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1.
An overview is presented of a 4-year study by the Äspö Task Force on Modelling of Groundwater Flow and Transport of Solutes, whose primary aim was to build a bridge between the approaches used for site characterisation (SC) and performance assessment (PA) associated with nuclear waste repositories. Eleven modelling teams representing six national radioactive waste organisations participated in eight modelling exercises whose objectives were: to assess simplifications used in PA models; to determine how, and to what extent, experimental tracer and flow experiments can constrain the range of parameters used in PA models; to support the design of SC programmes to assure that the results have optimal value for PA calculations; and to improve the understanding of site-specific flow and transport behaviour at different scales using SC models. The modelling tasks were concerned with flow and transport through single and multiple near-planar features on SC and PA timescales, including the diffusion of solutes into multiple immobile zones adjacent to fracture surfaces. In general, tracer tests provide only limited quantitative constraints on retention parameter values relevant to PA but nevertheless provide insight about the flow and transport processes, which is a key element of the bridge between SC and PA.  相似文献   

2.
We present two-feldspar thermometry and diffusion chronometry from sanidine, orthopyroxene and quartz from multiple samples of the Bishop Tuff, California, to constrain the temperature stratification within the pre-eruptive magma body and the timescales of magma mixing prior to its evacuation. Two-feldspar thermometry yields estimates that agree well with previous Fe–Ti oxide thermometry and gives a ~80 °C temperature difference between the earlier- and later-erupted regions of the magma chamber. Using the thermometry results, we model diffusion of Ti in quartz, and Ba and Sr in sanidine as well as Fe–Mg interdiffusion in orthopyroxene to yield timescales for the formation of overgrowth rims on these crystal phases. Diffusion profiles of Ti in quartz and Fe–Mg in orthopyroxene both yield timescales of <150 years for the formation of overgrowth rims. In contrast, both Ba and Sr diffusion in sanidine yield nominal timescales 1–2 orders of magnitude longer than these two methods. The main cause for this discrepancy is inferred to be an incorrect assumption for the initial profile shape for Ba and Sr diffusion modelling (i.e. growth zoning exists). Utilising the divergent diffusion behaviour of Ba and Sr, we place constraints on the initial width of the interface and can refine our initial conditions considerably, bringing Ba and Sr data into alignment, and yielding timescales closer to 500 years, the majority of which are then within uncertainty of timescales modelled from Ti diffusion in quartz. Care must be thus taken when using Ba in sanidine geospeedometry in evolved magmatic systems where no other phases or elements are available for comparative diffusion profiling. Our diffusion modelling reveals piecemeal rejuvenation of the lower parts of the Bishop Tuff magma chamber at least 500 years prior to eruption. Timescales from our mineral profiling imply either that diffusion coefficients currently used are uncertain by 1–2 orders of magnitude, or that the minerals concerned did not experience a common history, despite being extracted from the same single pumice clasts. Introduction of the magma initiating crystallisation of the contrasting rims on sanidine, quartz, orthopyroxene and zircon was prolonged, and may be a marker of other processes that initiated the Bishop Tuff eruption rather than the trigger itself.  相似文献   

3.
Cementitious materials will be used for the construction of the engineered barrier of the planned repositories for radioactive waste in Switzerland. Superplasticizers (SPs) are commonly used to improve the workability of concretes and, along with a set accelerator (Acc), to produce shotcrete. In this study the influence of a polycarboxylate- (PCE) and a polynaphthalene-sulphonate-based (PNS) SP on the hydration process, mineral composition and the sorption behaviour of metal cations has been investigated using an ordinary Portland cement (OPC), a low-alkali cement mix (LAC) consisting of CEM III-type cement and nanosilica, and a shotcrete-type cement mix (ESDRED) consisting of a CEM I-type cement and silica fume prepared in the presence of an alkali-free set accelerator.Both the PCE and PNS SP do not significantly influence the amount and quantity of hydrates formed during hydration. The concentration of both SPs decreased rapidly in the early stage of the hydration process for all cements due to sorption onto cement phases. After 28 days of hydration and longer, the concentration of the PNS SP in the pore fluids of all cements was generally lower than that of the PCE SP, indicating stronger uptake of the PNS SP. The formate present in the Acc sorbs only weakly onto the cement phases, which led to higher aqueous concentration of organics in the ESDRED cement than in OPC and LAC.Sorption experiments with 63Ni, 152Eu and 228Th on a cation exchange resin indicate that, at concentrations above 0.1 g L−1, the two SPs could reduce sorption of metal cations. Thermodynamic modelling further indicates that radionuclide complexation by formate at the concentration level in Acc can be excluded, suggesting that the apparent effect of Acc in the sorption measurements on the resin can be attributed to colloids formed owing to the high concentrations of Al and S in Acc. Sorption studies with the same radionuclides on hardened cement paste (HCP) in the presence of concrete admixture solutions and pore fluids squeezed from cement pastes further revealed no significant effect on sorption by either the concrete admixtures or their degradation products that were potentially present in the pore fluids. This finding suggests that the investigated concrete admixtures (PNS, PCE, Acc) and their degradation products have no significant impact on radionuclide mobilisation.  相似文献   

4.
《Applied Geochemistry》2002,17(3):207-223
Many designs for geological disposal facilities for radioactive and toxic wastes envisage the use of cement together with bentonite clay as engineered barriers. However, there are concerns that the mineralogical composition of the bentonite will not be stable under the hyperalkaline pore fluid conditions (pH > 12) typical of cement and its properties will degrade over long time periods. The possible extent of reaction between bentonite and cement pore fluids was simulated using the reaction-transport model, PRECIP. Key minerals in the bentonite (Na-montmorillonite, analcite, chalcedony, quartz, calcite) were allowed to dissolve and precipitate using kinetic (time-dependent) reaction mechanisms. Simulations were carried out with different model variants investigating the effects of: temperature (25 and 70 °C); cement pore fluid composition; dissolution mechanism of montmorillonite; rates of growth of product minerals; solubilities of product minerals; and aqueous speciation of Si at high pH. Simulations were run for a maximum of 3.2 ka. The results of all simulations showed complex fronts of mineral dissolution and growth, driven by the relative rates of these processes for different minerals. Calcium silicate hydrate (CSH) minerals formed closest to the cement-bentonite boundary, whereas zeolites and sheet silicates formed further away. Some growth of primary bentonite minerals (analcite, chalcedony, calcite and montmorillonite) was observed under certain conditions. Most alteration was associated with the fluid of highest pH, which showed total removal of primary bentonite minerals up to 60 cm from the contact with cement after ∼1 ka. The maximum porosity increase observed was up to 80–90% over a narrow zone 1–2 cm wide, close to the cement pore fluid- bentonite contact. All simulations (except that with alternative aqueous speciation data for Si) showed total filling of porosity a few cms beyond this interface with the cement, which occurred after a maximum of 3.2 ka. Porosity occlusion was principally a function of the growth of CSH minerals such as tobermorite. There was very little difference in the alteration attained using different model variants, suggesting that bentonite alteration was not sensitive to the changes in parameters under the conditions studied, so that transport of pore fluid through the bentonite governed the amount of alteration predicted. Principal remaining uncertainties associated with the modelling relate to assumptions concerning the evolution of surface areas of minerals with time, and the synergy between changing porosity and fluid flow/diffusion.  相似文献   

5.
The uptake of methanol, ethanol, formaldehyde, acetaldehyde, formic acid and acetic acid by cement paste was determined in hydrating cement after 1 h, 28 d and 390 d hydration. The sorption values determined for formate and acetate were critically assessed by investigating through- and out-diffusion of these compounds in fully hydrated cement paste and their uptake by individual cement phases. Diffusion studies included inverse modelling of four data sets for each compound and an uncertainty analysis based on a Latin hypercube sampling procedure. Solid–liquid distribution ratios determined from the hydration experiments are on the order of 10−4 m3 kg−1 in the case of alcohols and aldehydes indicating non-specific (very weak) bonding onto the surface of the cement phases, e.g. through hydrogen bonding. Hydration and diffusion studies reveal slightly higher distribution ratios and reversible uptake by cement paste and cement phases in the case of acetate indicating specific adsorption (electrostatic interaction) onto partially positively charged surface sites of the cement phases. Selective binding of a small fraction of formate is evidenced from both sorption and out-diffusion experiments suggesting the presence of sorption sites capable of strongly bonding the anion, presumably by SO42−/HCOO− replacement in the ettringite structure.  相似文献   

6.
A numerical code has been developed to track the distribution of trace elements in crustal rocks undergoing melting. The model handles diffusion with moving boundaries and accounts for the processes of diffusion, dissolution and precipitation in a partially molten system. Among the various input parameters for modelling, source composition (i.e. modal abundance) variations, diffusion coefficients and partition coefficients are found to exert a significant control on the melt chemistry. The other inputs such as melt reaction stoichiometry, kinetics of melting and grain size of protolith have lesser influence. Exploration of the general behaviour indicates that for systems in which disequilibrium melting of the kind considered in this paper occurs, trace element concentrations may be used to constrain the composition of the protolith or the timescales of melting, depending on the specific circumstances. After exploring some general features of melting in a pelitic system, the model is applied to calculate trace element distributions in migmatites from the Lesser Himalayan rocks in Sikkim, India. We focus on the distribution of trace elements during the initial stages of melt formation. These partially molten rocks show disequilibrium distribution of trace elements, and the numerical code is capable of quantitatively reproducing many of the observed patterns. The results of the modelling indicate that the observed melts in this zone were formed within 50,000 years and that segregation of melts (into leucosome and restite) was complete between 50,000 and 250,000 years. These short timescales may point to deformation-enhanced melt segregation at least on a hand specimen scale. It is important to distinguish between timescales of segregation over these scales and timescales of removal of melt on an outcrop scale to form plutons—the latter, requiring higher degrees of melting and larger distances of migration, take longer.  相似文献   

7.
The integrity of wells, which are key components for CO2 sequestration, depends mainly on the seal between the wellbore cement and the geologic formation. To identify the reaction products that may alter the cement/caprock interface, batch experiments and computer modelling were conducted and analysed. Over time, the dissolution and precipitation of minerals alters the physical properties of the interface, including its tightness. One main objective of the simulation was thus to analyse the evolution of the porosity of cement and caprock over time. The alteration of the cement/caprock interface was identified as a complex problem and differentiated depending on rock type. The characteristic feature of a cement/shale contact zone is the occurrence of a highly carbonated, compacted layer within the shale, which in turn causes cement/shale detachment. In the case of a cement/anhydrite interface, the most important reaction is severe anhydrite dissolution. Secondary calcite precipitation takes place in deeper parts of the rock. The cement/rock contact zone is prone to rapid mineral dissolution, which contributes to increased porosity and may alter the well integrity. Comparison of computer simulations with autoclave experiments enabled the adjustment of unknown parameters. This enhances the knowledge of these particular assemblages. Overall, a good match was obtained between experiments and simulations, which enhances confidence in using models to predict longer-term evolution.  相似文献   

8.
Distinctive peritidal tepee antiform structures, buckled margins of saucer-like megapolygons are common in marine vadose fenestral and pisolitic limestones and/or dolomites of carbonate platform sequences and occur in intertidal and supratidal carbonates ranging in age from Silurian to Holocene. These megapolygons commonly form and are sometimes truncated before the deposition of the next sedimentary layer. The megapolygons result from the expansion of surface sediments by as much as 15%. The expansion is caused by the following continuously repeated sequence of processes: (1) Desiccation and thermal contraction causing small fractures; (2) phases of wetting causing enlargement of fractures; (3) phases of crystallization of calcium carbonate and other minerals causing the enlargement, fill and cementation of the fractures. Precipitation is from brines and meteoric waters; (4) hydration of minerals, thermal expansion, breaking waves and faulting may add to this disruption. The development of the tepee fabric can be traced from an initially cemented subaerial fenestral crust, exhibiting expansion and compressional structures, to a completely disrupted and brecciated sediment riddled by a labyrinth of fractures and solution cavities. These spaces are filled by numerous phases of internal marine and fresh-water cement and sediment, the latter containing penecontemporaneous or younger marine faunas. Peritidal tepees are useful tools for geologic reconstruction and provide evidence of subaerial exposure; a tropical to subtropical climate; and back-beach or back-barrier deposition. Proper identification of tepees is of economic importance, because they provide good early porosity and permeability for petroleum entrapment and a site for mineralization. Aesthetically, tepee rocks are a fine kaleidoscopic decorative stone.  相似文献   

9.
The interaction of groundwater with cement in a geological disposal facility (GDF) for intermediate level radioactive waste will produce a high pH leachate plume. Such a plume may alter the physical and chemical properties of the GDF host rock. However, the geochemical and mineralogical processes which may occur in such systems over timescales relevant for geological disposal remain unclear. This study has extended the timescale for laboratory experiments and shown that, after 15 years two distinct phases of reaction may occur during alteration of a dolomite-rich rock at high pH. In these experiments the dissolution of primary silicate minerals and the formation of secondary calcium silicate hydrate (C–S–H) phases containing varying amounts of aluminium and potassium (C–(A)–(K)–S–H) during the early stages of reaction (up to 15 months) have been superseded as the systems have evolved. After 15 years significant dedolomitisation (MgCa(CO3)2 + 2OH− → Mg(OH)2 + CaCO3 + CO32−(aq)) has led to the formation of magnesium silicates, such as saponite and talc, containing variable amounts of aluminium and potassium (Mg–(Al)–(K)–silicates), and calcite at the expense of the early-formed C–(A)–(K)–S–H phases. This occured in high pH solutions representative of two different periods of cement leachate evolution with little difference in the alteration processes in either a KOH and NaOH or a Ca(OH)2 dominated solution but a greater extent of alteration in the higher pH KOH/NaOH leachate. The high pH alteration of the rock over 15 years also increased the rock’s sorption capacity for U(VI). The results of this study provide a detailed insight into the longer term reactions occurring during the interaction of cement leachate and dolomite-rich rock in the geosphere. These processes have the potential to impact on radionuclide transport from a geodisposal facility and are therefore important in underpinning any safety case for geological disposal.  相似文献   

10.
In this paper, a comparative modelling exercise from the DECOVALEX-2015 project is presented. The exercise is based on in situ experiments, performed at the Tournemire Underground Research Laboratory (URL), run by the IRSN (Institut de Radioprotection et de Sûreté Nucléaire), in France. These experiments aim at identifying conditions (e.g. technical specifications, design, construction, and defects) that will affect the long-term performance of swelling clay-based sealing systems, which is of key importance for the safety of underground nuclear waste disposal facilities. A number of materials are being considered as seals; the current work focusses on a 70/30 MX80 bentonite–sand mixture initially compacted at a dry density of 1.94 Mg/m3. The performance of the sealing plug involves at least three different important components, which are the hydro-mechanical behaviour of the bentonite–sand core, the overall permeability of the surrounding argillite, and the influence of the technological gap between the core and the argillite. Two particular tests have been selected for a comparative modelling exercise: the WT-1 test, which was designed to study the rock mass permeability, and the PT-A1 test, which aimed at quantifying the evolution of the hydro-mechanical field within the bentonite–sand core. A number of independent teams have worked towards modelling these experiments, using different codes and input parameters calibrated on additional small-scale laboratory experiments. Their results are compared and discussed.  相似文献   

11.
Fractures in wellbore cement and along wellbore-cement/host-rock interfaces have been identified as potential leakage pathways from long-term carbon sequestration sites. When exposed to carbon-dioxide-rich brines, the alkaline cement undergoes a series of reactions that form distinctive fronts adjacent to the cement surface. However, quantifying the effect of these reactions on fracture permeability is not solely a question of geochemistry, as the reaction zones also change the cement’s mechanical properties, modifying the fracture geometry as a result.This paper describes how these geochemical and geomechanical processes affect fracture permeability in wellbore cement. These competing influences are discussed in light of data from a core-flood experiment conducted under carbon sequestration conditions: reaction chemistry, fracture permeability evolution over time, and comparative analysis of X-ray tomography of unreacted and reacted cement samples. These results are also compared to predictions by a complementary numerical study that couples geochemical, geomechanical and hydrodynamic simulations to model the formation of reaction fronts within the cement and their effect on fracture permeability.  相似文献   

12.
The geological storage of nuclear waste includes multibarrier engineered systems where a large amount of cement-based material is used. Predicting the long term behaviour of cement is approached by reactive transport modelling, where some of the boundary conditions can be defined through studying natural cement analogues (e.g. at the Maqarin natural analogue site). At Maqarin, pyrometamorphism of clay biomicrites and siliceous chalks, caused by the in-situ combustion of organic matter, produced various clinker minerals. The interaction of infiltrating groundwater with these clinker phases resulted in a portlandite-buffered hyperalkaline leachate plume, which migrated into the adjacent biomicrite host rock, resulting in the precipitation of hydrated cement minerals.In this study, rock samples with different degrees of interaction with the hyperalkaline plume were investigated by various methods (mostly SEM-EDS). The observations have identified a paragenetic sequence of hydrous cement minerals, and reveal how the fractures and porosity in the biomicrite have become sequentially filled. In the alkaline disturbed zone, C-A-S-H (an unstoichiometric gel of Ca, Al, Si and OH) is observed to fill the pores of the biomicrite wallrock, as a consequence of reaction with a high pH Ca-rich fluid circulating in fractures. Porosity profiles indicate that in some cases the pores of the rock adjacent to the fractures became tightly sealed, whereas in the veins some porosity is preserved. Later pulses of sulphate-rich groundwater precipitated ettringite and occasionally thaumasite in the veins, whereas downstream in the lower pH distal regions of the hyperalkaline plume, zeolite was precipitated.Comparing our observations with the reactive transport modelling results reveals two major discrepancies: firstly, the models predict that ettringite is precipitated before C-A-S-H, whereas the C-A-S-H is observed as the earlier phase in Maqarin; and, secondly, the models predict that ettringite acts as the principal pore-filling phase in contrast to the C-A-S-H observed in the natural system. These discrepancies are related to the fact that our data were not available at the time the modelling studies were performed. However, all models succeeded in reproducing the porosity reduction observed at the fracture–rock interface in the natural analogue system.  相似文献   

13.
In global carbon cycle models, orogenesis is often viewed as a sink for atmospheric CO2, acting on tectonic timescales. However, recent attempts to quantify fluxes for CO2 produced by metamorphic reactions and released to the atmosphere suggest that these are an order‐of‐magnitude greater than CO2 uptake by chemical weathering of silicate minerals, and that metamorphic CO2 is released on millennial timescales. These hypotheses have gained support from both measurements of CO2 emissions from present‐day orogenic hot springs and chromatographic modelling of carbonation reactions in metamorphic rocks from ancient orogens. In this article I review research that attempts to quantify metamorphic CO2 release fluxes, focussing specifically on studies conducted in the SW Scottish Highlands.  相似文献   

14.
黏土矿物组构对水化作用影响评价   总被引：6，自引：0，他引：6  
泥页岩水化过程中黏土矿物起着主要的作用,但目前还缺少相关的定量描述研究。为此,利用SEM、X-粉晶衍射技术,对采自不同地区的泥岩和板岩在干燥状态、不同浸泡时间后的微观结构和含量进行分析及研究,分析黏土矿物的组构随浸泡时间的变化过程,并定量地分析其对水化过程的影响规律,研究泥页岩的软化过程。研究认为,（1）泥页岩、板岩中影响水化过程的内在因素是蒙脱石、高岭石、绿泥石和伊利石等黏土矿物的含量;（2）黏土矿物定向排列时水化作用效果较无序排列时的明显;（3）泥页岩的水化作用是一个渐进的过程,即在水化过程中流体介质首先使表面的黏土矿物软化,产生掉块;随着时间延长,流体沿裂缝、层理面向岩石内部渗透,黏土土矿物发生膨胀;无围岩限制作用时坍塌掉块持续发生;（4）泥浆中加入一定的无机盐有助于抑制水化过程的发生;压力增加将抑制水化过程的产生;温度升高则能促进泥页岩的水化过程。  相似文献   

15.
Partial melting has been shown to be an important mechanism for intracrustal differentiation and granite petrogenesis. However, a series of compositional differences between granitic melt from experiments and natural granites indicate that the processes of crustal differentiation are complex. To shed light on factors that control the processes of crustal differentiation, and then the compositions of granitic magma, a combined study of petrology and geochemistry was carried out for granites (in the forms of granitic veins and parautochthonous granite) from a granulite terrane in the Tongbai orogen, China. These granites are characterized by high SiO2 (>72 wt%) and low FeO and MgO (<4 wt%) with low Na2O/K2O ratios (<0.7). Minerals in these granites show variable microstructures and compositions. Phase equilibrium modelling using P–T pseudosections shows that neither anatectic melts nor fractionated melts match the compositions of the target granites, challenging the conventional paradigm that granites are the crystallized product of pure granitic melts. Based on the microstructural features of minerals in the granites, and a comparison of their compositions with crystallized minerals from anatectic melts and minerals in granulites, the minerals in these granitoids are considered to have three origins. The first is entrained garnets, which show comparable compositions with those in host granulites. The second is early crystallized mineral from melts, which include large plagioclase and K-feldspar (with high Ca contents) crystals as well as a part of biotite whose compositions can be reproduced by crystallization of the anatectic melts. The compositions of other minerals such as small grained plagioclase, K-feldspar and anorthoclase in the granites with low Ca contents are not well reconstructed, so they are considered as the third origin of crystallized products of fractionated melts. The results of mass balance calculation show that the compositions of these granites can be produced by mixing between different proportions of crystallized minerals and fractionated melts with variable amounts of entrained minerals. However, the calculated modal proportions of different crystallized minerals (plagioclase, K-feldspar, biotite and quartz) in the granites are significantly different from those predicted by melt crystallization modelling. Specifically, some rocks have lower modes of biotite and plagioclase, whereas others show lower K-feldspar modes than those produced by melt crystallization. This indicates that the crystallized minerals would be differentially separated from the primary magmas to form the evolved magmas that produce these granites. Therefore, the crystal entrainment and differential melt-crystal separation make important contributions to the composition of the target granites. Compared with leucogranites worldwide, the target granites show comparable compositions. As such, the leucogranites may form through the crystal fractionation of primary granitic magmas at different extents in addition to variable degrees of partial melting.  相似文献   

16.
《Applied Geochemistry》2004,19(11):1699-1709
One of the French options for the final disposal of high-level radioactive waste is a deep geological repository. The Callovo-Oxfordian formation in the Meuse and Haute-Marne (France) was proposed, by the French agency for the management of radioactive wastes (ANDRA), to be the site of a research laboratory in order to evaluate in situ the interaction between the host formation and the engineered barriers.In the previous experimental part, secondary minerals such as zeolites, tobermorite and katoite have been observed after the alteration of the Callovo-Oxfordian clay under alkaline conditions. Three different reactions of phyllosilicates alteration have been proposed as a function of both pH and chemical composition of the reacting solutions. The aim of this work was to simulate the reaction between the Callovo-Oxfordian clay and high-pH solutions in order to validate the proposed alteration reactions from experimental data.The thermodynamic modelling of stability relationships among minerals in the Callovo-Oxfordian clay was performed using the solution speciation solubility modelling code KINDIS at 120 °C for different chemical media (NaOH, KOH and Ca(OH)2). Input data were the mineralogical composition of the <2 μm fraction of Callovo-Oxfordian clay at nearly the same burial depth of the underground laboratory construction as well as the neoformed minerals observed after the experimental alteration of this clay (zeolites and cement phases). In the NaOH and KOH runs, anacime, phillipsite and chabazite, respectively were the first stable minerals which appeared at the beginning of modelling. In the Ca(OH)2 runs, oversaturated with respect to portlandite, katoite and then tobermorite were the first minerals occurring at the beginning of the alteration. Smectites and illites were undersaturated whatever the chemical composition. Both minerals and the interstratified illite-smectite were less stable in Ca(OH)2 than in NaOH and KOH solutions. Concerning the secondary minerals, a discussion is developed in order to improve modelling and to predict the long term reactions between clays and alkaline solutions.  相似文献   

17.
准噶尔盆地陆1井砂岩成岩作用及其对储层的影响   总被引：1，自引：1，他引：0  
本文探讨了陆1井岩屑砂岩的成岩作用及其对砂岩储层的影响.研究表明,压实作用使岩屑砂岩的孔隙度随埋深迅速减小,成岩早期的胶结物使大部分原生孔隙被充填。水化作用在成岩早期及有机质半成熟和成熟期成岩作用过程中,制约着各个阶段的成岩作用特点。在水化作用和有机质热演化作用的共同影响下,使得方解石胶结物发生选择性溶蚀形成了深部(上乌尔禾组)次生孔隙发育带。  相似文献   

18.
Mudstones are one of the least permeable rocks in most sedimentary sequences. Accordingly they can act as seals for fluid flow leading to abnormal overpressures. Nevertheless, mudstone compaction and related permeability and porosity decrease are not adequately described in current basin modelling software, because only mechanical compaction is taken into account. In reality, however, clay minerals undergo severe chemical diagenesis which certainly influences petrophysical properties and compaction. In this context a mathematical approach which has been originally developed in soil mechanics has been adapted to basin modelling. The underlying mathematical equations are carefully explained in the text. In the basic equation the compression coefficient is a function of void ratio and effective stress. Using these equations, overpressure can be predicted by using petroleum systems modelling techniques. This is shown for a real 3D case study in the North Sea, in which strong overpressure occurs. A compaction model for mudstones that depends strongly on the clay content of the individual stratigraphic units is used for the calibration of porosities in the 3D case study. In addition, a chemical compaction model that reduces porosities by using a kinetic reaction is used for the deeper part of the basin where mechanical compaction processes are less important. The pressure generation process depends strongly on permeability and compressibility of the porous medium. Therefore, the use of mudstone compaction and permeability models is sufficient to produce pore overpressures. In the case studied, abnormal overpressures are generated during burial together with the petroleum generation process. The mechanical and chemical compaction mechanisms ensure that the pressures are preserved in the deeper part of the basin.  相似文献   

19.
《Applied Geochemistry》1998,13(4):491-507
Rock–fluid interactions induced by steamflood enhanced oil recovery were investigated in laboratory simulations to determine the geochemical reactions and the effects of these reactions on reservoir permeability. Flow-through laboratory experiments using mixtures of quartz, kaolinite, and siderite were performed in a high temperature/high pressure permeameter at a confining pressure of 1200 psi and temperatures between 150–250°C. Fluid compositions used in the experiments simulated the vapor and residual liquid phases encountered in steamflood operations as well as an intermediate fluid composition. Effects of fluid pH, fluid salinity and flow rate were systematically investigated in the experiments.The most extensive fluid–rock interactions were observed in the vapor phase simulations and high temperature/high pH condition simulations. Smectite, chlorite, illite, mixed-layer clays, greenalite, analcime, and K-feldspar were all identified as products of rock fluid interaction in the experiments. Smectite was the dominant authigenic phase to reduce permeability in the experiments. The experiments showed that the formation of smectite in Fe-rich environments does not require a clay precursor.Smectite is likely the most damaging neoformed mineral to reservoir permeability under different hydrogeochemical conditions for several reasons including: (1) its relatively high surface area (including microporosity in the “honeycomb texture”), (2) its propensity to migrate and block pore throats during fluid flow in porous media because of its small particle size, pore-lining texture, and electrochemical surface properties, and (3) the wide range of stability of smectites in the physical and chemical conditions that exist in reservoirs undergoing steamflood EOR.The rapid precipitation of authigenic minerals in these experiments suggests that the period required for fluids and rock to reach equilibrium in diagenetic environments are extremely short when considering geologic time scales. The armoring of pre-existing minerals by grain-coating authigenic minerals appears to result in the attainment of local equilibrium conditions prior to when one would predict assuming a continuous supply of reactant minerals was present.  相似文献   

20.
利用X射线衍射、TG-DSC综合热分析以及环境扫描电子显微分析技术等,研究了矿渣微细粉对水泥水化产物钙矾石、Ca(OH)2、CSH凝胶等的影响规律。研究结果表明,在水化早期,矿渣微细粉即参与水泥水化进程,显著影响水泥水化产物钙矾石、Ca(OH)2和CSH凝胶等的生成速度和生成量及微观形貌,并且随着其掺量增大及水化时间延长,矿渣微细粉参与水泥水化反应程度逐渐提高。  相似文献   

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