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1.
以皂石、高岭石、绿泥石和伊利石为原材料,分别与赖氨酸进行反应,研究赖氨酸在上述粘土矿物上的吸附行为, 并运用粉末X-射线衍射技术（XRD）、傅里叶变换红外吸收光谱术（FTIR）和热重（TG）等分析方法,表征反应前后粘土 矿物的变化。实验结果表明,不同粘土矿物对赖氨酸的吸附等温线均符合Freundlich等温方程,且不同粘土矿物对赖氨酸的 饱和吸附量大小顺序为：皂石>蒙脱石>绿泥石>高岭石>伊利石;XRD结果表明皂石对赖氨酸的吸附发生在矿物层间,而绿 泥石、高岭石和伊利石对赖氨酸的吸附主要在矿物表面进行;FTIR和TG结果表明赖氨酸主要取代粘土矿物层间吸附水,以 氢键的形式与Si-O-Si(IVAl)键合。实验结果将有助于进一步探明环境中粘土矿物对有机质的吸附机理。  相似文献   

2.
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   

3.
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   

4.
Elevated concentrations of arsenic in the sediment and pore water in the Sundarban wetlands pose an environmental risk. Adsorption and desorption are hypothesized to be the major processes controlling arsenic retention in surface sediment under oxic/suboxic condition. This study aims to investigate sorption kinetics of As(III & V) and its feedback to arsenic mobilization in the mangrove sediment. It ranges from sand to silty clay loam and shows the adsorption of As(III & V) following the Langmuir relation. Estimates of the maximum adsorption capacity are 59.11 ± 13.26 μg g−1 for As(III) and 58.45 ± 8.75 μg g−1 at 30°C for As(V) in the pH range 4 to 8 and salinity 15–30 psu. Extent of adsorption decreases with increasing pH from 4 to 8 and desorption is the rate-limiting step in the reaction of arsenic with sediment. Arsenic in the sediment could be from a Himalayan supply and co-deposited organic matter drives its release from the sediment. Arsenic concentration in the sediment is well below its maximum absorption capacity, suggesting the release of sorbed arsenic in pore water by the microbial oxidation of organic matter in the sediment with less feedback of adsorption.  相似文献   

5.
Iheya‐North‐Knoll is one of the small knolls covered with thick sediments in the Okinawa Trough back‐arc basin. At the east slope of Iheya‐North‐Knoll, nine hydrothermal vents with sulfide mounds are present. The Integrated Ocean Drilling Program (IODP) Expedition 331 studied Iheya‐North‐Knoll in September 2010. The expedition provided us with the opportunity to study clay minerals in deep sediments in Iheya‐North‐Knoll. To reveal characteristics of clay minerals in the deep sediments, samples from the drilling cores at three sites close to the most active hydrothermal vent were analyzed by X‐ray diffraction, scanning electron microscope and transmission electron microscope. The sediments are classified into Layer 0 (shallow), Layer 1 (deep), Layer 2 (deeper) and Layer 3 (deepest) on the basis of the assemblage of clay minerals. Layer 0 contains no clay minerals. Layer 1 contains smectite, kaolinite and illite/smectite mixed‐layer mineral. Layer 2 contains chlorite, corrensite and chlorite/smectite mixed‐layer mineral. Layer 3 is grouped into three sub‐layers, 3A, 3B and 3C; Sub‐layer 3A contains chlorite and illite/smectite mixed‐layer mineral, sub‐layer 3B contains chlorite/smectite and illite/smectite mixed‐layer minerals, and sub‐layer 3C contains chlorite and illite. Large amounts of di‐octahedral clay minerals such as smectite, kaolinite, illite and illite/smectite mixed‐layer mineral are found in Iheya‐North‐Knoll, which is rarely observed in hydrothermal fields in mid‐ocean ridges. Tri‐octahedral clay minerals such as chlorite, corrensite and chlorite/smectite mixed‐layer mineral in Iheya‐North‐Knoll have low Fe/(Fe + Mg) ratios compared with those in mid‐ocean ridges. In conclusion, the characteristics of clay minerals in Iheya‐North‐Knoll differ from those in mid‐ocean ridges; di‐octahedral clay minerals and Fe‐poor tri‐octahedral clay minerals occur in Iheya‐North‐Knoll but not in mid‐ocean ridges.  相似文献   

6.
In the oxidized zone of Rakha-Chapri Block of the Singhbhum Copper Belt, alteration of biotite, chlorite and muscovite extends down to ∼ 60 m. Below this level, these minerals are not altered, implying a supergene origin for the clay alteration products. The altered host-rock profile consists of an upper, predominantly kaolinitic zone and a lower illite-chlorite rich zone, with the clay minerals showing an overall tendency to decrease with depth. Kaolinite is the dominant clay mineral, the proportion of which varies considerably with depth, and chlorite, illite and halloysite are the other clay minerals of the oxidized zone. Incipient removal of copper even from the cap rocks, in-situ transformation of sulphides to oxidized compounds, and the unusual mode of occurrence of copper in the oxidized zone are the characteristic features of the Rakha-Chapri Block. Insufficient localized hydrolysis of silicates is considered responsible for relatively low acidity in the oxidized zone as a whole. Copper forms a component of the clay minerals probably as surface adsorbed or/lattice-bound ions.  相似文献   

7.
Microbial reduction of Fe(III) in clay minerals is an important process that affects properties of clay-rich materials and iron biogeochemical cycling in natural environments. Microbial reduction often ceases before all Fe(III) in clay minerals is exhausted. The factors causing the cessation are, however, not well understood. The objective of this study was to assess the role of biogenic Fe(II) in microbial reduction of Fe(III) in clay minerals nontronite, illite, and chlorite. Bioreduction experiments were performed in batch systems, where lactate was used as the sole electron donor, Fe(III) in clay minerals as the sole electron acceptor, and Shewanella putrefaciens CN32 as the mediator with and without an electron shuttle (AQDS). Our results showed that bioreduction activity ceased within two weeks with variable extents of bioreduction of structural Fe(III) in clay minerals. When fresh CN32 cells were added to old cultures (6 months), bioreduction resumed, and extents increased. Thus, cessation of Fe(III) bioreduction was not necessarily due to exhaustion of bioavailable Fe(III) in the mineral structure, but changes in cell physiology or solution chemistry, such as Fe(II) production during microbial reduction, may have inhibited the extent of bioreduction. To investigate the effect of Fe(II) inhibition on CN 32 reduction activity, a typical bioreduction process (consisting of lactate, clay, cells, and AQDS in a single tube) was separated into two steps: (1) AQDS was reduced by cells in the absence of clay; (2) Fe(III) in clays was reduced by biogenic AH2DS in the absence of cells. With this method, the extent of Fe(III) reduction increased by 45-233%, depending on the clay mineral involved. Transmission electron microscopy observation revealed a thick halo surrounding cell surfaces that most likely resulted from Fe(II) sorption/precipitation. Similarly, the inhibitory effect of Fe(II) sorbed onto clay surfaces was assessed by presorbing a certain amount of Fe(II) onto clay surfaces followed by AH2DS reduction of Fe(III). The reduction extent consistently decreased with an increasing amount of presorbed Fe(II). The relative reduction extent [i.e., the reduction extent normalized to that when the amount of presorbed Fe(II) was zero] was similar for all clay minerals studied and showed a systematic decrease with an increasing clay-presorbed Fe(II) concentration. These results suggest a similar inhibitory effect of clay-sorbed Fe(II) for different clay minerals. An equilibrium thermodynamic model was constructed with independently estimated parameters to evaluate whether the observed cessation of Fe(III) reduction by AH2DS was due to exhaustion of reaction free energy. Model-calculated reduction extents were, however, over 50% higher than experimentally measured, indicating that other factors, such as blockage of the electron transfer chain and mineralogy, restricted the reduction extent. Another important result of this study was the relative reducibility of Fe(III) in different clays: nontronite > chlorite > illite. This order was qualitatively consistent with the differences in the crystal structure and layer charge of these minerals.  相似文献   

8.
Industrial uranium orebodies have recently been found through in-depth uranium exploration in the Luohe Formation in the southwestern Ordos Basin, which is an important breakthrough in deep prospecting for sandstone-type uranium deposits. The composition, content and characteristics of clay minerals in the Luohe Formation in the Zhenyuan area were systematically studied by means of thin section identification, scanning electron microscopy, X-ray diffraction and altered mineral spectral scanning. Unlike the most important uranium-bearing rock series in the Zhiluo Formation in the northeast and southwest of the basin, the ore-bearing Luohe Formation sandstone has low contents of clay minerals while the clay mineral assemblages vary in different sand bodies. Among them, the main types of mudstone, oxidized sandstone, calcareous sandstone and mineralized sandstone are illite-smectite mixed-layer mineral and illite, followed by kaolinite and chlorite, the main types uranium-rich sandstone and gray-green sandstone are kaolinite and illite-smectite mixed-layer mineral, followed by illite and chlorite. Even though adsorption of clay minerals, such as chlorite, illite-smectite mixed-layer mineral, kaolinite, and illite may contribute to U enrichment and uranium mineral precipitation, no correlation between clays and uranium minerals have been observed, indicating that clay minerals are not the main factor affecting uranium enrichment during the deep metallogenic process. The study of clay minerals in the Luohe Formation sandstone demonstrated that there are at least two phases of chlorite and one phase of kaolinite in the study area, which respectively represent two phases of alkaline fluid and one phase of acid fluid activities, revealing a fluid phase transition of alkaline-acidic-alkaline. Therefore, the clay minerals can be used as an important indicator for uranium mineralization. © 2020, Science Press. All right reserved.  相似文献   

9.
Siliciclastic sediments on the insular shelf of Puerto Rico are derived from a volcanic arc. The sands are feldspatholithic and subquartzose. They confirm predictions about sandstones of arc derivation in the following ways. The quartz content is low, usually less than 25 %. Feldspar is more abundant than quartz, but less so than lithic fragments. If mud rip-up clasts are excluded from the lithic suite, the ratio V/L (volcanic lithic grains to total unstable lithic grains) assumes values near 0.75. Most of the volcanic lithic grains have textures suggesting intermediate volcanics as source rocks. Ratios of plagioclase to total feldspar are high. Values of the parameter C/Q (stable lithic fragments to total lithic grains) are higher than expected for sandstones of volcanic provenance. Four compositionally and areally distinct assemblages of clay minerals are recognized. Clay suites characterized by major concentrations of both halloysite and smectite are found off the north-west coast. Sediments off the north-central and north-east coasts contain major concentrations of halloysite and lesser amounts of smectite, illite and chlorite. Major concentrations of kaolinite are present off the south-east coast. An assemblage of poorly crystallized smectite with lesser amounts of illite and chlorite occurs off the south-west and south-central coasts. Variation in the mineralogic composition of clays around the perimeter of the island reflects changes in the intensity of chemical weathering and the type of rock exposed in the immediate source area and, in instances, either early diagenetic alteration or, more likely, sorting within the clay fraction by currents on the shelf.  相似文献   

10.
The Shurijeh Reservoir Formation of Neocomian age is represented by a sandstone sequence, occasionally interbedded with shale, in the Gonbadli gas field, Kopet-Dagh Basin, Northeastern Iran. In this study X-ray diffraction (XRD) and X-ray fluorescence (XRF) techniques were used together to characterize the Shuirjeh clay minerals in 76 core samples collected from two deep Gonbadli wells. The results of XRF analysis showed high percentages of silicon and moderate to low percentages of aluminum, sulfur, calcium, potassium, sodium, magnesium, and iron in both wells. The XRD analysis indicated that the above elements were concentrated in the form of quartz, anhydrite, dolomite, calcite, plagioclase, K-feldspar, hematite, and clay minerals. Further XRD examination of the clay fraction revealed that illite, chlorite, and kaolinite were the major types of clay minerals. Unlike, glauconite, smectite, and a mixed layer clays of both the illite–smectite and chlorite–smectite types were observed only in very few samples. The percentages of individual clay minerals were determined using external standard calibration curves and successfully validated by a system of simultaneous linear equations acquired from detailed elemental information based on the XRF analysis. The error reached ± 5% for the main mineral constituent and ± 15% for minor minerals. A local regression relationship was also derived, based on the XRF elemental information, which can be used to estimate the clay contents of other Shurijeh drilled wells with data of pulsed-neutron spectroscopy tools. According to the proposed quantitative approach, the amount of illite varied considerably, reaching 18.3%. In contrast, the amounts of kaolinite and chlorite were generally small, i.e., less than 8.4%. The amount of total clay minerals changed greatly from a minimum of 5% to a maximum of 32.5%. An increase in illite with increasing burial depth and temperature was an obvious indication of deep burial diagenesis in this formation.  相似文献   

11.
Burial Metamorphism of the Ordos Basin in Northern Shaanxi   总被引：1，自引：0，他引：1  
Burial metamorphism has been found in the Ordos basin of northern Shaanxi. On the basis of a rather intensive study of burial metamorphism of sandstone, it has been shown that the evolution from diagenesis to metamorphism involves four stages: cementation of clay minerals, regrowth of pressolved quartz and feldspar, cementation of carbonates and formation of laumontite. On that basis it has been put forward that the laumontite is formed by burial metamorphism of clay and carbonate minerals. According to the thermodynamic data of minerals, the conditions under which laumontite is formed are T<250℃ and X_(CO_2)<0.17. High-resolution SEM and TEM studies of clay minerals in mudstone show that there occur a mixed layer assemblage of bertherine and illite/chlorite and transformation from bertherine to chlorite. On that basis coupled by the X-ray diffraction analysis the author suggests the following transformation of clay minerals during burial metamorphism: the earliest smectite-kaolinite assemblage changes into the bertherine-illite mixture with increasing depth, then into the illite/chlorite mixed layer assemblage and finally into dispersed individual illite and chlorite. The reaction of the transformation is:smectite+kaolinite+K~+=illite+chlorite+quartz According to the study of the oxygen isotope thermometry of the coexisting illitequartz pair, the temperature of the above transformation is lower than 180℃.  相似文献   

12.
贵州碳酸盐岩红土中的粘土矿物及其形成机理   总被引：13，自引：2，他引：13  
朱立军  傅平秋 《矿物学报》1996,16(3):290-297,T001
本文运用Ｘ射线衍射、红外光谱、差热、透射电镜和扫描电镜等方法对贵州碳酸盐岩红土中的粘土矿物进行了系统研究。高岭石和０．７ｎｍ埃洛石是碳酸盐岩红土中的主要粘土矿物，其次为伊利石、蛭石、绿泥石、绿泥石／蛭石混层矿物，水铝英石和三水铝石等。  相似文献   

13.
A 54-m long core was raised from the bed of the Nal Sarovar, a large shallow lake located in the middle of the low-lying region linking the Gulfs of Kachchh and Khambhat, in western India. A three-layer sequence comprising: Zone-1 (top 3 m), predominantly silty-clay/clayey; Zone-2 (3–18 m), sandy; and Zone-3 (18–54 m), dominated by sticky silty-clay/clayey-silt with occasional thin sand layers and basalt fragments was identified. Smectite and illite are the dominant clay minerals with minor amounts of kaolinite and chlorite. Very high content of smectite (53–97%) in the clays of the lowermost zone (18–54 m) and the geomorphic features of the surrounding region suggested that the sediments were derived from the basaltic terrain of Saurashtra and/or via the Gulf of Khambhat. The clay content in the middle zone (3–18 m), dominantly sandy, is very low. Therefore, provenance for this zone was derived using heavy minerals in the sand fraction. The heavy mineral species in this zone suggested the mixed metamorphic and igneous terrain of Aravallis as the major source. The grain-size distribution of this zone closely matched with the sediments underlying the modern Sabarmati riverbed at Ahmedabad, suggesting fluvial depositional environment. Clays also dominate sediments of the topmost (0–3 m) zone with illite as the dominant (74–81%) specie followed by smectite suggesting derivation from the mixed metamorphic and igneous terrain of Aravallis.  相似文献   

14.
This study collected the early Oligocene to middle Miocene sediments from the Gerze Basin of Tibet, and used X-Ray diffraction （XRD） and Scanning Electron Microscope （SEM） to discuss their clay mineralolgy, clay indices, better understand the clay mineralogy and its paleoclimatic significance. The results show that clay minerals of the Gerze Basin sediments are mainly composed of iilite and chlorite, with minor amounts of smectite and kaolinite, and their relative content varies along the section. Variations of relative contents and clay indices suggest that the Gerze Basin has experienced three-stage evolution of paleoclimate： I ） high ilUte and chlorite contents, with fluctuant smectite and low （I＋Ch）/（K＋S） ratio, indicative of a dominant seasonal arid climate from the early Oligoeene to late Oligocene; Ⅱ） higher illite and chlorite contents and larger （I＋Ch）/（K＋S） ratio but absence of kaolinite, indicating a colder and drier climate from the late Oligocene to early Miocene; Ⅲ） high iilite and chlorite contents with fluctuant （I＋Ch）/（K＋S） ratios and occasional occurrence of kaolinite, suggesting that the climate became warmer and more humid compared with that of stage Ⅱ in the mid-Miocene. These conclusions were also reinforced by the clay morphology, which suggests that physical weathering dominated in stage Ⅱ, while relatively strong chemical weathering was dominant in stages Ⅰ and Ⅲ Clay minerals of the sediments mainly consist of illite and chlorite, indicating that the source rock played a significant role in clay origin. It is inferred that global cooling and the enhancement of denudation and obstruction of northward moisture due to the uplift of the Qinghai-Tibet Plateau were responsible for the provenance of iUite and chlorite under weak chemical weathering. Though the Qinghai-Tibet Plateau reached a certain elevation by the mid-Miocene, yet the mid-Miocene widespread warming might have largely impacted the Gerze climate.  相似文献   

15.
对江西赣南6个地区风化淋滤型稀土矿中全风化层的粘土矿物进行了研究,为进一步了解粘土矿物对该类型稀土矿中稀土元素分异的影响奠定了基础。X射线衍射自然定向片、甲酰胺片、饱和乙二醇片和加热片、红外光谱及扫描电镜观察结果表明该区粘土矿物以片状高岭石和针管状7埃洛石为主,其中坳背塘、长坑屋、上堡、杨村样品主体为高岭石,足洞样品中发育大量埃洛石,而石排样品中高岭石与埃洛石比例相当。电感耦合等离子体质谱分析表明稀土元素在粘土矿物中大量富集,其稀土元素配分不仅受到原岩的影响,而且受到粘土矿物本身性质的影响。Ce元素在足洞和石排样品的粘土矿物中表现出正异常,而在其他样品粘土矿物中表现为负异常,可能与其中发育的埃洛石密切相关。Ce元素可能以方铈矿胶膜的形式包裹在针状埃洛石中,和/或以离子形式被选择性吸附于埃洛石表面。  相似文献   

16.
Summary ?Sheet silicates of the serpentine–kaolin-group (serpentine, kaolinite, dickite, nacrite, halloysite), the talc–pyrophyllite-group (talc, pyrophyllite), the smectite-group (montmorillonite), and illite (as a mineral of the mica-group) were investigated to obtain information concerning their cathodoluminescence behaviour. The study included analyses by cathodoluminescence (CL microscopy and spectroscopy), electron paramagnetic resonance (EPR), X-Ray diffraction (XRD), scanning electron microscopy (SEM) and trace element analysis. In general, all dioctahedral clay minerals exhibit a visible CL. Kaolinite, dickite, nacrite and pyrophyllite have a characteristic deep blue CL, whereas halloysite emission is in the greenish-blue region. On the contrary, the trioctahedral minerals (serpentine, talc) and illite do not show visible CL. The characteristic blue CL is caused by an intense emission band around 400 nm (double peak with two maxima at 375 and 410 nm). EPR measurements indicate that this blue emission can be related to radiation induced defect centres (RID), which occur as electron holes trapped on apical oxygens (Si–O centre) or located at the Al–O–Al group (Al substituting Si in the tetrahedron). Additional CL emission bands were detected at 580 nm in halloysite and kaolinite, and between 700 and 800 nm in kaolinite, dickite, nacrite and pyrophyllite. Time-resolved spectral CL measurements show typical luminescence kinetics for the different clay minerals, which enable differentiation between the various dioctahedral minerals (e.g. kaolinite and dickite), even in thin section. Received December 3, 2001; revised version accepted February 27, 2002  相似文献   

17.
The clay mineralogy of the Newark Supergroup (Upper Triassic/Lower Jurassic) in the Connecticut Valley was studied by X-ray diffraction analysis. Clay minerals identified in 126 samples are illite, chlorite, smectite, kaolinite, vermiculite, expandable chlorite, mixed-layer illite/smectite, mixed-layer chlorite/smectite, and mixed-layer chlorite/vermiculite. In general, the rocks are illitic with subordinate amounts of chlorite. However, the various lithofacies in the Newark Supergroup are characterized by distinct clay-mineral assemblages. Red beds of floodplain origin contain clays mainly of detrital nature with 2M illite most abundant. Subordinate amounts of chlorite, smectite, vermiculite, kaolinite and mixed-layer illite/smectite are also present. An interstratified chlorite/vermiculite occurs in red mudstone underlying basalt flows. Lacustrine gray beds are generally characterized by the clay-mineral assemblage 1Md illite + chlorite with minor amounts of smectite ane expandable chlorite. An interstratified chlorite/smectite predominates in gray mudstone associated with perennial lake cycles in the East Berlin Formation. Black shales of deeper lacustrine origin contain the assemblage 1Md ifillite + trioctahedral smectite and traces of chlorite. Illite and smectite also occur as mixed-layer phases.In many respects, the distribution of clay minerals in the Connecticut Valley can be likened to the general scheme proposed for the Permo-Triassic basins of Europe and Africa. These display both vertical and horizontal variations in clay-mineral assemblages that reflect the chemical and spatiotemporal evolution of intrabasin depositional and diagenetic environments. Chemical data indicate that magnesium, especially, was concentrated in the black muds of large perennial lakes that intermittently occupied the Connecticut rift valley. Pore waters derived from these sediments played an important role in the development of Mg-rich 2 : 1 and interstratified clay minerals during early diagenesis.  相似文献   

18.
Laboratory experiments indicate that clay particles of the <2-üm fraction can be considerably degraded by the bivalve Mytilus edulis: dickite, kaolinite, smectite, chlorite and illite particles are partially dissolved and rounded by the digestive processes. Structural changes and a decrease in crystallinity of kaolinites, dickites and illites are striking. Investigations of clay minerals from tidal flat sediments highly populated by marine invertebrates, from marine suspensions and samples from profiles across Mytilis edulis beds on the North Sea coast of Germany show, however, that these materials have a uniform mineral composition. This uniformity of clay mineralogy can be explained by the hydrodynamic conditions in the nearshore area, where tidal currents and waves cause a periodic resuspension and transport of sediments introduced into the Wadden Sea from different sources (glacial, fluviatile). Processes of bioturbation also redistribute the sedimentary material. These mixing processes effectively erase any evidence of local enrichment of the biogenically degraded clays. However, the disordered clays should react more sensitively (i.e. have higher adsorption capacities for organic substances, hydroxides and metals) in sediments than untreated materials, so that biodegradation is of basic importance for clay diagenesis. During these processes, Pb, V, Ni and Fe are dissolved from the digested particles.  相似文献   

19.
巴州坳陷下白垩统—中侏罗统的粘土矿物特征   总被引：1，自引：1，他引：0       下载免费PDF全文
根据岩石薄片、Ｘ衍射和扫描电镜分析资料,本文研究了巴州坳陷下白垩统—中侏罗统粘土矿物特征,发现粘土矿物分为伊利石、伊／蒙混层和绿泥石三种类型。粘土矿物的类型和含量随深度而变化,形成了伊／蒙混层带、混层迅速转化带和伊利石带。粘土矿物的转化和自生粘土矿物的形成是沉积地层非常重要的成岩变化。  相似文献   

20.
为了从深层次揭示控制黏土矿物天然气吸附能力的主要因素, 选择不同来源和成因的泥页岩中的常见黏土矿物进行了甲烷等温吸附实验.分析显示不同类型的黏土矿物气体吸附能力差异明显, 各种黏土矿物甲烷吸附容量次序为蒙脱石＞＞伊蒙混层＞高岭石＞绿泥石＞伊利石＞粉砂岩＞石英岩.黏土矿物结晶结构决定了矿物片层之间的层间孔隙和聚合体颗粒之间粒间孔隙的形态和大小, 从而决定着其表面积和气体吸附性能.黏土矿物甲烷吸附能力与电镜扫描所反映的微孔隙发育程度密切相关.研究表明, 黏土矿物的气体吸附能力不仅与黏土类型有关, 而且明显受成岩演化程度和岩石成因的影响.此外, 随粒度减小孔隙连通性和内表面积的不断增加, 黏土矿物气体吸附能力有所升高.   相似文献   

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