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 15 毫秒
1.
The incorporation of hydrogen in enstatite in a hydrous system containing various amounts of NaCl was investigated at 25 kbar. The hydrogen content in enstatite shows a clear negative correlation to the NaCl-concentration in the system. The most favourable explanation is the reduction of water fugacity due to dilution. Other reasons for the limited hydrogen incorporation at high NaCl levels, such as a significant influence of Na+ on the defect chemistry or an exchange between OH- and Cl−in enstatite, appear much less important. A partition coefficient D Na En/Fluid = 0.0013 could be determined, demonstrating that Na is less incompatible in enstatite than H. The new results support the idea that dissolved components have to be considered when the total hydrogen storage capacity in nominally anhydrous minerals is estimated, especially in geological settings with high levels of halogens, such as subduction zones.  相似文献   

2.
An extraction-quench apparatus was used to measure calcite solubilities in supercritical CO2H2O mixtures. Experiments were conducted at 1 kbar and 2 kbar, between 240°C and 620°C and from XCO2 = .02 toXCO2 = .15 in order to determine the solubility behavior as a function of pressure, temperature and CO2 content. The results indicate that calcite solubilities under these conditions behave similarly to previously investigated calcite solubilities at lower pressures and temperatures (SHARP and Kennedy, 1965). At constant XCO2, the solubility increases with increasing pressure, but it decreases with increasing temperature. When the temperature and pressure are constant, the calcite solubility rises with increasing XCO2 to a maximum value at XCO2 between 0.02 and 0.05. For higher CO2 contents, up to XCO2 = .15, the calcite solubility decreases, probably due to the decrease of H2O activities to values significantly below unity.The solubility behavior can be successfully modeled by making the assumption that Ca++ is the dominant calcium species and that the carbon-bearing species are CO2(aq) and HCO−3. Since for these dilute H2OCO2 fluids, all activity coefficients can be assumed to not differ significantly from unity, ionization constants for the reaction H2O + CO2(aq) H+ + HCO−3 can be calculated at 1 and 2 kbar between 250°C and 550°C. These calculated values are in good agreement with the low temperature determinations of the ionization constants for this reaction determined by Read (1975). Values of the molal Gibbs free energy of CO2(aq) obtained in our study exhibit a much greater positive departure from ideality than those calculated with the modified Redlich-Kwong equations of either Flowers (1979) or Kerrick and Jacobs (1981) for dilute CO2 aqueous solutions.  相似文献   

3.
  相似文献   

4.
We examine the star-forming region in a molecular cloud with the coordinates l = 33.30°, b = 0.25° at a distance of 1.7 kpc, in which the nebula GM 2–30 is embedded. Apart from the previously known Herbig—Haro object HH 172, several new HH objects have been found, comprising at least two HH flows. The internal structure of these objects is studied. The relationship between the line emission and kinematic data obtained through multi-pupil spectroscopy suggest the presence of bipolar outflow associated with the nebula GM 2–30 and HH 172/HH 721, which show mirror symmetry according to a number of characteristics. No optical source of this flow is observed, although the source of energy of the second flow may be a weak star associated with HH 723. The linear dimensions of the flows (more than one parsec) suggest that they are the giant outflows.  相似文献   

5.
It has been proved to be one effective means to reduce emissions of CO2 to mitigate the worsening global climate change through lots of projects and tests about CO2 geological storage. The sites that are suitable for CO2 geological storage include coal seams that can not be mined, deep saline aquifers, oil fields, and depleted gas fields. The emission of CO2 from fuel combustion is about 3.54 Gt in China in 2003, which is the second biggest in the world. Because the energy consumption in C…  相似文献   

6.
It has been proved to be one effective means to reduce emissions of CO2 to mitigate the worsening global climate change through lots of projects and tests about CO2 geological storage. The sites that are suitable for CO2 geological storage include coal seams that can not be mined, deep saline aquifers, oil fields, and depleted gas fields. The emission of CO2 from fuel combustion is about 3.54 Gt in China in 2003, which is the second biggest in the world. Because the energy consumption in China mainly depends on fossil fuels for a long time in the future, China will become a country with the biggest emission of CO2 in the world, which will make China have to reduce the emissions of CO2 by some methods including geological storage. Based on lots of information about the reserves of coal seam methane and the rank of coal in the 68 coal basins in China, the total CO2 storage capacity in these coal basins was estimated according to the recovery coefficient and exchange ratio of CO2 to CHa.The total storage capacity in deep saline aquifers can be regarded as the total quantity of CO2 that can be dissolved in the saline aquifers at the depth from 1000m to 3000m under ground. The quantity can be estimated by multiplying the solubility of CO2 in the saline water and the volume of the appropriate aquifers. According to the reserve and quality of crude oil in 46 main oil basins in China, the CO2 storage capacity and the quantity of enhanced oil were calculated. The storage capacity of depleted gas fields can be derived from the reserve and depth of the gas fields. The total CO2 geological storage capacity is about 196.2 Gt CO2 that is as against 55.4 times the CO2 emission from fuel combustion in China in 2003. According to the results of the finished projects and tests about CO2-EOR and CO2-ECBM, the CO2 geological storage capacities in coal seams, deep saline aquifers, oil fields and depleted gas fields will be estimated.  相似文献   

7.
The solubility of water in coexisting enstatite and forsterite was investigated by simultaneously synthesizing the two phases in a series of high pressure and temperature piston cylinder experiments. Experiments were performed at 1.0 and 2.0 GPa at temperatures between 1,100 and 1,420°C. Integrated OH absorbances were determined using polarized infrared spectroscopy on orientated single crystals of each phase. Phase water contents were estimated using the calibration of Libowitzky and Rossman (Am Mineral 82:1111–1115, 1997). Enstatite crystals, synthesized in equilibrium with forsterite and an aqueous phase at 1,350°C and 2.0 GPa, contain 114 ppm H2O. This is reduced to 59 ppm at 1,100°C, under otherwise identical conditions, suggesting a strong temperature dependence. At 1,350°C and 1.0 GPa water solubility in enstatite is 89 ppm, significantly lower than that at 2.0 GPa. In contrast water solubility in forsterite is essentially constant, being in the range 36–41 ppm for all conditions studied. These data give partition coefficients in the range 2.28–3.31 for all experiments at 1,350°C and 1.34 for one experiment at 1,100°C. The incorporation of Al2O3 in enstatite modifies the OH stretching spectrum in a systematic way, and slightly increases the water solubility.  相似文献   

8.
Fractal-like adsorption kinetics of Pb^2＋ in rocks   总被引：1，自引：0，他引：1  
The adsorption kinetics of Pb^2＋ in rocks has been studied using ion selective electrodes and atomic absorption spectrophotometer. The results showed that the adsorption process is a fractal-like reaction. The adsorption rate was relatively high before 30 minutes, and then dropped. The saturated adsorption capacity （a） of Pb^2＋ and kinetic parameters （b, a, D and k） increased with increasing initial concentrations of Pb^2＋. These parameters （except a） decreased while Na^＋ was present in the solution. Furthermore, the smaller the rocks were in grain size, the bigger these kinetic parameters would be, though the parameter a was almost constant.  相似文献   

9.
This paper studies the CO2 distribution of soil atmosphere in the Shilin National Park. The measurement sites were chosen according to different topographic features and different vegetations. Seven measurement sites on 3 cross sections were chosen to pass through 3 karstic depressions or on the slopes of depressions. All measurement results show soils with pH values lower than 7.0 (from 5.4 to 6.6). There are 2 cases for the pH values of soil in different topographic features: the pH values of 2 profiles on the ridges or upper slopes of depressions are lower than those in the depressions; and the pH values of 2 soil profiles on the slopes of depressions are higher than those in the depressions. Most samples show relatively low humidity and CO2 contents on the ridges or slopes of depressions compared with soil profiles in the depressions. High CO2 contents occur at depths from -40 to -80 cm and high and dense grassland shows high CO2 contents in the soil atmosphere. Grass roots may grow and are distribu  相似文献   

10.
INTRODUCTIONThermohaline circulation(THC)is normally de-fined as the density-driven global-scale oceanic circu-lation,which flows northwardin the upper layer andsouthward in the deeper layer in the Atlantic.Itplays ani mportant role in the global meridional heatand the freshwater transports(Marotzke,2000).Thus,changes in the THC alter the global oceanheat transport and affect the global cli mate(Broeck-er,1991).The increase in the concentration of greenhousegases will reduce the effici…  相似文献   

11.
A number of different impurities are located in the open channels of natural beryl crystals. The rare Maxixe beryl contains an unusual amount of NO2. The isoelectronic CO2 − radical is found in the irradiated Maxixe-type beryl. The NO2 radicals are distributed in the Be–Al plane of the crystal, with the nitrogen atom close to the oxygens of the beryl cavity wall. These oxygens repel the negative CO2 − radical, which is located at the center of the beryl cavity and rotates around its O–O axis, which is parallel to the crystal c-axis. When there is a nearby alkali ion at the center of the beryl channel, it reorients the CO2 − radical so that its bisector is parallel to the c-axis and points toward the positive ion. Different signals are analyzed for Li+, Na+, and another counter-ion, which probably is Cs+. The related NO3 and CO3 − radicals are the color centers in the investigated deep blue beryls. The slow decay of the color, which makes these beryls useless as gem stones, is related to the decay of the hydrogen atoms which are present in these crystals. Evidence is given that NO3 is created in Maxixe beryl by a natural process, while CO3 − in Maxixe-type beryl has been created by irradiation. The temperature dependence of the EPR signals of these two radicals was investigated, but a definitive proof that they rotate at the center of the beryl cavity could not be given. EPR signals from some other radicals in beryl have been observed and described.  相似文献   

12.
Saturation index with respect to calcite (SIc) and equilibrium CO2 partial pressure are important parameters to study groundwater in limestone aquifers. Aside from their use in time series, CO2 and SIc are used to estimate the baseline of CO2 in the vadose zone. The objective of this paper is to present conceptual examples on the use of the CO2–SIc relationship to have new information from usual parameters. Case study was considered as an example of use from Cussac site, a limestone aquifer in southwest of France. The result showed that CO2 baseline in unsaturated zone is found close to 25,000 ± 1,000 ppm.  相似文献   

13.
  相似文献   

14.
We present observations of H2O maser emission from the complex region of active star formation Sgr B2 performed in 2005–2012. The observations were carried out with the 22-m radio telescope of the Pushchino Radio Astronomy Observatory. Seven flares with flux densities higher than 1000 Jy were detected. The flares occurred in all three main sites of star formation in Sgr B2, N,M, and S. The highest peak flux densities were 3200 Jy (60.9 km/s), 2350 Jy (69.4 km/s), and 7300 Jy (69.3 km/s) in N, M, and S, respectively. This last flare was the strongest during our monitoring campaign from 1982 to 2012, both in S and in the entire Sgr B2 complex. Possible associations of the flares were determined. High-velocity, short-lived emission was detected at 124–128 km/s. Emission at 127 km/s with a flux density of 23 Jy is associated with region M. Emission at 80.6 and 84.6 km/s, at radial velocities higher than those observed previously, was detected in region S.  相似文献   

15.
In order to elucidate the solution behavior of carbon and hydrogen in iron-bearing magmatic melts in equilibrium with a metallic iron phase and graphite at oxygen fugacity (fO2) values 2–5 orders of magnitude below the iron-wustite buffer equilibrium, fO2 (IW), experiments were carried out at 4 GPa and 1550°C with melts of FeO-Na2O-SiO2-Al2O3 compositions. Melt reduction in response to an fO2 decrease was accompanied by a decrease in FeO content. The values of fO2 in the experiments were determined on the basis of equilibrium between Fe-C-Si alloy and silicate liquid. Infrared and Raman spectroscopy showed that carbon compounds are formed in FeO-Na2O-SiO2-Al2O3 melts: CH4 molecules, CH3 complexes (Si-O-CH3), and complexes with double C=O bonds. The content of CO2 molecules and carbonate ions (CO 3 2? ) is very low. In addition to carbon-bearing compounds, dissolved hydrogen occurs in melt as H2 and H2O molecules and OH? groups. The spectral characteristics of FeO-Na2O-SiO2-Al2O3 glasses indicate the occurrence of redox reactions in the melt, which are accompanied at decreasing fO2 by a significant decrease in H2O and OH?, a slight decrease in H2, and a significant concomitant increase in CH4 content. The content of species with the double C=O bond increases considerably at decreasing fO2 and reaches a maximum at ΔlogfO2(IW) = ?3. According to the obtained IR spectra, the total water content (OH? + H2O) in the glasses is 1.2–5.8 wt % and decreases with decreasing fO2. The high H2O contents are due largely to oxygen release related to FeO reduction in the melt. The total carbon content at high H2O (4.9–5.8 wt %) is approximately 0.4 wt %. The carbon content in liquid iron alloys depends on silicon content and, probably, oxygen solubility and ranges from 0.3 to 3.65 wt %. Low carbon contents were observed at a significant increase in Si content in liquid iron alloy, which may be as high as ～13 wt % at fO2 values 4–5 orders of magnitude below fO2(IW).  相似文献   

16.
This paper is devoted to experimental investigations of the hydro-mechanical–chemical coupling behaviour of sandstone in the context of CO2 storage in aquifers. We focused on the evolution of creep strain, the transport properties and the elastic modulus of sandstone under the effect of CO2–brine or CO2 alone. A summary of previous laboratory results is first presented, including mechanical, poromechanical and hydro-mechanical–chemical coupling properties. Tests were then performed to investigate the evolution of the creep strain and permeability during the injection of CO2–brine or CO2 alone. After the injection of CO2–brine or CO2 alone, an instantaneous volumetric dilatancy was observed due to the decrease in the effective confining stress. However, CO2 alone had a significant influence on the creep strain and permeability compared to the small influence of CO2–brine. This phenomenon can be attributed to the acceleration of the CO2–brine–rock reaction by the generation of carbonic acid induced by the dissolution of CO2 into the brine. The original indentation tests on samples after the CO2–brine–rock reaction were also performed and indicated that the elastic modulus decreased with an increasing reaction time. The present laboratory results can advance our knowledge of the hydro-mechanical–chemical coupling behaviour of sandstone in CO2 storage in aquifers.  相似文献   

17.
Single crystals of (Ca1–xSrx)2MgSi2O7 slightly doped with 1000 ppm Mn2+ and with x ranging from 0.04 to 0.32 were grown from the melt in a mirror furnace applying the Czochalski technique. Transmission electron microscopy (TEM) revealed incommensurately modulated structures at room-temperature for all compositions in accordance with earlier studies by electron paramagnetic resonance (EPR). Electron diffraction patterns clearly show satellite reflections typical for two-dimensional modulation, and their successive destabilization with increasing Sr content. The modulation is of tartan-like appearance. Beyond a Sr/(Sr+Ca) ratio of about 0.32 the synthesis of stable solid solution åkermanite type crystals was proved not to be feasible, indicating the existence of a miscibility gap in the Sr åkermanite system. As presumed from the diffuse scattering around the satellite reflections, and suggested more conclusively by crystallographic processing of high resolution EM images the Sr ions incorporated into the incommensurate crystal phase are distributed in an ordered fashion and are partly adapted to the displacive modulation of the pure åkermanite. This means, occupational modulation even makes a contribution to the overall modulation characteristics in (Ca1–xSrx)2 MgSi2O7.  相似文献   

18.
Cristobalite, a high temperature phase of silica, SiO2, undergoes a (metastable) first-order phase transition from a cubic, , to a tetragonal, P43212 (or P41212), structure at around 220° C. The cubic C9-type structure for -cristobalite (Wyckoff 1925) is improbable because of two stereochemically unfavorable features: a 180° Si-O-Si angle and an Si-O bond length of 1.54 Å, whereas the corresponding values in tetragonal -cristobalite are 146° and 1.609 Å respectively. The structure of the -phase is still controversial. To resolve this problem, a symmetry analysis of the (or P41212) transition in cristobalite has been carried out based on the Landau formalism and projection operator methods. The starting point is the ideal cubic ( ) C9-type structure with the unit cell dimension a (7.432 Å) slightly larger than the known a dimension (7.195 Å at 205° C) of -cristobalite, such that the Si-O-Si angle is still 180°, but the Si-O bond length is 1.609 Å. The six-component order parameter driving the phase transition transforms according to the X4 representation. The transition mechanism essentially involves a simultaneous translation and rotation of the silicate tetrahedra coupled along 110. A Landau free-energy expression is given as well as a listing of the three types of domains expected in -cristobalite from the transition. These domains are: (i) transformation twins from a loss of 3-fold axes, (ii) enantiomorphous twins from a loss of the inversion center, and (iii) antiphase domains from a loss of translation vectors 1/2 110 (FP). These domains are macroscopic and static in -cristobalite, and microscopic and dynamic in -cristobalite. The order parameter , couples with the strain components as 2, which initiates the structural fluctuations, thereby causing the domain configurations to dynamically interchange in the -phase. Hence, the - cristobalite transition is a fluctuation-induced first-order transition and the -phase is a dynamic average of -type domains.  相似文献   

19.
Model of Reflection Spectra of Rock Surface in 2π Space   总被引：5，自引：0，他引：5  
This paper deals with reflection spectra and polarized reflection spectra of 20 sorts of rock in 2π space, and then creates a model of reflection spectra of rock surface in 2π space. We measured the change of reflection and polarized reflection spectra as altering the incidence angle, vertex angle, azimuth angle, band and polarization. The results show that influence of the incidence angle on spectral curves is very strong. And when the vertex angle is constant, the horizontal azimuth polarizes rock spectra, and distorts the circular spectrum to become elliptic. The polarization influences the reflection intensity of rock spectra, but has no evident influence on the characteristics of wave forms of rock in 2π space. Therefore, we can describe the whole reflection spectral characteristics, including polarization, of rock surface in 2π space by measuring and calculating the e and p values in several key directions.  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