首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 31 毫秒
1.
The mechanisms for storage of CO2 in rock formations include structural/stratigraphic, mineral, solubility and residual trapping. Residual trapping is very important in terms of both containment security and storage capacity. However, to date, the contribution from residual trapping (i.e. immobilisation of supercritical fluid via capillarity in pore spaces) is still relatively difficult to quantify accurately. Using a laboratory-based testing program, this study demonstrates the feasibility of using reactive ester tracers (i.e. triacetin, propylene glycol diacetate and tripropionin), which partition between a mobile water phase and a stationary supercritical CO2 phase, to quantify the residual CO2 saturation, Sgr, of a rock formation. The proposed single-well test involves injecting these tracers into the subsurface, followed by CO2 saturated water, where the ester tracers slowly hydrolyse to form products with differing partition coefficients. After a suitable period of time, allowing for partial hydrolysis, water containing the tracer mixture is produced from the subsurface and analysed using gas chromatography mass spectrometry (GCMS). A numerical simulator of the tracer behaviour in a reservoir is used to explain the differential breakthrough of these tracer compounds during water production to estimate Sgr. Computer modelling suggests that the use of esters tracers to determine CO2 residual saturation is a potentially robust method. The supercritical CO2/water partition coefficients directly dictate the amount of time that each tracer spends in the CO2 and water phases. As such for modelling of tracer behaviour and estimating Sgr, knowing the tracer partition coefficient is essential; in this paper, the first laboratory study to determine the partition coefficients of these reactive ester tracers is described.  相似文献   

2.
李木子  万力 《地学前缘》2016,23(5):301-309
多孔介质中重非水相液体(Dense Non Aqueous Phase Liquid,DNAPL)与水相的界面面积是影响DNAPL在地下水中溶解速率的关键参数。本文通过二维均质砂箱实验,运用界面分配示踪法和体积分配示踪法分别测定DNAPL与水相的界面面积(单位介质体积内的面积,Anw)和DNAPL饱和度(Sn),并研究两者之间的相关关系。使用C18H29NaO3S(SDBS)作为界面分配示踪剂,Alcohol(2,4 Dimethyl 3 Pentanol)作为体积分配示踪剂,CaBr2作为保守示踪剂。利用Fe2+催化的Na2S2O8对DNAPL进行原位氧化修复,改变Anw和Sn。结果表明,通过定量(用孔隙体积数PV值衡量)加入Na2S2O8,Anw由206 cm2逐渐降为37 cm2,下降速率约为14 cm2/PV;Sn由1.34%逐渐降为0.33%,下降速率约为0.1%/PV;Anw和Sn之间具有良好的线性关系(Anw=146×Sn,R2=0.987)。此关系可用于估算多孔介质中DNAPL与水相之间的界面面积。对实验影响因素的分析表明,孔隙度的增大(变化率为20.7%)使示踪剂穿透曲线出现肩现象和拖尾现象,导致保守示踪剂的保留时间增加5.6%,界面面积减小6.8%。  相似文献   

3.
Pollution source characterization by the Partitioning Interwell Tracer Test method requires the assessment of the partitioning coefficient of the tracers with the pollutant. Experiments conducted on batch tests (static) and laboratory columns (dynamic) indicated a partitioning kinetics between the reactive tracer (4-methyl 2-pentanol) and the organic phase (trichlorethene); the partitioning coefficient decreases when the flow velocity through the porous medium increases. This partitioning kinetics has been confirmed by the interpretation of the tracer breakthrough curves with a first-order kinetic transfer model. To cite this article: M. Bohy et al., C. R. Geoscience 336 (2004).  相似文献   

4.
The effective site assessment is crucial to the successful remediation of the subsurface contaminated with light nonaqueous phase liquids (LNAPLs). Recent studies showed that large spatial volumes of the subsurface contaminated with LNAPLs could be investigated with the partitioning tracer method. This study investigated the applicability of the partitioning tracer method for detecting and quantifying refined petroleum products in a saturated aquifer containing alluvial soil or weathered granite soil. In the batch-partitioning experiments, the partition coefficients of alcohol tracers between the petroleum mixture and water were measured, and they were found to be increased in proportion to the boiling points of the alcohol tracers when the molecular weights of the alcohol tracers were similar. The sorption isotherm experiments indicated that a considerable amount of 4-methyl-2-pentanol was sorbed into Jumunjin sand (JS) or weathered granite soil (WGS). In the column experiments, it was confirmed that the partitioning tracer method could be used as a method for detecting the presence of the petroleum mixture in saturated soil, and the residual saturation of the petroleum mixture in the soil column prepared by firstly contaminating with the petroleum mixture and secondly saturating with water was measured higher than that in the soil column prepared by firstly saturating and secondly contaminating. The highest accuracy of estimation using the partitioning tracer method was found for 2-ethyl-1-butanol and the lowest accuracy was found for 4-methyl-2-pentanol.  相似文献   

5.
Perfluorocarbon compounds (PFCs) have high chemical and thermal stability, low background levels in natural systems, and easy detectability. They are proposed as tracers for monitoring potential CO2 leakage associated with geological carbon sequestration (GCS). The fate of the PFCs in porous media, and in particular, the transport of these compounds relative to CO2 gas in geological formations, has not been thoroughly studied. We conducted column tests to study the transport of perfluoro-methylcyclo-pentane (PMCP), perfluoro-methylcyclo-hexane (PMCH), ortho-perfluoro-dimethylcyclo-hexane (ortho-PDCH), and perfluoro-trimethylcyclo-hexane (PTCH) gas tracers in a variety of porous media. The influence of water content and sediment minerals on the retardation of the tracers was tested. The transport of PFC tracers relative to 13CO2 and the conservative tracer sulfur hexafluoride (SF6) was also investigated. Results show that at high water content, the PFCs and SF6 transported together. In dry and low-water-content sediments, however, the PFCs were retarded relative to SF6 with the degree of retardation increasing with the molecular weight of the PFC. When water was present in the medium, the transport of CO2 was greatly retarded compared to SF6 and the PFC tracers. However, in dry laboratory sediments, the migration of CO2 was slightly faster than all the tracers. The type of minerals in the sediments also had a significant impact on the fate of the tracers. In order to use the PFC tracer data obtained from the ground surface or shallow subsurface in a GCS site to precisely interpret the extent and magnitude of CO2 leakage, the retardation of the tracers and the interaction of CO2 with the reservoir overlying formation water should be carefully quantified.  相似文献   

6.
This study investigates the influence of two factors—geological heterogeneity and variability in water infiltration—on non-aqueous phase liquid (NAPL) migration in the unsaturated zone. NAPL migration under three-phase flow conditions resulting from a ground surface spill is modeled for multiple heterogeneous realizations of a porous medium with various water infiltration scenarios. Increased water infiltration before the spill has two counteracting effects: NAPL relative permeability (k rn) increases with increasing water saturation (S w) for a given NAPL saturation, while higher S w in the soil near the NAPL source zone leads to less NAPL mass infiltration. It is found that the former effect is overwhelmed by the latter effect, the net effect being that with longer infiltration durations before the spill, both the infiltrated NAPL mass and the depth of the front migration decrease. Simulation results also show strong effect of the medium heterogeneity. Results suggest that total infiltrated mass, front depth and plume spread increase with an increasing standard deviation of log-permeability. Also variability in modeling results among realizations is largely impacted by the log-permeability standard deviation. Spatial correlation in permeability also strongly influences NAPL infiltration. An increase in the isotropic correlation length from 0.75 to 1.5 m leads to a decrease in total infiltrated mass, plume migration depth as well as vertical spread. Lateral spread in this case is not shown to be affected by the correlation length.  相似文献   

7.
The partitioning behavior of cerium, europium, gadolinium and ytterbium between an aqueous “vapor” phase and water saturated silicate melt have been experimentally examined using a new experimental approach employing radioactive tracers and a double-capsule technique. Equilibrium was established by reversing the partition coefficient1 and by betatrack autoradiography. Aqueous solution compositions were varied by adding different amounts of chloride and in some cases fluoride or carbon dioxide. The H2O contents of the Spruce Pine pegmatite melts were varied by conducting experiments at 4.0 kb, 800°C and at 1.25 kb, 800°C. A jadeite-nepheline composition (75 wt% Jadeite) also was employed at 4.0 kb, 800°C.The chloride experiments (Spruce Pine 4 kb, 800°C) show a linear relationship between the cube of the chloride molality and the partition coefficients of the trivalent rare earths. Europium, under the experimental fO2 conditions (quartz-fayalite-magnetite buffer), varied linearly as the fifth power of the chloride molality. At the chloride molalities examined (<1.1 mC1), all the rare earths partitioned preferentially into the melt phase (KPRE <1). Relative to pure water, the presence of chloride and fluoride fon increased the partitioning of the individual rare earths into the vapor phase, while carbon dioxide did not. Europium anomalies were recorded 1n all experiments, particularly those involving the Spruce P1ne melt at 4.0 kb and 800°C which displayed a large positive europium anomaly at all chloride molalities. Furthermore, a relative fractionation of the trivalent rare earths was also observed in these experiments, such that KPCe>KPGd>KPYb. The smaller ytterbium ion was consistently concentrated in the melt phase relative to the other rare earths in all experiments on the Spruce Pine composition. Experiments on the jadeite-nepheline composition showed no relative fractionation and a positive europium anomaly. The 1.25 kb experiment on the Spruce Pine composition showed a negative europium anomaly in plots of KpRE vs. REE.The overall rare earth partitioning at a constant chloride molality (mCl = .914) was such that KPSP(1.25 kb) > KPSP(4.0 kb) > KPJd-Ne(4.0 kb), where SP = Spruce Pine, Jd-Ne = jadeitenepheli Using the model of Burnnam (1975), It is suggested that the trivalent rare earth partitioning is related to the cube of the melt octahedral site concentration; a property which 1n hydrous melts 1s dependent on melt composition and hydroxyl molality. Excellent agreement was found for the Spruce Pine melt, whereas the jadeite-nepheline melt gave apparent hydroxyl molalities which were too high for the measured partition coefficient. Additional octahedral sites are proposed for this unusual composition perhaps due to some aluminum in 6-fold coordination. The apparent compositional variation of europium partitioning at a constant oxygen fugacity is believed to be related to both the octahedral melt site concentration for trlvalent europium and an 8-coordinated site concentration for divalent europium. Any parameter which affects the numbers of these sites (PH2O, melt composition) will affect the rare earth partitioning. The observed dependency of the partition coefficient on the structural state of the melt could be as significant as its dependency on crystalline structural constraints. Furthermore, since PH2O can drastically effect the melt structural state, its effects could be reflected in melt/crystal partition coefficients.  相似文献   

8.
Chemical tracers have been used in various C capture and storage (CCS) projects worldwide primarily to provide information regarding subsurface migration of CO2 and to verify CO2 containment. Understanding the movement and interactions of CO2 in the subsurface is a challenging task considering the variety of states in which it exists (i.e. gas, liquid, supercritical, dissolved in water) and the range of possible storage mechanisms (i.e. residual or capillary trapping, dissolved in water, structural trapping or incorporation into minerals). This paper critically reviews several chemical tracer applications and case studies for CCS projects. In many instances, there are parallels (e.g. tracer classes and applications) between tracers in the oil and gas industry and in CCS. It has been shown that chemical tracers can complement geophysical measurements (e.g. seismic) in understanding the formation behaviour of CO2. Although tracers have been successfully used in many CCS projects, some fundamental information, for example partitioning and adsorption, about the behaviour of tracers is still lacking and this can be an issue when interpreting tracer data (e.g. determining leakage rates). In this paper the deployment and recovery of chemical tracers and their use on various CCS projects are described.  相似文献   

9.
对于重非水相污染场地,传统的钻孔取样方式因经费和取样个数的限制,往往无法准确估计含水层中重非水相污染物的残留量。井间分溶示踪法费用较低,且不会对污染源区造成破坏,可适用于推估重非水相污染物残留量,但目前该方法的准确性尚未得到验证。本文基于数值模拟方法探讨了示踪剂注入速率、示踪剂类型以及污染源区结构等多因素对井间分溶示踪估计重非水相污染物残留量准确性的影响。数值算例结果表明:井间分溶示踪实验估计重非水相污染物残留量的误差小于15%;降低示踪剂的注入速率使得分溶性示踪剂在非水相和水相流体间作用更充分,能够提高井间分溶示踪估计重非水相污染物残留量的精度,实验中示踪剂注入速率由500 m3/d降为250 m3/d后,多种情景的平均精度由91.68%提高至93%;选取低分溶系数的示踪剂有利于提高示踪剂的回收率,从而提高推估精度,实验中示踪剂由2,2-二甲基-3-戊醇改为己醇后,平均精度由87.83%提高至96.85%;复杂的重非水相液体污染源区结构易于出现示踪剂绕流等现象,导致井间分溶示踪估计重非水相污染物残留量的误差增大,实验中含水层由均质变为非均质后,平均精度由93.03%变为91.65%。重非水相污染场地调查时,建议结合数值模拟方法选择适宜的示踪剂和示踪剂注入速率,以提高污染场地的刻画精度。  相似文献   

10.
The single-well injection-withdrawal (SWIW) tracer test is a method used to estimate the tracer retardation properties of a fracture or fracture zone. The effects of single-fracture aperture heterogeneity on SWIW-test tracer breakthrough curves are examined by numerical modelling. The effects of the matrix diffusion and sorption are accounted for by using a particle tracking method through the addition of a time delay added to the advective transport time. For a given diffusion and sorption property (P m) value and for a heterogeneous fracture, the peak concentration is larger compared to a homogeneous fracture. The cumulative breakthrough curve for a heterogeneous fracture is similar to that for a homogeneous fracture and a less sorptive/diffusive tracer. It is demonstrated that the fracture area that meets the flowing water, the specific flow-wetted surface (sFWS) of the fracture, can be determined by matching the observed breakthrough curve for a heterogeneous fracture to that for a homogeneous fracture with an equivalent property parameter. SWIW tests are also simulated with a regional pressure gradient present. The results point to the possibility of distinguishing the effect of the regional pressure gradient from that of diffusion through the use of multiple tracers with different P m values.  相似文献   

11.
 Incorporation of hydrocarbons (CH4, C2H6, C3H8, C4H10) in cordierite channels was experimentally studied at 700 °C and at pressures from 200 to 1000 MPa, (avoiding recrystallization). The maximum concentrations of hydrocarbons determined by gas chromatographic analysis are CH4=78.3, C2H6=134, C2H4 + C2H6=26, C3H8=28, C4H10=32, C5H12=23, and C6H14=7 × 10−3 wt%). According to IR spectroscopy data, the channel forms of hydrocarbons differ from the forms on the surface. As a result of interactions with the framework oxygen, normal hydrocarbons are converted to saturated oligomers and their fragments. Small amounts of water molecules of the first and second types (up to 0.3 wt%) are formed in the same way. As pressure grows from 200 to 1000 MPa, the total content of structural hydrocarbons is nearly doubled. Special runs on cordierite saturation in mixtures of hydrocarbons with water showed that low contents of hydrocarbons in natural cordierites correspond to their large concentrations in fluid. Received: 7 May 2001 / Accepted: 17 July 2001  相似文献   

12.
Rb and Sr partitioning between haplogranitic melts and aqueous solutions   总被引：2，自引：0，他引：2  
Rubidium and strontium partitioning experiments between haplogranitic melts and aqueous fluids (water or 1.16-3.56 m (NaCl + KCl) ± HCl) were conducted at 750-950 °C and 0.2-1.4 GPa to investigate the effects of melt and fluid composition, pressure, and temperature. In addition, we studied if the applied technique (rapid and slow quench, and in-situ determination of trace element concentration in the fluid) has a bearing on the obtained data. There is good agreement of the data from different techniques for chloridic solutions, whereas back reactions between fluid and melt upon cooling have a significant effect on results from the experiments with water.The Rb fluid-melt partition coefficient shows no recognizable dependence on melt composition and temperature.For chloridic solutions, it is ∼0.4, independent of pressure. In experiments with water, it is one to two orders of magnitude lower and increases with pressure. The strontium fluid-melt partition coefficient does not depend on temperature. It increases slightly with pressure in Cl free experiments. In chloridic fluids, there is a sharp increase in the Sr partition coefficient with the alumina saturation index (ASI) from 0.003 at an ASI of 0.8 to a maximum of 0.3 at an ASI of 1.05. At higher ASI, it decreases slightly to 0.2 at an ASI of 1.6. It is one to two orders of magnitude higher in chloridic fluids compared to those found in H2O experiments. The Rb/Sr ratio in non-chloridic solutions in equilibrium with metaluminous melts increases with pressure, whereas the Rb/Sr ratio in chloridic fluids is independent of pressure and decreases with fluid salinity.The obtained fluid-melt partition coefficients are in good agreement with data from natural cogenetic fluid and melt inclusions. Numerical modeling shows that although the Rb/Sr ratio in the residual melt is particularly sensitive to the degree of fractional crystallization, exsolution of a fluid phase, and associated fluid-melt partitioning is not a significant factor controlling Rb and Sr concentrations in the residual melt during crystallization of most granitoids.  相似文献   

13.
Halogens show a range from moderate (F) to highly (Cl, Br, I) volatile and incompatible behavior, which makes them excellent tracers for volatile transport processes in the Earth’s mantle. Experimentally determined fluorine and chlorine partitioning data between mantle minerals and silicate melt enable us to estimate Mid Ocean Ridge Basalt (MORB) and Ocean Island Basalt (OIB) source region concentrations for these elements. This study investigates the effect of varying small amounts of water on the fluorine and chlorine partitioning behavior at 1280?°C and 0.3 GPa between olivine and silicate melt in the Fe-free CMAS+F–Cl–Br–I–H2O model system. Results show that, within the uncertainty of the analyses, water has no effect on the chlorine partitioning behavior for bulk water contents ranging from 0.03 (2) wt% H2O (DCl ol/melt = 1.6?±?0.9 × 10?4) to 0.33 (6) wt% H2O (DCl ol/melt = 2.2?±?1.1 × 10?4). Consequently, with the effect of pressure being negligible in the uppermost mantle (Joachim et al. Chem Geol 416:65–78, 2015), temperature is the only parameter that needs to be considered for the determination of chlorine partition coefficients between olivine and melt at least in the simplified iron-free CMAS+F–Cl–Br–I–H2O system. In contrast, the fluorine partition coefficient increases linearly in this range and may be described at 1280?°C and 0.3 GPa with (R 2?=?0.99): \(D_{F}^{\text{ol/melt}}\ =\ 3.6\pm 0.4\ \times \ {{10}^{-3}}\ \times \ {{X}_{{{\text{H}}_{\text{2}}}\text{O}}}\left( \text{wt }\!\!\%\!\!\text{ } \right)\ +\ 6\ \pm \ 0.4\times \,{{10}^{-4}}\). The observed fluorine partitioning behavior supports the theory suggested by Crépisson et al. (Earth Planet Sci Lett 390:287–295, 2014) that fluorine and water are incorporated as clumped OH/F defects in the olivine structure. Results of this study further suggest that fluorine concentration estimates in OIB source regions are at least 10% lower than previously expected (Joachim et al. Chem Geol 416:65–78, 2015), implying that consideration of the effect of water on the fluorine partitioning behavior between Earth’s mantle minerals and silicate melt is vital for a correct estimation of fluorine abundances in OIB source regions. Estimates for MORB source fluorine concentrations as well as chlorine abundances in both mantle source regions are within uncertainty not affected by the presence of water.  相似文献   

14.
We report an experimental study of the partitioning of Sm in a natural plagioclase/melt system as a function of concentration of Sm at constant pressure, temperature and bulk composition. Both radioactive 151Sm and non-radioactive Sm2O3 were used. In experiments in which the sample was initially held at a temperature above the liquidus for only one hour, we find that the plagioclase/ melt partition coefficient for Sm increases with decreasing concentration of Sm. There is also evidence for isotopic heterogeneity in the initially molten charge. In experiments in which the sample was initially held at the same temperature above the liquidus for 24 hours, the partition coefficient was constant as a function of concentration and no evidence for isotopic heterogeneity was observed. These experiments indicate that partition coefficients obtained from experiments involving tracer isotopes are very sensitive to experimental procedure. Our experiments also indicate that the partition coefficient for Sm between plagioclase and melt is constant over the range 3 to 50,000 ppm Sm in the melt. That range encompasses most concentrations in natural systems.  相似文献   

15.
A three-dimensional model for contaminant transport resulting from the dissolution of multicomponent nonaqueous phase liquid (NAPL) pools in three-dimensional saturated subsurface formations is developed. The solution is obtained numerically by a finite-difference scheme, and it is suitable for homogeneous porous media with unidirectional interstitial velocity. Each dissolved component may undergo first-order decay and may sorb under local equilibrium conditions. It is also assumed that the dissolution process is mass transfer limited. The nonaqueous phase activity coefficients of the NAPL pool components are evaluated at each time step. The model behavior is illustrated through a synthetic example with a NAPL pool consisting of a mixture of TCA (1,1,2-trichloroethane) and TCE (trichloroethylene). The numerical solution presented in this work is in good agreement with a recently developed analytical solution for the special case of a single component NAPL pool. The results indicate the importance of accounting for the necessary changes in the organic phase activity which significantly affects the equilibrium aqueous solubility.Notation C liquid phase solute concentration (solute mass/liquid volume) (M L–3) - C s single component aqueous saturation concentration (solubility) (M L–3) - C w equilibrium aqueous solubility (M L–3) - D molecular diffusion coefficient (L2 t –1) - D e effective molecular diffusion coefficient (L2 t –1) - D x longitudinal hydrodynamic dispersion coefficient (L2 t –1) - D y lateral hydrodynamic dispersion coefficient (L2 t –1) - D z hydrodynamic dispersion coefficient in the vertical direction (L2 t –1) - I() integer mode arithmetic operator - k local mass transfer coefficient (Lt –1) - k * average mass transfer coefficient (Lt –1) - L length - l x ,l y pool dimensions inx andy directions (L) - ll x ,l y x andy Cartesian coordinates of the pool origin (L) - M number of moles remaining in a pool (moles) - M initial number of moles (moles) - n finite-difference scheme time level - R retardation factor (dimensionless) - t time (t) - U x average interstitial velocity (Lt –1) - x, y, z spatial Cartesian coordinates (L) - X dimensionless mole fraction - dimensionless activity coefficient - w viscosity of water (=0.8904 cp at 25°C) - decay coefficient (t –1) - * tortuosity ( 1) - i,j, k finite-difference scheme grid indicators - p component number indicator - P total number of components - s pure single component - o nonaqueous phase - w aqueous phase  相似文献   

16.
Several lines of evidence point to the existence of a pre-eruptive fluid phase in the magmas erupted in 1912 at the Valley of Ten Thousand Smokes, Alaska. The discovery of rare, Cu-rich bubbles in some melt inclusions is best explained by the random entrapment of a low-density, fluid phase within growing phenocrysts. The H2O, S and Cl concentrations of the high-silica rhyolite are also consistent with fluid saturation in the rhyolite. Water contents, as determined by infrared spectroscopy on doubly polished melt inclusions, cluster between 3.5 and 4.5 wt% H2O, without any apparent differences between magmas vented explosively and effusively. These concentrations would be sufficient for H2O saturation at a pressure of 100 MPa, though the presence of other volatiles such as CO2 and SO2 could allow saturation with respect to a fluid phase at higher pressures. The S, Cu and Cl contents of the phenocryst assemblages, as determined by XRF analyses, are too low to account for the decrease in the concentrations of S and Cu in the melt, and only modest increase in Cl, with differentiation. Therefore, the behavior of these volatile elements was controlled either by eryptic fractionation if phenocryst phasese or, more likely, by partitioning into a coexisting fluid phase. The presence of this low-density phase apparently provided metals such as Cu with a volatile phase into which they could partition; the concentration of Cu in this fluid reached tens to hundreds of times that of the coexisting silicate melt and may have been as rich as 0.05 wt% Cu. The distribution of Cu in the magma was also controlled by sulfides such as intermediate solid solution and pyrrhotite, which cyrstallized directly from the silicate melt.  相似文献   

17.
赵斌  赵劲松  许德如 《岩石学报》2017,33(6):1841-1858
矽卡岩矿床各种硅酸盐矿物中熔融包裹体和流体-熔融包裹体的显微测温资料和相成分让我们提出过大量矽卡岩是岩浆成因的建议。在本文中,我们提供沿长江中下游成矿带的许多矽卡岩矿床包含在石榴子石和辉石里的熔融包裹体和流体-熔融包裹体的激光拉曼分析结果,目的是证明所研究的并与Cu-Fe-Au矿床共生的矽卡岩系岩浆成因。我们的研究结果显示,熔融包裹体只含固体相和微量气相。流体-熔融包裹体除了含大量固相外,还含微量流体和气相以及没有被仪器检测到的气体。固体相与包裹体寄主矿物相同或类似。流体相主要为水或盐水溶液和包括C6H6、C3H6、C3H8、CH4、CO2和O2的气体。我们提出,熔融包裹体和流体-熔融包裹体是原始岩浆的最好代表。这就证明,矽卡岩组合是由一个原生岩浆直接结晶而成。此外,我们还讨论了岩浆矽卡岩形成的温度、分布范围和规模、形成机制和与Cu-Fe-Au矿化作用的联系。  相似文献   

18.
An analytical solution is given to evaluate the number and duration of pumping cycles required for the remediation by pumping of contaminants, both single component and multi-component non-aqueous phase liquids (NAPLs), when no free product is present in the system. The method can be applied in a homogenous medium if the contamination zones have been delineated and residual total NAPL concentrations assessed. Based on the principle of the NAPL partitioning in unsaturated or saturated porous media, analytical closed-form solutions are provided for both cases of remediation by pumping in saturated and unsaturated conditions: “pump-and-treat” and “soil vapor extraction”. In each case we determine the number of pumping cycles required to reach the residual required concentration of NAPL (for example, according to health-based standards), considering one or more chemicals simultaneously present in an aquifer. The method requires information on the aquifer saturation state and the properties of the chemicals of interest. Calculations are based on the assumption of equilibrium partitioning of chemicals between the pore water, the soil solids, and the soil gas (in the case of unsaturated conditions), and no presence of a NAPL phase.  相似文献   

19.
The barium deposits in Ankang and Xunyang counties,Shaanxi Province,China,occur in the northernmost part of the world-class barium metallogenic belt in south Qinling.The deposits are hosted by the Lower Silurian carbonaceous siliceous rocks,with a unique combination of barite and witherite.The homogenization temperatures of fluid inclusions in the barite are mainly concentrated between 135 and 155 ℃,whereas those from the witherite have two peaks of 165-175 ℃,and 215-225℃,respectively.Laser Raman analysis of fluid inclusions indicates that the vapor phase of fluid inclusions in barite is dominated by H_2O,although some contains N_2,H_2S,and CH_4.The compositions of the vapor and liquid phases of fluid inclusions in witherite can be divided into two end-members,one dominated by H_2O without other volatiles,and the other containing CH_4,C_2H_6,C_3H_8,C_2H_4,and C_6H_6 in addition to H_2O.CO_2,H_2S,and some CH_4 are interpreted as products of chemical reactions during mineralization.Organic gases(CH_4,C_2H_6,C_3H_8,C_2H_4,and C_6H_6) in the fluids were critical in the formation of barium sulfate versus carbonate.The δ~(34)S values of barite range from 38.26‰ to54.23‰(CDT),the δ~(34)S values of sulfides coexisting with barium minerals vary from 22.44‰ to25.11‰(CDT),and those in the wall rock from 11.60‰ to 19.06‰(CDT).We propose that the SO_4~(2-)generally experienced bacterial sulfate reduction in seawater before mineralization,and some SO_4~(2-)also experienced thermochemical sulfate reduction in hydrothermal system during mineralization.The δ~(13)C values of witherite range from-27.30‰ to-11.80‰(PDB),suggesting that carbon was sourced from organic substances(like CH_4,C_2H_4,and C_2H_6).The formation of witherite was possibly associated with thermochemical sulfate reduction,which caused the consumption of the organic gases and SO_4~(2-) in the hydrothermal solutions,consequently inhibiting barite formation.The important conditions for forming witherite include high fluid temperatures,high Ba~(2+) concentrations,CO_2 in the fluids,low HS~- concentrations,and the subsequent rapid diffusion of H_2S during thermochemical sulfate reduction of the fluids.  相似文献   

20.
  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号