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1.
Ran Liu Amy L. Wolfe David A. Dzombak Colin P. Horwitz Brian W. Stewart Rosemary C. Capo 《Applied Geochemistry》2009
Electrochemically controlled pyrite dissolution was performed with three pyrite materials from different geological origins under mixed potential and high overpotential conditions. Both solid electrodes and C paste electrodes of powdered pyrite were used. The rate of pyrite dissolution increased with applied positive potential and was strongly affected by temperature. Current density measurements over the applied potential range successfully described the rate of pyrite dissolution of each pyrite electrode. Controlled dissolution performed under mixed potential conditions on the solid electrodes successfully reflected the same pyrite reactivity and dissolution rate order as in batch reactor dissolution studies with the same pyrite materials. Therefore, the relative reactivity of different pyrite materials can be determined through current density measurements on their solid electrodes under mixed potential conditions. This technique could be a useful tool to compare rapidly the relative reactivity for different pyrite materials. In contrast, electrochemically controlled dissolution studies with C paste electrodes constructed with fine-grained pyrite and paraffin/graphite mixture did not result in accurate ranking of pyrite samples by dissolution rate. 相似文献
2.
Comparison of dissolution under oxic acid drainage conditions for eight sedimentary and hydrothermal pyrite samples 总被引：1，自引：0，他引：1
Ran Liu Amy L. Wolfe David A. Dzombak Brian W. Stewart Rosemary C. Capo 《Environmental Geology》2008,56(1):171-182
The abiotic oxidative dissolution behaviors of eight natural pyrite samples, five sedimentary and three hydrothermal, from
various geological environments were compared under oxic conditions at pH 3 and 6 in a highly controlled batch reactor dissolution
system. The three sedimentary pyrite samples associated with coal had greater specific surface areas and also exhibited greater
apparent dissolution rates and extent than the other two sedimentary and three hydrothermal samples under both pH conditions.
However, after normalizing for surface area, the dissolution rate constants for the different pyrite samples were similar;
the greatest difference was between the two non-coal sedimentary pyrite samples. Pyrite morphology and the presence of trace
metals could contribute to the differences in dissolution behavior as reflected in the normalized dissolution rates. The sulfur:iron
ratio observed in the aqueous solution at pH 3 increased with time, but was always less than 2.0 (predicted from the stoichiometry
of dissolution) for all the pyrite samples during the 24-h experimental duration. This can be explained by the disproportionation
dissociation of thiosulfate, an initial product of pyrite dissolution, to elemental sulfur and sulfate which does not occur
in a 1:1 ratio. The results of this work indicate the importance of extracting and using the specific pyrite(s) relevant to
particular mining areas in order to understand pyrite dissolution rates and the influence of environmental conditions on those
rates. 相似文献
3.
《Applied Geochemistry》2001,16(7-8):803-819
Sulfide mineral oxidation, primarily pyrite and pyrrhotite, generates acid mine drainage during weathering. Successful management of acid generating wastes entails the suppression of the initiation of oxidation reactions. The reactivity of pyrite depends on ore mineralogy, including the effects of associated sulfide impurities. The electrochemical surface characterization study using cyclic voltammetry with carbon paste electrodes containing minerals particles (CPE-Mineral) is an effective tool for demonstrating how the various mineral characteristics work together to influence the overall reactivity of the mineral. This study was supported by chemical, mineralogical and leachate chemistry data. The results show that the presence of other sulfides in contact with pyrite at the beginning of the weathering process is the most important parameter affecting pyrite reactivity, which is likely to be oxidized and passivated. In more advanced stages of leaching, mineral coatings which passivate the pyrite surfaces tend to play the most important role in defining the reactivity of pyrite. The electrochemical response of pyritic samples in conjunction with the evolution of the chemical quality of the leach solution in the simple experimental device here used, could then provide valuable information on acid mine drainage generation. 相似文献
4.
The Wilcox aquifer is a major groundwater resource in the northern Gulf Coastal Plain (lower Mississippi Valley) of the USA, yet the processes controlling water chemistry in this clastic aquifer have received relatively little attention. The current study combines analyses of solutes and stable isotopes in groundwater, petrography of core samples, and geochemical modeling to identify plausible reactions along a regional flow path ～300 km long. The hydrochemical facies evolves from Ca-HCO3 upgradient to Na-HCO3 downgradient, with a sequential zonation of terminal electron-accepting processes from Fe(III) reduction through SO4 2? reduction to methanogenesis. In particular, decreasing SO4 2? and increasing δ34S of SO4 2? along the flow path, as well as observations of authigenic pyrite in core samples, provide evidence of SO4 2? reduction. Values of δ13C in groundwater suggest that dissolved inorganic carbon is contributed both by oxidation of sedimentary organic matter and calcite dissolution. Inverse modeling identified multiple plausible sets of reactions between sampled wells, which typically involved cation exchange, pyrite precipitation, CH2O oxidation, and dissolution of amorphous Fe(OH)3, calcite, or siderite. These reactions are consistent with processes identified in previous studies of Atlantic Coastal Plain aquifers. Contrasts in groundwater chemistry between the Wilcox and the underlying McNairy and overlying Claiborne aquifers indicate that confining units are relatively effective in limiting cross-formational flow, but localized cross-formational mixing could occur via fault zones. Consequently, increased pumping in the vicinity of fault zones could facilitate upward movement of saline water into the Wilcox. 相似文献
5.
通过构建产电微生物—黄铁矿双室体系, 应用电化学方法对以黄铁矿单晶电极作为产电微生物电子受体时, 两者间的电子转移过程进行表征和分析.结果显示, 与惰性石墨电极相比, 以黄铁矿单晶作为产电微生物电子受体时, 体系最大功率密度提升132.9%;电化学阻抗谱显示, 黄铁矿单晶电极极化电阻降低98.8%, 表现出优良的电化学反应特性, 表明产电微生物与黄铁矿单晶间具有良好的电子转移活性.籍由产电微生物对底物的氧化作用, 与黄铁矿单晶接受产电微生物电子在0.34 V(相对于饱和甘汞电极)处发生的还原反应, 构成了两者间完整的协同电子转移过程. 相似文献
6.
Pedro J. Marenco Frank A. Corsetti Douglas E. Hammond Alan J. Kaufman David J. Bottjer 《Chemical Geology》2008,247(1-2):124-132
The sulfur isotopic composition of carbonate associated sulfate (CAS) has been used to investigate the geochemistry of ancient seawater sulfate. However, few studies have quantified the reliability of δ34S of CAS as a seawater sulfate proxy, especially with respect to later diagenetic overprinting. Pyrite, which typically has depleted δ34S values due to authigenic fractionation associated with bacterial sulfate reduction, is a common constituent of marine sedimentary rocks. The oxidation of pyrite, whether during diagenesis or sample preparation, could thus adversely influence the sulfur isotopic composition of CAS. Here, we report the results of CAS extractions using HCl and acetic acid with samples spiked with varying amounts of pyrite. The results show a very strong linear relationship between the abundance of fine-grained pyrite added to the sample and the resultant abundance and δ34S value of CAS. This data represents the first unequivocal evidence that pyrite is oxidized during the CAS extraction process. Our mixing models indicate that in samples with much less than 1 wt.% pyrite and relatively high δ34Spyrite values, the isotopic offset imparted by oxidation of pyrite should be much less than ? 4‰. A wealth of literature exists on the oxidation of pyrite by Fe3+ and we believe this mechanism drives the oxidation of pyrite during CAS extraction, during which the oxygen used to form sulfate is taken from H2O, not O2. Consequently, extracting CAS under anaerobic conditions would only slow, but not halt, the oxidation of pyrite. Future studies of CAS should attempt to quantify pyrite abundance and isotopic composition. 相似文献
7.
Synthetic pyrite crystals doped with As, Co, or Ni, undoped pyrite, and natural arsenian pyrite from Leadville, Colorado were investigated with electrochemical techniques and solid-state measurements of semiconducting properties to determine the effect of impurity content on pyrite’s oxidation behavior. Potential step experiments, cyclic voltammetry, and AC voltammetry were performed in a standard three-electrode electrochemical cell setup. A pH 1.78 sulfuric acid solution containing 1 mM ferric iron, open to atmospheric oxygen, was chosen to approximate water affected by acid drainage. Van der Pauw/Hall effect measurements determined resistivity, carrier concentration and carrier mobility.The anodic dissolution of pyrite and the reduction of ferric iron half-reactions are taken as proxies for natural pyrite oxidation. Pyrite containing no impurities is least reactive. Pyrite with As is more reactive than pyrite with either Ni or Co despite lower dopant concentration. As, Co, and Ni impurities introduce bulk defect states at different energy levels within the band gap. Higher reactivity of impure pyrite suggests that introduced defect levels lead to higher density of occupied surface states at the solid-solution interface and increased metallic behavior. The current density generated from potential step experiments increased with increasing As concentration. The higher reactivity of As-doped pyrite may be related to p-type conductivity and corrosion by holes. The results of this study suggest that considering the impurity content of pyrite in mining waste may lead to more accurate risk assessment of acid producing potential. 相似文献
8.
Iron-rich smectite is commonly described in the diagenetic fraction of deep-sea sediment, as millimeter to centimeter aggregates dispersed in the sediment, or as a coating on sedimentary particles or nodules. This study examines several factors to elucidate formation mechanisms of a particular iron-rich smectite and its potential transformation to glauconite. The study combines a detailed mineralogical investigation on natural samples and a chemical modeling approach to assess mineralogical reactions and pathways.Transmission electron microscopy (TEM) observations and analytical electron microscopy (TEM-AEM) analyses were conducted on microtomed samples of millimeter- to centimeter-long green grains. These grains are widespread in pelagic calcareous sediment from the Costa Rica margin. They are composed of pyrites that are partially dissolved and are surrounded by amorphous or very poorly crystallized iron-rich particles. Iron-rich montmorillonite grows from an amorphous precursor and its formation requires the input of Si, O, Mg, K, Na and Ca; our results suggest that these inputs are supported by the dissolution of sedimentary phases such as volcanic glasses, siliceous fossils and silicates.Thermodynamic modeling of fluid-sediment interactions was conducted with the geochemical computer code PhreeqC, using mineralogical and pore fluid compositions from sediment samples and calculated estimates for thermodynamic constants of smectites that are not maintained by the computer code. Simulations confirm the possibility that the green grains are the product of pyrite alteration by seawater under oxidizing conditions. The extent of smectite production is controlled by the kinetics of pyrite dissolution and fluid migration. The absence of aluminum in the Costa Rica margin system explains the formation of an iron-rich montmorillonite instead of glauconite, whereas the presence of calcite that buffers the system explains the formation of an iron-rich montmorillonite instead of iron oxides. 相似文献
9.
沉积地层中的黄铁矿形态及同位素特征初探——以华南埃迪卡拉纪深水相地层为例 总被引：1，自引：1，他引：0
地质历史时期新元古代大气氧含量普遍较低。在硫酸盐还原细菌作用下,作为海洋重要的氧化性离子,陆源硫酸根离子有效促进了深层海水的氧化进程。在此过程中,硫元素在硫酸根和黄铁矿之间发生显著同位素分馏,其分馏程度可反推当时古海洋的氧化还原状态。沉积地层中的黄铁矿普遍具有多种形态,不同形态黄铁矿的形成环境多有不同。如草莓状黄铁矿多形成于底层缺氧水体或沉积物的浅表面,而大颗粒单晶黄铁矿或脉状黄铁矿则多沉积于成岩早期的沉积物孔隙或形成于成岩后期的热液改造。与草莓状黄铁矿不同,大颗粒单晶或脉状黄铁矿的硫同位素组成并不能反映沉积时期的古海洋氧化还原条件。判定沉积地层中不同形态的黄铁矿及形成过程,是获得有效反映海洋沉积环境硫同位素组成特征的基本前提。简要总结了地质历史时期沉积地层中的黄铁矿类型及矿物形成过程,并以华南埃迪卡拉纪蓝田组岩芯样品为例,识别出各个样品中的黄铁矿形态组成特征,对比分析了全岩黄铁矿与样品中大颗粒黄铁矿硫同位素组成差异。研究结果表明:不同岩性样品中黄铁矿的形态种类及含量均存在差异。页岩样品保存有更好形态的自形晶以及草莓状黄铁矿;碳酸盐岩样品中具有较多自形晶以及他形晶黄铁矿,并且其中的少量草莓状黄铁矿遭受后期成岩作用而发生不同程度的晶体蚀变。样品中大颗粒黄铁矿的硫同位素值（δ34SL-pyr）通常显著高于全岩黄铁矿的硫同位素值（δ34ST-pyr）,最大差值可达48.5‰。在利用黄铁矿的硫同位素组成来反推当时古海洋环境时,需要区分不同形态黄铁矿,仔细剔除大颗粒黄铁矿,降低成岩期黄铁矿对样品中硫同位素组成的影响。更细致的微区黄铁矿硫同位素分析工作将依赖于SIMS分析测试手段进行。 相似文献
10.
The stable enrichment of pyrite from magnesite ores in δ34S isotope (from 5.4 to 6.9‰) compared with pyrite from the host (sedimentary and igneous) rocks was established in the classical Satka sparry magnesite ore field. Concretionary segregations of fine-grained pyrite in dolomite are depleted in the heavy sulfur isotope (δ34S, from–9.1 to–5.8‰). Pyrite from dolerite is characterized by δ34S values (–1.1 and 1.7‰) close to the meteorite sulfur. The δ34S values in barite from the underlying dolomite horizon vary in the range of 32.3–41.4‰. The high degree of homogeneity of the sulfur isotope composition in pyrite from magnesite is a result of thermochemical sulfate reduction during the syngenetic crystallization of pyrite and magnesite from epigenetic brines, formed during dissolution of evaporite sulfate minerals at the stage of early catagenesis of the Riphean deposits.
相似文献11.
黄铁矿特征研究可为页岩沉积环境恢复与页岩气富集保存规律预测提供依据。以贵州岑巩地区岑页1井牛蹄塘组为研究对象,基于岩心、薄片、扫描电镜及微量元素、硫同位素地球化学,确定牛蹄塘组页岩沉积环境及页岩气富集地质条件。研究表明,牛蹄塘组页岩黄铁矿发育为草莓状、自形-半自形及他形(主要为胶状他形)三种形态,不同形态的黄铁矿形成于不同沉积环境,草莓状黄铁矿形成于缺氧还原环境,自形-半自形黄铁矿形成于贫氧环境,胶状他形黄铁矿指示沉积过程有热液活动的参与。测试井牛蹄塘组整体处于较开放的沉积水体,上段为含氧-贫氧环境,硫同位素整体变轻且发生负漂;中段为较缺氧环境,硫同位素跨度大且发生正漂;下段为还原性更强的沉积环境,硫同位素小幅度负漂。黄铁矿含量与有机质富集密切相关,与黄铁矿有关的孔隙为页岩气吸附、保存及运移提供载体,且草莓状黄铁矿指示的缺氧硫化环境更利于有机质保存。研究工作系统梳理了黄铁矿对牛蹄塘组页岩沉积环境及储层页岩气富集的指示作用,为页岩气勘探提供指示。 相似文献
12.
The Taupo Volcanic Zone (TVZ) on the North Island of New Zealand is located above the subducting Pacific slab and hosts hydrothermal systems related to subduction, arc magmatism and crustal extension. In these systems, gold is transported primarily as sulphide complexes, with gold being deposited in response to boiling and mixing of the deep geothermal fluids. Conglomerate cobbles and hydrothermal fumaroles from the upper Retaruke River in the western TVZ are mineralised deposits that have been eroded from the nearby Miocene alluvial sedimentary plateau. Abundant gold-bearing pyrite was precipitated in the conglomerates and fumaroles by late hydrothermal process, primarily occurring as veinlets, disseminations and fine-grained aggregates which consists discrete euhedral microcrystals. Scanning electron microscopy combined with X-ray energy disperses spectroscopy shows that pyrites are commendably affected by late hydrothermal fluids, possibly by the carbonate fluid. Electron probe microanalysis revealed that the pyrite contains 20–120 ppm Au (averaging 60 ppm). Wavelength dispersive spectral elemental mapping suggests that gold is distributed uniformly in pyrite, indicating structurally bound gold (solid solution) in pyrite. Gold mineralisation recognised in the conglomerates and fumaroles demonstrates that the upper Retaruke River is a promising target for future gold exploration. 相似文献
13.
A portable, battery-operated electrochemical instrument which enables the method of staircase voltammetry to be implemented may be coupled with the method of abrasive stripping voltammetry for the direct identification of minerals in the field. Small amounts of solid mineral samples are mechanically transferred to a paraffin-impregnated graphite electrode by rubbing the electrode against the crushed mineral. The electrode is then transferred to a conventional electrochemical cell containing electrolyte, and experiments analogous to the well known method of stripping voltammetry are then completed to provide an “electrochemical spectrum” or fingerprint of the mineral. Since the technique can be applied directly with battery-operated equipment, the method can be used by geochemists and mineralogists undertaking field work in areas remote from sophisticated laboratories and mains-powered instruments normally used to characterize minerals. The method has been successfully applied to the identification of minerals such as galena, stibnite, cuprite, pyrite and chalcopyrite, although further work is required to investigate any limitations that might apply with complex mixtures or minerals, and, at the present stage of development, the method is qualitative rather than quantitative. 相似文献
14.
The assessment of the aluminosilicate buffering potential during acid weathering of the Estonian alum shale is provided.
It is found that the stoichiometric interaction between dissolved pyrite oxidation products and illite of the shale best describe
the buffering process and are consistent with earlier field studies. The scheme includes incongruent dissolution of illite
with smectite and K-jarosite precipitating. This complex mechanism involves buffering of 8% of the acidity by K+ and temporary precipitation of 25% of the acidity as K-jarosite. Dissolution proceeds at a low pH (1.5–3) until all pyrite
in the shale particle is oxidised. Hence, if the total amount of illite present is larger than needed for stoichiometric interactions,
only part of it is involved in a buffering process, neutralising a certain percentage of acidity. The next stage in shale
weathering is the incongruent dissolution of K-jarosite with the release of the precipitated acidity and the formation of
ferric oxyhydroxide.
Received: 3 August 1998 · Revised paper: 26 January 1999 · Accepted: 23 February 1999 相似文献
15.
Zahra Badrzadeh Timothy J. Barrett Jan M. Peter Domingo Gimeno Mossaieb Sabzehei Mehraj Aghazadeh 《Mineralium Deposita》2011,46(8):905-923
The Sargaz Cu–Zn massive sulfide deposit is situated in the southeastern part of Kerman Province, in the southern Sanandaj–Sirjan Zone of Iran. The stratigraphic footwall of the Sargaz deposit is Upper Triassic to Lower Jurassic (?) pillowed basalt, whereas the stratigraphic hanging wall is andesite. Mafic volcanic rocks are overlain by andesitic volcaniclastics and volcanic breccias and locally by heterogeneous debris flows. Rhyodacitic flows and volcaniclastics overlie the sequence of basaltic and andesitic rocks. Based on the bimodal nature of volcanism, the regional geologic setting and petrochemistry of the volcanic rocks, we suggest massive sulfide mineralization in the Sargaz formed in a nascent ensialic back-arc basin. The current reserves (after ancient mining) of the Sargaz deposit are 3 Mt at 1.34% Cu, 0.38% Zn, 0.08%Pb, 0.24 g/t Au, and 7 g/t Ag. The structurally dismembered massive sulfide lens is zoned from a pyrite-rich base, to a pyrite?±?chalcopyrite-rich central part, and a sphalerite–chalcopyrite-rich upper part, with a sphalerite-rich zone lateral to the upper part. The main sulfide mineral is pyrite, with lesser chalcopyrite and sphalerite. The feeder zone, comprised of a vein stockwork consists of quartz–sulfide–sericite pesudobreccia and, in the deepest part, chlorite–quartz–pyrite pesudobreccia. Footwall hydrothermal alteration extends at least 70–80 m below the massive sulfide lens and more than a hundred meters along strike from the massive sulfide lens. Jasper and Fe–Mn bearing chert horizons lateral to the sulfide deposit represent low-temperature hydrothermal precipitates of the evolving hydrothermal system. Based on mineral textures and paragenetic relationships, the growth history of the Sargaz deposit is complex and includes: (1) early precipitation of sulfides (protore) on the seafloor as precipitation of fine-grained anhedral pyrite, sphalerite, quartz, and barite; (2) anhydrite precipitation in open spaces and mineral interstices within the sulfide mound followed by its subsequent dissolution, formation of breccia textures, and mound clasts and precipitation of coarse-grained pyrite, sphalerite, tetrahedrite–tennantite, galena and barite; (3) replacement of pre-existing sulfides by chalcopyrite precipitated at higher temperatures (zone refining); (4) continued “refining” led to the dissolution of stage 3 chalcopyrite and formation of a base-metal-depleted pyrite body in the lowermost part of the massive sulfide lens; (5) carbonate veins were emplaced into the sulfide lens, replacing stage 2 barite. The δ34S composition of the sulfides ranges from +2.8‰ to +8.5‰ (average, +5.6‰) with a general increase of δ34S ratios with depth within the massive sulfide lens and underlying stockwork zone. The heavier values indicate that some of the sulfur was derived from seawater sulfate that was ultimately thermochemically reduced in deep hydrothermal reaction zones. 相似文献
16.
HANS PIRLET LAURA M. WEHRMANN BENJAMIN BRUNNER NORBERT FRANK JAN DEWANCKELE DAVID VAN ROOIJ ANNELEEN FOUBERT RUDY SWENNEN LIEVEN NAUDTS MATTHIEU BOONE VEERLE CNUDDE JEAN‐PIERRE HENRIET 《Sedimentology》2010,57(3):786-805
Authigenic gypsum was found in a gravity core, retrieved from the top of Mound Perseverance, a giant cold‐water coral mound in the Porcupine Basin, off Ireland. The occurrence of gypsum in such an environment is intriguing, because gypsum, a classic evaporitic mineral, is undersaturated with respect to sea water. Sedimentological, petrographic and isotopic evidence point to diagenetic formation of the gypsum, tied to oxidation of sedimentary sulphide minerals (i.e. pyrite). This oxidation is attributed to a phase of increased bottom currents which caused erosion and enhanced inflow of oxidizing fluids into the mound sediments. The oxidation of pyrite produced acidity, causing carbonate dissolution and subsequently leading to pore‐water oversaturation with respect to gypsum and dolomite. Calculations based on the isotopic compositions of gypsum and pyrite reveal that between 21·6% and 28·6% of the sulphate incorporated into the gypsum derived from pyrite oxidation. The dissolution of carbonate increased the porosity in the affected sediment layer but promoted lithification of the sediments at the sediment‐water interface. Thus, authigenic gypsum can serve as a signature for diagenetic oxidation events in carbonate‐rich sediments. These observations demonstrate that fluid flow, steered by environmental factors, has an important effect on the diagenesis of coral mounds. 相似文献
17.
Voltammetric methods using direct insertion of a gold-amalgam microelectrode with a sensitive, computercontrolled voltammeter detected soluble iron(II) sulfide, [FeS]aq, in the porewaters of anoxic, sulfidic, fine-grained sediments from the Loughor Estuary, Wales. The voltammetric results are reproducible. Studies of cores stored in sealed, refrigerated containers for up to 21 d reveal no measurable oxidation. [FeS]aq forms in this estuarine environment as a result of the dissolution of amorphous FeS, and appears to be involved in the formation of pyrite. [FeS]aq makes no significant contribution to the total sulfide and iron contents of the sediment but could constitute an important component of the dissolved Fe(II) and S(−II) contents of the porewater. Mass balance calculations show pyrite forms in this system by the addition of sulfur to FeS rather than by the loss of iron from FeS. The overall process appears to involve [FeS]aq as an intermediary. Although the porewaters of the Loughor Estuary sediments are iron-rich relative to seawater, the iron sulfide-forming process is iron-limited rather than sulfide-limited. Reactive iron is bound to sulfide rapidly in the sediment. After the reactive iron is bound to sulfide, additional sulfide produced is fixed as pyrite. 相似文献
18.
安徽庐枞盆地矾山酸性蚀变岩帽形成时代及其地质意义 总被引：3，自引：1，他引：2
酸性蚀变岩帽是岩浆热液流体和围岩在近地表相互作用的产物,是斑岩-浅成低温热液成矿系统的重要指标。发育在长江中下游成矿带庐枞盆地内的矾山酸性蚀变岩帽产出面积较大( 20km~2)。前人对该酸性蚀变岩帽中的明矾石矿床的地质和地化特征进行了相关研究,但详细的年代学研究工作尚未开展。为精确厘定矾山酸性蚀变岩帽的形成时代,本文开展了明矾石~(40)Ar-~(39)Ar法和金红石原位U-Pb法定年。矾山酸性蚀变岩帽中明矾石共有三种类型:ⅠA型明矾石主要呈交代蚀变发生在热液蚀变早阶段,与石英、粒状黄铁矿或赤铁矿、少量金红石共生;ⅠB型明矾石形成于热液蚀变晚阶段,主要呈叶片状集合体充填在开放空间中,与石英、星点状赤铁矿、粒状金红石集合体共生,少量金红石和赤铁矿沿明矾石解理裂隙分布;Ⅱ型明矾石是表生明矾石,主要呈细粒集合体沿裂隙分布,与赤铁矿、高岭石、地开石共生。三类明矾石形成于不同环境下:ⅠA和ⅠB型明矾石形成于岩浆热液环境下,是大矾山明矾石矿区的主要产物;Ⅱ型细粒明矾石分布在矾山酸性蚀变岩帽的非明矾石矿区,是表生环境下的产物。ⅠA型明矾石的~(40)Ar-~(39)Ar定年的坪年龄为131±6Ma,代表了矾山酸性蚀变岩帽的形成时代。与Ⅱ型明矾石密切共生的金红石U-Pb定年结果为32. 7±4Ma,在该期间,整个盆地内无岩浆活动发生,该年龄反映了矾山酸性蚀变岩帽经历表生氧化作用的时间。明矾石和金红石定年结果分别对应岩浆热液和表生明矾石的形成时代。在利用明矾石进行找矿工作时需先明确明矾石成因,矾山酸性蚀变岩帽中深成明矾石是下一阶段的找矿研究的基础。 相似文献
19.
新疆吐拉苏盆地京希-伊尔曼德金矿地质和地球化学特征研究 总被引：2，自引：1，他引：1
京希-伊尔曼德金矿位于新疆北天山吐拉苏盆地的西北缘,赋存于泥盆纪-早石炭世火山-沉积地层底部的凝灰岩、凝灰质砂岩中,围岩经历了绢云母化、黄铁矿化、多期硅化和角砾化、碳酸盐化和重晶石化,金矿化与硅化围岩紧密伴生。矿体呈透镜状、层状和似层状,产状与围岩基本一致,主要由热液角砾岩型矿石组成,其热液演化期由四个阶段组成:I:硅化及绢云母化——在围岩凝灰岩和凝灰质砂岩中形成大量浸染状石英、绢云母和少量黄铁矿;II:角砾化及硅化——形成含金热液角砾岩a,角砾为早期蚀变围岩,胶结物为烟灰色玉髓状石英、黄铁矿、毒砂和少量金矿物;III:角砾化及硅化——形成含金热液角砾岩b,角砾为热液角砾岩a和蚀变围岩,胶结物为细粒石英、黄铁矿、毒砂和少量金矿物;IV:方解石-重晶石阶段——形成大量粗大的方解石-重晶石脉。京希-伊尔曼德金矿成矿流体本身富集V、Cr、Ni、Cu、Sb,且其中的Mn、Co、Zn、Bi以及大离子亲石元素LILE主要来自火山岩围岩。从成矿早期到晚期,成矿流体轻稀土元素逐渐富集、氧化性增强。水-岩体系氢、氧同位素组成模拟计算表明,京希-伊尔曼德金矿成矿流体主要为与区内火山岩再平衡的岩浆水,其中金浓度为1×10-6～2×10-6,形成该矿需要约1×108～0.5×108t岩浆热液,蚀变围岩和矿石中黄铁矿富集轻稀土元素。角砾化作用及其伴随的氧逸度升高是导致金沉淀的主要机制。 相似文献
20.
Determining the source of sulfur in an ore deposit is key to understanding the nature of the ore forming processes. The Neoarchaean Paulsens sediment-hosted gold deposit (∼1 Moz @ 7.6 g/t) located in the Pilbara Craton of Western Australia exhibits many of the characteristics of Phanerozoic shale hosted gold deposits (e.g. Huijiabao Trend, Northern Carlin Trend and Sukhoi Log), in that 1) black shales are the dominant host rock, 2) gold is hosted in pyrite as both free gold and dissolved gold in the lattice of the pyrite, and 3) multiple generations of pyrite have formed due to a variety of geological processes. In this contribution we utilised Secondary Ion Mass Spectrometer (SIMS) to measure the in-situ quadrupole (32S, 33S, 34S and 36S) sulfur isotope compositions of the different generations of pyrite. Our results indicate that the both diagenetic and hydrothermal pyrite generations display similar and anomalous Δ33S signatures (up to +0.4‰). Further, the Δ33S-Δ36S arrays in the hydrothermal pyrite generations lie on a slope which is similar to that of the diagenetic pyrite. These data support the hypothesis that the sulfur in the ore zones came from the host Hardey Formation black shales.We also performed trace element analyses of syn-sedimentary and early diagenetic pyrite from the Hardey Formaiton using Nano Secondary Ion Mass Spectrometry (NanoSIMS), Electron Probe Microanalysis (EPMA) and Laser Ablation-inductively coupled plasma-mass spectrometry (LA-ICPMS), all of which show that the syn-sedimentary and early diagenetic pyrite contain high concentrations of many trace elements (As, Ni, Co, Cu, Ag, Se, Te, Bi), including up to 1.5 ppm Au. These metals contents are also abundant in the several generations of mineralised hydrothermal pyrite and form clear patterns of growth associated with couple dissolution reprecipitation reactions. These findings clearly indicate that the fluid that transported the Au must have also been enriched in the base and precious metals that are contained in the early, syn-diagenesis pyrite.Data from this study clearly support the hypothesis that in some sediment-hosted gold systems, all the sulfur and gold required to form the deposit are sourced from the local sedimentary package. By using the presence of anomalous mass independent sulfur isotope signatures as chemically conservative and indelible tracers, it is possible to fingerprint the source of sulfur in a wide range of mineral systems, thus enhancing predictive exploration strategies at the regional to camp scales. 相似文献