The free, adsorbed and inclusion oils were recovered by sequential extraction from eleven oil and tar containing reservoir rocks in the Tazhong Uplift of Tarim Basin. The results of gas chromatography (GC) and GC–mass spectrometry analyses of these oil components and seven crude oils collected from this region reveal multiple oil charges derived from different source rocks for these oil reservoirs. The initially charged oils show strong predominance of even over odd n-alkanes in the range n-C12 to n-C20 and have ordinary maturities, while the later charged oils do not exhibit any predominance of n-alkanes and have high maturities. The adsorbed and inclusion oils of the reservoir rocks generally have high relative concentrations of gammacerane and C28 steranes, similar to the Cambrian-Lower Ordovician source rocks. In contrast, the free oils of these reservoir rocks generally have low relative concentrations of gammacerane and C28 steranes, similar to the Middle-Upper Ordovician source rocks. There are two interpretations of this result: (1) the initially charged oils are derived from the Cambrian-Lower Ordovician source rocks while the later charged oils are derived from the Middle-Upper Ordovician source rocks; and (2) both the initially and later charged oils are mainly derived from the Cambrian-Lower Ordovician source rocks but the later charged oils are contaminated by the oil components from the Silurian tar sandstones and the Middle-Upper Ordovician source rocks. 相似文献
Carbon isotopic compositions were determined by GC–IRMS for individual n-alkanes in crude oils and the free, adsorbed and inclusion oils recovered by sequential extraction from reservoir rocks in the Tazhong Uplift and Tahe oilfield in the Tabei Uplift of Tarim Basin as well as extracts of the Cambrian–Ordovician source rocks in the basin. The variations of the δ13C values of individual n-alkanes among the 15 oils from the Tazhong Uplift and among the 15 oils from the Triassic and Carboniferous sandstone reservoirs and the 21 oils from the Ordovician carbonate reservoirs in the Tahe oilfield demonstrate that these marine oils are derived from two end member source rocks. The major proportion of these marine oils is derived from the type A source rocks with low δ13C values while a minor proportion is derived from the type B source rocks with high δ13C values. Type A source rocks are within either the Cambrian–Lower Ordovician or the Middle–Upper Ordovician strata (not drilled so far) while type B source rocks are within the Cambrian–Lower Ordovician strata, as found in boreholes TD2 and Fang 1. In addition, the three oils from the Cretaceous sandstone reservoirs in the Tahe oilfield with exceptionally high Pr/Ph ratio and δ13C values of individual n-alkanes are derived, or mainly derived, from the Triassic–Jurassic terrigenous source rocks located in Quka Depression.The difference of the δ13C values of individual n-alkanes among the free, adsorbed and inclusion oils in the reservoir rocks and corresponding crude oils reflects source variation during the reservoir filling process. In general, the initial oil charge is derived from the type B source rocks with high δ13C values while the later oil charge is derived from the type A source rocks with low δ13C values.The δ13C values of individual n-alkanes do not simply correlate with the biomarker parameters for the marine oils in the Tazhong Uplift and Tahe oilfield, suggesting that molecular parameters alone are not adequate for reliable oil-source correlation for high maturity oils with complex mixing. 相似文献
The Halahatang Depression in the Tabei Uplift of the Tarim basin is an active exploration area because it has substantial reservoir potential and contains or is near to many commercial oil fields. Geochemical analysis indicates that Halahatang oils were derived from marine carbonate source rocks deposited under anoxic reducing conditions. The maturities for Halahatang oils are corresponding to the peak of the oil window and slightly higher than the neighboring Tahe oils. The Halahatang oils feature low Pr/Ph, C21/C23 tricyclic terpane and, C28/C29 sterane ratios, high C29/C30 hopane and C35/C34 hopane ratios, a “V” shape in the distribution of C27–C28–C29 steranes and light carbon isotope ratios, similar to the Tahe oils and correlate well with the Middle-Upper Ordovician source rock. However, some source-related biomarker parameters imply a more reducing source organofacies with more zooplanktonic contribution than that for the Tahe oils. 相似文献
1 Introduction Since the 1990’s of the 20th century, oil & gas geochemists have shifted their research focus on hydrocarbon source rocks in the past to that on reservoir rocks and oil reservoirs at present; their research field has been expanded from oil & gas exploration to the assessment of oil reservoirs and production & management. Therefore, reservoir geochemistry as a branch disciplinary of organic geochemistry is now attracting great concern of many oil & gas explorers and oilfield en… 相似文献
Research on the molecular fossil characteristics of heavy oil from Well Tadong-2 is of great importance to constrain the source
of marine crude oils in the Tarim Basin, Xinjiang, China. The authors synthetically applied the isotope mass spectrograph,
chromatography and chromatography-mass spectrography to the studies of molecular fossil characteristics of heavy oil from
Well Tadong-2 in the Tarim Basin, and the results obtained revealed that heavy oil from Well Tadong-2 is characterized by
high gammacerane, high C28 sterane, low rearranged sterane and high C27-triaromatic steroid, these characteristics are similar to those of Cambrian-Lower Ordovician source rocks, demonstrating
that Cambrian crude oils came from Cambrian-Lower Ordovician source rocks; condensed compounds (fluoranthene, pyrene, benzo[a]anthracene,
bow, benzo fluoranthene, benzopyrene) of high abundance were detected in heavy oil from Well Tadong-2, and the carbon isotopic
values of whole oil are evidently heavy, all the above characteristics revealed that hydrocarbons in the crude oils became
densified in response to thermal alteration. 相似文献
Forty-six crude oil samples were selected from the Ordovician in the northwestern part of the Tahe oilfield for detailed molecular geochemical and isotopic analysis, including group compositions, carbonhydrogen isotopes and gas chroma-tograms of saturated hydrocarbons, as well as the characteristics of terpane, sterane and other biomarkers, indicating that crude oils are of the same origin from different districts in the Tahe oilfield and were derived from the same source kitchen (or oil source formation), i.e., mainly stemming from marine hydrocarbons. Detailed studies of oil physical properties of 25-honpane revealed that such oils have heavy or thick oil qualities due to biodegradation. Comprehensive assessment in terms of five maturity parameters shows that the oils from the Ordovician with Ro values varying from 0.80% to 1.59% are widely distributed in the northwest of the Tahe oilfield. 相似文献
Two oil families in Ordovician reservoirs from the cratonic region of the Tarim Basin are distinguished by the distribution of regular steranes, triaromatic steroids, norcholestanes and dinosteroids. Oils with relatively lower contents of C28 regular steranes, C26 20S, C26 20R + C27 20S and C27 20R regular triaromatic steroids, dinosteranes, 24-norcholestanes and triaromatic dinosteroids originated from Middle–Upper Ordovician source rocks. In contrast, oils with abnormally high abundances of the above compounds are derived from Cambrian and Lower Ordovician source rocks. Only a few oils have previously been reported to be of Cambrian and Lower Ordovician origin, especially in the east region of the Tarim Basin. This study further reports the discovery of oil accumulations of Cambrian and Lower Ordovician origin in the Tabei and Tazhong Uplifts, which indicates a potential for further discoveries involving Cambrian and Lower Ordovician sourced oils in the Tarim Basin. Dinosteroids in petroleum and ancient sediments are generally thought to be biomarkers for dinoflagellates and 24-norcholestanes for dinoflagellates and diatoms. Therefore, the abnormally high abundance of these compounds in extracts from the organic-rich sediments in the Cambrian and Lower Ordovician and related oils in the cratonic region of the Tarim Basin suggests that phytoplankton algae related to dinoflagellates have appeared and might have flourished in the Tarim Basin during the Cambrian Period. Steroids with less common structural configurations are underutilized and can expand understanding of the early development history of organisms, as well as define petroleum systems. 相似文献
Up until now, it has been assumed that oil in the Palaeozoic reservoirs of the Tazhong Uplift was derived from Upper Ordovician source rocks. Oils recently produced from the Middle and Lower Cambrian in wells ZS1 and ZS5 provide clues concerning the source rocks of the oils in the Tazhong Uplift, Tarim Basin, China. For this study, molecular composition, bulk and individual n-alkane δ13C and individual alkyl-dibenzothiophene δ34S values were determined for the potential source rocks and for oils from Cambrian and Ordovician reservoirs to determine the sources of the oils and to address whether δ13C and δ34S values can be used effectively for oil–source rock correlation purposes. The ZS1 and ZS5 Cambrian oils, and six other oils from Ordovician reservoirs, were not significantly altered by TSR. The ZS1 oils and most of the other oils, have a “V” shape in the distribution of C27–C29 steranes, bulk and individual n-alkane δ13C values predominantly between −31‰ to −35‰ VPDB, and bulk and individual alkyldibenzothiophene δ34S values between 15‰ to 23‰ VCDT. These characteristics are similar to those for some Cambrian source rocks with kerogen δ13C values between −34.1‰ and −35.3‰ and δ34S values between 10.4‰ and 21.6‰. The oil produced from the Lower Ordovician in well YM2 has similar features to the ZS1 Cambrian oils. These new lines of evidence indicate that most of the oils in the Tazhong Uplift, contrary to previous interpretations, were probably derived from the Cambrian source rocks, and not from the Upper Ordovician. Conversely, the δ13C and δ34S values of ZS1C Cambrian oils have been shown to shift to more positive values due to thermochemical sulfate reduction (TSR). Thus, δ13C and δ34S values can be used as effective tools to demonstrate oil–source rock correlation, but only because there has been little or no TSR in this part of the section. 相似文献
Sequential extraction was performed on two oil sandstones from the Upper Carboniferous oil columns of TZ401 well.The free oils of these two oil sandstones and a crude oil from the Lower Carboniferous oil column of this well have low ratios of C28/C27+C28+ C29) steranes and gammacerane/C31 hopanes,ranging of 0.11-0.16 and 0.09-0.15,respectively,similar to those from the Middle-Upper Ordovician source rock.However,these two ratios for the adsorbed and inclusion oils of these two oil sandstones are relatively high,ranging of 0.29-0.31 and 0.26-0.40,respectively,similar to those of the Cambrian-Lower Ordovician source rock.This result demonstrates that the initial oil charging the reservoirs was derived from the Cambrian-Lower Ordovician source rock,whereas the later charging oil was derived from the Middle--Upper Ordovician source rock. 相似文献
The Masila Basin is an important hydrocarbon province in Yemen, but the origin of hydrocarbons and their generation history are not fully understood. In this regard, 10 crude oils from different petroleum reservoir sections in the Masila Basin were characterized by a variety of biomarker and non-biomarker parameters using GC, GC-MS and stable carbon isotope techniques. Oils from the Masila Basin display pristane/phytane (Pr/Ph) ratios ranging from 1.7 to 2.0, low sulfur content, high C35 homohopane index, relatively high C27 sterane concentrations and relatively high tricyclic terpanes suggesting a marine clay source rock that was deposited in mildly anoxic to suboxic conditions with dominantly algal organic matter. C29 20S/(20S + 20R) steranes and ββ/(ββ + αα) sterane ratios indicate that the Masila oils have reached peak oil window maturity. Another related feature of these oils is the absence of 18α (H)-oleanane, which suggests a source age older than Cretaceous. The carbon isotope compositions are similar to those of the potential source rocks, which range from −25.4‰ to −28.3‰, indicating a marine environment. The new data presented in this paper suggest that the Masila oils constitute one oil family and that the oil originated from the Upper Jurassic Madbi source rock in the basin. 相似文献
The Qinjiatun and Qikeshu oilfields are new Mesozoic petroleum exploration targets in Lishu Fault Depression of Songliao Basin, northeastern China. Currently, researches on geochemistry of crude oils from Qinjiatun and Qikeshu oilfields have not been performed and the genesis of oils is still uncertain. Based on bulk analyses, the crude oils in the Qinjiatun and Qikeshu oilfields of Lishu Fault Depression from the Lower Cretaceous can be classified as three types. TypeⅠoils, from Quantou and Denglouku formations of Qikeshu oilfield, are characterized by high C24tetracyclic terpane/C26tricyclic terpanes ratios, low gammacerance/C30hopane ratios, tricyclic terpanes/hopanes ratios, C29Ts/C29norhopane ratios and 17α(H)-diahopane/17α(H)-hopane ratios, indicating a brackish lacustrine facies. TypeⅡoils, from Shahezi Formation of Qikeshu oilfield show low C24tetracyclic terpane/C26tricyclic terpanes, high gammacerance/C30hopane ratios, tricyclic terpanes/hopanes ratios, C29Ts/C29 norhopane and C30diahopane/C30hopane ratios, thus suggesting that they originated from source rocks deposited in a weak reducing brackish lacustrine environment, or clay-rich sediments. Type oilsⅢ, from some wells of Qikeshu oilfield have geochemical characteristics intermediate between those two types and may be mixture of typeⅠand Ⅱoils. 相似文献
The parameter S1 + S2 (genetic potential) of Rock-Eval analysis is widely used as an evaluation of the genetic potential for the source rocks. Oligocene–Miocene saline lacustrine source rocks in the western Qaidam basin have low total organic C contents (TOC), most around 0.5% with a few exceptions >1.0%. Mineral matrix effects are substantial for source rocks with low TOC, resulting in relatively low S1 and S2 peaks. Based on the results of confined pyrolyses (sealed Au capsules) on 6 Oligocene–Miocene source rocks from the western Qaidam basin, with TOC ranging between 0.48% and 2.22%, the relationship between the S1 + S2 parameter and the maximum amount of extracted bitumen or saturated and aromatic hydrocarbons (SA) after the confined pyrolysis has been established as follows: bitumen (mg/g rock) = 1.4924 × (S1 + S2) + 0.3201 (r = 0.987), or SA (saturates + aromatics) (mg/g rock) = 0.7083 × (S1 + S2) + 0.4045 (r = 0.992). Based on these formulas, the amounts of hydrocarbons generated from source rocks can be reasonably estimated. The typical crude oils with low biomarker maturities in this region appear substantially different to the pyrolysates of these six rocks at 180–300 °C but comparable to the pyrolysates at 320 °C and higher temperatures based on molecular parameters. This result, in combination with the physical and gross compositions of the crude oils, suggests that the majority of these crude oils were generated from the source rocks during the main oil-generative stage, possibly at a maturity higher than Ro 0.74%. 相似文献
A large amount of deep oil has been discovered in the Tazhong Uplift, Tarim Basin whereas the oil source is still controversial. An integrated geochemical approach was utilized to unravel the characteristics, origin and alteration of the deep oils. This study showed that the Lower Cambrian oil from well ZS1C (1x) was featured by small or trace amounts of biomarkers, unusually high concentration of dibenzothiophenes (DBTs), high δ34S of DBTs and high δ13C value of n-alkanes. These suggest a close genetic relationship with the Cambrian source rocks and TSR alteration. On the contrary, the Middle Cambrian oils from well ZS1 (2a) were characterized by low δ13C of n-alkanes and relatively high δ34S of individual sulfur compounds and a general “V” shape of steranes, indicating a good genetic affinity with the Middle–Upper Ordovician source rocks. The middle Cambrian salt rock separating the oils was suggested to be one of the factors responsible for the differentiation. It was suggested that most of the deep oils in the Tazhong Uplift were mixed source based on biomarkers and carbon isotope, which contain TSR altered oil in varied degree. The percentage of the oils contributed by the Cambrian–Lower Ordovician was in the range of 19–100% (average 57%) controlled by several geological and geochemical events. Significant variations in the δ34S values for individual compounds in the oils were observed suggesting a combination of different extent of TSR and thermal maturation alterations. The unusually high DBTs concentrations in the Tazhong-4 oilfield suggested as a result of mixing with the ZS1C oil (1x) and Lower Ordovician oils based on δ34S values of DBT. This study will enhance our understanding of both deep and shallow oil sources in the Tazhong Uplift and clarify the formation mechanisms of the unusually high DBTs oils in the region. 相似文献
Unusually high dibenzothiophene (DBT) concentrations are present in the oils from the Tazhong-4 Oilfield in the Tazhong Uplift, Tarim Basin. Positive-ion electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) was used in combination with conventional geochemical approaches to unravel the enrichment mechanisms. Significant amounts of S1 species with relatively low DBE values (0–8), i.e., sulfur ethers, mercaptans, thiophenes and benzothiophenes, were detected in three Lower Ordovician oils with high thermal maturity, which were suggested to be the products of thermochemical sulfate reduction (TSR) in the reservoir. The occurrence of TSR was also supported by the coexistence of thiadiamondoids and abundant H2S in the gases associated with the oils. Obviously low concentrations of the DBE = 9 S1 species (mainly equivalent to C0–C35 DBTs) compared to its homologues were observed for the three oils which were probably altered by TSR, indicating that no positive relationship existed between TSR and DBTs in this study. The sulfur compounds in the Tazhong-4 oils are quite similar to those in the majority of Lower Ordovician oils characterized by high concentrations of DBTs and dominant DBE = 9 S1 species with only small amounts of sulfur compounds with low thermal stability (DBE = 0–8), suggesting only a small proportion of sulfur compounds were derived from TSR. It is thermal maturity rather than TSR that has caused the unusually high DBT concentrations in most of the Lower Ordovician oils. We suggest that the unusually high DBT oils in the Tazhong-4 Oilfield are caused by oil mixing from the later charged Lower Ordovician (or perhaps even deeper), with high DBT abundances from the earlier less mature oils, which was supported by our oil mixing experiments and previous relevant investigations as well as abundant authigenic pyrite of hydrothermal origin. We believe that TSR should have occurred in the Tazhong Uplift based on our FT-ICR MS results. However, normal sulfur compounds were detected in most oils and no increase of δ13C2H6–δ13C4H10 was observed for the gas hydrocarbons, suggesting only a slight alteration of the oils by TSR currently and/or recently. We suspect that the abnormal sulfur compounds in the Lower Ordovician oils might also be a result of deep oil mixing, which might imply a deeper petroliferous horizon, i.e., Cambrian, with a high petroleum potential. This study is important to further deep petroleum exploration in the area. 相似文献
Geochemical characterisation of 18 crude oils from the Potwar Basin (Upper Indus), Pakistan is carried out in this study. Their relative thermal maturities, environment of deposition, source of organic matter (OM) and the extent of biodegradation based on the hydrocarbon (HC) distributions are investigated. A detailed oil-oil correlation of the area is established. Gas chromatography-mass spectrometry (GC-MS) analyses and bulk stable carbon and hydrogen isotopic compositions of saturated and aromatic HC fractions reveals three compositional groups of oils. Most of the oils from the basin are typically generated from shallow marine source rocks. However, group A contains terrigenous OM deposited under highly oxic/fluvio-deltaic conditions reflected by high pristane/phytane (Pr/Ph), C30 diahopane/C29Ts, diahopane/hopane and diasterane/sterane ratios and low dibenzothiophene (DBT)/phenanthrene (P) ratios. The abundance of C19-tricyclic and C24-tetracyclic terpanes are consistent with a predominant terrigenous OM source for group A. Saturated HC biomarker parameters from the rest of the oils show a predominant marine origin, however groups B and C are clearly separated by bulk δ13C and δD and the distributions of the saturated HC fractions supporting variations in source and environment of deposition of their respective source rocks. Moreover, various saturated HC biomarker ratios such as steranes/hopanes, diasteranes/steranes, C23-tricyclic/C30 hopane, C28-tricyclic/C30 hopane, total tricyclic terpanes/hopanes and C31(R + S)/C30 hopane show that two different groups are present. These biomarker ratios show that group B oils are generated from clastic-rich source rocks deposited under more suboxic depositional environments compared to group C oils. Group C oils show a relatively higher input of algal mixed with terrigenous OM, supported by the abundance of extended tricyclic terpanes (up to C41+) and steranes.Biomarker thermal maturity parameters mostly reached to their equilibrium values indicating that the source rocks for Potwar Basin oils must have reached the early to peak oil generation window, while aromatic HC parameters suggest up to late oil window thermal maturity. The extent of biodegradation of the Potwar Basin oils is determined using various saturated HC parameters and variations in bulk properties such as API gravity. Groups A and C oils are not biodegraded and show mature HC profiles, while some of the oils from group B show minor levels of biodegradation consistent with high Pr/n-C17, Ph/n-C18 and low API gravities. 相似文献
