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This book explores water geothermometry, a highly relevant topic in the exploration and exploitation of geothermal energy. Presenting theoretical geothermometers and indicators of CO2 fugacity, it describes a rigorous new approach entirely based on thermodynamics. The book will appeal to geothermal geoscientists, especially those working in research institutions and companies around the globe. It is also of interest to students on advanced courses in applied geochemistry, water–rock interaction and other related areas.
Volume 76 of Reviews in Mineralogy and Geochemistry presents an extended review of the topics conveyed in a short course on Geothermal Fluid Thermodynamics held prior to the 23rd Annual V.M. Goldschmidt Conference in Florence, Italy (August 24-25, 2013). It covers Thermodynamics of Geothermal Fluids, The Molecular-Scale Fundament of Geothermal Fluid Thermodynamics, Thermodynamics of Aqueous Species at High Temperatures and Pressures: Equations of State and Transport Theory, Mineral Solubility and Aqueous Speciation Under Hydrothermal Conditions to 300 °C – The Carbonate System as an Example, Thermodynamic Modeling of Fluid-Rock Interaction at Mid-Crustal to Upper-Mantle Conditions, Speciation and Transport of Metals and Metalloids in Geological Vapors, Solution Calorimetry Under Hydrothermal Conditions, Structure and Thermodynamics of Subduction Zone Fluids from Spectroscopic Studies and Thermodynamics of Organic Transformations in Hydrothermal Fluids.
Illustrates the usefulness of the thermodynamic approach to geological problems by means of examples based on natural rock systems.
This book includes innovative gas-geothermometers and geobarometers, which are urgently needed to estimate the increasingly higher temperatures and pressures present at depth below the Solfatara volcano, owing to its on-going unrest. Therefore, in this book, new gas geoindicators, applicable up to ca. 1000°C and 3 kbar, have been implemented and applied to Solfatara fluids. The innovations of this book include: methane, having a sluggish behavior, was treated separately from fast-reacting carbon monoxide; deviations from the ideal gas behavior were considered; the effects of reaction kinetics were taken into account. This was possible because a dataset including many geochemical parameters and extending from 1983 to 2020 with a good sampling frequency is available for Solfatara, making it a case history probably unique worldwide. Nevertheless, the gas geoindicators described in this book can be applied to other similar systems. Thus, this book is of interest to many scientists studying gas geochemistry, geothermometry, and geobarometry for volcanic surveillance and the mitigation of the volcanic risk.
Volume 70 of Reviews in Mineralogy and Geochemistry represents an extensive review of the material presented by the invited speakers at a short course on Thermodynamics and Kinetics of Water-Rock Interaction held prior to the 19th annual V. M. Goldschmidt Conference in Davos, Switzerland (June 19-21, 2009). Contents: Thermodynamic Databases for Water-Rock Interaction Thermodynamics of Solid Solution-Aqueous Solution Systems Mineral Replacement Reactions Thermodynamic Concepts in Modeling Sorption at the Mineral-Water Interface Surface Complexation Modeling: Mineral Fluid Equilbria at the Molecular Scale The Link Between Mineral Dissolution/Precipitation Kinetics and Solution Chemistry Organics in Water-Rock Interactions Mineral Precipitation Kinetics Towards an Integrated Model of Weathering, Climate, and Biospheric Processes Approaches to Modeling Weathered Regolith Fluid-Rock Interaction: A Reactive Transport Approach Geochemical Modeling of Reaction Paths and Geochemical Reaction Networks
In order to evaluate the performance of proposed processes utilizing geothermal energy, it is essential to determine the thermodynamic properties of fluid streams at various points in the system. The method described ascertains the values of these properties for either pure water or salt solution, correlating temperature, pressure, enthalpy, and entropy in the liquid, two-phase, and vapor regions. The corresponding FORTRAN computer formulation is coded in one subroutine and twenty-six function subprograms, sixteen of which represent correlations of the properties of pure water. The subroutine chooses the appropriate correlations, validates input data, and embodies a large fraction of the salt solution algorithms. Including nonexecutable comment lines, the entire formulation requires less than 910 lines of code. (MHR).
Geothermometry is an important tool for estimating deep reservoir temperature from the geochemical composition of shallower and cooler waters. The underlying assumption of geothermometry is that the waters collected from shallow wells and seeps maintain a chemical signature that reflects equilibrium in the deeper reservoir. Many of the geothermometers used in practice are based on correlation between water temperatures and composition or using thermodynamic calculations based a subset (typically silica, cations or cation ratios) of the dissolved constituents. An alternative approach is to use complete water compositions and equilibrium geochemical modeling to calculate the degree of disequilibrium (saturation index) for large number of potential reservoir minerals as a function of temperature. We have constructed several "forward" geochemical models using The Geochemist's Workbench to simulate the change in chemical composition of reservoir fluids as they migrate toward the surface. These models explicitly account for the formation (mass and composition) of a steam phase and equilibrium partitioning of volatile components (e.g., CO2, H2S, and H2) into the steam as a result of pressure decreases associated with upward fluid migration from depth. We use the synthetic data generated from these simulations to determine the advantages and limitations of various geothermometry and optimization approaches for estimating the likely conditions (e.g., temperature, pCO2) to which the water was exposed in the deep subsurface. We demonstrate the magnitude of errors that can result from boiling, loss of volatiles, and analytical error from sampling and instrumental analysis. The estimated reservoir temperatures for these scenarios are also compared to conventional geothermometers. These results can help improve estimation of geothermal resource temperature during exploration and early development.