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1.
本文分析了不同矿石中Ａｇ与Ｐｂ、Ｚｎ、Ｃｕ、Ｓ等元素的相关性，并根据银含量变化规律，银矿物组合特征，划分Ｐｂ（Ｚｎ）－Ａｇ－Ｓｎ－Ｓｂ和Ｃｕ（Ｍｏ）－Ａｇ－Ｔｅ－Ｂｉ两个不贩银的矿化组合。 相似文献
2.
内蒙古大井矿床中银矿物的研究 总被引：1，自引：0，他引：1
本文总结了内蒙古大井矿床中银矿物的类型，产出特征以及矿物命名的问题，详细描述了黝铜矿族，浓红银矿，脆银矿，自然银以及含银的铅－铋（锑）硫盐类矿物等主要银矿物的产出状态和化学成分特征，并讨论了相应的形成条件，同时指出本区银矿物主要形成于两个矿化阶段，即：早期黄铜矿－黄铁矿阶段，主要形成了黝铜矿族的含银矿物以及辉锑银矿，硫锑铜银矿等含铜的硫盐类矿物，晚期方铅矿－闪锌矿阶段，形成的银矿物种类较为繁杂，除形成黝铜矿族矿物外，多数含铅，铋的硫盐矿物以及自然银、硫化物和浓红银矿、脆银矿等无铜的简单硫盐等均是在这一阶段形成。 相似文献
3.
4.
吉林小西南岔金铜矿床的金属矿物及矿石特征。 总被引：3，自引：0，他引：3
小西南岔矿床是与燕山期花岗岩有关的斑岩矿床，以金、铜为主，伴有银、铋矿化。金属硫化物主要是黄铁矿、毒砂、磁黄铁矿、黄铜矿。金矿物是金－银系列的自然金、银金矿及金银矿。金的成色低，平均成色７２８，且变化在３０５～９９３这一较大范围内。另外，还发现了碲银矿、硫碲银铋铅矿、自然铋、赫啼铋矿、富硫铋铅矿等多种银、铋矿物。成矿早期只有微弱的铜（钼）矿化，大量金和铜富集于成矿中期（２１０～４７５℃），而银、铋矿化则出现在成矿作用晚期（１６０～２４０℃）。 相似文献
5.
夏塞银多金属矿床中硫化物和硫盐系列矿物特征及其意义 总被引：4，自引：1，他引：3
夏塞矿主档是大型的热液脉型银多金属矿床,通过对大量矿石光（薄）片观察和电子探针分析表明,除主要（方铅矿、富铁闪锌矿）和次要（黄铁矿、毒砂、磁黄铁矿、黄铜矿等）硫化物外,硫盐毓硫物十分发育,主要有Ｃｕ－Ｓｂ－Ａｇ硫盐（黝铜矿、含银黝铜矿和银黝铜矿）、Ｓｂ－Ａｇ硫盐（深红银矿、辉锑银矿）、Ｐｂ－Ｓｂ硫盐（脆硫锑铅矿、硫锑铅矿）和Ｂｉ－Ｐｂ硫盐（斜方辉饿铅矿）。此外,尚有少（微）量黄锡矿、锡石、自然饿和银金矿等。银的硫盐硫物和硫化物（辉银矿）乃是获得银的主要工业矿物,这些硫盐毓矿物常与硫化物伴生,多沿方铅矿、富铁闪锌矿、黄铁矿等的解理、裂隙或粒间产出,这些研究结果不仅有助于了解矿化作用过程,而且为矿床评价,组分综合利用和选冶提供重要依据。 相似文献
6.
福建碧田矿床成因上是与燕山晚期次火山岩有关的,以银为主的大型铜金银矿床。该矿床产于燕山早期花岗岩中,在其铜矿石内发现了较多的锌砷黔铜矿、铋砷黝铜矿、铋锑黝铜矿、碲砷黝铜矿,针硫铋铅矿、硫铋铜矿、硫砷铜矿等硫盐矿物及少见的钨锡矿化物－硫锡铁铜矿,硫铁锡铜矿和硫钨锡铜矿。 相似文献
7.
四川石棉碲矿床地球化学特征研究 总被引：5，自引：0，他引：5
研究了世界首例碲矿床的地球化学特征，特别是微量分散元素碲富集成矿的地球化学条件。此矿床属Ｔｅ－Ｂｉ－Ａｕ－Ａｇ组合型中温热液矿床，矿体为碳酸盐脉和磁黄铁矿脉，矿石平均品位：Ｔｅ５．９８％、Ｂｉ８．０２％、Ａｕ９．７３×１０－６、Ａｇ３７．４５×１０－６。成矿元素Ｔｅ、Ａｕ、Ａｇ主要来源于深部富含ＣＯ２、Ｓ的热流体。此热流体沿深大断裂上升至地壳浅部时，从围岩中浸取了大量的成矿元素Ｂｉ、Ｆｅ等。热液中的硫优先与铁结合生成磁黄铁矿析出，降低了热液中的硫浓度，从而促使分散元素碲与其沉淀剂Ｂｉ、Ａｇ、Ａｕ相结合呈碲铋矿物、碲银矿和碲金矿等独立矿物形式沉淀，并富集成矿。 相似文献
8.
新疆包古图斑岩铜矿伴生元素金和银赋存状态初步研究 总被引：13，自引：0，他引：13
新疆西准噶尔包古图斑岩铜矿床Au平均含量0.25g/t,Ag为2.56g/t,Cu为0.30%,属于富金斑岩铜矿。伴生金和银矿化作用有两期:早期为斑岩矿化,形成了Cu-Mo-Au矿化组合,是主矿化期;后期叠加了Cu-Au-Ag-Te-Bi矿化,规模不大,出露于矿床的局部部位,但对矿石起到了加富作用。通过对钻孔薄片和光薄片的镜下观察及电子探针成分分析,认为早期矿化中Au和Ag主要呈固溶体形式存在于硫化物中,分布比较均匀,基本上不出现独立矿物,Au含量明显高于Ag;晚期矿化形成了复杂的Cu-Au-Ag-Te-Bi矿物,矿石呈浸染状和脉状叠加在早期矿化之上,以银矿物为主,与多种碲铋类矿物共生,主要银矿物有碲银矿、铋-碲银矿(?)、银-辉碲铋矿(?)、银-硫铋铜矿、银金矿等。晚期矿化规模不大,但对于提高矿床的经济价值具有重要意义。 相似文献
9.
本研究成果建立在对产于晚太古代录岩带中的５５个中温热液金矿床的１３７个大样的约７０种元素的分析基础上，尺管这些矿床在成矿省和单外矿床的元素共生组合和富集上有明显差别，但总体来看，Ａｕ，Ｔｅ，Ｓ，Ａｓ，Ｗ，Ｂｉ，Ａｇ和Ｓｅ依然是金矿勘探中最重要的元素，Ｔｅ，Ａｓ，Ｂｉ和Ｓｅ的富集一般大于玄武岩平均丰度的１０００－１００倍，Ｗ、Ｓ和Ａｇ的富集系数则为１００－１０。Ｓｂ，Ｂ，Ｍｏ，Ｃｕ，Ｕ，Ｈｇ，Ｐｂ， 相似文献
10.
目前,我国金属矿床中见到铋硫盐矿物共４６种,其中有８种未定名矿物。在ＰｂＳ＿Ｂｉ２Ｓ３系列矿物中,实验矿物学（Ｌ．Ｌ．Ｙ．Ｃｈａｎｇ）上已有的１０种ＰｂＳ－Ｂｉ２Ｏ３系列矿物,即由富硫铋铅矿→硫铋铅矿→针辉铋铅矿→柱辉铋铅矿→斜方辉铋铅矿→卡辉铋铅矿→辉铋铅矿→杂硫铅铋矿→斜方硫铋铅矿→柱硫铋铅矿,我国应有尽有外,还发现有４种ＰｂＳ－Ｂｉ２Ｓ３的未定名的矿物。块辉铋铅银矿中暂定的３个亚各,我 辄全 相似文献
11.
《Russian Geology and Geophysics》2015,56(3):435-445
The spatial coexistence and synchronous formation of magmatogene porphyry Cu–Mo mineralization and epithermal gold mineralization are due to the genetic relationship between their formation processes. This relationship might be due to the generation of metal-bearing fluids of different geochemical compositions by the porphyry ore-magmatic system, which then participate in the formation of magmatogene porphyry Cu–Mo(Au) and associated epithermal gold deposits. Synthesis of fluid inclusions in quartz was performed for experimental study of the behavior of Cu, Mo, W, Sn, Au, As, Sb, Te, Ag, and Bi in heterophase fluids similar in composition and aggregate state to natural ore-forming fluids of porphyry Cu–Mo(Au) deposits. We have established that at 700 °C, a pressure decrease from 117 to 106 MPa leads to a significant enrichment of the gas phase of heterophase chloride fluid with Au, As, Sb, and Bi. The heterophase state of carbonate–chloride–sulfate fluids is observed at 600 °C and 100–90 MPa. It characterizes the highly concentrated liquid carbonate–sulfide phase–liquid chloride phase–low-density gas phase equilibrium. A decrease in the pressure of heterophase carbonate–chloride–sulfate fluid leads to a noticeable enrichment of its chloride phase with Cu, Mo, Fe, W, Ag, Sn, Sb, and Zn relative to the carbonate–sulfate phase. The processes of redistribution of ore elements between the phases of heterophase fluids can be considered a model of generation of metal-bearing chloride fluids, which occurs in nature during the formation of porphyry Cu–Mo(Au) deposits, as well as a model of generation of gas fluids supplying Au, Te, As, and other ore elements to the place of formation of epithermal Au–Cu and Au–Ag mineralization.© 2015, V.S. Sobolev IGM, Siberian Branch of the RAS. Published by Elsevier B.V. All rights reserved. 相似文献
12.
《Resource Geology》2018,68(3):209-226
Shin‐Otoyo, Suttsu, Teine, Date, Chitose, and Koryu are sites rich in precious and base metal Miocene–Pleistocene epithermal deposits, and located in southwestern Hokkaido, Japan. The deposits are predominantly hosted by the Green Tuff Formation of Middle Miocene age. Ore petrographic study of these deposits shows the occurrence of variable quantities of Cu–As–Sb–Ag–Bi–Pb–Te sulfosalt minerals. Determination of mineralogical and chemical compositions of the sulfosalt minerals was undertaken to elucidate the time and spatial changes of the sulfide‐sulfosalt minerals. Various types of sulfosalt minerals identified from gold–silver and base metal quartz–sulfide veins represented some sulfosalt mineralization phases, such as the Cu–Fe–Sn–S phase of mawsonite and stannite; Cu–(As,Sb)–S phase of tetrahedrite–tennantite and luzonite–famatinite series minerals; (Cu,Ag)–Bi–Pb–S phase of emplectite, pavonite, friedrichite, aikinite, and lillianite–gustavite series minerals; (Ag,Cu)–(As,Sb)–S phase of proustite–pyrargyrite and pearceite–polybasite series minerals; and Bi–Te–S phase of tetradymite and kawazulite minerals. There are some trends in the paragenetic sequence of sulfosalt mineralization in southwestern Hokkaido (in complete or partial) as follows: sulfide → Cu–Fe–Sn–S → (Cu,Ag)–Bi–Pb–S → (Bi–Te–S) → Cu–(As,Sb)–S → ([Ag,Cu]–[As,Sb]–S). The formation of sulfosalt minerals is characterized by the introduction of some elements such as Sn, Bi, and Te at an earlier stage and an increase or decrease of some elements such as As and Sb, followed by the introduction of Ag at the later stage of ore mineral paragenesis sequence. Mineral composition of the Chitose and Koryu deposits are slightly different from those of Shin‐Otoyo, Suttsu, Teine, and Date due to their lack of Sn (tin) and Bi (bismuth) mineralization. The variable concentrations and relationships are not simply with redistributed trace elements from the original sulfide minerals of chalcopyrite, pyrite, galena, and sphalerite. Some heavier elements were also introduced during the replacement reaction, which is consistent with the occurrence of their associated minerals. 相似文献
13.
The chemistry and mode of occurrences of native tellurium in the epithermal gold ores from Teine, Kobetsuzawa, Mutsu, Kawazu, Suzaki and Iriki in Japan are examined. Mineral assemblages in contact with native tellurium are: quartz‐sylvanite at Teine, quartz‐hessite‐sylvanite‐tellurantimony at Kobetsuzawa, quartz at Mutsu, quartz‐stutzite‐hessite‐sylvanite‐tetradymite at Kawazu, quartz at Suzaki, and quartz‐goldfieldite at Iriki. The peak patterns of XRD for native tellurium from these six ores are nearly identical to that of JCPDS 4–554. Their chemical compositions of Te range from 98.16 to 100.73 wt.%, showing nearly pure tellurium. Other elements detected are: Se of 0–0.85 and Cu of 0–0.74 at Teine, Sb of 0.45–0.47 and Se of 0.19–0.27 at Kawazu, Se of 0.22–1.11 and Sb of 0–0.49 at Suzaki, and Cu of 0.69–0.98, As of 0.22–0.28 and Bi of 0–0.22 wt.% at Iriki. No other elements are detected in the ores of Kobetsuzawa and Mutsu. The ranges of associated minor compositions are consistent with those of the experimental phase. The differences would be related to associate minerals. The mineral assemblages in these ores agree well with the previously proposed experimental phase relations in Au‐Ag‐Te ternary system for 120–280°C. The Suzaki ore has high Te‐Au assemblage: from calaverite‐sylvanite‐krennerite via native tellurium to petzite, with changing mineralization stage, whereas the Kobetsuzawa and the Kawazu ores have high Te‐Ag assemblage of tellurium‐hessite, and native tellurium‐stutzite‐hessite‐sylvanite, respectively. The Teine ore has intermediate assemblage of native tellurium‐sylvanite. The mineral assemblages in the Au‐Ag‐Te system are related to the hydrothermal environment especially to the pH condition, i.e. Au rich assemblages under acidic and Ag rich assemblages under intermediate pH conditions, being supported by alteration mineral species. The other telluriferous epithermal gold deposits not in association with native tellurium such as Agawa, Date, Takeno, Chugu, Chitose, Sado and Kushikino are estimated to have been formed under higher pH conditions as adularia and calcite occur in these deposits. The pH‐Eh diagram for aqueous tellurium species and tellurium minerals at 250°C indicates that the region of native tellurium occurs between those of aqueous telluride and tellurous species at lower pH, being consistent with their mineral assemblages in ores and alteration envelopes. 相似文献
14.
K. N. Dobroshevsky V. I. Gvozdev S. A. Shlykov V. A. Stepanov D. G. Fedoseev 《Russian Journal of Pacific Geology》2017,11(5):368-382
The mineral composition and geochemical characteristics of the ores of the Malinovskoe gold-ore deposit are studied by the data from mining works (ditches, cleanings, and boreholes). It is found that the ore–magma system of the deposit was formed in several stages of mineralization characterized by two phases of magmatism differing in age. In terms of the set of features (the geological–structural position of the deposit, as well as the material composition and geochemical characteristics of the ores), the deposit is attributed to the gold–tourmaline type of mineralization associated spatially and genetically with the “raremetal” granitoid magmatism. This type has not previously been found in Primorskii Krai. The studies of the material composition and geochemical characteristics of the ores allow us to ascertain the correlations between the elements along with the reasons of their origination. By analogy with other gold-ore formations of the Russian Far East, the mineralogical and geochemical model of the deposit is developed (Be–Sn–Cr–Ba–Au–Cu–Mo–Pb–V–Ti–Co–W–Ag–Bi–Ni–Mn–Sr–Zn–Sb–As modeling element series of vertical zoning), which enables us to estimate the levels of the erosion section of the ore bodies and to evaluate their prospects. It is found that the most productive associations in the deposit are the gold–bismuth geochemical association (Au–Ag–Bi–Cu–As–Co) and, to a lesser degree, the gold–tungsten association (W–Au–Ag–Cu–Bi–As). 相似文献
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16.
为预测和评价那仁陶勒盖金矿的成矿潜力,运用多元统计方法,结合地球化学各参数信息,对那仁陶勒盖金矿原生晕进行系统研究.结果显示:那仁陶勒盖金矿赋矿花岗闪长岩中Au、Ag、Bi等元素浓集克拉克值明显偏高,与那仁陶勒盖金成矿作用关系密切;矿石中Au与Sb、Cu、Pb、Ag、Hg、Zn、As、Bi等关系最为密切;矿体原生晕轴向分带序列出现尾晕元素W、Sn等与前缘晕元素As叠加的现象,同时(As+Sb)/(Bi+Mo)、100Sb/(Bi·Mo)等分带性指数出现转折,指示深部存在盲矿体.依据上述矿体原生晕特征,建立矿体叠加晕预测模型,预测盲矿体赋存位置在海拔710m以下的岩体与地层接触带附近. 相似文献
17.
新疆富蕴县希勒库都克钼铜矿床地球化学特征 总被引：1，自引：0，他引：1
通过对希勒库都克钼铜矿床的矿床地质、矿区地层、岩浆岩微量元素含量特征进行研究,认为下石炭统南明水组上亚组地层富集成矿元素,为矿区的主要含矿层位,该地层中强蚀变砂岩、凝灰质粉砂岩的成矿元素含量较高,为矿区的主要赋矿围岩。岩浆岩中成矿元素及主要伴生元素的含量特征显示,海西中晚期侵入的花岗闪长岩、花岗闪长斑岩和闪长斑岩（玢岩）与成矿作用密切,可能直接或间接提供了成矿物质来源。矿床在水平和垂直方向上均具有良好的分带特征,水平上由矿床中心向外呈现Mo、Cu（Au）、→V、Ti、Co、Cr、Ni、Mn、As、Sb、Hg、W、Sn、Bi→Ag、Zn、B、F的分带特征,垂向上自上而下呈现F、B、As（Cr、Ni）→Au、Cu、W（Mo、V、Co、Bi）→Mn（Au、V、Bi、Mo）的分带特征,对指导找矿具有一定意义。 相似文献
18.
五龙金矿是辽东地区大型岩浆热液型金矿床,163矿脉是矿区内目前发现的最大含矿构造。为进一步探测深部找矿潜力,近几年矿山对163矿脉进行了大量的探采工程,其中在-762 m坑道实施了600 m钻孔。本文在详细编录该钻孔的基础上,对全孔样品进行成矿元素测试工作,利用SPSS软件对所得测试数据进行元素相关性、聚类、因子分析。相关性分析显示,具有显著正相关的元素主要为Bi、W、Cu、Ag、Au和As、Sb、Sn、Zn两组;Mo元素与Sn、Ag、Cu、Bi、W、Sb地素具有显著正相关性,而Pb元素与Cu、Mo、Au、W元素呈显著负相关性,Hg元素与其它元素相关性不明显。聚类分析结果表明,R型聚类在类的距离为5的水平上,这些元素明显可分为3组：Hg、Cu、Pb、Zn、Sn、Mo、As、W;Ag、Au、Sb、Bi。因子分析结果表明,提取3个因子可以反映出12个元素变量64.42%的地球化学信息,F1的主要载荷因子组成为Sn、Ag、As、Zn、Sb, F2的主要载荷因子组成为Au、W、Bi、-Pb, F3的主要载荷因子组成为Hg。根据成矿元素随深度变化特征,结合前人构造叠加晕研究成果,推测该钻孔深部还... 相似文献
19.
Concentrations of platinum group elements (PGE), Ag, As, Au, Bi, Cd, Co, Mo, Pb, Re, Sb, Se, Sn, Te, and Zn, have been determined
in base metal sulfide (BMS) minerals from the western branch (402 Trough orebodies) of the Creighton Ni–Cu–PGE sulfide deposit,
Sudbury, Canada. The sulfide assemblage is dominated by pyrrhotite, with minor pentlandite, chalcopyrite, and pyrite, and
they represent monosulfide solid solution (MSS) cumulates. The aim of this study was to establish the distribution of the
PGE among the BMS and platinum group minerals (PGM) in order to understand better the petrogenesis of the deposit. Mass balance
calculations show that the BMS host all of the Co and Se, a significant proportion (40–90%) of Os, Pd, Ru, Cd, Sn, and Zn,
but very little (<35%) of the Ag, Au, Bi, Ir, Mo, Pb, Pt, Rh, Re, Sb, and Te. Osmium and Ru are concentrated in equal proportions
in pyrrhotite, pentlandite, and pyrite. Cobalt and Pd (∼1 ppm) are concentrated in pentlandite. Silver, Cd, Sn, Zn, and in
rare cases Au and Te, are concentrated in chalcopyrite. Selenium is present in equal proportions in all three BMS. Iridium,
Rh, and Pt are present in euhedrally zoned PGE sulfarsenides, which comprise irarsite (IrAsS), hollingworthite (RhAsS), PGE-Ni-rich
cobaltite (CoAsS), and subordinate sperrylite (PtAs2), all of which are hosted predominantly in pyrrhotite and pentlandite. Silver, Au, Bi, Mo, Pb, Re, Sb, and Te are found predominantly
in discrete accessory minerals such as electrum (Au–Ag alloy), hessite (Ag2Te), michenerite (PdBiTe), and rhenium sulfides. The enrichment of Os, Ru, Ni, and Co in pyrrhotite, pentlandite, and pyrite
and Ag, Au, Cd, Sn, Te, and Zn in chalcopyrite can be explained by fractional crystallization of MSS from a sulfide liquid
followed by exsolution of the sulfides. The early crystallization of the PGE sulfarsenides from the sulfide melt depleted
the MSS in Ir and Rh. The bulk of Pd in pentlandite cannot be explained by sulfide fractionation alone because Pd should have
partitioned into the residual Cu-rich liquid and be in chalcopyrite or in PGM around chalcopyrite. The variation of Pd among
different pentlandite textures provides evidence that Pd diffuses into pentlandite during its exsolution from MSS. The source
of Pd was from the small quantity of Pd that partitioned originally into the MSS and a larger quantity of Pd in the nearby
Cu-rich portion (intermediate solid solution and/or Pd-bearing PGM). The source of Pd became depleted during the diffusion
process, thus later-forming pentlandite (rims of coarse-granular, veinlets, and exsolution flames) contains less Pd than early-forming
pentlandite (cores of coarse-granular). 相似文献
20.
内蒙花敖包特Pb-Zn-Ag多金属矿床原生晕分带特征与深部矿体预测模型 总被引：4，自引：1，他引：3
花敖包特Pb-Zn-Ag多金属矿床构造上位于滨西太平洋成矿域内蒙古大兴安岭成矿带南段, 是一个近年来发现的与白垩纪早期构造岩浆活动有关的隐伏热液脉状矿床.研究表明: (1)矿体原生晕发育, 且分带明显.据其异常强度建立的元素横向分带顺序(从强到弱)为Cd→Pb→Zn→Ag→Sb→In→Hg→As→Cu→Sn→W→Mo→Bi, 排在序列前面的Cd、Pb、Zn、Sb、Ag等5种元素, 可作为远矿指示元素; 排在序列后端的As、Bi、Mo、W等4种元素, 可作为近矿指示元素.(2)根据Grigorian原生晕分带计算方法, 获得矿体原生晕轴向分带序列(自矿体头部至尾部)为Sb→Pb→Cd→Ag→Zn→Hg→Cu→In→As→Bi→Sn→Mo→W, 与Grigorian建立热液矿床标准分带基本一致.(3)构建深部矿体找矿模型, 其预测评价指标(Sb×Pb×Cd×Ag)D/(As×Sn×Mo×W)D在矿体头部为1.30、矿体中上部为0.35、矿体中下部为0.056、矿体尾部为0.005, 这表明该指标随深度的增加有规律地降低, 是预测深部矿体资源潜力的有效指标. 相似文献