FixAl及同位素方法在EGS返排液研究中的应用

增强地热系统(EGS)是开采低渗透率热岩体中热能的技术,属于广义的地热储工程。其中,作为换热介质被注入岩体并在换热后返回地表的返排液,不仅是岩体地球化学特征的信息载体,而且其物理化学行为直接影响着EGS系统的运行效果。FixAl化学热力学模拟和水同位素十三线图解在天然水热系统评价中得到了广泛应用,对返排液研究的实用性则是文章的核心问题。文中收集了全球主要EGS项目的返排液资料,基于FixAl方法分析矿物与返排液的化学平衡状态,并计算了流体在深部的热交换温度,用同位素模型验证了EGS系统中原生卤水的驱替过程。研究结果表明,上述方法在EGS返排液研究中是适用的。此外,返排液的化学特征对EGS的指示意义还包括厘定原生卤水在返排液中所占比例,识别岩浆挥发分溶解及储层改造时的添加剂残留,预测结垢趋势和流体腐蚀性等。未来需要通过更多的实验和模拟方法深入研究返排液的化学特征,建立EGS的热-水-力-化学(THMC)耦合模型,为科学开发深层地热能提供依据。     

Fluid inclusions

Fluid inclusions in crystals provide a valuable insight into the nature and origin of ancient mineral-forming fluids. Fluid inclusions are established geothermometers and geobarometers, but their use as chemical indicators has in the past been hampered by their extremely small size. With the rapid development of a range of modern instrumental microanalytical techniques it is becoming increasingly possible to determine in detail the compositions of various phases present within minute inclusions down to the parts-per-million level     

Evolution of interstitial waters along the passive margin of the Southeast Basin of France: WELCOM (Well Chemical On-line Monitoring) applied to Balazuc-1 well (Ardèche)

As part of the Géologie Profonde de la France [GPF (Deep Geology of France)] Programme investigating the passive margin of the Southeast Basin of France, studies are being made on the possibility of modelling mass transfer. In the summer of 1990, when the first hole in the area (Balazuc-1) was being drilled along a basement-rooted fault, chemical monitoring of the drilling fluids (WELCOM) enabled the composition of the interstitial fluids contained within the intersected rocks to be reconstructed. The computations were compared to on-core leaching carried out during the drilling, following which the WELCOM results were calibrated. The interstitial fluids from the drilled formations show very contrasted compositions. From the top to the bottom of the hole it has been possible to distinguish: diagenetically evolved seawater within the Hettangian limestone, modified continental fluids within the upper part of the Triassic sandstone reservoirs, and evaporated seawater within the Middle Triassic evaporites. Several zones of intensive fluid circulation are also indicated by: dolomitization of the basal Hettangian limestone, circulation of fluids expelled from the evaporites within the upper part of Triassic sandstone reservoirs, and continental-derived hydrothermal fluid flow within the Lower Triassic sandstone reservoir and Carboniferous silty shale. The results show that chemical logging of drilling fluids can provide valuable data concerning interstitial fluids where other techniques are not available.     

The influence of coupled physical swelling and chemical reactions on deformable geomaterials

Coupled thermo‐hydro‐mechanical‐chemical modelling has attracted attention in past decades due to many contemporary geotechnical engineering applications (e.g., waste disposal, carbon capture and storage). However, molecular‐scale interactions within geomaterials (e.g., swelling and dissolution/precipitation) have a significant influence on the mechanical behaviour, yet are rarely incorporated into existing Thermal‐Hydro‐Mechanical‐Chemical (THMC) frameworks. This paper presents a new coupled hydro‐mechanical‐chemical constitutive model to bridge molecular‐scale interactions with macro‐physical deformation by combining the swelling and dissolution/precipitation through an extension of the new mixture‐coupling theory. Entropy analysis of the geomaterial system provides dissipation energy, and Helmholtz free energy gives the relationship between solids and fluids. Numerical simulation is used to compare with the selected recognized models, which demonstrates that the swelling and dissolution/precipitation processes may have a significant influence on the mechanical deformation of the geomaterials.     

Modelling chemo‐hydro‐mechanical behaviour of unsaturated clays: a feasibility study

Effective capabilities of combined chemo‐elasto‐plastic and unsaturated soil models to simulate chemo‐hydro‐mechanical (CHM) behaviour of clays are examined in numerical simulations through selected boundary value problems. The objective is to investigate the feasibility of approaching such complex material behaviour numerically by combining two existing models. The chemo‐mechanical effects are described using the concept of chemical softening consisting of reduction of the pre‐consolidation pressure proposed originally by Hueckel (Can. Geotech. J. 1992; 29 :1071–1086; Int. J. Numer. Anal. Methods Geomech. 1997; 21 :43–72). An additional chemical softening mechanism is considered, consisting in a decrease of cohesion with an increase in contaminant concentration. The influence of partial saturation on the constitutive behaviour is modelled following Barcelona basic model (BBM) formulation (Géotech. 1990; 40 (3):405–430; Can. Geotech. J. 1992; 29 :1013–1032). The equilibrium equations combined with the CHM constitutive relations, and the governing equations for flow of fluids and contaminant transport, are solved numerically using finite element. The emphasis is laid on understanding the role that the individual chemical effects such as chemo‐elastic swelling, or chemo‐plastic consolidation, or finally, chemical loss of cohesion have in the overall response of the soil mass. The numerical problems analysed concern the chemical effects in response to wetting of a clay specimen with an organic liquid in rigid wall consolidometer, during biaxial loading up to failure, and in response to fresh water influx during tunnel excavation in swelling clay. Copyright © 2005 John Wiley & Sons, Ltd.     

Characteristics of Compositional Migration in Mylonites from the Ductile Shear Zones of the Southern Tancheng-Lujiang Fault Belt, Eastern Anhui Province

On the basis of field geology, three typical ductile shear zones in the southern part of the Tancheng-Lujiang fault belt have been chosen for a detailed study. Altogether ten samples of the tectonites have been collected for this study. The paper is focused on a comprehensive study of the tectonites in the medium-lower horizons of the ductile shear zones. The mineral compositions of the rocks are analyzed with EPMA and some typical whole-rock samples analyzed by chemical and ICP methods. Based on the comprehensive study of the characteristics of the deformation, the mineral assemblages and the changes of chemical composition of the bulk rocks, this paper presents a discussion on the relationship between the volume loss, the fluid flow and compositional changes during mylonitization of the ductile shear zones in this region. Our study shows that there are a large amount of fluids flowing through the shear zones during the process of mylonization, accompanied by the loss of rock volume and migration of el     

Mantle hornblendites of Naein ophiolite (Central Iran): Evidence of deep high temperature hydrothermal metasomatism in an upper mantle section

The Naein ophiolite is the most complete ophiolitic exposure in Cental Iran and considered as a remnant of the Mesozoic Central East Iranian microcontinent (CEIM) confining oceanic crust. In the northeastern part of this ophiolite (Darreh Deh area) within the mantle peridotites, a few hundred meters below the top of the Moho transition zone (MTZ), the hornblendites are present as dykes (former cracks and joints) from a few millimeters to nearly 50 cm wide. They have sharp boundaries with the surrounding mantle harzburgites and dunites. These hornblendites are pale green and coarse-grained in hand specimen and composed of magnesio-hornblende (Mg# = 0.93), chlorite (penninite and clinochlore, Mg# = 0.95), Cr-spinel (chromite, Cr# = 0.67 and Mg# = 0.55), tremolite, calcite and dolomite. Tremolites were formed by retrograde metamorphism of hornblendes. Calcite and dolomite occur as late-stage veins. Very high amount of primary hydrous phases (~94 vol % hornblende and chlorite), as well as peculiar mineralogical and chemical characteristics of the Naein ophiolite mantle hornblendites, do not match a magmatic origin. They are possibly products of the reaction between mantle peridotites and seawater-originated supercritical fluids, rich in silicate components. The presence of primary hydrous phases (hornblende and chlorite) may reveal high activity of H₂O in the involved solution. The chemical composition of chromite in the hornblendites is near to the average chromite composition from the surrounding harzburgite and dunite. This suggests that the main source of Cr should be chromites of nearby peridotites, which were totally or partly dissolved by hydrothermal fluids. The positive anomaly of Eu in the chondrite-normalized REE patterns of hornblendes, high modal abundance of Ca-rich hornblende, as well as presence of calcite and dolomite, point to seawater ingression through the gabbros in to the uppermost mantle peridotites. The higher value of MgO than CaO, presence of high-Cr chromite and Cr-enrichment of hornblendes and chlorites indicate a higher contribution of peridotites rather than gabbros to the chemical characteristics of the involved fluids. This study shows that circulation of possibly seawater-derived high temperature hydrous fluids in the upper mantle can leach and provide necessary elements to form hornblendite in joints and cracks of the uppermost mantle.     

流体成矿系统与成矿作用研究

对几乎所有金属矿床类型来说，其形成过程均与金属从源岩的活化、原始渗滤、矿质运移和金属沉淀富集成矿关系密切，这些过程主要是由流体的运动和作用完成的。因此，识别金属和流体的来源，追溯流体从源区将金属运载至最终成矿部位所经过的路径，以及查明金属和流体沿运移通道发生的物理、化学和时间上的各种变化及其特殊性质，可以为矿床评价与勘查提供很有价值的定量成矿信息。成矿流体的来源－运移－沉淀（－堆积）过程会以流体成矿系统的形式保留下来。对流体成矿系统和作用的全面了解可通过调查活动的和古代的两种系统获得。活动流体成矿系统是目前正在进行原始矿质搬运的系统，调查这些系统可对运移通道中的含矿流体进行取样和监测研究。古流体成矿系统包括各时代从含金石英脉到铅－锌矿脉系统的所有热液脉型矿床以及沉积喷气型和所谓层控矿床。对含矿矿物和岩石的广泛岩石学、化学、流体包裹体和同位素研究将为定量评价与预测矿床的分布和变化提供至关重要的资料。流体成矿系统内具有一些重要特征，如各种地质要素的方向性、相关性和指示性变化。     

Interaction of chemical and physical processes during deformation at fluid-present conditions: a case study from an anorthosite–leucogabbro deformed at amphibolite facies conditions

We present microstructural and chemical analyses of chemically zoned and recrystallized plagioclase grains in variably strained samples of a naturally deformed anorthosite–leucogabbro, southern West Greenland. The recorded microstructures formed in the presence of fluids at mid-crustal conditions (620–640 °C, 7.4–8.6 kbar). Recrystallized plagioclase grains (average grain size 342 μm) with a random crystallographic orientation are volumetrically dominant in high-strain areas. They are characterized by asymmetric chemical zoning (An₈₀ cores and An₆₄ rims) that are directly associated with areas exhibiting high amphibole content and phase mixing. Analyses of zoning indicate anisotropic behaviour of bytownite plagioclase with a preferred replacement in the $ \left\langle {0 10} \right\rangle $ direction and along the (001) plane. In areas of high finite strain, recrystallization of plagioclase dominantly occurred by bulging recrystallization and is intimately linked to the chemical zoning. The lack of CPO as well as the developed asymmetric zoning can be explained by the activity of grain boundary sliding accommodated by dissolution and precipitation creep (DPC). In low-strain domains, grain size is on average larger and the rim distribution is not related to the inferred stress axes indicating chemically induced grain replacement instead of stress-related DPC. We suggest that during deformation, in high-strain areas, pre-existing phase mixture and stress induced DPC-caused grain rotations that allowed a deformation-enhanced heterogeneous fluid influx. This resulted in local plagioclase replacement through interface-coupled dissolution and precipitation and chemically induced grain boundary migration, accompanied by bulging recrystallization, along with neocrystallization of other phases. This study illustrates a strong interaction and feedback between physical and chemical processes where the amount of stress and fluids dictates the dominant active process. The interaction is a cause of deformation and external fluid infiltration with a result of strain localization and chemical re-equilibration at amphibolite facies conditions.     

金矿成矿流体特点及深-浅部流体相互作用成矿机制

以中国一些典型金矿研究资料为基础 ,结合前人关于深部流体研究成果 ,分析对比了金矿成矿流体和深部流体的特点 ,总结了深部流体参与金矿成矿作用的主要表现 ,然后计算了深部富气流体的能量传递效应和富水流体在不同深度上的密度变化规律。认为深部富气流体主要是向浅部输送大量热能和部分有利于成矿的物质 ,而浅部富水流体下渗提供足够的水体 ,二者在中地壳的“低速层”附近交汇 ,发生相互作用并作用于围岩 ,在有利条件下演化形成成矿流体 ,最终上升到地壳浅部沉淀成矿。     

Critical issues in modelling the long-term hydro-thermomechanical performance of natural clay barriers

Performance assessment of deep repositories for heat-generating radioactive waste requires the capability of predicting reliably the evolution of the system during a time period commensurate with the hazardous life of the waste. In many repository designs clay barriers represent important elements of the waste isolation system.

In order to provide reasonable assurance that clay barriers will ensure long-term waste isolation, it is essential to understand their behaviour under a variety of conditions. Due to the variability of argillaceous materials, to the complexity of the phenomena that might take place in a waste repository and to the longevity of the required isolation, an adequate understanding of the behaviour and the capability to model the evolution of the clay barriers are not easy tasks. The factors that need to be understood and modelled include stress evolution, long-term strain or creep, thermal effects on solid skeleton, on interstitial fluids and on mineralogy. The difficulty of the task is increased by the facts that many effects are coupled, that their rates must be extremely low, in order to be realistic, and that the time period to be modelled defies the possibility of direct experimental observation. Several critical issues are identified and discussed briefly, such as: constitutive law to describe the thermo-mechanical behaviour of the clay skeleton, modelling of the fluid phase in clays and its response to heating, thermal fracturing and healing. Strategies are suggested for a rational approach to the experimental investigation of some relevant processes. The study of suitable natural analogues, for example the thermo-metamorphic halo occurring at Orciatico in Tuscany, could provide valuable insights in the thermal effects of heating clay barriers. It is conceivable that models describing a variety of relevant phenomena, such as dehydration, fracturing and permeability changes could be tested through the study of the Orciatico analogue.

In the end performance assessments of clay barriers would benefit through improvements in modelling: this would involve progress in understanding the basic phenomena and their coupled nature, improved conceptual and mathematical models and increased reliability for their calibration/validation. The improved understanding of phenomena requires additional experimental activities on various levels: molecular, microscopic, macroscopic, medium scale and in situ.     

Proposal for applying a component-based mixture approach for ecotoxicological assessment of fracturing fluids

Hydraulic fracturing is increasingly being used to produce gas from unconventional resource sites for energy supply. Therefore, concerns about risks of this technology related to human health and the environment have to be addressed. Among the major issues is the potential contamination of surrounding water systems by chemical additives used in fracturing fluids. In this study, the ecotoxicological hazards of fracturing fluids, both, their individual components (chemicals) as well as their mixtures (product) were assessed using a component-based mixture approach. For five exemplary fracturing fluids, 40–90 wt% of the contained substances could unambiguously be defined in their chemical identity. The concentrations used in the applied fluid mixture were considered as (maximum) exposure concentrations. For components with mass fractions between 10 and 74 wt%, the effect concentrations for acute and chronic toxicity of fish, daphnia and algae were retrieved from experimental databases and through predictive modeling. The hazard indices calculated from the ratio of exposure to effect concentration were >1 for all fracturing fluids, using different scenarios. This indicated a hazard from the undiluted fracturing fluids. The assessment framework presented in this study allows for dealing with data gaps and uncertainties in a tiered fashion and in particular accommodates for combined effects resulting from chemical mixtures. It might be employed for ecotoxicological risk assessment of products containing chemical mixtures and optimization of their environmental performance.     

Trinidad mud volcanoes: where do the expelled fluids come from?

In order to establish the origin of fluids expelled from mud volcanoes in Trinidad, we analyzed their major-element, trace-element, and isotopic (H, O, Sr) compositions. The mineralogical, chemical, and Sr isotope compositions of associated expelled muds were also determined.On the basis of their chemical and Sr isotope compositions, the fluids were divided into two groups—those southwest and northeast of a major right lateral wrench fault (the Los Bajos fault) that both controls the chemical quality of the fluids and acts as a drain. Strontium isotopes were derived via mixing between a radiogenic source (0.71135) and a nonradiogenic source (≤0.70671) for both southwest and northeast groups. However, the nonradiogenic source possibly feeding the northeast group showed a lower Sr concentration than that of the southwest group. H and O isotope data show that the fluids became enriched in δ¹⁸O through interaction with wall rocks. The fluids were originally oceanic, but their properties were subsequently modified by diagenesis as evidenced by chemical data, and mixing between fluids issued from two deep-seated reservoirs and surface aquifer end-members.The gas phase expelled with the mud and the fluid through the mud volcanoes is composed mainly of methane with minor carbon dioxide. The amount of expelled gas seems the same in samples from both sides of the Los Bajos fault. The almost unique methane content of the gas phase and the large positive δ¹⁸O shifts of the reservoir end-member, as well as B, Li, and Ba contents, reveal that the fluids from the deep-seated reservoirs inherited their chemical compositions at high-temperature fluid–rock interactions. Estimates of equilibrium temperatures of the two deep-seated reservoirs suggest that, to acquire the estimated higher temperature (150°C), the mud volcanoes must have been fed partly by a reservoir located at a depth of more than 3 km. This depth corresponds to previous geologic information, which located the deep-seated reservoir in Miocene sediments at such a comparable depth. The mixing of the original fluids with a less deep-seated reservoir and meteoric waters on the ascending path suggests the presence of a recharge mechanism and contributes to the dynamics of the expulsion itself.     

贵州省水热型地热资源分布及流体水化学特征

为分析总结贵州省水热型地热资源分布特征和水化学特征,对省内天然温泉和地热井流体进行调查和采样测试,在全面收集已有最新地热勘查资料的基础上,通过地热资源地质勘查、评价相关标准和规范以及流体水化学Piper三线图分析等,划分地热资源类型,分析资源分布、资源富集和热储特征,研究不同构造区、不同热储中流体水文地球化学、微量元素等特征。结果表明: 贵州省水热型地热资源主要分布于黔中及黔北地区,属低温地热资源,类型以隆起(褶皱)断裂型为主,以层状兼带状热储分布最广; 地热流体富集和出露受构造控制明显,在石阡、遵义、贵阳、息烽等地形成以震旦系、寒武系白云岩热储为主的4大地热资源富集区,动态较稳定; 相同构造区和热储中流体水化学特征基本相似,水化学类型总体以重碳酸盐型为主,具有矿化度低、富含锶、偏硅酸、氟、氡等对人体有益的微量元素和放射性成分等特征。     

Fluid evolution during burial and Variscan deformation in the Lower Devonian rocks of the High-Ardenne slate belt (Belgium): sources and causes of high-salinity and C–O–H–N fluids

Fluid inclusions in quartz veins of the High-Ardenne slate belt have preserved remnants of prograde and retrograde metamorphic fluids. These fluids were examined by petrography, microthermometry and Raman analysis to define the chemical and spatial evolution of the fluids that circulated through the metamorphic area of the High-Ardenne slate belt. The earliest fluid type was a mixed aqueous/gaseous fluid (H₂O–NaCl–CO₂–(CH₄–N₂)) occurring in growth zones and as isolated fluid inclusions in both the epizonal and anchizonal part of the metamorphic area. In the central part of the metamorphic area (epizone), in addition to this mixed aqueous/gaseous fluid, primary and isolated fluid inclusions are also filled with a purely gaseous fluid (CO₂–N₂–CH₄). During the Variscan orogeny, the chemical composition of gaseous fluids circulating through the Lower Devonian rocks in the epizonal part of the slate belt, evolved from an earlier CO₂–CH₄–N₂ composition to a later composition enriched in N₂. Finally, a late, Variscan aqueous fluid system with a H₂O–NaCl composition migrated through the Lower Devonian rocks. This latest type of fluid can be observed in and outside the epizonal metamorphic part of the High-Ardenne slate belt. The chemical composition of the fluids throughout the metamorphic area, shows a direct correlation with the metamorphic grade of the host rock. In general, the proportion of non-polar species (i.e. CO₂, CH₄, N₂) with respect to water and the proportion of non-polar species other than CO₂ increase with increasing metamorphic grade within the slate belt. In addition to this spatial evolution of the fluids, the temporal evolution of the gaseous fluids is indicative for a gradual maturation due to metamorphism in the central part of the basin. In addition to the maturity of the metamorphic fluids, the salinity of the aqueous fluids also shows a link with the metamorphic grade of the host-rock. For the earliest and latest fluid inclusions in the anchizonal part of the High-Ardenne slate belt the salinity varies respectively between 0 and 3.5 eq.wt% NaCl and between 0 and 2.7 eq.wt% NaCl, while in the epizonal part the salinity varies between 0.6 and 17 eq.wt% NaCl and between 3 and 10.6 eq.wt% for the earliest and latest aqueous fluid inclusions, respectively. Although high salinity fluids are often attributed to the original sedimentary setting, the increasing salinity of the fluids that circulated through the Lower Devonian rocks in the High-Ardenne slate belt can be directly attributed to regional metamorphism. More specifically the salinity of the primary fluid inclusions is related to hydrolysis reactions of Cl-bearing minerals during prograde metamorphism, while the salinity of the secondary fluid inclusions is rather related to hydration reactions during retrograde metamorphism. The temporal and spatial distribution of the fluids in the High-Ardenne slate belt are indicative for a closed fluid flow system present in the Lower Devonian rocks during burial and Variscan deformation, where fluids were in thermal and chemical equilibrium with the host rock. Such a closed fluid flow system is confirmed by stable isotope study of the veins and their adjacent host rock for which uniform δ¹⁸0 values of both the veins and their host rock demonstrate a rock-buffered fluid flow system.     

Metamorphic and post-metamorphic fluid flow in the low-grade rocks of the Harlech Dome, north Wales

A combination of fluid inclusion, stable isotope and geochemical techniques has been used to study the nature of fluids present and their behaviour during Caledonian low-grade metamorphism of the Harlech Dome, north Wales. Fluid inclusion studies show that in most of the metasedimentary sequence the peak metamorphic fluid was an aqueous Na–K–Cl brine but in the graphitic Clogau Formation and in parts of the overlying Maentwrog Formation immiscible H₂O-rich and CH₄-rich fluids coexisted. Late-stage inclusions are of calcium-rich brine and a dilute aqueous fluid. The chemical composition of chlorite in metamorphic veins and rocks varies between different formations and quartz-oxygen isotopic compositions show considerable variation between different units. Both of these features are taken to indicate that there was little or no pervasive movement of fluid between different units at the peak of metamorphism. After the metamorphic peak there was focused flow of fluid upward through the sequence along fractures, in response to end-Caledonian uplift and unloading. Where the migrating fluid crossed the graphitic shales, interaction between the fluid and the shales gave rise to the formation of the auriferous veins of the Dolgellau Gold Belt. Subsequent to this mineralizing event there was widespread development of ¹⁸O-enriched calcites and micas. In the case of vein minerals it is possible that these crystallized directly from late-stage fluids at lower temperature than the quartz in the same veins. Alternatively, the original vein minerals may have re-equilibrated with later ¹⁸O-enriched or cooler fluid. In the case of muscovites in the rock matrix it is proposed that the isotopically heavy compositions are the result of re-equilibration of initially light grains with an introduced fluid, requiring considerable influx of fluid. This event may relate to either of two late-stage fluids observed as inclusions.     

The isotopic and chemical composition of CO2-rich thermal waters in the Mont-Dore region (Massif-Central,France)

Chemical and isotope compositions of fluid samples, collected between 1974 and 1986 from 52 springs or shallow boreholes located in the Mont-Dore region (Massif Central, France), were examined. Some springs and wells were sampled several times during this period. The fluids emerge from Quaternary volcanic rocks or Paleozoic granite at temperatures between 4 and 62°C, and the origin of the H₂O is meteoric. The waters can be classified into three groups: bicarbonate fluids, mixed bicarbonate-chloride fluids (with a mineralization up to 8 g/l), and acid-sulfate fluids. Only two fluids contain sufficient Cl⁻ to be considered as ‘mature’ waters. Previous work has demonstrated that they all contain partly mantle-derived CO₂ gas, and that the CO₂-rich gas phase and bicarbonate-chloride waters are separated at substantial depth.Mineralized fluids circulate at depth and undergo several processes, such as cooling or dilution with recent freshwater, during their ascent to the surface. Therefore, the CO₂-rich gas phase can be partly dissolved in the freshwater, or in deep fluids after their dilution. This process leads to the dissolution of surrounding rocks; such dissolution is discussed on the basis of major-element concentrations (Na, K, Ca, Mg), as well as the Sr 87/86 isotope ratio. Dissolution of S-bearing minerals has also been demonstrated. The presence of the CO₂-rich gas phase also leads to isotope exchange between CO₂ and H₂O. Some mineralized fluids are less affected by these processes than others, in which case they display the chemical and isotopic characteristics of the original deep fluids.It was shown that the applicability of geothermometer calculations for these waters is hampered by several processes that modify the chemical composition. However, some geothermometers can be used for estimating the temperature of the deep fluids using the chemical composition of the less modified fluids. They indicate that fluids emerging from volcanic rocks in the Dordogne valley reach temperatures of around 100–130°C at depth, while the temperature of the fluid that issues from the granite at Saint-Nectaire is 160–175°C at depth.     

河南省鹤壁市新区地热流体特征及成因分析

地热资源属于一种宝贵矿产资源,它的形成需要特定的地质构造环境。本文在分析鹤壁市新区古近系、奥陶—寒武系热储地热流体化学特征的基础上,分别对其热水进行了医疗热矿水等质量评价。利用水文地球化学方法、同位素分析方法等,对地下热水和二氧化碳气体的成因进行了分析;依据放喷试验和二氧化碳的产状对驱动喷发的机理进行了探讨。从而为合理开发利用地热流体资源提供了地质依据。