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1.
天然沸石是岩石圈上部分布最广的硅酸盐矿物之一,它普遍地见于各种火山岩和火山-沉积岩中。沸石不仅在岩浆期后热液阶段生成,而且在沉积-成岩作用阶段、表生作用(风化)阶段、低级变质阶段都可以生成。由于沸石对周围的物理化学条件和热、动力变质作用反应灵敏,因此,它是了解地质体形成时的地质环境及其变化的良好的指示矿物。本文概述了我国东部中生代火山岩中沸石岩的分布、时代、产出的地层岩性剖面、原岩类型、矿物组合及其生成顺序,并探讨了它的形成条件和成因类型,其中主要涉及具有工业意义的斜发沸石岩和丝光沸石岩。 相似文献
2.
Current concepts of oil and gas generation by thermal decomposition of kerogen are reviewed. Primary oil migration mechanisms requiring large quantities of water to serve as a carrier for the movement of oil from source rock to reservoir are discussed. Previous investigators regarded the expulsion of interlayer water from montmorillonite and montmorillonite-illite mixed-layer minerals by transformation during diagenesis as the most important source of the carrier water.The process of diagenesis is subdivided into three stages based on the results of experimental compaction studies on montmorillonite clay, on studies of the expulsion mechanism of interlayer and interstitial waters, and on the observed changes in pores and mineral grains in argillaceous sediments during these stages. As a result, we concluded that the migration of oil chiefly occurs during the late compaction stage when the sediment's porosity ranges from 30 to 10%.This conclusion implies that a large amount of oil can move during the period when the active generation of oil corresponds with the primary migration of carrier water. For instance, in the oil-bearing Miocene sediments of the Akita area of northern Japan, the oil generation temperature ranged from 100 to 150°C and the average migration depth was between 1300 and 2600 m. Therefore, the possibility of large oil pool formation will be high in the basin where the paleo-geothermal gradient is about 5.0°C/100 m. In fact, it is expected that the paleo-geothermal gradients in the vicinities of large oil fields will be very close to this value.Prediction of the type and amount of hydrocarbons in the exploration area will be possible by an examination of the paleo-geothermal gradient in the area and by a study of the relation between absolute porosity and burial depth of argillaceous rocks. 相似文献
3.
The results of the study of clay mineral alterations in Upper Pleistocene sediments of the southern trough in the Guaymas Basin (Gulf of California) due to the influence of hydrothermal solutions and heat produced by sill intrusions are discussed. Core samples from DSDP Holes 477 and 477A were taken for the analysis of clay minerals. Application of the method of modeling X-ray diffraction patterns of oriented specimens of the finely dispersed particles made it possible to establish the phase composition of clay minerals, determine their structural parameters, and obtain reliable quantitative estimates of their contents in natural mixtures. The modeling data allowed us to characterize reliably the transformation of clay minerals in sediments of the hydrothermally active southern trough in the Guaymas Basin. In Upper Pleistocene sandy–clayey sediments of the southern trough, changes in the composition of clay minerals occurred under the influence of a long-living hydrothermal system. Its lower part (interval 170.0–257.5 m) with maximum temperatures (~300°C) was marked by the formation of chlorite. Terrigenous clay minerals are not preserved here. Saponite appears at a depth of 248 m in the chlorite formation zone. Higher in the sedimentary section, the interval 146–170 m is also barren of terrigenous clay minerals. Sediments of this interval yielded two newly formed clay minerals (chlorite and illite), which were formed at lower temperatures (above 180°C and below 300°C, approximately up to ~250°C), while the relatively low-temperature upper part (110–146 m) of the hydrothermal system (from ~140°C to ~180°C) includes the mixture of terrigenous and newly formed clay minerals. Terrigenous illite is preserved here. Illitization of the mixed-layer illite–smectite was subjected to illitization. The terrigenous montmorillonite disappeared, and chlorite–smectite with 5–10% of smectite layers were formed. In the upper interval (down to approximately 110 mbsf), the composition of terrigenous clay minerals remains unchanged. They are composed of the predominant mixed-layer illite–smectite and montmorillonite, the subordinate illite, mixed-layer chlorite–smectite with 5% of smectite layers, mixed-layer kaolinite–smectite with 30% of smectite layers, and kaolinite. This composition of clay minerals changed under the influence of sill intrusions into the sedimentary cover at 58–105 m in the section of Hole 477. The most significant changes are noted in the 8-m-thick member above the sill at 50–58 m. The upper part of this interval is barren of the terrigenous mixed-layer illite–smectite, which is replaced by the newly formed trioctahedral smectite (saponite). At the same time, the terrigenous dioctahedral smectite (montmorillonite) is preserved. The composition of terrigenous clay minerals remains unchanged at the top of the unit underlying the sill base. 相似文献
4.
Results of thermic transformations of ore minerals from genetically different oceanic ferromanganese rocks in the course of their heating up to 1000°C are considered. Manganese minerals with various types of crystalline lattice have different grades of thermic stability. Layered manganese minerals (buserite I, asbolane-buserite, and birnessite) are stable up to 120–150°C; asbolane up to 180°C, vernadite, up to ～500°C; todorokite and pyrolusite (minerals of the tunnel group), up to 600 and 670°C, respectively. Sorbed cations of heavy metals govern the transformation temperature and mineral composition of products of the calcination of ferromanganese rocks. Study of birnessite and todorokite demonstrated that genesis of ferromanganese rocks do not affect thermic properties of minerals in them. 相似文献
5.
ABSTRACT Sandstones occur in back-arc basins of the western Pacific at DSDP sites 299 (Sea of Japan), 297 (northern Shikoku Basin), 445 and 446 (Daito-Ridge-and-Basin Province), 453 (Mariana Trough), 286 (New Hebrides Basin) and 285 (South Fiji Basin). These sandstones are dominantly volcaniclastic arenites derived from andesitic island arcs. The degree of sandstone diagenesis is dependent on original composition, burial rate, heat flow history of the basin, and timing of sandstone deposition with respect to rifting processes and associated high heat flow.
Sandstones containing a larger proportion of volcaniclastic components showed more diagenetic effects than sandstones containing a significant volume of other rock fragments and mineral components. Sandstones deposited during early stages of rifting (sites 445, 446) with a slow burial rate and high crustal heat flow showed the greatest degree of downhole diagenetic change. These diagenetic changes include early pore-space reduction and rim cementation by clay minerals followed later by calcite, and subsequent pore-fill cementation by clinoptilolite, heulandite, analcite and later calcite. Replacement of recognizable volcanic rock fragments by chert, calcite and zeolites was observed in the deepest part of the hole. Sandstones deposited after rifting under conditions of associated lower heat flow showed considerably less diagenetic changes, particularly if burial was rapid.
The high heat flow associated with earliest rifting, associated fluid circulation driven by thermal convection, and slow burial rate controlled the diagenetic history of these sandstones. Thus, timing of sandstone deposition with rifting stage and associated burial rates were key factors in controlling sandstone diagenesis in back-arc basins. 相似文献
Sandstones containing a larger proportion of volcaniclastic components showed more diagenetic effects than sandstones containing a significant volume of other rock fragments and mineral components. Sandstones deposited during early stages of rifting (sites 445, 446) with a slow burial rate and high crustal heat flow showed the greatest degree of downhole diagenetic change. These diagenetic changes include early pore-space reduction and rim cementation by clay minerals followed later by calcite, and subsequent pore-fill cementation by clinoptilolite, heulandite, analcite and later calcite. Replacement of recognizable volcanic rock fragments by chert, calcite and zeolites was observed in the deepest part of the hole. Sandstones deposited after rifting under conditions of associated lower heat flow showed considerably less diagenetic changes, particularly if burial was rapid.
The high heat flow associated with earliest rifting, associated fluid circulation driven by thermal convection, and slow burial rate controlled the diagenetic history of these sandstones. Thus, timing of sandstone deposition with rifting stage and associated burial rates were key factors in controlling sandstone diagenesis in back-arc basins. 相似文献
6.
Clinoptilolite, a zeolite of the heulandite group, occurs commonly in sediments as an authigenic mineral. In the Middle Eocene of southern Israel, it constitutes from a few per cent up to 80 per cent of the insoluble residue of the chalks and limestones. It is associated with opal C-T, montmorillonite and palygorskite. These chalks and limestones overlie the Danian-Palaeocene Taqiya marls which also contain a well-established clay mineral sequence consisting of opal C-T, montmorillonite, palygorskite, sepiolite, and clinoptilolite. This paragenesis of minerals is shown to be typical of the Upper Cretaceous to Eocene times. It is world-wide, occurs in deep-sea sediments as well as in shallow water sediments, and results from the abundance of silica which probably reflects a warmer climate during this time period. The concentration of magnesium in the sea-water and its ratio to the other cations seem to determine which authigenic silicate will be formed. 相似文献
7.
The Hvalfjördur area, 30 km north of Iceland’s capital Reykjavik, belongs to the sequence of Late Tertiary to early Quaternary flood basalts with minor intercalations of hyaloclastites and rhyolites. The basalts are affected by progressive low-temperature metamorphism, caused by the burial of the lava succession and higher heat flow from nearby central volcanoes. Low-grade zeolite facies metamorphism of basaltic lavas in the Hvalfjördur area results in two distinct mineral parageneses that can be correlated to events in the burial and hydrothermal history of the lava pile. Stage Ia represents syn-eruptive near-surface alteration in which celadonite and silica were precipitated along primary pores. During regional burial metamorphism (stage Ib), hydrolysis of olivine and glass led to the formation of mixed-layer chlorite/smectite clays. The chlorite content of stage Ib phyllosilicate vesicle rims increases with increasing burial depth and temperature. Stage II occurred after the burial and is marked by zeolite mineralization caused by higher heat flow from the Laxárvogur and Hvalfjördur central volcanoes. Altogether 11 different zeolites were found in the Hvalfjördur area: analcime, chabazite, epistilbite, heulandite, laumontite, levyne, mesolite, stilbite, stellerite, thomsonite and yugawaralite. In total, three separate depth and temperature-controlled “zeolite zones” occur in the Hvalfjördur area. 相似文献
8.
Fayalite, hypersthene, basalt, and obsidian were dissolved in buffered solutions (25°C; pH 4.5 and 5.5) under air, N2 or O2 atmospheres, in order to follow the kinetics of dissolution. Each dissolved more rapidly at lower pH values, dissolving most rapidly in the initial few days, followed by slower dissolution for periods up to six months. Dissolution was more rapid when air was excluded. In oxygen atmospheres an Fe(OH)3 precipitate armors mineral surfaces, thus inhibiting further dissolution, and further affects the solution by scavenging dissolved silica and cations. Dissolution reactions include initial exchange between cations and H+, incongruent dissolution of silicate structures, oxidation of Fe2+ in solution, precipitation of Fe(OH)3, and scavenging of dissolved silica and cations by Fe(OH)3. Dissolution kinetics may explain weathering of mafic rocks and minerals at the Earth's surface, the formation of Fe-oxide coatings on mineral grains, weathering of submarine mafic rocks and intrastratal solution of mafic minerals in buried sandstones. Early Precambrian weathering would have been more rapid before the appearance of large amounts of oxygen in the atmosphere, and continental denudation rates may have been higher than at present because of this effect and the predominance of mafic igneous rocks at an early stage of continent formation and growth. 相似文献
9.
渤海湾盆地辽河坳陷西部凹陷雷家地区古近系沙河街组四段杜家台油层发现方沸石白云岩及其组合类型。该套岩石具有复杂的矿物组分和沉积构造,以往被认为是一套泥质白云岩和白云质泥岩组合。利用岩石薄片鉴定、X衍射全岩分析、扫描电镜、电子探针等方法,首次发现该套岩石含有大量沉积成因方沸石,其呈纹层状与泥晶白云石混杂沉积,局部可成为方沸石岩。地球化学分析结果表明,该套岩石δ13C值偏正而 δ18O 值偏负,与已报道的热水白云石碳、氧同位素数据非常接近;稀土元素配分曲线特征与其同层位及其下伏房身泡组大套偏碱性玄武岩相似,具有很好的亲缘性。综合上述分析结果认为,方沸石白云岩的形成与房身泡组玄武岩的矿物转变以及湖底热液作用密切相关,为二者共同作用形成的热水沉积岩。 相似文献
10.
Diagenetic trends in the siliceous facies of the Monterey Shale in the Santa Maria region, California 总被引：2，自引：0，他引：2
KENNETH A. PISCIOTTO 《Sedimentology》1981,28(4):547-571
X-ray diffraction and oxygen isotopic analyses of outcrop and subsurface samples of siliceous rocks were used to reconstruct thermal and diagenetic histories of the Miocene Monterey Shale near Santa Maria, California. Within many stratigraphic sections soft, porous diatomaceous rocks change gradationally to underlying hard and brittle chert, porcellanite, and siliceous shale; the accompanying silica mineral zones are, in descending stratigraphic order: (1) biogenic silica (opal-A), (2) cristobalitic silica (opal-CT), and (3) microcrystalline quartz. Boundaries between silica mineral zones and stratigraphic horizons are often discordant. Within the opal-CT zone, the d(101)-spacing of opal-CT decreases in a smooth non-linear fashion from about 4 10 Å to 4-04 Å. In the Santa Maria Valley and Bradley oil field areas the thicknesses of the opal-CT zones are greater and the present thermal gradients less than in the adjacent Orcutt oil field. Thin opal-CT zones at shallow maximum burial depths apparently correlate with higher thermal gradients. Using present thermal gradients and reconstructed maximum burial depths from well data in the Santa Maria region, the ranges in temperatures for the top and base of the opal-CT zone are 38–54 °C and 55–110 °C, respectively. The temperature difference between these two boundaries ranges from 17 to 60 °C. In comparison, temperature ranges for these two boundaries computed from oxygen isotopic compositions of opal-CT and quartz, extrapolated experimental quartz-water fractionations, and assuming δO18= 0%o for the isotopic composition of the equilibrating fluid are 18–56 °C and 31–80 °C for the top and base of the opal-CT zone, respectively. The temperature difference between these boundaries is 11–36 °C using this method. Thermal gradients and sedimentation rates strongly influence rates of silica transformations. Reconstructed thermal and diagenetic histories of siliceous rocks of the Monterey Shale at four well sites in the Santa Maria region demonstrate that most silica conversions probably occurred during the last 3–4 Myr in response to accelerated rates of sedimentation (and therefore burial heating) during the Pliocene. 相似文献
11.
The differentiated Mesozoic alkali dolerite Prospect Intrusion contains a wide range of secondary minerals, including carbonates (primarily calcite), laumontite, prehnite and heulandite, whose stability relationships imply a formation temperature of <200°C. The δ18O data for carbonates define a higher temperature (160 – 195°C) suite, and a lower temperature (51 – 73°C) suite. The δ13C, δ18O and 87Sr/86Sr isotope systematics for these carbonates suggest derivation of the higher temperature group from magmatic fluids, whereas the other group had a major meteoric component that probably originated from porewater in the country rock. Source fluids for prehnite were meteoric rather than magmatic in origin based on their δD and δ18O ratios. Early in the intrusion's emplacement, CO2-rich hydrothermal fluids formed a carbonate rind sealing the upper part of the hydrothermal system and produced the higher temperature carbonates (calcite) and laumontite. Later, cooler fluids with a meteoric component infiltrated vesicles and fractures, depositing the lower temperature carbonates (calcite, aragonite), heulandite and prehnite. 相似文献
12.
Organic matter(OM)is intimately associated with minerals in clay-rich mudstones,leading to widespread organic-mineral interaction during hydrocarbon generation in argillaceous source rocks.What we are concerned is the effects of the different mineral properties on hydrocarbon generation process and mechanism during mineral transformation.In this way,pyrolysis experiments with smectite-octadecanoic acid complexes(Sm-OA and Ex-Sm-OA)were conducted to analyze correlation of mineralogy and pyrolysis behaviors.Based on organicmineral interaction,hydrocarbon generation process was divided into three phases.At 200–300℃,collapse of smectite led to desorption of OM,resulting in high yield of resin and slight increase in saturates.Subsequently,enhanced smectite illitization at 350–450℃was accompanied with large amounts of saturates and a mere gaseous hydrocarbon.Featured by neoformed plagioclase,ankerite,and illite,500C saw plenty of asphaltene and methane-rich gaseous hydrocarbons,revealing cracking reactions of OM.Noteworthy is that saturated and gaseous hydrocarbons in Ex-Sm-OA were considerably more than that in Sm-OA during second and third phases.Quantitative calculation of hydrogen revealed organic hydrogen provided by cross-linking of OM could not balance hydrogen consumed by cracking reactions,but supply of inorganic hydrogen ensured cracking could readily occur and consequently greatly promoted hydrocarbon generation.Further investigating characteristics of mineralogy and pyrolytic products,as well as effects of solid acidity on hydrocarbon generation,we concluded desorption of OM and decarboxylation promoted by Lewis acid were dominated at 200–300C,resulting in lowdegree hydrocarbon generation.While high yield of saturated and gaseous hydrocarbons in second and third phases,together with occurrence of ankerite,indicated predominance of decarboxylation and hydrogenation promoted by Lewis and Br?nsted acid,respectively.Variations in organic-mineral interactions indicated(1)the controls of mineral transformation on hydrocarbon generation process and mechanism include desorption,decarboxylation,and hydrogenation reactions;(2)clay minerals acted as reactants evolving together with OM rather than catalysts.These findings are profoundly significant for understanding the hydrocarbon generation mechanisms,organic-inorganic interactions,and carbon cycle. 相似文献
13.
Lauren C. Duarte Leo A. Hartmann Luiz H. Ronchi Zsolt Berner Thomas Theye Hans J. Massonne 《Mineralium Deposita》2011,46(3):239-255
Stable isotopes (C, O, S) and mineralogical studies of the world-class amethyst-geode deposits of the Los Catalanes gemological
district, Uruguay, constrain processes operative during mineral deposition. The mineralized basaltic andesites from the Cretaceous
Paraná volcanic province are intensely altered to zeolites (clinoptilolite) and clay minerals. Variations in the δ18O values of silica minerals in geodes (chalcedony, quartz, and amethyst) are much larger and the values generally somewhat
lower (21.2–31.5‰) in the Uruguayan deposits than in the Ametista do Sul area of southern Brazil. The range of δ34S values (−15.0 to −0.3‰) of altered basaltic rocks requires (in addition to sulfur of magmatic origin) the involvement of
34S-depleted sedimentary sulfur from bacterial sulfate reduction. The results delimit the mineralizing processes to a post-eruption
environment characterized by low temperature and strong interaction of the lava flows with meteoric water. 相似文献
14.
The Coniacian Arnager Limestone Formation is exposed on the Danish island of Bornholm in the Baltic Sea. It is composed of mound-bedded siliceous chalk, and X-ray diffraction and scanning electron microscopy indicate a content of 30–70% insoluble minerals, including authigenic opal-CT, quartz, clinoptilolite, feldspars, calcite, dolomite, and barite. Opal-CT and clinoptilolite are the most common and constitute 16–53% and 2–9%, respectively. The content of insoluble minerals varies laterally both within the mounds and in planar beds, and the opal-CT content varies by up to 10% vertically. The mounds consist of two microfacies, spiculitic wackestone and bioturbated spiculitic wackestone, containing 10–22% and 7–12% moulds after spicules, respectively.Subsequent to deposition and shallow burial, dissolution of siliceous sponge spicules increased the silica activity of the pore water and initiated precipitation of opal-CT. The opal-CT formed at temperatures around 17 °C, the precipitation lowered the silica activity and the Si/Al ratio of the pore water, resulting in precipitation of clinoptilolite, feldspar and smectite. Calcite formed synchronously with the latest clinoptilolite. Minor amounts of quartz precipitated in pore water with low silica activity during maximum burial, probably to depths of 200–250 m. The dissolution of sponge spicules and decomposition of the sponge tissue also resulted in the release of Ba2+, Sr2+, Mg2+, Ca2+ and CO32?, facilitating precipitation of barite and dolomite. Precipitation of especially opal-CT reduced the porosity to an average of 40% and cemented the limestone. The study highlights the diagenetic pathways of bio-siliceous chalk and the effects on preservation of porosity and permeability. 相似文献
15.
Heat-induced changes in speciation and extraction of uranium associated with sheet silicate minerals
《Applied Geochemistry》2003,18(8):1121-1135
Three samples of gouge from a U-mineralised fault, and two model samples, montmorillonite and muscovite, spiked with U, were heat-treated at a range of temperatures up to 1100 °C. Mineralogical changes were followed by thermal analysis, powder XRD and electron microscopy, and U extractability was measured by extraction with NH4+. Changes in U speciation in the montmorillonite sample were followed using EXAFS spectroscopy. On heating, the minerals progressively dehydrate, dehydroxylate and eventually decompose to form new phases in a glassy matrix. In the case of montmorillonite (90% of U extractable from unheated material), U extractability increased slightly on heating to temperatures around 400 °C. Almost 50% of U was extracted from unheated muscovite, and this increased slightly by 450 °C. Above 500–600 °C, U extractability from both montmorillonite and muscovite declined to very low levels, reflecting dehydration of the uranyl ion and trapping in the new phases and glassy matrix. Uranium extractability from the natural samples was much lower in all cases (0.25–5% of the total before heating). In 2 samples, a significant increase in U extraction was associated with dehydroxylation at around 600 °C, followed by a decrease to very low levels at higher temperatures. Uranium extraction from the third natural sample, which contained X-ray amorphous U minerals, decreased steadily on heating. The results show that changes in U extraction can be related to structural and morphological changes in sheet silicate minerals. Heat treatment has potential to fix U but only if temperatures above 800 °C are reached. If only lower temperatures, in the range 400–600 °C, are used, then U extraction may increase. 相似文献
16.
Isotopic and mineralogic data from an 8500-m thick section of the Great Valley sequence, northern California, indicate that changes in the δ18O values of authigenic minerals resulted from the conversion of smectite to a 10 Å clay-mineral as temperature increased with burial in the Jurassic- Cretaceous outer-arc basin. The clay-mineral assemblage in mudstone is characterized by a proportional increase of the 10 Å clay-mineral with increasing stratigraphic depth, and by a depletion in the δ18O value of the mixed-layer smectite/10 Å clay-mineral with descending stratigraphic position from +21.9 to + 15.5%. SMOW. Modeling of the oxygen isotopic data from authigenic phases, based on equilibrium fractionation during clay-mineral diagenesis, indicates that δ18O values of calcite in mudstones and of calcite cements in sandstone precipitated along a temperature gradient of about 25°C/km during maximum burial to about 6–7 km. δD values of the mixed-layer smectite/10 Å clay-mineral range between ?69 to ?44%. SMOW. Using temperatures calculated from the oxygen isotopic data, the deuterium and oxygen isotopic data indicate that the smectite underwent late-stage dehydration and probably buffered the composition of formation waters from sea water values to isotopic compositions of δ18O ≈ +8%. SMOW and δD ≈ ?25%. SMOW. The δ13C values of calcite from mudstone and sandstone imply that crystallization of authigenic calcite was linked to organic diagenesis during which dissolved HCOt-3 was continuously enriched in 13C as temperature increased with burial. At the base of the sequence and immediately overlying the ophiolitic basement rocks, several hundred meters of strata were altered by more oxygen-depleted (δ18O ? +4 to +5%.) hydrothermal fluids emanating from the ophiolitic rocks, probably at maximum burial depth. 相似文献
17.
M. S. Babushkina L. P. Nikitina A. G. Goncharov N. I. Ponomareva 《Geology of Ore Deposits》2009,51(8):712-722
Hydrous species and the amount of water (OH? ions and crystal hydrate H2O) in structures of nominally anhydrous rock-forming minerals (olivine, ortho- and clinopyroxenes) were studied with Fourier spectroscopy in peridotite nodules (19 samples) from Cenozoic alkali basalts of the Baikal-Mongolia region (Dariganga Plateau, Taryat Depression, and Vitim Plateau). Single-crystal samples oriented relative to the crystallographic axes of minerals were examined with an FTIR spectrometer equipped with an IR microscope at the points of platelets free from fluid inclusions. FTIR spectra were measured in regions of stretching vibrations of OH? and H2O (3800–3000 cm?1) and deformation vibrations of H2O (1850–1450 cm?1). The water content in mineral structures was determined from integral intensities. To estimate the conditions of entrapment and loss of structural water in minerals, their chemical composition, including Fe2+ and Fe3+ contents, was determined with an electron microprobe analysis and Mössbauer spectroscopy. The bulk chemical composition of some nodules was determined with XRF and ICP MS. The total water content (OH? + H2O) varies from 150 to 1140 ppm in olivines, from 45 to 870 ppm in clinopyroxenes, and from 40 to 1100 ppm in orthopyroxenes. Both water species in the mineral structures are retained down to a depth of 150–160 km in wide temperature and pressure ranges (1100–1500 °C, 32–47 kbar) at the oxygen fugacity of ?1.4 to ?0.1 log units relative to that of the quartz-fayalite-magnetite buffer. 相似文献
18.
Thermodynamic modeling of the hydrothermal exposure of the rocks of the Bazhenov Formation resulted in revealing the equilibrium mineral associations at 50–350°C and the pressure of saturated water vapor. The calculation results show that mineral parageneses varied slightly with the increase of temperature. Thus, zeolites were characterized by the stilbite–laumontite–wairakite series; kaolinite, pyrite, dolomite, and brannerite were replaced by montmorillonite and/or albite, pyrrhotite, calcite, and uraninite, respectively. The modeling results were confirmed in experiments. 相似文献
19.
《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
20.
台地泥质组分沉积记录了源—汇过程和环境演化等沉积学领域信息,可作为古气候和古环境重建的重要载体。然而,利用沉积物中的泥质组分进行古气候和古环境恢复时仍存在相当大的复杂性和局限性。鉴于此,笔者以上寺剖面中二叠统茅口组为例,通过研究该层位富泥质组分灰岩—泥灰岩韵律的宏微观形貌学和矿物学特征,发现其泥质组分主要由成岩黏土矿物海泡石构成,其次为少量滑石和蒙脱石。基于前人认识,进一步运用电子探针和激光原位元素地球化学分析手段,综合认为海泡石中镁元素来源于继承海水的孔隙水以及亚稳定矿物的转化释放,硅元素可能来源于上扬子台地的同沉积期断裂热液。此外,滑石主要形成于海泡石埋藏过程中的成岩转化,蒙脱石可能也具有类似成因,但不排除有少量蒙脱石来源于火山物质的海底改造。结合区域资料,华南中二叠统浅水碳酸盐台地上广泛发育自生成因（早期成岩作用和埋藏成岩作用）泥质组分。因此,在利用泥质组分来恢复古环境的时候,需要谨慎识别其成因,这将有利于提高沉积旋回识别和环境解释的准确性;另一方面,对自生成因泥质组分进行专门研究,在成岩过程以及成岩地球化学信号识别上也具有参考价值。 相似文献