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1.
The occurence and temporal variations of a variety of low to medium polarity organic compounds in the volatility range bracketed by n-heptane and n-octadecane have been studied in seawater from a station in Vineyard Sound, Massachusetts, and from a tidal creek in Sippewisset Marsh, Massachusetts. The closed-loop vapor phase stripping method of Grob and Zürcher (J. Chromatogr., v. 117, p. 285–294), high resolution glass capillary gas chromatography, and gas chromatography-mass spectrometry were used. Approximately 50 compounds were found at ≥ 2 ng/kg; most were recovered at less than 10 ng/kg, while the 20 ng/kg level was only rarely exceeded by a few components. The total material recovered was 0.2–1.0 μg organic carbon equivalent/kg seawater. The major compound classes found were normal alkanes, alkenes, aromatic and alkylaromatic hydrocarbons, n-aldehydes, dimethyldisulfide and dimethyltrisulfide, and a few halogenated hydrocarbons. The preliminary results suggest that both biogenic and anthropogenic sources were representted. Also, air-sea gas exchange and other physical processes may be important non-biological sinks.  相似文献   

2.
为了解广州地区蔬菜基地有机污染物的分布情况,选取了6个代表性基地进行调查采样,测试分析了表层土壤、蔬菜及灌溉水中15种邻苯二甲酸酯(PAEs)化合物、16种多环芳烃(PAHs)化合物和19种有机氯农药(OCPs)化合物的质量分数及质量浓度.结果表明:在15种PAEs化合物的总质量分数(w(ΣPAEs))中,土壤样品为158.0~4 321.0 ng/g,蔬菜样品为1 134.0~48 576.0 ng/g;水样中15种PAEs化合物的总质量浓度(ρ(ΣPAEs))为632.0~14 271.0 ng/L;就单个化合物而言,以DiBP、DBP、DEHP三种污染物为主,其三项之和占所有PAEs质量分数的97.5%~99.1%;在16种PAHs化合物的总质量分数(w(ΣPAHs))中,土壤样品为28.48~1 121.96 ng/g,蔬菜样品为238.09~1 000.61 ng/g;水样中16种PAHs化合物的总质量浓度(ρ(ΣPAHs))为338.21~1 239.78 ng/L;在19种OCPs化合物的总质量分数(w(ΣOCPs))中,土壤为0.04~71.28 ng/g,蔬菜为1.08~9.18 ng/g.总体上看,各基地土壤中DBP质量分数均超标,多环芳烃类在灵山、花东、黄埔菜地土壤中存在轻微污染,有机氯农药均未出现污染.  相似文献   

3.
The organic composition of produced water samples from coalbed natural gas (CBNG) wells in the Powder River Basin, WY, sampled in 2001 and 2002 are reported as part of a larger study of the potential health and environmental effects of organic compounds derived from coal. The quality of CBNG produced waters is a potential environmental concern and disposal problem for CBNG producers, and no previous studies of organic compounds in CBNG produced water have been published. Organic compounds identified in the produced water samples included: phenols, biphenyls, N-, O-, and S-containing heterocyclic compounds, polycyclic aromatic hydrocarbons (PAHs), aromatic amines, various non-aromatic compounds, and phthalates. Many of the identified organic compounds (phenols, heterocyclic compounds, PAHs) are probably coal-derived. PAHs represented the group of organic compounds most commonly observed. Concentrations of total PAHs ranged up to 23 μg/L. Concentrations of individual compounds ranged from about 18 to <0.01 μg/L. Temporal variability of organic compound concentrations was documented, as two wells with relatively high organic compound contents in produced water in 2001 had much lower concentrations in 2002.  相似文献   

4.
The Tunisian environmental legislation that follows the EC Directives requires monitoring of persistent, toxic and bio-accumulated substances commonly considered as hazardous substances. In order to comply with this requirement, samples of sea water, sediment and biota from the urbanized and industrialized coast line of Sfax city are investigated. This study presents the results of petroleum hydrocarbon content, distribution and probable origin (anthropogenic and/or biogenic) in 16 intertidal sediments of Sfax coastal area. Alkane distribution indices and hydrocarbon distribution patterns are used to identify natural and anthropogenic input. Non-aromatic hydrocarbons present a high concentration with a range varying from 180 to 1,400 μg/g of dry sediment. The total concentrations of polycyclic aromatic hydrocarbons (PAHs) varied from 0.41 to 5.6 μg/g dry weight. These concentrations are comparable to other marine areas that receive important inputs. n-Alkanes with carbon number ranging from 15 to 35 are identified to be derived from both biogenic and anthropogenic sources in varying proportions. Pristane/phytane ratio shows values lower than 1.4 suggesting the presence of petroleum contamination. This is confirmed by the presence of a large group of unresolved complex mixture and the identification of hopanes with predominant C29 and C30 compounds and steranes with predominance of C27 over C28 and C29 compounds. Ratios of selected PAH concentrations indicate petrogenic and pyrolytic origin of hydrocarbons. Anthropogenic hydrocarbon inputs were more apparent at sites associated with industrial discharges, shipping activities and sewage outfalls.  相似文献   

5.
Small diameter core samples were taken from outcrops of the Permian Phosphoria Formation and the Cretaceous Pierre Shale of the Western United States to determine the effects of weathering on organic matter in shale outcrops. While the Pierre Shale core showed no evidence of weathering, the Phosphoria Formation showed significant reduction of overall organic content and pronounced changes in organic composition over the near-surface interval of the core. Total organic carbon is lower by as much as 60% over the upper 2 ft of the core. Chloroform-soluble organic matter and total hydrocarbon (C15+) concentrations are 50% lower over this same interval. The ratio of saturated to aromatic hydrocarbons decreases steadily with core depth over the upper 2.6 ft of the core. Aromatic hydrocarbons are enriched in the stable carbon-13 isotope by an average of 1.7%. over this same interval. Shallow core samples also show a loss of n-paraffins relative to branched/cyclic compounds in the saturated C15+ fraction.Although the extent of weathering is variable, certain characteristic effects are recognizable and can be applied to the interpretation of outcrop data in organic geochemical studies.  相似文献   

6.
A set of 14 samples—both extracted and unextracted from the Toarcian of the Paris Basin have been investigated using Curie-point pyrolysis-mass spectrometry and Curie-point pyrolysis gas chromatography mass spectrometry. The relative amount of n-alkenes and n-alkanes in the pyrolyzates increases with increasing maximum burial depth of the samples. Comparison of the pyrolysis data of extracted and unextracted samples shows that generation of hydrocarbons from the kerogen starts at a maximum burial depth of ~ 1000m. The increase of pristane and phytane in the extracts of the deeper samples is correlated with the gradual decrease of the characteristic pyrolysis product prist-1-ene. Three samples yield pyrolyzates with high relative amounts of aromatic compounds. This phenomenon probably reflects a different type of contributing organic matter and/or a different environment of sedimentation.  相似文献   

7.
Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous organic pollutants in urban environments and are considered as the priority pollutants. The main objectives of this study were (1) to assess the contamination extent of 16 PAHs compounds in urban street dust and (2) to identify the anthropogenic sources of contamination. Forty-nine samples were analysed for 16 PAHs by gas chromatography/mass spectrometry. Results showed that total PAHs concentrations varied from 2174 to 24,499 ng/g with an average value of 6616 ng/g. Total PAHs concentrations showed a significant correlation with the total organic carbon (TOC) content (r = 0.599, p < 0.0001), suggesting likely that TOC can influence the distribution of PAHs in Xuzhou street dust. Source identification indices suggested that the primary source of PAHs was automobile exhausts. A factor analysis was performed, and three factors were extracted from the available dataset, explaining a total variance of approximately 84.7%. Results from the factor analysis could be indicative of PAHs with different origins.  相似文献   

8.
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   

9.
建立了同时测定土壤中23种挥发性氯代烃和苯系物的吹扫捕集-气相色谱-质谱法.优化了试验条件,标准曲线在0.32×10-9~200.0×10-9范围内呈线性关系,方法检出限（3S/N）为0.077×10-9~0.69×10-9,样品标准添加平均回收率86.5%~117.5%,相对标准偏差（n=7）在1.6%~8.2%之间.  相似文献   

10.
Study of a series of twenty-six German high volatile bituminous B to low volatile bituminous coals of Upper Carboniferous age by recently refined analytical methods (‘flow-blending’ extraction, medium pressure liquid chromatography, HPLC, glass capillary gas chromatography and spectral fluorescence microscopy) reveals that yield and composition of soluble organic matter are strongly controlled by rank. In particular, the following points of inflection are noted in rank trends around 0.9% vitrinite reflectance: a maximum in yields of total soluble organic matter, aromatic hydrocarbons and n-alkanes; the most pronounced change in aromatic hydrocarbon composition; a trend reversal for pristane/ phytane ratios; a gradient change in the odd/even-predominance of long chain n-alkanes; appearance of a bimodal n-alkane distribution; and a sharp drop in concentration of individual n-, and isoprenoid alkanes. This discontinuity in rank trends around 0.9% Rm is interpreted to reflect a major change in reaction types, i.e. a shift from predominantly hydrocarbon generating to predominantly fragmentation reactions. Rank trends of maceral fluorescence exhibit the following pronounced changes over a similar but broader rank range: Different types of the maceral sporinite show a relatively abrupt shift of the fluorescence colour from yellow towards red between 0.8–0.9% Rm while up to about 1.0% Rm a sharp increase is recorded in the proportion of fluorescent vitrinite. This coincidence at a near-equal rank stage suggests a common cause for changes in yield and composition of the soluble organic matter and the maceral fluorescence of these coals.  相似文献   

11.
A solvent–water extraction method was proposed as an assessment tool to estimate the bioavailability of polycyclic aromatic hydrocarbons in coal–tar-contaminated soils. The approach taken was to measure the percent of polycyclic aromatic hydrocarbons extracted by a solvent–water mixture and comparing the results with the percent of polycyclic aromatic hydrocarbons degraded in a soil slurry reactor. Five soil samples from three former manufactured gas plant sites and a coal–tar disposal site which were operated between 1880 and 1947, and 1945 and 1950, respectively, in Iowa, USA were used in this study. Extraction experiments were conducted using acetone–water or ethanol–water mixtures with solvent volume fractions ranging from 1.0 to 0.4 (v/v). The percent of polycyclic aromatic hydrocarbons extracted from the various soils decreased as the volume fraction of the solvent in the solvent–water mixture was reduced. An acetone–water mixture of 0.6 was found to be appropriate in correlating the percent of polycyclic aromatic hydrocarbons degraded to the percent of polycyclic aromatic hydrocarbons extracted. For the first correlation, the percent extracted and the percent biodegraded were modified by using the molecular weights and log K ow of polycyclic aromatic hydrocarbons, respectively. For the second correlation, the equation relating the percent extracted and the percent biodegraded was modified using soil properties such as organic carbon content and percent of clay and silt. Although the experiments were conducted for a limited number of soils, the extraction method appeared to be a good starting point in estimating the bioavailability of polycyclic aromatic hydrocarbons in coal–tar-contaminated soils.  相似文献   

12.
Fifteen sediment samples were studied from five drill sites recovered by the ‘Glomar Challenger’ on Legs I and IV in the Gulf of Mexico and western Atlantic. This study concentrated on compounds derived from biogenic precursors, namely: (1) hydrocarbons, (2) fatty acids, (3) pigments and (4) amino acids.Carbon isotope (δC13) data (values < ? 26%, relative to PDB), long-chain n-alkyl hydrocarbons ( ?C277) with odd carbon numbered molecules dominating even carbon numbered species, and presence of perylene proved useful as possible indicators for terrigenous contributions to the organic matter in some samples. Apparently land-derived organic matter can be transported for distances over 1000 km into the ocean and their source still recognized.The study was primarily designed to investigate: (i) the sources of the organic matter present in the sediment, (ii) their stability with time of accumulation and (iii) the conditions necessary for in situ formation of new compounds.  相似文献   

13.
The objectives of this study were to identify the chlorinated volatile organic compounds near the water surface of two heavily polluted rivers in the south of Taiwan and compare their concentration distributions. Air samples were collected seasonally at the upstream, midstream and downstream water surfaces of each river and the chlorinated volatile organic compounds were analyzed qualitatively and quantitatively by gas chromatography and electron capture detector. Totally, twelve kinds of chlorinated volatile organic compounds were found at the water surfaces of both rivers and many of them were reported to be carcinogenic or probably carcinogenic to human. The results showed that each chlorinated volatile organic compound had its own distribution pattern and no good correlation of chlorinated volatile organic compounds between both rivers was obtained. The chlorinated volatile organic compounds identified at the river water surface of Fong Shan Stream showed much higher concentration than those of Chuen-Tsen River. Several chlorinated volatile organic compounds, including chlorodibromomethane, hexachlorobutadiene, 1,1,2,2-tetrachloroethene and 1,2-dibromo-3-chloropropane were found with much higher concentration (mean concentrations of 124.5 μg/m3, 334.5 μg/m3, 92.2 μg/m3, 268.4 μg/m3, respectively) at the water surface of Fong Shan Stream in some seasons (especially spring and summer, summer and winter, spring and winter, spring and summer, respectively) and they were reported to be possibly carcinogenic to human. Therefore, it may be concluded that the people living close to Fong Shan Stream possibly had higher health risks due to the release of volatile organic compounds from the heavily polluted river.  相似文献   

14.
In this work, we use Fourier transform infrared spectroscopy (FTIR) and nuclear magnetic resonance spectroscopy (13C NMR) data to quantify the changes of major chemical compound classes (carboxylic acid, amide, ester, aliphatic, aromatic and carbohydrate) in high molecular weight (HMW, >1 kDa) dissolved organic matter (DOM) isolated along a transect through the Elizabeth River/Chesapeake Bay system to the coastal Atlantic Ocean off Virginia, USA. Results show that carboxylic acids and aromatic compounds are lost along the transect, while HMW DOC becomes enriched in carbohydrate moieties that could have a mid-transect source, perhaps the intensive red tide bloom (Choclodinium polykrikoides) which occurred during our sampling period. Taking the second derivative of the FTIR spectra resolved three pools of de-protonated carboxylic acids at our Dismal Swamp site (used to represent terrestrial organic matter in this area): one carboxylic acid pool, complexed with iron, seems to be lost between the Dismal Swamp and river sites; the second appears biogeochemically active throughout the riverine transect, disappearing in the coastal ocean sample; the third seems refractory, with the potential to be transported to and to accumulate within the open ocean. Five-member ring esters (γ-lactones) were the major ester form in the Dismal Swamp; aliphatic and acetate esters were the dominant esters in the estuary/marine DOM. No amide groups were detectable in Dismal Swamp DOM; secondary amides were present at the estuarine/marine sites. Coupling FTIR with 13C NMR provides new insights into the biogeochemical roles of carboxylic acid, amide and ester compounds in aquatic ecosystems.  相似文献   

15.
High concentrations of hydrocarbons (500–3000 μg/g dry weight) together with a complex and wide molecular weight range of composition, and low 14C activity of δ14C = ?833 ± 50%. strongly indicate that fossil fuel hydrocarbons make up the bulk of hydrocarbons in and near the New York Bight dump site areas. The composition and concentrations of hydrocarbons in Hudson Channel sediments suggest some transport of dump site hydrocarbons to areas in the channel midway to the edge of the continental shelf. Sediments at 16 stations in other areas of the continental shelf, continental slope and abyssal plain have hydrocarbon concentrations and compositions indicating that no more than 1 μg/g dry weight of fossil fuel hydrocarbons are present.N-alkanes from land sources were among the most predominant hydrocarbons in all samples except those in the New York Bight region. Their presence in abyssal plain surface sediments documents transport of some land derived organic matter to these deep ocean areas. Two 25-carbon cycloalkenes are among the more predominant hydrocarbons in continental shelf surface sediments except for the dump site areas. These two compounds are present in lower concentrations in slope sediments and are not detected in abyssal plain sediments.  相似文献   

16.
Sediment samples from the coastal zone of the Gulf of Suez contain a variety of organic compounds from anthropogenic and natural sources. A total of 12 surface samples of bottom sediments were collected with an Ekman grab sampler along an off-shore transect south of Ras Abu el-Darag. The samples were extracted with a mixture of dichloromethane and methanol (3:1 v/v) after drying and sieving through 250 μm mesh. The extracts were derivatized and analyzed by gas chromatography–mass spectrometry in order to characterize the chemical composition and sources of the organic components. Marine with minor terrestrial biota were the major natural sources of organic tracers and included n-alkanoic acids, sterols and saccharides (5.7–76.7%). Anthropogenic sources, from petroleum related activities, detergent usage for spill cleaning and littering, are indicated by the presence of n-alkanes with carbon preference index ≤1.0, hopanes, steranes, unresolved complex mixture of branched and cyclic hydrocarbons, alkyl nitriles, alkamides and plasticizers. Their total relative concentrations ranged from 23.3 to 97.3% of the total extracts. Petroleum residues from natural seepage may also be part of these hydrocarbons. The levels of anthropogenic inputs decrease from about 94% in coastal zone sediments to about 20% in sediments from the reef front.  相似文献   

17.
Distribution of volatile organic compounds around a polluted river   总被引：2，自引：2，他引：0  
The objectives of this study were to investigate the species and the concentration distribution of volatile organic compounds around a heavily polluted river. Air samples were collected seasonally at different locations near the polluted river. Samples were then analyzed by gas chromatography (electron capture detector for chlorinated organic compounds and flame ionization detector for ordinary hydrocarbons). The data was then analyzed by the statistical product and service solutions software. The results showed that total of 26 species of volatile organic compounds were identified. Each individual had its own concentration distribution pattern at different seasons and aliphatic volatile organic compounds displayed much higher concentrations than most benzenoic volatile organic compounds. In aliphatic volatile organic compounds, 1,2-dibromo-3-chloropropane, hexachlorobutadiene and 1,2-dibromoetane had much higher concentrations at the nearby environment of the river and they have been claimed to be carcinogenic to some experimental animals and possibly to human. Therefore, It is in doubt that for a long term, the volatile organic compounds evaporating out of the stream may threat the health of the residents living very close to the river. The concentrations of tetrachloroethene, 1,1,2,2-tetrachloroethane, hexachlorobutadiene, dibromoetane, dichlorobenzene and sec-butylbenzene appeared at the nearby environment of the river had significant correlations (P < 0.05) with those of each other or many other volatile organic compounds.  相似文献   

18.
Supercritical CO2 (scCO2) is a good solvent for organic compounds such as benzene, toluene, ethyl-benzene, and xylene (BTEX), phenols, and polycyclic aromatic hydrocarbons (PAHs). Monitoring results from geological carbon sequestration (GCS) field tests have shown that organic compounds are mobilized following CO2 injection. Such results have raised concerns regarding the potential for groundwater contamination by toxic organic compounds mobilized during GCS. Knowledge of the mobilization mechanism of organic compounds and their transport and fate in the subsurface is essential for assessing risks associated with GCS. Extraction tests using scCO2 and methylene chloride (CH2Cl2) were conducted to study the mobilization of volatile organic compounds (VOCs, including BTEX), the PAH naphthalene, and n-alkanes by scCO2 from representative reservoir rock and caprock obtained from depleted oil reservoirs and coal from an enhanced coal-bed methane recovery site. Results showed that the extent of mobilization for the organic compounds was a function of the source rock. In fate and transport sand column experiments, moisture content was found to have an important influence on the transport of the organic compounds. In dry sand columns the majority of the compounds were retained in the column except benzene and toluene. In wet sand columns the mobility of the BTEX was much higher than that of naphthalene. Based upon the results determined for the reservoir rock, caprock, and coal samples studied here, the risk to aquifers from contamination by organic compounds appears to be relatively low; however, further work is necessary to fully evaluate the risks.  相似文献   

19.
This study aimed to evaluate the total concentration of polycyclic aromatic hydrocarbons in sediments of Iguassu River in Southern Brazil. Alongside the concentration, the amount of such compounds bioavailable was also evaluated. This is accomplished by comparing its total amount present in sediments and the amount extracted by n-butanol. The results showed that the total concentration of polycyclic aromatic hydrocarbons presented in sediment ranged from 4.49 to 58.75???g/g. The total amount of polycyclic aromatic hydrocarbons extracted by n-butanol ranged from 1.22 to 17.07???g/g. The use of n-butanol represents the mimetic conditions that hydrocarbons, derived from oil, could be taken up by organisms. Most of the hydrocarbons extracted by n-butanol were those with lower octanol?Cwater partition constant, usually those with three and four rings. Compounds with more than four rings were extracted in lower or insignificant amounts. Even the hydrocarbons with lower molecular weight available may be degraded or eliminated by organisms, when accumulated. Estimating bioavailability of hydrocarbons represents what specific hydrocarbons could be available to be taken up by organisms.  相似文献   

20.
Polycyclic aromatic hydrocarbons and polychlorinated biphenyls were investigated in sediment of bitumen deposit impacted area of Agbabu, Nigeria, to determine the present level of contamination with these toxic compounds prior to exploitation. Samples were collected during the dry season (March) and the wet season (August) of year 2008. Analysis was carried out with gas chromatography using mass spectrometry detector for polycyclic aromatic hydrocarbons and flame ionization detector for polychlorinated biphenyls. In the dry season sum of concentration of PAHs ranged from zero to 0.12 ± 0.06 ppm, while in the wet season the minimum was 0.18 ± 0.07 ppm and the maximum was 1.04 ± 0.16 ppm. Most of these values were higher than sum of polycyclic aromatic hydrocarbons concentrations of 1–10 μg/kg indicating that they were likely to come from anthropogenic sources. Average concentrations of PAHs such as naphthalene and benzo (a) pyrene obtained in sediment in the wet season in some of the stations were higher than recommended limits. The linear regression analysis between sum of concentrations and percentage organic carbon showed no significant correlation in sediment in the dry season (r2 = 0.0025) and in the wet season (r2 = 0.1345). The predominance of 4–6 ringed polycyclic aromatic hydrocarbons and the ratios between pairs of individual polycyclic aromatic hydrocarbons showed that they are likely to have come from pyrolytic sources. No polychlorinated biphenyl congener was detected in the samples.  相似文献   

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