The Atlantis II Deep is a location of modern submarine hydrothermal activity along the slowly spreading Red Sea rift axis. Venting of high-temperature hydrothermal fluids, similar to those associated with black smokers, takes place in a brine pool and has led to the accumulation of 90 Mt (dry, salt free) of stratiform, metalliferous sediment. The conditions of mineralization are unique in the modern oceans, but have been widely suggested as a possible analog of some important ancient stratiform base metal ore deposits. This study shows that many of the proposed genetic models for these ancient deposits may be highly simplified and do not take into account rapid diagenetic transformations, widespread non-equilibrium processes, and many other aspects of metal deposition. Sediment cores of the Atlantis II muds were last studied more than 30 years ago. High-resolution sampling and careful re-examination of the mineralogy and geochemistry of the sediments, using modern analytical techniques has significantly improved the understanding of the different processes responsible for the formation of the finely layered metallifeous sediments. The geochemistry of the individual layers is controlled by highly variable detrital, hydrogenic and hydrothermal input. Primary depositional pathways from the brine pool are the main control on basin-wide metal distribution (e.g., increasing Cu/Zn away from the vents) including variable enrichment in trace metals via scavenging from the brine pool and from the enriched pore waters. Cu and Zn have been deposited not only as sulfides but also with poorly crystalline Si-Fe-(oxy)hydroxides. A significant proportion of the original non-sulfide Cu and Zn are diagenetically transformed into sulfides, but also carbonates and clays, in large part reflecting sulfide deficient pore waters. Negative δ34S values, previously unrecognized in the sulfide- and metal-rich units, indicate a source of bacteriogenic sulfide. Syn-diagenetic processes also appear to have been responsible for the sharp laminations in the sediments, as well as distinctive zoning of carbonate and clay minerals around the vent source. The early diagenetic transformations observed in the Atlantis II Deep may not be preserved in the ancient rock record but nevertheless have important implications for metal deposition in some of the world’s largest and richest base metal ore deposits.

Les circulations de fluides aux interfaces entres les socles cristallins et leur couvertures sédimentaires sont des événements majeurs de transferts élémentaires dans la croûte. Dans de nombreux contextes, des fluides de bassins peuvent pénétrer dans les socles de faible perméabilité, interagir avec eux, y lessiver des métaux, et donner lieu à des concentrations métalliques, notamment en Pb, Zn, Cu, Ag et U. Les gisements d’uranium de type discordance du bassin d’âge protérozoïque de l’Athabasca (Canada), sont des témoins essentiels de ce type de circulations de fluides, et sont des objets modèles pour comprendre les mécanismes et les conséquences de tels événements. Les inclusions fluides permettent d’échantillonner et d’analyser directement les paléofluides. Malgré les difficultés d’analyse, ces objets de taille micrométriques apportent des informations importantes sur les propriétés des fluides. Les techniques d’analyse disponibles (microthermométrie, LA-ICP-MS, écrasement-lessivage, écrasement sous vide) permettent de reconstituer la température, la pression, la composition chimique détaillée des fluides, dont les teneurs en métaux, ainsi que la composition isotopique de l’hydrogène de l’eau, du chlore et du carbone du CO2 dissous. De plus, l’analyse de la composition isotopique de l’oxygène et du carbone des minéraux dans lesquels sont piégées les inclusions fluides apporte des informations complémentaires sur la température des fluides et les interactions fluides-roches. Cette approche a été utilisée sur six gisements d’uranium du Bassin de l’Athabasca, et a permis d’apporter les résultats suivants, potentiellement généralisables à l’ensemble du bassin. (1) Deux saumures, une calcique et une sodique ont circulé et se sont mélangées à la base du bassin et dans le socle au cours de la formation des gisements à environ 150 ± 30°C. (2) Ces deux saumures ont transporté de l’uranium, dont les concentrations exceptionnelles et très hétérogènes (entre 0.2 et 600 ppm) indiquent qu’il a été lessivé dans le socle. (3) Ces saumures ont une origine commune et se sont formées essentiellement par évaporation en surface de l’eau de mer, et mélange avec des fluides issus de la dissolution de minéraux évaporitiques. (4) La saumure calcique s’est formée par interaction entre la saumure sodique et les roches du socle. (5) Les interactions des saumures avec les minéraux et le graphite du socle, la radiolyse de l’eau, et la synthèse de bitumes ont contrôlé la composition isotopique en oxygène, hydrogène et carbone de ces saumures. / Fluid circulations between crystalline basements and their sedimentary covers are major events for element transfer in the crust. In numerous settings, basinal fluids penetrate the low-permeability basement, interact with basement lithologies, leach metals, leading to metal concentrations, notably Pb, Zn, Cu, Ag and U. Unconformity-related uranium deposits from the Proterozoic Athabasca Basin (Canada) are crucial witnesses and useful tools for the understanding of mechanisms and consequences of such fluid events. Fluid inclusions allow us to directly sample and analyze paleofluids. Despite analytical difficulties, these micrometer size objects provide key information on fluid properties. Available analytical techniques (microthermometry, LA-ICP-MS, crush-leach, in-vacuo crushing) provide reconstruction of temperature, pressure, detailed fluid chemistry, including metal concentrations, as well as isotopic composition of water hydrogen, chlorine and of dissolved CO2 carbon. In addition, analysis of isotopic composition of oxygen and carbon from minerals in which fluid inclusions are trapped provide supplementary information on fluid temperatures and fluid-rock interactions. This approach was used on six uranium deposits from the Athabasca Basin and provided the following results, which can be potentially generalized to the entire basin. (1) Two brines, a calcium-rich brine and a sodium-rich brine have circulated and mixed at the base of the basin and in the basement at the time of formation of uranium deposits, at temperature close to 150 ± 30°C. (2) Both brines have transported uranium, whose exceptional and highly heterogeneous concentrations (0.2 to 600 ppm) indicate that it was leached in the basement. (3) Both brines share a common origin and were formed mainly by surface evaporation of seawater and mixing with fluids originating from dissolution of evaporitic minerals. (4) The calcium-rich brine was formed by interaction between the sodium-rich brine and basement lithologies. (5) Interaction with basement minerals and graphite, water radiolysis, and bitumen synthesis were the main controls on the oxygen, hydrogen and carbon isotopic composition of brines.

Eine grundlegende Herausforderung bei der Gewinnung von Lithiumsalzen aus den Brines der südamerikanischen Salzseen stellt die Trennung von Lithium- und Magnesiumsalzen dar. Bei der klassischen salaren Eindunstung fallen schwer zu trennende Salzgemische und Doppelsalze an. Eine effektive Möglichkeit zur Abtrennung von Magnesiumsalzen kann die fraktionierte Kristallisation von Salar-Brines bei tiefen Temperaturen sein. Die vorliegende Arbeit untersucht die Lösegleichgewichte und Prozesse im System 2Li+ , Mg2+ || 2Cl - , SO42- – H2O bei Temperaturen zwischen 25°C und -30°C experimentell und stellt thermodynamische Modelle (Ionenwechselwirkungsmodell nach Pitzer und modifiziertes BET-Modell) zu deren Beschreibung zur Verfügung. Diese Modelle bieten eine Grundlage für die Simulation und Umsetzung von Tieftemperatur-Prozessschritten zur Gewinnung reiner Lithiumsalze. Ein möglicher Prozess zur Abreicherung von Magnesium aus hochkonzentrierten Lithiumchlorid-Lösungen durch Tiefkühlung wurde experimentell im Pilotmaßstab und modell-rechnerisch nachvollzogen.

Le procédé Solvay génère d’énormes quantités de saumures résiduaires au pH alcalin contenant portlandite, brucite et silicates de calcium hydratés. La carbonatation conduit à un abaissement du pH, ce qui favorise la formation de deux phases majoritaires : la calcite et le gypse. L’objectif de la thèse est de valoriser les saumures résiduaires carbonatées par séparation des phases en colonne de flottation. L’étude de la carbonatation en réacteur batch, puis en colonne de carbonatation pilote montre qu’il est préférable de ne pas carbonater les saumures résiduaires jusqu’à l’équilibre thermodynamique. En effet, la mise en solution de métaux lourds intervient à partir d’un pH de l’ordre de 7,5, ce qui limiterait les rejets des saumures dans l’environnement. En outre, une carbonatation brusque et incomplète est souhaitable pour une meilleure séparation des phases par flottation. Les essais de flottation réalisés sur une colonne de 7,6 cm de diamètre et de 3 m de haut ont montré une faisabilité de la séparation des deux minéraux calciques avec l’oléate de sodium comme collecteur malgré une abondante littérature incitant à la prudence. La différence entre la taille des particules de carbonates et celle des particules de sulfates et leurs hydratations de surfaces, ainsi qu’une force ionique élevée du milieu permettent une bonne séparation des phases. Une étude des saumures synthétiques permet de mettre en évidence le rôle des cations métalliques (nature, rayon, charge…) sur la coalescence des bulles dans les conditions dynamiques et dans un milieu à forte force ionique. Une étude des paramètre de fonctionnement effectué sur une colonne de 30,5 cm de diamètre et de 10 m de haut ont permis la modélisation du procédé de flottation en colonne dans le but de proposer une procédure de dimensionnement du procédé industriel. La confrontation des résultats de simulation aux résultats réels permet la détermination des intensités des microprocessus de flottation (attachement/détachement), et conduit à la proposition d’une installation industrielle avec deux colonnes de flottation en série / Solvay process generates huge amounts of waste brines at alkaline pH containing portlandite, brucite and calcium silicate hydrates. Carbonation leads to lowering of pH which favors formation of two predominant phases: calcite and gypsum. The aim of this thesis is to develop carbonated waste brines valorization by phase separation in flotation column Study of carbonation in a batch reactor and in a carbonation pilot column shows it is preferable not to carbonate waste brines until thermodynamic equilibrium. Indeed dissolution of heavy metals occurs from a pH of about 7.5 thereby limiting discharge of brines in the environment. In addition, a sudden and incomplete carbonation is appropriate for phase separation by flotation. Flotation tests carried out in a 7.6 cm diameter and 3 m high column showed feasibility of the separation of the two calcium minerals using sodium oleate as a collector despite abundant literature for caution. The differences between the particle size of carbonates and sulfates and their surface hydration, as well as the high ionic strength of the medium allow an efficient separation of phases. Study of synthetic brines highlights the role of metal cations (nature, radius, charge…) on bubble coalescence in dynamic conditions in an environment with high ionic strength. Study of operation parameter performed on a 30.5 cm diameter and 10 m high column enabled the modeling of the column flotation process in order to provide a scale-up procedure of industrial process. Comparison of simulation results with actual results allows the determination of intensities of flotation subprocesses (attachment/detachment), and led to the proposal of an industrial plant with two flotation columns in series

Mémoire (M.Sc.T.)-- Université du Québec à Chicoutimi, 1993. / Document électronique également accessible en format PDF. CaQCU

This thesis demonstrates that geological setting, depositional facies, open system flux of hot basinal brines and descending of shallow waters have a strong impact on the distribution of the diagenetic alterations within continental and paralic/shallow marine sandstones which in turn control the quality and heterogeneities of the reservoirs. Geological setting controls the mineralogical and textural maturity of sandstone, whereas depositional facies control the pore water chemistry (marine, brackish or meteoric), sedimentary texture and sand body geometry. Eogenetic alterations in the fluvial deposits are dominated by precipitation of infiltrated clays, kaolinitization of detrital silicates, whereas the shallow marine deposits are dominated by precipitation of early calcite and kaolinite. Conversely mesogenetic alterations are dominated by clay minerals transformation, quartz overgrowths and Ferroan- carbonates, barite and anhydrite. Flux of hot basinal brines is evidenced by precipitation of mesogenetic minerals that lack of internal sources (e.g. barite, anhydrite and ferroan carbonate cements), which is evidenced by: (1) restricted occurrence of these minerals in downthrown blocks. (2) The high fluid inclusion homogenization temperatures (Th) of quartz overgrowths (Th &gt; 110-139°C), and carbonate cements (T &gt; 80-140°C), which also have light δ18OV-PDB(-17.6‰ to -6.7‰). Flux of hot basinal brines is further evidenced by occurrence of saddle Fe-dolomite along stylolites. Fluid inclusion microthermometry further revealed a dramatic shift in pore- water chemistry from NaCl dominated brines during precipitation of quartz overgrowths to NaCl-CaCl2 dominated brines during cementation by Fe-dolomite. Presence of mixed brine (NaCl+CaCl2) systems in the fluid inclusions suggests flux of descending waters, which have circulated in the overlying carbonate-evaporite successions. The restricted occurrence of oil- filled inclusion to quartz overgrowths and methane to Fe-carbonate cements suggest migration of oil during precipitation by quartz and migration of methane during precipitation by Fe- carbonate cements. The extensive mesogenetic cements in the down thrown blocks is attributed to flux of basinal brines along deep seated faults, i.e. open system diagenesis. Integration of fluid inclusion microthermometry, isotopes, Raman spectrometry and thermal tectonic evolution of basins are essential techniques for unraveling the evolution of basinal fluids, cementation conditions and relative timing of hydrocarbons migration. / <p>Errata: Felaktigt disputationsdatum på spikbladet.</p>

Numerous glacial advances over the past 2 million years have covered the entire Canadian and Fennoscandian Shield outcrop. During glacial advance and retreat, permafrost is expected to form in front of the glacier. The question of how permafrost and freezing impact the formation and evolution of brines in natural systems may be vital to understanding the chemistry of groundwater in crystalline rocks. Investigations of groundwater conditions beneath thick permafrost can provide valuable information that can be applied to assessing safety of deep, underground nuclear waste repositories and understanding analogues to potential life-bearing zones on Mars. However, very little scientific investigation of cryogenic processes and hydrogeology deep within crystalline systems has been published. The purpose of this research is to evaluate the impacts of thick permafrost (>300m) formation on groundwater chemical and flow system evolution in the crystalline rock environment over geologic timescales. A field investigation was conducted at the Lupin Mine in Nunavut, Canada, to characterize the physical and hydrogeochemical conditions within and beneath a thick permafrost layer. Taliks, or unfrozen channels within the permafrost, are found beneath large lakes in the field area, and provide potential hydraulic connections through the permafrost. Rock matrix waters are dilute and do not appear to affect groundwater salinity. Permafrost waters are Na-Cl and Na-Cl-SO4 type, and have been contaminated with chloride and nitrate by mining activities. Sulfide oxidation in the permafrost may be naturally occurring or is enhanced by mining activities. Basal permafrost waters (550 to 570 mbgs) are variably affected by mining. The less contaminated basal waters have medium sulfate concentrations and are Ca-Na dominated. This is similar to deeper, uncontaminated subpermafrost waters, which are Ca-Na-Cl or Na-Ca-Cl type with a wide range of salinities (2.6 to 40 g•L-1). The lower salinity subpermafrost waters are attributed to dissociation of methane hydrate and drawdown of dilute talik waters by the hydraulic gradient created by mine dewatering. This investigation was unable to determine the influence of talik waters to the subpermafrost zone in undisturbed conditions. Pressures are also highly variable, and do not correlate with salinity. Fracture infillings are scarce and calcite δ18O and δ13C values have a large range. Microthermometry indicates a large range in salinities and homogenization temperatures as well, indicative of a boiling system. In situ freezing of fluids and methane hydrate formation may have concentrated the remaining fluids. Field activities at the Lupin mine also provided an opportunity to study the nature of gases within crystalline rocks in a permafrost environment. Gases were generally methane-dominated (64 to 87), with methane δ13C and δ2H values varying between -56 and -42‰ VPDB and -349 to -181 ‰ VSMOW, respectively. The gases sampled within the Lupin mine have unique ranges of chemical and isotopic compositions compared with other Canadian and Fennoscandian Shield gases. The gases may be of thermogenic origin, mixed with some bacteriogenic gas. The generally low δ2H-CH4 ratios are somewhat problematic to this interpretation, but the geologic history of the site, a metaturbidite sequence, supports a thermogenic gas origin. The presence of gas hydrate in the rock surrounding Lupin was inferred, based on temperature measurements and hydrostatic pressures. Evidence also suggests fractures near the mine have been depressurized, likely due to mine de-watering, resulting in dissipation of methane hydrate near the mine. Modeling results indicate methane hydrates were stable throughout the Quaternary glacial-interglacial cycles, potentially limiting subglacial recharge. The effects of deep permafrost formation and dissipation during the Pleistocene glacial/interglacial cycle to deep groundwaters in the Canadian Shield were also investigated by compiling data from thirty-nine sites at twenty-four locations across the Canadian Shield. Impacts due to glacial meltwater recharge and surficial cryogenic concentration of fluids, which had been previously considered by others, and in situ freeze-out effects due to ice and/or methane hydrate formation were considered. At some Canadian Shield sites, there are indications that fresh, brackish, and saline groundwaters have been affected by one of these processes, but the data were not sufficient to differentiate between mixed, intruded glacial meltwaters, or residual waters resulting from either permafrost or methane hydrate formation. Physical and geochemical data do not support the cryogenic formation of Canadian Shield brines from seawater in glacial marginal troughs. The origin and evolution of Canadian and Fennoscandian Shield brines was explored with a survey of chlorine and bromine stable isotope ratios. The δ37Cl and δ81Br isotopic ratios varied between -0.78 ‰ and 1.52 ‰ (SMOC) and 0.01 ‰ and 1.52 ‰ (SMOB), respectively. Variability of chlorine and bromine isotope ratios decreases with increasing depth. Fennoscandian Shield groundwaters tend to be more enriched than Canadian Shield groundwaters for both 37Cl and 81Br. Other sources and processes which may affect δ37Cl and δ81Br composition are also explored. Primary processes such as magmatic and/or hydrothermal activity are thought to be responsible for the isotopic composition of the most concentrated fluids at each site. Positive correlations between δ81Br, and δ37Cl with δ2H-CH4 and δ13C-CH4 were noted. At this time the cause of the relationship is unclear, and may be a result of changing redox, pH, temperature, and/or pressure conditions during hydrothermal, metamorphic, or volcanogenic processes. The data suggest solute sources and fluid evolution at individual sites would be better constrained utilizing a multi-tracer investigation of δ37Cl, δ81Br, and 87Sr/86Sr ratios comparing fluids, rocks, and fracture filling minerals (including fluid inclusions).

Numerous glacial advances over the past 2 million years have covered the entire Canadian and Fennoscandian Shield outcrop. During glacial advance and retreat, permafrost is expected to form in front of the glacier. The question of how permafrost and freezing impact the formation and evolution of brines in natural systems may be vital to understanding the chemistry of groundwater in crystalline rocks. Investigations of groundwater conditions beneath thick permafrost can provide valuable information that can be applied to assessing safety of deep, underground nuclear waste repositories and understanding analogues to potential life-bearing zones on Mars. However, very little scientific investigation of cryogenic processes and hydrogeology deep within crystalline systems has been published. The purpose of this research is to evaluate the impacts of thick permafrost (>300m) formation on groundwater chemical and flow system evolution in the crystalline rock environment over geologic timescales. A field investigation was conducted at the Lupin Mine in Nunavut, Canada, to characterize the physical and hydrogeochemical conditions within and beneath a thick permafrost layer. Taliks, or unfrozen channels within the permafrost, are found beneath large lakes in the field area, and provide potential hydraulic connections through the permafrost. Rock matrix waters are dilute and do not appear to affect groundwater salinity. Permafrost waters are Na-Cl and Na-Cl-SO4 type, and have been contaminated with chloride and nitrate by mining activities. Sulfide oxidation in the permafrost may be naturally occurring or is enhanced by mining activities. Basal permafrost waters (550 to 570 mbgs) are variably affected by mining. The less contaminated basal waters have medium sulfate concentrations and are Ca-Na dominated. This is similar to deeper, uncontaminated subpermafrost waters, which are Ca-Na-Cl or Na-Ca-Cl type with a wide range of salinities (2.6 to 40 g•L-1). The lower salinity subpermafrost waters are attributed to dissociation of methane hydrate and drawdown of dilute talik waters by the hydraulic gradient created by mine dewatering. This investigation was unable to determine the influence of talik waters to the subpermafrost zone in undisturbed conditions. Pressures are also highly variable, and do not correlate with salinity. Fracture infillings are scarce and calcite δ18O and δ13C values have a large range. Microthermometry indicates a large range in salinities and homogenization temperatures as well, indicative of a boiling system. In situ freezing of fluids and methane hydrate formation may have concentrated the remaining fluids. Field activities at the Lupin mine also provided an opportunity to study the nature of gases within crystalline rocks in a permafrost environment. Gases were generally methane-dominated (64 to 87), with methane δ13C and δ2H values varying between -56 and -42‰ VPDB and -349 to -181 ‰ VSMOW, respectively. The gases sampled within the Lupin mine have unique ranges of chemical and isotopic compositions compared with other Canadian and Fennoscandian Shield gases. The gases may be of thermogenic origin, mixed with some bacteriogenic gas. The generally low δ2H-CH4 ratios are somewhat problematic to this interpretation, but the geologic history of the site, a metaturbidite sequence, supports a thermogenic gas origin. The presence of gas hydrate in the rock surrounding Lupin was inferred, based on temperature measurements and hydrostatic pressures. Evidence also suggests fractures near the mine have been depressurized, likely due to mine de-watering, resulting in dissipation of methane hydrate near the mine. Modeling results indicate methane hydrates were stable throughout the Quaternary glacial-interglacial cycles, potentially limiting subglacial recharge. The effects of deep permafrost formation and dissipation during the Pleistocene glacial/interglacial cycle to deep groundwaters in the Canadian Shield were also investigated by compiling data from thirty-nine sites at twenty-four locations across the Canadian Shield. Impacts due to glacial meltwater recharge and surficial cryogenic concentration of fluids, which had been previously considered by others, and in situ freeze-out effects due to ice and/or methane hydrate formation were considered. At some Canadian Shield sites, there are indications that fresh, brackish, and saline groundwaters have been affected by one of these processes, but the data were not sufficient to differentiate between mixed, intruded glacial meltwaters, or residual waters resulting from either permafrost or methane hydrate formation. Physical and geochemical data do not support the cryogenic formation of Canadian Shield brines from seawater in glacial marginal troughs. The origin and evolution of Canadian and Fennoscandian Shield brines was explored with a survey of chlorine and bromine stable isotope ratios. The δ37Cl and δ81Br isotopic ratios varied between -0.78 ‰ and 1.52 ‰ (SMOC) and 0.01 ‰ and 1.52 ‰ (SMOB), respectively. Variability of chlorine and bromine isotope ratios decreases with increasing depth. Fennoscandian Shield groundwaters tend to be more enriched than Canadian Shield groundwaters for both 37Cl and 81Br. Other sources and processes which may affect δ37Cl and δ81Br composition are also explored. Primary processes such as magmatic and/or hydrothermal activity are thought to be responsible for the isotopic composition of the most concentrated fluids at each site. Positive correlations between δ81Br, and δ37Cl with δ2H-CH4 and δ13C-CH4 were noted. At this time the cause of the relationship is unclear, and may be a result of changing redox, pH, temperature, and/or pressure conditions during hydrothermal, metamorphic, or volcanogenic processes. The data suggest solute sources and fluid evolution at individual sites would be better constrained utilizing a multi-tracer investigation of δ37Cl, δ81Br, and 87Sr/86Sr ratios comparing fluids, rocks, and fracture filling minerals (including fluid inclusions).

Thesis (Ph.D.); Submitted to the University of California, Berkeley, CA (US); 18 Dec 2003. / Published through the Information Bridge: DOE Scientific and Technical Information. "LBNL--54280" Garcia, Julio Enrique. USDOE Director. Office of Science. Basic Energy Sciences (US) 12/18/2003. Report is also available in paper and microfiche from NTIS.

Cette thèse s’est déroulée dans le cadre du projet FONGEOSEC, qui vise à développer la filière de la géothermie profonde en France avec la conception d’un démonstrateur d’une centrale de production d’énergie géothermique dans le bassin Rhénan. Ce projet est piloté par Fonroche Géothermie, qui gère un consortium de plus de dix acteurs du milieu académique et industriel. Le financement du projet est réalisé avec participation de l’Agence de l’Environnement et de la Maîtrise de l’Énergie (ADEME). Ainsi, les travaux exposés dans ce document se sont intéressés à la caractérisation thermodynamique des fluides géothermaux (saumures chaudes contenant des gaz dissous) de la région ciblée par le projet. Il est nécessaire de déterminer la solubilité de chacun des gaz dissous dans ces saumures aux conditions de pression, température et salinité de l’exploitation géothermique. Des modèles thermodynamiques de prévision des équilibres entre phases liquide et vapeur peuvent être utilisés pour estimer ces solubilités. Néanmoins, en absence des mesures expérimentales dans les conditions de pression, température et salinité d’intérêt, pour effectuer la régression de paramètres de ces modèles, il sera difficile d’obtenir avec précision ces solubilités à partir de simulations. Ainsi, cette thèse est centrée sur l’étude expérimentale des solubilités des gaz dans des saumures représentatives des fluides du bassin Rhénan. La gamme de pression de FONGEOSEC va de 6.0 MPa à 40.0 MPa pour des températures de 333.15 K et 453.15 K. Le dispositif expérimental utilisé dans cette thèse fonctionne dans ces conditions. Les gaz dissous dans les saumures visées par le projet sont constitués essentiellement de dioxyde de carbone (CO2), puis d’azote (N2) et enfin de méthane (CH4) en plus faibles quantités. Les sels dissous dans ces fluides sont surtout du chlorure de sodium et du chlorure de calcium, à molalité de 1.2 mol NaCl-0.2 mol CaCl2.Kg H2O-1. Dans cette thèse, nous avons effectué la détermination expérimentale de la solubilité du dioxyde de carbone dans des saumures typiques du bassin Rhénan aux conditions de pression et de température du projet FONGEOSEC. Des réflexions sont proposées quant à une méthodologie d’analyse de solubilité du méthane et de l’azote dans des phases aqueuses. Nous observons aussi que dans les conditions de pression et température de fond du puits, la solubilité du dioxyde de carbone dans les saumures typiques du bassin Rhénan est la plus élevée parmi toutes les conditions caractérisées. Une étude du sating-out effect dans ces saumures est également proposée dans cette thèse. Enfin, il est remarqué que le modèle de Pitzer (Pitzer.dat sur PhreeqC) semble prédire de façon correcte nos mesures expérimentales à 333.15 K, mais il perd son efficacité à 453.15 K. Dans cette condition, le modèle E-NRTL (Simulis®) semblerait être plus approprié. / This thesis was part of the FONGEOSEC project, which aims to develop the deep geothermal energy sector in France through the the design of a geothermal power pilot plant on the Upper Rhine Graben. This project is controled by Fonroche Géothermie, which manages a consortitium of more than ten academic and industrial partners. The French Environment & Energy Management Agency (ADEME) participates at the fundings of the project.Therefore, the work exposed in this document concerns the thermodynamic characterisation of geothermal fluids (hot brines containing dissolved gases) from the target region of this project. It is thus necessary to determine the solubility of each gas dissolved in these brines at the pressure, temperature and salinity conditions of geothermal energy exploitation.Thermodynamic models that predict liquid-vapour phase equilibrium can be used to estimate these solubilities. However, if there is a lack of experimental measures on the pressure, temperature and salinity conditions of interest, it will not be possible to regress these models interaction parameters and, therefore, it will be difficult to have precise solubility results from these thermodynamic simulations. Thus, this thesis has focused on the experimental study of gas solubilities in brines representing the Upper Rhine Graben fluids. The pressure range of the FONGEOSEC project goes from 6.0 MPa to 40.0 MPa for temperatures of 333.15 K and 453.15 K. The experimental setup used on this thesis can operate at these conditions. Dissolved gases in the brines concerned by this project are mainly composed by carbon dioxyde (CO2), and then by nitrgen (N2) and methane (CH4) at lower quantitites. Dissolved salts in these fluids are basically chloride sodium and chloride calcium, at molalities of 1.2 mol NaCl-0.2 mol CaCl2.Kg H2O-1.On the scope of this thesis, we have performed the experimental determination of carbon dioxyde solubility in Upper Rhine Graben-type brines at the pressure and temperature conditions of the FONGEOSEC project. We propose a discussion about an analysis methodology for measuring nitrogen and methane solubility in aqueous phases. We also observed that at the pressure and temperature conditions found at the bottom of the production well, carbon dioxyde solubility in the Upper Rhine Graben-type brines reaches its highest value among all the conditions studied in this thesis. A salting-out effect study in these brines is also proposed in this document. Finally, it is noticed that the Pitzer model (Pitzer.dat at PhreeqC) seems to predict properly our experimental data at 333.15 K, but it is less efficient at 453.15 K. In this condition, the E-NRTL model (Simulis®) seems to be more appropriate.