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1.
Light hydrocarbons (LHs) are one of the main petroleum fractions in crude oils, and carry much information regarding the genetic origin and alteration of crude oils. But secondary alterations—especially biodegradation—have a significant effect on the composition of LHs in crude oils. Because most of the LHs affected in oils underwent only slight biodegradation (rank 1 on the biodegradation scale), the variation of LHs can be used to describe more the refined features of biodegradation. Here, 23 crude oils from the Dawanqi Oilfield in the Tarim Basin, NW China, eleven of which have been biodegraded to different extents, were analyzed in order to investigate the effect of slight to minor biodegradation on C6–C7 LHs. The study results showed that biodegradation resulted in the prior depletion of straight-chained alkanes, followed by branched alkanes. In slight and minor biodegraded oils, such biodegradation scale could not sufficiently affect C6–C7 cycloalkanes. For branched C6–C7 alkanes, generally, monomethylalkanes are biodegraded earlier than dimethylalkanes and trimethylalkanes, which indicates that branched alkanes are more resistant to biodegradation, with the increase of substituted methyl groups on parent rings. The degree of alkylation is one of the primary controlling factors on the biodegradation of C6–C7 LHs. There is a particular case: although 2,2,3-trimethylbutane has a relative higher alkylation degree, 2,2-dimethylpentane is more resistant to biodegradation than 2,2,3-trimethylbutane. 2,2-Dimethylpentane is the most resistant to biodegradation in branched C6–C7 alkanes. Furthermore, the 2-methylpentane/3-methylpentane and 2-methylhexane/3-methylhexane ratios decreased steadily with increasing biodegradation, which implies that isomers of bilateral methyl groups are more prone to bacterial attack relative to mid-chain isomers. The position of the alkyls on the carbon skeleton is also one of the critical factors controlling the rate of biodegradation. With increasing biodegradation, Mango’s LH parameters K1 values decrease and K2 values increase, the values of n-heptane and isoheptane decrease, and the indices of methylcyclohexane and cyclohexane increase. LH parameters should be applied cautiously for the biodegraded oils. Because biodegraded samples belong to slight or minor biodegraded oils, the values of n-heptane and isoheptane from Dawanqi Oilfield can better reflect and determine the “Biodegraded” zone. When the heptane value is 0–21 and the isoheptane value is 0–2.6, the crude oil in Dawanqi Oilfield is defined as the “Biodegraded” zone. 相似文献
2.
煤成气轻烃地球化学特征及其影响因素——以四川盆地须家河组为例 总被引：3，自引：0，他引：3
轻烃在天然气中含量虽低,但因其含有丰富的地球化学信息,在天然气成因等研究方面引起了关注。作者以四川盆地须家河组煤成气和雷三段油型气为例,采用GC和GC-IR-MS技术对煤成气轻烃的地球化学分布特征及其影响因素进行了系统分析。煤成气C7轻烃组成具有甲基环己烷分布优势,在甲基环己烷、正庚烷和二甲基环戊烷相对组成中,甲基环己烷含量最高,分布在48%~73%,平均为63.9%,煤成气轻烃单体烃碳同位素重,δ13C分布在-25.1‰~-20.0‰之间,大部分分布在-23.0‰~-21.0‰。轻烃的分布受到多种因素影响,天然气成熟度对轻烃中芳烃含量变化影响复杂,在成熟和高成熟阶段,天然气轻烃中芳烃含量低,成熟度对芳烃的含量影响较小,而在过成熟阶段,芳烃含量高,成熟度对芳烃含量影响大。通过凝析油和天然气轻烃组成对比,蒸发分馏作用对热演化参数Ctemp和庚烷值、甲苯/正庚烷等影响较大,但对成因类型参数如(2-MH+2,3-DMP)/C7与(3-MH+2,4-DMP)/C7,P2/C7与N2/P3,正庚烷、甲基环己烷和二甲基环戊烷相对含量关系等影响小。天然气成因类型对轻烃Mango参数K1值、正庚烷、甲基环己烷和二甲基环戊烷相对含量关系以及轻烃单体烃碳同位素影响大,因此,可以利用这些参数进行天然气成因类型判识。 相似文献
3.
Different types of crude oils have different light hydrocarbon compositional and geochemical characteristics. Based on the light hydrocarbon data from two kinds of oils, i.e., coal-generated oils and marine oils in China, light hydrocarbons in marine oils in the Tazhong area are generally relatively enriched in n-heptane, and coal-generated oils from the Turpan Basin are enriched in methylcyclohexane. The K1 values, reported by Mango （1987）, range from 0.97 to 1.19 in marine oils, basically consistent with what was reported by Mango on light hydrocarbons in terms of the majority of the crude oil data. But the K1 values of coal-generated oils are particularly high （1.35-1.66） and far greater than those of marine oils; heptane values in marine oils, ranging from 32.3% to 45.4%, and isoheptane values, ranging from 1.9 to 3.7, are respectively higher than those of coal-generated oils, indicating that the oils are in the high-maturity stage. In addition, expulsion temperatures of coal-generated oils from the Turpan Basin are obviously lower than those of marine oils from the Tazhong area. 相似文献
4.
1IntroductionTheTarimBasin ,NWChina,istheonlybasininChinawherenotonlymarine ,butalsoter restrialindustrialoilandgaspoolsaredeveloped .TheterrestrialoilandgaspoolshavebeenfoundintheKuchedepressioninthenorthernpartofthebasinanditsfrontupliftarea (Fig .1) .ThesourcerocksoftheterrestrialoilandgaspoolsareTriassicandJurassiclacustrinemudstonesandswampcoals.ThebiomarkersfromthesaturatedfractionsofTriassicandJurassicterrestrialsourcerocksandFig .1 .LocationofTriassicandJurassicterrestrialsource… 相似文献
5.
Ten series of aromatic hydrocarbon compounds (biphenyl, naphthalene, phenanthrene, anthracene, retene, chrysene, benzoanthracene, dibenzofuran, fluorene, dibenzothiophene) isolated from seven Triassic and Jurassic lacustrine mudstone samples and three swamp coal samples, as well as five crude oil samples collected in the Kuche depression of the Tarim Basin,NW China, have been analysed by GC-MS techniques. It is found that the relative abundances of dibenzofuran series are higher in the three swamp coal samples than those in the lacustrine mudstone samples. Based on the similar relative abundances of dibenzofuran series, especially dibenzofuran compound, in the TICs of aromatic hydrocarbons, crude oils from wells SA3 (K), YTK5(E,K) and QL1 (E) are thought to have been derived predominantly from the coals of the Lower Jurassic Yangxia Formation or Middle Jurassic Kezilenuer Formation, whereas those from wells YM7 (O) and YHI (E) were derived mainly from Triassic and Jurassic lacustrine mudstones in the Kuche depression. This is the first report about how to distinguish coal-generated oils from lacustrine mudstone-generated oils in the Kuche depression in terms of the dibenzofuran series.The present paper has enlightening and directive significance for further oil-source rock correlations and oil and/or gas exploration in the Kuche depression of the Tarim Basin. 相似文献
6.
Molecular fossils and sources of Cambrian heavy oil of Well Tadong-2 in the Tarim Basin,Xinjiang, China 总被引：1，自引：1，他引：0
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
7.
塔里木盆地气－液溶解平衡机制下的原油轻烃行为及其地质意义 总被引：3，自引：0，他引：3
塔北地区普遍存在气顶型凝析气藏和带油环的凝析气藏。与传统烃类热演化理论相矛盾的是：１）天然气的成熟度远高于油环原油或凝析油；２）高－过成熟天然气与同藏的原油间存在明显的物性不匹配。结合地质背景，认为这种矛盾是由后期形成的干气进入已形成的油藏并溶解原油轻烃这一过程所致，凝析气中的轻烃是气－液溶解平衡的产物。地质历史时期凝析气与油环分离或产生凝析油气藏或混入其它油藏的蒸发分馏作用过程导致了轻烃的油藏再分配，形成了塔北地区纵向上原油轻烃的“反序”分布趋势及某些参数的异常分布。认为烃类的气－液相溶解平衡作用是原始原油轻烃分布特征后期演变的主要控制机制之一。其实质是不同性质轻烃气液两相差异性分配基础上的物理化学分异过程。 相似文献
8.
How to quantitatively evaluate the maturity of crude oils is still an open question. Mango discovered a remarkable compositional invariance of four isoheptane ratios in crude oils, and proposed a steady-state catalytic model for the origin of light hydrocarbons. According to this model, 2,4/2,3 dimethylpentane ratio is a pure temperature parameter. Bement, Mango et al. established the functional equation between the two parameters--light hydrocarbon temperature and burial temperature and applied it to the calculation of hydrocarbon-generating temperature, which provided a new choice for the study of oil maturity. In this paper, the Mango＇s parameters for hydrocarbons from the Tazhong area were calculated, the average K1 value is 1.06, which is in good consistency with the Mango＇s proposal that the K1 value is relatively stable. Calculated with the functional formula of hydrocarbon-generating temperature, the hydrocarbon-generating temperatures are with the range of 120-129℃, and the converted vitrinite reflectance （Ro） varies from 0.88% to 0.90%. This is well consistent with the maturity characteristics of neohopanes. The results have verified the reliability of this method. 相似文献
9.
塔北地区普遍存在气顶型凝析气藏和带油环的凝析气藏。与传统烃类热演化理论相矛盾的是:１）天然气的成熟度远高于油环原油或凝析油；２）高－过成熟天然气与同藏的原油间存在明显的物性不匹配。结合地质背景，认为这种矛盾是由后期形成的干气进入已形成的油藏并溶解原油轻烃这一过程所致，凝析气中的轻烃是气－液溶解平衡的产物。地质历史时期凝析气与油环分离或产生凝析油气藏或混入其它油藏的蒸发分馏作用过程导致了轻烃的油藏再分配，形成了塔北地区纵向上原油轻烃的“反序”分布趋势及某些参数的异常分布。认为烃类的气－液相溶解平衡作用是原始原油轻烃分布特征后期演变的主要控制机制之一。其实质是不同性质轻烃气液两相差异性分配基础上的物理化学分异过程。 相似文献
10.
Ercin Maslen Kliti Grice Pierre. Le MétayerDaniel Dawson Dianne Edwards 《Organic Geochemistry》2011,42(4):387-398
The present study aims to establish the factors controlling the stable carbon isotopic compositions (δ13C) of individual aromatic hydrocarbons analysed by compound specific isotope analysis (CSIA) in crude oils from western Australian petroleum basins of varying age and facies type. This paper reports δ13C values of individual aromatic hydrocarbons, like alkylbenzenes, alkylnaphthalenes, alkylphenanthrenes and methylated biphenyls. The main aims are to confirm the origin (source) and age of these oils based on CSIA of selected aromatic compounds and to understand why the Sofer plot is ineffective in establishing the source of western Australian petroleum systems. The bulk δ13C of saturated and aromatic hydrocarbon fractions of crude oils have been previously used to differentiate sources, however, many Australian crude oils are not classified correctly using this method. The oils were classified as marine by the δ13C values of individual aromatic compounds and as terrigenous based on the bulk δ13C data (Sofer plot).The oils where the δ13C values of 1,6-DMN and 1,2,5-TMN isomers are most negative are indicative of a marine source, whereas oils with a less negative values for the 1,6-DMN and 1,2,5-TMN isomers are derived from marine source rocks that contain a significant terrigenous component. Similarly, oils with the least negative δ13C values for the 1-MP and 1,9-DMP isomers reflect varying inputs of terrigenous organic matter to the their marine source rocks. Plots of P/DBT and Pr/Ph concentration ratios versus δ13C values of DMP, 1,6-DMN, 1,2,5-TMN, 1-MP and 1,9-MP are constructed to establish the relative amount of terrigenous organic matter contributing to the source rock of a series of marine oils. The ratios of P/DBT and Pr/Ph plotted against the δ13C values of the aromatic isomers (such as 1,6-DMN, 1,2,5-TMN, 1-MP and 1,9-MP) provide a novel and convenient way to discriminate crude oils derived from different source rocks that contain varying amounts of marine and terrigenous organic matter. 相似文献
11.
Based on the chromatograms of oils and saturated hydrocarbons, biomarkers and stable carbon isotope analyses, the geochemical characteristics and oil family Classification of crude oils from the Markit Slope in the southwest of the Tarim Basin were investigated. The results showed that crude oils from the Markit Slope are divided into two oil family Classification. Oils collected from the Bashituo oilfield in the western part of the Markit Slope are characterized by high contents of tricyclic terpanes, pregnane, and homopregnane, low contents of garmmacerane (G/H<0.20), dibenzofuran, and methyl cyclohexane, and light stable carbon isotopic values (the δ13C values of satu-rated hydrocarbons and aromatic components are less than -34‰ and -32‰, respectively), with the distribution type of steranes being C27>>C28 -32‰ and -30.6‰, respectively), with the distribution type of steranes being C27>C28<相似文献
12.
塔里木盆地大宛齐油田的部分原油经受了不同程度的微生物降解作用,通过对该油田原油中轻烃分布特征的研究,
能更深入地认识微生物降解作用对轻烃的影响。结果表明,微生物优先消耗正构烷烃,其次为异构烷烃和环烷烃;从而导致
C6、C7轻烃三角图发生相应变化。在大宛齐原油中,随微生物降解程度的增加,正庚烷值和异庚烷值逐渐减小;当庚烷值
为0~21,异庚烷值为0~2.6时,为“微生物降解”原油。微生物降解作用亦能使苯/正己烷、甲苯/正庚烷两个比值增大,而
使正庚烷/甲基环己烷比值减小;基于甲苯/正庚烷、正庚烷/甲基环己烷两个比值建立的判别次生蚀变作用的模板,当原油
处于轻微微生物降解作用时,该模板易与蒸发分馏趋势混淆,需谨慎使用。 相似文献
13.
PAUL Philp 《中国地球化学学报》2012,31(3):264-275
Based on the systematic analyses of fifteen typical crude oils and ten typical potential source rocks col-lected from the Qaidam,Tarim and Turpan basins,Northwest China,the geochemical characteristics of the oils and source rocks were investigated and oil-source rock correlations undertaken.The oils and source rocks deposited in saline lacustrine environment from the western Qaidam Basin were characterized by n-alkanes with even car-bon-number preference in the C20-C28 range,low pristane/phytane(Pr/Ph) ratios(less than 0.5),and high abundances of C27 steranes,gammacerane and C35 hopanes.The oils and source rocks deposited in marine environment from the Tarim Basin were characterized by n-alkanes with even carbon-number preference in the C14-C18 range,relatively low Pr/Ph ratios(near to 1),high abundance of C28 steranes,and relatively high gammacerane.In contrast,the oils and source rocks deposited in terrigenous bog environment from the Turpan Basin were characterized by relatively high Pr/Ph ratios(oil samples greater than 6) high abundance of C29 steranes,and relatively low gammacerane and C31-35 hopanes.The higher amounts of C37 and C38 n-alkanes of source rocks from the western Qaidam Basin and the Tarim Basin suggest an origin of these alkanes from functionalized C37 and C38 n-alkadienes and alkenones in prymnesiophytes living in lacustrine and marine environments.Oil-source rock correlations suggest oils in the west-ern Qaidam Basin were derived from the Oligocene Lower Ganchaigou Formation(E3),oils in the Tabei and Tazhong uplifts from the Tarim Basin have a genetic relationship with the Middle-Upper Ordovician source beds.Oils in the Turpan Basin generally fall into two genetic types.Most oils in the Taibei depression from the Turpan Basin were derived from the Lower-Middle Jurassic coal measures,but the fewer oils in this region are a mixed source derived from the Lower-Middle Jurassic coal measure and the Upper Permian source rocks. 相似文献
14.
塔北隆起雅克拉油气田原油成因特征 总被引：1，自引：0，他引：1
针对雅克拉油气田多个含油气层位的原油,进行了一系列的地球化学测试分析,对雅克拉油气田原油的地球化学特征、成因特征进行了解剖。研究结果表明,雅克拉油气田深浅不同层位原油轻烃组成与轻烃单体烃碳同位素、类异戊二烯烷烃组成以及原油与馏分碳同位素组成具有明显的海相原油特征;深浅层原油三环萜烷、C28甾烷、三芳甾烷和甲基三芳甾烷以及原油与馏分碳同位素组成皆具有典型上奥陶统来源油的特征,与寒武-下奥陶统来源油特征差异明显,暗示雅克拉油气田原油来源于上奥陶统烃源层。 相似文献
15.
对Mango的轻烃稳态成因理论进行了综述：基于大量实际分析资料,Mango发现轻烃的形成受一种化学过程控制,且有4个C,异构化合物的相对组成有显著的不变性,即轻烃稳态成因模式;基于该模式,Mango建立了轻烃参数与生油层最大埋深温度的关系,同时发现参数K1、1（2的不同来源于有机质类型不同。在该理论基础上,通过对苏北盆地湖相油和海相油气轻烃的分析,探讨了轻烃参数K1、K2在确定油气母质类型方面的应用,同时依据轻烃参数2,4．／2,3-DMP与最大埋深温度关系式计算了苏北湖相油与海相油气的生成温度,结果显示湖相油生成温度与甾烷C2920S／（S＋R）参数有较好的相关性,处于成熟阶段;海相油气生成温度显著高于湖相油,处于成熟晚期阶段。 相似文献
16.
塔里木盆地一类新海相原油的地球化学特征 总被引：1，自引：0，他引：1
对塔中52等井奥陶系储层产出的原油进行的分析结果表明,它们的三环萜烷系列较为特殊,主要表现为其相对丰度呈C19>C20>C21>C23>C24>C25>C26阶梯状的模式,C24四环萜烷异常丰富,且其丰度远高于C26三环萜烷,这一分布模式一般出现在淡水沼泽相和浅湖相沉积地层与原油中。在三萜烷分布特征上,其伽马蜡烷含量很低,甾烷系列和藿烷系列的分布与组成特征与该地区来源于中上奥陶统烃源岩的海相原油十分接近,同时它们的全油均具有轻的碳同位素组成,其δ13Ｃ值都小于-30‰,具有海相成因原油的特征。而塔中12井上奥陶统良里塔格组4-5段烃源岩中生物标志物的分析结果进一步证实了该类原油与那些富含宏观藻残片,且有机质类型偏腐殖型的上奥陶统海相烃源岩关系密切,是该地区油气勘探中值得关注的对象。 相似文献
17.
The Variance of Mango‘s Light—Hydrocarbon Parameter K 总被引：1，自引：0，他引：1
The analyses of light hydrocarbons in oils from the Tarim Basin show that the Mango‘s parameter K is about unity except those oils trapped in the eastern part of the Tazhong (Central Tarim)Fault Uplift,The regular variance of K may indicates the accumulation and admixture of the oil populations in the eastern part of the Tazhong Fault Uplift. 相似文献
18.
石油碳、氢同位素组成的研究 总被引：12，自引：1，他引：11
通过对我国18个含油气区、385个石油样品进行碳、氢同位素和部分馏份碳同位素分析,将所获数据对两种不同性质的石油如正常原油和轻质（凝析）油分别研究其碳、氢同位素地球化学特征,提出轻质（凝析）油的碳同位素值（δ13C为-32.5‰～ -24.3‰）比正常原油δ13C为-34.4‰～ -24.6 ‰．6‰）相对偏高;石油馏份中芳烃碳同位素组成的变化受母质继承效应更为明显。因此,用芳烃碳同位值可以判识不同母质来源的石油。与海相有关的轻质（凝析）油的氢同位素值大于-15.0‰,而非海相轻质（凝析）油的δD值( δD为-21.0‰～-1.05‰）基本覆盖了海相轻质油的分布范围,从淡水－微咸水－半咸水和海水环境其氢同位素有明显变重趋势,表明氢同位素主要与沉积环境密切相关。 相似文献
19.
20.
油层不同开采时期原油组分变化特征 总被引：1，自引：0，他引：1
运用有机地球化学分离、分析技术对取自塔里木盆地的东河、塔中和轮南油田不同时期开采出的原油样品进行剖析,研究其宏观组成和微观分子在时空上的变化规律。分析结果表明,原油饱 /芳比值随开采时间的推移呈下降的趋势;饱和烃与非烃 +沥青质的含量变化有很好的相关性。随着开采时间的增长,原油中正构烷烃的主峰碳数后移,原油的轻 /重组分比降低。原油碱性氮、有机酸等非烃类化合物随开采时间的推移也呈降低的趋势。这些变化与原油在驱替过程中的自然色层吸附作用机理和原油中各种组分的相互作用关系有关。该项研究对于深入探索驱油机理、预测原油润湿性和提高采收率具有重要的实际意义。 相似文献