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Computer-controlled scanning electron microscopy is introduced as a faster, reliably and cost-reducing alternative to conventional electron microprobe analyses on kimberlite indicator minerals. The method is based on conventional scanning electron microscopy and energy dispersive X-ray spectrometry, but due to extended counting times, optimised settings and computer-controlled particle recognition valid data can be obtained on a low amount of operator and machine time. A comparison of the results between both methods yields that computer-controlled scanning electron microscopy is able to investigate major and minor element concentrations in indicator minerals with almost the same precision as the electron microprobe. 相似文献
3.
Summary The Ni-Mo Huangjiawan mine, Guizhou Province, People’s Republic of China, occurs in Lower Cambrian black shale (stone coal)
in an area where other mines have recently extracted ore from the same horizon. Detailed electron microprobe (EMPA) and scanning
electron microscope (SEM) analyses of representative thin sections have revealed a complex assemblage of sulfides and sulfarsenides.
Early sulfidic and phosphatic nodules and host matrix have been lithified, somewhat fractured, and then mineralized with later-stage
sulfides and sulfarsenides. Gersdorffite, millerite, polydymite, pyrite, sphalerite, chalcopyrite, galena, and clausthalite
have been recognized. EMPA data are given for the major phases. Pyrite trace-element distributions and coeval Ni-, As-sulfides
indicate that in the main ore layer, the last sulfide deposition was Ni-As-Co-rich. Mo and V deposition were early in the
petrogenesis of these rocks. The assemblages gersdorffite-millerite-polydymite (pyrite) and millerite-gersdorffite (pyrite)
and the composition of gersdorffite indicate a formation temperature of between 200° and 300 °C suggesting that the last solutions
to infiltrate and mineralize the samples were related to hydrothermal processes.
Environmentally sensitive elements such as As, Cd, and Se are hosted by sulfides and sulfarsenides and are the main source
of these elements to residual soil. Crops grown on them are enriched in these elements, and they may be hazardous for animal
and human consumption.
Authors’ addresses: H. E. Belkin, U.S. Geological Survey, 956 National Center, Reston, VA 20192, USA; Kunli Luo, Institute of Geographical Sciences and Natural Resources Research, Chinese Academy of Sciences, 11A Datun Road, Beijing
100101, People’s Republic of China 相似文献
4.
V. A. Kovalenker N. V. Trubkin V. D. Abramova O. Yu. Plotinskaya G. D. Kiseleva S. E. Borisovskii Yu. I. Yazykova 《Geology of Ore Deposits》2018,60(1):62-81
The paper presents pioneering data on the composition, texture, and crystal structure of molybdenite from various types of molybdenum mineralization at the Bystrinsky Cu–Au–Fe porphyry–skarn deposit in the eastern Transbaikal region, Russia. The data were obtained using electron microprobe analysis (EMPA), laser ablation–inductively coupled plasma mass spectrometry (LA-ICP-MS), and high-resolution transmission electron microscopy (HRTEM). Molybdenite found at the deposit in skarn, sulfide-poor quartz veins, and quartz–feldspar alteration markedly differs in the concentrations of trace elements determined by their species in the mineral, as well as in its structural features. Molybdenite-2H from skarn associated with phyllosilicates occurs as ultrafine crystals with uniform shape and texture; no dislocations or inclusions were found but amorphous silica was. The molybdenite composition is highly contrasting in the content and distribution of both structure-related (Re, W, and Se) and other (Mn, Co, Ni, Cu, Zn, As, Ag, Cd, Sb, Te, Ag, Pd, Au, Hg, Pb, and Bi) metals. In the sulfide-poor quartz veins, highly structurally heterogeneous (2H + 3R) molybdenite microcrystals with abundant defects (dislocations and volumetrically distributed inclusions) are associated with illite, goethite, and barite. Some single crystals are unique three-phase (2H + 3R polytypes + amorphous MoS2). The mineral has a low concentration of all trace elements, which are uniformly distributed. However, individual domains with uniquely high Pd, Te, Ni, Hg, and W concentrations caused by mineral inclusions are found in some grains. Molybdenite from quartz–feldspar alteration is characterized by low concentrations of all trace elements except for Re and Se, which enrich some domains of the grains. Our data indicate that the compositional and structural heterogeneity of molybdenite from the Bystrinsky deposit are its crucial features, which obviously correlate with the types of Mo mineralization. 相似文献
5.
介绍了扫描电镜能谱、透射电镜、二次离子质谱、激光微探针质谱、显微傅立叶红外光谱等几种微束分析技术的性能特点，系统地论述了其在有机岩石学在应用现状与进展，并较详细地阐述了利用上述技术研究塔里木盆地烃源岩显微组分的结果。 相似文献
6.
Nickel geochemistry of a Philippine laterite examined by bulk and microprobe synchrotron analyses 总被引：1，自引：0，他引：1
Rong Fan 《Geochimica et cosmochimica acta》2011,75(21):6400-6415
The Ni geochemistry of limonite and saprolite laterite ores from Pujada in the Philippines has been investigated using a mixture of laboratory and synchrotron techniques. Nickel laterite profiles are typically composed of complicated mineral assemblages, with Ni being distributed heterogeneously at the micron scale, and thus a high degree of spatial resolution is required for analysis. This study represents the first such analysis of Philippine laterite ores. Synchrotron bulk and microprobe X-ray absorption spectroscopy (XAS), comprising both X-ray absorption near edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) spectroscopies, together with synchrotron microprobe X-ray fluorescence microscopy (XFM) and diffraction (XRD) have been applied to provide quantitative analysis of the mineral components and Ni speciation.Synchrotron microprobe EXAFS spectroscopy suggests that the limonite Ni is associated with phyllomanganate via adsorption onto the Mn oxide layers and substitution for Mn within these layers. Laboratory scanning electron microscopy, coupled to electron dispersive spectroscopy analyses, indicates that Ni is also associated with concentrated Fe containing particles and this is further confirmed by synchrotron bulk and microprobe investigation. Linear combination fitting of the bulk EXAFS limonite data suggests 60 ± 15% of the Ni is associated with phyllomanganate, with the predominant fraction adsorbed above vacancies in the MnO6 layers with the remainder being substituted for Mn within these layers. The remaining 40 ± 10% of the Ni in the limonite ore is incorporated into goethite through replacement of the Fe. In the saprolite ore, 90 ± 23% of the Ni is associated with a serpentine mineral, most likely lizardite, as a replacement for Mg. The remaining Ni is found within phyllomanganate adsorbed above vacancies in the MnO6 layers. 相似文献
7.
Environmental legislation has had significant impact on coal utilization, especially coal combustion for power generation, in limiting emissions of potentially hazardous materials to the environment. For the most part, such emissions derive from the inorganic constituents in coal. However, as such legislation becomes ever more encompassing, it has increased the need to understand better the behavior of the inorganic species in coal processing to ensure, in part, that such legislation is not unduly burdensome. Consequently, it has led to significant development of new models for the behavior of inorganics in coal combustion and a complementary enhancement of many analytical methods for determining inorganics in coal.In this paper, analytical methods for inorganics in coal are reviewed on three fronts: (i) methods for determining elemental concentrations; (ii) methods for determining the mineralogy of coals; and (iii) methods for determining modes of occurrence (speciation) of trace elements in coal. The concept of association with respect to mineral–maceral and mineral–mineral occurrences is also discussed. Where possible, comparison of different analysis methods has been made by reference to data on well-characterized suites of coals, such as the Argonne premium coal samples.Incremental enhancements will continue to be made in analytical methods for elemental concentrations; however, major improvements are needed in the other two areas. There is a great need to verify and corroborate by direct speciation methods, the many inferences made by indirect methods regarding trace element speciation. Also, improvements in the measurement of mineral association and its integration into the coal mineral analysis by means of the computer-controlled scanning electron microscopy (CCSEM) would be a significant advance. Accurate determinations of both association and coal mineralogy would lead to significant and much-needed refinements of models for the behavior of inorganics in both coal cleaning processes and coal combustion. 相似文献
8.
通过电子显微镜及电子探针分析,对鄂尔多斯盆地东南部店头地区砂岩型铀矿物的赋存状态、主要伴生元素及其沉淀机制进行了初步探讨。研究区主要的铀矿物类型为沥青质铀矿,以显微浸染状充填于砂岩孔隙及胶结物中;与U密切伴生的元素有Fe、Se、Pb、Si、Ti、Cr、S等,与铀矿物伴生的矿物组合有黄铁矿、方铅矿、钛铀矿以及与其关系密切的硒矿化;主要含铀层位富含有机质及黄铁矿,夹有透镜状、条带状煤线,具备丰富的还原物质,有利于铀元素的还原富集,因此认为影响研究区铀沉淀的主要地球化学障是还原障和吸附障。 相似文献
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《International Journal of Coal Geology》1988,10(2):177-191
A preliminary mineralogical/geochemical investigation of low-rank coals from Leicestershire, England, has been carried out with a view to their future beneficiation. Analytical scanning electron microscopy (SEM) and X-ray powder diffraction (XRD) have been used to identify and assess the distribution of mineral phases likely to give corrosion-producing or slag-forming materials during combustion, and those minerals which would be potentially valuable by-products of beneficiation processes. Differences in the mineral petrography of borehole samples from the Vale of Belvoir Prospect and coal from Bagworth Colliery are compared. Samples from both areas contain substantial amounts of epigenetic minerals: calcite, dolomite, kaolinite and fluor-apatite are important phases in the Bagworth sample, whilst gypsum, illite, quartz, kaolinite, barytocelestine, pyrite, chalcopyrite, anatase, galena and sphalerite occur in the Vale of Belvoir samples. Whereas the presence of halides in the Bagworth coal would seem to be a possible source of boiler-corrosion problems, the major undesirable characteristic of the Vale of Belvoir coal is the presence of significant amounts of metal sulphides. However, extraction of sulphides from this coal prior to combustion could provide a valuable source of metals as a by-product. Certain trace element concentrations in the Vale of Belvoir samples have also been determined by instrumental neutron activation analysis (INAA) and higher levels of lanthanide elements are present in the whole coal relative to mineral veins (mainly gypsum). Trace-element signatures may provide a useful distinction between syngenetic and epigenetic mineral formation. 相似文献
10.
为了进一步深化铀矿物的富集机理.利用α径迹放射性照相、扫描电镜、电子探针等方法对鄂尔多斯盆地北部铀矿床中铀矿物的赋存状态进行了系统研究.发现该区铀矿物主要为铀石，少量沥青铀矿和含铀钛矿物.沉积-成岩期碎屑铀矿物赋存在碎屑颗粒内部，吸附在锐钛矿周围，为铀储层中预富集的铀.成矿期铀矿物大部分赋存在碎屑颗粒填隙部位，与黄铁矿、碳质碎屑相伴生，与石英颗粒及方解石胶结关系密切；部分吸附在包裹碎屑颗粒的蒙脱石薄膜上.另外发现了，沥青铀矿-赤铁矿-黄铁矿的矿物组合，以及硒铅矿（PbSe）和白硒铁矿（FeSe2）与铀矿物相伴生，并伴有REE含量明显升高.分析得出，沥青铀矿形成于成矿早期，氧化酸性流体与还原碱性流体的过渡界面，偏向于氧化酸性一侧；而铀石主要形成于成矿晚期的还原碱性环境.双重铀源供给、丰富的还原介质、多源流体的耦合，局部的热液流体叠加改造，共同造就了鄂尔多斯盆地北部大矿、富矿的形成. 相似文献
11.
The elemental composition of the individual macerals in a suite of Australian coals has been determined in polished sections using light-element electron microprobe techniques. The analyses of the individual macerals in each coal were combined with data on maceral abundance to produce an inferred chemical composition for the organic matter of the respective whole-coal samples, and this was compared, for each sample, to the respective whole-coal ultimate analysis data, corrected to a dry, ash-free (daf) basis. Except for slightly lower values in some lower-rank coals, the inferred percentages of whole-coal C estimated from the microprobe data were found to be very close to the respective whole-coal C percentages as determined by conventional ultimate analysis. The proportion of O in the coals indicated by the microprobe study, however, appears to be as much as 2% higher than that derived from the ultimate analysis data, especially in the lower-rank coal samples. The difference it may represent errors in calculating the O percentages in ultimate analysis, errors in the microprobe analysis due to difficulties in calibration or measurement, or increased proportions of O in the coals due to factors such as take-up with storage of the polished sections. The percentages of whole-coal N calculated from the microprobe data are up to 0.5% (absolute) below the proportion of N determined directly by whole-coal ultimate analysis. This may reflect the inherent difficulty of dealing with a light element at low concentrations by the microprobe technique, or it may indicate that some of the N occurs in the coals in mineral form. The percentages of whole-coal (organic) S calculated from the microprobe study are close to the percentages of organic S determined for each sample by more conventional techniques. With the exception of (organic) O, which may be affected by other factors, and also possibly of N, the electron microprobe technique appears from the study to provide results that are consistent with ultimate analysis over a wide rank range. 相似文献
12.
鄂尔多斯盆地东北缘准格尔煤田煤中超常富集勃姆石的发现 总被引：10，自引：0，他引：10
运用X射线衍射分析(XRD)、带能谱仪的扫描电镜(SEM-EDX)和光学显微镜等技术,首次在鄂尔多斯盆地东北缘准格尔矿区6号巨厚煤层中发现了超常富集的勃姆石及其特殊的矿物组合,勃姆石含量可高达13.1%,与勃姆石伴生的矿物有磷锶铝石、锆石、金红石、菱铁矿、方铅矿、硒铅矿和硒方铅矿。重矿物的组合特征与华北地区本溪组铝土矿中的重矿物组合特征相似,高含量的勃姆石主要来源于聚煤盆地北偏东方向本溪组风化壳铝土矿,三水铝石以胶体溶液的形式从铝土矿中被短距离带入泥炭沼泽中,在泥炭聚积阶段和成岩作用早期经压实作用脱水凝聚而形成勃姆石。 相似文献
13.
Franck Poitrasson 《Contributions to Mineralogy and Petrology》2002,142(4):485-500
Allanite is, with monazite, the main repository for light rare earth elements (REE) in the continental crust and can be used in U-Th-Pb geochronology. This mineral has been shown to be prone to alteration. The geochemical exchanges occurring between allanite and hydrothermal fluids were explored using backscattered scanning electron microscopy, electron microprobe, and laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS). The alteration mechanisms found show the restricted role of metamictization and correspond to the allanite to epidote transformation or to the leaching of the allanite A-crystallographic sites. Hence, the REE are mostly removed from this phase during fluid-mineral interactions, although a heavy rare earth-rich fluid may imprint its geochemical signature on the allanite altered zones. It appears that even if this REE holder presents evidence of alteration, the bulk mineral and whole-rock REE and Sm-Nd isotope signatures were not significantly affected in the cases studied. Alteration results mostly in the input of common lead, thus restricting the usefulness of allanite for U-Th-Pb dating when alteration occurs. Finally, the alteration mechanisms found here confirm the much more limited flexibility of silicates crystalline lattice as compared to phosphates. 相似文献
14.
Mineralogy and geochemistry of the No. 6 Coal (Pennsylvanian) in the Junger Coalfield, Ordos Basin, China 总被引：16，自引：3，他引：16
Shifeng Dai Deyi Ren Chen-Lin Chou Shengsheng Li Yaofa Jiang 《International Journal of Coal Geology》2006,66(4):253-270
This paper discusses the mineralogy and geochemistry of the No. 6 Coal (Pennsylvanian) in the Junger Coalfield, Ordos Basin, China. The results show that the vitrinite reflectance (0.58%) is lowest and the proportions of inertinite and liptinite (37.4% and 7.1%, respectively) in the No. 6 Coal of the Junger Coalfield are highest among all of the Late Paleozoic coals in the Ordos Basin. The No. 6 Coal may be divided vertically into four sections based on their mineral compositions and elemental concentrations. A high boehmite content (mean 6.1%) was identified in the No. 6 Coal. The minerals associated with the boehmite in the coal include goyazite, rutile, zircon, and Pb-bearing minerals (galena, clausthalite, and selenio-galena). The boehmite is derived from weathered and oxidized bauxite in the weathered crust of the underlying Benxi Formation (Pennsylvanian). A high Pb-bearing mineral content of samples ZG6-2 and ZG6-3 is likely of hydrothermal origin. The No. 6 coal is enriched in Ga (44.8 μg/g), Se (8.2 μg/g), Sr (423 μg/g), Zr (234 μg/g), REEs (193.3 μg/g), Hg (0.35 μg/g), Pb (35.7 μg/g), and Th (17.8 μg/g). Gallium and Th in the No. 6 Coal mainly occur in boehmite, and the Pb-bearing selenide and sulfide minerals contribute not only to Se and Pb contents in the coal, but also probably to Hg content. A high Zr content is attributed to the presence of zircon, and Sr is related to goyazite. The REEs in the coal are supplied from the sediment-source region, and the REEs leached from the adjacent partings by groundwater. 相似文献
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利用电子探针、扫描电镜分析技术在产自山东碱性玄武岩的刚玉巨晶中发现了尖晶石族氧化物包体,并有许多刚玉、钛铁矿、高硅氧化物、辉石、长石、方解石等包体.这些包体矿物的化学成分明显与该地区相应的巨晶矿物不同,具有深源性的特征.刚玉巨晶具有世代现象,其生长具有明显的阶段性,是在一种高度演化的富含SiO_2岩浆中生成,生长过程极其复杂. 相似文献
17.
运用扫描电子显微镜（SEM）及其配套的背散射电子像功能、能谱仪（EDS）鉴定功能以及电子探针波谱分析功能,初步查明了江浪矿田内里伍矿床、黑牛铜矿床、挖金沟矿床、笋叶林矿床、中咀矿床中的主要成矿元素Cu、Zn、Fe、S及其重要伴生元素Au、Ag的赋存状态。该研究成果可为矿产资源的选矿、资源的合理充分利用、环境保护等提供有价值的参考资料。 相似文献
18.
A. Cepedal M. Fuertes-Fuente A. Martín-Izard S. González-Nistal L. Rodríguez-Pevida 《Mineralogy and Petrology》2006,87(3-4):277-304
Summary Gold ores in skarns from the Río Narcea Gold Belt are associated with Bi–Te(–Se)-bearing minerals. These mineral assemblages
have been used to compare two different skarns from this belt, a Cu–Au skarn (calcic and magnesian) from the El Valle deposit,
and a Au-reduced calcic skarn from the Ortosa deposit. In the former, gold mineralization occurs associated with Cu–(Fe)-sulfides
(chalcopyrite, bornite, chalcocite-digenite), commonly in the presence of magnetite. Gold occurs mainly as native gold and
electrum. Au-tellurides (petzite, sylvanite, calaverite) are locally present; other tellurides are hessite, clausthalite and
coloradoite. The Bi-bearing minerals related to gold are Bi-sulfosalts (wittichenite, emplectite, aikinite, bismuthinite),
native bismuth, and Bi-tellurides and selenides (tetradymite, kawazulite, tsumoite). The speciation of Bi-tellurides with
Bi/Te(Se + S) ≤ 1, the presence of magnetite and the abundance of precious metal tellurides and clausthalite indicate fO2 conditions within the magnetite stability field that locally overlap the magnetite-hematite buffer. In Ortosa deposit, gold
essentially occurs as native gold and maldonite and is commonly related to pyrrhotite and to the replacement of l?llingite
by arsenopyrite, indicating lower fO2 conditions for gold mineralization than those for El Valle deposit. This fact is confirmed by the speciation of Bi-tellurides
and selenides (hedleyite, joséite-B, joséite-A, ikunolite-laitakarite) with Bi/Te(+ Se + S) ≥ 1. 相似文献
19.
和田玉（透闪石玉）的研究 总被引：12，自引：0，他引：12
用电子探针、X射线衍射、扫描电镜等测试方法,对新疆和田玉进行了研究,结果表明和田玉的主要矿物组成为透闪石,主要结构为毛毡状结构.本文还论述了其成因,指出了进一步找矿及考古意义. 相似文献
20.
The distribution of trace elements in the lower Eocene coal seam mined in the Yeniceltek, Kucukkohne and Ayridam coal mines from the Sorgun Basin was investigated in relation to ash content and maceral composition. The coal seam is mainly composed of huminite. In the present study, 35 samples from five seam sections were collected on the basis of megascopic characteristics. Results were determined using an energy dispersive polarised X-ray fluorescence (EDP-XRF) spectrometer on a whole-coal dry basis. Most of the major and trace elements studied are enriched in high-ash samples, while Ba, Br, Mn and W show relative enrichments in low-ash samples. Most of elements studied, such as Ga, Ce, La, Th, Nb, Rb, Zr, V, Cu, U, Pb, Sb, Cs, Sn, Cr, Se, Y and Zn, are primarily associated with mineral matter (clay minerals). Arsenic and a part of Zn, Se and Sb are probably concentrated in pyrites in the samples. Element concentrations show statistically significant negative correlations with many macerals and positive relationships with only attrinite that is mainly mixed with mineral matter (clay minerals and small quartz grains) in the samples. Nine trace elements (As, Cr, Mn, Ni, Pb, Sb, Se, Th and U), considered as potentially Hazardous Air Pollutants, are present in low to moderate concentrations. The mean values of trace element concentrations display relative enrichments in Se (2.8 ppm), Th (21 ppm) and W (26 ppm) in the investigated samples in comparison with other coals in the world. 相似文献