海南乐东地区抱伦金矿矿石特征及其成因矿物学意义

抱伦金矿为大型中温热液石英脉型矿床,矿石以含金石英脉型为主,次为含金蚀变岩型。主要金属矿物为黄铁矿和磁黄铁矿,次要金属矿物20多种;脉石矿物有石英、方解石、绢云母和绿泥石等。金矿物主要为自然金,次为金、铋和银的固溶体,含Au8.20%～99.30%,Ag≤52.71%,Bi≤91.20%。铋、碲矿物有自然金属、硫化物、铋化物、硫盐和碲化物等类型。金矿石含Bi0.18×10-6～16×10-6,平均4.11×10-6,富矿石中达419×10-6。该矿床属较特殊的富铋类型,与琼西戈枕剪切带的金矿有相似之处,在琼西-粤东金矿带大陆一侧存在类似矿床,它们在成因上均应与岩浆和韧—脆性断裂活动有关。     

陕西洛南县大王西峪金矿床矿石特征及金的赋存和富集规律

大王西峪金矿床位于大月坪复背斜南翼近轴部部位,属小秦岭金矿田的西(峪)—闵(峪)含金石英脉密集区。该矿床为岩浆热液成因的石英脉型金矿,矿石类型主要为金—黄铁矿—脉石英型和金—多金属硫化物—脉石英型。组成矿石的矿物成分较复杂,脉石矿物以石英为主,局部有绢云母、长石、绿泥石及碳酸盐矿物;金属矿物以黄铁矿为主,次有方铅矿、黄铜矿、磁铁矿和微量白钨矿、钼铅矿、泡铋矿、闪锌矿、自然金、银金矿等。次生矿物有褐铁矿、白铅矿、蓝辉铜矿、铅矾及孔雀石等。金的载体矿物主要为黄铁矿,次有方铅矿、黄铜矿、石英等,金以微细粒度的包体金、裂隙金、粒间金状态赋存于载体矿物晶体中。根据单矿物样品分析结果,金主要赋存在黄铁矿等金属硫化物中,故金主要富集在多金属硫化物—脉石英类型的矿石中。     

论浙江火山岩区金矿床的成矿模式和找矿标志

文中给出了一个包含两大类五亚类八个型式的金矿床成矿模式图。浙江省火山岩区金矿的找矿标志有:矿床产出条件、围岩蚀变、同位素组成、包裹体、矿物共生组合、矿物组构及其标型特征。例如,该火山岩区重要金矿床的黄铁矿中,相对富含Pb、Zn、Mo、Sn、As,Sb和Bi,而贫Co、Ni、Se和Te;并且S/se、Ag/Au、Pb/Ni、Se/Te和(As+Sb+Bi)/(Se+Te)比值较高,Co/Ni、Ag/Pb、Ag/Zn、Cu/Zn和(Co+Ni)/(Pb+Zn)比值较低。Ⅰ、Ⅵ、Ⅶ式金银矿床中闪锌矿的化学成分富Fe、Mn,贫Cd、Hg;尤其贫Ge、Ga、Tl而富Au、Ag、Sn、Bi;晶体结构αo值约为5.4167～5.4191A。闪锌矿比重较低(d<4.05)、反射率(R)较高(高于纯闪锌矿0.24～1.61％),并且只有一个红外吸收峰(310～313cm~(-1))的特点。     

金矿床主要矿物标型特征研究综述

总结了金矿床中金矿物、黄铁矿、方铅矿、闪锌矿及黄铜矿等金属矿物和石英、碳酸盐矿物、云母类矿物及金红石等非金属矿物的产状，晶体形态、比重、硬度、颜色、反射率、导电性、热发光性等物理性质，谱学特征以及化学成分特征。从中提取出不同类型金矿床成因信息，含矿与非矿矿物特征以及判定金矿化程度、矿床规模和矿体剥蚀程度的指标。     

新疆鄯善康古尔塔格金矿床地质地球化学特征及成矿模式

康古尔塔格金矿床位于天山东段。附近还有一些金矿点和金化探异常,构成长达110km、宽约5km的金矿化带。容矿岩石为一套海相火山-沉积岩系,以火山岩为主。主要岩石类型有安山岩、英安斑岩、凝灰岩、霏细岩、流纹岩夹浅变质砂岩、粉砂岩、含砾砂岩及灰岩等。金矿体呈层状、似层状,有膨胀狭缩、分支复合现象。矿体最长850m,厚0.5～11m,向下延伸380m,含金2.6～8.7(g/t)。主要金属矿物有黄铁矿、磁铁矿、赤铁矿、黄铜矿、方铅矿、闪锌矿、自然金等。脉石矿物主要为绿泥石、石英、绢云母、方解石、重晶石。     

夏日哈木岩浆硫化物矿床中钴和镍关键金属的赋存状态及分布规律

东昆仑夏日哈木超大型岩浆镍钴硫化物矿床的工业价值，不仅取决于矿石中Co、Ni的含量，还取决于钴和镍关键金属的赋存状态和分布规律。笔者利用全自动矿物分析系统钻孔样品分析，确定Co和Ni在样品中有2种赋存状态：独立钴、镍矿物和含Co、Ni矿物。对钴、镍金属矿物进行原位主、微量元素分析发现，Co在钴、镍金属矿物中含量由高到低为：辉砷钴矿>砷镍矿、方硫铁镍矿、镍黄铁矿>红砷镍矿、磁铁矿>磁黄铁矿、黄铜矿；Ni在钴、镍金属矿物中含量由高到低为：砷镍矿、红砷镍矿>硫铋镍矿、方硫铁镍矿、镍黄铁矿>辉砷钴矿>磁铁矿、磁黄铁矿、黄铜矿。选择钻孔中体积分数占比最高的磁黄铁矿、镍黄铁矿和黄铜矿，进行原位核–边微量元素及面扫描分析发现，Co、 Ni在镍黄铁矿和黄铜矿单颗粒尺度上是均一分布的，两种矿物的Co/Ni值变化不大，表明矿物没有受到热液作用影响。然而，Ni在磁黄铁矿中分布不均一，并且矿物的Co/Ni值变化较大，表明磁黄铁矿对热液作用更为敏感。矿物原位主、微量元素分析结果显示，镍黄铁矿中的Co、Ni含量与镍、钴独立矿物接近，远超岩体中其他含钴、镍金属硫化物。因此，含Ni...     

利用电子探针研究甘肃陇南赵家庄金矿载金矿物特征

应用偏光显微镜与电子探针相结合的手段是研究载金矿物的主要方法。本文采用镜下鉴定和电子探针分析技术,对赵家庄金矿中载金矿物含量、形态特征及其与其他矿物的空间关系开展研究,并对载金矿物进行定性和定量分析,探寻具有找矿意义的载金矿物和总结标志矿物特征。结果表明:研究区金矿石中主要载金矿物为黄铁矿,少量为黄铜矿、闪锌矿,这些载金矿物中Au含量依次为:细晶黄铁矿粗晶黄铁矿草莓状黄铁矿黄铜矿。不同时期的黄铁矿(粗晶黄铁矿、细晶黄铁矿、草莓状黄铁矿)中Au的分布均匀,但存在差异性,主要表现为细晶黄铁矿和草莓状黄铁矿中的Au含量较高(平均含量0. 14%～0. 18%),这种现象表明此类矿物为构造热液期形成,金易富集。Au以两种形式存在,一种是"可见金"包裹于脉石矿物中,或以裂隙金的形式嵌布在矿物晶隙及裂隙中;另一种是"不可见金"以纳米级颗粒金的形式存在于载金矿物中,也是Au的主要存在形式。本研究为后期矿床的成因、成矿过程和成矿机理研究提供了佐证,同时易于根据含金矿物的特征选择合适的选冶方法。     

肯德可克铁多金属矿床矿石矿物标型特征及成因意义

肯德可克矿床是祁漫塔格成矿带最重要的铁多金属矿床之一。前人对肯德可克矿床的地质特征、地球化学特征、成矿年代与物质来源以及成因进行了研究,但对于成矿类型与成矿环境存在不同的认识。肯德可克矿床中的黄铁矿、黄铜矿、磁铁矿、磁黄铁矿、闪锌矿和方铅矿电子探针分析结果表明,黄铁矿与磁黄铁矿均富Co贫Ni,且磁黄铁矿以单斜磁黄铁矿为主;黄铜矿、闪锌矿与方铅矿硫含量较高,且早期磁铁矿较晚期磁铁矿更富集MnO、TiO2。综合各矿物标型特征认为,肯德可克矿床为具矽卡岩型和热液型特征的中低温矿床。     

西天山智博铁矿床黄铁矿成分特征及硫同位素研究

智博大型磁铁矿床位于新疆西天山阿吾拉勒铁铜成矿带东段,主要矿石矿物为磁铁矿,主要共生金属矿物为黄铁矿。文章通过对黄铁矿进行矿物成因研究来推测矿床成因及特征。本次研究选择2个成矿期的矿石及围岩中的黄铁矿进行电子探针及硫同位素研究。电子探针数据显示岩浆期黄铁矿w(Co)平均为4703×10~(-6),大于热液期w(Co)(735.71×10~(-6)),Co/Ni比值(平均18.53)也大于热液期黄铁矿Co/Ni比值(平均0.96);S/Se比值多数集中于1000～8000之间。部分Co/Ni、Se/Te、S/Se比值落入热液成因范围内,暗示了热液流体参与成矿的可能性。而Co-Co/Ni图解显示岩浆期矿石和热液期矿石具有一定的继承性。黄铁矿中δ~(34)S值介于-1.2‰和0.3‰之间,表明硫主要来源于幔源硫。智博铁矿床矿石主要为岩浆成因,但岩浆期后热液及其他热液流体也参与了晚阶段的成矿作用。     

山东省平度市大庄子金矿区黄铁矿、方铅矿与金的共生关系研究

通过对山东省平度市大庄子金矿区黄铁矿、方铅矿三个蚀变阶段特征研究,发现金矿化主要发生在第二阶段,强烈的石英-黄铁矿-碳酸盐化与金矿化的关系最为密切。金多数以包体的形式赋存于黄铁矿等金属硫化物中,并且在黄铁矿、方铅矿、闪锌矿等矿物共同产出时更有利于金的富集。研究认为石英和黄铁矿组合以及黄铁矿、黄铜矿、方铅矿、闪锌矿的组合可作为金的富集指示性矿物组合,伴生矿物之中方铅矿含金性最好。方铅矿、黄铜矿、闪锌矿和磁黄铁矿呈细脉状、网脉状、斑杂状产于含金石英脉和团块状黄铁矿的裂隙中,研究发现细脉状较团块状黄铁矿含金性要好。     

Isotopic systematics of He,Ar, S,Cu, Ni,Re, Os,Pb, U,Sm, Nd,Rb, Sr,Lu, and Hf in the rocks and ores of the Norilsk deposits

This paper reports the first results of a study of 11 isotope systems (³He/⁴He, ⁴⁰Ar/³⁶Ar, ³⁴S/³²S, ⁶⁵Cu/⁶³Cu, ⁶²Ni/⁶⁰Ni, ⁸⁷Sr/⁸⁶Sr, ¹⁴³Nd/¹⁴⁴Nd, ^206–208Pb/²⁰⁴Pb, Hf–Nd, U–Pb, and Re–Os) in the rocks and ores of the Cu–Ni–PGE deposits of the Norilsk ore district. Almost all the results were obtained at the Center of Isotopic Research of the Karpinskii All-Russia Research Institute of Geology. The use of a number of independent genetic isotopic signatures and comprehensive isotopic knowledge provided a methodic basis for the interpretation of approximately 5000 isotopic analyses of various elements. The presence of materials from two sources, crust and mantle, was detected in the composition of the rocks and ores. The contribution of the crustal source is especially significant in the paleofluids (gas–liquid microinclusions) of the ore-forming medium. Crustal solutions were probably a transport medium during ore formation. Air argon is dominant in the ores, which indicates a connection between the paleofluids and the atmosphere. This suggests intense groundwater circulation during the crystallization of ore minerals. The age of the rocks and ores of the Norilsk deposits was determined. The stage of orebody formation is restricted to a narrow age interval of 250 ± 10 Ma. An isotopic criterion was proposed for the ore-bearing potential of mafic intrusions in the Norilsk–Taimyr region. It includes several interrelated isotopic ratios of various elements: He, Ar, S, and others.     

高压微波消解法测定醋酸纤维过滤器采集的微尘粒子中的砷镉钴铬铜铁锰镍铅钒锌

最新的流行病学研究表明,空气中较高浓度的悬浮细颗粒可能对人类的健康有不利的影响。根据该项研究显示,由于心脏病、慢性呼吸问题和肺功能指标恶化而导致死亡率的升高与细尘粒子有关。这些研究结果已经促使欧盟于1999年4月出台了限制空气中二氧化硫、二氧化氮、氧化氮、铅和颗粒物含量的法案(1999/30/EC),对各项指标包括对可吸入PM10颗粒的浓度提出了新的限制性指标。PM10颗粒是指可以通过预分级器分离采集的气体动力学直径小于10μm的细颗粒。目前研究的兴趣重点逐步偏向PM2.5这些更细微颗粒物,PM2.5这种颗粒物对健康有明显的不利影响。在欧盟指令2008/50/EC中,对PM10和PM2.5都提     

Wavelength-dispersive X-ray fluorescence spectrometric determination of Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, Pb, and Th in komatiites

Komatiites are mantle-derived ultramafic volcanic rocks. Komatiites have been discovered in several States of India, notably in Karnataka. Studies on the distribution of trace-elements in the komatiites of India are very few. This paper proposes a simple, accurate, precise, rapid, and non-destructive wavelength-dispersive x-ray fluorescence (WDXRF) spectrometric technique for determining Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, Pb, and Th in komatiites, and discusses the accuracy, precision, limits of detection, x-ray spectral-line interferences, inter-element effects, speed, advantages, and limitations of the technique. The accuracy of the technique is excellent (within 3%) for Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Zr, Nb, Ba, Pb, and Th and very good (within 4%) for Y. The precision is also excellent (within 3%) for Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, Pb, and Th. The limits of detection are: 1 ppm for Sc and V; 2 ppm for Cr, Co, and Ni; 3 ppm for Cu, Zn, Rb, and Sr; 4 ppm for Y and Zr; 6 ppm for Nb; 10 ppm for Ba; 13 ppm for Pb; and 14 ppm for Th. The time taken for determining Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, Pb, and Th in a batch of 24 samples of komatiites, for a replication of four analyses per sample, by one operator, using a manual WDXRF spectrometer, is only 60 hours.     

Regional distribution of Al,B, Ba,Ca, K,La, Mg,Mn, Na,P, Rb,Si, Sr,Th, U and Y in terrestrial moss within a 188,000 km2 area of the central Barents region: influence of geology,seaspray and human activity

Five hundred and ninety-eight samples of terrestrial moss (Hylocomium splendens and Pleurozium schreberi) collected from a 188,000 km² area of the central Barents region (NE Norway, N Finland, NW Russia) were analysed by ICP-AES and ICP-MS. Analytical results for Al, B, Ba, Ca, K, La, Mg, Mn, Na, P, Rb, Si, Sr, Th, U and Y concentrations are reported here. Graphical methods of data analysis, such as geochemical maps, cumulative frequency diagrams, boxplots and scatterplots, are used to interpret the origin of the patterns for these elements. None of the elements reported here are emitted in significant amounts from the smelting industry on the Kola Peninsula. Despite the conventional view that moss chemistry reflects atmospheric element input, the nature of the underlying mineral substrate (regolith or bedrock) is found to have a considerable influence on moss composition for several elements. This influence of the chemistry of the mineral substrate can take place in a variety of ways. (1) It can be completely natural, reflecting the ability of higher plants to take up elements from deep soil horizons and shed them with litterfall onto the surface. (2) It can result from naturally increased soil dust input where vegetation is scarce due to harsh climatic conditions for instance. Alternatively, substrate influence can be enhanced by human activity, such as open-cast mining, creation of ‘technogenic deserts’, or handling, transport and storage of ore and ore products, all of which magnify the natural elemental flux from bedrock to ground vegetation. Seaspray is another natural process affecting moss composition in the area (Mg, Na), and this is most visible in the Norwegian part of the study area. Presence or absence of some plant species, e.g., lichens, seems to influence moss chemistry. This is shown by the low concentrations of B or K in moss on the Finnish and Norwegian side of the (fenced) border with Russia, contrasting with high concentrations on the other side (intensive reindeer husbandry west of the border has selectively depleted the lichen population).     

Petrographic, mineralogy, and geochemistry of coals of Pabedana, Kerman Province, Central Iran

This paper discusses the result of the detailed investigations carried out on the coal characteristics, including coal petrography and its geochemistry of the Pabedana region. A total of 16 samples were collected from four coal seams d2, d4, d5, and d6 of the Pabedana underground mine which is located in the central part of the Central-East Iranian Microcontinent. These samples were reduced to four samples through composite sampling of each seam and were analyzed for their petrographic, mineralogical, and geochemical compositions. Proximate analysis data of the Pabedana coals indicate no major variations in the moisture, ash, volatile matter, and fixed carbon contents in the coals of different seams. Based on sulfur content, the Pabedana coals may be classified as low-sulfur coals. The low-sulfur contents in the Pabedana coal and relatively low proportion of pyritic sulfur suggest a possible fresh water environment during the deposition of the peat of the Pabedana coal. X-ray diffraction and petrographic analyses indicate the presence of pyrite in coal samples. The Pabedana coals have been classified as a high volatile, bituminous coal in accordance with the vitrinite reflectance values (58.75–74.32 %) and other rank parameters (carbon, calorific value, and volatile matter content). The maceral analysis and reflectance study suggest that the coals in all the four seams are of good quality with low maceral matter association. Mineralogical investigations indicate that the inorganic fraction in the Pabedana coal samples is dominated by carbonates; thus, constituting the major inorganic fraction of the coal samples. Illite, kaolinite, muscovite, quartz, feldspar, apatite, and hematite occur as minor or trace phases. The variation in major elements content is relatively narrow between different coal seams. Elements Sc,, Zr, Ga, Ge, La, As, W, Ce, Sb, Nb, Th, Pb, Se, Tl, Bi, Hg, Re, Li, Zn, Mo, and Ba show varying negative correlation with ash yield. These elements possibly have an organic affinity and may be present as primary biological concentrations either with tissues in living condition and/or through sorption and formation of organometallic compounds.     

Coprecipitation of Ti,Mo, Sn and Sb with fluorides and application to determination of B,Ti, Zr,Nb, Mo,Sn, Sb,Hf and Ta by ICP-MS

We examined the coprecipitation behavior of Ti, Mo, Sn and Sb in Ca–Al–Mg fluorides under two different fluoride forming conditions: at < 70 °C in an ultrasonic bath (denoted as the ultrasonic method) and at 245 °C using a Teflon bomb (denoted as the bomb method). In the ultrasonic method, small amounts of Ti, Mo and Sn coprecipitation were observed with 100% Ca and 100% Mg fluorides. No coprecipitation of Ti, Mo, Sn and Sb in Ca–Al–Mg fluorides occurred when the sample was decomposed by the bomb method except for 100% Ca fluoride. Based on our coprecipitation observations, we have developed a simultaneous determination method for B, Ti, Zr, Nb, Mo, Sn, Sb, Hf and Ta by Q-pole type ICP-MS (ICP-QMS) and sector field type ICP-MS (ICP-SFMS). 9–50 mg of samples with Zr–Mo–Sn–Sb–Hf spikes were decomposed by HF using the bomb method and the ultrasonic method with B spike. The sample was then evaporated and re-dissolved into 0.5 mol l^− 1 HF, followed by the removal of fluorides by centrifuging. B, Zr, Mo, Sn, Sb and Hf were measured by ID method. Nb and Ta were measured by the ID-internal standardization method, based on Nb/Mo and Ta/Mo ratios using ICP-QMS, for which pseudo-FI was developed and applied. When 100% recovery yields of Zr and Hf are expected, Nb/Zr and Ta/Hf ratios may also be used. Ti was determined by the ID-internal standardization method, based on the Ti/Nb ratio from ICP-SFMS. Only 0.053 ml sample solution was required for measurement of all 9 elements. Dilution factors of ≤ 340 were aspirated without matrix effects. To demonstrate the applicability of our method, 4 carbonaceous chondrites (Ivuna, Orgueil, Cold Bokkeveld and Allende) as well as GSJ and USGS silicate reference materials of basalts, andesites and peridotites were analyzed. Our analytical results are consistent with previous studies, and the mean reproducibility of each element is 1.0–4.6% for basalts and andesites, and 6.7–11% for peridotites except for TiO₂.     

Roles of xenomelts,xenoliths, xenocrysts,xenovolatiles, residues,and skarns in the genesis,transport, and localization of magmatic Fe-Ni-Cu-PGE sulfides and chromite

Most sulfide-rich magmatic Ni-Cu-(PGE) deposits form in dynamic magmatic systems by partial melting S-bearing wall rocks with variable degrees of assimilation of miscible silicate and volatile components, and generation of barren to weakly-mineralized immiscible Fe sulfide xenomelts into which Ni-Cu-Co-PGE partition from the magma. Some exceptionally-thick magmatic Cr deposits may form by partial melting oxide-bearing wall rocks with variable degrees of assimilation of the miscible silicate and volatile components, and generation of barren Fe ± Ti oxide xenocrysts into which Cr-Mg-V ± Ti partition from the magma. The products of these processes are variably preserved as skarns, residues, xenoliths, xenocrysts, xenomelts, and xenovolatiles, which play important to critical roles in ore genesis, transport, localization, and/or modification. Incorporation of barren xenoliths/autoliths may induce small amounts of sulfide/chromite to segregate, but incorporation of sulfide xenomelts or oxide xenocrysts with dynamic upgrading of metal tenors (PGE > Cu > Ni > Co and Cr > V > Ti, respectively) is required to make significant ore deposits. Silicate xenomelts are only rarely preserved, but will be variably depleted in chalcophile and ferrous metals. Less dense felsic xenoliths may aid upward sulfide transport by increasing the effective viscosity and decreasing the bulk density of the magma. Denser mafic or metamorphosed xenoliths may also increase the effective viscosity of the magma, but may aid downward sulfide transport by increasing the bulk density of the magma. Sulfide wets olivine, so olivine xenocrysts may act as filter beds to collect advected finely dispersed sulfide droplets, but other silicates and xenoliths may not be wetted by sulfides. Xenovolatiles may retard settling of – or in some cases float – dense sulfide droplets. Reactions of sulfide melts with felsic country rocks may generate Fe-rich skarns that may allow sulfide melts to fractionate to more extreme Cu-Ni-rich compositions. Xenoliths, xenocrysts, xenomelts, and xenovolatiles are more likely to be preserved in cooler basaltic magmas than in hotter komatiitic magmas, and are more likely to be preserved in less dynamic (less turbulent) systems/domain/phases than in more dynamic (more turbulent) systems/domains/phases. Massive to semi-massive Ni-Cu-PGE and Cr mineralization and xenoliths are often localized within footwall embayments, dilations/jogs in dikes, throats of magma conduits, and the horizontal segments of dike-chonolith and dike-sill complexes, which represent fluid dynamic traps for both ascending and descending sulfides/oxides. If skarns, residues, xenoliths, xenocrysts, xenomelts, and/or xenovolatiles are present, they provide important constraints on ore genesis and they are valuable exploration indicators, but they must be included in elemental and isotopic mass balance calculations.