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.
Dajing Cu-Sn-Ag-Pb-Zn ore deposit, in the Inner Mongolia Autonomous Region of China, is a fissure-filling hydrothermal ore deposit. The δD values of quartz-hosted inclusion water are centered at −100%.– −130%.. The δ34S values of sulfide ore minerals and δ13 C values of carbonate gangue minerals vary from −0.3%. to 2.6%. and from −2.9%. to −7.0%., respectively. Integrated isotopic data point to two major contributions to the mineralizing fluid that include a dominant meteoric-derived groundwater, and sulfur and carbon species from hypogene magma. Linear trends are exhibited on the gaseous H2O versus CO2 plot, and plots of CO, N2, CH4, and C2H6. It is shown by quantitative simulation that magma degassing cannot explain the linear trends. Hence, these linear trends are interpreted in terms of mixing of CO2-rich magmatic fluid with meteoric-derived groundwater. The groundwater circulated in Paleozoic sedimentary rocks and absorbed CO, N2, CH4, C2H6 and radiogenic Ar from organic matter. Cooling effects resulting from mixing have caused the precipitation of ore minerals.  相似文献   

2.
Step heating experiments on ultra-high pressure (UHP) mcks from the Dabie Mountain shows a majority of CO2 in fluid inclusion (excluding H2O); CO is also a significant component, with a small content of N2 and CH4. Carbon isotopic composition of CO2 in fluid of metamorphic climax stage (-25%0- -30%0) is different from that of mantle carbon, indicating that UHP rocks did not experience obvious transformation by mantle fluids despite their subduction depth. CO2 was derived from carbon matter in the pmtoliths of UHP rocks in a relatively confined system, showing that the UHP rocks subsided quickly and uplifted quickly from the mantle. Current organization: Research Institute of Petroleum Exploration and Development, Beijing 100083, China.  相似文献   

3.

This paper presents gas compositions and H-, O-isotope compositions of sulfide- and quartz-hosted fluid inclusions, and S-, Pb-isotope compositions of sulfide separates collected from the principal Stage 2 ores in Veins 3 and 210 of the Jinwozi lode gold deposit, eastern Tianshan Mountains of China. Fluid inclusions trapped in quartz and sphalerite are dominantly primary. H-and O-isotopic compositions of pyrite-hosted fluid inclusions indicate two major contributions to the ore-forming fluid that include the degassed magma and the meteoric-derived but rock 18O-buffered groundwater. However, H- and O-isotopic compositions of quartz-hosted fluid inclusions essentially suggest the presence of groundwater. Sulfide-hosted fluid inclusions show considerably higher abundances of gaseous species CO2, N2, H2S, etc. than quartz-hosted ones. The linear trends among inclusion gaseous species reflect the mixing tendency between the gas-rich magmatic fluid and the groundwater. The relative enrichment of gaseous species in sulfide-hosted fluid inclusions, coupled with the banded ore structure indicating alternate precipitation of quartz with sulfide minerals, suggests that the magmatic fluid has been inputted to the ore-forming fluid in pulsation. Sulfur and lead isotope compositions of pyrite and galena separates indicate an essential magma derivation for sulfur but the multiple sources for metallic materials from the mantle to the bulk crust.

  相似文献   

4.
This paper presents gas compositions and H-, O-isotope compositions of sulfide- and quartz-hosted fluid inclusions, and S-, Pb-isotope compositions of sulfide separates collected from the principal Stage 2 ores in Veins 3 and 210 of the Jinwozi lode gold deposit, eastern Tianshan Mountains of China. Fluid inclusions trapped in quartz and sphalerite are dominantly primary. H-and O-isotopic compositions of pyrite-hosted fluid inclusions indicate two major contributions to the ore-forming fluid that include the degassed magma and the meteoric-derived but rock 18O-buffered groundwater. However, H- and O-isotopic compositions of quartz-hosted fluid inclusions essentially suggest the presence of groundwater. Sulfide-hosted fluid inclusions show considerably higher abundances of gaseous species CO2, N2, H2S, etc. than quartz-hosted ones. The linear trends among inclusion gaseous species reflect the mixing tendency between the gas-rich magmatic fluid and the groundwater. The relative enrichment of gaseous species in sulfide-hosted fluid inclusions, coupled with the banded ore structure indicating alternate precipitation of quartz with sulfide minerals, suggests that the magmatic fluid has been inputted to the ore-forming fluid in pulsation. Sulfur and lead isotope compositions of pyrite and galena separates indicate an essential magma derivation for sulfur but the multiple sources for metallic materials from the mantle to the bulk crust.  相似文献   

5.
This paper reveals the physicochemical properties such as component, formulation, genesis, tem-perature, pH, Eh, salinity and pressure of all main alteration fluid of interlayer oxidation zone sand-stone-type uranium deposits after studying the geologic process and geochemistry of internal typical sandstone-type uranium deposits such as Shihongtan deposit in the Turpan-Hami basin, 512 deposit in the Yili basin, Dongsheng deposit in the Ordos basin. The composition of fluid can be divided into two parts based on the analysis of inclusion: one can be affirmed as atmospheric water with ordinary temperature epigenesist according to the character of hydrogen and oxygen isotope of inclusion, the other is natural gas containing gaseous hydrocarbon like CH4, and CO2 as well as a little H2S, CO, H2, N2 and so on, it always contains a small quantity of hydrocarbon liquid in petroliferous basins. The fluid property of oxidation alteration zone is always oxidation alkaline, and neutrality or weak acid-weak alkaline and reducibility during the metallizing process, but at secondary reduction or deoxidization zone it becomes strong reduction alkaline. Oxygenic groundwater in the fluid is the activate and mig-ratory medium of uranium element, but the gaseous hydrocarbon like CH4 as well as H2, H2S, CO from natural gas is the important sedimentary reducer of uranium mineral; the transformation of pH,Eh in fluid environment is the main reason for the formation of uranium metallization.  相似文献   

6.
Two kinds of inclusions, fluid-melting inclusion and gas-liquid inclusion, are present in the Huanggangliang deposit in eastern Inner Mongolia. Temperature ranges from 1050°C of fluid-melting inclusion to 150°C of liquid inclusion. Away from intrusion, the inclusions of orebodies intend to be characterized by simpler type, lower temperature and lower salinity, as well as weakened relation to intrusion. The metallization of the Huanggangliang deposit is characterized by multiple activities of ore-forming fluid, multi-source, multi-stage accumulation of ore-forming material, F-rich environment, enrichment of F, organic gas, CO2 and N2, and involving of residual magma.  相似文献   

7.
Noncondensible gases from hot springs, fumaroles, and deep wells within the Valles caldera geothermal system (210–300°C) consist of roughly 98.5 mol% CO2, 0.5 mol% H2S, and 1 mol% other components. 3He/4He ratios indicate a deep magmatic source (R/Ra up to 6) whereas δ13C–CO2 values (−3 to −5‰) do not discriminate between a mantle/magmatic source and a source from subjacent, hydrothermally altered Paleozoic carbonate rocks. Regional gases from sites within a 50-km radius beyond Valles caldera are relatively enriched in CO2 and He, but depleted in H2S compared to Valles gases. Regional gases have R/Ra values ≤1.2 due to more interaction with the crust and/or less contribution from the mantle. Carbon sources for regional CO2 are varied. During 1982–1998, repeat analyses of gases from intracaldera sites at Sulphur Springs showed relatively constant CH4, H2, and H2S contents. The only exception was gas from Footbath Spring (1987–1993), which experienced increases in these three components during drilling and testing of scientific wells VC-2a and VC-2b. Present-day Valles gases contain substantially less N2 than fluid inclusion gases trapped in deep, early-stage, post-caldera vein minerals. This suggests that the long-lived Valles hydrothermal system (ca. 1 Myr) has depleted subsurface Paleozoic sedimentary rocks of nitrogen. When compared with gases from many other geothermal systems, Valles caldera gases are relatively enriched in He but depleted in CH4, N2 and Ar. In this respect, Valles gases resemble end-member hydrothermal and magmatic gases discharged at hot spots (Galapagos, Kilauea, and Yellowstone).  相似文献   

8.
Abundant fluid inclusions in olivine of dunite xenoliths (～1–3 cm) in basalt dredged from the young Loihi Seamount, 30 km southeast of Hawaii, are evidence for three coexisting immiscible fluid phases—silicate melt (now glass), sulfide melt (now solid), and dense supercritical CO2 (now liquid + gas)—during growth and later fracturing of some of these olivine crystals. Some olivine xenocrysts, probably from disaggregation of xenoliths, contain similar inclusions.Most of the inclusions (2–10 μm) are on secondary planes, trapped during healing of fractures after the original crystal growth. Some such planes end abruptly within single crystals and are termed pseudosecondary, because they formed during the growth of the host olivine crystals. The “vapor” bubble in a few large (20–60 μm), isolated, and hence primary, silicate melt inclusions is too large to be the result of simple differential shrinkage. Under correct viewing conditions, these bubbles are seen to consist of CO2 liquid and gas, with an aggregate ? = ～ 0.5–0.75 g cm?3, and represent trapped globules of dense supercritical CO2 (i.e., incipient “vesiculation” at depth). Some spinel crystals enclosed within olivine have attached CO2 blebs. Spherical sulfide blebs having widely variable volume ratios to CO2 and silicate glass are found in both primary and pseudosecondary inclusions, demonstrating that an immiscible sulfide melt was also present.Assuming olivine growth at ～ 1200°C and hydrostatic pressure from a liquid lava column, extrapolation of CO2P-V-T data indicates that the primary inclusions were trapped at ～ 220–470 MPa (2200–4700 bars), or ～ 8–17 km depth in basalt magma of ? = 2.7 g cm?3. Because the temperature cannot change much during the rise to eruption, the range of CO2 densities reveals the change in pressure from that during original olivine growth to later deformation and rise to eruption on the sea floor. The presence of numerous decrepitated inclusions indicates that the inclusion sample studied is biased by the loss of higher-density inclusions and suggests that some part of these olivine xenoliths formed at greater depths.  相似文献   

9.
The density, and therefore the pressure, of CO2 fluid inclusions in minerals can be estimated from the Fermi diad splitting of Raman spectra of CO2. An accurate determination of the pressure of CO2 fluid inclusions enables the estimation of the depth origin of rocks from the deep Earth. A micro-Raman densimeter was applied to ultramafic–mafic xenoliths sampled along the Ohku coast of Oki-Dogo Island in the Sea of Japan (East Sea). The density of CO2 fluid inclusions in the mafic granulite was 1.02–1.05 g/cm3, while those of lherzolites were 0.98–1.02 g/cm3. In contrast, the density of CO2 fluid inclusions measured in olivine gabbro, clinopyroxenite, and harzburgite were lower ranging from 0.86–to 0.99 g/cm3. Taking into account the temperature condition estimated using a pyroxene thermometer, the mafic granulite originated from a depth of 27–30 km and the lherzolites from 25–29 km. The overlapping depth of 27–29 km can be interpreted as the depth including the Moho discontinuity under Oki-Dogo Island 3.3 Ma. This estimation is consistent with geophysical observations.  相似文献   

10.
The equilibrium distribution of CO2H2O fluids in synthetic rock samples (principally dunite and quartzite) has been characterized by measurements of the dihedral wetting angle, θ, resulting from 5-day annealing periods at 950–1150°C and 1 GPa. For fluids in equilibrium with polycrystalline quartz, θ varies systematically from 57° for pure H2O to 90° at XCO2 0.9. Similarly, for San Carlos olivine, θ varies from 65° for pure H2O to 90° at XCO2 0.9. The addition of solutes (NaCl, KCl, CaF2, Na2CO3) to H2O causes a major decrease in θ in the quartz/fluid system (to values as low as 40°), but has no effect on fluid wetting in dunite. Reconnaissance experiments on other mono- and polymineralic aggregates indicate universally high wetting angles (θ 60°) in upper mantle assemblages and for CO2 in felsic compositions. For diopside + H2O, θ 80°, with large variation due to crystalline anisotropy. In no case does θ approach 0°, the condition necessary for fluid to be present along all grain boundaries.Because a value of θ greater than 60° precludes the existence of an interconnected fluid phase in a rock, our results have important implications not only for fluid transport but also for the physical properties of the bulk fluid/rock system. Any static fluid present in the upper mantle must exist as isolated pores located primarily at grain corners, and transport can occur only by hydrofracture. In the continental crust, aqueous fluids (especially saline ones) are likely to form an interconnected network along grain edges, thus contributing to high electrical conductivity and allowing the possibility of fluid transport by porous flow or surface energy-driven infiltration.  相似文献   

11.
The Okinawa trough is a spreading back-are basin featuring emitting hydrothermal solutions (black chimney type) and modem sulfide precipitation on the sea floor. The study of fluid inclusions in water-rock interaction products in the Jade hydrothermal field indicates that the deep hydrothermal system beneath the sea floor is fairly rich in gas and there are two independent and coexisting fluids-CO2-hydrocarbon fluid and salt aqueous fluid. On the whole, the composition of CO2-hydrocarbon fluid inclusions is similar to that of the fluid inclusions in natural gas fields. The dominant composition of the inclusions in aqueous fluid is H2O with CO2 and CH4 being oversaturated. The salt aqueous fluid of the Jade hydrothermal system might be emitted through a black chimney, whereas CO2-rich fluids discharge CO2 bubbles and CO2 hydrate through fissures. Hydrocarbons in gas phase or in fluid might be enclosed somewhere under the sea. Large storage of CO2-CH4-H2S gas or fluid and reaction of this gas or fluid with salt water will lead to commercial sulfide deposits.  相似文献   

12.
Fluid inclusion studies have been used to derive a model for fluid evolution in the Hohi geothermal area, Japan. Six types of fluid inclusions are found in quartz obtained from the drill core of DW-5 hole. They are: (I) primary liquid-rich with evidence of boiling; (II) primary liquid-rich without evidence of boiling; (III) primary vapor-rich (assumed to have been formed by boiling); (IV) secondary liquid-rich with evidence of boiling; (V) secondary liquid-rich without evidence of boiling; (VI) secondary vapor-rich (assumed to have been formed by boiling). Homogenization temperatures (Th) range between 196 and 347°C and the final melting point of ice (Tm) between −0.2 and −4.3°C. The CO2 content was estimated semiquantitatively to be between 0 and 0.39 wt. % based on the bubble behavior on crushing. NaCl equivalent solid solute salinity of fluid inclusions was determined as being between 0 and 6.8 wt. % after minor correction for CO2 content.Fluid inclusions in quartz provide a record of geothermal activity of early boiling and later cooling. The CO2 contents and homogenization temperatures of fluid inclusions with evidence of boiling generally increase with depth; these changes, and NaCl equivalent solid solute salinity of the fluid can be explained by an adiabatic boiling model for a CO2-bearing low-salinity fluid. Some high-salinity inclusions without CO2 are presumed to have formed by a local boiling process due to a temperature increase or a pressure decrease. The liquid-rich primary and secondary inclusions without evidence of boiling formed during the cooling process. The salinity and CO2 content of these inclusions are lower than those in the boiling fluid at the early stage, probably as a result of admixture with groundwater.  相似文献   

13.
In a series of experiments at 0.5–1.3 GPa and 1050–1200°C we have monitored the transport, via crack propagation, of CO2 into well-annealed olivine and quartz aggregates. The objectives were to determine (1) the extent and rate of fluid penetration; (2) the effect of varying both P-T conditions and microstructure; and (3) the fluid penetration pathways. Experiments on CO2 penetration into dunite annealed in the absence of MgO indicate rapid and pervasive fluid transport on a grain-dimension scale, but a limited penetration distance ( 1 mm). Additional experiments on dunite annealed in the presence of MgO (either dispersed or present at both ends), however, resulted in CO2 penetration that was both pervasive on the scale of individual grains and almost always completely through the 5 mm long samples. The abundance of fine (10 μm) grains in the MgO-free dunite, in contrast to the much larger grain sizes of the samples annealed with MgO present, suggests the difference in fluid penetration behavior may arise because the strength variation in dunite scales with the grain size. Effects arising from changes in olivine point defect chemistry, however, are an additional possibility. The response of synthetic quartzite to CO2 overpressure is distinct from that of dunite: Quartzite experiences rapid and complete penetration of CO2, via a macroscopically visible system of transgranular fractures, over the range of P-T conditions investigated.The small amount of porosity ( 2–3%) present in most rock samples fabricated for this study, lacks three-dimensional connectivity, thus precluding any enhanced fluid penetration via porous flow. Pores could possibly enhance fluid penetration as the result of a small reduction in resistance to fracture, but the probable abundance of strength-controlling flaws in natural rocks is likely to produce similar behavior.The results of our experiments on olivine and olivine + MgO suggest that the transport of pressurized CO2 in very olivine-rich mantle environments will be pervasive on the scale of individual grains and its extent may be dependent on rock microstructure and/or crystal chemical effects. Such pervasive fluid transport, perhaps associated with magma decarbonation, may have interesting implications for both magma transport and local LREE enrichment of adjacent mantle wall-rock. The ease with which quartzite is penetrated by CO2 at the conditions of our experiments underscores the possible role of decarbonation reactions in crustal permeability-enhancement processes.  相似文献   

14.
Clarification of the molecular mechanism underlying the interaction of coal with CH4, CO2, and H2O molecules is the basis for an in-depth understanding of the states of fluid in coal and fluid-induced coal swelling/contraction. In terms of instrumental analysis, molecular simulation technology based on molecular mechanics/dynamics and quantum chemistry is a powerful tool for revealing the relationship between the structure and properties of a substance and understanding the interaction mechanisms of physical-chemical systems. In this study, the giant canonical ensemble Monte Carlo (GCMC) and molecular dynamics (MD) methods were applied to investigate the adsorption behavior of a Yanzhou coal model (C222H185N3O17S5). We explored the adsorption amounts of CH4, CO2, and H2O onto Yanzhou coal, the adsorption conformation, and the impact of oxygen-containing functional groups. Furthermore, we revealed the different adsorption mechanisms of the three substances using isosteric heat of adsorption and energy change data. (1) The adsorption isotherms of the mono-component CH4, CO2, and H2O were consistent with the Langmuir model, and their adsorption amounts showed an order of CH4<CO2<H2O. In addition, high temperatures were non-conducive to adsorption. When the three components of CH4/CO2/H2O were mixed (at a molar ratio of 1:1:1) for adsorption, only the adsorption curve of H2O was consistent with the Langmuir model. (2) The mean values of the isosteric heat of adsorption of CH4, CO2, and H2O were 22.54, 36.90, and 37.82 kJ/mol, respectively; that is, H2O>CO2>CH4. In addition, at higher temperatures, the isosteric heat of adsorption decreased; pressure had no significant effect on the heat of adsorption. (3) CH4 molecules displayed an aggregated distribution in the pores, whereas CO2 molecules were cross arranged in pairs. Regarding H2O molecules, under the influence of hydrogen bonds, the O atom pointed to surrounding H2O molecules or the H atoms of coal molecules in a regular pattern. The intermolecular distances of the three substances were 0.421, 0.553, and 0.290 nm, respectively. The radial distribution function (RDF) analysis showed that H2O molecules were arranged in the most compact fashion, forming a tight molecular layer. (4) H2O molecules showed a significantly stratified distribution around oxygen-containing functional groups on the coal surface, and the bonding strength showed a descending order of hydroxyl> carboxyl>carbonyl. In contrast, CO2 and CH4 showed only slightly stratified distributions. (5) After the adsorption of CH4, CO2, and H2O, the total energy, the energy of valence electrons, and the non-bonding interaction of the system in the Yanzhou coal model all decreased. The results regarding the decrease in the total energy of the system indicated an order of H2O>CO2>CH4 in terms of the adsorption priority of the Yanzhou coal model. The results regarding the decrease in the energy of valence electrons showed that under certain geological conditions, a pressure-induced “coal strain” could lead to a structural rearrangement during the interaction of coal with fluid to form a more stable conformation, which might be the molecular mechanism of coal swelling resulting from the interaction between fluid and coal. An analysis of the contribution of Van der Waals forces, electrostatic interactions and hydrogen bonds to the decrease in non-bonding interactions revealed the mechanism underlying the interactions between coal molecules and the three substances. The interaction between coal molecules and CH4 consisted of typical physical adsorption, whereas that between coal molecules and CO2 consisted mainly of physical adsorption combined with weak chemical adsorption. The interaction between coal molecules and H2O is physical and chemical.  相似文献   

15.
To reduce the negative effect of climate change on Biodiversity, the use of geological CO2 sequestration has been proposed; however leakage from underwater storages may represent a risk to marine life. As extracellular homeostasis is important in determining species’ ability to cope with elevated CO2, we investigated the acid–base and ion regulatory responses, as well as the density, of sea urchins living around CO2 vents at Vulcano, Italy. We conducted in situ transplantation and field-based laboratory exposures to different pCO2/pH regimes. Our results confirm that sea urchins have some ability to regulate their extracellular fluid under elevated pCO2. Furthermore, we show that even in closely-related taxa divergent physiological capabilities underlie differences in taxa distribution around the CO2 vent. It is concluded that species distribution under the sort of elevated CO2 conditions occurring with leakages from geological storages and future ocean acidification scenarios, may partly be determined by quite subtle physiological differentiation.  相似文献   

16.
Interfacial interactions, namely interfacial tension, wettability, capillarity and interfacial mass transfer are known to govern fluid distribution and behavior in porous media. Therefore the interfacial interactions between CO2, brine and oil and/or gas reservoirs have a significant influence on the effectiveness of any CO2 storage operations. However, data and knowledge of interfacial properties in storage conditions are scarce. This issue becomes particularly true in the case of deep saline aquifers where limited, economically driven, data collection and archiving are available. In this paper, we present a complete set of brine–CO2 interfacial tension data at pressure, temperature and salinity conditions, representative of a CO2 storage operation. A semi-empirical correlation is proposed to calculate the interfacial tension from the experimental data. Wettability is studied at pore scale, using glass micromodels in order to track fluids distribution as a function of the thermodynamic properties and wettability conditions for water–CO2 systems. With this approach, we show that, in strongly hydrophilic porous media, the CO2 does not wet the solid surface whereas; if the porous media has less hydrophilic properties the CO2 significantly wets the surface.  相似文献   

17.
To investigate the relationship between volatile abundances and eruption style, we have analyzed major element and volatile (H2O, CO2, S) concentrations in olivine-hosted melt inclusions in tephra from the 2000 yr BP eruption of Xitle volcano in the central Trans-Mexican Volcanic Belt. The Xitle eruption was dominantly effusive, with fluid lava flows accounting for 95% of the total dense rock erupted material (1.1 km3). However, in addition to the initial, Strombolian, cinder cone-building phase, there was a later explosive phase that interrupted effusive activity and deposited three widespread ash fall layers. Major element compositions of olivine-hosted melt inclusions from these ash layers range from 52 to 58 wt.% SiO2, and olivine host compositions are Fo84–86. Water concentrations in the melt inclusions are variable (0.2–1.3 wt.% H2O), with an average of 0.45±0.3 (1σ) wt.% H2O. Sulfur concentrations vary from below detection (50 ppm) to 1000 ppm but are mostly ≤200 ppm and show little correlation with H2O. Only the two inclusions with the highest H2O have detectable CO2 (310–340 ppm), indicating inclusion entrapment at higher pressures (700–900 bars) than for the other inclusions (≤80 bars). The low and variable H2O and S contents of melt inclusions combined with the absence of less soluble CO2 indicates shallow-level degassing before olivine crystallization and melt inclusion formation. Olivine morphologies are consistent with the interpretation that most crystallization occurred rapidly during near-surface H2O loss. During cinder cone eruptions, the switch from initial explosive activity to effusive eruption probably occurs when the ascent velocity of magma becomes slow enough to allow near-complete degassing of magma at shallow depths within the cone as a result of buoyantly rising gas bubbles. This allows degassed lavas to flow laterally and exit near the base of the cone while gas escapes through bubbly magma in the uppermost part of the conduit just below the crater. The major element compositions of melt inclusions at Xitle show that the short-lived phase of renewed explosive activity was triggered by a magma recharge event, which could have increased overpressure in the storage reservoir beneath Xitle, leading to increased ascent velocities and decreased time available for degassing during ascent.  相似文献   

18.
The Main Endeavour Field, northern Juan de Fuca Ridge, experienced intense seismic activity in June 1999. Hydrothermal vent fluids were collected from sulfide structures in September 1999 and July 2000 and analyzed for the abundance of H2, H2S, CH4, CO2, NH3, Mg and Cl to document temporal and spatial changes following the earthquakes. Dissolved concentrations of CO2, H2, and H2S increased dramatically in the September 1999 samples relative to pre-earthquake abundances, and subsequently decreased during the following year. In contrast, dissolved NH3 and CH4 concentrations in 1999 and 2000 were similar to or less than pre-earthquake values. Aqueous Cl abundances showed large decreases immediately following the earthquakes followed by increases to near pre-earthquake values. The abundances of volatile species at the Main Endeavour Field were characterized by strong inverse correlations with chlorinity. Phase separation can account for 20-50% enrichments of CO2, CH4, and NH3 in low-chlorinity fluids, while temperature- and pressure-dependent fluid-mineral equilibria at near-critical conditions are responsible for order of magnitude greater enrichments in dissolved H2S and H2. The systematic variation of dissolved gas concentrations with chlorinity likely reflects mixing of a low-chlorinity volatile-enriched vapor generated by supercritical phase separation with a cooler gas-poor hydrothermal fluid of seawater chlorinity. Decreased abundances of sediment-derived NH3 and CH4 in 1999 indicate an earthquake-induced change in subsurface hydrology. Elevated CO2 abundances in vent fluids collected in September 1999 provide evidence that supports a magmatic origin for the earthquakes. Temperature-salinity relationships are consistent with intrusion of a shallow dike and suggest that the earthquakes were associated with movement of magma beneath the ridge crest. These data demonstrate the large and rapid response of chemical fluxes at mid-ocean ridges to magmatic activity and associated changes in subsurface temperature and pressure.  相似文献   

19.
The concentration of greenhouse gases – particularly carbon dioxide (CO2) – in the atmosphere has been on the rise in the past decades. One of the methods which have been proposed to help reduce anthropogenic CO2 emissions is the capture of CO2from large, stationary point sources and storage in deep geological formations. The caprock is an impermeable geological layer which prevents the leakage of stored CO2, and its integrity is of utmost importance for storage security. Due to the high pressure build-up during injection, the caprock in the vicinity of the well is particularly at risk of fracturing. Biofilms could be used as biobarriers which help prevent the leakage of CO2 through the caprock in injection well vicinity by blocking leakage pathways. The biofilm could also protect well cement from corrosion by CO2-rich brine.  相似文献   

20.
We suggest that different equations of state (EOS) algorithms can and frequently will provide very different predictions of CO2 migration following injection for sequestration. Rather than carry out an exhaustive examination of all EOS algorithms available, we elected to evaluate this general hypothesis by making detailed comparisons of simulation results of two very common EOS algorithms. We simulated and compared CO2 migration patterns using two fundamentally different EOS algorithms – Modified Redlich-Kwong EOS (MRKEOS) and Span and Wagner EOS (SWEOS). In general, the predictions of thermophysical properties for both algorithms are close, except for a contrast in the predicted fugacity coefficient of CO2, which subsequently propagates to a contrast in predicted solubility in water/brine. Typically, MRKEOS underestimates solubility of CO2 compared to both SWEOS and experimental solubility data. In simulations of CO2 migration, dissolution rates of separate-phase CO2 predicted from the two EOS algorithms were significantly different, even for small contrasts in predicted fluid properties from EOS algorithms, resulting in markedly different migration patterns.  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