Ultrahigh-pressure（UHP） metamorphic rocks are distinctive products of crustal deep subduction,and are mainly exposed in continental subduction-collision terranes. UHP slices of continental crust are usually involved...Ultrahigh-pressure（UHP） metamorphic rocks are distinctive products of crustal deep subduction,and are mainly exposed in continental subduction-collision terranes. UHP slices of continental crust are usually involved in multistage exhumation and partial melting, which has obvious influence on the rheological features of the rocks, and thus significantly affect the dynamic behavior of subducted slices. Moreover,partial melting of UHP rocks have significant influence on element mobility and related isotope behavior within continental subduction zones, which is in turn crucial to chemical differentiation of the continental crust and to crust-mantle interaction.Partial melting can occur before, during or after the peak metamorphism of UHP rocks. Post-peak decompression melting has been better constrained by remelting experiments; however, because of multiple stages of decompression, retrogression and deformation, evidence of former melts in UHP rocks is often erased. Field evidence is among the most reliable criteria to infer partial melting. Glass and nanogranitoid inclusions are generally considered conclusive petrographic evidence. The residual assemblages after melt extraction are also significant to indicate partial melting in some cases. Besides field and petrographic evidence, bulk-rock and zircon trace-element geochemical features are also effective tools for recognizing partial melting of UHP rocks. Phase equilibrium modeling is an important petrological tool that is becoming more and more popular in P-T estimation of the evolution of metamorphic rocks; by taking into account the activity model of silicate melt, it can predict when partial melting occurred if the P-T path of a given rock is provided.UHP silicate melt is commonly leucogranitic and peraluminous in composition with high SiO_2,low MgO, FeO, MnO, TiO_2 and CaO, and variable K_2 O and Na_2 O contents. Mineralogy of nanogranites found in UHP rocks mainly consists of plagioclase ＋ K-feldspar ＋ quartz, plagioclase being commonly albite-rich.Tr展开更多
研究区位于大别造山带晓天—磨子潭断裂附近(图1)。晓天—磨子潭断裂是北大别杂岩带和北淮阳带之间的边界断裂,部分研究者认为该断裂带为华北板块和扬子板块之间的缝合线以及大别山超高压变质岩折返的重要边界(Faure et al.,1999;徐树桐...研究区位于大别造山带晓天—磨子潭断裂附近(图1)。晓天—磨子潭断裂是北大别杂岩带和北淮阳带之间的边界断裂,部分研究者认为该断裂带为华北板块和扬子板块之间的缝合线以及大别山超高压变质岩折返的重要边界(Faure et al.,1999;徐树桐等,2002),但对此仍存在较大争议。展开更多
To study the feasibility of CO2 geological sequestration,it is needed to understand the complicated mul- tiple-phase equilibrium and the densities of aqueous solution with CO2 and multi-ions under wide geological cond...To study the feasibility of CO2 geological sequestration,it is needed to understand the complicated mul- tiple-phase equilibrium and the densities of aqueous solution with CO2 and multi-ions under wide geological condi- tions(273.15—473.15K,0—60MPa),which are also essential for designing separation equipments in chemical or oil-related industries.For this purpose,studies on the relevant phase equilibria and densities are reviewed and ana- lyzed and the method to improve or modify the existing model is suggested in order to obtain more reliable pre- dictions in a wide temperature and pressure range.Besides,three different models(the electrolyte non random two-liquid(ELECNRTL),the electrolyte NRTL combining with Helgeson model(ENRTL-HG),Pitzer activity co- efficient model combining with Helgeson model(PITZ-HG))are used to calculate the vapor-liquid phase equilib- rium of CO2-H2O and CO2-H2O-NaCl systems.For CO2-H2O system,the calculation results agree with the experi- mental data very well at low and medium pressure(0—20MPa),but there are great discrepancies above 20MPa.For the water content at 473.15K,the calculated results agree with the experimental data quite well.For the CO2-H2O-NaCl system,the PITZ-HG model show better results than ELECNRTL and ENRTL-HG models at the NaCl concentration of 0.52mol·L -1 .Bur for the NaCl concentration of 3.997mol·L -1 ,using the ELECNRTL and ENRTL-HG models gives better results than using the PITZ-HG model.It is shown that available experimental data and the thermodynamic calculations can satisfy the needs of the calculation of the sequestration capacity in the temperature and pressure range for disposal of CO2 in deep saline aquifers.More experimental data and more accu- rate thermodynamic calculations are needed in high temperature and pressure ranges(above 398.15K and 31.5MPa).展开更多
Due to the density contrast between the hydrate and methane gas,the pore pressure is accumulated in the sediment during the decomposition process of methane hydrate.This accumulation of pore pressure decreases the mag...Due to the density contrast between the hydrate and methane gas,the pore pressure is accumulated in the sediment during the decomposition process of methane hydrate.This accumulation of pore pressure decreases the magnitude of effective stress,further triggering potential geological disasters such as landslide.This paper establishes a theoretical framework to investigate the evolution of fluid pressure in the hydrate-bearing sediments during the decomposition process.This model consists of two parts:an unsaturated thermo-poromechanical constitutive law as well as a phase equilibrium equation.Compared with the existing studies,the present work incorporates the effect of pore volume change into the pressure built-up model.In addition,the capillary effect is considered,which plays a nontrivial role in fine-grained sediments.Based on this model,the evolution of fluid pressure is investigated in undrained conditions.It is shown that four mechanisms mainly contribute to the pressure built-up:the density contrast between decomposing hydrate and producing fluid,the variation of pore volume,the compaction of hydrate due to variation of capillary pressure,and the thermal deformation of pore constituents induced by temperature change.Among these mechanisms,the density contrast dominates the pore pressure accumulation.Under the combined effect of these contributions,the evolution of fluid pressure exhibits a strong nonlinearity during the decomposition process and can reach up to dozens of mega Pascal.Nevertheless,this high-level pressure built-up results in a significant tensile strain,yielding potential fracturing of the sediment.展开更多
A high temperature equilibration experiment was carried out to investigate the effect of oxygen partial pres- sure on the phase equilibria and liquidus in CaO-Al2O3- FeOx system with the intermediate oxygen partial pr...A high temperature equilibration experiment was carried out to investigate the effect of oxygen partial pres- sure on the phase equilibria and liquidus in CaO-Al2O3- FeOx system with the intermediate oxygen partial pressures of 10.13 Pa and 1.01 × 10^-3 Pa. The equilibrated phases and their compositions of the quenched samples were analyzed by using SEM/EPMA （Scanning Electron Microscope/Electron Probe Micro Analysis） and XRD （X Ray Diffraction）. The phase equilibrium results include two cases, the two phase coexistence and the three-phase coexistence in the high Al2O3 region with oxygen partial pressure of either 10.13 Pa or 1.01 × 10^-3 Pa. Effects of oxygen partial pressure and temperature on the liquidus along the primary phase fields of CaO · Al2O3 and CaO · 2Al2O3 were nota hle. With the decrease of oxygen partial pressure, the liquid area expands and the liquidus of CaO · Al2O3 and CaO · 2Al2O3 primary fields moves to the Al2O3-FeOx region. On the other hand, the liquid area of CaO Al2O3-FeOx sys tem extends extremely to the high Al2O3 region with the temperature increasing from 1 400 to 1 500℃, especially at lower oxygen partial pressure. The present experiment results are in good agreement with the calculated ones by FactSage.展开更多
基金financially supported by the National Basic Research Program of China (Grant No. 2015CB856104)the National Natural Science Foundation of China (Grant No. 41273036)
文摘Ultrahigh-pressure（UHP） metamorphic rocks are distinctive products of crustal deep subduction,and are mainly exposed in continental subduction-collision terranes. UHP slices of continental crust are usually involved in multistage exhumation and partial melting, which has obvious influence on the rheological features of the rocks, and thus significantly affect the dynamic behavior of subducted slices. Moreover,partial melting of UHP rocks have significant influence on element mobility and related isotope behavior within continental subduction zones, which is in turn crucial to chemical differentiation of the continental crust and to crust-mantle interaction.Partial melting can occur before, during or after the peak metamorphism of UHP rocks. Post-peak decompression melting has been better constrained by remelting experiments; however, because of multiple stages of decompression, retrogression and deformation, evidence of former melts in UHP rocks is often erased. Field evidence is among the most reliable criteria to infer partial melting. Glass and nanogranitoid inclusions are generally considered conclusive petrographic evidence. The residual assemblages after melt extraction are also significant to indicate partial melting in some cases. Besides field and petrographic evidence, bulk-rock and zircon trace-element geochemical features are also effective tools for recognizing partial melting of UHP rocks. Phase equilibrium modeling is an important petrological tool that is becoming more and more popular in P-T estimation of the evolution of metamorphic rocks; by taking into account the activity model of silicate melt, it can predict when partial melting occurred if the P-T path of a given rock is provided.UHP silicate melt is commonly leucogranitic and peraluminous in composition with high SiO_2,low MgO, FeO, MnO, TiO_2 and CaO, and variable K_2 O and Na_2 O contents. Mineralogy of nanogranites found in UHP rocks mainly consists of plagioclase ＋ K-feldspar ＋ quartz, plagioclase being commonly albite-rich.Tr
基金Supported by the Chinese National Science Foundation for 0utstanding Young Scholars （No.29925616）, the Joint Research Fund for Young Scholars in Hong Kong and Abroad （No.20428606）, the National Natural Science Foundation of China （Nos.20236010, 20246002, 20376032）, the Natural Science Foundation of Jiangsu Province （Nos.BK2002016, BK2004215） and Chinese National Fundamental Research Development Program （973 Program： 2003CB615700）.
文摘To study the feasibility of CO2 geological sequestration,it is needed to understand the complicated mul- tiple-phase equilibrium and the densities of aqueous solution with CO2 and multi-ions under wide geological condi- tions(273.15—473.15K,0—60MPa),which are also essential for designing separation equipments in chemical or oil-related industries.For this purpose,studies on the relevant phase equilibria and densities are reviewed and ana- lyzed and the method to improve or modify the existing model is suggested in order to obtain more reliable pre- dictions in a wide temperature and pressure range.Besides,three different models(the electrolyte non random two-liquid(ELECNRTL),the electrolyte NRTL combining with Helgeson model(ENRTL-HG),Pitzer activity co- efficient model combining with Helgeson model(PITZ-HG))are used to calculate the vapor-liquid phase equilib- rium of CO2-H2O and CO2-H2O-NaCl systems.For CO2-H2O system,the calculation results agree with the experi- mental data very well at low and medium pressure(0—20MPa),but there are great discrepancies above 20MPa.For the water content at 473.15K,the calculated results agree with the experimental data quite well.For the CO2-H2O-NaCl system,the PITZ-HG model show better results than ELECNRTL and ENRTL-HG models at the NaCl concentration of 0.52mol·L -1 .Bur for the NaCl concentration of 3.997mol·L -1 ,using the ELECNRTL and ENRTL-HG models gives better results than using the PITZ-HG model.It is shown that available experimental data and the thermodynamic calculations can satisfy the needs of the calculation of the sequestration capacity in the temperature and pressure range for disposal of CO2 in deep saline aquifers.More experimental data and more accu- rate thermodynamic calculations are needed in high temperature and pressure ranges(above 398.15K and 31.5MPa).
基金The authors acknowledge that this work was supported by National Natural Science Foundation of China(U20B6005).
文摘Due to the density contrast between the hydrate and methane gas,the pore pressure is accumulated in the sediment during the decomposition process of methane hydrate.This accumulation of pore pressure decreases the magnitude of effective stress,further triggering potential geological disasters such as landslide.This paper establishes a theoretical framework to investigate the evolution of fluid pressure in the hydrate-bearing sediments during the decomposition process.This model consists of two parts:an unsaturated thermo-poromechanical constitutive law as well as a phase equilibrium equation.Compared with the existing studies,the present work incorporates the effect of pore volume change into the pressure built-up model.In addition,the capillary effect is considered,which plays a nontrivial role in fine-grained sediments.Based on this model,the evolution of fluid pressure is investigated in undrained conditions.It is shown that four mechanisms mainly contribute to the pressure built-up:the density contrast between decomposing hydrate and producing fluid,the variation of pore volume,the compaction of hydrate due to variation of capillary pressure,and the thermal deformation of pore constituents induced by temperature change.Among these mechanisms,the density contrast dominates the pore pressure accumulation.Under the combined effect of these contributions,the evolution of fluid pressure exhibits a strong nonlinearity during the decomposition process and can reach up to dozens of mega Pascal.Nevertheless,this high-level pressure built-up results in a significant tensile strain,yielding potential fracturing of the sediment.
基金Item Sponsored by National Natural Science Foundation of China(50974034,51074039)
文摘A high temperature equilibration experiment was carried out to investigate the effect of oxygen partial pres- sure on the phase equilibria and liquidus in CaO-Al2O3- FeOx system with the intermediate oxygen partial pressures of 10.13 Pa and 1.01 × 10^-3 Pa. The equilibrated phases and their compositions of the quenched samples were analyzed by using SEM/EPMA （Scanning Electron Microscope/Electron Probe Micro Analysis） and XRD （X Ray Diffraction）. The phase equilibrium results include two cases, the two phase coexistence and the three-phase coexistence in the high Al2O3 region with oxygen partial pressure of either 10.13 Pa or 1.01 × 10^-3 Pa. Effects of oxygen partial pressure and temperature on the liquidus along the primary phase fields of CaO · Al2O3 and CaO · 2Al2O3 were nota hle. With the decrease of oxygen partial pressure, the liquid area expands and the liquidus of CaO · Al2O3 and CaO · 2Al2O3 primary fields moves to the Al2O3-FeOx region. On the other hand, the liquid area of CaO Al2O3-FeOx sys tem extends extremely to the high Al2O3 region with the temperature increasing from 1 400 to 1 500℃, especially at lower oxygen partial pressure. The present experiment results are in good agreement with the calculated ones by FactSage.
