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1.
Copper–Gold Skarn Mineralization at the Karavansalija Ore Zone,Rogozna Mountain,Southwestern Serbia 
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下载免费PDF全文 Zhivko D. Budinov Kotaro Yonezu Thomas Tindell Jillian Aira Gabo‐Ratio Stanoje Milutinovic Adrian J. Boyce Koichiro Watanabe 《Resource Geology》2015,65(4):328-344
Karavansalija ore zone is situated in the Serbian part of the Serbo‐Macedonian magmatic and metallogenic belt. The Cu–Au mineralization is hosted mainly by garnet–pyroxene–epidote skarns and shifts to lesser presence towards the nearby quartz–epidotized rocks and the overlying volcanic tuffs. Within the epidosites the sulfide mineralogy is represented by disseminated cobalt‐nickel sulfides from the gersdorfite‐krutovite mineral series and cobaltite, and pyrite–marcasite–chalcopyrite–base metal aggregates. The skarn sulfide mineralization is characterized by chalcopyrite, pyrite, pyrrhotite, bismuth‐phases (bismuthinite and cosalite), arsenopyrite, gersdorffite, and sphalerite. The sulfides can be observed in several types of massive aggregates, depending on the predominant sulfide phases: pyrrhotite‐chalcopyrite aggregates with lesser amount of arsenopyrite and traces of sphalerite, arsenopyrite–bismuthinite–cosalite aggregates with subordinate sphalerite and sphalerite veins with bismuthinite, pyrite and arsenopyrite. In the overlying volcanoclastics, the studied sulfide mineralization is represented mainly by arsenopyrite aggregates with subordinate amounts of pyrite and chalcopyrite. Gold is present rarely as visible aggregate of native gold and also as invisible element included in arsenopyrite. The fluid inclusion microthermometry data suggest homogenization temperature in the range of roughly 150–400°C. Salinities vary in the ranges of 0.5–8.5 wt% NaCl eq for two‐phase low density fluid inclusions and 15–41 wt% NaCl eq for two‐phase high‐salinity and three‐phase high‐salinity fluid inclusions. The broad range of salinity values and the different types of fluid inclusions co‐existing in the same crystals suggest that at least two fluids with different salinities contributed to the formation of the Cu–Au mineralization. Geothermometry, based on EPMA data of arsenopyrite co‐existing with pyrite and pyrrhotite, suggests a temperature range of 240–360°C for the formation of the arsenopyrite, which overlaps well with the data for the formation temperature obtained through fluid inclusion microthermometry. The sulfur isotope data on arsenopyrite, chalcopyrite, pyrite and marcasite from the different sulfide assemblages (ranging from 0.4‰ to +3.9‰ δ34SCDT with average of 2.29 δ34SCDT and standard deviation of 1.34 δ34SCDT) indicates a magmatic source of sulfur for all of the investigated phases. The narrow range of the data points to a common source for all of the investigated sulfides, regardless of the host rock and the paragenesis. The sulfur isotope data shows good overlap with that from nearby base‐metal deposits; therefore the Cu–Au mineralization and the emblematic base‐metal sulfide mineralization from this metallogenic belt likely share same fluid source. 相似文献
2.
This paper reports on different styles of gold mineralization observed in Archean gold deposits hosted by Algoma-type Banded Iron-Formations (BIF) in southern Africa. Genetic aspects of various occurrences are discussed in the context of mineralogical as well as geochemical data of BIFs from the greenstone terranes of the Zimbabwe and Kaapvaal cratons. The study revealed that, in spite of their different provenance and age (3.5 to 2.6 Ga), the BIFs are geochemically similar, whereas observed mineralogical differences reflect various degrees of metamorphic overprint. Generally, the BIFs belong to mixed oxide-carbonate-(±sulfide)-facies. REE distribution patterns of the investigated Archean BIF samples exhibit positive Eu-anomalies, which suggest a strongly reducing nature of the solutions which also provided the distinctive element contents now present in the chemical sediments. Irrespective of their formation, gold enrichment in BIF only occurs if the S- and/or As-contents of the BIFs exceed specific threshold values, i.e. gold mineralization is always associated with increased contents of the iron-sulfides pyrite, arsenopyrite and pyrrhotite. The studies indicate that BIF-hosted gold occurrences are not products of a single universal metallogenic process, but may be explained by several different genetic processes such as primary syn-sedimentary formation, diagenetic changes, metamorphic remobilization, and epigenetic hydrothermal emplacement. 相似文献
3.
The Ohori deposit, one of the base metal deposits in the Green-Tuff region, NE Japan, is composed of two types of mineralization; a skarn-type (Kaninomata orebody) made by the replacement of the Miocene calcareous layer, and a vein-type (Nakanomata orebody). While the ore mineral assemblage of the deposit (chalcopyrite, pyrite, sphalerite and galena) has been known for being rather simple, some Pb-Bi-S minerals have been discovered for the first time in the present study. The minerals mainly occur in the chalcopyrite-rich ores of both orebodies. They essentially belong to the Pb-Bi-S system and contain Cu and Ag in minor amounts, which correspond to the lillianite–gustavite solid solution series (phases Z and X), cosalite, neyite, felbertalite, krupkaite and Bi-bearing galena. The chalcopyrite-rich (Bi-bearing) ores from both orebodies are richer in chalcopyrite, pyrite and chlorite, and have higher homogenization temperatures (>300°C) of fluid inclusions, and higher FeS contents in sphalerite compared to the Bi-free ores. In the Green-Tuff region, Bi-minerals have been reported from many base metal deposits. Most of these Bi-bearing ore deposits are referred to as xenothermal-type deposits, and are characterized by the following common features; composite mineralization of high- and low-temperatures in the shallower environments, and close relationships with the Tertiary granitic rocks. The whole mineralization at the Ohori deposit also has a similar xenothermal character because of the coexistence of high-temperature chalcopyrite-rich ores with Pb-Bi-S minerals, which were formed by the influence of the Tertiary granitic rocks at a shallow depth. 相似文献
5.
新疆哈密卡拉塔格块状硫化物矿床金银赋存状态研究 总被引：3，自引：0，他引：3
新疆哈密红海黄土坡VMS矿床位于东天山卡拉塔格隆起带,是卡拉塔格矿集区内新发现的块状硫化物矿床。矿体产于卡拉塔格隆起带核部火山沉积岩建造中,具有典型的VMS型矿床“上层下脉”二元结构特征。该矿床中含金硫化物矿石主要有块状黄铁矿黄铜矿、块状黄铁矿黄铜矿闪锌矿、块状黄铁矿闪锌矿黄铜矿和块状闪锌矿。文中在对各类含金硫化物矿石进行详细的矿相学研究基础上,结合扫描电子显微镜与能谱仪联用技术(SEM/EDS),对硫化物样品中金、银的赋存状态进行研究。结果表明,4种块状硫化物中的主要矿物形成于多个期次,主要包括VMS成矿期(黄铁矿阶段、闪锌矿黄铜矿黝铜矿方铅矿阶段、石英重晶石阶段)、热液叠加期(石英黄铁矿黄铜矿闪锌矿方铅矿阶段)和表生期(铜蓝纤铁矿阶段)。矿区首次发现4颗金银金属互化物(银金矿、碲银矿),其较大的化学成分差异指示了热液环境由中酸性中性转变为更有利于Au、Ag迁移沉淀的偏碱性。后期的偏碱性热液对VMS成矿期形成矿物产生了交代作用,使得Au、Ag活化再富集。由于后期热液叠加改造,红海VMS型矿床中Au、Ag不仅赋存于VMS成矿期后期中低温闪锌矿黄铜矿阶段,也赋存于VMS成矿期早期中高温黄铁矿阶段,并贯穿整个热液叠加期。各含金矿物组合中除4颗金银金属互化物外Au多呈显微不可见状态,推测Au、Ag主要以原子或离子形式赋存于矿物晶格中或矿物空位处。 相似文献
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7.
江西武山铜矿床海底喷流与岩浆热液叠加成矿作用: 控矿地质条件、矿石结构构造与矿床地球化学制约 总被引：4，自引：2，他引：2
长江中下游成矿带存在一套产于泥盆系五通组砂岩和石炭系黄龙组白云质灰岩层间的层状含铜硫化物矿体,对其成因存在很大争议。本文以产出典型层状矿体的武山铜矿为解剖重点,结合区域控矿地质要素、矿石结构构造特征及矿石中黄铁矿的稀土元素地球化学,提出层状矿体是海底喷流同生沉积与岩浆热液叠加成矿作用的产物。对武山铜矿层状矿体中的胶黄铁矿和黄铁矿、矽卡岩矿体中黄铁矿和脉状矿体中黄铁矿进行的稀土元素含量分析发现,从层状矿体胶黄铁矿、层状矿体黄铁矿、到矽卡岩和脉状矿体黄铁矿,稀土总量和稀土配分曲线显示递变规律,即层状矿体胶黄铁矿具有较低的稀土总量和轻重稀土分异不明显的较平坦型配分曲线;而矽卡岩和脉状矿体黄铁矿具有较高的稀土总量和轻重稀土分异较明显的右倾型配分曲线。层状矿体黄铁矿的稀土特征则介于两者之间,反映了岩浆热液的叠加作用。根据矿物组合共生关系及矿石结构构造的研究,可将武山铜矿黄铁矿分为3个期次:I期为微球粒、草莓状、条带状、纹层状沉积型黄铁矿; II期为半自形、自形粒状和港湾状黄铁矿,可见与长英质斑晶、岩屑或晶屑凝灰岩伴生或共生, 说明黄铁矿形成与同沉积期火山凝灰岩的密切关系。III期为块状、粗晶状、碎裂状黄铁矿。黄铜矿的形成晚于I、II期黄铁矿,成微粒状、脉状交错穿插或包裹早期球粒状、粒状黄铁矿及长英质矿物。对新发现的灰泥丘构造的详细研究表明,武山铜矿中含矿的灰泥丘与武山外围乌石街出露的不含矿的灰泥丘具有不同的特征,其中前者具有封闭的孔洞系统,而后者为开放的孔洞系统。总之,武山铜矿控矿地质条件、矿石结构构造及不同类型矿石黄铁矿的稀土元素证据表明矿床存在两期成矿事件,即海西期海底喷流同生沉积成矿期和燕山期岩浆热液叠加成矿期。 相似文献
8.
铜官山矿田是铜陵矿集区内五大矿田之一,矿田内顺层产出的层状硫化物矿体是铜金矿床的主矿体,矿体内含有较多的胶状黄铁矿,其成因的争议制约了对铜金矿床成矿作用的解析。本文主要利用场发射扫描电镜(FE-SEM)等纳米矿物学手段,并结合光学显微镜、粉晶X射线衍射(XRD)、微区激光拉曼光谱分析等方法,对矿田内铜官山矿床及天马山矿床内层状硫化物矿体中胶状黄铁矿矿石的矿物组成、微形貌、微结构等特征进行系统研究,结果表明胶状黄铁矿矿石多呈胶状、鲕状结构,具有同心环状构造,同心环被赤铁矿、菱铁矿与黄铜矿脉穿切。同心环主要由白铁矿+有机质与胶状黄铁矿交替组成。胶状黄铁矿的黄铁矿颗粒粒径从纳米至亚微米均有分布,以自形-半自形立方体为主,少数呈他形,脉体边部胶状黄铁矿颗粒较大,自形程度较高,重结晶显著。矿石中含有少量白云石、伊利石微晶体,与胶状黄铁矿紧密共存,显示典型沉积特征。共存石英磨圆度较高,存在次生加大现象,表面存在胶状黄铁矿印模,显示为碎屑成因。这些综合信息表明胶状黄铁矿非岩浆热液成因,而是与石炭系地层同沉积成岩成因,并可能有微生物作用参与。高孔隙率、高化学活性及较高有机质含量的胶状黄铁矿可能为燕山期岩浆热液演化的含铜成矿流体提供了沉淀剂,对矿田内铜金硫化物矿体的层控性发挥了重要的控制作用。 相似文献
9.
Magmatic sulfide deposits typically occur in ultramafic-mafic systems, however, mineralisation can occur in more intermediate and alkaline magmas. Sron Garbh is an appinite-diorite intrusion emplaced into Dalradian metasediments in the Tyndrum area of Scotland that hosts magmatic Cu-Ni-PGE-Au sulfide mineralisation in the appinitic portion. It is thus an example of magmatic sulfide mineralisation hosted by alkaline rocks, and is the most significantly mineralised appinitic intrusion known in the British Isles. The intrusion is irregularly shaped, with an appinite rim, comprising amphibole cumulates classed as vogesites. The central portion of the intrusion is comprised of unmineralised, but pyrite-bearing, diorites. Both appinites and diorites have similar trace element geochemistry that suggests the diorite is a more fractionated differentiate of the appinite from a common source that can be classed with the high Ba-Sr intrusions of the Scottish Caledonides. Mineralisation is present as a disseminated, primary chalcopyrite-pyrite-PGM assemblage and a blebby, pyrite-chalcopyrite assemblage with significant Co-As-rich pyrite. Both assemblages contain minor millerite and Ni-Co-As-sulfides. The mineralisation is Cu-, PPGE-, and Au-rich and IPGE-poor and the platinum group mineral assemblage is overwhelmingly dominated by Pd minerals; however, the bulk rock Pt/Pd ratio is around 0.8. Laser ablation analysis of the sulfides reveals that pyrite and the Ni-Co-sulfides are the primary host for Pt, which is present in solid solution in concentrations of up to 22 ppm in pyrite. Good correlations between all base and precious metals indicate very little hydrothermal remobilisation of metals despite some evidence of secondary pyrite and PGM. Sulfur isotope data indicate some crustal S in the magmatic sulfide assemblages. The source of this is unlikely to have been the local quartzites, but S-rich Dalradian sediments present at depth. The generation of magmatic Cu-Ni-PGE-Au mineralisation at Sron Garbh can be attributed to post-collisional slab drop off that allowed hydrous, low-degree partial melting to take place that produced a Cu-PPGE-Au-enriched melt, which ascended through the crust, assimilating crustal S from the Dalradian sediments. The presence of a number of PGE-enriched sulfide occurrences in appinitic intrusions across the Scottish Caledonides indicates that the region contains certain features that make it more prospective than other alkaline provinces worldwide, which may be linked the post-Caledonian slab drop off event. We propose that the incongruent melting of pre-existing magmatic sulfides or ‘refertilised’ mantle in low-degree partial melts can produce characteristically fractionated, Cu-PPGE-Au-semi metal bearing, hydrous, alkali melts, which, if they undergo sulfide saturation, have the potential to produce alkaline-hosted magmatic sulfide deposits. 相似文献
10.
The Laloki and Federal Flag deposits are two of the many (over 45) polymetallic massive sulfide deposits that occur in the Astrolabe Mineral Field, Papua New Guinea. New data of the mineralogical compositions, mineral textures, and fluid inclusion studies on sphalerite from Laloki and Federal Flag deposits were investigated to clarify physiochemical conditions of the mineralization at both deposits. The two deposits are located about 2 km apart and they are stratigraphically hosted by siliceous to carbonaceous claystone and rare gray chert of Paleocene–Eocene age. Massive sulfide ore and host rock samples were collected from each deposit for mineralogical, geochemical, and fluid inclusion studies. Mineralization at the Laloki deposit consists of early‐stage massive sulfide mineralization (sphalerite‐barite, chalcopyrite, and pyrite–marcasite) and late‐stage brecciation and remobilization of early‐stage massive sulfides that was accompanied by late‐stage sphalerite mineralization. Occurrence of native gold blebs in early‐stage massive pyrite–marcasite‐chalcopyrite ore with the association of pyrrhotite‐hematite and abundant planktonic foraminifera remnants was due to reduction of hydrothermal fluids by the reaction with organic‐rich sediments and seawater mixing. Precipitation of fine‐grained gold blebs in late‐stage Fe‐rich sphalerite resulted from low temperature and higher salinity ore fluids in sulfur reducing conditions. In contrast, the massive sulfide ores from the Federal Flag deposit contain Fe‐rich sphalerite and subordinate sulfarsenides. Native gold blebs occur as inclusions in Fe‐rich sphalerite, along sphalerite grain boundaries, and in the siliceous‐hematitic matrix. Such occurrences of native gold suggest that gold was initially precipitated from high‐temperature, moderate to highly reduced, low‐sulfur ore fluids. Concentrations of Au and Ag from both Laloki and Federal Flag deposits were within the range (<10 ppm Au and <100 ppm Ag) of massive sulfides at a mid‐ocean ridge setting rather than typical arc‐type massive sulfides. The complex relationship between FeS contents in sphalerite and gold grades of both deposits is probably due to the initial deposition of gold on the seafloor that may have been controlled by factors such as Au complexes, pH, and fO2 in combination with temperature and sulfur fugacity. 相似文献
11.
位于华北克拉通南缘的小秦岭地区是我国仅次于胶东的大型金矿床集中区,但金矿床的成矿物质来源及成因问题一直存在较大争议.以华北南缘小秦岭矿集区东桐峪金矿床中的黄铁矿作为研究对象,在黄铁矿显微结构研究的基础上利用LA-ICP-MS对黄铁矿的微量元素进行原位分析,为进一步认识东桐峪金矿床及区内其他同类型矿床的成因提供新的资料和制约.东桐峪金矿床的黄铁矿从早到晚依次划分为3个世代(PyⅠ、PyⅡ和PyⅢ).PyⅠ主要形成于粗粒黄铁矿-石英阶段,颗粒粗大且自形程度高,呈星点状或斑点状赋存于乳白色石英脉中.PyⅡ主要形成于石英-中细粒黄铁矿阶段,呈半自形-他形结构且裂隙发育,常被晚期石英、多金属硫化物、自然金等矿物充填.PyⅢ主要形成于多金属硫化物阶段,常呈他形粒状结构与黄铜矿、方铅矿及闪锌矿等硫化物密切共生.LA-ICP-MS分析结果显示,PyⅠ中As平均含量为16.63×10-6,Au、Ag和Te含量较低且常位于检测限以下;相较而言,PyⅡ中As含量稍低,而Au、Ag和Te含量略高(其中Au含量为0.10×10-6~0.59×10-6);PyⅢ中Au、Ag和Te含量差异较大且显著升高,其中Au、Te含量最高可达35.58×10-6和79.79×10-6,而As含量较低且大部分数值低于检测限;不同世代黄铁矿的Co/Ni比值基本上都大于1,且PyⅢ的Co、Ni含量和Co/Ni比值明显低于PyⅡ和PyⅠ.以上结果表明,东桐峪金矿床的载金矿物黄铁矿中As的含量很低,金的富集与As无关;不同世代的黄铁矿中Au、Ag和Te之间存在显著且稳定的线性正相关关系,暗示金矿化与Te关系密切.另外,第3世代黄铁矿(PyⅢ)中Au、Ag及Te存在显著富集,指示Te(而不是As)在金和银的迁移、搬运、富集、沉淀等过程中具有重要作用.华北克拉通南缘小秦岭地区晚中生代大规模的金成矿作用及金矿床中普遍存在Te-Au-Ag矿物,且黄铁矿中As含量低、Te含量高等特征,暗示该区金矿床的成矿物质/成矿流体可能来自深部岩浆的脱挥发分或地幔脱气作用,而与区域变质作用的关系不大. 相似文献
12.
《Ore Geology Reviews》2003,22(1-2):61-90
Quantitative laser ablation (LA)-ICP-MS analyses of fluid inclusions, trace element chemistry of sulfides, stable isotope (S), and Pb isotopes have been used to discriminate the formation of two contrasting mineralization styles and to evaluate the origin of the Cu and Au at Mt Morgan.The Mt Morgan Au–Cu deposit is hosted by Devonian felsic volcanic rocks that have been intruded by multiple phases of the Mt Morgan Tonalite, a low-K, low-Al2O3 tonalite–trondhjemite–dacite (TTD) complex. An early, barren massive sulfide mineralization with stringer veins is conforming to VHMS sub-seafloor replacement processes, whereas the high-grade Au–Cu ore is associated with a later quartz–chalcopyrite–pyrite stockwork mineralization that is related to intrusive phases of the Tonalite complex. LA-ICP-MS fluid inclusion analyses reveal high As (avg. 8850 ppm) and Sb (avg. 140 ppm) for the Au–Cu mineralization and 5 to 10 times higher Cu concentration than in the fluids associated with the massive pyrite mineralization. Overall, the hydrothermal system of Mt Morgan is characterized by low average fluid salinities in both mineralization styles (45–80% seawater salinity) and temperatures of 210 to 270 °C estimated from fluid inclusions. Laser Raman Spectroscopic analysis indicates a consistent and uniform array of CO2-bearing fluids. Comparison with active submarine hydrothermal vents shows an enrichment of the Mt Morgan fluids in base metals. Therefore, a seawater-dominated fluid is assumed for the barren massive sulfide mineralization, whereas magmatic volatile contributions are implied for the intrusive related mineralization. Condensation of magmatic vapor into a seawater-dominated environment explains the CO2 occurrence, the low salinities, and the enriched base and precious metal fluid composition that is associated with the Au–Cu mineralization. The sulfur isotope signature of pyrite and chalcopyrite is composed of fractionated Devonian seawater and oxidized magmatic fluids or remobilized sulfur from existing sulfides. Pb isotopes indicate that Au and Cu originated from the Mt Morgan intrusions and a particular volcanic strata that shows elevated Cu background. 相似文献
13.
Zircon U–Pb and pyrite Re–Os age constraints on pyrite mineralization in the Yinjiagou deposit,China
《International Geology Review》2012,54(13):1616-1625
We report new zircon U–Pb and pyrite Re–Os geochronological studies of the Yinjiagou poly-metallic deposit, sited along the southern margin of the North China Craton (SMNCC). In this deposit, pyrite, the most important economic mineral, is intergrown/associated with Mo, Cu, Au, Pb, Zn, and Ag. Prior to our new work, the age of chalcopyrite–pyrite mineralization was known only from its spatial relationship with molybdenite mineralization and with intrusions of known ages. The U–Pb and Re–Os isotope systems provide an excellent means of dating the mineralization itself and additionally place constraints on the ore genesis and metal source. Zircons separated from the quartz–chalcopyrite–pyrite veins include both detrital and magmatic groups. The magmatic zircons confine the maximum age of chalcopyrite–pyrite mineralization to 142.0 ± 1.5 Ma. The Re–Os results yield an age of 141.1 ± 1.1 Ma, which represents the age of the chalcopyrite–pyrite mineralization quite well. The common Os contents are notably low (0.5–20.1 ppt) in all samples. In contrast, the Re contents vary considerably (3.0–199.2 ppb), most likely depending on intensive boiling, which resulted in an increase of Re within the pyrite. This study demonstrates that the main chalcopyrite–pyrite mineralization occurred late in the magmatic history and was linked to a deeper intrusion involving dominant mantle-derived materials. This mineralization event might be related to the Early Cretaceous lithospheric destruction and thinning of the SMNCC. 相似文献
14.
B. De Vivo L.G. Closs A. Lima R. Marmolino V. Perrone 《Journal of Geochemical Exploration》1984,21(1-3)
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
15.
The effect of sulfide concentrate mineralogy and texture on Reactive Oxygen Species (ROS) generation
The generation of Reactive Oxygen Species (ROS), H2O2 and OH, has been observed from sulfide mineral containing particles in acidic solutions. The implications of this phenomenon, as a potential microbial stress-causing effect, have been studied previously with respect to thermophilic bioleaching performance in the presence of finely milled pyrite and chalcopyrite concentrates. In this study, the effect of sulfide mineralogy on ROS generation in the absence of microbes under physicochemical conditions typical for the bioleach environment was investigated. The mineralogical and elemental composition of eleven different samples containing sulfide mineral was obtained. These Au, Cu and other base metal-containing sulfide mineral concentrates as well as a milled whole ore of low Cu grade were tested for ROS generation. The whole ore sample and two refractory Au concentrates containing approximately 50% pyrite, generated significantly less ROS compared to the base metal-containing concentrates when compared on a constant surface area loading basis. Sulfide mineral-related variables were correlated with ROS generation. A significant difference was observed between FeS2 and CuFeS2 grades separately, whereas a combined measure of both minerals present in samples showed a consistently strong correlation to ROS generation. The Cu grade, total Cu-containing sulfides and the chalcopyrite content of Cu-containing samples correlated well with ROS generation. However, a common deterministic variable with a strong association to increased ROS generation was not found. A sub-set of samples were subjected to QEMSCAN® for textural analysis. Results suggested that a decrease in sulfide mineral liberation, caused by gangue silicate mineral occlusion to solution, resulted in decreased reactivity as shown in one of the Au-containing samples. Well-liberated chalcopyrite and pyrite phases corresponded to increased reactivity of samples. Pyrite, which was present in all of the reactive samples, was shown to be associated with other sulfide minerals, implicating its importance in galvanic interactions. Micro-analysis of chalcopyrite and pyrite phases from highly reactive samples showed an abundance of particles with extensive cracking and the possible presence of secondary transformation phases (szomolnokite). These results suggest that sulfide mineralogy, liberation and extent of physical processing affect sulfide mineral concentrate reactivity in acidic solutions. 相似文献
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17.
近年来,在相山铀矿田的西部牛头山地区深部发现了铅锌矿化体,其成因机制不明.为探讨牛头山铅锌矿化体物质来源,开展了硫化物原位硫同位素分析研究.根据硫化物矿物之间的充填和包裹关系判断,铅锌矿化体金属硫化物形成的先后顺序是:黄铁矿形成最早,方铅矿和闪锌矿次之,细脉状黄铜矿形成最晚.利用LA-MC-ICP-MS技术对矿化体中几种金属硫化物分别进行了系统的原位硫同位素分析.结果显示:黄铁矿、闪锌矿、方铅矿、细脉状黄铜矿的δ34S值介于-4.8‰~+5.4‰之间,各硫化物矿物之间硫同位素未达到完全平衡分馏,利用黄铁矿δ34S值得到的矿化流体δ34SΣS值（总硫同位素组成）近似为+3.7‰,与共生矿物对（闪锌矿-方铅矿）图解法得到的闪锌矿和方铅矿沉淀时矿化流体的δ34SΣS值（+3.2‰）相近,表明形成牛头山铅锌矿化体的矿化流体δ34SΣS值大约为+3.7‰,为岩浆硫.结合前人的岩浆岩年龄数据,我们判断该铅锌矿化体金属硫化物的硫可能主要来自次火山岩相花岗斑岩岩浆热液.同一薄片中闪锌矿δ34S值高于共生的方铅矿,表明两者硫同位素基本平衡,利用共生矿物对（闪锌矿-方铅矿）硫同位素温度计计算得出平衡温度为197~476℃,与前人通过脉石矿物流体包裹体得到的铅锌矿化流体温度基本一致.相山火山盆地与相邻的北武夷黄岗山、梨子坑等产铅锌矿的火山盆地具有相似的成矿条件及成矿物质来源,使相山火山盆地具有良好的铅锌多金属找矿前景. 相似文献
18.
The Dabaoshan polymetallic deposit, located in the middle Nanling metallogenic belt, is an important and representative W-Mo-Cu-Pb-Zn deposit in the northern Guangdong. The deposit is characterized by a complex combination of ore-forming elements, containing 0.86 Mt Cu, 0.85 Mt Zn, 0.31 Mt Pb, 0.14 Mt WO3 at grades of 0.86%, 12%, 1.77% and 0.12%, respectively. Due to different mineral association and occurrence, mineralization at Dabaoshan can be defined as three types: porphyry W-Mo mineralization, skarn Mo-W mineralization and strata-bound sulfide mineralization. Pyrite from the three-mineralization types has different textures and element compositions. EMPA mapping analysis suggested that distribution of Co, Ni, and As is nearly homogeneous, whilst As in pyrite from the stratabound sulfides shows weak irregular zoning. LA-ICP-MS analyses of pyrite suggested that the three type have distinctive trace element characteristics even though the concentrations of the trace elements are relatively low. Cobalt, Ni, As and Se substitutes Fe and S in pyrite respectively while Cu, Zn, Sn Sb are mainly represented by chalcopyrite, sphalerite, cassiterite and stibnite inclusions enclosed in pyrite. Ni and Ag are rich in the pyrite from the stratabound mineralization. The results suggested that the trace element characteristic of pyrite can be used to: a) study the occurrence of trace element in pyrite; b) imply the chemical-physical conditions; c) trace the regional ore-forming substance and ore forming process. The stratabound mineralization is formed during the volcano eruption during the Devonian then and overprinted by the deep source material and multiple ore-forming fluids in the Yanshanian period. © 2018, Science Press. All right reserved. 相似文献
19.
铊(Tl)是一种战略性关键金属,在高科技领域具有重要用途。作为“稀散元素”之一,Tl主要富集于低温贱金属硫化物矿床中,黄铁矿和白铁矿是其主要载体矿物。滇东北火德红MVT铅锌矿床中黄铁矿和白铁矿显示Tl的富集,其中白铁矿中Tl含量显著高于黄铁矿,为探究Tl在不同矿物之间的差异性富集机制提供了理想对象。本文对火德红矿床共生黄铁矿-白铁矿开展系统的结晶学、矿物学和地球化学研究。电子背散射衍射(EBSD)结果表明,热液黄铁矿、白铁矿晶粒组构具有一定继承性,与闪锌矿紧密共生,暗示为同一成矿事件的产物。激光剥蚀耦合等离子体质谱(LA-ICPMS)原位微量元素含量分析结果显示,黄铁矿和白铁矿中的Tl含量分别为127×10^(-6)~516×10^(-6)和356×10^(-6)~1046×10^(-6),不同含量测点Tl的激光剥蚀时间分辨元素信号曲线均较为平滑,暗示Tl主要以类质同象形式进入黄铁矿和白铁矿晶格。透射电镜(TEM)进一步证实Tl类质同象直接替换Fe为主,即2Tl^(+)←→□(空位)+Fe^(2+)。结合黄铁矿和白铁矿中Tl与Zn含量的正相关关系,本文认为白铁矿中Tl的超常富集可能与偏酸性条件下富Tl、Zn和Fe等金属成矿流体有关。综合研究表明,火德红矿床黄铁矿与白铁矿中Tl的差异性富集与晶体结构、Tl赋存状态无关,而是流体成分、物化条件共同制约的结果,受到矿物和矿床等不同尺度苛刻成矿条件的影响。与闪锌矿共生的白铁矿是未来寻找铊资源的重要方向。 相似文献
20.
I.V. Gas’kov Tran Tuan Anh Tran Trong Hoa Pham Thi Dung P.A. Nevol’ko Pham Ngoc Can 《Russian Geology and Geophysics》2012,53(5):442-456
The Sin Quyen Cu–Fe–Au–REE deposit is localized in the Proterozoic deposits of the Phan Xi Pang zone, northern Vietnam. The mineralization is formed by lenticular and sheet-like bodies occurring concordantly with the host rocks. Seventeen orebodies have been recognized in the deposit, which form an ore horizon up to 140 m in total thickness, about 2 km in strike, and up to 350 m in dip. The ores are of simple mineral composition: Au-rich copper and iron sulfides (chalcopyrite, pyrite, pyrrhotite) and iron oxides (magnetite, hematite). Gold and silver are distributed unevenly in the ores: Their contents vary from hundredths and tenths of ppm to 1.8 ppm. Copper sulfide ores are the main concentrator of gold and silver. All ores are characterized by high REE contents, tens and hundreds of times exceeding the element clarkes. The highest contents have been revealed for Ce and La. Orthite is the main carrier of REE. No correlation between REE and ore elements of sulfide-oxide ores has been revealed, which points to the independent formation of the mineralization. Orebodies together with the host rocks underwent metamorphism at 500–600 to 630–685 °C and 3–7 kbar. The spatial association of the mineralization with amphibolites (metamorphosed basites) and the mineral composition of ores suggest that the Sin Quyen deposit is of Cyprian volcanogenic type. 相似文献