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1.
《Geochimica et cosmochimica acta》1987,51(6):1457-1466
Aliphatic and aromatic hydrocarbons in sediments of the middle and lower Mississippi Fan and two intraslope basins in the Gulf of Mexico are derived from terrestrial organic matter and thermogenic, mature hydrocarbons. The terrestrial hydrocarbon component consists primarily of terrigenous, plant biowaxes (n-alkanes with 21 to 33 carbons). The occurrence of thermogenic hydrocarbons in immature near-surface sediments, their molecular distributions and concentration variations with depth suggest that the majority of these mature hydrocarbons have migrated from a source much deeper in the sediment column. A portion of the thermogenic hydrocarbons may be derived from recycled material and includes phenanthrene, methyl phenanthrenes, chrysene and benzopyrenes. The migrated, thermogenic hydrocarbons include normal and isoprenoid alkanes with less than 21 carbons, naphthalene, methyl naphthalenes, ethyl naphthalenes and other aromatics of similar volatility (i.e., biphenyl, acenaphthene and fluorene). Triterpane, sterane and aromatized sterane distributions suggest that the thermogenic hydrocarbons at both sites have a common source and are overprinted with immature sediment hydrocarbons. The biomarker distributions and carbon isotopic compositions of the thermogenic hydrocarbons are atypical for petroleum produced in the Gulf of Mexico. Molecular distributions of the hydrocarbons are constant, regardless of the present depth of occurrence, suggesting that they have migrated in a separate phase. The upward migration of hydrocarbons from deeper sources is a wide-spread phenomenon in the Gulf of Mexico with several documented cases of massive seepage (visible oil) as well as the more diffuse permeation of Pleistocene sediments of the Mississippi Fan and two intraslopes reported here. 相似文献
2.
Surface sediments from the Outer Continental Shelf of Alaska were analyzed for hydrocarbons as part of an environmental survey sponsored by NOAA/BLM. Sediments were collected from the proposed oil lease areas of Beaufort Sea, southeastern Bering Sea, Norton Sound, Navarin Basin, Gulf of Alaska, Kodiak Shelf and lower Cook Inlet. Data on normal and branched alkanes and di- and triterpenoids from capillary gas chromatography (GC) and gas chromatography-mass spectrometry (GC/ MS) indicate that the area displays little evidence of petroleum hydrocarbons (i.e., seeps) except at a few isolated stations. Beaufort Sea sediments have the highest hydrocarbon budget, whereas Kodiak Shelf sediments have the lowest. The molecular markers of the hydrocarbons are of a mixed marine autochthonous and terrestrial allochthonous origin. Norton Sound and Cook Inlet sediments contain the highest levels of terrigenous lipids and Kodiak Shelf the lowest. The abundance of alkenes implies that relatively low oxidizing conditions exist in some of the depositional areas studied, suggesting that extraneous petroleum hydrocarbons introduced into these sediments would be expected to have a relatively long residence time. The distribution of polynuclear aromatic hydrocarbons (PAH) is complex and shows a pyrolytic origin. The data on perylene strongly favor the hypothesis that it is “performed” from terrigenous precursors and transported into the marine environment with no apparent in situ generation. Polynuclear aromatic hydrocarbons of diagenetic origin are probably dominant in Gulf of Alaska and Kodiak Shelf sediments.Two stations, north of Kalgin Island, in lower Cook Inlet and one in southeastern Bering Sea show typical weathered petroleum distribution of n-alkanes and triterpenoids. Probable pathways of transport and fate of petroleum hydrocarbons in case of an oil spill are also briefly discussed. 相似文献
3.
This work considers results of the study of Holocene cover sediments of Iceland largely composed of wind-transported palagonitized hyaloclastite particles and coeval horizons of acid and basic tephra. It is established that polyciclic aromatic hydrocarbons (PAH) are released from the basaltic glass in natural environments only in the case of intense physicochemical alteration and destruction of its structure. This process does not influence the composition of polycyclic aromatic hydrocarbons and their quantitative proportions. No new polyclic aromatic hydrocarbons formed during several thousands of years of the Holocene section accumulation. Hydrocarbons are transferred from fixed the state in basaltic glass into the free state in palagonites practically without any changes. Polyciclic aromatic hydrocarbons were mainly redeposited by winds, derived together with palagonite from weathered hyaloclastites, and precipitated from atmosphere with tephra during eruptions. 相似文献
4.
珠江口盆地番禺低隆起-白云凹陷北坡干酪根热演化模拟与生烃 总被引：1，自引：0，他引：1
通过密封金管-高压釜体系对珠江口盆地番禺低隆起-白云凹陷北坡恩平组炭质泥岩的干酪根(PY),在24.1 MPa压力、20℃/hr(373.5~526℃)和2℃/h(343~489.2℃)两个升温速率条件下进行热模拟生烃实验,分析气态烃(C1 5)和液态烃(C6 14和C14+)的产率,以及沥青质和残余有机质碳同位素组成。同时与Green River页岩(GR)和Woodford泥岩(WF)的干酪根,分别代表典型的I型和II型干酪根进行对比研究。结果显示PY热演化产物中总油气量明显低于GR和WF干酪根,且气态烃(C1 5)最高产率是液态烃的1.5倍,揭示恩平组炭质泥岩主要以形成气态烃为主。在热演化过程中,有机质成熟度和母质类型是控制油气比的主要因素,气态烃和轻烃的产率比值主要受热演化成熟度的影响。干酪根残余有机质碳同位素和沥青质碳同位素在热演化过程中受有机质成熟度的影响较小,δ13C残余和δ13C沥青质可以间接反映原始母质的特征,为高演化烃源岩油气生成提供依据。 相似文献
5.
I. A. Nemirovskaya 《Geochemistry International》2008,46(4):378-385
Aliphatic and polycyclic aromatic hydrocarbons were examined in the surface layer of bottom sediments from the eastern part of the Sakhalin shelf (the materials were sampled in the summer of 2002). The concentrations of hydrocarbons were determined to have changed since the beginning of the development of oil fields (compared with earlier years). According to the distribution of markers in the hydrocarbon compositions, the bottom sediments are dominated by allochthonous (terrigenous) hydrocarbons, which are the most stable compounds. The presence of transformed anthropogenic oil alkanes, which have never been found before, may be indicative of the increasing pollution of the region. 相似文献
6.
利用气相色谱、气相色谱-质谱分析法从北京市西北城区四个季节大气可吸入颗粒物（PM10）中检测出种类丰富的饱和烃,主要包括正构烷烃、萜烷及甾烷等系列化合物。利用饱和烃的多项参数（如主峰碳数、碳优势指数CPI、藿烷22S/(22S+22R)比值等）对大气PM10中可溶有机物的来源及分布作了探讨。北京市西北城区PM10中正构烷烃的主峰碳数均介于23和27之间,而CPI值介于1和3之间,表明北京市西北城区PM10中的饱和烃均不同程度地受到了高等植物等现代生物和化石燃料（石油、煤等）不完全燃烧产物两种来源的影响,其中在春、夏季以高等植物、花粉、微生物等生物来源占比重较大,而在秋、冬季,尤其在冬季,化石燃料的不完全燃烧造成的污染比较明显。萜烷类物质的检出,表明北京市西北城区四个季节PM10中部分饱和烃来自于石油等化石燃料的不完全燃烧。甾烷类物质的检出,表明北京市西北城区四个季节PM10中部分饱和烃是来自于车辆释放的机油等。 相似文献
7.
《Applied Geochemistry》2005,20(2):367-381
Several series of saturated, diaromatic, triaromatic C-ring cleaved and triaromatic diterpenoids and triterpenoids have been detected in 4 immature coal and mudstone samples. A number of these compounds appear to represent intermediates in a series of postulated pathways for progressive aromatization of biogenic diterpenoids and triterpenoids. Diagenetic pathways for the formation of tricyclic aromatic hydrocarbons from abietane and pimarane type diterpenoid precursors and for the formation of diaromatic, triaromatic C-cleaved and triaromatic hydrocarbons from β-amyrin and other triterpenoid precursors are proposed. Saturated and aromatized abietanes, pimaranes and phyllocladanes, which are the most abundant compounds in all 4 samples, indicate a predominant higher plant input which can be related to the Coniferales group but not to individual plant families. β-Amyrin and other triterpenoid-derived triaromatic and triaromatic C-ring cleaved hydrocarbons with triterpenoid structures are thought to be characteristic for angiosperms. The relative concentrations of the triaromatic and triaromatic C-ring cleaved hydrocarbons are higher in samples 9602 (mudstone) and 9603 (coal) than samples 9601 (coal) and 9604 (mudstone) indicating samples 9602 (mudstone) and 9603 (coal) contain relatively more angiosperm derived organic matter than samples 9601 (coal) and 9604 (mudstone). The distribution patterns and the relative concentrations of saturated and aromatic diterpenoids and triterpenoids thus are valuable markers for the determination of the relative contents of biological sources of organic material in geological samples. 相似文献
8.
Levels of polycyclic aromatic hydrocarbons and polychlorinated biphenyls in sediment of bitumen deposit impacted area 总被引：5，自引：5，他引：0
E. O. Fagbote E. O. Olanipekun Ph.D. 《International Journal of Environmental Science and Technology》2010,7(3):561-570
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
9.
Numerous potentially toxic compounds are entering Louisiana’s inshore and nearshore coastal environments. To a large degree there is insufficient information for predicting the fate and effect of these materials in aquatic environments. Studies documenting the impact of petroleum hydrocarbons entering Louisiana coastal wetlands are summarized. Also included are research findings on factors affecting the persistence of petroleum hydrocarbons and other toxic organics (pentachlorophenol (PCP), 2,4-dichlorophenoxyacetic acid (2,4-D), creosote, etc.) in sediment-water systems. Sediment pH and redox conditions have been found to play an important role in the microbial degradation of toxic organics. Most of the hydrocarbons investigated degrade more rapidly under high redox (aerobic) conditions although there are exceptions (e.g., 1,1,1-trichloro-2,2-bis(4-chlorophenyl) (DDT) and polychlorobiphenyls (PCBs)). Some of these compounds, due to their slow degradation in anaerobic sediment, may persist in the system for decades. 相似文献
10.
Ultrasonic wave extraction and simultaneous analysis of polycyclic aromatic hydrocarbons (PAHs) and phthalic esters in soil 
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下载免费PDF全文 ZHANG Yong-tao ZHAO Guo-xing LIU Jing-shang ZHANG Li LI Xiao-ya GUI Jian-ye ZHANG Chen-ling 《地下水科学与工程》2017,5(3):249-253
A method is developed for detection of polycyclic aromatic hydrocarbons(PAHs) and Phthalic Acid Esters(PAEs) in soil samples. Ultrasonic Wave Extraction under airtight circumstances is adopted to extract the analytes in soil samples with n-hexane–acetone(V:V=1:1) as extraction solvent. This method has several advantages, including high extraction efficiency, short time, convenience and simplicity. It can be used to detect polycyclic aromatic hydrocarbons(PAHs) and Phthalic Acid Esters(PAEs) in soil. 相似文献
11.
A study of two classes of hydrocarbons (HCs)—aliphatic and polycyclic aromatic—in suspended matter of the surface waters and bottom sediments of the Northern and Middle Caspian Sea (R/V Nikifor Shurekov, October 2015) is described. It has been determined that oil pollution transported by river runoff and fluid streams flowing from sedimentary formations in the northeastern part are the main sources of hydrocarbons in the river–sea boundaries of the Volga, Terek, and Sulak rivers. 相似文献
12.
A. R. Bahrami I. Mohammad Fam J. Donaldson 《International Journal of Environmental Science and Technology》2004,1(3):165-169
An investigation for the analysis of polycyclic aromatic hydrocarbons in airborne particulates using thermal desorption and gas chromatography-mass spectrometry is described. Samples are obtained from ambient air using fibreglass filters and the volatile material from the filter is thermally desorbed to gas chromatograph. A 30 meter capillary column is used to separate the hydrocarbons and eight polyaromatic hydrocarbons are used to test the method and recovery is >95%. The eight polycyclic aromatic hydrocarbons anthracene, phenanthrene, fluoranthrene, pyrene, benzo (a) anthracene, chrysene, benzo (a) pyrene and benzo (e) pyrene were the most abundant PAHs found in the samples of ambient air with current method at Uxbridge-London. Application of the measurement of polycyclic aromatic hydrocarbons in ambient air samples shows that the hydrocarbons trapped in the particle phase to a lesser degree at higher ambient temperature. In conclusion a method has been developed to transfer the PAHs in particle phase from a filter to GC-MS by thermal desorption. A standard mixture of PAHs, when absorbed onto the filter, did lead to strong analyte absorbent interactions by the high percent recovery of the sample. 相似文献
13.
油气藏微观不均一性及其意义 总被引：18，自引：3，他引：15
油气储集岩中不同孔隙类型（开放型与封闭型）中的油气组分、孔隙中自由状态的油气组分、矿物颗粒表面吸附（束缚状态）的油气组分、以及矿物内部油气包裹体之间常规生物标志化合物组成（甾、萜分布）存在明显的差异,反映了不同成藏阶段油气组成的地球化学特征,展示了油气充填过程,同时为油源对比提供了新方法。 相似文献
14.
K. Opuene Ph.D. I. E. Agbozu Ph.D. L. E. Ekeh M.Phil M.Sc. 《International Journal of Environmental Science and Technology》2007,4(4):457-462
Perylene and penta-aromatic hydrocarbons were determined in sediments as part of a study that was dedicated to the aquatic ecosystem of Elelenwo Creek (Southern Nigeria) in order to carry out a critical corroboration of occurrence and diagenetic evolution of perylene in the sediments of the creek. The results show that the annual mean levels of Benzo [g, h, i] Perylene ranged from 209.00–245.28 ?g/kg dry weight at the various stations sampled. Meanwhile, Station 3 recorded the highest mean level of 245.28 ?g/kg dry weight. The observed values for total penta-aromatic hydrocarbons were high (787.00–1154.36?g/kg dry weight) in all the stations sampled. In addition, the highest mean value of 1154.36?g/kg dry weight was again recorded at station 3 for the penta-aromatic hydrocarbons. One origin index or concentration ratio of Ip/Ip+BghiP was also used to evaluate the suitability of the penta-aromatic hydrocarbons as a tracer to distinguish between contaminations arising from different sources. The values for the sampling stations therefore ranged from 0.41 to 0.43. A critical appraisal of the PAH index, consequently, suggested that petroleum combustion is the major penta-aromatic hydrocarbon source in sediments of the creek. The PAH group profile shows that perylene was high in the sediments and would pose apparent effects in fauna. The high concentration of perylene in the sediments was also indicative of an in situ biogenic derivation. Furthermore, a concentration of perylene > 10 % of total penta-aromatic hydrocarbons established a credible diagenetic origin. 相似文献
15.
16.
现代松粉的温－压热模拟实验中，产出的轻质烃和氯仿抽提物芳烃馏份的GC－MS分析均检出大量偶数碳优势明显的脂肪酸类分子生物标志物，轻烃主要为C16，C18烷酸及其甲，乙酯，芳烃组分相对比较复杂，包括饱和脂肪酸（酯），不饱和脂肪酸（酯）和脂肪酸内酯，前者碳数分布为C15－，C30，C16，C18碳酸（酯）相对丰度占绝对优势为特征，后者碳数分布为C20-C30,以C26，C28和C30脂肪酸内酯为主，在250℃以下样品中检测出相对丰度较高的不饱和C18碳酸（酯），脂肪酸酯化合物在极低的温度条件下便可排出，并分别在200－300℃和300－400℃之间形成两次产出高峰；花粉内质体中的游离态脂肪酸及不饱和脂肪酸形成低温阶段的第一次高峰；花粉壁脂质结构中的脂肪酸及饱和脂肪酸在较高温度阶段形成第二次高峰，原样及低温样品以脂肪酸酯为主，250℃及其以上温度条件下因水解产生较多的脂肪酸，随温率继续升高，脂肪酸酯易发生脱羰反应而生成链烷烃。400℃以后因强烈降解脂肪酸酯含量大大降低，这与350－450℃之间奇数碳优势正构烷烃在轻质烃和饱和烃中的大量产出相吻合，研究表明，植物花粉是沉积有机质中饱和及不饱和C16，C18脂肪酸酯的重要母源之一。 相似文献
17.
Petroleum source-rock evaluations by pyrolysis are based on the concept that free hydrocarbons in rock samples are volatilized below 300°C while hydrocarbons cracked from kerogen come off at higher temperatures. The pyrolysis of pure hydrocarbons with different mineral matrices shows that free hydrocarbons containing 16 or more carbon atoms may not be evolved eblow 300°C, but at varying higher temperatures. The extent to which this occurs depends on the hydrocarbon volatility, the mineral matrix and the pyrolysis instrument design. Source-rock parameters which use the P1 (S1) peak may be not be reproducible between instruments if the rock contains appreciable amounts of high molecular weight hydrocarbons. 相似文献
18.
原油生物降解模拟实验及其定量化评价 总被引：1，自引：0，他引：1
利用筛选到的优势烃降解复合菌(I菌)对大庆油田3口不同油井的油(西5-P10、三元后和G1131-262)进行不同时间的降解实验和全油GC-MS定量分析,探讨饱和烃、芳烃化合物分布情况变化。实验研究表明I菌为高效烃降解菌;相同微生物对此3种不同原油的降解能力存在明显的差异,所以烃污染现场生物修复试验需要根据不同原油性质选择不同的高效降解菌;对于饱和烃和芳烃生物降解的顺序既有对过去结论的验证又提出新的看法。藿烷的降解在重排甾烷之后,萘比菲先开始降解,三甲基萘比三甲基菲更早开始遭受生物降解,三甲基和四甲基萘在深度生物降解后会达到一个平衡,之后的降解速度减慢。当生物降解到一定阶段,抗生物降解能力强的多环芳烃富集会加重对环境的毒害,因此,多环芳烃降解菌或萘、菲降解菌等特效菌是未来烃污染环境修复工作的重点。 相似文献
19.
1 Introduction As a linkage between the biosphere and the geosphere, organic geochemistry, especially molecular markers, has become a powerful tool for investigating important geological events and the evolutionary history of ancient life on Earth (Kvenvo… 相似文献
20.
Jaap S. Sinninghe Damst W. Irene C. Rijpstra Jan W. de Leeuw P.A. Schenck 《Organic Geochemistry》1988,13(4-6)
The distribution patterns of Organic Sulphur Compounds (OSC), occurring in certain sediments and immature crude oils, were compared with those of the corresponding hydrocarbons. Because of the complexity of the OSC mixtures, they were desulphurized to hydrocarbons (n-alkanes, isoprenoid alkanes, steranes, triterpanes and branched alkanes). The hydrocarbons produced by desulphurization of the OSC exhibited distribution patterns different from those of the hydrocarbons originally present. Therefore reaction of elemental sulphur with these hydrocarbons at elevated temperatures must be considered as an unlikely origin for these OSC. Sulphur incorporation reactions on an intramolecular basis with suitable functionalized precursors at the early stages of diagenesis are probably the major origin for these OSc. Desulphurization of high molecular weight fractions also produced hydrocarbons, dominated by n-alkanes up to C40. Therefore it is assumed that these substances contain n-alkanes, 2,5-dialkyl-thiophenes and -thiolanes linked to each other by sulphur briddges. These findings stronly suggest that sulphur-containing high molecular weight substances are formed by the same sulphur incorporation reactions as OSC, but in an intermolecular fashion. 相似文献