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1.
Kaolinitic clays associated with sedimentary rocks cover widespread in the Yeniköy formation from the Akhar?m district, (Afyonkarahisar, W Anatolia). Due to the proximity to the ceramic industry areas such as Kütahya and U?ak Province of Turkey, the clays in the Akhar?m district have been intensively exploited for the last few years. The Akhar?m kaolinitic clays were hosted by Middle-Upper Miocene-aged Yeniköy formation and divided into two parts as northeastern and southwestern via normal fault. The alteration degree increases from lower levels to surface in the NE part of deposit. Besides layered structure in their N70° W/30° SW direction and gray-beige, yellowish brown colored in SW part. This study focused on mineralogy, geochemistry, and ceramic properties of kaolinitic clays. X-ray diffraction (XRD) and scanning electron microscope (SEM) analysis, chemical, physical, and mechanical tests were conducted on studied samples from the wall of clay quarry. Akhar?m clay deposits consist of mainly kaolinite and quartz. Additionally, they include smectite, biotite, feldspar, jarosite, calcite, and hematite minerals. Akhar?m clays are characterized with their moderate plasticity (PL = 17.07–24.09), low water absorption (3.64–9.53 wt.%), low linear shrinkage (8.08–15.55 wt.%), high bending strength (17.72–32.69 N/mm2), and ideal lightness values (L* = 46.50–82.74) and color values (a* = 4.71–29.87; b* = 14.67–28.72). These properties vary related with mineralogical and geochemical features of Akhar?m clays. In conclusion, Akhar?m clays have desired specifications for floor and wall t to their mineralogical, geochemical, and ceramic properties.  相似文献   

2.
This work presents the main characteristics of 97 quarry wastes, collected in 23 gravel pits, from the Jarama river area, Madrid province, Spain. In this area, more than 2.5 × 106 ton of silty-clay waste are generated every year, and no applications have as yet been defined for them. This work is the first systematic study of the fine fractions generated from the Jarama river quaternary deposits, playing part in the comprehension of this complex terrace systems. Quartz, potassium feldspar, plagioclase, calcite, and complex mixtures of phyllosilicates, such as smectite, illite, kaolinite, chlorite and illite/smectite mixed layer, have been detected. Two sets of waste which are recognized according to the calcite content, have been directly related with the terrace level beneficed in the Jarama river, and the position along the valley. Calcite concentrates in the wastes produced in the lower course, where Henares and Tajuña tributaries promote an extensive change in the geochemistry of underground water, and locally, in the petrology of quarried conglomerates. This clear distinction by location between calcite-bearing and calcite-free wastes is essential for potential applications, such as soil conditioning, raw materials for brick or tiles, etc. The wastes studied can be considered as a potential source of industrial raw materials because of their uniformity and large volume. This suggestion is now being carried out, with an attempt at assessing the possibilities of using these mining wastes as ceramic raw materials.  相似文献   

3.
Gouges formed in north-northeast-striking fault zones of the Sydney region and associated host-rocks were investigated by XRD, SEM, TEM and optical microscopy in order to determine their mineralogy. XRD studies reveal that illite, illite–smectite, kaolinite, quartz and dickite are present in varying proportions. Kübler Indices (0.54–0.71) and low smectite contents in illite–smectite (<10% smectite) in most gouges and host-rocks, indicate the assemblages formed at temperatures between 120 and 150°C. Those at the Heathcote Road, Lucas Heights location formed at lower temperatures (<100°C). SEM images of the clays in host sublitharenites and gouges show a variety of sizes and habits that reflect variations in fluid temperature and rate of crystallisation. SEM studies also reveal that detrital quartz grains exhibit overgrowths and etch pits of varying density, size and shape that are more strongly developed in the gouges than in the host-rocks. These features are thought to be related to higher fluid/rock ratios brought about by major ingress of fluids into the fault zones. The mineral assemblage present and the features exhibited are believed to have formed in response to a thermal event associated with the early stages of the breakup of Gondwana.  相似文献   

4.
Abstract

The characteristics and distribution of clay minerals and their effects on reservoir quality in the Huagang sandstones in the Xihu Sag, East China Sea Basin were studied by using X-ray diffraction, casting thin-sections, scanning electron microscopy, electron microprobe analysis, fluid inclusion analysis, constant-rate mercury injection and nuclear magnetic resonance. Clay minerals consist of kaolinite, chlorite, illite and illite–smectite mixed layer (I/S); kaolinite forms from dissolved feldspars, chlorite occurs as clay coatings that are transformed from clay precursors owing to the flocculation of suspended detrital clays or the crystallisation of pore fluids, and illite forms from the illitisation of detrital smectite, authigenic kaolinite and K-feldspars. Clay distribution is controlled by sedimentary environments, burial history and lithologies. Typical reservoirs in the western sub-sag are thin and developed in braided river facies at relatively shallow burial depths with clays dominated by kaolinite. However, typical reservoirs in the central inversion tectonic zone are thicker and developed in a braided delta front facies at deeper burial depths with clays mainly consisting of chlorite, illite and I/S. High-quality reservoirs are characterised by coarse granularity, high quartz content and low clay content with widespread development of chlorite coatings that inhibit quartz cements at low temperatures. At higher temperatures, the high-quality reservoirs develop more pores providing growth space for quartz cements and result in the coexistence of chlorite coatings and quartz cements. The high-quality reservoirs are controlled by their lithological characteristics rather than chlorite coatings. Illite and I/S clays create severe damage to reservoirs by reducing the size and connectivity of pore-throats.  相似文献   

5.
In order to investigate changes caused in clay mineralogy and potassium (K) status by different land-use types, 42 soils samples (0–30 cm) were monitored and analyzed. Soil samples belonging to Reference Soil Groups of Cambisols and Vertisols were collected from three neighboring land uses involving cropland (under long-term continuous cultivation), grassland, and forestland. The soils reflected an alkaline and calcareous aspect as were characterized by high pH (mean of 7.1 to 7.5) and calcium carbonate equivalent (mean of 35 to 97 g?kg?1) in the three land-use types. X-ray diffraction patterns of the clay fraction showed that the soils were mainly composed of illite, smectite, chlorite, and kaolinite. Chlorite and kaolinite remained unweathered irrespective of land use and soil types, soil processes, and physicochemical attributes assessed. Some changes in the XRD diffractograms of illite and smectite (the intensity or the position of peaks) were observed in the cultivated soils compared to those of the adjoining grassland that may explain the dynamics of the K trapped in illite interlayer sites. Potassium issues reflected a heterogeneous response to changes in land-use types. In light of this, a pronounced variation in soluble K (4–22 mg?kg?1), exchangeable K (140–558 mg?kg?1), and non-exchangeable K (135–742 mg?kg?1) appeared among the land-use types for both Cambisols and Vertisols, corresponding to variability in clay content, nature and type of clay mineral (mainly illite and smectite), cation exchange capacity (CEC), and soil organic carbon (SOC). In general, the largest amounts of soluble K and exchangeable K were recorded in the forestland, whereas the highest contents of non-exchangeable K were found in the grassland for both Cambisols and Vertisols. Exchangeable K, available K, CEC, and clay contents in the soils with higher smectite values (25–50 %) were significantly different (P?≤?0.05) compared to those of the lower smectite values (10–25 %). This suggests that smectite is a major source for surface sorption of K in the studied soils.  相似文献   

6.
The smectite-to-chlorite conversion is investigated through long-duration experiments (up to 9 years) conducted at 300 °C. The starting products were the Wyoming bentonite MX80 (79 % smectite), metallic iron and magnetite in contact with a Na–Ca chloride solution. The predominant minerals in the run products were an iron-rich chlorite (chamosite like) and interstratified clays interpreted to be chlorite/smectite and/or corrensite/smectite, accompanied by euhedral crystals of quartz, albite and zeolite. The formation of pure corrensite was not observed in the long-duration experiments. The conversion of smectite into chlorite over time appears to take place in several steps and through several successive mechanisms: a solid-state transformation, significant dissolution of the smectite and direct precipitation from the solution, which is over-saturated with respect to chlorite, allowing the formation of a chamosite-like mineral. The reaction mechanisms are confirmed by X-ray patterns and data obtained on the experimental solutions (pH, contents of Si, Mg, Na and Ca). Because of the availability of some nutrients in the solution, total dissolution of the starting smectite does not lead to 100 % crystallization of chlorite but to a mixture of two dominant clays: chamosite and interstratified chlorite/smectite and/or corrensite/smectite poor in smectite. The role of Fe/(Fe + Mg) in the experimental medium is highlighted by chemical data obtained on newly formed clay particles alongside previously published data. The newly formed iron-rich chlorite has the same composition as that predicted by the geothermometer for diagenetic to low-grade metamorphic conditions, and the quartz + Fe-chlorite + albite experimental assemblage in the 9-year experiment is close to that fixed by water–rock equilibrium.  相似文献   

7.
《Applied Geochemistry》1998,13(7):905-916
Experiments measuring kaolinite and smectite dissolution rates were carried out using batch reactors at 35° and 80°C. No potential catalysts or inhibitors were present in solution. Each reactor was charged with 1 g of clay of the ≤2 μm fraction and 80, 160 or 240 ml of 0.1–4 M KOH solution. An untreated but sized kaolinite from St. Austell and two treated industrial smectites were used in the experiments. One smectite is a nearly pure montmorillonite, while the second has a significant component of beidellitic charge (35%). The change in solution composition and mineralogy was monitored as a function of time. Initially, the 3 clays dissolved congruently. No new formed phases were observed by XRD and SEM during the pure dissolution stage. The kaolinite dissolution is characterized by a linear release of silica and Al as a function of the log of time. This relationship can be explained by a reaction affinity effect which is controlled by the octahedral layer dissolution. Far from equilibrium, dissolution rates are proportional to a0.56±0.12OH− at 35°C and to a0.81±0.12OH− at 80°C. The activation energy of kaolinite dissolution increases from 33±8 kJ/mol in 0.1 M KOH solutions to 51±8 kJ/mol in 3 M KOH solutions. In contrast to kaolinite, the smectites dissolve at much lower rates and independently of the aqueous silica or Al concentrations. The proportionality of the smectite dissolution rate constant at 35 and 80°C was a0.15±0.06OH−. The activation energy of dissolution appears to be independent of pH for smectite and is found to be 52±4 kJ/mol. The differences in behavior between the two kinds of minerals can be explained by structural differences. The hydrolysis of the tetrahedral and the octahedral layer appears as parallel reactions for kaolinite dissolution and as serial reactions for smectite dissolution. The rate limiting step is the dissolution of the octahedral layer in the case of kaolinite, and the tetrahedral layer in the case of smectite.  相似文献   

8.
The composition of river water, sediments, and pore waters (down to 30 cm below the bed) of Las Catonas Stream was studied to analyze the distribution of trace elements in a peri-urban site. The Las Catonas Stream is one of the main tributaries of Reconquista River, a highly polluted water course in the Buenos Aires Province, Argentina. The semi-consolidated Quaternary sediments of the Luján Formation are the main source of sediments for Las Catonas Stream. The coarse-grained fraction in the sediments is mainly composed of tosca (calcretes), intraclasts, bone fragments, glass shards, quartz, and aggregates of fine-grained sediments together with considerably amounts of vegetal remains. The clay minerals are illite, illite–smectite, smectite, and kaolinite. For the clay-sized fraction, the external surface area values are mostly between 70 and 110 m2g?1, although the fraction at 15 cm below the bottom of the river shows a lower surface area of 12 m2g?1. The N2 adsorption–desorption isotherms at 77 K for this sample display a behavior indicative of non-porous or macroporous material, whereas the samples above and below present a typical behavior of mesoporous materials with pores between parallel plates (slit-shaped). As, Cr, Cu, and Cd concentrations increase down to 15 cm depth in the sediments, where the highest trace element and total organic carbon (TOC) concentrations were found, and then decrease toward the bottom of the core. Except for As, the levels of the other heavy metals show higher concentration in surficial waters than in pore waters. Distribution coefficients between the sediments, pore water, and surficial water phases indicate that As is released from the sediments to the pore and surficial waters. Cu content strongly correlates with TOC (mainly from vegetal remains), suggesting that this element is mainly bound to the organic phase.  相似文献   

9.
Clay minerals associated with intra-volcanic bole horizons of varied colours and thicknesses contain montmorillonite, halloysite and kaolinite, show distinct microstructures and microaggregates. In kaolinite, Fe3+ ions substitute for Al3+ at octahedral sites. Most of these clays are dioctahedral type, show balance between net layer and interlayer charges. The interstratified illite — smectite (I/S) mixed layers containing variable proportions of montmorillonite. Illite contains sheet-like, well oriented microaggregates. The parallel stacks of chlorite sheets show chlorite/smectite (C/S) mixed layers. Progressive enrichment of Fe and depletion of Al ions with the advancement of kaolinization process is observed. High order of structural and compositional maturity observed in these bole clays, indicate long hiatus between the two volcanic episodes.  相似文献   

10.
The incorporation of OH defects in quartz as a function of Li content in the bulk system and pressures was investigated. Quartz crystals were grown in water-saturated granitic systems, containing various amounts Li, B and P, supplied as accessory phases such as spodumene, tourmaline or apatite in the starting mixtures. High pressure experiments were performed at temperatures between 900 and 1100 °C, and pressures between 5 and 20 kbar with a piston cylinder apparatus, and the synthesized quartz crystals were analyzed by IR spectroscopy, electron microprobe and LA-ICP-MS spectroscopy. All IR absorption spectra revealed absorption features that can be assigned to AlOH (3313, 3379 and 3431 cm?1) and (4H)Si defects (3585 cm?1), whereas quartz grown in the Li and B systems exhibited two additional bands related, respectively, to LiOH (3483 cm?1) and BOH defects (3596 cm?1). It was further observed that LiOH incorporation increases with higher spodumene content in the starting material and decreases with pressure, until no LiOH defects are observed at pressure higher than 15 kbar. Specifically, the most pronounced reduction of LiOH defects occurs in a rather narrow pressure interval (10–15 kbar) close to the high-quartz/low-quartz transition. However, the link between the transition and the defect incorporation remains unclear. Li total concentrations always exceed the Li-coupled LiOH defects, suggesting the simultaneous presence of dry AlLi defects. Results of this study suggest that LiOH defects are detectable only in quartz crystals grown from middle and upper crustal sections (such as hydrothermal quartz) and not in quartz from deep roots of orogenic granitoids.  相似文献   

11.
Soil total porosity is, rather than measured by water desorption method, more often estimated from bulk density (BD) and assumed particle density. Measured and estimated total porosities of even kaolinitic tropical soils (which have low tendency to expand upon wetting) usually differ by an extent that depends on soil structural stability, but such differences are scarcely documented. Seventy samples of coarse-textured soils under different fallow- and cultivation-management systems in the southeastern region of Nigeria were analyzed for texture, mean-weight diameter (MWD) of aggregates, BD and organic matter (OM) concentration. Soil total porosities measured by water desorption method were compared with those estimated from BDs (with particle density fixed at 2.70 g cm?3), after grouping the soils by structural stability, assessed by OM/(silt + clay) for 50 of the samples from fallowed plots (BD > 1.48 g cm?3) and MWD for the rest from cultivated plots (BD < 1.48 g cm?3). The fallowed plots showed a wider stability range than the cultivated plots. Irrespective of land use, structural stability tended to increase with decreasing soil BD. Measured total porosities were consistently higher than their estimated counterparts, with the differences closing up with increasing soil structural stability up till a mean BD of 1.41 ± 0.05 g cm?3 (corresponding to MWD of 2.66 ± 0.12 mm), beyond which the trend reversed. These results suggest that, as the soil structural stability increases, soil particle density decreases while entrapped air and transitory drainage of saturated samples at weighing increase. Estimating total porosity with a fixed particle density of 2.70 g cm?3 appears suitable only in highly stable soils, with BD of ≤1.40 ± 0.08 g cm?3 and/or MWD of ≥2.92 ± 0.05 mm [corresponding to OM/(silt + clay) of ≥16.38 ± 0.28 %].  相似文献   

12.
This study focused on typical injection layers of deep saline aquifers in the Shiqianfeng Formation used in the Carbon Capture and Sequestration Demonstration Projects in the Ordos Basin, Northwest China. The study employed experiments and numerical simulations to investigate the mechanism of CO2 mineral sequestration in these deep saline aquifers. The experimental results showed that the dissolved minerals are plagioclase, hematite, illite–smectite mixed layer clay and illite, whereas the precipitated minerals are quartz (at 55, and 70 °C) and kaolinite (at 70 °C). There are rare carbonate mineral precipitations at the experimental time scale, while the precipitation of quartz as a product of the dissolution of silicate minerals and some intermediate minerals rich in K and Mg that transform to clay minerals, reveals the possibility of carbonate precipitation at the longer time scale. These results are consistent with some results previously reported in the literature. We calibrated the kinetic parameters of mineral dissolution and precipitation by these experimental results and then simulated the CO2 mineral sequestration under deep saline aquifer conditions. The simulation results showed that the dissolved minerals are albite, anorthite and minor hematite, whereas the precipitated minerals are calcite, kaolinite and smectite at 55 and 70 °C. The geochemical reaction of illite is more complex. At 55 °C, illite is dissolved at the relatively lag time and transformed to dawsonite; at 70 °C, illite is precipitated in the early reaction period and then transformed to kaolinite. Based on this research, sequestrated CO2 minerals, which are mainly related to the temperature of deep saline aquifers in Shiqianfeng Fm., are calcite and dawsonite at lower temperature, and calcite at higher temperature. The simulation results also establish that calcite could precipitate over a time scale of thousands of years, and the higher the temperature the sooner such a process would occur due to increased reaction rates. These characteristics are conducive, not only to the earlier occurrence of mineral sequestration, but also increase the sequestration capacity of the same mineral components. For a sequestration period of 10,000 years, we determined that the mineral sequestration capacity is 0.786 kg/m3 at 55 °C, and 2.180 kg/m3 at 70 °C. Furthermore, the occurrence of mineral sequestration indirectly increases the solubility of CO2 in the early reaction period, but this decreases with the increase in temperature.  相似文献   

13.
The newly independent country of Timor Leste is located in the eastern half of Timor Island (Indonesian archipelago). Geological studies of the country’s mineral resources and extractive activities are practically non-existent. There is evidence of the exploitation of ceramic raw materials at outcrop level and two small brick kilns, nowadays inactive, in the Dili and Aileu areas. Near Aileu, there are light-coloured silt-rich deposits, interpreted as overbank deposits, interbedded with ancient river terraces (post-Pliocene) overlying metamorphic bedrock. These sediments are the subject of this study, which encompassed geological mapping and preliminary characterisation. Tectonically, the area is a graben, preserving alluvium and colluvium deposits. Five channel samples representative of the silt-rich deposits were collected. Semi-quantitative mineralogical analysis shows that the samples are made of illite, quartz and kaolinite clays, with accessory illite/vermiculite interstratified minerals and K-feldspar. The chemical data show agreement with the estimated mineralogical composition. The grain size distribution points to a silt-dominated assemblage. Most samples have a satisfactory extrudability but deficient moulding properties. After firing, the sampled raw materials form a final product with possible ceramic capability for whiteware production.  相似文献   

14.
Natural and constructed clay liners are routinely used to contain waste and wastewater. The impact of acidic solutions on the geochemistry and mineralogy of clays has been widely investigated in relation to acid mine drainage systems at pH > 1.0. The impact of H2SO4 leachate characterized by pH < 1.0 and potentially negative pH values on the geochemistry and mineralogy of clays is, however, not clear. Thus, laboratory batch experiments were conducted on three natural clay samples with different mass ratios of smectite, illite and kaolinite to investigate the impact of H2SO4 on the geochemistry and mineralogy of aluminosilicates from pH 5.0 to −3.0. Batch testing was conducted at seven pH treatments (5.0, 3.0, 1.0, 0.0, −1.0, −2.0 and −3.0) using standardized H2SO4 solutions for four exposure periods (14, 90, 180, and 365 d). Aqueous geochemical and XRD analyses showed: increased dissolution of aluminosilicates with decreasing pH and increasing exposure period, that smectite was more susceptible to dissolution than illite and kaolinite, precipitation of an amorphous silica phase occurred at pH ? 0.0, and anhydrite precipitated in Ca-rich clays at pH ? −1.0. In addition, global dissolution rates were calculated for the clays and showed good agreement to literature smectite, illite and kaolinite dissolution rates, which suggests global dissolution rates for complex clays could be determined from monomineralic studies. A stepwise conceptual model of the impact of H2SO4 on aluminosilicate geochemistry and mineralogy between pH 5.0 and −3.0 is proposed.  相似文献   

15.
Gold mineralization in the Velvet District occurs in an eastward dipping sequence of late Tertiary rhyolitic ash-flow tuffs, flows, and tuffaceous sediments in northwestern Nevada. Minor gold and silver concentrations are associated with irregular zones of brecciation, argillic alteration, and quartz veining along north-northeast trending normal faults. Reaction of mineralizing fluids with wallrock produced an argillic alteration assemblage of illite, mixed-layer clays, smectite, and kaolinite. Illite alteration and highest gold concentrations appear to be associated with zones of high water/rock ratios. Kaolinite, smectite, alunite, and opal are postulated to have formed during a steam-dominated episode of alteration.Fluid inclusion studies indicate that the quartz veins were deposited in the temperature range 230 to 280°C from fluids which had salinities equivalent to 0.2–0.8 weight percent NaCl. δ 18O of quartz veins varies from ?2.5 to +6.7 ‰ and indicates that the ore fluid must have been Tertiary meteroric water. Stable isotope data appear to define a zone of concentrated fluid flow and potential subsurface mineralization in the southeastern part of the district. Fluid inclusion and isotope studies can be used in combination with more standard geochemical, geophysical, and geological information to provide site-specific targets for epithermal metal concentrations.  相似文献   

16.
The vein system in the Arinem area is a gold‐silver‐base metal deposit of Late Miocene (8.8–9.4 Ma) age located in the southwestern part of Java Island, Indonesia. The mineralization in the area is represented by the Arinem vein with a total length of about 5900 m, with a vertical extent up to 575 m, with other associated veins such as Bantarhuni and Halimun. The Arinem vein is hosted by andesitic tuff, breccia, and lava of the Oligocene–Middle Miocene Jampang Formation (23–11.6 Ma) and overlain unconformably by Pliocene–Pleistocene volcanic rocks composed of andesitic‐basaltic tuff, tuff breccia and lavas. The inferred reserve is approximately 2 million tons at 5.7 g t?1 gold and 41.5 g t?1 silver at a cut‐off of 4 g t?1 Au, which equates to approximately 12.5t of Au and 91.4t of Ag. The ore mineral assemblage of the Arinem vein consists of sphalerite, galena, chalcopyrite, pyrite, marcasite, and arsenopyrite with small amounts of pyrrhotite, argentite, electrum, bornite, hessite, tetradymite, altaite, petzite, stutzite, hematite, enargite, tennantite, chalcocite, and covellite. These ore minerals occur in quartz with colloform, crustiform, comb, vuggy, massive, brecciated, bladed and calcedonic textures and sulfide veins. A pervasive quartz–illite–pyrite alteration zone encloses the quartz and sulfide veins and is associated with veinlets of quartz–calcite–pyrite. This alteration zone is enveloped by smectite–illite–kaolinite–quartz–pyrite alteration, which grades into a chlorite–smectite–kaolinite–calcite–pyrite zone. Early stage mineralization (stage I) of vuggy–massive–banded crystalline quartz‐sulfide was followed by middle stage (stage II) of banded–brecciated–massive sulfide‐quartz and then by last stage (stage III) of massive‐crystalline barren quartz. The temperature of the mineralization, estimated from fluid inclusion microthermometry in quartz ranges from 157 to 325°C, whereas the temperatures indicated by fluid inclusions from sphalerite and calcite range from 153 to 218 and 140 to 217°C, respectively. The mineralizing fluid is dilute, with a salinity <4.3 wt% NaCl equiv. The ore‐mineral assemblage and paragenesis of the Arinem vein is characteristically of a low sulfidation epithermal system with indication of high sulfidation overprinted at stage II. Boiling is probably the main control for the gold solubility and precipitation of gold occurred during cooling in stage I mineralization.  相似文献   

17.
A series of natural silica impactite samples from Chicxulub (Mexico) was investigated by Raman microprobe (RMP) analysis. The data yield evidence for high-pressure shock metamorphism in the rock. The impactite contains three polymorphs of silica: the original α-quartz, and two high-pressure varieties – coesite and disordered quartz representing various degrees of crystallinity. We found systematic changes in frequencies and half-widths of the Raman bands, caused by increasing irregularities of bond-lengths and bond-angles and a general breaking-up of the structure as a result of impact events. Therefore, RMP is an adequate tool for measuring the crystallinity of disordered quartz. The half-width Γ and the frequency ω of the symmetric SiOSi stretching vibrational band (A1 mode) of the SiO4 tetrahedra are the most amenable parameters for estimating the degree of crystallinity. In well-crystallized quartz, Γ=5 cm?1 and ω=464 cm?1, while in highly disordered quartz this line shifts up to ω=455 cm?1 and broadens up to Γ=30 cm?1. The Raman lineshapes appear to depend strongly on the degree of lattice disorder subsequent to impact events. To cite this article: M. Ostroumov et al., C. R. Geoscience 334 (2002) 21–26  相似文献   

18.
The clay mineralogy of the clay intervals interbedded with siliceous mudstones across the Permian-Triassic boundary (PTB) in Pengda, Guiyang, Guizhou province, was investigated by X-ray diffraction (XRD) and high resolution transmission electron microscopy (HRTEM). The clay mineral assemblages of the sediments are mainly I/S clays and minor smectite, kaolinite, and illite as reveled by XRD analyses. The peak-shape parameters BB1 and BB2 of I/S clays of the representative clay bed PL-01 are 4.7° and 4.4°, and the peak position of the low angle reflection is at 6.8° 2θ (13.6 ), suggesting that the I/S clays has a IS type of ordering. However, the presence of multi-order reflections and their intensities are different from those of completely ordered 1∶1 mixed-layer I/S clay rectorite, indicating that I/S clays of the Pengda section have partially ordered IS structures. HRTEM observations show that most of the I/S clays exhibit an IS stacking ordering. However, in some areas within a IS particle, smectite layer is observed in doublets, triplets, and quartets, which are interstratified by various amounts of illite layers, suggesting the presence of other irregular stacking in addition to the major 1∶1 IS ordered stacking. Transformation of smectite layer into illite layers is also observed in the I/S clays, suggesting that the Pengda I/S clays are derived from smectite illitization, in good agreement with the clay mineral assemblage. The I/S clays of the Pengda section contain up to 45% to 95% smectite layer, the notably higher contents of smectite layer relative to those of other PTB stratigraphic sets in south China can be attributed to difference in alteration and smectite illitization processes due to different sedimentary environments.  相似文献   

19.
We investigated the speciation of Fe in bulk and in suspended respirable quartz dusts coming from ceramic and iron-casting industrial processes via X-ray absorption spectroscopy, with the aim of contributing to a better understanding of the variability of crystalline silica toxicity. Four different bulk industrial quartz powders, nominally pure quartz samples with Fe contents below 200 ppm, and three respirable dusts filters were selected. Fe speciation was determined in all samples through a coupled study of the X-ray absorption near-edge structure and extended X-ray absorption fine structure regions, operating at the Fe–K edge. Fe speciation revealed common features at the beginning of the different production processes, whereas significant differences were observed on both respirable dusts and bulk dusts exiting from the production process. Namely, a common pollution of the raw quartz dusts by elemental Fe was evidenced and attributed to residuals of the industrial production of quartz materials. Moreover, the respirable samples indicated that reactivity occurs after the suspension of the powders in air. The gravitational selection during the particle suspension consistently allowed us to clearly discriminate between suspended and bulk dusts. On the basis of the obtained results, we provide an apparent spectroscopic discrimination between the raw materials used in the considered industrial processes, and those that are effectively inhaled by workers. In particular, an amorphous FeIII oxide, with an unsaturated coordination sphere, can be related to silica reactivity (and health consequences).  相似文献   

20.
《Chemical Geology》2003,193(3-4):273-293
The El Berrocal granite/U-bearing quartz vein (UQV) system has been studied as a natural analogue of a high-level radioactive waste repository. The main objective was to understand the geochemical behaviour of natural nuclides under different physicochemical conditions. Within this framework, the argillization processes related to fracturing and formation of the uranium–quartz vein were studied from a mineralogical and isotopic standpoint in order to establish their temperatures of formation and thus complete the geothermal history of the system. For this purpose, δ18O values were determined for pure mineral from the unaltered granite and quartz from the uranium–quartz vein, as well as for mixture samples from the hydrothermally altered granite (sericitised granite) and clayey samples from fracture fillings, including the clayey walls of the uranium–quartz vein. The isotopic signature of quartz from the uranium–quartz vein and the monophasic nature of its fluid inclusions led us to conclude that the isotopic signature of water in equilibrium with quartz was approximately in the range from −8.3‰ to −5.7‰ V-SMOV, its temperature of formation being around 85–120 °C. The δ18O values of pure sericite from the hydrothermally altered granite, calculated by means of the oxygen fraction molar method, indicate that its temperature of formation, in equilibrium with the aforementioned waters, is also in the range from 70 °C to approximately 120 °C. Clays from fracture fillings and clayey walls of the uranium–quartz vein are usually mixtures, in different proportions, of illite, approximately formed between 70 and 125 °C; two generations of kaolinite formed at approximately 90–130 °C and at around 25 °C, respectively; smectite, formed at ≤25 °C; and occasionally palygorskite, formed either between 30 and 45 °C or 19 and 32 °C, depending on the fractionation equation used. These data suggest that sericite from the hydrothermally altered granite, quartz from the uranium–quartz vein, illite and the first generation of kaolinite from the fracture fillings resulted from the same hydrothermal process affecting the El Berrocal granite in relation to fracturing. Under certain physicochemical conditions (T≈100 °C, pH≈8 and log [H4SiO4] between −4 and −3), illite and kaolinite can be paragenetic. As a result of weathering processes, smectite was formed from hydrothermal illite and inherited albite under alkaline weathering, while the second generation of kaolinite was formed from smectite, under acid conditions and close to the sulphide-rich uranium–quartz vein. Palygorskite is an occasional mineral formed probably either during the thermal tail of the above-described hydrothermal process or during weathering processes. In both cases, palygorskite must have formed from alkaline Si–Mg-rich solutions. Finally, these data and processes are discussed in terms of natural analogue processes, drawing some implications for the performance assessment of a deep geological radwaste repository (DGRR).  相似文献   

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