion were important in downtown and rural area, respectively, which indicated they were main sources of HMW PAHs and presumably of BC.  相似文献   

5.
山东半岛海岸带面临着各类复杂的环境问题,尤其是受到了多环芳烃(PAHs)等持久性有机物的污染,本文研究了整个山东半岛典型海岸带62个站点表层沉积物中PAHs的含量及其分布特征,并对其来源和潜在风险进行解析与评价。研究表明,该地区表层沉积物中16种PAHs总含量为0.06~3191.40 ng/g(平均值262.08 ng/g),与国内外海岸带相比,山东半岛海岸带表层沉积物中PAHs整体污染状况处于较低水平,但个别站点的PAHs含量偏高。运用特征比值法、相关性分析及主成分分析法解析研究区PAHs主要来源为木柴、煤炭、油类的燃烧以及油类泄露的联合作用。采用效应区间低值法(ERL)和中值法(ERM)对PAHs进行生态风险评价,结果表明莱州湾周边所有站点及威海、青岛周边个别站点苊、芴浓度位于ERL值与ERM值之间,但多数站点对生态环境潜在负面效应很小。山东半岛典型海岸带中PAHs对生物的毒副作用尚在安全可控范围内,极少对生态环境产生负面效应。  相似文献   

6.
Concentrations and sources of polycyclic aromatic hydrocarbons (PAHs) were investigated in surface sediments of the Yellow River Estuary (YRE). The isobath-parallel tidal and residual currents play important roles in the variation of PAH distribution, such that the contamination level of PAHs in fine-grained sediments is significantly higher than in the relatively coarse grain size sediments. Both diagnostic ratios and principal component analysis (PCA) with multivariate linear regression (MLR) were used to apportion sources of PAHs. The results revealed that pyrogenic sources are important sources of PAHs. Further analysis indicated that the contributions of coal combustion, traffic-related pollution and mixed sources (spills of oil products and vegetation combustion) were 35, 29 and 36 %, respectively, using PCA/MLR. Pyrogenic sources (coal combustion and traffic-related pollution) contribute 64 % of anthropogenic PAHs in sediments, which indicates that energy consumption could be a predominant factor in PAH pollution of YRE. Acenaphthylene and acenaphthene are the two main species of PAHs with more ecotoxicological concern in YRE.  相似文献   

7.
Oyster and sediment samples collected from six sites in Galveston Bay from 1986 to 1998 were analyzed for polynuclear aromatic hydrocarbons (PAHs). Total concentrations of parent PAHs in oysters ranged from 20 ng g−1 at one site to 9,242 ng g−1 at another and varied randomly with no clear trend over the 13 year period at any site. Concentrations of alkylated PAHs, which are indications of petroleum contamination, varied from 20 to 80,000 ng g−1 in oysters and were in higher abundance than the parent PAHs, indicating that one source of the PAH contaminants in Galveston Bay was petroleum and petroleum products. Four to six ring parent PAHs, which are indicative of combustion source , were higher than those of 2–3 ring parent PAHs, suggesting incomplete combustion generated PAHs was another source of PAHs into Galveston Bay. Concentrations of parent PAHs in sediments ranged from 57 to 670 ng g−1 and were much lower than those in oysters. Sediments from one site had a high PAH concentration of 5,800 ng g−1. Comparison of the compositions and concentrations of PAHs between sediment and oysters suggests that oysters preferentially bioaccumulate four to six ring PAHs. PAH composition in sediments suggests that the sources of PAH pollution in Galveston Bay were predominantly pyrogenic, while petroleum related PAHs were secondary contributions into the Bay.  相似文献   

8.
Twenty-five drinking water samples collected from the household property and from the Sydney Regional Municipality well bores and lakes were analyzed to evaluate the various inorganic parameters, level of concentrations of the priority elements and polyaromatic hydrocarbons (PAHs). The pH of the majority of the water samples was below the guidelines adopted by Health and Welfare Canada (1996), although the drinking waters supplied by the Sydney Regional Municipality were within the guidelines. Only three water samples (13 and 14: Point Aconi area and 16: Port Morien fish plant) have elevated concentrations of various PAHs compared to the detection limit. Eight samples have higher concentrations of manganese and two samples (number 7: Sydney Airport and number 1: RCMP Office; Reserve Mines) have higher concentrations of priority elements (especially lead) than the recommended guidelines (>0.05 mg/l). These priority elements and the PAHs in the drinking water samples may have originated from the leaching of the individual coal seams within that part of the Sydney Basin. Other potential sources of these elements and PAHs (Power Plant disposal, Sydney Tar Pond, metalliferous rocks, hydrocarbon reservoir rocks) are not located close enough to the sampling sites of the water samples. Therefore, they are not considered the source of these elements and PAHs.  相似文献   

9.
Concentration, distribution, and sources of 16 polycyclic aromatic hydrocarbons (PAHs) were investigated in surface sediments of Laizhou Bay, China. Total PAH concentrations ranged from 97.2 to 204.8 ng/g, with a mean of 148.4 ng/g. High concentrations of PAHs were found in the fine-grained sediments on both sides of the Yellow River estuary (YRE). In contrast, low levels of PAHs were observed in relatively coarse grain sediments, suggesting hydrodynamics influence the accumulation of sedimentary PAHs. The YRE and its adjacent area is the main sink for Yellow River-derived PAHs. Both PAH isomer ratios and principal component analysis (PCA) with multivariate linear regression (MLR) were applied to apportion sources of PAHs. Results indicated that both pyrogenic and petrogenic PAH sources were important. Further PCA/MLR analysis showed that the contributions of coal combustion, petroleum combustion and a combined source of spilled oil and biomass burning were 41, 15 and 44%, respectively. From an ecotoxicological viewpoint, the studied area appears to have low levels of PAH pollution.  相似文献   

10.
《Organic Geochemistry》1999,30(8):881-889
The 13C/12C isotopic ratios for coal-derived polycyclic aromatic hydrocarbons (PAHs) from a number of processes encompassing low and high temperature carbonisation, gasification and combustion have been determined using gas chromatography–isotope ratio mass spectrometry (δ13C GC–IRMS). The results, in conjunction with those for PAHs released under controlled laboratory pyrolysis conditions, indicate that the primary control on the isotopic values of coal-derived PAHs is likely to be the extent of ring growth required to form PAHs during processing. Thus, for relatively mild conversion processes such as low temperature carbonisation where the major aromatics are alkyl substituted 2–3 ring PAHs, the isotopic signatures are similar to those of the parent coals (−24 to −25‰ for UK bituminous coals). However, the δ13C values for the PAHs become lighter in going to high temperature carbonisation (−25 to −27‰), gasification (−27 to −29‰ for old Town gas plants in the UK) and combustion (−29 to −31‰) as the extent of ring condensation increases and confirming that the PAHs are not released as primary volatiles. To demonstrate the potential of applying these differences to source apportion environmental PAHs where major inputs from coals can be expected, soil and vegetation samples taken close to a low temperature carbonisation plant (Bolsover, North Derbyshire) have been analysed. In addition to low temperature coal tar, significant inputs of PAHs from transport fuels, high temperature carbonisation and possibly combustion (coal/biomass) have been inferred from the isotopic ratios, taken in conjunction with the differences in alkyl substitution patterns.  相似文献   

11.
Joanna Kinsey 《Geoforum》1981,12(4):331-347
Liverpool developed round the Port which brought prosperity to the region dating from the 18th century. Over the last twenty years, however, changes in trading patterns and cargo-handling methods have had a distinct and drastic impact upon the Port. Today it is struggling to compete with South and East coast rivals. Its economic impact on the local economy is also declining. Through examining activity linked with the Port it was found that (a) jobs totally dependent upon the Port number less than 15,000, (b) firms supplying the Port are generally only dependent upon it for an extremely small proportion of their total turnover and (c) the Port's customers, which tend to be located in the North West, West Midlands and Yorkshire-Humberside, are decreasing in number and are frequently constrained by shipping companies for their choice of port.  相似文献   

12.
Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous organic pollutants in urban environments including urban soils. Elevated concentrations of PAHs in urban soils are caused by incomplete combustion of petroleum and coal. This study assesses 16 individual PAH compounds in a total of 112 surficial soil samples. The objective was to assess and compare the levels of contamination as well as examine the main sources of PAHs in four urban agricultural soils using molecular ratios of some specific hydrocarbons. The study showed that PAH levels in soil ranged from 1.23 ng/kg in soil collected from Dzorwulu to 2.95 ng/kg in soil collected from Ghana Broadcasting Cooperation (GBC) vegetable irrigation site. Of the total PAHs, the more water soluble PAHs (2–4 rings), which tend to be concentrated in the vapour phase were found to dominate the soils. The percentage dominance were Dzorwulu (52.8 %), Marine Drive (62.5 %), CSIR (53.2 %) and GBC (49.2 %). However, there were significant levels of the more carcinogenic PAHs (5–6 rings) present with percentages as 47.1, 37.5 46.8 and 50.8 % for Dzorwulu, Marine Drive, CSIR and GBC vegetable irrigation sites, respectively, and therefore, may impact negatively on public health. Based on the classification by the Institute of Soil Science and Plant Cultivation in Pulawy, Poland, urban soils in Accra could be classified as contaminated to different levels. Molecular ratios of Flu/pyr and PA/Ant were calculated to determine the main sources of PAHs. Results showed that PAHs could originate mainly from incomplete combustion of petroleum products, especially from atmospheric fallout from automobile exhausts. The study further showed that B(a)P concentration of 0.05 ng/kg in soil from GBC urban vegetable irrigation site requires immediate clean-up exercise and monitoring to mitigate human health impact.  相似文献   

13.
The distribution and sources of PAHs in soil as well as PAHs profiles have been investigated in areas with anthropogenic pollution in the Niger Delta (Nigeria) such as Warri and Ughelli. PAHs were identified in 21 soil samples (0–10cm upper layer) collected in May, 2003. The typical total PAHs level in Niger Delta soil ranged from 182 ± 112 - to - 433 ±256 íg/kg dw. PAH concentrations in soil samples from Warri Refinery, Tanker Loading point and Ugboko via Rapele oil field were quite high ( the mean ÓPAH concentrations were 433, 402 and 384 íg/kg dry weight respectively). The dominant PAHs in soil samples were pyrene, naphthalene and benzo[k]fluoranthene. The soil total PAHs (PAHtot.) concentration, normalized to organic carbon content (OC), ranged from 11.4 to 47.2 mg PAHtot. /kg OC; and showed that organic matter of the soil samples from Quality Control Centre, Ugelli West is highly contaminated with PAHs and had a value of 47.2 ± 31.2 mg PAHtot./kg OC. Two and three ring aromatic hydrocarbons predominated in soil samples from Ughelli West, Tanker Loading point and Delta Steel Company, which is indicative of petrogenic origin.  相似文献   

14.
The history records of polycyclic aromatic hydrocarbons (PAHs), lead and its stable isotope ratios were determined in a sediment core to receive anthropogenic impacts on the Shilianghe Reservoir in eastern China. The historical changes of PAHs concentrations, PAHs fluxes, Pb/Al and Pb isotope ratios showed a synchronous trend throughout the core, suggesting changes in energy usage and correlating closely with the experience of a rapid economic and industrial development of the catchment, Linyi City in eastern China. PAHs isomer ratios results reveal PAHs in sediments are dominantly anthropogenic pyrogenic source, dominated by the combustion of coal and biomass. Furthermore, the Pb isotopic composition also clearly indicates that coal combustion dust mainly contributed to the Pb burden in the reservoir sediments. Based on mix end member model of Pb isotope ratios, coal combustion dust dominated anthropogenic Pb sources over fifty years contributing from 31% to 62% of total Pb in sediment. And the contribution of leaded gasoline was low than average 25%. In addition, a stable increase of coal combustion source was found in sediment core, while the contribution of leaded gasoline had declined in recent decades, with the phase-out of leaded gasoline in China.  相似文献   

15.
太原市区土壤中多环芳烃污染特征研究   总被引:2,自引:0,他引:2  
采用1个样/km2的密度,1个分析组合样/25km2的方法,对太原市区土壤中多环芳烃进行了调查。结果表明,太原市区土壤中多环芳烃的平均含量为8.65μg/g;空间分布上北高南低,高值点主要位于工业区及交通要道地段;组成上以四环及四环以上的多环芳烃为主。通过与国内外城市土壤的对比可知,太原市土壤PAHs污染已相当严重,其来源主要是煤炭的燃烧。太原市工业布局、能耗类型和地理位置是造成土壤PAHs污染的主要原因。  相似文献   

16.
Polycyclic aromatic hydrocarbons (PAHs) in soil originate from various sources under different spatial scales. Coregionalization analysis is more revealing than univariate geostatistical analysis. Scale-dependent spatial features of variables reflect different sources of spatial variability. In this study, 188 topsoil samples in the Tianjin area were collected. The contents of 16 PAHs and soil background properties were determined for all samples. A multivariate geostatistical approach was used for multi-scale spatial analysis for PAH compounds. Results show that coal combustion was the major source for the spatial distribution patterns of PAHs in the topsoil of the studied area. It worked mainly at the short-range scale (5–10 km). Significant spatial variation patterns were identified. In contrast, no significant spatial distribution trends at the nugget (0–5 km) or long-range scales (10–50 km) were seen. Long-range transport and site contamination of PAHs might not be key contributors in forming the distribution pattern of PAHs in the topsoil of Tianjin area.  相似文献   

17.
环境中的多环芳烃及其生物恢复技术   总被引:9,自引:0,他引:9  
多环芳烃是一大类广泛存在于环境中的有机污染物。天然燃烧、火山爆发、矿物资料及其它有机物的不完全燃料和热解产生的PAH进入大气中,气态沉降、城市地表径流、城市污水、废水及油的溢涵和渗漏等是PAH进行地表水的主要途径,大气中PAH的干、湿沉降,污水灌溉,地面及地下储油装置的渗漏,地面固体废物堆的淋滤等是土壤中PAH的主要来源,沉积物和土壤是PAH的主要环境归宿。生物恢复是一种处理有机污染的新方法。  相似文献   

18.
19.
Pyrolysis-GC/MS is advantageous as a tool for rapid sediment contamination assessment because of the small sample size required, minimal sample preparation and its ability to detect a wide variety of organic pollutants as well as naturally-occurring biological materials. Py-GC/MS was applied, together with determination of organic carbon, and major and minor element concentrations, to evaluate potentially contaminated sediments in the port of Barcelona (Spain) and the adjacent Llobregat River delta. Detected contaminant markers, most evident in the Old Port (Port Vell) area, included hopanes and alkylated PAHs (petroleum), sterenes (sewage), C16–C19 phenylalkanes (detergents) and parent PAHs (combusted fuels).  相似文献   

20.
Previous studies have suggested that coal from the 1891 shipwreck of a collier off Victoria, BC, Canada is responsible for elevated parent (unsubstituted) PAH concentrations in sediments near deep marine outfalls from Esquimalt and Victoria in the Strait of Juan de Fuca. To resolve this question, we analysed a comprehensive suite of resolved and unresolved complex mixture (UCM) alkanes, tricyclic terpane, hopane and sterane biomarkers, and parent and alkyl polycyclic aromatic hydrocarbons (PAHs) in samples of coal, wastewater and sediments. Composition patterns, principal components analysis (PCA) models and PAH and biomarker ratios all indicate that coal from the collier does not make a dominant contribution to any sediment sample. Mass balance calculations based on the n-C24 content and 24/4 tetracyclic terpane to 26/3R tricyclic terpane ratio in coal provide a particularly good match between predicted and observed alkyl PAH concentrations for sediments with high alkyl naphthalenes and phenanthrene/anthracenes and low UCM, but the predicted coal contribution substantially underestimates the measured parent PAHs for all sediment samples. Methylbenz[a]anthracene/chrysene profiles for sediments with a dominance of parent PAHs are very close to coal tar, with a marked predominance of methylbenz[a]anthracenes and the possible 10-methylbenz[a]anthracene as a major constituent, while the methylchrysenes predominate in coal. Hence, coal from the collier could account for most alkyl PAHs in the sediments, but dredged sediment containing pyrolised coal waste from a former coal gas plant in Victoria Harbour is a more likely source for the samples with elevated parent PAHs. PAH ratios indicate that these sources are superimposed on combustion PAHs introduced by a combination of atmospheric deposition and delivery via stormwater and the outfalls. Parent PAH distributions also suggest that PAHs in wastewater that originate from oils and soot in liquid fossil fuel combustion are dispersed and degraded, while the larger wood char particles (containing PAHs more protected from degradation) settle closer to the outfalls. Overall, results suggest that PAHs have predominant sources in wood combustion, coal and possibly coke, with a likelihood of much lower bioavailability than would be expected from wastewater dominated by oils and soot from vehicle combustion.  相似文献   

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