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1.
In the paper, we investigate the core width of superpartials and dissociated width of the 〈110〉{1–10} superdislocations in CaSiO3 perovskite under pressures of 30 and 100 GPa by using the modified P–N dislocation equation. Our results show that when taking into account the discrete effect correction, core width of superpartials and dissociated width become much wider, and both of them increase significantly with the increase of the superdislocation angle. Furthermore, it is found that the dissociated width and core width of superpartials are determined by value of the unstable stacking fault energy and antiphase boundary energy, which are independent of the position of unstable stacking energy. Interestingly, the Peierls stress of superpartials can be predicted by using the variational method to solve the modified P–N dislocation equation.  相似文献   

2.
Several new radiation defects with total electron spin S?=?1 occurring in electron-irradiated, synthetic ??-quartz have been observed by using electron paramagnetic resonance spectroscopy. These defects are considered to be biradicals, i.e., pairs of S?=?1/2 species. The concentration of these centers depends on the condition of the fast-electron irradiation. They have different decay behaviors that allow measurements of any individual species especially when it predominates over the others. The primary spin Hamiltonian parameter matrices g 1, g 2, D have now been determined for two similar defects, which herein are labeled $ E_{2}^{\prime \prime } $ and $ E_{4}^{\prime \prime } $ . Inter-electron distances estimated by using the magnetic dipole model, suggest that the structures of centers $ E_{2}^{\prime \prime } $ and $ E_{4}^{\prime \prime } $ both involve the unpaired electrons each located in orbitals of two silicon atoms next to a common oxygen vacancy but which have slightly different Si?CSi distances at 0.90 and 0.79?nm, respectively. This model is consistent with previous DFT calculations of the triplet configurations with local energetic minima. Observed decay behaviors suggest a transformation of centers $ E_{2,4}^{\prime \prime } $ to the analogous $ E_{1}^{\prime \prime } $ center. These triplet centers in quartz provide new insights into the structures of analogous defects in amorphous silica.  相似文献   

3.
In-situ powder diffraction measurements between 90 and 935?K on four anorthite-rich plagioclase samples (An100, An96Ab4, An89Ab11 and An78Ab22) were used to determine the detailed evolution of these samples through the $I \overline{1} $ $P \overline{1} $ phase transition. The c-type reflections indicative of $P \overline{1} $ symmetry were detected only in An100, An96Ab4, whereas deviations in the evolution of the unit-cell parameters with temperature were observed in all samples, most prominently in the β unit-cell angle. The c-type reflections disappear at ~510 and ~425?K in An100 and An96Ab4 respectively, and their intensity decreases according to a tricritical trend $ I^{2} \propto \left( {T - T_{\text{c}} } \right) $ . The cell parameter changes were used to determine the spontaneous strains arising from the transition which were modelled with Landau theory, allowing for low-temperature quantum saturation, in order to determine the thermodynamic behaviour. In An100 tricritical behaviour was observed [T c?=?512.7(4)?K; θs?=?394(4)] in good agreement with previous studies, and the c-type superlattice reflections indicative of $P \overline{1} $ symmetry persist up to the T c determined from the spontaneous strain, and then disappear. The evolution of the spontaneous strain in An96Ab4 is tricritical at low temperatures [T c?=?459(1) K, θs?=?396(5)] up to the temperature of disappearance of c-type reflections, but becomes second order beyond ~440?K. In An89Ab11 the strain displays second-order behaviour throughout [T c?=?500(1) and θs?=?212(5)], and the c-type reflections are not detected in the powder diffraction patterns at any temperature. The apparent discrepancy between the absence of c-type reflections in temperature ranges where the cell parameters display significant spontaneous strain is resolved through consideration of the sizes of the anti-phase domains within the crystals. It is deduced that the tricritical phase transition occurs in well-ordered crystals with large domains in which the behavior of individual domains is dominant (i.e. in pure anorthite) or where the $P \overline{1} $ distortions within the domains are large enough to dominate the structural coherency strains between the domains. When both the magnitude of the $P \overline{1} $ pattern of displacements of the tetrahedral framework become smaller and the influence of the structural coherency between anti-phase domains becomes significant, the thermodynamic behavior becomes 2nd-order in character, the c-type reflections disappear, and the orientation of the spontaneous strain changes.  相似文献   

4.
Oxygen isotope ratios (\(^{18}\hbox {O}/^{16}\hbox {O}\)) of surface seawater and rainwater samples from the Indian Ocean region (10°N–60°S) during austral summer collected onboard ORV Sagar Nidhi during 2011–2013 have been measured along with salinity, sea surface temperature and relative humidity. The rainwater is isotopically lighter (by \(4.6\pm 2.7\permille )\) compared to the equilibrium condensation of the vapour arising from the seawater at the ambient condition. The isotopic composition of the vapour at high altitude responsible for the rain formation at the sampling location is estimated from a global atmospheric water isotope model (IsoGSM2). The apparent deficit of \(\sim \)5\(\permille \) can be explained by invoking a high degree of rainout (on average, about 70% of the overhead atmospheric moisture) during transport of the source vapour to the sampling location undergoing a Rayleigh fractionation. The required rainout fraction is higher (\(\sim \)80%) in the latitude belt 40°–60°S compared to the equatorial belt (\(\sim \)60%). The pattern of variation in the rainout fraction with latitude is consistent with the well-known evaporation/precipitation processes in the Indian Ocean.  相似文献   

5.
Mathematical Geosciences - A weighted compressed sensing (WCS) algorithm is proposed for the problem of channelized facies reconstruction from pixel-based measurements. This strategy integrates...  相似文献   

6.
Mineralization of groundwater in volcanic aquifers is partly acquired through silicates weathering. This alteration depends on the dissolution of atmospheric, biogenic, or mantellic gaseous CO2 whose contributions may depend on substratum geology, surface features, and lava flow hydrological functionings. Investigations of $ {\text{P}}_{{{\text{CO}}_{ 2} {\text{eq}}}} $ and δ13CTDIC (total dissolved inorganic carbon) on various spatiotemporal scales in the unsaturated and saturated zones of volcanic flows of the Argnat basin (French Massif Central) have been carried out to identify the carbon sources in the system. Mantellic sources are related to faults promoting CO2 uplift from the mantle to the saturated zone. The contribution of this source is counterbalanced by infiltration of water through the unsaturated zone, accompanied by dissolution of soil CO2 or even atmospheric CO2 during cold periods. Monitoring and modeling of δ13CTDIC in the unsaturated zone shows that both $ {\text{P}}_{{{\text{CO}}_{ 2} {\text{eq}}}} $ and δ13CTDIC are controlled by air temperature which influences soil respiration and soil-atmosphere CO2 exchanges. The internal geometry of volcanic lava flows controls water patterns from the unsaturated zone to saturated zone and thus may explain δ13C heterogeneity in the saturated zone at the basin scale.  相似文献   

7.
8.
It is shown that the gas and water phases of the thermal nitrogen–methane waters in the Talysh fold zone of the Lesser Caucasus mountain system contain helium and strontium with mantle isotope signatures (3Не/4Не from 200 × 10–8 to 401 × 10–8 and 87Sr/86Sr from 0.70490 to 0.70562). At the same time, clear signs of the mantle component in other gases (nitrogen, methane, and carbon dioxide) are absent. The δ15N value in nitrogen varies from +0.3 to +1.7‰, methane is mainly characterized by δ13C from–57.4 to–38.0‰, while δ13C(CО2) varies from–24.4 to–11.3‰. An increase of the CО2 content is accompanied by the decrease of δ13C in CО2, against the background of increasing SO4 content in the salt composition of waters. This indicates a microbial nature of CO2 in the studied gases. Thus, the presence of mantle helium and strontium in the thermal waters is likely related to their leaching from the Pleogene–Neogene host volcanic rocks. The studies of the oxygen and hydrogen isotope composition in water revealed quite different mechanisms for the formation of cold and thermal waters of the region. The cold waters are mainly fed by local infiltration, whereas the feeding of thermal nitrogen–methane waters is strongly provided by transit atmogenic waters (>50%), which are formed in the mountain ranges at altitudes no less than 1600 m and spaced at 20–40 km or more from the thermal discharge sites.  相似文献   

9.
Hao  Guocheng  Wang  Panpan  Hu  Xiangyun  Guo  Juan  Wang  Guocheng  Tan  Songyuan 《Natural Hazards》2022,110(3):1869-1885
Natural Hazards - The Earth's natural pulse electromagnetic field (ENPEMF) signal, is generally considered to be a nonlinear or nonstationary signal received from our instrument, placed on the...  相似文献   

10.
Geology of Ore Deposits - The status of lazurite as a valid mineral species has been confirmed. The neotype specimen from the Malaya Bystraya gem lazurite deposit, Baikal Lake area has been studied...  相似文献   

11.
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   

12.
《Chemical Geology》2003,193(1-2):93-107
In situ atomic force microscopy (AFM) experiments, scanning electron microscopy (SEM) imaging and composition analysis, and X-ray diffraction have provided information about the growth, dissolution and transformation processes promoted by Sr2+–Ca2+–CO32− aqueous solutions in contact with calcite {101̄4} surfaces. Experiments have shown a wide variety of surface phenomena, such as the influence of the Sr-bearing newly-formed surface on the subsequent growth (template effect), the growth and subsequent dissolution of surfaces and the nucleation of secondary three-dimensional nuclei on calcite surfaces. These phenomena reveal the metastability of the crystallisation system and are a consequence of the interplay between thermodynamics (the relative stability of the two calcite and aragonite structure solid solutions that can be formed), supersaturation of the aqueous solution with respect to the two possible solid solutions, and the crystallographic control of the surfaces on cation incorporation.  相似文献   

13.
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   

14.
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   

15.
In situ high-temperature synchrotron radiation powder diffraction patterns were taken from room temperature to T = 740°C from synthetic feldspars along the join CaAl2Si2O8–SrAl2Si2O8 (An–SrF). Three samples of composition An95SrF5, An90SrF10 and An85SrF15 were investigated, and the evolution of cell parameters with T was determined by Rietveld analysis of powder X-ray diffraction patterns. The high-temperature $P\bar 1{\text{-}}I\bar 1$ phase transition, previously observed with T c = 241°C in anorthite, was found in An95SrF5, An90SrF10 and An85SrF15 feldspars at T c = 233(5)°, 195(2)° and 174(2)°C respectively. The transition was revealed by the disappearance of critical reflections and variations in the rate of change of cell parameters with temperature. A significant, although small (between 0.0025 and 0.0012 at room temperature), spontaneous strain could be measured, allowing the thermodynamic behaviour of the transition to be modelled. A second-order trend for An90SrF10 and An85SrF15 [β = 0.504(7) and 0.505(7) respectively] or nearly second-order for An95SrF5[β = 0.458(4)] was observed in contrast with tricritical behaviour of end member anorthite. An extrapolation of the T c versus composition to room temperature indicates that the critical composition for the $P\bar 1$ phase is An60SrF40.  相似文献   

16.
The impact of CO2 sequestration on the host formation is an issue occurring over geologic time. Laboratory tests can provide important results to investigate this matter but have limitations due to a relatively short timeline. Based on literature review and core sample observation, naturally occurred geological phenomena, stylolites are studied in this paper for understanding CO2 sequestration in deep carbonate formations. Stylolites are distinctive and pervasive structures in carbonates that are related to water-assisted pressure solution. Pressure solution involving stylolitization is thought to be the main mechanism of compaction and cementation for many carbonates. In parallel, CO2 sequestration in carbonate formation involves extensive chemical reactions among water, CO2 and rock matrix, favoring chemical compaction as a consequence. An analogue between stylolites and CO2 sequestration induced formation heterogeneity exists in the sense of chemical compaction, as both pressure solution in stylolites and CO2 enriched solution in CO2 sequestration in carbonate formations may all introduce abnormal porous regions. The shear and/or tension fractures associated with stylolites zones may develop vertically or sub-vertically; all these give us alert for long-term safety of CO2 sequestration. Thus a study of stylolites will help to understand the CO2 sequestration in deep carbonate formation in the long run.  相似文献   

17.
18.
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   

19.
δ18 O and δ13C of G.sacculifer have been measured in five cores from the northern Indian Ocean. In addition, high resolution analysis (1 to 2 cm) was performed on one core (SK-20-185) for both δ18O and gd13C in five species of planktonic foraminifera. CaCO3 variation was measured in two cores. The results, presented here, show that
–  • the summer monsoon was weaker during 18 ka and was stronger during 9 ka, relative to modern conditions;
–  • δ13C variations are consistent with independent evidence that shows that during the last glacial maximum (LGM; 18 ka) the upwelling was reduced while during 9 ka it was vigorous;
–  • calculation of CaCO3 flux shows that the LGM was characterized by low biogenic productivity in the Arabian Sea while during the Holocene productivity increased by ∼65%, as a direct consequence of the changes in upwelling. Similar changes (of lesser magnitude) are also seen in the equatorial Indian Ocean. The amount of terrigenous input into the Arabian Sea doubled during LGM possibly due to the higher erosion rate along the west coast.
–  • δ18O values indicate that the Arabian Sea was saltier by 1 to 2%o during LGM. The northern part was dominated by evaporation while in the equatorial part there was an increased precipitation.
  相似文献   

20.
《Chemical Geology》2004,203(1-2):139-151
Aragonite is precipitated by a new CO2-diffusion technique from a Ca2+–Mg2+–Cl solution between 10 and 50 °C. Crystallisation of aragonite instead of calcite occurs by maintaining a [Mg2+]/[Ca2+] ratio of 2 in the fluid. The dissolved inorganic carbon (DIC) is received by diffusion of CO2 through a polyethylene membrane (diffusion coefficient: DCO2=10−6.4 cm2 s−1 at 19 °C). It is suggested that significant amounts of DIC may be transferred by diffusion of CO2 in natural systems if the CO2 gradient is high. The CO2-diffusion technique is used as a kind of simple mixed flow reactor for the co-precipitation of barium and strontium with aragonite. The distribution coefficients of Ba2+ and Sr2+ decrease from 10 to 50 °C according to DBa,a*=2.42−0.03595T (°C) and DSr,a*=1.32−0.005091T (°C). At 25 °C, the distribution coefficients are DBa,a*=1.5±0.1 and DSr,a*=1.19±0.03. The effect of temperature on DBa,a* is about one order of magnitude higher versus that on DSr,a*. Thus, Ba2+ may be a potential paleotemperature indicator if the composition of the solution is known.  相似文献   

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