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1.
The wide existence of immature oils throughout the world especially in China broke through the hydrocarbon generation theory through kerogen thermal degradation. Studies have shown that soluble and insoluble organic matter are organically connected in the sedimentary rock, both contributing to hydrocarbon generation. In the diagenesis,kerogen can not produce oils, so immature oils derive directly from the soluble lipids. Hydrocarbon generation process through kerogen thermal degradation takes place mainly in the early catagenesis(R o= 0.2% ～1.2%), and the oils generated are normal. In the late catagenesis, hydrocarbon generation comes into wet gas stage(R o=1.2%～2.0%), with pyrrobitumen degenerating into high mature light oils and oils cracking into gases. In this paper,the author presented a new generating hydrocarbon and evolutionary model with soluble and insoluble organic matter both contributing to the generation of hydrocarbon. 相似文献
2.
Mohammed Hail Hakimi Mukhtar A. Nasher Shadi A. Saeed Hitham Al-Hakame Tareq Al-Moliki Kholah Qaid Al-Sharabi 《Journal of the Geological Society of India》2017,89(3):325-330
The Tertiary volcanic rocks are widely exposed in the Sharab area of Taiz Governorate, southwestern Yemen. The Jurassic calcareous shale and black limestone deposits collected closely to theTertiary volcanic rocks were investigated to provide information regarding the thermal effects of Tertiary volcanic rocks on organic materials. The bulk geochemical results indicate that the analysed Jurassic deposits are organically lean with present-day TOC values less than 0.95% and very low HI values (< 50 mg HC/g TOC), with a predominantly Type IV kerogen (inert carbon). This is attributed to thermal effect on the original organic matter as indicated by high thermal maturity data, consistent with post-mature to metagenesis stage. The present study also suggests that the high thermal maturity of the Jurassic marine deposits is due to the presence of the alkali basalts which have invaded the Jurassic rocks during late Oligocene to early Miocene (~10 Ma). Thus, the heat flow caused by Tertiary basaltic rocks further increased the temperature level and led to metamorphosis of organic matter and converted it to graphitic materials (inert carbon). 相似文献
3.
Haiyan Hu 《中国地球化学学报》2014,33(4):425-430
To determine the effect of thermal maturity on the methane sorption in shale gas system, two different thermal maturity kerogens of type II isolated from Barnett shale of Fort Worth Basin were used to measure the methane adsorption amount under the pressure ranging from 0 to 14 MPa at constant temperatures. One kerogen was called Lee C-5-1 with 0.58% of vitrinite reflectance; the other was called Blakely#1 kerogen with 2.01% of vitrinite reflectance. The results suggested that the methane sorption capacity of kerogen Blakely#1 was higher than the immature kerogen Lee C-5-1, and its Langmuir constant and Langmuir maximum sorption amount, which were reached by fitting the measured data for at least square method, greater than the immature kerogen Lee C-5-1. This may be associated with that nanopores opened up during the degradation of organic matter, and which increased the specific surface area of kerogen. Therefore, the over mature kerogen has greater methane adsorption capacity. 相似文献
4.
5.
阿拉善右旗杭乌拉地区下二叠统埋汗哈达组烃源岩特征 总被引：4，自引：0，他引：4
通过对阿拉善右旗杭乌拉地区下二叠统埋汗哈达组岩性特征、暗色泥页岩油气地球化学特征研究,总结了烃源岩纵向分布、有机质丰度、干酪根类型和热演化特征。下二叠统埋汗哈达组烃源岩分布层段集中,暗色泥页岩累计厚度160.1 m,占碎屑岩厚度的33.3%。有样品控制的暗色泥页岩厚度94.1 m,w（TOC）平均为0.75%,大于0.3%的样品占93.5%。其中:w（TOC）大于1.0%的好烃源岩厚度22.2 m,占样品控制厚度的23.6%;w（TOC）为0.5%~1.0%的中等烃源岩厚度45.5 m,占48.3%;w（TOC）为0.3%~0.5%的差烃源岩厚度16.5 m,占17.5%。甾烷相对含量具有明显的C27优势,族组分饱和烃含量显著高于芳烃含量,干酪根类型为II型。Rc平均为0.77%,表明干酪根演化进入成熟阶段,最高热解温度（Tmax）分布范围为350~550 ℃,属成熟-高成熟阶段。综合评价认为,下二叠统埋汗哈达组具有较好的生烃条件,以生气为主。 相似文献
6.
许多研究者认为,烃源岩干酪根C同位素组成主要受干酪根类型的影响,可以作为评价烃源岩类型、沉积环境和进行油气源对比的重要指标,并得到广泛应用.对额济纳旗及邻区典型剖面石炭系-二叠系烃源岩有机碳(TOC)的丰度、地球化学特征、热演化特征和干酪根C同位素分布的研究表明.研究区石炭系-二叠系烃源岩为浅海陆棚相沉积环境形成的泥质岩,TOC含量中等,以Ⅱ类干酪根为主,烃源岩演化进入成熟-过成熟阶段,干酪根C同位素县有显著偏重的特点.并且干酪根C同位素组成明显与热演化程度和有机碳丰度有关,随着烃源岩演化程度的不断提高,重碳同位素不断富集,在成熟-过成熟阶段,对C同位素的影响可达4‰～6‰随着TOC含量的增加,干酪根C同位素显著偏轻,影响值可达4‰以上.由于研究区烃源岩已进入成熟-过成熟阶段,干酪根C同位素的分布在演化过程中已经发生较大变化,干酪根类型的影响相对降低或已不显著,不能再作为评价烃源岩干酪根类型的指标. 相似文献
7.
海相碳酸盐岩中矿物结合有机质的组成及成烃演化 总被引：6，自引：0，他引：6
对高成熟程度的碳酸盐岩有机质进行了地球化学研究,发现在可溶有机质与干酪根之间存在着成熟度上的差异,这种差异是矿物对沥青组份的保护作用所致.矿物结合有机质无论在组成还是在分布上都与游离态有机质有较大不同,随着成熟度的增加,由于结合态有机质的释放,这种不同逐渐消失,研究表明,矿物结合有机质的释放约在过成熟阶段早期,其量可达几百个ppm.因而在碳酸盐岩地层中,除了干酷根成油气外,在高成熟区亦可能存在着由矿物结合有机质形成的“高温”石油. 相似文献
8.
Organic-rich (18.2%) Monterey Formation diatomite from California was studied. The organic matter consist of 94% bitumen and 6% kerogen. Biological markers from the bitumen and from pyrolysates of the coexisting asphaltenes and kerogen were analyzed in order to elucidate the relationship between the various fractions of the organic matter. While 17 alpha(H), 18 alpha(H), 21 alpha(H)-28,30-bisnorhopane was present in the bitumen and in the pryolysate of the asphaltenes, it was not detected in the pyrolysates of the kerogen. A C40-isoprenoid with "head to head" linkage, however, was present in pyrolysates of both kerogen and asphaltenes, but not in the bitumen from the diatomite. The maturation level of the bitumen, based on the extent of isomerization of steranes and hopanes, was that of a mature oil, whereas the pyrolysate from the kerogen showed a considerably lower maturation level. These relationships indicate that the bitumen may not be indigenous to the diatomite and that it is a mature oil that migrated into the rock. We consider the possibility, however, that some of the 28,30-bisnorhopane-rich Monterey Formation oils have not been generated through thermal degradation of kerogen, but have been expelled from the source rock at an early stage of diagenesis. 相似文献
9.
The Menilite Shales (Oligocene) of the Polish Carpathians are the source of low-sulfur oils in the thrust belt and some high-sulfur oils in the Carpathian Foredeep. These oil occurrences indicate that the high-sulfur oils in the Foredeep were generated and expelled before major thrusting and the low-sulfur oils in the thrust belt were generated and expelled during or after major thrusting. Two distinct organic facies have been observed in the Menilite Shales. One organic facies has a high clastic sediment input and contains Type-II kerogen. The other organic facies has a lower clastic sediment input and contains Type-IIS kerogen. Representative samples of both organic facies were used to determine kinetic parameters for immiscible oil generation by isothermal hydrous pyrolysis and S2 generation by non-isothermal open-system pyrolysis. The derived kinetic parameters showed that timing of S2 generation was not as different between the Type-IIS and -II kerogen based on open-system pyrolysis as compared with immiscible oil generation based on hydrous pyrolysis. Applying these kinetic parameters to a burial history in the Skole unit showed that some expelled oil would have been generated from the organic facies with Type-IIS kerogen before major thrusting with the hydrous-pyrolysis kinetic parameters but not with the open-system pyrolysis kinetic parameters. The inability of open-system pyrolysis to determine earlier petroleum generation from Type-IIS kerogen is attributed to the large polar-rich bitumen component in S2 generation, rapid loss of sulfur free-radical initiators in the open system, and diminished radical selectivity and rate constant differences at higher temperatures. Hydrous-pyrolysis kinetic parameters are determined in the presence of water at lower temperatures in a closed system, which allows differentiation of bitumen and oil generation, interaction of free-radical initiators, greater radical selectivity, and more distinguishable rate constants as would occur during natural maturation. Kinetic parameters derived from hydrous pyrolysis show good correlations with one another (compensation effect) and kerogen organic-sulfur contents. These correlations allow for indirect determination of hydrous-pyrolysis kinetic parameters on the basis of the organic-sulfur mole fraction of an immature Type-II or -IIS kerogen. 相似文献
10.
Precambrian cherts from the Fig Tree and Onverwacht groups of South Africa contain unusually high concentrations of chromium and nickel. The organic carbon content of these cherts (0.02–1.58%) shows a considerable variation with a maximum abundance in the Onverwacht group. Atomic H/C ratios (0.08–1.38) of the associated organic matter (kerogen) support the suggestion that the carbon isotopic values of kerogen have not been isotopically enriched by metamorphic processes. Chemically bound alipathic structures amount to about 10% by weight of the organic carbon content of a chert from the lowermost Theespruit succession. 相似文献
11.
《Applied Geochemistry》1993,8(4):317-324
Two crude oils with relatively high (0.60 wt%) and low (0.18 wt%) oxygen contents were heated in the presence of water in gold-plated reactors at 300°C for 2348 h. The high-oxygen oil was also heated at 200°C for 5711 h. The compositions of aqueous organic acid anions of the oils and of the headspace gases were monitored inn order to investigate the distribution of organic acids that can be generated from liquid petroleum.The oil with higher oxygen content generated about five times as much organic anions as the other oil. The dominant organic anions produced were acetate, propionate and butyrate. Small amounts of formate, succinate, methyl succinate and oxalate were also produced. The dominant oxygen-containing product was CO2, as has been observed in similar studies on the hydrous pyrolysis of kerogen. These results indicate that a significant portion (10–30%) of organic acid anions reported i be generated by thermal alteration of oils in reservoir rocks. The bulk of organic acid anions present in formation waters, however, is most likely generated by thermal alteration of kerogen in source rocks. Kerogen is more abundant than oil in sedimentary basins and the relative yields of organic acid anions reported from the hydrous pyrolysis of kerogen are much higher than the yields obtained for the two oils. 相似文献
12.
Kerogen plays an important role in shale gas adsorption, desorption and diffusion. Therefore, it is necessary to characterize the molecular structure of kerogen. In this study, four kerogen samples were isolated from the organic-rich shale of the Longmaxi Formation. Raman spectroscopy was used to determine the maturity of these kerogen samples. High-resolution transmission electron microscopy (HRTEM), 13C nuclear magnetic resonance (13C NMR) , X-ray diffraction (XRD) and Fourier transform infrared (FT-IR) spectroscopy were conducted to characterize the molecular structure of the shale samples. The results demonstrate that VReqv of these kerogen samples vary from 2.3% to 2.8%, suggesting that all the kerogen samples are in the dry gas window. The macromolecular carbon skeleton of the Longmaxi Formation kerogen is mainly aromatic (fa’=0.56). In addition, the aromatic structural units are mainly composed of naphthalene (23%), anthracene (23%) and phenanthrene (29%). However, the aliphatic structure of the kerogen macromolecules is relatively low (fal*+falH=0.08), which is presumed to be distributed in the form of methyl and short aliphatic chains at the edge of the aromatic units. The oxygen-containing functional groups in the macromolecules are mainly present in the form of carbonyl groups (fac=0.23) and hydroxyl groups or ether groups (falO=0.13). The crystallite structural parameters of kerogen, including the stacking height (Lc=22.84 ?), average lateral size (La=29.29 ?) and interlayer spacing (d002=3.43 ?), are close to the aromatic structural parameters of anthracite or overmature kerogen. High-resolution transmission electron microscopy reveals that the aromatic structure is well oriented, and more than 65% of the diffractive aromatic layers are concentrated in the main direction. Due to the continuous deep burial, the longer aliphatic chains and oxygen-containing functional groups in the kerogen are substantially depleted. However, the ductility and stacking degree of the aromatic structure increases during thermal evolution. This study provides quantitative information on the molecular structure of kerogen samples based on multiple research methods, which may contribute to an improved understanding of the organic pores in black shale. 相似文献
13.
P. K. Mukhopadhyay F. Goodarzi M. A. Kruge M. H. Alimi 《International Journal of Coal Geology》1997,34(3-4)
Organic-rich from the Schei Point group (middle to late Triassic in age) and the Ringnes formation (late Jurassic) from the Sverdrup basin of the Canadian arctic archipelago have been geochemically evaluated for source rock characterization. Most samples from the Schei Point group are organic-rich (> 2% TOC and are considered as immature to mature oil-prone source rocks [kerogen types I, I–II (IIA) and II (IIA)]. These kerogen types contain abundant AOM1, AOM2 and alginite (Tasmanales, Nostocopsis, Leiosphaeridia, acritarch and dinoflagellate) with variable amounts of vitrinite, inertinite and exinite. Samples from the Ringnes formation contain dominant vitrinite and inertinite with partially oxidized AOM2, alginite and exinite forming mostly immature to mature condensate- and gas-prone source rocks [kerogen type II–III (IIB), III and a few II (IIA)]. Schei Point samples contain higher bitumen extract, saturate hydrocarbons and saturate/ aromatic ratio than the Ringnes samples. Triterpane and sterane (dominant C30) distribution patterns and stable carbon isotope of bitumen and kerogen suggest that the analyzed samples from the Schei Point group are at the onset of oil generation and contain a mixture of sapropelic (algal) and minor terrestrial humic organic matter. Sterane carbon number distributions in the Ringnes formation also suggest a mixed algal and terrestrial organic matter type. There are some variations in hopane carbon number distributions, but these are apparently a function of thermal maturity rather than significant genetic differences among samples. Pyrolysis-gas chromatography/mass spectrometry of the two samples with similar maturity shows that the Schei Point sample generates three times more pyrolyzate than the Ringnes sample. Both samples have a dominant aliphatic character, although the Ringnes sample contains phenol and an aromaticity that is higher than that of the Schei Point sample. 相似文献
14.
The ash yield and concentrations of twenty-four minor and trace elements, including twelve potentially hazardous trace elements were determined in Mukah coal from Sarawak, Malaysia. Comparisons made to the Clarke values show that Mukah coal is depleted in Ag, Ba, Be, Cd, Co, Mn, Ni, Se, U, and V. On the other hand, it is enriched in As, Cr, Cu, Pb, Sb, Th, and Zn. Among the trace elements studied, V and Ba are associated predominantly with the clay minerals. Manganese, Cr, Cu, Th, and Ni are mostly bound within the aluminosilicate, sulphide and/or carbonate minerals in varying proportions, though a portion of these elements are also organically bound. Arsenic, Pb and Sb are mostly organically bound, though some of these elements are also associated with the sulphide minerals. Zinc is associated with both the organic and inorganic contents of the coal. Among the potentially hazardous trace elements, Be, Cd, Co, Mn, Ni, Se, and U may be of little or no health and environmental concerns, whereas As, Cr, Pb, Sb and Th require further examination for their potential health and environmental concerns. Of particular concern are the elements As, Pb and Sb, which are mostly organically bound and hence cannot be removed by physical cleaning technologies. They escape during coal combustion, either released as vapours to the atmosphere or are adsorbed onto the fine fly ash particles. 相似文献
15.
Beukes NJ Klein C Kaufman AJ Hayes JM 《Economic geology and the bulletin of the Society of Economic Geologists》1990,85(4):663-690
The transition zone comprises Campbellrand microbialaminated (replacing "cryptalgalaminate") limestone and shale, with minor dolomite, conformably overlain by the Kuruman Iron Formation of which the basal part is characterized by siderite-rich microbanded iron-formation with minor magnetite and some hematite-containing units. The iron-formation contains subordinate intraclastic and microbialaminated siderite mesobands and was deposited in deeper water than the limestones. The sequence is virtually unaltered with diagenetic mineral assemblages reflecting a temperature interval of about 110 degrees to 170 degrees C and pressures of 2 kbars. Carbonate minerals in the different rock types are represented by primary micritic precipitates (now recrystallized to microsparite), early precompactional sparry cements and concretions, deep burial limpid euhedral sparites, and spar cements precipitated from metamorphic fluids in close contact with diabase sills. Paragenetic pathways of the carbonate minerals are broadly similar in all lithofacies with kerogen intimately associated with them. Kerogen occurs as pigmentation in carbonate crystals, as reworked organic detritus in clastic-textured carbonate units, and as segregations of kerogen pigment around late diagenetic carbonate crystals. Locally kerogen may also be replaced by carbonate spar. Carbon isotope compositions of the carbonate minerals and kerogen are dependent on their mode of occurrence and on the composition of the dominant carbonate species in a specific lithofacies. Integration of sedimentary, petrographic, geochemical, and isotopic results makes it possible to distinguish between depositional, early diagenetic, deep burial, and metamorphic effects on the isotopic compositions of the carbonate minerals and the kerogen in the sequence. Major conclusions are that deep burial thermal decarboxylation led to 13C depletion in euhedral ferroan sparites and 13C enrichment in kerogen (organic carbon). Metamorphic sparites are most depleted in 13C. Carbonates in oxide-rich iron-formations are more depleted in 13C than those in siderite-rich iron-formation whereas the kerogens in oxide banded iron-formations (BIF) are more enriched. This implies that the siderite-rich iron-formations were not derived from oxide-rich iron-formation through reduction of ferric iron by organic matter. Organic matter oxidation by ferric iron did, however, decrease the abundance of kerogen in oxide-rich iron-formation and led to the formation of isotopically very light sparry carbonates. Siderite and calcmicrosparite both represent recrystallized primary micritic precipitates but differ in their 13C composition, with the siderites depleted in 13C by 4.6 per mil on average relative to calcmicrosparite. This means that the siderites were precipitated from water with dissolved inorganic carbon depleted in 13C by about 9 per mil relative to that from which the limestones precipitated. This implies an ocean system stratified with regard to total carbonate, with the deeper water, from which siderite-rich iron-formation formed, depleted in 13C. Iron-formations were deposited in areas of very low organic matter supply. Depletion of 13C may, therefore, derive not from degradation of organic matter but from hydrothermal activity, a conclusion which is supported by 18O composition of the carbonate minerals and trace element and rare earth element (REE) compositions of the iron-formations. 相似文献
16.
封闭体系有机质与有机碳氢氮恢复动力学研究 总被引：3，自引：0，他引：3
在封闭体系的条件下,对典型的Ⅰ、Ⅱ、Ⅲ型干酪根在热演化过程中的损失进行生烃动力学研究,获得了Ⅰ、Ⅱ、Ⅲ型干酪根的总量、有机碳、氢以及氮质量损失动力学参数。用Kinetics软件计算了封闭体系干酪根有机碳丰度、氢碳原子比和氮碳原子比的恢复系数。认为在对高成熟—过成熟干酪根进行生烃评价时,Ⅰ、Ⅲ型干酪根残余有机碳丰度需要进行恢复,而Ⅱ型干酪根残余有机碳丰度不需要恢复。三种类型干酪根的氢碳原子比均需要进行恢复。 相似文献
17.
扬子地块西北缘及西南缘卡林型金矿的有机质地质地球化学 总被引：7，自引：0，他引：7
扬子地块西北缘，西南缘卡林型金矿床的有机碳含量为０．０５％－８．７３％。含金建造形成的环境不同，其改造成的金矿床的有机碳含量不同；矿化主岩的岩性不同，基有机碳的含量不同。由浊积岩型含金建筑改造成的卡林型金矿床，其干酪根属Ⅱ型酪根，原始有机母质属还原环境沉积的海相菌藻类生物演化成的腐泥型有机质。 相似文献
18.
This article prognosticates the hydrocarbon generation potential of core samples from fields A, B, C and D in Niger delta, Nigeria. The objectives of this study are to characterize the quality of these core samples by organic geochemical analyses. A total of ten core samples collected from fields A, B, C and D in Niger delta were analyzed using total organic carbon （TOC） content analysis, rock-eval pyrolysis technique. The analytical results of the stud- ied core samples reveal that they have generally high total organic carbon contents （TOC）, suggesting that conditions in the Niger delta favour organic matter production and preservation. There is a variation in the kerogen types and this may be attributed to the relative stratigraphic positions of the core samples within the Niger delta. The rock-eval results indicate that the samples from fields C and D contain predominantly Type II kerogen with a capacity to gen- erate oil and gas and hence have good generative potential. The samples from fields A and B contain mainly Type III kerogen and are gas-prone with moderate generative potential. 相似文献
19.
为揭示鄂尔多斯盆地东缘上古生界海陆过渡相页岩及页岩气地球化学特征,选取临兴地区页岩样,开展薄片鉴定、全岩和黏土含量、扫描电镜、有机碳、岩石热解、干酪根显微组分和干酪根碳同位素测试,分析页岩解吸气的气体组分和碳同位素组成。结果表明:临兴地区过渡相页岩矿物组分主要是石英和黏土矿物,含少量方解石、斜长石、钾长石、白云石和黄铁矿等。受矿物成因、沉积环境等多方面的影响,不同矿物组分与有机质赋存方式各异。石英与有机质存在2种赋存方式,黏土矿物存在3种赋存方式,黄铁矿存在4种赋存方式。有机质类型为Ⅱ2–Ⅲ型,有机碳含量平均值大于2.0%,干酪根碳同位素介于–24.5‰~–23.2‰。镜质体反射率介于0.92%~1.30%,tmax值介于427~494℃,有机质热演化达到成熟阶段。页岩气中烃类气以甲烷为主,含有少量乙烷、丙烷,总体属于干气。甲烷碳同位素均值为–40.0‰,介于海相页岩气和陆相页岩气甲烷碳同位素之间;乙烷碳同位素值介于–26.8‰~–22.56‰,均大于–29‰,整体呈现出δ13C1＜δ13C2＜δ13C3正碳序列。研究认为,该区页岩具备大量生成页岩气的潜力,页岩气主要来源于上古生界偏腐殖型页岩,属于由干酪根裂解而生成的有机热成因煤成气。 相似文献
20.
Two samples from the upper and lower horizons of the Irati oil shale of the Paraná Basin, Brazil were sampled in a single borehole, and analysed using organic petrography and geochemistry. The results are interpreted in terms of the kerogen type, maturity and depositional environment of the two horizons.Organic petrography shows the oil-shales to be composed of a mineral groundmass, mainly clay minerals, carbonate and pyrite, associated, and sometimes impregnated, with fluorescing organic material and disseminated phytoclasts. Humic material is fairly rare and mostly present as very small particles. The liptinitic particles are mostly alginite (A and B), sporinite and more rarely resinite. Reflectance measurements (upper seam = 0.34% R0; lower seam = 0.40% R0) indicate an equivalent rank of lignite/sub-bituminous coal (ASTM), i.e. immature with respect to oil and gas generation. Different organic geochemical methods (Rock-Eval pyrolysis, solvent extraction, GC and GC-MS) demonstrate both samples to be immature, rich oil-shales (100–114 kg/ton) containing Type I kerogen, of a dominantly bacterially-degraded algal origin deposited in a lacustrine environment. The presence of Botryococcus suggests deposition under fresh/brackish water conditions.A tentative interpretation of the extract and vitrinite reflectance data suggests a maximum paleo-burial of between 1.3 and 2.8 km for the analysed section of the Irati Formation. 相似文献