In situ Raman spectroscopic quantification of CH4–CO2 mixture: application to fluid inclusions hosted in quartz veins from the Longmaxi Formation shales in Sichuan Basin, southwestern China

We re-evaluate the Raman spectroscopic quantification of the molar ratio and pressure for CH4–CO2 mixtures.Firstly,the Raman quantification factors of CH4 and CO2 increase with rising pressure at room temperature,indicating that Raman quantification of CH4/CO2 molar ratio can be applied to those fluid inclusions(FIs)with high internal pressure(i.e.,>15 MPa).Secondly,the v1(CH4)peak position shifts to lower wavenumber with increasing pressure at constant temperature,confirming that the v1(CH4)peak position can be used to calculate the fluid pressure.However,this method should be carefully calibrated before applying to FI analyses because large discrepancies exist among the reported v1(CH4)-P curves,especially in the highpressure range.These calibrations are applied to CH4-rich FIs in quartz veins of the Silurian Longmaxi black shales in southern Sichuan Basin.The vapor phases of these FIs are mainly composed of CH4 and minor CO2,with CO2 molar fractions from4.4%to 7.4%.The pressure of single-phase gas FI ranges from 103.65 to 128.35 MPa at room temperature,which is higher than previously reported.Thermodynamic calculations supported the presence of extremely high-pressure CH4-saturated fluid(218.03–256.82 MPa at 200°C),which may be responsible for the expulsion of CH4 to adjacent reservoirs.

Determining Fluid Compositions in the H_2O-NaCl-CaCl_2 System with Cryogenic Raman Spectroscopy:Application to Natural Fluid Inclusions

Previous cryogenic Raman spectroscopic analysis of H_2O-NaCl-CaCl_2 solutions has identified the Raman peaks of various hydrates of NaCl and CaCl_2,and established a linear relationship between Raman band intensity of the hydrates and the composition of the solution（NaCl/（NaCl＋CaCl_2） molar ratio,or X_（NaC1）） using synthetic fluids,which created the opportunity to quantitatively determine the solute composition of aqueous fluid inclusions with cryogenic Raman spectroscopy.This paper aims to test the feasibility of this newly established method with natural fluid inclusions.Twenty-five fluid inclusions in quartz from various occurrences which show a high degree of freezing during the cooling processes were carefully chosen for cryogenic Raman analysis.X_（Na）Cl was calculated using their spectra and an equation established in a previous study.These inclusions were then analyzed with the thermal decrepitation-SEM-EDS method.The X_（NaCl） values estimated from the two methods show a 1：1 correlation,indicating that the new,non-destructive cryogenic Raman spectroscopic analysis method can indeed be used for fluid inclusion compositional study.

CO_2 Density-Raman Shift Relation Derived from Synthetic Inclusions in Fused Silica Capillaries and Applications

The density of CO2 inclusions in minerals is commonly used to determine the crystallizing conditions of the host minerals.However,the conventional microthermometry method is difficult to apply for inclusions that are small in size（【5-10μm） or low in density.Raman analysis is an alternative method for determining CO2 density,provided that

小秦岭地区花岗岩体中CO_2-H_2O包裹体的找矿意义

小秦岭地区与金矿成因有关的燕山期文峪花岗岩及其派生石英脉中发育了非常丰富的ＣＯ２－Ｈ２Ｏ包裹体，其流体为富含ＣＯ２的低盐度（＜１０％ＮａＣｌ）流体，这与含金石英脉内的包裹体类型及金矿成矿流体性质上十分相似。与金矿成因无关的华山岩体内包裹体类型则为水溶液包裹体，流体性质为贫ＣＯ２的低盐度流体。与金矿有关，但其周围矿化很差的娘娘山岩体内ＣＯ２－Ｈ２Ｏ包裹体数量很少。因此，ＣＯ２－Ｈ２Ｏ包裹体可以作为与金矿成因有关的花岗岩体关联程度的判别标志。

Evolution of Diagenetic Fluid of the Dawsonite-Bearing Sandstone in the Jiyang Depression,Eastern China

Based on the petrology,isotope geochemistry and fluid inclusions analysis,we established the evolutionary mode of the diagenetic fluid of dawsonite-bearing sandstone in the Jiyang Depression.Dawsonite-bearing sandstone is characterized by double injection of CO_(2)and oil-gas in the Jiyang Depression that have experienced a relatively complex diagenetic fluid evolution process.The diagenetic sequence of secondary minerals involves secondary enlargement of quartz,kaolinite,first-stage calcite,dawsonite,second-stage calcite,ferrocalcite,dolomite and ankerite.Hydrocarbon charging in the dawsonite-bearing sandstone occurred at around 2.6–0 Myr.The CO_(2)charging event occurred during Dongying tectonism,forming the Pingfangwang CO_(2)gas reservoir,which provided an abundant carbon source for dawsonite precipitation.Carbon and oxygen isotopic compositions of dawsonite demonstrate that CO_(2)forming the dawsonite was of an inorganic origin derived from the mantle,and that water mediating the proc-ess during dawsonite precipitation was sequestered brine with a fluid temperature of 82℃.The evolutionary sequence of the diagenetic fluid in the dawsonite-bearing sandstone was:alkaline syngenetic fluids,weak alkaline fluids during organic acid forma-tion,acidic fluids in the early stage of CO_(2)injection,alkaline fluids in the late stage of CO_(2)injection,and weak alkaline fluids during oil and gas charging.The mode indicates an increase in-HCO_(3)because of the CO_(2)injection,and the loss of Ca^(2+)and Mg^(2+)due to the precipitation of carbonate minerals.Therefore,the evolutionary mode of diagenetic fluids is in good agreement with high HCO_(3)^(-),low Ca^(2+)and low Mg^(2+)composition of the present formation water in the dawsonite-bearing sandstone.

A New Method for Determining Fluid Compositions in the H_2O-NaClCaCl_2 System with Cryogenic Raman Spectroscopy

Raman peaks of various hydrates in the H20-NaCl-CaCl2 system have been previously identified, but a quantitative relationship between the Raman peaks and XNaCl （i.e.,NaCl/ （NaCl＋CaCl2）） has not been established, mainly due to the difficulty to freeze the solutions. This problem was solved by adding alumina powder to the solutions to facilitate nucleation of crystals. Cryogenic （-185℃） Raman spectroscopic studies of alumina-spiced solutions indicate that XNaCl is linearly correlated with the total peak area fraction of hydrohalite. Capsules of solutions made from silica capillary were prepared to simulate fluid inclusions. Most of these artificial fluid inclusions could not be totally frozen even at temperatures as low as -185℃, and the total peak area fraction of hydrohalite is not correlated linearly with XNaCI. However, the degree of deviation （△XNaCl） from the linear correlation established earlier is related to the amount of residual solution, which is reflected by the ratio （r） of the baseline ＂bump＂ area, resulting from the interstitial unfrozen brine near 3435 cm^-1, and the total hydrate peak area between 3350 and 3600 cm^-1. A linear correlation between △XNaCl and r is established to estimate XNaCl from cryogenic Raman spectroscopic analysis for fluid inclusions.

Discovery and Significance of High CH_4 Primary Fluid Inclusions in Reservoir Volcanic Rocks of the Songliao Basin,NE China

Comparing compositions of the fluid inclusions in volcanic rocks to the contents and isotopes of the gases in corresponding volcanic reservoirs using microthermometry, Raman microspectroscopy and mass spectrum analysis, we found that： （1） up to 82 mole% methane exists in the primary inclusions hosted in the reservoir volcanic rocks; （2） high CH4 inclusions recognized in the volcanic rocks correspond to CH4-bcaring CO2 reservoirs that are rich in helium and with a high ^3He/^4He ratio and which show reversed order of 813C in alkane; （3） in gas reservoirs of such abiotic methane （〉80%） and a mix of CH4 and CO2, the enclosed content of CH4 in the volcanic inclusions is usually below 42 mole%, and the reversed order of δ^13C in alkane is sometimes irregular in the corresponding gas pools; （4） a glassy inclusion with a homogeneous temperature over 900℃ also contains a small portion of CH4 although predominantly CO2. This affinity between gas pool and content of inclusion in the same volcanic reservoirs demonstrates that magma-originated gases, both CH4 and CO2, have contributed significantly to the corresponding gas pools and that the assumed hydrocarbon budget of the bulk earth might be much larger than conventionally supposed.

Applications of the SW96 formulation in the thermodynamic calculation of fluid inclusions and mineral-fluid equilibria

The SW96 formulation explicit in Helmholtz free energy proposed by Span and Wagner(1996)is the most accurate multifunction equation of state of CO_2 fluid,from which all thermodynamic properties can be obtained over a wide temperature-pressure range from 216.592 to 1100 K and from 0 to 8000 bar with or close to experimental accuracy.This paper reports the applications of the SW96 formulation in fluid inclusions and mineral-fluid equilibria.A reliable and highly efficient algorithm is presented for the saturated properties of CO_2 so that the formulation can be conveniently applied in the study of fluid inclusions,such as calculation of homogenization pressures,homogenization densities(or molar volumes),volume fractions of vapor phase and isochores.Meanwhile,the univariant curves of some typical decarbonation reactions of minerals are calculated with the SW96 formulation and relevant thermodynamic models of minerals.The computer code of the SW96 formulation can be obtained from the corresponding author.

Experimental Study on Water-rock Reactions with CO2 Fluid in a Deep Sandstone Formation under High Temperature and Pressure

Qiongdongnan Basin has a tectonic geological background of high temperature and high pressure in a deep reservoir setting,with mantle-derived CO2.A water-rock reaction device was used under high temperature and high pressure conditions,in conjunction with scanning electron microscope(SEM)observations,to carry out an experimental study of the diagenetic reaction between sandstone at depth and CO2-rich fluid,which is of great significance for revealing the dissolution of deep clastic rock reservoirs and the developmental mechanism of secondary pores,promoting deep oil and gas exploration.In this study,the experimental scheme of the water-rock reaction system was designed according to the parameters of the diagenetic background of the deep sandstone reservoir in the Qiongdongnan Basin.Three groups of single mineral samples were prepared in this experiment,including K-feldspar samples,albite samples and calcite samples.Using CO2 as a reaction solution,a series of diagenetic reaction simulation experiments were carried out in a semi-closed high temperature and high pressure simulation system.A field emission scanning electron microscope(SEM)was used to observe the microscopic appearance of the mineral samples after the water-rock reaction,the characteristics of dissolution under high temperature and high pressure,as well as the development of secondary pores.The experimental results showed that the CO2-rich fluid has an obvious dissolution effect on K-feldspar,albite and calcite under high temperature and high pressure.For the three minerals,the main temperature and pressure window for dissolution ranged from 150℃to 300℃and 45 MPa to 60 MPa.Scanning electron microscope observations revealed that the dissolution effect of K-feldspar is most obvious under conditions of 150℃and 45 MPa,in contrast to conditions of200℃and 50 MPa for albite and calcite.Through the comparative analysis of experimental conditions and procedures,a coupling effect occurred between the temperature and pressure change and the dissolution strength and calcite.Under high temperature and high pressure,pressure changed the solubility of CO2,furthermore,the dissolution effect and strength of the sandstone components were also affected.The experiment revealed that high temperature and high pressure conditions with CO2-rich fluid has a significant dissolution effect on aluminosilicate minerals and is conducive to the formation of secondary pores and effective reservoirs.Going forward with the above understanding has important implications for the promotion of deep oil and gas exploration.

Research on Fluid Inclusions of the Yinshan Polymetallic Deposit, Jiangxi Province, China

In this paper some new advances in the study of fluid inclusions of the Yinshan deposit in Jiangxi Province, China, are presented. The fluid inclusions of the deposit can be divided into four types: 1) gas rich inclusions; 2) liquid rich inclusions; 3) salt saturated H 2O inclusions; and 4) single phase or multiphase CO 2 rich inclusions. Homogenization temperatures of the fluid inclusions range from 100 to 520℃, mainly in the range 120-400℃. The daughter crystal bearing multiphase inclusions present in quartz porphyries (including Nos. 13 and 4 dikes) have been observed. In ore veins, some daughter crystal bearing multiphase inclusions have been observed, too. On the basis of the results of fluid inclusion research, the authors suggest that the ore forming fluid must have a close genetic relation to magmatic hydrothermal solution. The ore forming fluid was dominantly originated from the depth and the mixing of magmatic solution with meteoric water was enhanced during ascending of the fluid, accompanying immiscibility and boiling of fluid. There may be a concealed igneous body at the depth of the Yinshan deposit, which furnishes the scientific basis for metallogenic prognosis at the depth of the Yinshan deposit.

滇西北兰坪铅锌银铜矿田含烃富CO_2成矿流体及其地质意义

在流体包裹体显微冷热台系统观测基础上,通过显微激光拉曼探针揭示出兰坪中—新生代盆地内金顶及外围矿床成矿主阶段原生流体包裹体含烃富CO_2,成分变化大。流体成分的耦合关系研究,并配合O、C同位素分析认为成矿流体中部分CO_2来自地幔,部分是沉积地层中碳酸盐岩和有机质分解成因,H_2O和烃主要起源于大气成因盆地卤水和地层有机质。地幔源CO_2对贱金属元素的搬运可能贡献突出,而烃类对金属元素的沉淀意义重大。成矿流体成分具有幔源(富CO_2和金属元素)和壳源(盆地流体富烃类和H_2O)两种流体混合的特征,暗示不同性质流体的混合可能是成矿作用基本方式。

用均匀设计CO_2超临界混合萃取当归、川芎、香附中挥发性成分及提取物β-CD包合的研究

目的 考察超临界流体CO2 萃取当归、川芎和香附中挥发性成分及所得混合挥发油的 β 环糊精包合物的制备工艺。方法 均匀设计方法 ,正交实验法。结果 萃取条件是 :萃取压力 30Pa ,萃取温度 6 0℃ ,解析温度Ⅰ 6 0℃ ,解析温度Π30℃ ,萃取时间 4 .0h。β CD包合物的制备最佳工艺条件是 :水 ,油与 β CD之比为 1∶10 (mL) ,研磨法 ,时间 6 0min。结论 确定了CO2 超临界混合萃取方法及挥发油的 β

高密度流体He+H_2混合物物态方程研究

选择高密度流体He +H2 混合物作为研究对象 ,用Ree混合规则和vanderWaals单组分流体变分微扰理论加量子力学一级修正模型编制计算程序。作为对计算模型及其程序的检验 ,首先用已有的α exp 6优化势参数 ,计算了T =30 0K的He +H2 混合物的等温相平衡线 ,得到了与实验值和分子动力学 (MD)数值模拟一致的结果 ,然后进一步计算了 0～ 60GPa和 5 0～ 70 0 0K压力温度范围内的流体He+H2 混合物 (He∶H2 分别为 1∶1、1∶3、3∶1摩尔比 )的高压物态方程。与Monte Carlo模拟数据所进行的比较表明 ,在低温下 。

High-precision analysis of carbon isotopic composition for individual CO_(2)inclusions via Raman spectroscopy to reveal the multiple-stages evolution of CO_(2)-bearing fluids and melts

The carbon isotopic composition of CO_(2)inclusions trapped in minerals reflects the origin and evolution of CO_(2)-bearing fluids and melts,and records the multiple-stages carbon geodynamic cycle,as CO_(2)took part in various geological processes widely.However,the practical method for determination isotope composition of individual CO_(2)inclusion is still lacking.Developing a microanalytical technique with spatial resolution in micrometers to precisely determinate theδ^(13)C value of individual CO_(2)inclusion,will make it possible to analyze a tiny portion of a zoning mineral crystal,distinguish the differences in micro-scale,and possible to find many useful information that could not be obtained with the bulk extraction and analysis techniques.In this study,we systematically collected Raman spectra of CO_(2)standards with different d13C values(34.9‰to 3.58‰)at 32.0℃and from 7.0 MPa to 120.0 MPa,and developed a new procedure to precisely determinate theδ^(13)C value of individual CO_(2)inclusion.We investigated the relationship among the Raman peak intensity ratio,d13C value,and CO_(2)density,and established a calibration model with high accuracy(0.5‰1.5‰),sufficient for geological application to distinguish different source of CO_(2)with varyingδ^(13)CO_(2).As a demonstration,we measured theδ^(13)C values and the density of CO_(2)inclusions in the growth zones of alkali basalt-hosted corundum megacrysts from Changle,Shandong Province.We found the significant differences of density and d13C between the CO_(2)inclusions in the core of corundum and those inclusions in the outer growth zones,the d13C value decreases from core to rim with decreasing density:δ^(13)C values are from7.5‰to9.2‰for the inclusions in the core,indicating the corundum core was crystallized from mantle-derived magmas;from13.5‰to18.5‰for CO_(2)inclusions in zone 1 and from16.5‰to–22.0‰for inclusions in zone 2,indicating the outer zones of corundum grew in a lowδ^(13)C value environment,resulted from an infilling of low d13C value fluid and/or degassing of the ascending basaltic magma.

Raman and infrared spectroscopic quantification of the carbonate concentration in K_(2)CO_(3)aqueous solutions with water as an internal standard

Carbonate-bearing fluids widely exist in different geological settings,and play important roles in transporting some elements such as the rare earth elements.They may be trapped as large or small fluid inclusions(with the size down to<1μm sometimes),and record critical physical-chemical signals for the formations of their host minerals.Spectroscopic methods like Raman spectroscopy and infrared spectroscopy have been proposed as effective methods to quantify the carbonate concentrations of these fluid inclusions.Although they have some great technical advantages over the conventional microthermometry method,there are still some technical difficulties to overcome before they can be routinely used to solve relevant geological problems.The typical limitations include their interlaboratory difference and poor performance on micro fluid inclusions.This study prepared standard ion-distilled water and K_(2)CO_(3)aqueous solutions at different molarities(from 0.5 to 5.5 mol/L),measured densities,collected Raman and infrared spectra,and explored correlations between the K_(2)CO_(3)molarity and the spectroscopic features at ambient P-T conditions.The result confirms that the Raman O-H stretching mode can be used as an internal standard to determine the carbonate concentrations despite some significant differences among the correlations,established in different laboratories,between the relative Raman intensity of the C-O symmetric stretching mode and that of the O-H stretching mode.It further reveals that the interlaboratory difference can be readily removed by performing one high-quality calibration experiment,provided that later quantifying analyses are conducted using the same Raman spectrometer with the same analytical conditions.Our infrared absorption data were collected from thin fluid films(thickness less than~2μm)formed by pressing the prepared solutions in a Microcompression Cell with two diamond-II plates.The data show that both the O-H stretching mode and the O-H bending mode can be used as internal standards to determine the carbonate concentrations.Since the IR signals of the C-O antisymmetric stretching vibration of the CO32ion,and the O-H stretching and bending vibrations from our thin films are very strong,their relative IR absorbance intensity,if well calibrated,can be used to investigate the micron-sized carbonate-bearing aqueous fluid inclusions.This study establishes the first calibration of this kind,which may have some applications.Additionally,our spectroscopic data suggest that as the K_(2)CO_(3)concentration increases the aqueous solution forms more large water molecule clusters via more intense hydrogen-bonding.This process may significantly alter the physical and chemical behavior of the fluids.

A Fluid Inclusion Study of Vein-type Copper Mineralization in the East Wulasigou Pb-Zn-Cu Deposit,Altay,Northwestern China

The Wulasigou Cu-Pb-Zn deposit,located 15 km northwest of Altay city in Xinjiang,is one of many Cu-Pb-Zn polymetallic deposits in the Devonian Kelan volcanic-sedimentary basin in southern Altaids.Two mineralizing periods can be distinguished：the marine volcanic sedimentary PbZn mineralization period,and the metamorphic hydrothermal Cu mineralization period,which is further divided into an early bedded foliated quartz vein stage（Q1） and a late sulfide-quartz vein stage（Q2） crosscutting the foliation.Four types of fluid inclusions were recognized in the Q1 and Q2 quartz from the east orebodies of the Wulasigou deposit：H2O-CO2 inclusions,carbonic fluid inclusions,aqueous fluid inclusions,and daughter mineral-bearing fluid inclusions.Microthermometric studies show that solid CO2 melting temperatures（T（m,CO2）） of H2O-CO2 inclusions in Ql are from-62.3℃ to-58.5C,clathrate melting temperatures（T（m,clath）l） are from 0.5 C to 7.5 C,partial homogenization temperatures（T（h,CO2）） vary from 3.3℃ to 25.9℃（to liquid）,and the total homogenization temperatures（T（h,tot）） vary from 285℃ to 378℃,with the salinities being 4.9%-15.1%NaCl eqv.and the CO2-phase densities being 0.50-0.86 g/cm-3.H2O-CO2 inclusions in Q2 have T（m,CO2） from-61.9℃ to-56.9℃,T（m,clath）from 1.3℃ to 9.5℃,T（h,CO2） from 3.4℃ to 28.7℃（to liquid）,and T（h,tot） from 242℃ to 388℃,with the salinities being 1.0%-15.5%NaCl eqv.and the CO2-phase densities being 0.48-0.89 g/cm-3.The minimum trapping pressures of fluid inclusions in Q1 and Q2 are estimated to be 260-360 MPa and180-370 MPa,respectively.The δ-（34）S values of pyrite from the volcanic sedimentary period vary from2.3‰ to 2.8‰（CDT）,and those from the sulfide-quartz veins fall in a narrow range of-1.9‰ to 2.6‰（CDT）.The δD values of fluid inclusions in Q2 range from-121.0‰ to-100.8‰（SMOW）,and theδ-（18）O（H2O） values calculated from δ-（18）O of quartz range from-0.2‰ to 8.3‰（SMOW）.The δD-δ-（18）O（H2O）data are close to the magmatic and metamorphic fields.The fluid inclusion and stable isotope data documented in this study indicate that the vein-type copper mineralization in the Wulasigou Pb-Zn-Cu deposit took place in an orogenic-metamorphic enviroment.

Raman Micro-Spectroscopic Study of Sulfate Ion in the System Na_2SO_4-H_2O

This work aims to quantify sulfate ion concentrations in the system Na_2SO_4-H_2O using Raman micro-spectroscopy.Raman spectra of sodium sulfate solutions with known concentrations were collected at ambient temperature（293 K） and in the 500 cm^（_1）-4000 cm^（-1） spectral region.The results indicate that the intensity of the SO_4^（2-） band increases with increasing concentrations of sulfate ion.A linear correlation was found between the concentration of SO_4^（2-）（c） and parameter I_1,which represents the ratio of the area of the SO_4^（2-） band to that of the O-H stretching band of water（A_s/A_w）：I_1=-0.00102＋0.01538 c.Furthermore,we deconvoluted the O-H stretching band of water（2800 cm^（-1）-3800 cm^（-1）） at 3232 and 3430 cm^（-1） into two sub-Gaussian bands,and then defined Raman intensity of the two sub-bands as A_（Bi）（3232 cm^（-1）） and A_（B2）（3430 cm^（-1））,defined the full width of half maximum（FWHM） of the two sub-bands as W_（B1）（3232 cm^（-1）） and W_（B2）（3430 cm^（-1））.A linear correlation between the concentration of SO_4^（2-）（c） and parameter I_2,which represents the ratio of Raman intensity of SO_4^（2-）（A_s）（in 981 cm^（-1）） to（A_（B1）＋A_（B2））,was also established：I_2=-0.0111＋0.3653 c.However,no correlations were found between concentration of SO_4^（2-）（c） and FWHM ratios,which includes the ratio of FWHM of SO_4^（2-）（W_s） to W_（B1） W_（B2） and W_（B1＋B2）（the sum of W_（B1） and W_（B2））,suggesting that FWHM is not suitable for quantitative studies of sulfate solutions with Raman spectroscopy.A comparison of Raman spectroscopic studies of mixed Na_2SO_4 and NaCI solutions with a constant SO_4^（2-） concentration and variable CI^- concentrations suggest that the I／ parameter is affected by CI^-,whereas the I_2 parameter was not.Therefore,even if the solution is not purely Na_2SO_4-H_2O,SO_4^（2-） concentrations can still be calculated from the Raman spectra if the H_2O band is deconvoluted into two sub-bands,making this method potentially applicable to analysis of natural fluid inclusions.

库车克拉2气田多期油气充注的古流体证据

对库车前陆盆地克拉2气田储集层进行流体包裹体分析、荧光光谱分析、场发射扫描电镜观察、岩心显微CT扫描及油气地球化学分析,从古流体证据的角度综合研究克拉2气田多阶段油气充注过程。克拉2气田经历了中新世早中期(N1)原油充注、上新世库车组沉积期(N2)高成熟油气充注与破坏、第四系(Q1以来)高—过成熟煤成气充注的3期成藏过程。储集层中广泛分布的残余干沥青、较发育的气液两相烃包裹体、纳米孔中的残余油、现今气层和水层中较高的颗粒(抽提物)荧光指数、储集层岩石较大的热解值等均是早期原油充注的证据;残余干沥青、含沥青的3相烃包裹体、凝析油轻质正构烷烃大量损失、石蜡质和芳烃等重组分含量相对较高、金刚烷含量异常高等均是早期原油遭受气洗发生脱沥青作用的有力证据。

库车坳陷克拉2气田异常流体压力演化史

根据克拉2气田现今实测地层压力分析了异常高压发育的特征,并通过流体包裹体测试求取包裹体形成时期的古压力。计算结果表明:下白垩统和古近系库姆格列木群砂岩储层在距今8～6Ma(康村组沉积期末)时,古压力系数大致为1.09～1.18,发育过剩压力为4.6～9.6MPa的异常高压。在此基础上,以古、今压力数据为约束条件,利用数值模拟技术定量恢复出下白垩统与侏罗系异常流体压力的演化历史。研究发现:下白垩统储层流体压力经历了沉积型异常流体压力形成发展(白垩纪-库车组沉积期末)和沉积型异常流体压力萎缩—构造挤压型异常流体压力孕育(库车组沉积期末至今)两个阶段。康村组沉积早期沉积型超压开始出现,库车组沉积期末达到顶峰,过剩压力达40～50MPa;此后,在沉积型超压萎缩—构造挤压型超压孕育过程的耦合下,过剩压力曾降至25～30MPa,更新世起超压略有升高。侏罗系流体压力演化较为简单,吉迪克组沉积期开始出现超压,至库车组沉积期末达到高峰,此后异常高压逐渐萎缩。在克拉2气田的主要成藏时期(距今3～1Ma),烃源岩较储层具有更高的异常压力,源—储压力差为10～30MPa。

鄂尔多斯盆地下寺湾地区长2段储层流体包裹体特征及油气成藏

长2油层组为鄂尔多斯盆地下寺湾地区主要的含油气层段之一,为确定长2油层组油气的成藏时期,采用流体包裹体测试技术和分析方法,利用包裹体的均一温度,对该地区长2油层组储层流体包裹体样品进行了系统研究.通过对流体包裹体特征的分析,应用流体包裹体均一温度的资料,结合相应沉积埋藏史、热史和生烃史,探讨了下寺湾地区油气的运聚成藏历史.下寺湾地区长2油层组砂岩储层中发育三类流体包裹体:盐水包裹体、含液态烃包裹体和液态烃包裹体.与烃类包裹体共生的盐水包裹体均一温度具有明显的单峰特征,主要分布在105～115℃.根据埋藏史和热演化史分析结果,最终确定鄂尔多斯盆地下寺湾地区长2油层组油藏为一期成藏,其成藏时间距今110～125 Ma,为早白垩世晚期.