Stratigraphy, sedimentology and bulk organic geochemistry of black shales from the Proterozoic Vindhyan Supergroup (central India)

Four organic-rich shale units of the Proterozoic Vindhyan sedimentary succession have been scanned to reveal their origin and hydrocarbon potential. The wavy-crinkly nature of the carbonaceous laminae is suggestive of a microbial mat origin of the shales. These shales are thus different from Phanerozoic black shales which typically exhibit planar laminae. The hydrocarbon potential of the black shale units has been evaluated by Rock-Eval pyrolysis. Total organic carbon content of many of the shales exceeds 1%. The meanT _max for the black shales translate to a vitrinite reflectance range of 2.05-2.40% Rm based on standard conversion techniques. These shales have reached the catagenetic stage near the beginning of anthracite formation.     

Organism relics or kerogens in oils as oil-source rock correlation indicator

Organism relics or kerogens in oils are first obsenred by a confocal laser scanning microscope (CLSM) and a transmission electron microscope (TEM). The complexes of kerogens in oils are characterized by the presence of a great variety of microfossils or macerals. These kerogens in oils are mainly the residues of the original organic substances from which oil formed, and minor kerogens from enclosing rocks enter the oils, therefore, the components and types of the kerogens in crude oils can serve as an indirect indicator of oil-source rock correlation. This method was applied to Jurassic oils in the Junggar Basin and the Turpan-Hami Basin, and there are two types of the kerogens in oils: one containing a lot of macerals from terrestrial plants may derive from coals, and the other, characterized by a high content of microscopic algae, fungus spores and Acritarch, may originate from Permian organic matter. In addition, the reflectance of the vitrodetrinites in oils can be used as an indicator of oil-source rock correlation.     

结构动力模型试验相似理论及其验证

通过几何比尺为2的两个有机玻璃模型的结构动力试验，验证了结构动力模型试验的弹性相似律和弹性力一重力相似律。得到了以下结论：(1)大小模型频率符合相似律，一阶频率误差为2．7％、4．1％，二阶频率误差为O、6．05％。弹性相似律比弹性力一重力相似律更适合于频率预测的试验。(2)大小模型的加速度、应变符合相似律，弹性相似律的加速度误差为-1．55％～8．75％，应变误差为O．377％～7．297％。弹性力-重力相似律的加速度误差为3．07％～4．158％，应变误差为6．849％～12．959％。(3)不同相似律大小模型的时问比尺吻合很好。加速度与应变时程曲线的波形一致，既无漏峰也无错峰。     

Composition of Kerogen in Kupferschiefer from Southwest Poland

Thirty-seven Kupferschiefer samples from southwestern Poland were analyzed by microscopy, Rock-Eval approach and instrumental neutron activation analysis to understand the geochemical and morphological characteristics of kerogen present in the samples. The analytical results indicate that there are two different types of kerogens. One type was only subjected to thermal alteration processes, and the other was further oxidized after deposition of the sediment.In the oxidized samples migrabitumen was transformed into pyrobitumen. Rock-Eval analyses show a significant decrease in HI values in the oxidized samples and an increase in OI values in relation to the samples that were not influenced by oxidation. Variations in S2 versus Corg contents indicate a change in kerogen from Type II to Type III with progressing oxidation. The presence of pyrobitumen and the depletion of hydrogen in the altered kerogen allow one to conclude that the kerogen was used as hydrogen donor for thermochemical sulfate reduction(TSR).     

Contact-metamorphic effect on parameters for kerogen maturation

This study examines the effect of contact metamorphism by an igneous dyke on parameters for kerogen maturation, such as elemental composition (H/C, O/C, N/C), ¹H-NMR T₁, vitrinite reflectance and infrared spectra. Although elemental composition and ¹H-NMR T₁ of the kerogen changed only within 1.5 and 5.0 m from the dyke respectively, vitrinite reflectance of the kerogen was thermally affected beyond 10.0 m from the intrusion. It is concluded that vitrinite reflectance is the most sensitive of the parameters evaluated to assess thermal stress of kerogens.     

硒在干酪根中的两种不同赋存状态:TEM证据

对拉尔玛Se—Au矿床和渔塘坝硒矿床中干酪根的高分辨透射电镜(TEM)研究表明，两个矿床的Se在干酪根中的赋存状态是截然不同的。前者Se在干酪根中的富集可能主要以有机结合态的形式存在，主要是取代干酪根中的硫；而后者Se在干酪根中的富集主要以超微包体Se的形式吸附在干酪根中。两种不同的赋存状态可能主要取决于干酪根中硫含量的多少以及成矿时氧化还原条件的变化。研究表明，TEM是研究元素在干酪根中赋存状态的有效手段。     

Thermal depolymerization of kerogen and formation of immature oil

Two Chinese immature oil shales from the continental deposits of kerogen type I and II have been thermally treated combined with the technique of supercritical fluid extraction at 630–650 K and 15–25 MPa in a semi-continuous laboratory scale apparatus. Toluence is selected as the solvent. Up to 70–80% of the kerogen matrix can be converted to a thermal bitumen and extracted simultaneously. The chemical structural parameters from the NMR, IR, XRD, ESR and EA analyses of the kerogen and the thermal bitumen show striking resemblance in nature. It implies that the thermal bitumen is primarily a depolymerized product of the kerogen. Based on the GC/MS spectra of the aliphatic eluate of the thermal bitumen, the predominance of the odd/even ratio of the alkanes and the epimeric ratios, such as 20S(20S + 20R) of C-29 steranes and 22S/(22S + 22R) of C-32 terpanes, show that the maturity of the thermal bitumen from these oil shales is comparable to that of commercial immature oils from East China. The thermal bitumen is thought to be an intermediate product of the thermal degradation of kerogen.Since the thermal bitumen is mainly composed of asphaltenes and resins, it has a structure of gel. The gel-state bitumen may turn to sol-state readily due to its low aromaticity and polarity, or due to selective adsorption of asphaltenes by clay minerals. Then the migration potential of the bitumen is enhanced.Consequently, under favorable geological conditions, the thermal depolymerization of kerogen seems to be a probable mechanism to explain the formation of immature oils.     

The control of maturity and kerogen type on quantitative analytical pyrolysis data

Quantitative pyrolysis-gas chromatography has been performed on 96 kerogen samples isolated from 17 wells on the Norwegian Continental shelf. Petrographic and bulk geochemical measurements were also performed on the samples, and a combined data set of 117 variables for each sample was analysed using principal components analysis (PCA). This approach provides an objective and reproducible means of kerogen characterisation, which can be easily automated. In addition to objective kerogen characterisation and facile visualisation of facies and maturity related chemical trends, the method has the potential to allow objective prediction of key geochemical parameters such as maturity level from pyrogram data.     

3D chemical model for geological macromolecules

This study defines a chemical representation of the kerogen macromolecule based on data from physicochemical analyses. The model should permit: creation of various schematic drawings representing an average macromolecule; future integration of new analytical results (for instance on structures of biomarkers or biopolymers); and determination of the distribution of chemical bonds.The models developed in this study can be represented in a 3D space, using classical chemical symbols, in the form of cyclic groups linked to each other by aliphatic chains. One cyclic group is a connected set of aromatic, naphthenoaromatic or naphthenic rings. These cyclic groups are constructed using basic elements such as atoms and bonds defined by their length and direction.Modeling of kerogen is done in three successive steps. A library is first created to define atoms, bonds and cyclic groups. Secondly, starting from a set of equations describing the analytical results, cyclic and aliphatic groups are chosen in the appropriate stoechiometric amount to match the analytical data. Finally the construction is done: cyclic groups are placed randomly in a 3D space, connections are made by aliphatic chains, and functional groups are added.The molecular modeling software Xmol^TM can be operated on APOLLO stations. It allows the creation of libraries, the calculation of chemical bonds corresponding to the analyses and the construction of macromolecules. An example is given for a type III kerogen at the beginning of diagenesis.