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1.
To better understand glass alteration mechanisms, especially alteration layers formation, leaching experiments of a borosilicate glass (SON68) doped with a different rare earth element (La, Ce, or Nd) with solutions rich in 29Si and 18O were carried out. The coupled analyses of glass, alteration products, and solution led to a complete elemental and isotopic (29Si and 18O) budget. They revealed different behaviours of elements that depend not only on their structural role in the glass, but also on their affinity for alteration products (gel, phyllosilicates, phosphates). However, analyses of both glass and solution are not sufficient to describe the real exchanges occurring between glass and solution. The use of 29Si and 18O tracers gives new insights on the formation of alteration layers. During alteration the phyllosilicates records the isotopic variations of the leaching solution. Their isotopic signatures highlight a mechanism of dissolution/precipitation, which implies equilibrium between the secondary phases and the solution. On the other hand the gel isotopic signature, that is intermediate between the glass and the solution, substantiates the hypothesis that the gel is formed by hydrolysis/condensation reactions. This mechanism can thus explain the influence of the gel formation conditions (alteration conditions, solution saturation) on the structure (reorganisation) and texture (porosity) of this layer and on its protective effect. These hydrolysis/condensation reactions are also certainly involved in the aluminosilicate glass alteration and in the formation of palagonite.  相似文献   

2.
This investigation was carried out to assess the protective properties of the alteration film that develops during aqueous alteration of the French SON 68 (R7T7-type) nuclear glass, notably by examining the behavior of some network-forming cations in the presence of complexing anions. Glass alteration was studied here in the presence of orthophosphate ions. Comparisons were established between two series of tests performed with a solution containing orthophosphate ions and control tests performed under the same conditions but without phosphates. The first series of experiments was performed under initial rate conditions (i.e. in dilute media) to assess the effect of pH and phosphate concentration on the initial glass dissolution rate. Under these conditions, which ensure maximum chemical affinity of the glass dissolution reaction, phosphate adsorption occurs at the reaction interface only with acid pH values, at which the glass dissolution reaction is strongly inhibited. The elements that form complexes with the phosphates (Al, Fe, etc.) partially control glass dissolution in acidic media. Additional experiments carried out under saturated conditions — notably with respect to Si — in a solution enriched with phosphates showed that rare earth and Ca phosphates precipitated in the outer region of the alteration film, maintaining a glass dissolution rate significantly higher than in the control experiment. These observations have several implications. (1) Comparing the results obtained in the presence of phosphates and in the reference medium, the authors demonstrate deductively that glass dissolution is limited by the inner portion of the alteration film, i.e. the amorphous gel. (2) A kinetic law of SON 68 glass dissolution cannot be based on silica alone; the results of these experiments contradict Grambow’s model. (3) With regard to control of the glass dissolution kinetics by the protective properties of the gel, this type of experiment shows that the relation between the chemical composition and the microstructure of the gel is an important aspect in modeling the glass alteration kinetics, but that it is still poorly understood.  相似文献   

3.
Microscopic distribution and speciation of Na, Mg, Ni and Cs in a simulated (inactive) nuclear waste glass were studied using micro X-ray fluorescence (μ-XRF) and micro X-ray absorption spectroscopy (μ-XAS), after aqueous leaching during 12 years at 90 °C. Na and Mg are major constituents of the glass that can be used to determine the progress of the glass corrosion process and the nature of secondary alteration phases. Ni and Cs represent dose determining long-lived radionuclides (59Ni, 135Cs) in vitrified nuclear waste.The Na-Mg μ-XRF maps revealed that the core regions of the glass fragments are apparently unaltered and compositionally homogeneous, whereas rims and interstitial spaces are enriched with Mg-rich smectite formed during the leaching process. The micro X-ray absorption near edge structure (μ-XANES) spectra collected at the Mg K-edge in the altered zones show three sharp resonances typical for crystalline Mg-silicates. These resonances are distinctive of Mg occupying undistorted octahedral positions. In contrast, the μ-XANES spectra collected in the core zones of the glass fragments lack this resonance pattern and are identical to the spectra measured on the pristine (unleached) MW glass.Micro extended X-ray absorption fine structure (μ-EXAFS) and μ-XANES analyses at the Ni K-edge revealed three distinct Ni(II) species: (a) Ni uniformly distributed in the glass matrix, (b) micro-inclusions with high Ni concentrations and (c) Ni associated to the Mg-clay. The comparison with reference spectra of unleached MW and other Ni-bearing silicate glasses indicated that species (a) represents the original coordinative environment of Ni in the glass. The μ-EXAFS analyses revealed that species (b) is structural Ni in trevorite (NiFe2O4), which probably formed through unmixing processes during the cooling of the glass melt. The μ-EXAFS of species (c) could be successfully modeled assuming specific adsorption or incorporation of Ni into the lattice of trioctahedral Mg-clay minerals. Alternative models assuming other elements (Ni, Al, Fe) in addition to Mg in the second shell could not be fitted successfully.Aqueous concentration data were used to calculate the speciation of the leaching solutions. Saturation index (SI) calculations indicate undersaturation with respect to NiCO3 and NiSO4·7H2O, but oversaturation with respect to β-Ni(OH)2. The latter result is probably due to the omission of Ni borate and Ni silicate complexes in the speciation calculations, for which formation constants are not available. With the help of estimation techniques, we could infer that such complexes would dominate the Ni speciation and consequently reduce the SI below the saturation of β-Ni(OH)2.The μ-XRF maps show that Cs is uniformly distributed in the MW glass, since no region with high Cs concentration could be detected. The Cs LIII-edge μ-XAS spectra were all very similar independently of the degree of alteration, indicating similar coordination environments of Cs in the core regions of the glass as well as in the secondary clays. These spectra largely differ from that measured for pollucite (a potential secondary Cs-phase in altered glasses) implying that the coordination environments of Cs in the MW glass and in pollucite are fundamentally different.The present study shows that μ-XRF and μ-XAS are essential tools in determining the fate and the retention mechanisms of radionuclides released from nuclear waste during aqueous alteration. Our spectroscopic analyses allowed us to exclude formation of specific Ni and Cs secondary solids (e.g. nepouite, β-Ni(OH)2, pollucite) during the aqueous alteration. Ni and Cs are instead distributed as trace elements in the alteration phases formed by major elements during the leaching process. Our results imply that solid solution and/or adsorption equilibria, rather than pure phase solubility equilibria, are the adequate chemical models to determine Ni and Cs aqueous concentrations in performance assessments for radioactive waste repositories.  相似文献   

4.
The present study investigates the alteration of a fractured glass block in contact with iron and Callovo-Oxfordian claystone at 90 °C under anoxic and water-saturated conditions. The alteration rates and the nature of glass alteration products at the different compact interfaces (glass-clay, glass-iron) and in cracks were assessed by solution chemistry and microscopic-scale techniques (scanning electron microscopy coupled with energy-dispersive X-ray microscopy, microRaman spectroscopy, and X-ray absorption fine structure spectroscopy). A significant but modest (two-fold) increase in glass alteration in contact with steel was observed, leading to an average alteration rate over the experiment of about 0.007–0.014 g/m2/d. This rate is significantly lower than forward rate r0 in clay-equilibrated groundwater (1.7 g/m2/d), indicating that a decrease of the alteration rate was not hindered by the steel presence. The corrosion–alteration interface was made up of successive layers of corrosion products in contact with iron, a layer of Fe silicates, and an altered glass layer enriched in Fe. Characterization of the glass block in direct contact with claystone revealed that the thickness of altered glass was much more important than at the glass-iron interface. The altered glass layer in contact with clay was slightly enriched in Fe and Mg, and depleted in alkali cations. Altered glass layers in cracks were usually limited to fringes thinner than 2 μm, with a thickness decreasing from the crack mouth, indicating that alteration is controlled by transport in the cracks. The fractures were partially filled with calcite and lanthanide hydroxocarbonate precipitates. These results contribute to the understanding of nuclear vitrified waste-iron-corrosion products interactions in a deep geological repository.  相似文献   

5.
黄骅坳陷三马地区中-深部储层成岩作用及主控因素分析   总被引：12，自引：2，他引：12  
黄骅坳陷三马地区储集岩样品的显微特征及成岩矿物的组合关系分析结果表明，三马地区下第三系中深层储层主要处于晚成岩A期，成岩现象包括石英、长石的次生加大、碳酸盐矿物胶结作用、矿物交代作用、溶解作用和粘土矿物转化作用等。其中石英次生加大于2700m左右开始出现，随埋深增大，石英增生加强；长石次生加大现象不十分普遍；碳酸盐胶结作用包括早期自生泥晶方解石胶结作用、连晶方解石和晚期白云石(或铁方解石)的胶结作用。在扫描电镜下可见到方解石与含铁方解石集合体充填在粒间孔隙中或与石英、钠长石及粘土矿物共生，白云岩多呈菱形粒状分布于粒间；常见的交代现象主要有方解石交代长石、石英及粘土矿物，粘土矿物交代长石、石英等；溶解作用主要有长石的溶解、碳酸盐颗粒的溶解和方解石胶结物的溶解等，粘土矿物的转化主要为蒙脱石、高岭石向伊利石(或绿泥石)转化。还讨论了储层岩相、岩性特征、孔隙水中有机酸含量、早期方解石的充填、烃类早期注入等因素对储层成岩演化的控制作用。  相似文献   

6.
The paper presents data on the contents of macro- and microelements (rare earth elements included) determined in grain size fractions of the Upper Pleistocene hydrothermally altered and unaltered sediments from the Guaymas Basin (Gulf of California). Sediments subjected to high-temperature hydrothermal alteration were recovered by DSDP Hole 477A. In the finely dispersed fractions, which are mainly composed of clay minerals, alteration of the chemical composition was provoked by the hydrothermal transformation of terrigenous clay minerals. The concentration of microelements in these fractions takes place primarily at the cost of the hydrothermal finely dispersed ore minerals. Alteration of the chemical composition of the coarse-grained fractions is related to the replacement of clastogenic minerals by the secondary varieties and the formation of new minerals (including ore minerals and native metals) from the solutions. Hydrothermal alterations of the chemical composition of bulk samples depend on the degree of chemical element concentration in fractions and their content in samples.  相似文献   

7.
《Applied Geochemistry》1996,11(4):511-521
It is difficult to measure accurately the natural long-term corrosion rates of highly durable nuclear waste glasses. Care should be taken when using data from high temperature experiments to predict corrosion rates under ambient repository conditions as there are many factors (such as the precipitation of secondary compounds, the chemistry of the water in contact with the glass, or circulation of this water through the repository) that can influence the temperature dependence of aqueous reactions. In this study, some standard leach tests using pure water, in continuous flow and direct sampling autoclaves, were performed on a synthetic medieval glass. Archaeological glass samples of a similar composition and which had suffered several centuries of corrosion in damp soil had been the subject of previous studies. The corrosion of the archaeological samples in damp soil was well understood and the aim was to determine how well standard leach tests would predict the observed corrosion.The experimentally measured long-term corrosion rates were not simply dependent on temperature, therefore they could not be used to predict either the corrosion rates or products found on the archaeological samples. In continuous flow experiments this was largely because the release of some cations (e.g. Mg2+) was proportional to the flow rates used, and so the long-term corrosion was dependent on both flow rate and temperature. In the autoclave experiments, concentrations of dissolved ions climbed rapidly in the small water volume, leading to the precipitation of complex mineral phase assemblages. The experiments did not reach silica saturation, therefore the long-term rates measured were a function of both the temperature and the extent of reaction. The initial release rates of silica and of the network modifying cations showed an Arrhenius temperature dependence with an activation energy of about 78.5 kJmol−1. These results would have predicted the soil corrosion of the archaeological samples to within about 30%, i.e. the initial corrosion rate in pure water was similar to the long-term rate in damp soil. As an explanation of the experimental observations it is suggested that clay minerals in the soil consumed silica as the glass dissolved, maintaining under-saturated conditions and allowing corrosion at a rate similar to the initial rate in pure water.  相似文献   

8.
Obsidian glass alteration experiments under near hydrothermal conditions were performed to study mechanism and conditions of formation of altered minerals. X-ray diffraction patterns and cell dimensions of the specimens treated at 150, 200 and 300°C (pH = 8.03) revealed appearance of three main minerals — illite (9.5–10 Å), chlorite (7.04 Å) and halloysite (10.25Å). Further increase in the pH favours matrix dissolution with the formation of secondary altered layers. SEM-EDS study show that the alteration causes smoothing of the grain surfaces. These surfaces exhibits etch pits and series of depressions, formed by the process of dissolution. SEM — Back Scattered Electron images of obsidian specimens show thin laminae of smectite, with foliated bulky rims and cellular honeycomb texture, formed by precipitation from the solution as well as by direct transformation of glass during alteration. This mechanism is resulting from the alteration of alkalis by ionic inter-diffusion with H3O+ and H+ and inward diffusion of H2O, leading to free diffusion of silica into solution and then to a local rearrangement of the glass framework. Thus, a direct transformation of glass into clay minerals is the major reaction mechanism as evidenced by the mechanism of glass dissolution and subsequent mineral precipitation.  相似文献   

9.
近年来红外光谱技术作为一种绿色、快速、无损、精确探测矿物的技术手段而倍受关注,针对斑岩型矿床蚀变矿物高度叠加、蚀变分带界线不明显、细粒蚀变矿物多、黏土蚀变矿物多等特征,该技术在蚀变矿物识别和勘探信息解读等方面优势突出。本文应用红外光谱技术对云南普朗斑岩铜矿区钻孔ZK1801岩心进行矿物识别和蚀变分带划分的研究,识别出钾硅酸盐化带、绿帘石-绿泥石化带、绿泥石-伊利石化带、石英-伊利石化带和泥化带。研究表明:普朗铜矿整个钻孔的蚀变矿物主要有石英、钾长石、绢云母、绿泥石、绿帘石、高岭石、蒙脱石、伊利石等;根据矿化特征,发现铜矿体广泛赋存在钾硅酸盐化带和绿帘石-绿泥石化带中,与矿化关系密切的蚀变矿物"石英+钾长石+绢云母"和"绿帘石+绿泥石",可以作为普朗矿床勘查的标型蚀变矿物组合;研究区广泛发育的绢云母Al—OH波长随钻孔深度增加而逐渐从2210～2205nm减小到2202～2198nm, Al—OH波长2210～2205nm(长波绢云母)与矿化关系密切,可以作为普朗矿床勘查的指示信息。  相似文献   

10.
In this study, we have investigated and clarified the processes occurring during the alteration of SON68 glass – the reference nuclear glass for the waste arising from reprocessing of spent fuel from light water reactors – at 50 °C in Callovo-Oxfordian clay groundwater in presence of magnetite. Magnetite is known to be one of the iron corrosion products expected to be present in the vicinity of glass in geological disposal conditions. The effects of the amount of magnetite relative to the glass surface and the transport of aqueous species during glass alteration were studied. A first series of experiments was focused on the effect of various magnetite amounts by mixing and altering glass and magnetite powders. In a second series of experiments, magnetite was separated from the glass by a diffusive barrier in order to slow down the transport of aqueous species. Glass alteration kinetics were analyzed and solids were characterized by a multiscale approach using Raman Spectroscopy, Scanning and Transmission Electron Microscopy, Energy-Dispersive X-ray and Scanning Transmission X-ray Microscopy coupled with Fe L2,3-edge and C K-edge NEXAFS.It appears that glass alteration increases with the amount of magnetite and that the transport of aqueous species is a key parameter. Several processes have been identified such as (i) the silica sorption on the magnetite surface, (ii) the precipitation of Fe-silicates in the vicinity of the glass (iii) the precipitation of SiO2 on the magnetite surface, (iv) the incorporation of Fe within the alteration layer. Process (iv) was not frequently observed, suggesting local variations in geochemical conditions. Moreover, this process is strongly influenced by the transport of aqueous species as indicated by the morphology and composition of the alteration layers. Indeed, when glass and magnetite are homogeneously mixed, the glass alteration layer consists of a gel enriched in Fe having the same Fe(II)/Fe(III) ratio as in magnetite. When both materials are separated by a diffusive barrier, the glass alteration layer consists of a porous gel (not enriched in iron) in presence of a mixture of Fe-silicates with Fe having the same valence as in magnetite, rare-earth precipitates and phyllosilicates. These results suggest that Fe incorporation within the alteration layer changes depending on the distance and the time required for dissolved Fe originating from the magnetite to reach the glass.  相似文献   

11.
Glass-iron-clay setups were reacted at 90 °C for 6-18 months to investigate the coupled interactions between glass alteration, Fe corrosion and clay transformation. The reacted interfaces were probed at the microscopic level using complementary characterization methods (scanning electron microscopy coupled with energy-dispersive X-ray analysis, micro-Raman spectroscopy, micro X-ray diffraction, micro X-ray fluorescence spectroscopy, and micro X-ray absorption near-edge structure spectroscopy). The 10-μm thick Fe foil was fully corroded within 10 months, exposing glass to the pore solution. Iron corrosion led to the formation of a layer containing mostly magnetite, siderite and Fe-rich phyllosilicates with one tetrahedral and one octahedral sheet (TO) or two tetrahedral and one octahedral (TOT) sheet per layer. The clay in contact with this corrosion layer was enriched in siderite (FeCO3). Glass alteration resulted in the formation of a gel layer whose thickness increased with reaction time (from 20 μm after 6 months to 80 μm after 18 months) and a thin layer of secondary precipitates that concentrated lanthanides, P, and Mo. Assuming conservative behavior of Zr, the Si molar concentration in the gel is about 57% that in the glass. Glass dissolution remained at a rate close to the initial dissolution rate r0. The data are consistent with glass dissolution sustained by the uptake of dissolved Si and charge-compensating cations on secondary (corrosion) products, thus maintaining the gel porosity open and facilitating the leaching of easily soluble elements.  相似文献   

12.
下庄铀矿为一花岗岩型铀矿，矿田地处湿热气候条件下，沥青铀矿普遍产于破碎带中，这种特定的产出环境致使该区沥青铀矿经受了强烈的风化，形成种类繁多、数量丰富的铀酰矿物；而我国高放废物地质处置库拟建在花岗岩体中。因此，下庄铀矿田是开展核废料氧化的天然类比研究的理想地区，并对我国的高放废物地质处置库的安全性评价有重要的指导作用。下庄铀矿田的铀酰矿物组合为铀酰氢氧化物、铀酰硅酸盐和铀酰磷酸盐，包括柱铀矿、黄钙铀矿、calciouranoite、红铀矿、富硅铀酰相、硅钙铀矿、钙铀云母和盈江铀矿等。根据它们的空间分布特征可划分成两个风化系列，即硅酸盐风化系列和磷酸盐风化系列，其共生次序分别为：沥青铀矿→铀酰氢氧化物（氧化物）→富硅铀酰相→硅钙铀矿和沥青铀矿→铀酰氢氧化物（氧化物）→钙铀云母→盈江铀矿。在该矿田中，铀酰氢氧化物是亚稳定相矿物，常常被铀酰硅酸盐或磷酸盐取代，因此，铀酰氢氧化物仅出现在少数样品中，而铀酰硅酸盐和铀酰磷酸盐矿物则非常普遍。矿田中的铀酰矿物在化学成分上以富钙为其显著特征，由于核废料地质处置库近场地下水中的Ca^2＋含量应该明显比下庄矿田地下水中的高，因此，我们预测含Ca的铀酰硅酸盐和铀酰磷酸盐矿物等热力学上的稳定物相很可能是地质处置系统中最主要的铀酰矿物，处置库内放射性核素的迁移主要是由这些矿物控制的。  相似文献   

13.
The relationship between composition and physical parameters such as specific surface area, cationic exchange capacity and plasticity is studied with the aim of developing regression models that would permit the prediction of clay properties. These models could be useful for mineralogists and industrial applications. Nineteen representative clay samples were collected from Jebel Ressas in north-eastern Tunisia. Mineralogical data show that clay samples cover a very large variety of minerals. The main clay mineral is illite (50–60 wt%), secondary minerals including quartz, calcite and minor amounts of Na-feldspar. This study reveals that the average amount of silica (SiO2) and alumina (Al2O3) are 51.9 and 19.6 wt%, respectively. The contents of lime (CaO) and iron (Fe2O3) vary between 4 and 8 wt% whereas the amount of alkalis (Na2O + K2O) is on average 4.1 wt%. The grain size data indicates a significant amount of silt fraction, and the fraction <2 µm varies between 23 and 35 wt%. Values for plasticity index range from 16 to 28 wt%. The cation exchange capacity and the specific surface values are 34.1–45.7 meq/100 g of air-dried clay and 302–374 m2/g, respectively. Lastly, regression models are used to correlate the properties with the mineralogical and chemical compositions. The significance and the validity of models were confirmed by statistical analysis and verification experiments. The regression models can be used to select the clay properties (plasticity index, cation exchange capacity and specific surface) in relation with clay minerals proportions and the finer fraction amounts.  相似文献   

14.
Trace element concentrations of altered basaltic glass shards (layer silicates) and zeolites in volcaniclastic sediments drilled in the volcanic apron northeast of Gran Canaria during Ocean Drilling Program (ODP) leg 157 document variable element mobilities during low-temperature alteration processes in a marine environment. Clay minerals (saponite, montmorillonite, smectite) replacing volcanic glass particles are enriched in transition metals and rare earth elements (REE). The degree of retention of REE within the alteration products of the basaltic glass is correlated with the field strength of the cations. The high field-strength elements are preferentially retained or enriched in the alteration products by sorption through clay minerals. Most trace elements are enriched in a boundary layer close to the interface mineral-altered glass. This boundary layer has a key function for the physico-chemical conditions of the subsequent alteration process by providing a large reactive surface and by lowering the fluid permeability. The release of most elements is buffered by incorporation into secondary precipitates (sodium-rich zeolites, phillipsite, Fe- and Mn-oxides) as shown by calculated distribution coefficients between altered glasses and authigenic minerals. Chemical fluxes change from an open to a closed system behavior during prograde low-temperature alteration of volcaniclastic sediments with no significant trace metal flux from the sediment to the water column.  相似文献   

15.
鄂尔多斯盆地泥页岩储层纯页岩段黏土矿物含量高,储集空间体积小。因此,黏土矿物转化释放的二氧化硅缺乏足够的空间,不能生长成自生石英,只能以非晶态存在于黏土矿物之间;而其粉砂质泥岩夹层中常见微米级孔洞。孔洞由长石溶蚀和黏土矿物转化形成,内部则发育晶形完好的自生石英、绿泥石及含铁方解石。此外,粉砂质泥岩的碎屑颗粒间常发育结块状非晶态二氧化硅,碎屑石英颗粒周围则以次生加大边的形式发育粒状和席状(或片状)非晶态二氧化硅。二氧化硅主要来源于黏土矿物转化与石英碎屑颗粒溶蚀。  相似文献   

16.
The x-ray powder diffraction identification of clay minerals both in bulk samples and in separated clay fraction confirmed the presence of palygorskite in samples of cave sediments from Wadi Haqil (the western slopes of Musandam Mountains; Ras Al-Khaimah Emirate, UAE). Samples contain quartz, gypsum, smectite, kaolinite, calcite, and palygorskite, some of them chlorite, illite, feldspars, and goethite. Calcite dominates in most samples; smectite prevails in clay fraction. After heating, the 001 reflection of chlorite shifts to higher diffraction angles and its intensity decreases; these features indicate that the chlorite represent a Fe-dominant species. Unit-cell dimensions of major phases as refined by the Rietveld method are in agreement with literature data. Chemical composition of palygorskite was derived from unit-cell dimensions as follows: MgO content is 11–14 wt% and Al2O3 10–13 wt%. Clay mineralogy is only hard to ascertain from the scanning electron microscope (SEM) images even after being combined with the energy-dispersive spectrometer data. The SEM was also used to characterize gypsum grains; they often display flow deformation features. Studied cave sediments represent palygorskite-bearing weathering products and desert soils re-deposited from the cave surroundings by slope processes and wind and/or surface runoff. The mixture with other clay minerals, quartz, feldspars, etc. supports this interpretation. Fine-grained quartz fraction is probably wind-blown. Gypsum and calcite are the precipitates (crusts and/or cements), although gypsum can also be re-deposited from omnipresent gypsum-cemented surface sediments.  相似文献   

17.
赵文  何生  郭小文  王永诗  郝雪峰  熊伟 《地球科学》2020,45(9):3487-3501
石英次生加大是砂岩储层中常见且重要的成岩现象.本文通过对东营凹陷中央背斜带沙三段不同含油级别砂岩样品铸体薄片镜下观察、石英次生加大边宽度和含量的定量统计以及流体包裹体测温,分析了不同含油级别砂岩中石英次生加大边发育特征、期次和石英次生加大所需硅质的可能来源.砂岩样品中石英次生加大边最大宽度和加大边面积分布范围变化大,分别分布在4~90 μm和2.50~39 927.80 μm2之间.砂岩中与油气充注有关的石英次生加大主要有两期,结合埋藏-温度史图,该两期石英次生加大边发育时间分别为距今15~6 Ma和4~0 Ma.钾长石溶蚀和沙三段砂泥岩层中黏土矿物的转化是研究区不同含油级别砂岩石英次生加大边发育的主要硅质来源.东营凹陷中央背斜带沙三段不同含油级别砂岩石英次生加大边发育具有相似性和差异性两种特征:（1）不同含油级别砂岩中石英次生加大边最大宽度和单颗粒石英次生加大边面积整体统计分布特征具有相似性;（2）石英次生加大边宽度和单颗粒石英加大边面积普遍存在差异性.砂岩孔渗性、含烃流体充注造成的酸性水介质环境和油水分布特征是造成沙三段不同含油级别砂岩石英次生加大边发育相似性和差异性的主要原因,该区砂岩中石英次生加大可作为含烃流体充注的成岩示踪标志.   相似文献   

18.
《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   

19.
Microfocus X-ray computed tomography (µCT) measurements were performed on deltaic sandstone samples from the diagenetically altered Westphalian C strata (Campine basin, north-east Belgium) in order to collect three dimensional data on mineral (quartz, kaolinite, ankerite, etc.) and porosity distribution. The acquired µCT data were compared with point counting results of stained impregnated thin-sections to qualify the sensitivity of µCT. Comparison between techniques shows positive results with regard to the quantification of main mineral phases such as quartz and ankerite, and porosity distribution. However, major discrepancies exist when studying the clay minerals. This can be explained by the influence of microporosity associated with these clay minerals, resulting in partial volume effects.  相似文献   

20.
航空高光谱识别的高、中、低铝绢云母矿物成因学研究   总被引：2，自引：0，他引：2  
国内外学者在航空高光谱矿物填图时,根据Al-OH光谱特征吸收波长位置不同将浅色云母类矿物分为2~3类,分别命名为高铝绢云母、中铝绢云母、低铝绢云母,但对它们的成因特点却只有零星的讨论,没有比较系统的有针对性的研究。本文在新疆雪米斯坦铀多金属成矿带获取CASI/SASI航空高光谱数据,并开展矿物填图的基础上,针对高铝绢云母、中铝绢云母、低铝绢云母等三种矿物的成因学专门开展了比较系统的研究。采用的方法主要是在开展详细的野外地质观察、采样的基础上,对采集的上述三类矿物蚀变岩样品进行详细的室内光谱测量、Al-OH吸收波长位置统计、显微薄片观察、全岩X衍射分析、粘土X衍射分析等研究,并结流体成矿理论和已有矿物成因学知识,进行了详细深入的分析讨论。研究表明,高铝绢云母蚀变岩蚀变强烈,云母类蚀变矿物以绢云母、伊利石为主,且主要与叶腊石和微晶石英等矿物伴生,而低铝绢云母蚀变岩蚀变强度中等,以伊利石、伊蒙混层为主,绿泥石增加,主要与方解石、浊沸石等矿物伴生;高铝绢云母蚀变岩具有相对高的石英含量和粘土矿物总量,具有相对较低的钾长石、斜长石以及方解石含量;低铝绢云母蚀变岩则具有相对较低的石英和粘土含量,具有相对较高的斜长石、钾长石和方解石含量。通过深入分析讨论,本文提出了在研究区航空高光谱识别的高铝绢云母形成于相对高温、偏酸性的热液流体环境,低铝形成于相对低温、偏碱性的热液流体环境。这一新认识对航空高光谱遥感矿物填图结果的深入应用和深层次找矿信息反演具有重要意义。  相似文献   

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