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1.
挪威某些铜镍矿石中单斜磁黄铁矿出溶体的退火和粗化   总被引：4，自引：0，他引：4  
在挪威某些正岩浆铜镍矿床的矿石中，六万磁黄铁矿基质内的单斜磁黄铁矿叶片是高温时形成的磁黄铁矿固溶体在降温过程中出溶的产物。出溶叶片宽度和间距的加大、叶片的带状分布、楔形尖端、箱状扭曲和复杂叶片等结构，表明出溶产物在不高于单斜-六方转变温度（254℃）的条件下发生过显著的退火和粗化。重结晶的六方磁黄铁矿基质中所保存的单斜变种甚少，表明变质作用所引起的矿石重结晶，可使磁黄铁矿吸收其中的单斜出溶体而发生均匀化。  相似文献   

2.
为探讨新疆坡北岩体坡七侵入体中铜镍硫化物矿(化)体的成因,采用显微镜观察、磁性胶体浸润和电子探针分析等方法,对主要的金属矿物磁黄铁矿、镍黄铁矿开展了成因矿物学研究。结果表明,浸染状、稠密浸染状矿石中,磁黄铁矿为六方(NC型)磁黄铁矿,或六方磁黄铁矿与散点状单斜(4C型)磁黄铁矿构成的不规则状交生体。六方磁黄铁矿是高温结晶后缓慢降温的产物,而不规则状交生体是流体交代六方磁黄铁矿的结果。块状矿石中的磁黄铁矿是六方与单斜变体构成叶片状/箱状交生体,其成因与快速降温和热事件干扰有关。镍黄铁矿富集Co,在各类矿石中均可分为3个世代(Pn1,Pn2,Pn3),在结晶过程中硫逸度随着温度的降低而减小。等轴晶系辉砷钴矿、自形镍黄铁矿及高温黄铜矿的晶出暗示金属硫化物结晶温度普遍偏高。  相似文献   

3.
黄山东铜镍硫化物矿床产于东天山地区的黄山—镜儿泉韧性剪切带中,大地构造上属中亚造山带东天山觉罗塔格岛弧带。该铜镍矿所在的黄山东镁铁—超镁铁岩体呈纺锤状侵位于晚石炭世火山岩中,其边部发生了与区域剪切带总体走向一致的强烈糜棱岩化作用。矿床中的部分矿体发生强烈韧性变形,其中17号矿体完全产于韧性变形带内,岩石和矿石都发生了强烈的破碎和蚀变而形成矿石糜棱岩。在上述韧性变形带内,还发育一定规模的网脉状和细脉状富铜碳酸盐—硫化物脉。论文在野外地质和构造形迹观察的基础上,对黄山东矿床不同类型的矿石开展了细致的显微岩相和矿相学观察,识别出三种类型矿石:原生矿石、强烈变形矿石和热液叠加矿石。海绵陨铁结构的原生矿石中,脉石矿物几乎不发生蚀变和变形,矿石矿物仅发生脆性破裂;强烈变形矿石中,脉石矿物和矿石矿物均发生强烈变形,主要以纤闪石的波状消光和膝折、金云母的书斜构造、磁黄铁矿的定向拉长为特征;热液叠加矿石中的磁黄铁矿普遍发育颗粒的扁平化、重结晶,局部可见磁黄铁矿的退火平衡结构。黄山东铜镍硫化物矿床的侵位与变形时间与区域黄山-镜儿泉剪切带的韧性剪切作用时间相一致。岩体冷却过程经历的强烈韧性剪切变形作用不但造成矿石矿物的强烈韧性变形而形成矿石糜棱岩,还使伴生脉石矿物发生细粒化和热液蚀变,释放出流体和成矿元素,并叠加于变形的矿石和岩石之上,从而形成了网脉状和细脉状矿体。黄山东铜镍矿的原生硫化物固熔体铁含量较高,因而在硫化物熔体结晶过程只形成六方磁黄铁矿而无伴生单斜磁黄铁矿和黄铁矿。在热液叠加过程中,流体沿边缘和裂隙面交代早期六方磁黄铁矿,形成单斜磁黄铁矿反应边。本次研究还发现六方磁黄铁矿形成的新机制:即在高硫逸度和高氧逸度的条件下,随着体系温度的降低,单斜磁黄铁矿可从热液六方磁黄铁矿中出溶形成呈叶片状单斜—六方磁黄铁矿交生体。  相似文献   

4.
金川铜镍硫化物矿床磁黄铁矿矿物学特征及成因意义   总被引：1，自引：0，他引：1  
金川铜镍硫化物矿床矿石类型主要为浸染状矿石、海绵陨铁状矿石及块状矿石。采用矿相显微镜观察、磁性胶体浸润与电子探针分析等方法,对3种类型矿石中磁黄铁矿的结构状态、共生组合与成分特征作了研究,探讨了矿石成因及成矿过程。在浸染状矿石与海绵陨铁状矿石中,磁黄铁矿为单纯的六方(NC型)磁黄铁矿,或者六方与单斜(4C型)磁黄铁矿构成的不规则状交生体。这2类矿石中磁黄铁矿的成因很可能是岩(矿)浆中S含量低,且高温结晶后缓慢降温,后期又受到了富硫和/或高氧逸度流体的交代作用。在Ⅱ矿区块状矿石中,单斜与六方磁黄铁矿构成平行叶片状交生体,表明六方磁黄铁矿在高温下结晶后温度曾快速下降,这期间仅出溶了微量的黄铁矿,而当温度下降到254℃以下时,发生了六方磁黄铁矿中单斜磁黄铁矿出溶作用。磁黄铁矿的结晶类型、金属原子(Fe、Ni、Cu、Co)与硫原子比值M/S演化等佐证了块状矿石晚期贯入成因。依据Fe-S系统相图拟合曲线计算得到块状矿石中六方磁黄铁矿结晶温度为743~518℃,且在结晶过程中,硫逸度logf(S2)曾从0.427降至-3.767。  相似文献   

5.
王炳恩  秦宽 《矿物岩石》1997,17(2):22-27
本文对红旗岭矿区磁黄铁矿－镍黄铁矿矿石建造进行了研究。并通过矿石组特征，矿物形成温度，硫、锶同位素，岩体稀土元素特征等研究，进一步论述了磁黄铁矿与镍黄铁矿的物质来源于上地幔。属于深部岩浆熔离含矿熔浆冷凝而成。  相似文献   

6.
南秦岭南部构造带具备较好的金矿成矿条件与成矿背景,是该区域规模较大金矿带.金沟矿段是黄龙金矿床最主要的组成部分,该矿段矿石中磁黄铁矿和黄铁矿发育,其中磁黄铁矿矿石是矿床中含量最高的硫化物矿石.磁黄铁矿存在两种产出状态,分别为早期形成的呈浸染状、团块状分布的磁黄铁矿与晚期形成的脉状磁黄铁矿.成分分析结果表明以单斜磁黄铁矿为主.该矿床属中-低温矿床.微量元素结果显示富Co贫Ni,与金矿化关系密切.在含金性方面,脉状产出的磁黄铁矿优于团块状分布的磁黄铁矿,且脉体越细含金性越好,因此细脉状磁黄铁矿可作为该区重要的找矿标志.  相似文献   

7.
新疆萨尔托海铬铁矿中的Fe-Ni-As-S矿物研究   总被引：2，自引：1，他引：1  
谭娟娟  朱永峰 《岩石学报》2010,26(8):2264-2274
新疆萨尔托海铬铁矿是一个典型的与蛇绿岩有关的高铝型豆荚状铬铁矿,其中矿石铬尖晶石发生了明显的热液蚀变,发育了富Cr的蚀变环边,形成高铁铬铁矿,Cr#在蚀变后升高,发生了Cr元素的次生富集。在矿石颗粒间隙中的Fe-Ni-As-S矿物组合主要为镍黄铁矿-赫硫镍矿-针镍矿-砷镍矿。围岩纯橄岩普遍发育强烈的蛇纹石化,其中的Fe-Ni-As-S矿物组合为赫硫镍矿-镍黄铁矿-砷镍矿,还有少量的针镍矿和铜矿物。通过对硫化物的成分对比分析,认为矿石中的镍黄铁矿和赫硫镍矿都属于岩浆演化的产物(600℃),与赫硫镍矿和针镍矿一样,均从贫S的母岩浆中通过岩浆熔离过程形成。围岩和矿石中的含砷矿物以及围岩中的镍黄铁矿都是晚期热液活动的结果,其中砷镍矿具有特殊的蠕虫状-乳滴状结构,与围岩中的赫硫镍矿和镍黄铁矿共生。围岩和矿石中Fe-Ni-As-S矿物组合的形态和成分差异,说明金属矿物的整体演化从岩浆期到热液期经历了从贫S到富As的环境变化,最终形成了现在所观察到的复杂Fe-Ni-As-S矿物组合。  相似文献   

8.
通过差热-热重分析、X射线粉末衍射（XRD）及磁化率分析等手段,对天然黄铁矿样品在氮气中受热发生的矿物相 变过程进行了综合研究。不同温度下黄铁矿煅烧产物的XRD物相分析结果显示,低于500℃时,黄铁矿无显著变化;随着 温度的升高（500~600℃）,黄铁矿开始转变为单斜磁黄铁矿,进而生成六方磁黄铁矿,磁化率显著升高;700℃~800℃的 煅烧产物主要为六方磁黄铁矿,磁化率明显下降,直至900℃进一步形成更稳定的陨硫铁（FeS）,磁化率接近于零。在黄 铁矿物相开始转变的温度（500~600℃）区间,黄铁矿生成单斜磁黄铁矿的速率大于单斜磁黄铁矿转化为六方磁黄铁矿的速 率;高温（700~900℃）时,黄铁矿转化为单斜磁黄铁矿的速率低于单斜磁黄铁矿转化为六方磁黄铁矿的速率,表现为黄铁 矿直接生成六方磁黄铁矿。  相似文献   

9.
攀西会理县白草矿区以钒钛磁铁矿而闻名,但该钒钛磁铁矿床中还发育一定规模的富钴硫化物矿石,对该类型矿石的形成机制研究还不深入.本文选择白草矿区产出的浸染状、致密块状、网脉状和斑杂状富钴硫化物矿石中的磁黄铁矿做为研究对象,在野外地质调查的基础上,通过矿相学和电子探针等方法对磁黄铁矿的成分和晶体类型进行研究.利用磁性胶体可以鉴别磁黄铁矿晶体类型的原理,确定了研究区的磁黄铁矿具有单斜磁黄铁矿(Mpo)和六方磁黄铁矿(Hpo)两种晶体类型,厘定了细脉状、叶片状和不规则状交生体.通过研究磁黄铁矿中各主量元素特征,计算了磁黄铁矿形成温度、硫逸度和M/S值等参数.将磁黄铁矿形成划分岩浆成矿期(熔离阶段、接触交代阶段)和热液成矿期,并初步厘定了4类磁黄铁矿生成顺序:首先形成浸染状矿石磁黄铁矿与致密块状矿石磁黄铁矿,其次形成斑杂状矿石磁黄铁矿,最后形成网脉状矿石磁黄铁矿.  相似文献   

10.
辽东裂谷硫铁矿矿床内两类磁黄铁矿的特征及其研究意义   总被引：1，自引：0，他引：1  
磁黄铁矿是辽东硫化物成矿带内主要矿石矿物。在对该矿床成因研究过程中，发现矿床内的磁黄铁矿有两种同质多象变体。通过对两类磁黄铁矿的产状、共生组合、物理化学性质、Ｘ－衍射特征，成矿条件等方面的研究表明它们形成于不同的成矿阶段。其中单斜磁黄铁矿为海底喷气热水沉积成矿作用的产物；而六方磁黄铁矿则是在变质改造作用过程中由黄铁矿转变而成。进而为判断矿床成因，指导找矿提供了依据  相似文献   

11.
The paper presents concentrations of the platinum-group and chalcophile elements in the base metal sulfides (BMS) from the Jinchuan Ni–Cu sulfide deposit determined by laser ablation-inductively coupled plasma-mass spectrometry. Mass balance calculations reveal that pentlandite hosts a large proportion of Co, Ni and Pd (> 65%), and that pentlandite and pyrrhotite accommodate significant proportions of Re, Os, Ru, Rh, and Ag (~ 35–90%), whereas chalcopyrite contains a small amount of Ag (~ 10%) but negligible platinum-group elements. Iridium and Pt are not concentrated in the BMS and mostly occur in As-rich platinum-group minerals. The enrichments of Co, Ni, Re, Os, Ru, and Rh in pentlandite and pyrrhotite, and Cu in chalcopyrite are consistent with the fractionation of sulfide liquid and exsolution of pentlandite and pyrrhotite from the mono-sulfide solid solution (MSS). The Ir-bearing minerals exsolved from the MSS, depleting pentlandite and pyrrhotite in Ir, whereas sperrylite exsolved from the residual sulfide liquid on cooling. Diffusion of Pd from residual sulfide liquid into pentlandite during its exsolution from the MSS and crystallization of Pt-bearing minerals in the residual sulfide liquid resulted in the enrichment of Pd in pentlandite and decoupling between Pd and Pt in the Jinchuan net-textured and massive ores.  相似文献   

12.
Magmatic sulfide liquids are effective at concentrating a range of metals. Within magmatic sulfide systems pentlandite, an exsolution product of monosulfide solid solution (MSS), is the primary host of Ni, Co and significant concentrations of Pd. Over the last decade, LA-ICP-MS mapping has revealed non-uniform metal distributions and complexity to the metal patterns such as zonation and the linear alignment of elements. Whereas the compatibility and partitioning behavior of chalcophile elements during sulfide fractionation are well constrained, there is little knowledge on the crystallographic control exerted on metal distributions.In this study, LA-ICP-MS mapping of globular sulfides from the Crystal Lake Intrusion, Ontario (Canada), is complimented by EBSD analysis, revealing a strong crystallographic control on both the concentration of metals and pentlandite exsolutions. Elements considered incompatible in the high temperature monosulfide solid solution (MSS) phase (e.g., Cr, V, As, Pb, Ag, Bi and Pd) are preserved as a microfabric, showing preferential concentration in association with the (0001) basal plane of pyrrhotite and adjacent pentlandite. Where the [0001] axis is viewed perpendicular to the cut surface, the microfabric is considered to be an intersection lineation between the basal (0001) plane and the surface of the cut section.Pentlandite textures described in magmatic sulfide deposits include granular, fan and laths/blades. Our observations indicate that marginal pentlandite exsolutions, are in optical continuity with granular exsolutions, providing insights into the growth of pentlandite at MSS grain boundaries. We conclude that all pentlandite forms are crystallographically controlled by the hexagonal mineral system of MSS/pyrrhotite, with the [0001] c-axis of pyrrhotite corresponding to the 〈111〉 axis of pentlandite. This axis also acts as a twinning rotation axis for the two identified pentlandite orientations. Fan and lath textured exsolutions are considered geometrically equivalent structures, being reconstructed as flat disc–shapes developed parallel to the basal (0001) plane of pyrrhotite, which acts as a preferred nucleation site. A network of low-angle grain boundaries are recognized as hexagonal or rectangular structures within pyrrhotite, with the morphology shown to be dependent on the orientation of the crystals. As these features are again geometric equivalents, they can be reconstructed as intragrain hexagonal prisms. We speculate due to their localized development, that they could represent a plastic response of the pyrrhotite to accommodate the increase in volume suggested to be associated with late pentlandite exsolutions and thus are the result of static lattice recovery.The microstructural and trace element observations presented here provide new context to some of the common textural features of magmatic sulfide deposits, while importantly highlighting the strong crystallographic control on both metal distributions and sulfide textures. This study also importantly recognizes the dominance of hexagonal pyrrhotite within the ores of the Crystal Lake Intrusion and likely other magmatic sulfide deposits. This has implications for mineral processing as its non-magnetic properties can result in dilution of Ni-Cu-PGE ores and thus requires special attention for the flotation strategy.  相似文献   

13.
The Garson Ni–Cu–platinum group element deposit is a deformed, overturned, low Ni tenor contact-type deposit along the contact between the Sudbury Igneous Complex (SIC) and stratigraphically underlying rocks of the Huronian Supergroup in the South Range of the 1.85-Ga Sudbury structure. The ore bodies are coincident with steeply south-dipping, north-over-south D1 shear zones, which imbricated the SIC, its ore zones, and underlying Huronian rocks during mid-amphibolite facies metamorphism. The shear zones were reactivated as south-over-north, reverse shear zones during D2 at mid-greenschist facies metamorphism. Syn-D2 metamorphic titanite yields an age of 1,849?±?6 Ma, suggesting that D1 and D2 occurred immediately after crystallization of the SIC during the Penokean Orogeny. The ore bodies plunge steeply to the south parallel to colinear L1 and L2 mineral lineations, indicating that the geometry of the ore bodies are strongly controlled by D1 and D2. Sulfide mineralization consists of breccia ores, with minor disseminated sulfides hosted in norite, and syn-D2 quartz–calcite–sulfide veins. Mobilization by ductile plastic flow was the dominant mechanism of sulfide/metal mobilization during D1 and D2, with additional minor hydrothermal mobilization of Cu, Fe, and Ni by hydrothermal fluids during D2. Metamorphic pentlandite overgrows a S1 ferrotschermakite foliation in D1 deformed ore zones. Pentlandite was exsolved from recrystallized polygonal pyrrhotite grains after cessation of D1, which resulted in randomly distributed large pentlandite grains and randomly oriented pentlandite loops along the grain boundaries of polygonal pyrrhotite within the breccia ore. It also overgrows a S2 chlorite foliation in D2 shear zones. Pyrrhotite recrystallized and was flattened during D2 deformation of breccia ore along narrow shear zones. Exsolution of pentlandite loops along the grain boundaries of these flattened grains produced a pyrrhotite–pentlandite layering that is not observed in D1 deformed ore zones. The overprinting of the two foliations by pentlandite and exsolution of pentlandite along the grain boundaries of flattened pyrrhotite grains suggest that the Garson ores reverted to a metamorphic monosulfide solid solution at temperatures ranging between 550 and 600 °C during D1 and continued to deform as a monosulfide solid solution during D2.  相似文献   

14.
Magmatic sulfide deposits consist of pyrrhotite, pentlandite, chalcopyrite (± pyrite), and platinum-group minerals (PGM). Understanding the distribution of the chalcophile and platinum-group element (PGE) concentrations among the base metal sulfide phases and PGM is important both for the petrogenetic models of the ores and for the efficient extraction of the PGE. Typically, pyrrhotite and pentlandite host much of the PGE, except Pt which forms Pt minerals. Chalcopyrite does not host PGE and the role of pyrite has not been closely investigated. The Ni–Cu–PGE ores from the South Range of Sudbury are unusual in that sulfarsenide PGM, rather than pyrrhotite and pentlandite, are the main carrier of PGE, probably as the result of arsenic contribution to the sulfide liquid by the As-bearing metasedimentary footwall rocks. In comparison, the North Range deposits of Sudbury, such as the McCreedy East deposit, have As-poor granites in the footwall, and the ores commonly contain pyrite. Our results show that in the pyrrhotite-rich ores of the McCreedy East deposit Os, Ir, Ru, Rh (IPGE), and Re are concentrated in pyrrhotite, pentlandite, and surprisingly in pyrite. This indicates that sulfarsenides, which are not present in the ores, were not important in concentrating PGE in the North Range of Sudbury. Palladium is present in pentlandite and, together with Pt, form PGM such as (PtPd)(TeBi)2. Platinum is also found in pyrite. Two generations of pyrite are present. One pyrite is primary and locally exsolved from monosulfide solid solution (MSS) in small amounts (<2 wt.%) together with pyrrhotite and pentlandite. This pyrite is unexpectedly enriched in IPGE, As (± Pt) and the concentrations of these elements are oscillatory zoned. The other pyrite is secondary and formed by alteration of the MSS cumulates by late magmatic/hydrothermal fluids. This pyrite is unzoned and has inherited the low concentrations of IPGE and Re from the pyrrhotite and pentlandite that it has replaced.  相似文献   

15.
Concentrations of Ag, Au, Cd, Co, Re, Zn and Platinum-group elements (PGE) have been determined in sulfide minerals from zoned sulfide droplets of the Noril’sk 1 Medvezky Creek Mine. The aims of the study were; to establish whether these elements are located in the major sulfide minerals (pentlandite, pyrrhotite, chalcopyrite and cubanite), to establish whether the elements show a preference for a particular sulfide mineral and to investigate the model, which suggests that the zonation in the droplets is caused by the crystal fractionation of monosulfide solid solution (mss). Nickel, Cu, Ag, Re, Os, Ir, Ru, Rh and Pd, were found to be largely located in the major sulfide minerals. In contrast, less than 25% of the Au, Cd, Pt and Zn in the rock was found to be present in these sulfides. Osmium, Ir, Ru, Rh and Re were found to be concentrated in pyrrhotite and pentlandite. Palladium and Co was found to be concentrated in pentlandite. Silver, Cd and Zn concentrations are highest in chalcopyrite and cubanite. Gold and platinum showed no preference for any of the major sulfide minerals. The enrichment of Os, Ir, Ru, Rh and Re in pyrrhotite and pentlandite (exsolution products of mss) and the low levels of these elements in the cubanite and chalcopyrite (exsolution products of intermediate solid solution, iss) support the mss crystal fractionation model, because Os, Ir, Ru, Rh and Re are compatible with mss. The enrichment of Ag, Cd and Zn in chalcopyrite and cubanite also supports the mss fractionation model these minerals are derived from the fractionated liquid and these elements are incompatible with mss and thus should be enriched in the fractionated liquid. Gold and Pt do not partition into either iss or mss and become sufficiently enriched in the final fractionated liquid to crystallize among the iss and mss grains as tellurides, bismithides and alloys. During pentlandite exsolution Pd appears to have diffused from the Cu-rich portion of the droplet into pentlandite.  相似文献   

16.
The bulk composition, mineralogy and mineral chemistry of base-metal sulfides have been investigated in the Fe-Ni-(Cu) ore deposits of the Ivrea-Verbano basic complex.The sulfide ores mostly display textural evidence of having been primarily deposited as an immiscible melt. Bulk compositions of the ores indicate that considerably low Ni/Fe and Ni/Co ratios are found in deposits developed close to metasedimentary country rocks, possibly as a result of mixing with sedimentary sulfur.Phase relations of primary sulfides indicate that early crystallization of the ore was dominated by a monosulfide solid solution (Mss) with a pyrrhotite composition, from which pentlandite and chalcopyrite were formed through subsolidus exsolution. Pentlandite from contaminated ores is typically enriched in Co. Troilite and hexagonal intermediate pyrrhotite intergrowths frequently occur due to low-temperature equilibration of metal-rich pyrrhotites, suggesting a low S fugacity of the original sulfide melt.The sulfides may be locally mobilized and redeposited along shear zones within the same host rock, giving rise to fairly massive ores having a typical cemented-breccia texture. Bulk composition and assemblages suggest that mobilization occurred at various temperatures during the cooling history of the ore, when sulfides were still in the molten state or at a lower temperature under the influence of abundant deuteric fluids. In this last case, growth of pyrite is seen as being possibly due to sulfurization and/or oxidation.  相似文献   

17.
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   

18.
The quasiequilibrium directed crystallization technique was used for experimental simulation of zoning characteristic of Cu-rich pyrrhotite-chalcopyrite and pyrrhotite-cubanite-mooihoekite-haycockite ores at the Oktyabr??sky deposit. Directed crystallization of samples I (Fe 32.55, Cu 10.70, Ni 5.40, S. 51.00, Pt = Pd = Rh = Ir= Au = Ag = 0.05 at %) and II (Fe 33.74, Cu 15.94, Ni 1.48, S. 48.75, Pt = Pd = 0.05 at %) was performed. These samples approximate average composition of the ore. Monosulfide (mms) and intermediate (iss) solid solutions progressively crystallized from the melt. The curves of ore element distribution in samples have been drawn. The partition coefficients (k) of ore elements between solid solutions and sulfide melt have been determined depending on melt composition. The paths of melt, mss, and iss compositions are supplemented by tie lines connecting compositions of equilibrium liquid and solid phases. The phase composition of samples after cooling was studied using an optical microscope, XRD, and microprobe. The zoning of sample I is described by the following sequence of phases: monoclinic pyrrhotite ?? hexagonal pyrrhotite + tetragonal chalcopyrite ?? tetragonal and cubic chalcopyrite + pentlandite + bornite. Crystallized sample II consists of four zones: (1) hexagonal pyrrhotite and isocubanite; (2) hexagonal pyrrhotite, cubanite, and pentlandite; (3) low-S pc-phase close to haycockite and pentlandite; and (4) mooihoekite, pentlandite, and bornite mixtures. This sequence corresponds to the secondary zoning, which reflects both the primary fractionation of components and the solid-phase reactions during cooling of the crystallized sample. The Rh, Ru, and Ir partition coefficients between mss and melt have been measured, and speciation of PGM in samples has been identified. The results obtained are compared with typical natural Cu-rich sulfide ore of the Oktyabr??sky deposit.  相似文献   

19.
A refined Avrami method, that assumes that the activation energy is a function of reaction extent y, was used to analyze the kinetics of the exsolution of pentlandite from mss/pyrrhotite (bulk composition, (Fe0.77Ni0.19)S) over the temperature range 473 to 573 K. The experimental results show the reaction rates vary from 1.6 × 10−5 to 5.0 × 10−7 s−1 at 473 K and from 9.4 × 10−5 to 4.1 × 10−7 s−1 at 573 K. Examination of exsolution textures indicated that the mechanism of exsolution did not change significantly over the temperature range investigated. The activation energy (Ea) decreases from 49.6 to 20.7 kJ mol−1 over the course of the reaction. The decrease in Ea with y is related to the change in the dominant factor of pentlandite exsolution, from nucleation dominant at the beginning to metal ion diffusion dominant at the end. The classic Avrami method provides average values of kinetic parameters for the overall solid-state reaction while the refined Avrami method provides more a detailed indication of the variation of kinetic parameters over the course of the reaction. Previously published kinetic data for the exsolution of pentlandite from mss/pyrrhotite are reevaluated using the refined Avrami method.  相似文献   

20.
董宇  魏博  王焰 《岩石学报》2021,37(9):2875-2888
金川铜镍硫化物矿床是我国最主要的铂族元素(PGE)资源产地,其矿石受热液蚀变作用影响明显,并产出多种铂族矿物(PGM)。岩浆演化和热液蚀变过程中PGE的迁移富集机制和PGM的成因,一直是研究PGE地球化学行为非常关注的问题。本文对金川铜镍硫化物矿床中PGM的研究发现,其主要类型包括含PGE的硫砷化物(硫砷铱矿)和砷化物(砷铂矿),Pd的铋化物、碲化物和硒化物,以及少量其他铂族矿物。其中,硫砷铱矿可包裹于各种贱金属硫化物(镍黄铁矿、磁黄铁矿和黄铜矿)中,表明硫砷铱矿可能结晶于早期的含As硫化物熔体,随后被包裹于硫化物熔体冷凝分异产生的单硫化物固溶体(MSS)和中间硫化物固溶体(ISS)中。硫化物熔体中的As可能主要通过地壳混染作用加入幔源岩浆。大量铋钯矿(PdBi)呈微细乳滴状包裹于黄铜矿中,为晚期ISS冷凝形成黄铜矿过程中出溶的产物。少量铋钯矿(PdBi_2)呈不规则状充填于矿物裂隙,与次生磁铁矿脉紧密共生,并随矿石的蚀变程度增加,铋钯矿的化学成分由PdBi逐渐向PdBi_2转变,表明这部分铋钯矿为后期热液蚀变产物。铋碲钯矿和钯的硒化物则主要产出于镍黄铁矿裂隙且与次生磁铁矿紧密共生,指示明显的热液成因。钯的硒化物的出现表明,岩浆期后酸性、高盐度、高氧逸度的富Cl~-流体对金川铜镍硫化物矿床中Pd的迁移和富集起到了关键控制作用。  相似文献   

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