Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Hydrothermal Alteration Zoning and Kinetic Process of Mineral‐Water Interactions

View through CrossRef
AbstractThis study reports the kinetic experimental results of albite in water and in KCl solution at 22 MPa in the temperature range of 25 to 400°C. Kinetic experiments have been carried out in an open flow‐through reaction system (packed bed reactor). Albite dissolution is always incongruent in water at most temperatures, but becomes congruent at 300°C (close to the critical point 374°C). At temperatures from 25 to 300°C, the incongruent dissolution of albite is reflected by the fact that sodium and aluminum are easily dissolved into water, from 300 to 400°C it is reflected by silicon being more easily dissolved in water than Al and Na. Maximum albite dissolution rates in the flow hydrothermal systems have been repeatedly observed at 300°C, independent of flow rates.The kinetic experiments of albite dissolution in a KCl aqueous solution (0.1 mol KCl) indicate that the dissolution rate of albite increases with increasing temperature. Maximum silicon release rates of albite have been observed at 400°C, while maximum aluminum release rates of albite at 374°C. The reaction rates of albite also depend on the potassium concentration in the aqueous solution.These results can be used to interpret the mechanism for forming hydrothermal alteration. The kinetic experiments of mineral‐aqueous solutions interactions in the hydrothermal system from 25 to 400°C and at 22 MPa indicate that the formation of the feldspar‐mica‐kaolinite zoning occurring in some ore deposits may depend not only on the mineral stability but also on the kinetics of feldspar hydration, which is affected by the water property variation when crossing the critical point.
Title: Hydrothermal Alteration Zoning and Kinetic Process of Mineral‐Water Interactions
Description:
AbstractThis study reports the kinetic experimental results of albite in water and in KCl solution at 22 MPa in the temperature range of 25 to 400°C.
Kinetic experiments have been carried out in an open flow‐through reaction system (packed bed reactor).
Albite dissolution is always incongruent in water at most temperatures, but becomes congruent at 300°C (close to the critical point 374°C).
At temperatures from 25 to 300°C, the incongruent dissolution of albite is reflected by the fact that sodium and aluminum are easily dissolved into water, from 300 to 400°C it is reflected by silicon being more easily dissolved in water than Al and Na.
Maximum albite dissolution rates in the flow hydrothermal systems have been repeatedly observed at 300°C, independent of flow rates.
The kinetic experiments of albite dissolution in a KCl aqueous solution (0.
1 mol KCl) indicate that the dissolution rate of albite increases with increasing temperature.
Maximum silicon release rates of albite have been observed at 400°C, while maximum aluminum release rates of albite at 374°C.
The reaction rates of albite also depend on the potassium concentration in the aqueous solution.
These results can be used to interpret the mechanism for forming hydrothermal alteration.
The kinetic experiments of mineral‐aqueous solutions interactions in the hydrothermal system from 25 to 400°C and at 22 MPa indicate that the formation of the feldspar‐mica‐kaolinite zoning occurring in some ore deposits may depend not only on the mineral stability but also on the kinetics of feldspar hydration, which is affected by the water property variation when crossing the critical point.

Related Results

Zoning Report: Massachusetts
Zoning Report: Massachusetts
<div> Massachusetts is facing a housing affordability crisis. Rising home prices and rents from Cape Cod to the Berkshires are pushing long-time residents out of their commu...
Hydrothermal Alteration Processes of Xincheng Gold Deposit Jiaodong Peninsula, China: Constraints from Composition of Hydrothermal Rutile
Hydrothermal Alteration Processes of Xincheng Gold Deposit Jiaodong Peninsula, China: Constraints from Composition of Hydrothermal Rutile
Delineating the process of hydrothermal alteration is crucial for effectively enhancing exploration strategies and better understanding the gold mineralization process. Rutile, wit...
Origins and significance of alteration textures in hydrovolcanic products from active volcanoes
Origins and significance of alteration textures in hydrovolcanic products from active volcanoes
Abstract While mineralization processes in hydrothermal systems have been studied intensively from the viewpoint of economic geology, the composition, and textures of hydro...
Geology and hydrothermal alteration of the Fab lake region, Northwest Territories
Geology and hydrothermal alteration of the Fab lake region, Northwest Territories
Detailed mapping of the Fab Lake magnetite-group iron oxide-copper-gold (IOCG) system has defined an alteration footprint extending almost 10 by 5 km, with the long axis trending i...
Hydrothermal fluid signatures of the Yulong porphyry Cu-Mo deposit: Clues from the composition and U-Pb dating of W-bearing rutile
Hydrothermal fluid signatures of the Yulong porphyry Cu-Mo deposit: Clues from the composition and U-Pb dating of W-bearing rutile
AbstractHydrothermal rutile (TiO2) is a widely distributed accessory mineral in hydrothermal veins or alteration assemblages of porphyry deposits and provides important information...
Formation of various trace element zoning patterns in high-pressure metamorphic garnet
Formation of various trace element zoning patterns in high-pressure metamorphic garnet
Compositional zoning of trace elements in garnet serves as a valuable tool for reconstructing petrogenetic evolution, supplementing major element analyses. This is particularly app...
Hydrothermal Alteration and Mineralization of Middle Jurassic Dexing Porphyry Cu‐Mo Deposit, Southeast China
Hydrothermal Alteration and Mineralization of Middle Jurassic Dexing Porphyry Cu‐Mo Deposit, Southeast China
AbstractThe Dexing deposit is located in a NE‐trending magmatic belt along the southeastern margin of the Yangtze Craton. It is the largest porphyry copper deposit in China, consis...

Back to Top