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1.
恬矿库周围土壤中重金属存在形态特征研究   总被引：48，自引：4，他引：44  
通过对大冶铜绿山铜铁矿尾矿库周围土壤中重金属形态分析实验,研究了重金属各种形态在土壤中的分布特征。由对比实验可知,尾矿库周围土壤中Ｃｕ、Ｐｂ、Ｚｎ、Ｃｄ等重金属含量都显著地高于对照样品,书经受到重金属的严重污染。土壤中重金属形态分布征为：ｗ（Ｃｒ、Ｚｎ、Ｆｅ）;可变换态〈碳酸盐态〈有机态〈铁锰氧化态〈残渣态;ｗ（Ｃｕ、Ｐｂ）：可变换态〈碳酸盐态〈有机态〈残渣态〈铁锰氧化态;ｗ（Ｃｄ）：残渣态,有机  相似文献   

2.
为研究磁化率在沉积锰矿床中的应用,对广西下雷锰矿床的钻孔岩心进行了磁化率测量试验。结果表明,含锰岩系中矿层磁化率与围岩磁化率明显不同,通常碳酸锰矿磁化率值比围岩要高出1~2个数量级,而围岩中硅质岩、灰岩、泥岩的磁化率无明显差异。磁化率可作为野外快速判别含锰岩系的代用指标。通过讨论下雷原生碳酸锰矿的磁化率异常,认为碳酸盐矿物磁性很低,对磁化率的贡献极小,磁化率异常高值指示与其伴生的铁质矿物;碳酸锰矿中含有磁性矿物,其磁性强弱决定了矿层磁化率的大小;黏土矿物中的绿泥石可吸附含铁的强磁性物质,绿泥石及其含量是影响碳酸锰矿磁化率的一个重要因素。  相似文献   

3.
黔东北黑色泥岩盆地含锰岩系的铁锰地球化学特征   总被引：1，自引：0，他引：1  
黑色泥岩盆地内的菱锰矿矿床中常伴生大量黄铁矿,由于菱锰矿和黄铁矿的沉积过程难以直接观察,铁锰的富集关系尚不明确。为了探讨二者的相互关系,以黔东北西溪堡锰矿的典型剖面为例,根据岩石薄片、TOC分析和元素分析等手段,分析了含锰岩系及其顶底板的岩性序列、矿物组合和铁锰地球化学特征,与现代沉积的菱锰矿进行了对比分析。研究表明,在黄铁矿和菱锰矿富集关系上,西溪堡锰矿与现代波罗的海具有类似特征。含锰岩系顶板和底板的锰含量较低;含锰岩系内部的Mn含量波动很大,与铁含量呈负相关。黄铁矿和菱锰矿的沉淀析出具有先后顺序,通常黄铁矿从溶液中析出在先,菱锰矿沉淀在后。  相似文献   

4.
Sequential core sediments from northwestern Taihu Lake in China were analyzed for grain size, organic carbon and heavy metal content. The sediments are composed of organic-poor clayey-fine silts. The chemical speciations of Cu, Fe, Mn, Ni, Pb, and Zn were also analyzed using the BCR sequential extraction procedure. Cu, Fe, Ni, and Zn are mainly associated with the residue fraction; Mn is concentrated mainly in exchangeable/carbonate fraction and residue fraction; and Pb mainly in Fe/Mn oxide fraction and organic/sulfide fraction. The exchangeable/carbonate fractions of Cu, Fe, Ni, Zn and Pb are lower. The fractions of Ni, Pb and Zn bound to the Fe/Mn oxide have significant correlations with reducible Mn; the organic/sulfide fractions of Cu, Mn, Ni, Pb, and Zn have significant correlations with TOC. The extractable fractions of Cu, Mn, Ni, Pb, and Zn are high at the top 4 cm of the core sediments as compared to those in the deeper layers, showing the anthropogenic input of heavy metals is due to rapid industrial development. The heavy metal pollution history of the sediments has been recorded since the late 1970s, determined by the result of ^137Cs dating.  相似文献   

5.
Biogeochemical cycling of zinc is strongly influenced by sorption on birnessite minerals (layer-type MnO2), which are found in diverse terrestrial and aquatic environments. Zinc has been observed to form both tetrahedral (ZnIV) and octahedral (ZnVI) triple-corner-sharing surface complexes (TCS) at Mn(IV) vacancy sites in hexagonal birnessite. The octahedral complex is expected to be similar to that of Zn in the Mn oxide mineral, chalcophanite (ZnMn3O7·3H2O), but the reason for the occurrence of the four-coordinate Zn surface species remains unclear. We address this issue computationally using spin-polarized density functional theory (DFT) to examine the ZnIV-TCS and ZnVI-TCS species. Structural parameters obtained by DFT geometry optimization were in excellent agreement with available experimental data on Zn-birnessites. Total energy, magnetic moments, and electron overlap populations obtained by DFT for isolated ZnIV-TCS revealed that this species is stable in birnessite without a need for Mn(III) substitution in the octahedral sheet and that it is more effective in reducing undersaturation of surface O at a Mn vacancy than is ZnVI-TCS. Comparison between geometry-optimized ZnMn3O7·3H2O (chalcophanite) and the hypothetical monohydrate mineral, ZnMn3O7·H2O, which contains only tetrahedral Zn, showed that the hydration state of Zn significantly affects birnessite structural stability. Finally, our study also revealed that, relative to their positions in an ideal vacancy-free MnO2, Mn nearest to Zn in a TCS surface complex move toward the vacancy by 0.08-0.11 Å, while surface O bordering the vacancy move away from it by 0.16-0.21 Å, in agreement with recent X-ray absorption spectroscopic analyses.  相似文献   

6.
Manganese nodules and manganese carbonate concretions occur in the upper 10–15 cm of the Recent sediments of Loch Fyne, Argyllshire in water depths of 180–200 m. The nodules are spherical, a few mm to 3 cm in diameter, and consist of a black, Mn-rich core and a thin, red, Fe-rich rim. The carbonate occurs as irregular concretions, 0.5–8 cm in size, and as a cement in irregular nodule and shell fragment aggregates. It partially replaces some nodule material and clastic silicate inclusions, but does not affect aragonitic and calcitic shell fragments.The nodules are approximately 75% pure oxides and contain 30% Mn and 4% Fe. In the cores, the principal mineral phase is todorokite, with a Mn/Fe ratio of 17. The rim consists of X-ray amorphous Fe and Mn oxides with a Mn/Fe ratio of 0.66. The cores are enriched, relative to Al, in K, Ba, Co, Mo, Ni and Sr while the rims contain more P, Ti, As, Pb, Y and Zn.The manganese carbonate has the composition (Mn47.7 Ca45.1 Mg7.2) CO3. Apart from Cu, all minor elements are excluded from significant substitution in the carbonate lattice.Manganese nodules and carbonates form diagenetically within the Recent sediments of Loch Fyne. This accounts for the high Mn/Fe ratios in the oxide phases and the abundance of manganese carbonate concretions. Mn concentrations in the interstitial waters of sediment cores are high (ca. 10 ppm) as also, by inference, are the dissolved carbonate concentrations.  相似文献   

7.
Ore-stage carbonates of the Silvermines stratiform orebodies have increased Zn and Pb and high Fe and Mn content. A major microtexture observed is produced by the replacement of carbonate allochems by dolomite, Fe dolomite, and siderite followed by the replacement of carbonates by sulfides. Generally, the process of replacement took place while the former fabric of the host carbonates was preserved. The reactivity of metal carbonates with sulfur favored the concentration of Pb and Zn in the sulfide and of Fe and Mn in the carbonate form. Sulfide-carbonate reactions probably maintained a high permeability in the ore zone over an extended period of time eventually producing a high-grade ore from solutions rich in Fe and Mn but poor in Zn and Pb. Initial porosity and permeability created by gravity flows controlled the mineralizing process at the beginning, but later stages were probably controlled by replacements, i.e., sulfide-carbonate reactions.  相似文献   

8.
冀北坳陷中元古界长城系高于庄组下部发育一套含锰岩层,厚60～80m,主要为深灰色—黑色含锰白云岩,多含泥质。文章对高于庄组82件碳酸盐岩样品进行了微量元素分析,结合地史演化、沉积特征以及地球化学特征,表明研究区内Mn主要来源于串岭沟—大红峪期的海底火山喷发活动,一部分锰质随海底火山作用向海水中迁移,另一部分随岩浆喷溢冷却形成火山岩熔岩系,经风化作用后、搬运至区内,在闭塞、滞留和缺氧的碳酸盐岩潮下坪环境富集成岩。  相似文献   

9.
Several small Mn–Fe oxide and Mn-oxide ore bodies associated with Precambrian Iron Ore Group of rocks are located within Koira-Noamundi province of north Orissa, India. These deposits are classified into in situ (stratiform), remobilized (stratabound) and reworked categories based on their field disposition. Volcaniclastic/terrigenous shale in large geographic extension is associated with these ore bodies.The in situ ore bodies are characterised by cryptomelane-, romanechite- and hematite-dominating minerals, low Mn/Fe ratio (1.1) and relatively lower abundance of trace (1500–2500 ppm) constituents. In such type of deposits the stratigraphic conformity of oxides with the tuffaceous shale suggests precipitation of Mn and Fe at a time of decreased volcaniclastic/terrigenous contribution. The minor and trace elements were removed from solution by adsorption rather than by precipitation. Both Mn and Fe oxides when precipitated adsorb trace elements strongly but the partitioning of elements takes place during diagenesis. The inter-elemental relationship reveals that Cu, Co, Ni, Pb and Zn were adsorbed on precipitating hydrous Mn oxides and form manganates. Some of these elements probably get desorbed from Fe oxide because of their inability to substitute for Fe3+ in the lattice of its oxide. However, P, V, As and Mo were less partitioned and retained in Fe-oxide phase. Positive correlation between Al2O3 and SiO2, MgO, Na2O, TiO2 and some traces like Li, Nb, Sc, Y, Zr, Th and U points to their contribution through volcaniclastic/terrigenous detritus of both mafic and acidic composition.The remobilized ore bodies are developed in a later stage through dissolution, remobilization and reprecipitation of Mn oxides in favorable structural weak planes under supergene environment. Increase in average Mn/Fe ratio (8) and trace content (5000–8500 ppm) by 5–2.5 orders of magnitude, respectively, or more above its abundance in adjoining/underlying protore is characteristic of these deposits. The newly formed Mn ores constituting lithiophorite, cryptomelane/romanechite and goethite get quantitatively enriched in traces like Cu, Co, Ni, Pb and Zn. Positive correlation between Mn, Li, Co and Zn is due to the formation of mineral of lithiophorite–chalcophanite group during redistribution and reconcentration of Mn oxide. P and V, which were present in Fe oxide, also get dissolved and reprecipitate with Fe oxyhydroxide in these ores. Some other elements like Y, Th and U show positive relation with Fe. This is probably due to leaching of these elements during chemical weathering of associated shale and getting re-adsorbed in Fe-oxyhydroxide phase.However, under oxidizing environment selective cations like Ba, K, etc. resorb from Mn-structure, resulting in the development of pyrolusite (Mn/Fe>20). In such transformation, trace metals from pyrolusitic structure expels out, resulting thereby in a considerable reduction in total trace value (<3000 ppm).The reworked ore bodies are allochthonous in nature and developed through a number of stages during terrain evolution and lateritisation. Secondary processes such as reworking of pre-existing crust; solution and remobilization; precipitation and cementation and transport, etc. are responsible for their development. Such deposits are usually very low in Mn/Fe ratio (3) and trace content (<2000 ppm).  相似文献   

10.
矿区已查明6条矿化带,圈定银矿体29条。矿体成似层状、透镜状、囊状。银的赋存状态：一是呈类质同象或次显微矿物包体存在于载体矿物中,二是以吸附态或银的次显微包体存在于铅锰矿及铁、锰氧化矿物中。属于具有层控特征的变质中低温热液型银铅锌碳酸盐型矿床。  相似文献   

11.
东海DGKS9617岩芯物源研究   总被引：4，自引：1，他引：4  
东海内陆架东北部DGKS9617岩芯以55cm为界明显地分为两个沉积相,岩芯下部(55～851cm)潮流作用明显,为浅海潮流相,而上部(0～55cm)潮流作用不明显,为浅海相沉积。岩芯的重矿物含量特征,Fe、Mn、V、Cr、Ni、Cu、Zn等7个元素的判别函数计算结果,以及碳酸盐分析和Ba-Sr-Zn三角判别图均一致显示岩芯沉积物的重矿物和元素地球化学特征与长江沉积物类似,柱样沉积物主要来源于长江,虽然不同沉积相的沉积环境差别较大,但其物质来源并未发生变化。  相似文献   

12.
Acidic ion-exchanger was applied to the selective extraction of heavy metals in carbonate phases of recent lake sediments. Cr was not detected and Fe and Cu contents were reduced by factors of three to ten, relative to non-carbonate fractions of the sediment samples. Values obtained for Mn and Zn exemplify the effects of dilution was well as enrichment, both originating from increased carbonate percentages. Determinations on grain-sized fractions from Bodensee samples suggest that elevated inputs of dissolved Zn, which partly originate from human activities, may be immobilized by authigenic carbonate precipitation.  相似文献   

13.
It is now well established that a number of terrestrial and aquatic microorganisms have the capacity to oxidize and precipitate Mn as phyllomanganate. However, this biomineralization has never been shown to occur in plant tissues, nor has the structure of a natural Mn(IV) biooxide been characterized in detail. We show that the graminaceous plant Festuca rubra (red fescue) produces a Zn-rich phyllomanganate with constant Zn:Mn and Ca:Mn atomic ratios (0.46 and 0.38, respectively) when grown on a contaminated sediment. This new phase is so far the Zn-richest manganate known to form in nature (chalcophanite has a Zn:Mn ratio of 0.33) and has no synthetic equivalent. Visual examination of root fragments under a microscope shows black precipitates about ten to several tens of microns in size, and their imaging with backscattered and secondary electrons demonstrates that they are located in the root epidermis. In situ measurements by Mn and Zn K-edge extended X-ray absorption fine structure (EXAFS) spectroscopy and X-ray diffraction (XRD) with a micro-focused beam can be quantitatively described by a single-phase model consisting of Mn(IV) octahedral layers with 22% vacant sites capped with tetrahedral and octahedral Zn in proportions of 3:1. The layer charge deficit is also partly balanced by interlayer Mn and Ca. Diffracting crystallites have a domain radius of 33 Å in the ab plane and contain only 1.2 layers (8.6 Å) on average. Since this biogenic Mn oxide consists mostly of isolated layers, basal 00l reflections are essentially absent despite its lamellar structure. Individual Mn layers are probably held together in the Mn–Zn precipitates by stabilizing organic molecules. Zinc biomineralization by plants likely is a defense mechanism against toxicity induced by excess concentrations of this metal in the rhizosphere.  相似文献   

14.
Zhaxikang is one large Sb–Pb–Zn–Ag deposit located in the North Himalaya of southern Tibet. To date, the genesis of this deposit still remains controversial. Here, we present new pyrite Fe and sphalerite Zn isotopic data for the first three stages of mineralization, Fe–Zn isotopic data for Mn–Fe carbonate that formed during the first two stages of mineralization, and Zn isotopic data for the slate wall rocks of the Jurassic Ridang Formation to discuss the genesis of the Zhaxikang deposit. The overall δ56Fe and δ66Zn values range from −0.80‰ to 0.43‰ and from −0.03‰ to 0.38‰, respectively. The δ56Fe values of Mn–Fe carbonates are lighter than those of associated pyrite in six mineral pairs, indicating that the iron carbonates are preferentially enriched in light Fe isotopes relative to pyrite. The sphalerite has lighter δ66Zn values than associated Mn–Fe carbonates in three mineral pairs.The δ56Fe values of pyrite that formed during the first three stages of mineralization gradually increase from stage 1 (−0.33‰ to −0.09‰) through stage 2 (−0.30‰ to 0.19‰) to stage 3 (0.16‰–0.43‰). In comparison, the sphalerite that formed during these stages has δ66Zn values that gradually decrease from stage 1 (0.16‰–0.35‰) through stage 2 (0.09‰–0.23‰) to stage 3 (−0.03‰ to 0.22‰). These data, in conjunction with the observations of hand specimens and thin sections, suggest that the deposit was overprinted by a second pulse of mineralization. This overprint would account for these Fe–Zn isotopic variations as well as the kinetic Rayleigh fractionation that occurred during mineralization. The temporally increasing δ56Fe and decreasing δ66Zn values recorded in the deposit are also coincident with an increase in alteration, again supporting the existence of two pulses of mineralization. The δ56Fe values of the first pulse of ore-forming fluid were calculated using theoretical equations, yielding values of −0.54‰ to −0.34‰ that overlap with those of submarine hydrothermal solutions (−1‰ to 0‰). However, the δ56Fe values of the stage 3 pyrite are heavier than those of typical submarine hydrothermal solutions, which suggests that the second pulse of mineralization was probably derived from a magmatic hydrothermal fluid. In addition, the second pulse of ore-forming fluid has brought some Fe and taken away parts of Zn, which results the lighter δ66Zn values of sphalerite and heavier δ56Fe values of pyrite from the second pulse of mineralization. Overall, the Zhaxikang deposit records two pulses of mineralization, and the overprint by the second pulse of mineralization causes the lighter δ66Zn values and heavier δ56Fe values of modified samples.  相似文献   

15.
银额盆地哈日凹陷下白垩统热水沉积岩特征及成因   总被引：2，自引：0，他引：2       下载免费PDF全文
银额盆地哈日凹陷下白垩统具有独特的沉积构造和矿物组成.通过开展岩石矿物和地球化学研究,论证其热水成因,探讨沉积环境和形成模式.研究区下白垩统发育方沸石、菱铁矿和白云石等矿物,富含Fe、Mn和Ba等元素,具有高∑REE、LREE富集和负Eu异常的稀土元素特征.结合Fe vs.Mn vs.（Cu+Co+Ni）×10和Ni vs.Co vs.Zn三角图解,证实下白垩统普遍含有热液成分.微量元素及碳氧同位素分析指示热水沉积岩形成于缺氧、封闭的咸水湖泊环境;氧同位素计算形成温度为43.94~86.08 ℃.研究表明,丰富的断裂系统为湖水下渗和热液喷流提供通道,湖水与热液的对流活动为湖盆持续输入热量和成矿离子.此类湖相热水沉积持续时间长、影响范围广,主要受物源供给和热液性质控制,代表一类特殊的沉积模式.   相似文献   

16.
A new method for the speciation of Fe and Mn at mineral surfaces is proposed using X-ray absorption fine structure in conversion electron yield mode (CEY-XAFS). This method generally reflects information on the species at the sub-μm scale from the particle surface due to the limited escape depth of the inelastic Auger electron. The surface sensitivity of this method was assessed by experiments on two samples of granite showing different degrees of weathering. The XANES spectra of the Fe-K and Mn-K edge clearly gave different information for CEY and fluorescence (FL) modes. These XANES spectra of Fe and Mn show a good fit upon application of least-squares fitting using ferrihydrite/MnO2 and biotite as the end members. The XANES spectra collected by CEY mode provided more selective information on the secondary phases which are probably present at the mineral surfaces. In particular, CEY-XANES spectra of Mn indicated the presence of Mn oxide in unweathered granite despite a very small contribution of Mn oxide being indicated by FL-XANES and selective chemical-extraction analyses. Manganese oxide could not be detected by micro-beam XANES (beam size: 5 × 5 μm2) in unweathered granite, suggesting that Mn oxide thinly and ubiquitously coats mineral surface at a sub-μm scale. This information is important, since Mn oxide can be the host for various trace elements. CEY-XAFS can prove to be a powerful tool as a highly sensitive surface speciation method. Combination of CEY and FL-XAFS will help identify minor phases that form at mineral surfaces, but identification of Fe and Mn oxides at mineral surfaces is critical to understand the migration of trace elements in water-rock interaction.  相似文献   

17.
Sediment core was collected from Tokyo Bay. The surface enrichment of heavy metals due to human activities is recognized in the sediment. Partitioning of Cu, Zn, Fe and Mn into sulfide, carbonate, organic and silicate fractions has been determined with selective chemical leaching techniques for 210Pb-dated sediment core samples. The heavy metal contents of silicate fractions without exchangeable sites are almost constant against depth in sediment core. However, the Cu, Zn and Mn contents of sulfide, carbonate and organic fractions vary with depth. Most Cu and Zn in the polluted sediment layer are associated with the iron sulfide fraction.  相似文献   

18.
Sediment samples at 10 locations in the mainstem of the Yellow River were taken in 1994. Five forms (exchangeable, carbonate, organic, Fe/Mn oxide and residual) of metals were extracted by the Tessier method. The total contents and contents of the five forms of 16 metal elements (Li, Na, K, Ca, Sr, Ba, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, and Al) were determined by ICP-AES. In sediments of the Yellow River, except for Na, mobile elements (such as K, Ca) do not show a negative correlation with the immobile elements. Alkaline metals (Li, Na, and K), Ti, and Al exist mainly in the residual form. The exchangeable forms of alkaline-earth elements (Ca, Sr, and Ba) are the highest, and their residual forms go up with the increase of the period in the periodic table of elements. Half of Mn exists in the residual form, and its non-residual forms exist mainly in carbonate and oxide forms. Except Mn, the iron group elements (Fe, Co, Ni, V, Cr) mainly exist in the residual and oxide forms. High carbonate content of Ca does not cause high contents of other elements in carbonate form, showing that chemical weathering is not strong in the area.  相似文献   

19.
The chemical forms of Fe, Mn, Zn, Cu, Cr, Pb and Cd in the Huanghe River sediments have been studied by sequential extraction techniques and the comparison with data from the Rhine River sediments has been made. In the Huanghe River sediments the average contents of metals, without exception, are below their respective contents in average shales and very close to their levels in Ca-poor granites. The major portion of metals is combined with the detrital and moderately reducible phases. Both in the Huanghe River and in the Rhine River sediments the distribution ratios of metals between the moderately reducible and the easily reducible phases are generally more than unity. However, the distribution ratios of Mn, Zn and Cd are obviously lower than those of Fe, Cr, Cu and Pb. As a result of contamination, the ratios of Fe, Cr, Cu and Pb show an apparent increase, but no remarkable ratio variation is observed for Mn, Zn and Cd. Metals in the Huanghe River sediments, especially Cu and Zn, show a tendency to be associated with the organic phase. The effect of carbonate on metal association preference seems to be less important than that in the Rhine River although there is higher content of carbonate in the Huanghe River sediments. Cd has a greater percentage of the exchangeable phase, which is similar to the result from the Rhine River sediments.  相似文献   

20.
A governmental regional drainage survey assessed the mineral potential of Calabria in 1974. The Calabria area of southern Italy is a mineralized region in which Penninic and Austro-Alpine nappes, comprising ophiolites, metasedimentary rocks (phyllites, paragneiss, granulites, amphibolites) and granitic and granodiorite plutons, are overthrusting carbonate Apenninic nappes. Pre-Alpine stratabound and vein-type base-metal sulfide mineralization predominate, tectonically redistributed during the Alpine orogeny.A total of 5518 samples of the original 6999 active stream sediments from an area of 10,000 km2 were analyzed by X-ray fluorescence and atomic absorption for Cu, Pb, Zn, Hg, Fe, Mn, As, W, Mo, Sn, and Be on the minus 180 μm fraction. Follow-up investigation of a 39-km2 area around Bivongi-Ferdinandea using 760 soil samples analyzed for Fe, Mn, Zn, Cu, Pb, K, Mo, and Au, investigated molybdenite and chalcopyrite occurrences associated with granodiorite.A five-factor R-mode factor analysis reflected geological and mineralization features in the reconnaissance data. Factor 1 (Fe-Mn-Cu-Zn) is related to the Fe and Mn distribution in the stream sediments. Factor 2 (Be-Sn) reflects presence of pegmatites within metamorphic and magmatic rocks. Factor 5 (Mo) is essentially a single-element factor. Factor 4 (As-Pb-Zn-Hg-Cu) reflects mineralization. Factor 3 (W-Ba) does not cluster in association with any specific lithological unit. Significant metal associations, recognized from R-mode factor analysis, were used as independent variables and regressed against the original metal concentration of each sample. Residuals of multiple regression analysis, differentiated features representing mineralization from those related either to lithologic or geochemical parameters. New prospecting targets were identified and areas of known mineral occurrences were evident in the distinction of residuals.R-mode factor analysis of data from the follow-up investigation identified three factors. Factor 2 (Mo-K) reflects Mo mineralization and associated hydrothermally altered areas but does not suggest additional target areas.  相似文献   

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