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1.
The petrographic and geochemical composition of coal wastes exposed to fire in the minestone dump of Piekary Ślą1skie town (Upper Silesia, Poland) was investigated using samples collected at various distances from a recent fire site. The question as to whether geochemical biomarker maturity parameters could be applied to assess thermal changes in organic matter caused by waste dump fires, was examined using the data obtained. Geochemical parameters were correlated with observed petrographic changes in the organic matter caused by oxidation and heating. Petrographic analyses included the determination of maceral group contents (vitrinite, liptinite and inertinite), mineral matter and coke contents, and reflectance measurements on organic matter. All results were supported by proximate and ultimate analyses. Geochemical analysis included ultrasonic solvent extraction of bitumen followed by gas chromatography–mass spectrometry (GC–MS) of the extracts. In petrographic terms, the influence of heating was seen in reflectance variations and as oxidation rims, cracks, pores and coke development. Some zoned oxidation rims may be interpreted as re-heating episodes. In terms of chemical fingerprints, less thermally-stable compounds such as lighter n-alkanes, cyclic isoprenoids, methyl- and dimethylnaphthalenes, methyphenanthrenes and five-ring polycyclic aromatic hydrocarbons were destroyed or evaporated in the most fire-affected material. The presence/absence of particular compound groups was used to assess heating temperatures. Biomarker parameters of thermal maturity were used to assess alterations in organic matter around the waste dump fires, especially those indices and ratios with higher maturity ranges, e.g. (3-methylbiphenyl + 4-methylbiphenyl)/dibenzofurane and Σdimethylbiphenyls/Σmethyldibenzofuranes. 相似文献
2.
《Chemie der Erde / Geochemistry》2016,76(2):211-226
Occurrence and distributions of geochemical markers on vegetation and in soils covering two self-heating coal waste dumps were investigated with gas chromatography-mass spectrometry (GC–MS) and compared with those of bitumen expelled on the coal waste dump surface. Presence of biomarkers, alkyl aromatic hydrocarbons, polycyclic aromatic hydrocarbons (PAHs), and such polar compounds as phenols indicate that components of self-heating coal wastes indeed migrate to soils and plants surface and their characteristic fingerprints can be applied in passive monitoring to investigate migration of contaminants from self-heating coal wastes. Moreover, results allow to discriminate between the Upper- and Lower Silesian coal basins, notwithstanding value shifts caused by heating. Mechanisms enabling the migration of geochemical compounds into soils include mixing with weathered coal-waste material, transport in gases emitted due to self-heating and, indirectly, by deposition of biomass containing geochemical substances. Transport in gases involves mostly lighter compounds such as phenols, methylnaphthalenes, methylbiphenyls, etc. Distributions and values of geochemical ratios are related to differences in their boiling temperatures in the case of lighter compounds but preserve geochemical features in the case of heavier compounds such as pentacyclic trierpanes. 相似文献
3.
The composition of organic matter was investigated in the oil shales and country rocks of the Kashpir deposit. The analysis of the aromatic fraction of bitumen showed the presence of isorenieratene derivatives, which indicates the accumulation of the sequence under anoxic conditions in the bottom waters of a paleobasin. Special attention was given to the composition of organosulfur compounds from the bitumen of rocks and products of kerogen pyrolysis. The concentrations of hydrocarbon structures occurring in the bitumen in a free state and in sulfur-bearing derivatives are comparable. The composition of the pyrolysis products of kerogen depends on the concentration of organic carbon in the rock: carbon-rich rock varieties contain kerogen whose pyrolysis yields relatively high concentrations of organosulfur compounds and low total contents of n-alkanes/n-alkenes-1. 相似文献
4.
Matthias Radke Rainer G. Schaefer Detlev Leythaeuser Marlies Teichmüller 《Geochimica et cosmochimica acta》1980,44(11):1787-1800
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
5.
Adel Arfaoui 《Arabian Journal of Geosciences》2014,7(1):369-383
The current geochemical study of n-alkanes, steranes, and triterpanes in bitumen from the Late Maastrichtian–Paleocene El Haria organic-rich facies in West of Gafsa, southern Tunisia, was performed in order to characterize with accuracy their geochemical pattern. The type of organic matter as deduced from n-alkanes, steranes, and triterpanes distributions is type II/III mixed oil/gas prone organic matter. Isoprenoids and biomarkers maturity parameters (i.e., T s/T m, 22S/(22S?+?22R) of the C31 αβ-hopanes ratios, 20S/(20R?+?20S) and ββ/(ββ?+?αα) of C29 steranes), revel that the organic-rich facies were deposited during enhanced anoxic conditions in southern Tunisa. The organic matter is placed prior to the peak stage of the conventional oil window (end of diagenesis–beginning of catagenesis). All these result are suggested by total organic carbon analysis, bitumen extraction and liquid chromatography data. Thus, the n-alkanes, triterpane, and steranes study remains valuable and practical for geochemical characterization of sedimentary organic matter. 相似文献
6.
碳酸盐岩中有机质组成特征分析 总被引：2，自引：0，他引：2
对碳酸盐岩有机质组分进行分类时，有两种分类标准，一是主要采用煤岩学方法，二是采用孢粉学研究方法。本文使用煤岩学方法作为标准，对碳酸盐岩有机质的组成特征进行分析。按有机质来源和有机组分光性和形态等方面差别划分为内源有机质、次生有机质和陆源有机质三类。内源有机质类中分腐泥组和动物有机组，前者主要来源于菌藻类，后者则主要来源于浮游动物有机体；次生有机质中区分出微粒体、有机包裹体、沥青；陆源有机质类分类术语仍沿用煤显微组分分类系统和术语。碳酸盐岩烃源岩的有机质主要为腐泥型，有机质来源以低等藻类为主，且有机质组成特征与碳酸盐岩烃源岩的地质年代有关。碳酸盐岩还存在着差异演化的特征。 相似文献
7.
Solid bitumen occurs extensively in the paleo-reservoirs of marine sequences in southern China. The fluids in these paleo-reservoirs have usually experienced severe secondary alteration such as biodegradation and/or thermal maturation. The concentrations of extractable organic matter (EOM) in the resulting solid bitumens are too low to satisfy the amount required for instrumental analysis such as GC–MS and GC–IRMS. It is also difficult to get enough biomarkers and n-alkanes by dry pyrolysis or hydrous pyrolysis directly because such solid bitumens are hydrogen poor due to high maturities. Catalytic hydropyrolysis (HyPy) can release much more EOM from solid bitumen at mature to highly over-mature stages than Soxhlet extraction, dry pyrolysis and hydrous pyrolysis. However, whether the biomarkers in hydropyrolysates can be used for bitumen-source or bitumen–bitumen correlations has been questionable. In this study, a soft biodegraded solid bitumen sample of low maturity was thermally altered to various maturities in a closed system. HyPy was then employed to release bound biomarkers and n-alkanes. Our results show that the geochemical parameters for source and maturity based on biomarkers released from these thermally altered bitumen residues by HyPy are insensitive to the degree of thermal alteration. Furthermore, the maturity parameters are indicative of lower maturity than bitumen maturation products at a corresponding temperature. This suggests that biomarker source and maturity parameters, based on the products of HyPy, remain valid for bitumens which have suffered both biodegradation and severe thermal maturation. The distributions of δ13C of n-alkanes in hydropyrolysates are also insensitive to the temperature used for bitumen artificial maturation. Hence, the δ13C values of n-alkanes in hydropyrolysates may also provide useful information in bitumen–bitumen correlation for paleo-reservoir solid bitumens. 相似文献
8.
Suspended particle samples from the Yellow River estuary were sorted into five grain size fractions to explore the effect of grain size distribution on organic matter content and composition. The n-alkanes and PAHs were determined for each size fraction. PAHs and n-alkanes were more abundant in the finer fractions and the loading decreases steadily with increasing of grain size. However, the total n-alkanes or PAHs normalized to organic C were lower in the smaller size fractions than those in the larger size fractions, suggesting n-alkanes or PAHs may be diluted by the addition of organic matter or gradually decreased by degradation in the smaller size fractions. The particulate n-alkanes in the Yellow River estuary consist of a mixture of compounds from terrigenous and riverine biogenic n-alkanes and more biogenic n-alkanes accumulate in finer particles. Particulate PAHs are related to combustion/pyrolysis processes of coal/wood, and the relative contribution of petrogenic PAHs increase with increasing grain size. The total particulate n-alkane and PAH discharges passing the Lijin Station are about 3.94 t d−1 and 0.52 t d−1, respectively. Fine particles (<32 μm) play a significant role in organic matter transfer. 相似文献
9.
以场发射扫描电镜与Pores and Cracks Analysis System （PCAS） 图像处理软件为主要研究手段,以形状系数为孔隙形态表征参数,并选取低压N2吸附等为辅助研究手段,对四川盆地及周缘地区的典型钻井A-D 井龙马溪组及筇竹寺组黑色页岩中纳米孔隙的形态特征进行定量研究。研究发现黑色页岩纳米孔隙形态受孔隙类型（赋存位置）、有机质显微组分、地层埋藏深度、热成熟度及孔隙尺寸等因素综合控制。具体体现在：（1） 有机质孔、粒间孔和粒内孔所占比例、孔径分布与孔隙形态具有明显差异,反映这三类孔隙的演化受成岩作用的影响不同。（2） 固体沥青纳米孔隙比其他显微组分中的纳米孔隙更加规则。（3） 与埋藏深度密切相关的压实作用很可能会在垂向上压缩孔隙,一方面令孔径缩小,另一方面让孔隙形态往狭长–裂缝形发展。（4） 有机质孔形态随热成熟度升高总体上会变得更加规则,但这种趋势可能会被孔隙间的合并及压实作用等破坏。（5） 面积更小的孔隙形态往往比面积更大的孔隙更规则。初步研究显示固体沥青纳米孔隙形态代表着高过成熟页岩气储层中主体储集空间所处压力环境,但固体沥青纳米孔隙形态随孔隙压力的演化模式及利用固体沥青纳米孔隙形态表征其所在层系异常高压维持状况及页岩气保存状况的可能性尚需进一步研究。 相似文献
10.
以场发射扫描电镜与Pores and Cracks Analysis System （PCAS） 图像处理软件为主要研究手段，以形状系数为孔隙形态表征参数，并选取低压N2吸附等为辅助研究手段，对四川盆地及周缘地区的典型钻井A-D 井龙马溪组及筇竹寺组黑色页岩中纳米孔隙的形态特征进行定量研究。研究发现黑色页岩纳米孔隙形态受孔隙类型（赋存位置）、有机质显微组分、地层埋藏深度、热成熟度及孔隙尺寸等因素综合控制。具体体现在：（1） 有机质孔、粒间孔和粒内孔所占比例、孔径分布与孔隙形态具有明显差异，反映这三类孔隙的演化受成岩作用的影响不同。（2） 固体沥青纳米孔隙比其他显微组分中的纳米孔隙更加规则。（3） 与埋藏深度密切相关的压实作用很可能会在垂向上压缩孔隙，一方面令孔径缩小，另一方面让孔隙形态往狭长–裂缝形发展。（4） 有机质孔形态随热成熟度升高总体上会变得更加规则，但这种趋势可能会被孔隙间的合并及压实作用等破坏。（5） 面积更小的孔隙形态往往比面积更大的孔隙更规则。初步研究显示固体沥青纳米孔隙形态代表着高过成熟页岩气储层中主体储集空间所处压力环境，但固体沥青纳米孔隙形态随孔隙压力的演化模式及利用固体沥青纳米孔隙形态表征其所在层系异常高压维持状况及页岩气保存状况的可能性尚需进一步研究。 相似文献
11.
Several samples of peat from 6 bogs located in southern Poland were investigated for occurrence and distribution types of biomarkers present in their extractable organic matter fraction. It was found that there are inputs from two different sources of organic compounds differing in their characteristics and origin: (1) recent immature peat organic matter deposited in situ which is the source of all polar functionalized compounds, most of n-alkanes, and acyclic isoprenoids, and (2) mature fossil fuels, most probably bituminous coals from the Upper Silesia Coal Basin of vitrinite reflectance equivalent values of 0.9–1.1%. The latter compounds were most probably transported with fly ash to bogs from nearby settlements utilizing such fuel in domestic ovens. This group includes pentacyclic triterpenoids (hopanes and moretanes), minor amounts of n-alkanes, and numerous alkyl naphthalenes and alkyl phenanthrenes. All these compounds show distributions and values of geochemical ratios characteristic for mature organic matter confirming there ex situ origin. 相似文献
12.
The isotopic composition of carbon from the organic matter of late Jurassic oil shales from the Volgian-Pechora shale province
is studied. The existence of a dependence between Corg content in the rock and the isotopic composition of kerogen carbon is ascertained. The content of the heavy carbon isotope
increases with increasing Corg. This dependence is accounted for by the progressive accumulation of isotopically heavy hydrocarbons of the initial organic
matter due to sulfurization. The data on the isotopic composition of individual n-alkanes of bitumen in the rocks and the data on the absence of isotopic fractionation between thermobitumen and the residual
kerogen from oil shales from the Volgian-Pechora shale province obtained by treating shale in an autoclave in the presence
of water are presented first in this paper. 相似文献
13.
《Applied Geochemistry》2003,18(6):845-861
Recent sediments of the Andaman Backarc Basin, Indian Ocean, between the Andaman Nicobar islands and the Malay Peninsula have been analyzed for biomarker lipids. Three cores were selected: one each from the fault zone in a deep basin (a graben between two fault systems), another from a location adjacent to the fault, and the third from the topographic high in the rift valley. The molecular composition of the lipid classes (n-alkanes, isoprenoids, alkylbenzenes, alkylcyclohexanes, hopanoids, polycyclic aromatic hydrocarbons, steranes, alcohols, sterols and fatty acids) was examined by gas chromatography (GC) and GC/mass spectrometry to understand the nature and source of the hydrocarbons present and the processes of maturation of organic matter. The data show that the hydrocarbons are of hydrothermal origin, derived from thermal alteration of sedimentary organic matter, consisting of a mixture predominantly of marine-derived components with some terrestrial inputs. Normal alcohols and fatty acids also corroborate the distribution of n-alkanes. The distribution profiles and various parameters computed from the concentration of the target compounds suggest that oxidative reactions and microbial degradation in this environment are insignificant. Triterpane and PAH compositions indicate that the thermal maturity of the bitumen in the samples is comparable to or lower than that found at other hydrothermal regions such as the Northern Juan de Fuca Ridge, Guaymas Basin and Escanaba Trough. 相似文献
14.
The nature and distribution of organic matter in geological cherts of archaeological use can serve to estimate the sources and origins of some remains of lithic industry. For example, organic and biomarker analysis can provide information to allow a deeper insight into source catchment areas, artefact displacement or the way in which the artefacts were employed. In this work, soluble (bitumen) and insoluble (kerogen) organic matter were isolated from several chert samples with different depositional history and analysed by means of gas chromatography–mass spectrometry (GC–MS) and spectroscopic techniques such as infrared and Raman spectroscopy. Chemometric treatment of the results allowed observation of differences between organic matter content on the basis of the depositional setting of the cherts. Samples with a continental deposition seemed to preserve more organic matter with little alteration. The hydrocarbon profiles of these samples were dominated by high molecular weight n-alkanes, alkylcyclohexanes and isoprenoid groups which allowed distinguishing them from the rest of the analysed samples. 相似文献
15.
n-Alkanes in the soluble organic matter extracted from a series of vitrinite and sporinite concentrates have been analysed by gas chromatography. The macerals were isolated from coals ranging in rank from 77.1% to 86.6% carbon (vitrinite: dry, ash-free), and yields of n-alkanes ranged from 10 to 580 ppm for vitrinites and from 20 to 970 ppm for sporinites. The maximum yields were found at a rank of 85.4% C from vitrinites and 86.6% C from sporinites.Distribution maxima of the n-alkanes, as shown by gas chromatography, range from C27 and C29 at lower ranks to as low as C16 at higher ranks. The distributions also show a progressive decrease in the preference of odd-carbon-number homologues with increasing rank. Virtually smooth distributions were attained in high-volatile bituminous A coals. Quantitative data show that the loss of the odd-carbon-number preference occurred, for the most part, while individual long-chain homologues increased in concentration.There is a progressive increase in the amounts of shorter-chain n-alkanes with increasing rank. It is suggested that sequential processes may have occurred whereby the rate of formation of long-chain n-alkanes in high-volatile bituminous A rank macerals becomes slower than their rate of subsequent fragmentation to shorter chain lengths. Consequently, assuming derivation from the insoluble maceral matrices, the chain-length distributions of parent n-alkyl structures within the insoluble material may retain characteristics pertaining more to the nature of the source organic matter at the time of deposition than do the extractable n-alkane patterns, especially at higher ranks. 相似文献
16.
《Applied Geochemistry》2005,20(3):455-464
In order to characterize the H isotopic compositions of individual lipid compounds from different terrestrial depositional environments, the δD values of C-bound H in individual n-alkanes from typical terrestrial source rocks of the Liaohe Basin and the Turpan Basin, China, were measured using gas chromatography–thermal conversion–isotope ratio mass spectrometry (GC–TC–IRMS). The analytical results indicate that the δD values of individual n-alkanes in the extracts of terrestrial source rocks have a large variation, ranging from −140‰ to −250‰, and are obviously lighter than the δD of marine-sourced n-alkanes. Moreover, a trend of depletion in 2H(D) was observed for individual n-alkanes from different terrestrial depositional environments, from saline lacustrine to freshwater paralic lacustrine, and to swamp. For example, the δD values of n-alkanes from a stratified saline lacustrine environment vary from −140‰ to −200‰, δD for n-alkanes from swamp facies range from −200‰ to −250‰, while those from freshwater paralic lacustrine–lacustrine environments fall between the δD values of the end members. The shift toward lighter δD from saltwater to freshwater environments indicates that the source water δD is the major controlling factor for the H isotopic composition of individual compounds. In addition, H exchange between formation water and sedimentary organic matter may possibly be important in regard to the δD of individual n-alkanes. Therefore, other lines of geochemical evidence must be considered when depositional paleoenvironments of source rocks are reconstructed based on the H isotopic composition of individual n-alkanes. 相似文献
17.
Alkane hydrocarbon and n-fatty acid distributions have been examined in cores taken over a 550 ft thickness through the lower Jurassic, largely non-marine Evergreen Shale, Surat Basin, Queensland, Australia. No depth trends in compound abundances or carbon preference indices are discernible. There is no evidence for significant generation of n-alkanes from kerogen nor for cracking of long-chain n-alkanes. The present distribution patterns of the biochemicals probably reflect closely the nature of the original organic matter. The general strong dominance of long-chain (C20+) n-alkanes; the lack of evidence for diagenetic change; and the absence of correlation between abundances of n-alkanes and n-fatty acids (among both the longer- and shorter-chain compounds), lead to the conclusion that at least the long-chain n-alkanes were largely deposited as such in the sediment, having originated in land-plant material, remains of which are abundant in the samples. In the upper 170 ft. (possibly marine), n-alkanes with chain lengths below C20 become important, suggesting greater significance of aquatic life as a source of organic matter at the time of deposition, a conclusion which is in general accord with the geological history of the basin, although this history is not well known. 相似文献
18.
在南方下古生界海相页岩有机显微组分及其赋存状态研究的基础上,以场发射扫描电镜二维图像所展示的有机质纳米孔隙形貌特征为主要依据,将四川盆地龙马溪组页岩有机质纳米孔隙的成因类型划分为沥青球粒孔、气孔、铸模孔。分别论述了这3种纳米孔隙的成因、形貌、大小、演化、连通性、相互关系及其在页岩储层中的作用。研究表明,龙马溪组页岩的显微组分主要是沥青质体,气孔和沥青球粒孔均发育于沥青质体内部,形成于有机质降解和热演化过程,是页岩气生成、吸附和聚集的有力佐证与优先空间。龙马溪组底部富有机质页岩中,各种有机质纳米孔隙发育程度高,直接体现了强的生气和聚气作用。 相似文献
19.
CAO Taotao LIU Guangxiang LIU Hu DENG Mo HAN Yuanhong HUANG Yanran Andrew S. HURSTHOUSE 《《地质学报》英文版》2019,93(4):1025-1046
Nanoscale pore characteristics of the Upper Permian Longtan transitional mudrocks and their equivalent strata Wujiaping Formation marine mudrocks in and around the eastern Sichuan Basin was investigated using field emission scanning electron microscopy (FE-SEM) and low-pressure N2 adsorption experiments. The results indicate that the Upper Permian mudrock is at a mature stage with total organic carbon (TOC) values ranging between 0.47% and 12.3%. The Longtan mudrocks mainly contain vitrinite, and their mineral composition is primarily clay. In contrast, the Wujiaping mudrocks are dominated by sapropelinite and solid bitumen, and their mineral compositions are mainly quartz and a notably high amount of pyrite. The FE-SEM reveals that clay mineral pores and microcracks are the common pore types in the Longtan mudrocks. The specific surface area and pore volume depend on the clay content but are negatively correlated with the TOC. The generation of nanometer pores in the Longtan mudrocks is caused by high clay mineral contents. Meanwhile, the Wujiaping mudrock mainly contains OM pores, and the pore parameters are positively correlated with the TOC. The OM pore development exhibits remarkable differences in the Longtan and Wujiaping mudrocks, which might be related to their sedimentary facies and maceral fractions. Vitrinite and inertinite appear as discrete particles in these mudrocks and cannot generate pores during thermal maturation. Sapropelinite often contains many secondary pores, and solid bitumen with large particles, usually with several pores, is not the major contributor to the pore system of the investigated mudrock. 相似文献
20.
中国已获得湖相页岩气勘探开发的重要突破,但对于咸化湖盆环境泥页岩储集层特征的研究较少。作者对柴达木盆地西部地区古近系下干柴沟组湖相泥页岩储集层开展有机地化、岩矿组成、储集层孔隙结构等特征的研究。(1)研究区泥页岩有机质丰度在0.12％～1.35％之间,具有强烈的非均质性,有机质类型以Ⅱ型为主,氯仿沥青“A”含量较高。(2)泥页岩中碳酸盐岩矿物含量最高,平均27.8％,黏土矿物和石英含量次之,有38.2％的样品检测出硬石膏,反映典型的咸化环境特征。(3)扫描电镜观察有机质孔隙发育较少,形状不规则且孔径较大,粒(晶)间孔隙直径多以微米级为主,微裂缝宽多小于1μm;低温气体吸附测试显示,中孔提供了主要的孔比表面积和孔隙体积,氯仿沥青“A”的存在对样品孔隙结构产生影响。(4)研究区泥页岩储集层中黏土矿物含量低而脆性矿物含量高,与北美页岩气产层及四川盆地龙马溪组页岩储集层岩矿特征类似,易于产生裂缝,有利于页岩气的后期开采。 相似文献