This work presents new experimental results on the kinetics of mineral dissolution in near-critical and supercritical water in a temperature range (T) from 25 to 400°C and a constant pressure of 23 MPa. Kinetic e...This work presents new experimental results on the kinetics of mineral dissolution in near-critical and supercritical water in a temperature range (T) from 25 to 400°C and a constant pressure of 23 MPa. Kinetic experiments were carried out by using a flow reactor (packed bed reactor) of an open system. The dissolution rates of albite and magnetite were measured under these experimental conditions. Na, Al and Si release rates for albite dissolution in water were measured as a function of the temperature and flow velocity in the reaction system. The maximum release rates of Na, Al and Si of albite dissolution in the hydrothermal flow systems under different flow velocities were always obtained at 300°C, that is to say, the maximum albite dissolution rates in the flow systems, regardless of different flow rates, were repeatedly measured at 300°C. Results indicate a wide fluctuation in albite dissolution rates occurring close to the critical point of water. The dissolution rates increased when the temperatures increased from 25 to 300°C and decreased when the temperatures increase from 300 to 400°C. At some flow velocities, the dissolution rates rose as the temperature surpassed 374°C. Albite dissolution was incongruent in water at most temperatures. It was only at 300°C that albite dissolution was congruent. The albite dissolution from 25 to 300°C (at 23 MPa) will change from incongruent to congruent, whereas from subcritical 300 to 400°C (at 23 MPa), the dissolution will change from congruent to incongruent. The release ratio of Al/Si (or Na/Si) is positive at T<300°C, and it is negative at T>300°C. The dissolution rates of magnetite in water increased with increasing T until T at the critical point of water or around it. The authors believe that this is caused by the wide fluctuations in water properties under the conditions from the near-critical to supercritical state.展开更多
The phase relation and solution structure of water and NaCl aqueous solution have been observed and examined by using the hydrothermal diamond anvil cell (HDAC) at elevated temperatures and pressures and the in situ F...The phase relation and solution structure of water and NaCl aqueous solution have been observed and examined by using the hydrothermal diamond anvil cell (HDAC) at elevated temperatures and pressures and the in situ FT-IR spectroscopy. The temperature of observations ranges from 25 to 850°C and the pressure up to 10 or 30 kb. At first, we observed the phase transition process from halite+liquid+vapour (H+L+V) to L+H, then to L (or supercritical fluid, SCF), and another path: H+L+V→L+V→L (or SCF) in heating process. By means of the visual microscope, the authors found that in the L+V immiscibility field L+V exhibits an ordered structure, i.e. a large visual cluster of solvent around ions. The liquid phase is manifested by vapour bubbles. When phase transitions are observed, the authors examined their infrared spectra by using the FT-IR microscopy simultaneously. In the case of the phase transition from liquid (L) to liquid + vapor (L+V) immisciblity field of NaCl solutions, a sudden change (strong frequency shift) of infrared spectra of the aqueous solution is observed near the critical temperature of water as the temperature is raised from 25 to 650°C. The frequency of the maximum intensity of OH symmetric and asymmetric vibration varies with respect to temperature. The sharp peak of the OH stretching vibration of the maximum intensity appears in an interval from 300 to 400°C. It is indicated that the hydrogen bonding network is weakened and broken at last near the critical point of water, which causes the aqueous solution to become more associated. Besides, a pressure indicator (a mineral or compound) was introduced to the HDAC.展开更多
基金We would like to thank the Ministry of Science and Technology and the Ministry of Land and Resources for supporting our projectThe experimental results presented in this paper were obtained with the financial support of GTB basic research fund 9501115+1 种基金the“Climbing Project”95-Pre-39,G1999043212National Natural ScienceFoundation of China grant 29673008.
文摘This work presents new experimental results on the kinetics of mineral dissolution in near-critical and supercritical water in a temperature range (T) from 25 to 400°C and a constant pressure of 23 MPa. Kinetic experiments were carried out by using a flow reactor (packed bed reactor) of an open system. The dissolution rates of albite and magnetite were measured under these experimental conditions. Na, Al and Si release rates for albite dissolution in water were measured as a function of the temperature and flow velocity in the reaction system. The maximum release rates of Na, Al and Si of albite dissolution in the hydrothermal flow systems under different flow velocities were always obtained at 300°C, that is to say, the maximum albite dissolution rates in the flow systems, regardless of different flow rates, were repeatedly measured at 300°C. Results indicate a wide fluctuation in albite dissolution rates occurring close to the critical point of water. The dissolution rates increased when the temperatures increased from 25 to 300°C and decreased when the temperatures increase from 300 to 400°C. At some flow velocities, the dissolution rates rose as the temperature surpassed 374°C. Albite dissolution was incongruent in water at most temperatures. It was only at 300°C that albite dissolution was congruent. The albite dissolution from 25 to 300°C (at 23 MPa) will change from incongruent to congruent, whereas from subcritical 300 to 400°C (at 23 MPa), the dissolution will change from congruent to incongruent. The release ratio of Al/Si (or Na/Si) is positive at T<300°C, and it is negative at T>300°C. The dissolution rates of magnetite in water increased with increasing T until T at the critical point of water or around it. The authors believe that this is caused by the wide fluctuations in water properties under the conditions from the near-critical to supercritical state.
基金The Ministry of Science and Technology and the Ministry of Land and Resources also supported this study,basic research fund(9501115)Chinese NSF 29673008 supported this project+1 种基金project 95-pre39 G1999043212special suport fromThe Ministry Science and Technology.
文摘The phase relation and solution structure of water and NaCl aqueous solution have been observed and examined by using the hydrothermal diamond anvil cell (HDAC) at elevated temperatures and pressures and the in situ FT-IR spectroscopy. The temperature of observations ranges from 25 to 850°C and the pressure up to 10 or 30 kb. At first, we observed the phase transition process from halite+liquid+vapour (H+L+V) to L+H, then to L (or supercritical fluid, SCF), and another path: H+L+V→L+V→L (or SCF) in heating process. By means of the visual microscope, the authors found that in the L+V immiscibility field L+V exhibits an ordered structure, i.e. a large visual cluster of solvent around ions. The liquid phase is manifested by vapour bubbles. When phase transitions are observed, the authors examined their infrared spectra by using the FT-IR microscopy simultaneously. In the case of the phase transition from liquid (L) to liquid + vapor (L+V) immisciblity field of NaCl solutions, a sudden change (strong frequency shift) of infrared spectra of the aqueous solution is observed near the critical temperature of water as the temperature is raised from 25 to 650°C. The frequency of the maximum intensity of OH symmetric and asymmetric vibration varies with respect to temperature. The sharp peak of the OH stretching vibration of the maximum intensity appears in an interval from 300 to 400°C. It is indicated that the hydrogen bonding network is weakened and broken at last near the critical point of water, which causes the aqueous solution to become more associated. Besides, a pressure indicator (a mineral or compound) was introduced to the HDAC.
