首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 546 毫秒
1.
During weathering, elements enriched in black shale are dispersed in the environment by aqueous and mechanical transport. Here a unique evaluation of the differential release, transport, and fate of Fe and 15 trace elements during progressive weathering of the Devonian New Albany Shale in Kentucky is presented. Results of chemical analyses along a weathering profile (unweathered through progressively weathered shale to soil) describe the chemically distinct pathways of the trace elements and the rate that elements are transferred into the broader, local environment. Trace elements enriched in the unweathered shale are in massive or framboidal pyrite, minor sphalerite, CuS and NiS phases, organic matter and clay minerals. These phases are subject to varying degrees and rates of alteration along the profile. Cadmium, Co, Mn, Ni, and Zn are removed from weathered shale during sulfide-mineral oxidation and transported primarily in aqueous solution. The aqueous fluxes for these trace elements range from 0.1 g/ha/a (Cd) to 44 g/ha/a (Mn). When hydrologic and climatic conditions are favorable, solutions seep to surface exposures, evaporate, and form Fe-sulfate efflorescent salts rich in these elements. Elements that remain dissolved in the low pH (<4) streams and groundwater draining New Albany Shale watersheds become fixed by reactions that increase pH. Neutralization of the weathering solution in local streams results in elements being adsorbed and precipitated onto sediment surfaces, resulting in trace element anomalies.Other elements are strongly adsorbed or structurally bound to solid phases during weathering. Copper and U initially are concentrated in weathering solutions, but become fixed to modern plant litter in soil formed on New Albany Shale. Molybdenum, Pb, Sb, and Se are released from sulfide minerals and organic matter by oxidation and accumulate in Fe-oxyhydroxide clay coatings that concentrate in surface soil during illuviation. Chromium, Ti, and V are strongly correlated with clay abundance and considered to be in the structure of illitic clay. Illite undergoes minimal alteration during weathering and is concentrated during illuvial processes. Arsenic concentration increases across the weathering profile and is associated with the succession of secondary Fe(III) minerals that form with progressive weathering. Detrital fluxes of particle-bound trace elements range from 0.1 g/ha/a (Sb) to 8 g/ha/a (Mo). Although many of the elements are concentrated in the stream sediments, changes in pH and redox conditions along the sediment transport path could facilitate their release for aqueous transport.  相似文献   

2.
《Applied Geochemistry》2000,15(8):1219-1244
Arsenian pyrite, formed during Cretaceous gold mineralization, is the primary source of As along the Melones fault zone in the southern Mother Lode Gold District of California. Mine tailings and associated weathering products from partially submerged inactive gold mines at Don Pedro Reservoir, on the Tuolumne River, contain ∼20–1300 ppm As. The highest concentrations are in weathering crusts from the Clio mine and nearby outcrops which contain goethite or jarosite. As is concentrated up to 2150 ppm in the fine-grained (<63 μm) fraction of these Fe-rich weathering products.Individual pyrite grains in albite-chlorite schists of the Clio mine tailings contain an average of 1.2 wt.% As. Pyrite grains are coarsely zoned, with local As concentrations ranging from ∼0 to 5 wt.%. Electron microprobe, transmission electron microscope, and extended X-ray absorption fine-structure spectroscopy (EXAFS) analyses indicate that As substitutes for S in pyrite and is not present as inclusions of arsenopyrite or other As-bearing phases. Comparison with simulated EXAFS spectra demonstrates that As atoms are locally clustered in the pyrite lattice and that the unit cell of arsenian pyrite is expanded by ∼2.6% relative to pure pyrite. During weathering, clustered substitution of As into pyrite may be responsible for accelerating oxidation, hydrolysis, and dissolution of arsenian pyrite relative to pure pyrite in weathered tailings. Arsenic K-edge EXAFS analysis of the fine-grained Fe-rich weathering products are consistent with corner-sharing between As(V) tetrahedra and Fe(III)-octahedra. Determinations of nearest-neighbor distances and atomic identities, generated from least-squares fitting algorithms to spectral data, indicate that arsenate tetrahedra are sorbed on goethite mineral surfaces but substitute for SO4 in jarosite. Erosional transport of As-bearing goethite and jarosite to Don Pedro Reservoir increases the potential for As mobility and bioavailability by desorption or dissolution. Both the substrate minerals and dissolved As species are expected to respond to seasonal changes in lake chemistry caused by thermal stratification and turnover within the monomictic Don Pedro Reservoir. Arsenic is predicted to be most bioavailable and toxic in the reservoir’s summer hypolimnion.  相似文献   

3.
The northwestern Guizhou in the Yangtze Craton of south China has a tremendous potential of shale gas resource. In this paper, we present results from major and trace elements, total organic carbon, mineralogical composition analysis and petrophysical parameters to characterise shale weathering features. Further, the differences of black shale between underground and outcrops have also been presented to examine the changes of black shale after weathering. Our results show that the trace elements of shale have varying degrees of loss in the weathering leaching process, both in Niutitang shale and Longmaxi shale, the loss of B, V, Ni, Cu, Zn and Ba is obvious, but the element migration quantity in the former is greater than in the latter. Decomposition of minerals such as pyrite, feldspar and calcite result in the leaching of Na, Ca, Mg and Fe. The loss rate of total organic carbon (TOC) in black shales ranges from 18% to 70% with an average of 43%; moreover, the loss of organic carbon in samples with high TOC content is larger than in those samples with low TOC content. Results following the testing of porosity and permeability show that porosity increases significantly after weathering but permeability changes little. Furthermore, the increment of porosity is greater in the Niutitang shale (with more sulphide minerals) than in the Longmaxi shale, suggesting that the oxidation of sulphide minerals may have led to the formation of an acidic environment, causing the other minerals in the black shale to weather more quickly, thus resulting in increased porosity. The content of clay minerals in the core samples is slightly lesser than the outcrop samples, but the TOC content in the core samples is greater and has a larger specific surface area. This suggest that the TOC content played a decisive role on the specific surface area of shale. In addition, changes in the black shale caused by the weathering process mainly depend on the mineral composition and the TOC content in shale. In this study, we try to establish relations between outcrop samples and core samples, in order to better understand the underground characteristics of shale reservoir.  相似文献   

4.
The mineralogy and geochemistry data are presented for thirty-seven shales,four concretions,two carbonate sediments and seven lignites from the Marathousa coal field of the Megalopolis Basin in Greece.The argillaceous rocks consist of chlorite,illite,kaolinte,albite,quartz.opal-A,calcite and dolomite;the concretions of aragonite,gypsum and pyrite;and the carbonate rocks of calcite,quartz and illite.The mineral matter in the lignites consists of gypsum,quartz,albite,chlorite,illite,opal-A,dolomite,pyrite,and rarely calcite and kaolinite Athree-factor model explains the total variaition of major and trace elements in the argillaceous sediments.The first factor is an aluminosilicate factor and involves the following elements:Al,Si,Mg,Na,K,Ti,Mn,Nb,Y,Rb,Zn,Cu,Ni,Cr,Nband V,associated with chlorite,albite and illite.The second factor involves the elements Ca,Sr,Ba,Znand Sc and is related to carbonate lithology and mainly the carbonate concretions with gypsum.The third factor involves Fe and Ce with a weak association with Mn.The diagenesis of the Marathousa sediments and lignites was not very advanced as indicated by (a) the total thickness of the sequence (500m),(b) the presence of biogenic silica(opal-A) and (c) the age of the deposit(Pleistocene).FOr these reasons the rpresence of chlorite,illite and kaolinite in the sediments and lignite is due not to diagenetic reactions but to weathering of the flysch and metamorphic rocks at the edges of the Megalopolis Basin and transport of the weathering products(illite,chlorite,kaolinite)into the basin of deposition.The diagenetic minerals of the Marathousa sequence include pyrite,gypsum,dolomite and aragonite.  相似文献   

5.
铜陵矿区废矿石次生氧化产物及其成因初探   总被引：1，自引：0，他引：1  
对铜陵矿区废矿石的矿物组成及其成因进行研究,利用X射线衍射仪（XRD）和扫描电子显微镜（SEM）分析原生矿物及其风化产物的组成,探讨次生矿物的形成机制。XRD及SEM/EDS分析表明,废矿石中残留的主要原生矿物为黄铁矿,次生矿物为针铁矿、赤铁矿、水铁矿及次生硫酸盐矿物。原生矿物风化为次生矿物的过程是从黄铁矿的裂隙带等有缺陷的部位开始,逐步氧化成最终产物针铁矿。中间过程出现了矿物相及形态的多样性,局部可能会先形成中间产物水铁矿,由于水铁矿很不稳定,在不同的温、湿度条件下会很快转化成针铁矿或赤铁矿。针铁矿在风化过程中呈现出多种形态,针状矿物最先形成,随后重结晶成球状集合体和菱方双锥单晶,最后在废矿石表面完全覆盖一层土状针铁矿。SEM观察到的黄铁矿表面的生物矿物与最外层风化层上的菌丝类物质说明,在废矿石的风化过程中生物亦起了一定的作用。  相似文献   

6.
Mineral matter in three naturally weathered coals from Pennsylvania strip mines and in two laboratory-oxidized coals has been characterized by 57Fe Mössbauer spectroscopy, scanning electron microscopy and other techniques to determine mineralogical trasnformations that occur in coals during weathering. Pyrite was found to be the most readily oxidized mineral, forming a variety of iron sulfates initially and geethite eventually. The iron sulfates formed were different in the two laboratory-oxidized coals, despite identical oxidation treatments. Calcite disappeared from one calcite-rich coal with increasing oxidation, but was not replaced by an equivalent amount of gypsum. A severely weathered strip-mine coal was enriched in calcium, which was dispersed through the oxidized macerals. Extended X-ray absorption fine-structure spectroscopy indicated that this dispersed calcium was most likely present as salts of carboxylic acids. Siderite was suprisingly resistant to oxidation at room temperature. Less direct evidence indicates that clay minerals also take part in the alteration to some extent.The coals oxidized in the laboratory showed alteration behavior that differed in a number of respects from that of the strip-mine coals. For example, iron sulfates were much less common in the latter coals; also, the formation of geothite appeared to be controlled to a large extent by the pyrite particle size in the strip-mine coals, but not in the laboratory-oxidized coals.The oxidation of an individual pyrite grain is not only a function of general conditions (temperature, humidity, oxygen partial pressure), but also the immediate local (< 1 mm) chemistry, as a variety of iron sulfates were observed in the coals, often in close proximity. Also, assemblages of gypsum and goethite were observed in otherwise slightly oxidized coal, which indicates that the alteration of pyrite and calcite, when in close contact, proceeds most rapidly.  相似文献   

7.
Different from previous studies on effect of weathering upon geochemical variation along a single weathered profile, this paper provides a new methodology validated by comparing a weathered outcrop samples and their stratigraphic counterpart un-weathered core samples in a nearby shallow borehole. This outcrop and borehole penetrated the Ordovician-Silurian Wufeng–Longmaxi shales, located in the same anticline structure in the northern part of Guizhou Province, Southern China. The mineral composition, major, trace and rare earth elements (REEs) composition and Rock-Eval parameters of outcrop and core samples were analyzed and compared. Organic matter (OM) was observed in the microscope and extracted for elements analysis. The results show that short-term weathering still has significant influence on OM, mineral and elemental composition of black shales. The elements composition shows the outcrop profile was moderately weathered. The REEs compositions do not alter much during weathering process and the REEs composition and their relative ratios still are valid for rock origin determination. The OM, mainly composed by graptolite and bitumen, even entering the highly-over thermal maturity, is still sensitive to the weathering with a systematic loss 30–50% of TOC along the outcrop profile, which suggests that the OM consumption is predominantly controlled by weathering duration and the distance from the weathering surface. In turn, OM has significant influence on the trace elements transportation behavior during weathering. Some trace elements associated with the OM such as V, Cr, Th, U, Ni and Co, change significantly in their absolute concentration during weathering, but their relative ratios do not necessarily change too much and might be still reliable proxies for paleo-environmental determination. The mobility of shale minerals during weathering is in the following order: plagioclase?>?potassium feldspar and dolomite >pyrite and OM. Short-term weathering can also result in considerable transportation of elements and significant variation of minerals content in black shale, which may pose potentially high environmental and engineering risk in the regions rich in black shale.  相似文献   

8.
Bangladesh is situated in a subtropical to tropical climatic zone. A recently weathered crust has developed on sedimentary bedrock (sandstone, siltstone, shale and claystones) of Tertiary–Quaternary age. Weathered samples were collected from 16 sections totaling 68 samples and were analyzed mineralogically. The main primary minerals identified in the weathered crust of sedimentary rocks are quartz, plagioclase, K-feldspar, biotite, muscovite, sparse carbonate and epidote. The secondary minerals are kaolinite, illite, chlorite, gibbsite and goethite. Weathering initiated along the grain boundaries and cleavage planes of the minerals, forming small cloudy materials which were very difficult to identify. In the advanced stage of weathering, these cloudy materials have turned into secondary minerals. In region 1, high rain fall (7100 mm/yr) and monsoonic climate resulted in a kaolinite–gibbsite–goethite suite through the weathering of feldspars and biotite. The occurrence of gibbsite in the relatively elevated lands of Sylhet and Fe-kaolinite throughout the study areas is indicative of a humid–tropical climate during formation of the weathered crust.  相似文献   

9.
The Darrehzar porphyry Cu-Mo deposit is located in Southwestern Iran (～70 km southwest of Kerman City). The porphyries occur as Tertiary quartz-monzonite stocks and dikes, ranging in composition from microdiorite to diorite and granodiorite. The Darrehzar stock is highly altered, and even in the outermost part of the intrusion, it is not possible to find completely fresh rock. Surface weathering was developing ferrous Fe-rich lithologic units in leached zone and concentrated copper minerals in supergene zone. Unlike eastern areas which do not account for deep faults, the supergene zone is well developed in western areas with maximum of 118 m thickness. Hydrothermal alteration and mineralization at Darrehzar are centered on the stock and were broadly synchronous with its emplacement. Early hydrothermal alteration was dominantly potassic and propylitic, and was followed by later phyllic and argillic alteration. The hydrothermal system involved both magmatic and meteoric water and boiled extensively. Copper mineralization was accompanied by both potassic and phyllic alteration. Four main vein groups have been identified: (I) quartz?+?pyrite?±?molybdenite?±?anhydrite?±?K-feldspar?±?chalcopyrite?±?bornite?±?Cu and Fe oxidic minerals (peripheral); (II) quartz?+?chalcopyrite?+?pyrite?+?molybdenite; (III) quartz?+?pyrite?±?calcite?±?chalcopyrite?±?anhydrite (gypsum); and (IV) quartz or calcite, gypsum or ± pyrite. Based on abundance, nature, and phases number observed at room temperature, three types of fluid inclusions are typically observed in these veins: (1) vapor-rich, (2) liquid-rich, and (3) multi-phase. Early hydrothermal alteration was caused by high temperature, high salinity orthomagmatic fluid and produced a potassic assemblage. Phyllitic alteration was caused by high salinity and lower temperature orthomagmatic fluid. Magmatic and meteoric water mixture was developed in the peripheral part of the stock and caused propylitic alteration which is attributed to a liquid-rich, lower temperature.  相似文献   

10.
The Rio Tinto in SW Spain drains Cu and pyrite mines which have been in operation since at least the Bronze Age. Extensive metal mining, especially from 1873 to 1954, has resulted in contamination of the Rio Tinto alluvium with As, Cu, Pb, Ag and Zn. X-ray diffraction (XRD), wavelength-dispersive X-ray mapping, scanning electron microscope petrography and X-ray energy-dispersive (EDX) analysis has revealed that 4 major groups of contaminant metal and As-bearing minerals, including sulphides, Fe-As oxides, Fe oxides/hydroxides/oxyhydroxides, and Fe oxyhydroxysulphates, occur in the alluvium. Sulphide minerals, including pyrite, chalcopyrite, arsenopyrite and sphalerite, occur in alluvium near the mining areas. Iron hydroxides and oxyhydroxides such as goethite and possibly ferrihydrite occur in cements in both the mining areas and alluvium downstream, and carry minor amounts of As, Cu and Zn. Iron oxyhydroxysulphates, including jarosite, plumbojarosite and possibly schwertmannite, are the most common minerals in alluvium downstream of the mining areas, and are major hosts of Cu, Pb, Zn and of As, next to the Fe-As minerals. This work, and other field observations, suggest that (1) the extreme acidity and elevated metal concentrations of the river water will probably be maintained for some time due to oxidation of pyrite and other sulphides in the alluvium and mine-waste tips, and from formation of secondary oxide and oxyhydroxysulphates; (2) soluble Fe oxyhydroxysulphates such as copiapite, which form on the alluvium, are a temporary store of contaminant metals, but are dissolved during periods of high rainfall or flooding, releasing contaminants to the aqueous system; (3) relatively insoluble Fe oxyhydroxysulphates and hydroxides such as jarosite and goethite may be the major long-term store of alluvial contaminant metals; and (4) raising river pH will probably cause precipitation of Fe oxyhydroxides and oxides/hydroxides/oxyhydroxides and thus have a positive effect on water quality, but this action may destabilise some of these contaminant metal-bearing minerals, releasing metals back to the aqueous system.  相似文献   

11.
Oxidation of the relatively iron sulfide-poor Dugald River zinc-lead lode in northwest Queensland and reaction of the acid solutions with carbonate has resulted in an undifferentiated gossan profile. The gossan is composed predominantly of quartz, goethite, hematite, barite, adularia, plumbian jarosite, plumbogummite and minor mica, chlorite, kaolinite and montmorillonite. Barite and adularia are formed by the breakdown of the barium feldspar hyalophane (K, Na, Ba)[(Al, Si)4O8] which occurs in the lode.Lead in the gossan is contained within the secondary minerals plumbogummite and plumbian jarosite, and in traces of anglesite and cerussite, whereas Zn occurs in the barite, secondary lead minerals and coronadite structures, and is adsorbed by iron oxides, phyllosilicates and carbonaceous matter. Only traces of zinc minerals smithsonite, goslarite and hemimorphite were detected.Use of Gresens' general metasomatic equation has enabled quantitative determination of compositional changes resulting from the oxidation of the ore. Silicon, Al, Ti and Ba are essentially immobile under the mildly acidic oxidizing conditions. In decreasing order of mobility Cd, Ca, S, Na, K, Mn, Mg, Zn, Ni and Cu, together with CO2 and Tl, have been leached from the gossan profile, while Ag, Sb, Se, As, Fe and Pb appear to have been added to the gossan, notably in a zone of solution-deposited secondary minerals where they have been concentrated, possibly as a result of leaching from the surface gossan.  相似文献   

12.
A waste rock pile with initial high sulfide (10–20 wt.%) and low carbonate content (1–2 wt.%) located at Dlouhá Ves in the Czech Republic has been investigated in two profiles (excavation and outcrop) using powder X-ray diffraction, electron microprobe analysis, bulk composition analysis and Mössbauer spectroscopy. The mobility of arsenic and other contaminants was evaluated by leaching experiments. The primary source of the arsenic was arsenopyrite, which was significantly oxidized in both profiles. The principal As-bearing phase at the excavation profile was goethite, located at the top of the profile, and minerals of the jarosite group which were found down to its base. Melanterite, rich in copper and zinc, was found in a sulfide-rich, lower part of the profile together with anglesite. At the outcrop profile, minerals of the jarosite–beudantite group, scorodite and kaňkite prevail and no Fe(II)-minerals were found. The paste pH was lower at the excavation profile (minimum about 1.9) than at the outcrop profile (minimum of about 2.8). Processes in the pile are affected by the pyrite/arsenopyrite ratio, where high pyrite content decreases the As/S ratio and results in the formation of jarosite group minerals and low pH conditions. Where arsenopyrite predominates, sulphides are coated by scorodite and other Fe–As phases like schwertmannite, which limit their further oxidation.  相似文献   

13.
The Nkout deposit is part of an emerging iron ore province in West and Central Africa. The deposit is an oxide facies iron formation comprising fresh magnetite banded iron formation (BIF) at depth, which weathers and oxidises towards the surface forming caps of high grade hematite/martite–goethite ores. The mineral species, compositions, mineral associations, and liberation have been studied using automated mineralogy (QEMSCAN®) combined with whole rock geochemistry, mineral chemistry and mineralogical techniques. Drill cores (saprolitic, lateritic, BIF), grab and outcrop samples were studied and divided into 4 main groups based on whole rock Fe content and a weathering index. The groups are; enriched material (EM), weathered magnetite itabirite (WMI), transitional magnetite itabirite (TMI) and magnetite itabirite (MI). The main iron minerals are the iron oxides (magnetite, hematite, and goethite) and chamosite. The iron oxides are closely associated in the high grade cap and liberation of them individually is poor. Liberation increases when they are grouped together as iron oxides. Chamosite significantly lowers the liberation of the iron oxides. Automated mineralogy by QEMSCAN® (or other similar techniques) can distinguish between Fe oxides if set up and calibrated carefully using the backscattered electron signal. Electron beam techniques have the advantage over other quantitative mineralogy techniques of being able to determine mineral chemical variants of ore and gangue minerals, although reflected light optical microscopy remains the most sensitive method of distinguishing closely related iron oxide minerals. Both optical and electron beam automated mineralogical methods have distinct advantages over quantitative XRD in that they can determine mineral associations, liberation, amorphous phases and trace phases.  相似文献   

14.
渝东北黑色页岩元素迁移特征及化学风化程度   总被引：1，自引：0，他引：1       下载免费PDF全文
黑色页岩是富含有机质和硫化矿物的特殊沉积岩,但人们对其风化过程的元素活动性及矿物风化机制关注较少.为探讨不同地形位置的黑色页岩化学风化过程,采集了渝东北城口某山脊 (A)、近山顶 (B) 和沟谷 (C) 的下寒武统水井沱组黑色页岩风化剖面岩样,利用XRD、XRF和化学分析手段对采集样品的矿物成分、主量元素进行测定分析.元素和矿物的质量迁移系数 (τ) 和质量迁移通量 (Mj, flux) 的计算结果表明,黑色页岩风化过程中Ca、Mg和Na元素具有明显的贫化现象,近地表处存在Al元素的富集现象;矿物成分方面,黄铁矿和有机质氧化后形成的酸性水环境,造成方解石、白云石、斜长石等不稳定矿物溶解,并生成含水石膏、铁质氧化物、黏土矿物等次生矿物.不同赋存位置的黑色页岩风化程度有所差异,Na/K-CIA、K/Ca*-Al/Na、A-CN-K和A-CNK-FM图解显示:A剖面处于脱Ca过程的初级风化阶段,B剖面处于脱Ca、Na初期的初等-中等风化阶段,C剖面已发生脱Ca、Na过程,并伴随脱Si作用的中等-强烈风化阶段,结合不同风化指数 (如:CIA、CIW、PIA、MWPI等),得出各剖面的化学风化强弱程度依次为C＞B＞A.   相似文献   

15.
The x-ray powder diffraction identification of clay minerals both in bulk samples and in separated clay fraction confirmed the presence of palygorskite in samples of cave sediments from Wadi Haqil (the western slopes of Musandam Mountains; Ras Al-Khaimah Emirate, UAE). Samples contain quartz, gypsum, smectite, kaolinite, calcite, and palygorskite, some of them chlorite, illite, feldspars, and goethite. Calcite dominates in most samples; smectite prevails in clay fraction. After heating, the 001 reflection of chlorite shifts to higher diffraction angles and its intensity decreases; these features indicate that the chlorite represent a Fe-dominant species. Unit-cell dimensions of major phases as refined by the Rietveld method are in agreement with literature data. Chemical composition of palygorskite was derived from unit-cell dimensions as follows: MgO content is 11–14 wt% and Al2O3 10–13 wt%. Clay mineralogy is only hard to ascertain from the scanning electron microscope (SEM) images even after being combined with the energy-dispersive spectrometer data. The SEM was also used to characterize gypsum grains; they often display flow deformation features. Studied cave sediments represent palygorskite-bearing weathering products and desert soils re-deposited from the cave surroundings by slope processes and wind and/or surface runoff. The mixture with other clay minerals, quartz, feldspars, etc. supports this interpretation. Fine-grained quartz fraction is probably wind-blown. Gypsum and calcite are the precipitates (crusts and/or cements), although gypsum can also be re-deposited from omnipresent gypsum-cemented surface sediments.  相似文献   

16.
Summary The Lower Lias Clay at Blockley, 20 km due south of Stratford-upon-Avon, UK, is thought to be representative of this clay formation over much of the Severn Basin. As far as the mineralogy of the clay is concerned, illite is the dominant clay mineral, kaolinite being subsidiary, with quartz, calcite, pyrite and chlorite/vermiculite present in subsidiary or accessory amounts. Weathering changes the mineralogy, with illite being degraded and calcite and pyrite being removed. Furthermore free iron oxide coatings become important as a result of weathering, with the maximum concentrations being present in the highly weathered material.The unweathered clay possesses a preferred orientation associated with turbostratic structures. At certain horizons microfolding and remoulding occurs in the unweathered clay and silty layers are displaced. Weathering has progressively destroyed the micro-structures present in the weathered clay horizons.The fissures in the Lower Lias Clay occur in five uniplanar sets. In the unweathered clay the intensity is fairly constant but it increases in a narrow zone just below the weathered horizons. The number of curved fissures also increases at this depth. This intense fissuring continues into the lowest zone of weathered clay where weathering is confined to the fissure surfaces. Fissures become less apparent in the more weathered horizons as more and more degradation has taken place. However, new smaller fissure systems are developed in the weathered clay, as are desiccation cracks.Engineering index properties and values of shear strength are given. Relationships between moisture content and strength, liquid limit and iron (Fe) content were observed, and a relationship between weathering zones and the shear strength-depth curve was established.  相似文献   

17.
Visible near infrared and shortwave infrared (VNIR-SWIR, 350 to 2500 nm) reflectance spectra obtained from an analytical spectral device (ASD) have been used to define alteration zones adjacent to porphyry copper deposits (PCDs), in the central part of Kerman magmatic arc, SE Iran. The spectral analysis identified sericite, illite, halloysite, montmorillonite, dickite, kaolinite, pyrophyllite, biotite, chlorite, epidote, calcite, jarosite, and iron oxyhydroxides (e.g. hematite, goethite) of hydrothermal and supergene origin. Identified alteration zones are classified into six principal types namely phyllic, phyllic/propylitic, propylitic, potassic, argillic and advanced argillic. The iron oxide minerals in the oxidized zone were also identified using spectral analysis. Results of spectral analyses of samples are consistent with mineralogical data obtained from X-ray diffraction (XRD) and petrographic studies. Spectroscopic studies by ASD demonstrate that this tool is very useful for semi-quantitative and cost effective identification of different types of alteration mineral assemblages. Furthermore, it can provide a valuable tool for evaluating aerial distribution of alteration minerals while coupled with remote sensing data analysis.  相似文献   

18.
青海省阿尔金黄石山地区近红外蚀变矿物填图   总被引：1，自引：0，他引：1  
利用近红外光谱对羟基(OH-)等敏感的特性,可以区分多种蚀变矿物及其矿物的不同结晶度,如舍羟基之硅酸盐矿物(绿帘石、闪石等),碳酸盐矿物(方解石、白云石等),层状硅酸盐中单矿物(粘土矿物、绿泥石、蛇纹石等),硫酸盐矿物(明矾石、黄钾铁矾、石膏等)等;矿物的结晶度不同,其红外吸收峰形也不相同,而矿物的结晶度标志着矿化作用...  相似文献   

19.

Shephards Discordant Zone is a 500–600 m thick interlayered sequence of deformed, altered and metamorphosed magnetite metagabbro and about 50 layers or lenses of magnetitite (> 80–90% magnetite). The sequence shows progressive magmatic fractionation upwards: Ti and Ti/Fe increase, and V, V/Ti and Cr decrease upwards in magnetite and in whole‐rock compositions. The main magnetite‐rich sequence (about 400 m thick) is deeply weathered, with 40 m of saprolite showing vertical zonation of weathering minerals due to progressive weathering. Magnetitites (average 1% V2O3) are resistant to weathering and show little chemical change, but magnetite gabbros (average 0.27% V2O3) are extensively weathered and show progressive loss of Ca, Na, Mg and S. Plagioclase, magnetite (1.37% V2O3), chlorite (up to 0.35% V2O3), actinolite, epidote and minor sulfides in unweathered rocks weather to kaolinite, hematite, goethite and minor vermiculite, ilmenite remaining largely unaffected. Vanadium is essentially immobile during weathering and is unaffected during weathering of magnetitites (1% V2O3), but is slightly depleted during weathering of magnetite gabbros (0.23% V2O3).  相似文献   

20.
Apatites occurring in lateritic residues derived from high-grade metamorphic rocks from Sri Lanka are hydroxy-apatite as indicated by EPMA and XRD. Weathered phosphates and weathered crystalline products are composed of carbonate fluorapatite, crandallite, wardite, fluellite, kaolinite, goethite and gibbsite. EDAX, DTA and SIMS show the presence of amorphous materials, such as oxides of Fe, Al, Si, Al+Si, and S, on the surface of weathered phosphate. Using SEM, TEM, EDAX and electron diffraction techniques, the presence of these amorphous and crystalline materials with several transitions has been clearly identified in weathered phosphate. Recrystallization of phosphate occurred during weathering by dissolution, nucleation and precipitation. The lattice images of hydroxyapatite are gradually increased from 8.3-A basal spacings by weathering, and form mosaic bound fragments. Chondrite-, shale- and phosphorite concretion-normalized REE patterns of these apatites, known to have sedimentary origins, suggest enrichment and remobilisation during post-depositional reworking.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号