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1.
铂族元素矿物共生组合(英文) 总被引：1，自引：2，他引：1
由于铂族元素能有效地降低汽车尾气的污染 ,其需求量日益增加 ,对铂族元素矿床的寻找已是当务之急。着重从矿物矿床学角度对铂族元素的矿物共生特点进行了探讨。铂族元素可呈独立矿床产出 ,主要产于基性超基性层状侵入体、蛇绿岩套及阿拉斯加式侵入体中。铂族元素也伴生于铜镍矿床中 ,该类铜镍矿床主要与苏长岩侵入体、溢流玄武岩及科马提岩有关。产于基性超基性层状侵入体中的铂族矿物有铂钯硫化物、铂铁合金、钌硫化物、铑硫化物、铂钯碲化物、钯砷化物及钯的合金。这些铂族矿物可与硫化物矿物共生 ,也可与硅酸盐矿物共生 ,还可与铬铁矿及其他氧化物矿物共生。产于蛇绿岩套中的铂族矿物主要是钌铱锇的矿物 ,而铂钯铑的矿物则较少出现 ,这些铂族矿物可呈合金、硫化物、硫砷化物以及砷化物 4种形式出现。产于阿拉斯加式侵入体中的铂族矿物主要有铂铁合金、锑铂矿、硫铂矿、砷铂矿、硫锇矿及马兰矿等少数几种 ,其中铂铁合金与铬铁矿及与其同时结晶的高温硅酸盐矿物共生 ,而其他的铂族矿物则与后来的变质作用及蛇纹岩化作用中形成的多金属硫化物及砷化物共生。产于铜镍矿床中的铂族矿物主要是铂和钯的矿物。产于基性超基性层状侵入体、蛇绿岩套及阿拉斯加式侵入体中的铂族矿物的共同特点是它们均与铬铁矿? 相似文献
2.
S. Yu. Stepanov K. N. Malitch A. V. Kozlov I. Yu Badanina A. V. Antonov 《Geology of Ore Deposits》2017,59(3):244-255
The new data for the geology and mineralogy of the platinum group element (PGE) mineralization related to the chromite–platinum ore zones within the dunite of the Svetly Bor and Veresovy Bor massifs in the Middle Urals are discussed. The geological setting of the chromite–platinum ore zones, their platinum content, compositional and morphological features of the platinum group minerals (PGM) are compared to those within the Nizhny Tagil massif, the world standard of the zonal complexes in the Platinum Ural belt. The chromite–platinum orebodies are spatially related to the contacts between differently granular dunites. Majority of PGM are formed by Pt–Fe alloys that are close in terms of stoichiometry to isoferroplatinum (Pt3Fe), and associated with Os–Ir alloys, Ru–Os and Ir–Rh sulfides, and Ir–Rh thiospinels of the cuproiridsite–cuprorhodsite–ferrorhodsite solid solution. The tetraferroplatinum (PtFe)–tulameenite (PtFe0.5Cu0.5) solid solution and Pt–Cu alloys belong to the later PGM assemblage. The established features of the chromite–platinum ore zones testify to the highly probable identification of the PGE mineralization within the dunite of the Svetly Bor and Vesesovy Bor massifs and could be used in prospecting and exploration for platinum. 相似文献
3.
The Sopcheozero chromite deposit is hosted in dunite of the Monchegorsk layered intrusion as a sheetlike body of disseminated ore with a chromite grade varying from 20 to 60%. The total PGM content in the ore attains 0.5–0.8 g/t. The composition of host rocks varies from plagioclase peridotite to dunite, but PGM were found only in chromite-bearing dunite. PGM inclusions were detected in the interstices of chromite and olivine grains and within grains themselves. The data obtained confirm the known tendency toward variation in PGM composition with increasing sulfur and light PGE contents in the residual magmatic melt. The first particles of refractory Ir, Os, and Ru intermetallides appeared at the final stage of olivine crystallization, whereas laurite (Ru,Os,Ir)S2 and pentlandite (Fe,Ni)9S8 were formed at the final stage of chromite crystallization, when the sulfur concentration in the residual melt became sufficient. 相似文献
4.
GUO Guolin YANG Jingsui Paul T. ROBINSON LIU Xiaodong XU Xiangzhen XIONG Fahui 《《地质学报》英文版》2016,90(3):900-912
Voluminous platinum-group mineral(PGM) inclusions including erlichmanite(Os,Ru)S_2, laurite(Ru,Os)S_2, and irarsite(Ir,Os,Ru,Rh)As S, as well as native osmium Os(Ir) and inclusions of base metal sulphides(BMS), including millerite(NiS), heazlewoodite(Ni_3S_2), covellite(CuS) and digenite(Cu_3S_2), accompanied by native iron, have been identified in chromitites of the Zedang ophiolite, Tibet. The PGMs occur as both inclusions in magnesiochromite grains and as small interstitial granules between them; most are less than 10 μm in size and vary in shape from euhedral to anhedral. They occur either as single or composite(biphase or polyphase) grains composed solely of PGM, or PGM associated with silicate grains. Os-, Ir-, and Ru-rich PGMs are the common species and Pt-, Pd-, and Rh-rich varieties have not been identified. Sulfur fugacity and temperature appear to be the main factors that controlled the PGE mineralogy during crystallization of the host chromitite in the upper mantle. If the activity of chalcogenides(such as S, and As) is low, PGE clusters will remain suspended in the silicate melt until they can coalesce to form alloys. Under appropriate conditions of ?S_2 and ?O_2, PGE alloys might react with the melt to form sulfides-sulfarsenides. Thus, we suggest that the Os, Ir and Ru metallic clusters and alloys in the Zedang chromitites crystallized first under high temperature and low ?S_2, followed by crystallization of sulphides of the laurite-erlichmanite, solid-solution series as the magma cooled and ?S_2 increased. The abundance of primary BMS in the chromitites suggests that ?S_2 reached relatively high values during the final stages of magnesiochromite crystallization. The diversity of the PGE minerals, in combination with differences in the petrological characteristics of the magnesiochromites, suggest different degrees of partial melting, perhaps at different depths in the mantle. The estimated parental magma composition suggests formation in a suprasubduction zone environment, perhaps in a forearc. 相似文献
5.
Z. Johan 《Mineralogy and Petrology》2006,87(1-2):1-30
Summary The study of platinum-group minerals (PGM) concentrates from the Nizhni Tagil placers related to the Soloviev Mountain (Gora
Solovieva) Uralian-Alaskan-type intrusion revealed a predominance of (Pt, Fe) alloys over Ir-, and Os-bearing alloys. (Pt,
Fe) alloys (“isoferroplatinum-type”) are interstitial with respect to chromite and show important variations in their chemical
compositions, which are, however, falling within the experimentally determined stability field of isoferroplatinum. Tetraferroplatinum,
enriched in Cu and Ni and tulameenite represent low-temperature mineral phases replacing (Pt, Fe) alloys. Alloys belonging
to the Os–Ir–Ru ternary system have compositions corresponding to native osmium, iridium and ruthenium, respectively, and
to rutheniridosmine. Osmium exsolutions appear in Ir-, and (Pt, Fe) alloys, and iridium exsolutions in (Pt, Fe) alloys. Laurite
is a high-temperature phase included in native iridium and (Pt, Fe) alloys. Low-temperature PGM association comprises Ir-bearing
sulpharsenides, including a phase (Ir, Os, Fe, Pt, Ru, Ni)3(As, Sb)0.85S, and a palladium antimonide Pd20Sb7. These two phases were previously unknown in nature. Furthermore, native palladium occurs in the studied concentrates. This
low-temperature paragenesis indicates an interaction of Pt-, Os-, Ir- and Ru-bearing alloys with late fluids enriched in volatiles,
As and Sb. The chromite composition is characterized by the predominance of Cr3+ → Fe3+ substitution like in other Uralian-Alaskan-type intrusions; that indicates a fO2 variation during the chromite precipitation.
Monomineralic inclusions of euhedral clinopyroxene and chromite crystals in (Pt, Fe) alloys were observed. Furthermore, (Pt,
Fe) alloys contain polyphase silicate inclusions, which occupy the alloy negative crystals. Two types of silicate inclusions
were recognized: (1) Low-pressure inclusions composed of amphibole, biotite, Jd-poor clinopyroxene, magnetite, apatite and
glass; (2) High-pressure inclusions include: omphacitic clinopyroxene (up to 56 mol.% Jd), tremolite, muscovite, apatite,
titanite and glass. In this case, the clinopyroxene is strongly zoned, revealing a pressure drop from about 25 to 5 kbar.
The chemical composition of glass is corundum-normative and its H2O content varies from about 12 to 15 wt.%. The composition of magmatic melts, from which the silicate inclusions have originated
was estimated using EPMA and image analysis interpreted by stereology. Their compositions are close to those obtained experimentally
by hydrous partial melting of upper mantle rocks. The interpretation of analytical data shows that magmatic melts entrapped
by (Pt, Fe) alloys crystallized from about 1100 to 700 °C. The (Pt, Fe) alloys formed after the crystallization of chromite,
clinopyroxene and albite. Consequently, the precipitation temperature of (Pt, Fe) alloys is estimated at about 900 °C. The
significant pressure drop implies a decrease of volatile concentrations in the magmatic melt and the possible formation of
a fluid phase, which might have generated, the precipitation of chromite and PGM. 相似文献
6.
Extremely abundant PGE-minerals(PGM)hosted in chromitites from the Veria ophiolite complex in Macedonia(N.Greece)may be unique among ophiolite complexes.This study focuses on differences between the low-and high-PGE chromitites.New textural,mineralogical and geochemical constraints from those ores are presented,aiming to define factors controlling the PGE enrichment in a supra subduction environment,in the light of postmagmatic processes.The whole ore analyses for mmajor and trace elements indicated an unusually high-IPGE content(up to 25 ppm)and higher Fe,Ca,Mn,Zn and V contents in high-PGE compared to low-PGE in massive chromitites.The wide compositional variation of chromite,even in the same polished section,the occurrence of very fine PGM(less than 20μm)as inclusions within chromite and extremely large(>1000μm),angular or fine-grained PGM aggregates ones within a matrix of highly fragmented chromite-Cr-garnet matrix,may indicate crystallization/recrystallization of chromite from more than one precursor phases.Laurite(RuS2)is very limited,occurring as remnants surrounding by Ru–Os–Ir oxides/hydroxides,of a wide compositional variation.Irarsite occurs as euhedral crystals up to 200μm,surrounding by chromite,as anhedral exsolutions 1–200μm within laurite,or creating segregates with platarsite and relics of(Ru,Pt,Rh,Os)sulfarsenides.Platinum–Ru–Rh–Pd-minerals occur commonly as relatively fine-grained assemblages,up to 50μm,along with irarsite and other relics of(Ru,Pt,Rh,Os)sulfarsenides.Pt-alloys show a variation ranging from tetraferroplatinum to Pt–Ir–Fe–Ni alloys.The presence of laurite relics in large IPGM,awaruite,heazlewoodite,and carbon-bearing material reflecting a super-reducing environment,and the transformation of primary PGM into Os–Ir–Ru-alloys and oxides/hydroxides in association with Fe-chromite and Fe3t-bearing garnet(andradite-uvarovite solidsolution series)may reflect changes of the redox conditions from reducing to oxidizing.The relatively high Na content in hydrous mineral inclusions within high-PGE chromitites suggest a hydrous mantle source and provide the possibility for estimation of the P(average 3.0 kbar)and T(average 874C),indicating formation at a shallow mantle environment. 相似文献
7.
Keiko Hattori Louis J. Cabri Stanley R. Hart 《Contributions to Mineralogy and Petrology》1991,109(1):10-18
Osmium isotope ratios for two types of platinum group mineral (PGM) nuggets of eluvial (residual) origin, associated with the Freetown Layered Gabbro Complex, were determined in-situ using an ion microprobe. The values for erlichmanite nuggets are 1.08. Those for PGM inclusions in Pt–Fe alloy nuggets are higher, ranging from 1.2 to 2.1. Ratios of187Os/186Os vary between the nuggets, but they are consistent within individual nuggest. The data suggest early formation of the erlichmanite nuggets, prior to a postulated substantial contribution of crustal Os. The Pt–Fe alloy nuggets, on the other hand, were formed later in a residual melt which was contaminated by crustal Os due to the assimilation (<10%) or the gaseous/fluid transport of Os from Archaean host rocks into the magma. The lack of systematic mineralogical and chemical changes of the Complex and extensive granulitization in the adjacent host rocks and xenoliths may favor the latter process.The lack of high187Os/186Os ratios, consistent187Os/186Os values within individual nuggets and their textures and mineralogy suggest that the studied PGM nuggets were not formed during lateritization or in low-temperature depositional environments. 相似文献
8.
豆荚状铬铁矿以及其中铂族元素矿物的成因问题——进展与展望 总被引：1，自引：0，他引：1
铂族元素矿物(Platinum Group Mineral:简称PGM)资料的不断积累,丰富了人们对蛇绿岩中豆荚状铬铁矿成因的认识。文章总结近年来有关PGM的新资料和取得的新认识,探讨豆荚状铬铁矿以及其中PGM的成因问题。幔源岩浆结晶过程中,铬铁矿周边熔体减少将诱发那些易氧化的铂族元素(Os、Ir、Ru)在熔体中达到饱和状态,并结晶形成纳米级PGM。在地幔熔体中,随着硫逸度升高,PGM微粒与熔体中的硫反应并逐渐长大。多期次的熔体抽提和熔体-岩石反应事件,可以在地幔源区通过逐步降低硫逸度、促进含铂族元素的贱金属硫化物分解,形成PGM以及铂族元素合金。低硫逸度环境更有利于PGM的形成和保存。在变质环境或流体环境中,这些PGM往往会与流体反应,造就了PGM矿物的多样性。原生PGM与变质流体反应并发生原地去硫化作用,可以形成次生的PGM环边或者纳米级PGM包体。铬铁矿的多阶段蚀变/再平衡过程可以导致PGM溶解—沉淀—均一化,并扰动Os同位素体系。不同类型矿石在有限空间伴生的现象以及它们所具有显著差异的地球化学特征,说明蛇绿岩是不同地幔组分的机械混杂。随着俯冲板片,铬铁矿团块被拖曳到地幔深部,并通过地幔对流重新出现在扩张中心附近,最终混杂在蛇绿岩中。发生循环的铬铁矿团块因此可以与新生铬铁矿及其围岩伴生在同一蛇绿混杂岩中。 相似文献
9.
Mineralogical studies of the heavy fraction from a Holocene pyrope-rich garnet placer deposit at Vestřev (Krkonoše Piedmont Basin, Bohemian Massif) have identified the presence of very rare grains of platinum group minerals (PGM). Pt–Fe alloy grains are accompanied by Os–Ir–Ru minerals (native osmium, iridium, and ruthenium) with inclusions of Pt–Fe alloy and hongshiite (PtCu). This mineral assemblage is typical for several mantle settings including ophiolites. The chemistry of the Os–Ir–Ru minerals shows an enrichment of the PGM in Ru, which is typical of ophiolites. The grain morphology of PGM and pyrope-rich garnet (mostly rounded with numerous euhedral/subhedral grains) does not exclude a common source. In-situ laser-ablation MC-ICP-MS was used to measure the Re–Os isotopic compositions of single Os-rich grains, which show heterogeneous subchondritic Os isotopic compositions (187Os/188Os = 0.12082–0.12505 ± 0.00003). This precludes their low-temperature origin and indicates derivation of platinum-group elements (PGEs) essentially from mantle-derived rocks without a significant contribution of crustal Os. The mantle model age (TMA) and Re-depletion model age (TRD) model ages range from ~ 0.4 to ~ 1.0 Ga and most likely reflect a long history of melt depletion that affected the mantle sources of PGM. 相似文献
10.
İbrahim Uysal Mahmud Tarkian M. Burhan Sadiklar Federica Zaccarini Thomas Meisel Giorgio Garuti Stefanie Heidrich 《Contributions to Mineralogy and Petrology》2009,158(5):659-674
Ultramafic rocks around the city of Muğla in SW Turkey are represented by mantle peridotites depleted to various degrees,
ranging from cpx-rich harzburgites to depleted harzburgite and dunite. Cpx-rich harzburgites are thought to be the residua
left after extraction of MORB-type basalt, from which high-Al chromitite [49.2 < Cr# = 100 × Cr/(Cr + Al) < 53.5] crystallised
with a higher proportion of 187Os/188Os (average of 0.1361). However, depleted harzburgites are assumed to be the residua left after extraction of hydrous boninitic
melt produced by second stage partial melting of already depleted mantle due to a subducting slab, from which high-Cr chromitites
(64.2 < Cr# < 85.9) with lower and heterogeneous 187Os/188Os ratio (average of 0.1324) were crystallised as a result of melt–rock interaction in a supra-subduction environment. Dunites
around the chromite deposits are considered to be the product of melt–peridotite interaction. Most of the chromitites contain
high-Cr chromite and display enrichment in IPGE (Os, Ir, Ru) over PPGE (Rh, Pt, Pd), with PGE concentrations between 61 and
1,305 ppb. Consistently, laurite-erlichmanite series minerals with various Os concentrations are found to be the most abundant
PGM inclusions in chromite. Os–Ir–Ru alloy, irarsite, and kashinite, as well as Pt–Fe alloy and Pt-oxide, which are not common
in ophiolitic chromitites, were also detected as magmatic PGM inclusions. Pentlandite, millerite, and, rarely heazlewoodite
form the magmatic inclusions of base-metal sulphide. The presence of olivine and clinopyroxene, as well as hydrous silicate
inclusions such as amphibole and phlogopite, in high-Cr chromitite supports the idea that high-Cr chromitites were formed
in a supra-subduction environment. 相似文献
11.
Summary Occurrences of platinum-group minerals (PGM) from chromitites of the Great Serpentinite Belt of New South Wales are reported for the first time in this study. On the basis of their major components, these minerals are classified into various groups, including sulphides, sulpharsenides, arsenides, antimonides, amalgams, and alloys of Os-Ir-Ru-(Fe Ni), Pd Cu Sn, Ni-Fe-Pt-Pd, Pd-Pb-Cu, and Rh-Sn-Cu. They are present: (i) as inclusions within chromite, (ii) in interstitial silicates, (iii) in ferritchromite and (iv) along fractures in chromite. Ir-subgroup (Ir, Os, Ru) minerals (IPGM) dominate podiform chromitites hosted by upper mantle serpentinised harzburgite, whereas Pdsubgroup (Pd, Pt, Rh) minerals (PPGM) characterise banded chromitites in cumulates of the overlying magmatic series. A highly brecciated podiform chromitite, however, is distinguished by abundant disseminated PPGM containing Sb ± Cu. Primary magmatic PGM in podiform chromitite comprise IPGM sulphides, sulpharsenides, and alloys, whereas hydrothermal PGM are characterised by PPGM alloys with Hg, Sb, and Cu. Dominantly hydrothermal PGM in the banded chromitites formed by remobilisation of primary magmatic PGM during serpentinisation. The contrast in PGM association is related to the crystallisation of the host chromitites; IPGM crystallised early from the parental magma along with podiform chromitite, but PPGM formed later at lower temperatures during crystallisation of banded chromitite.[
Platingruppen-Minerale in den Chromititen aus dem Great Serpentinite Belt, NSW, Australien
Zusammenfassung In dieser Studie wird zum ersten Mal über das Vorkommen von PlatingruppenMineralen (PGM) in Chromititen der Great Serpentinite Belt berichtet. Die auftretenden Mineralphasen umfassen Sulfide, Sulfarsenide, Arsenide, Antimonide, Amalgam und Legierungen von Os-Ir-(Fe-Ni), Pd-Cu-Sn, Ni-Fe-Pt-Pd, Pd-Pb-Cu and Rh-Sn-Cu. Sie treten als i) Einschlüsse im Chromit, ii) in Silikaten der Grundmasse, iii) Im Ferritchromit und iv) in Frakturen des Chromit auf. Mineralphasen der Ir-Untergruppe (IPGM = Ir, Os, Ru) dominieren in podiformen Chromititen, die in serpentinisierten Harzburgiten des oberen Mantels auftreten. Minerale der Pd-Untergruppe (PPGM = Pd, Pt, Rh) charakterisieren gebänderte Chromitite, die innerhalb der über der Mantelsequenz liegenden Kumulatabfolge vorkommen. Ein deutlich brekzierter podiformer Chromitit unterscheidet sich von den übrigen podiformen Chromititen durch häufiges Auftreten von disseminierten PPGM, die auch Sb ± Cu führen. Primär magmatisch gebildete PGM in podiformen Chromititen umfassen IPGM in Form von Sulfide, Sulfarsenide und Legierungen, während PPGM als Legierungen mit Hg, Sb und Cu hydrothermale Phasen darstellen. Die hydrothermalen PGM in den gebänderten Chromititen wurden überwiegend durch Remobilisation aus primär magmatischen PGM während der Serpentinisierung gebildet. Der markante Unterschied in den während der Serpentinisierung gebildet. Der markante nterschied in den PGM-Assoziationen steht mit der Kristallisation des jeweiligen Chromitit in Verbindung: Während IPGM früh aus dem Magma zusammen mit den podiformen Chromititen kristallisierten, wurden PPGM später unter niedrigeren Temperaturen während der Kristallisation der gebänderten Chromitite gebildet.[相似文献
12.
Genesis of the Jinchuan PGE deposit, China: evidence from fluid inclusions, mineralogy and geochemistry of precious elements 总被引：3，自引：0，他引：3
Summary The Jinchuan deposit is a platinum group element (PGE)-rich sulfide deposit in China. Drilling and surface sampling show that
three categories of platinum group element (PGE) mineralization occur; type I formed at magmatic temperatures, type II occurs
in hydrothermally altered zones of the intrusion, and type III in sheared dunite and lherzolite. All ore types were analyzed
for Os, Ir, Ru, Rh, Pd, Pt and Au, as well as for Cu, Ni, Co and S. Type I ore has (Pt + Pd)/(Os + Ir + Ru + Rh) ratios of
<7 and relatively flat chondrite-normalized noble metal patterns; the platinum group minerals (PGM) are dominated by sperrylite
and moncheite associated with chalcopyrite, pyrrhotite and pentlandite. Type II has (Pt + Pd)/(Os + Ir + Ru + Rh) ratios from
40 to 330 and noble metal distribution patterns with a positive slope; the most common PGM are sperrylite and Pd bismuthotelluride
phases concentrated mostly at the margins of base metal sulfides. Type III ores have the highest (Pt + Pd)/(Os + Ir + Ru +
Rh) ratios from 240 to 710; the most abundant PGM are sperrylite and phases of the Pt–Pd–Te–Bi–As–Cl system. It is concluded
that the Jinchuan deposit formed as a result of primary magmatic crystallization followed by hydrothermal remobilization,
transport, and deposition of the PGE. 相似文献
13.
A. G. Mochalov 《Geology of Ore Deposits》2013,55(3):145-161
A genetic model has been developed for platinum group minerals (PGM) hosted in plutonic gabbro-pyroxenite-dunite (GPD) complexes of the Koryak Highland. The following mineralogical-geochemical and genetic PGM types have been distinguished: (1) magmatic platinum (Pt), (2) magmatic-fluid-metasomatic platinum (Pt) and osmium-platinum (Pt > Os), (3) fluid-metamorphic iridium-platinum (Pt > Ir), and (4) hydrothermal metasomatic platinum-copper (Pt-Cu). PGM of the magmatic Pt type were formed under conditions of monocyclic petrogenesis of Cr-spinel-olivine and olivine-clinopyroxene cumulates as products of picritic magma fractionation in the conduit chamber. The magmatic-fluid-metasomatic platinum Pt and osmium-platinum Pt > Os types were formed by interaction of these early cumulates with magma. The abundance of these types is proportional to injections of picritic magma into the conduit chamber. PGM of the fluid-metamorphic iridium-platinum Pt > Ir type accumulated as a result of synmagmatic recrystallization of GPD cumulates. Their development depends on (1) mono- or polycyclic GPD cumulative complex and (2) the degree of GPD cumulate recrystallization from partial to complete and the degree of transformation of PGM pertaining to the magmatic and magmatic-fluid-metasomatic Pt types. The monocyclic GPD complexes are low-prospective in respect to magmatic Pt deposit formation. The polycyclic GPD complexes differ in their prospectivity from ore occurrences to unique magmatic-fluid-metasomatic Pt and Pt > Os deposits, as well as deposits of the fluid-metamorphic Pt > Ir type. The genetic types of PGM accumulation imply a multifactor system of ore-forming processes with the participation of platinum-group elements (PGE) in GPD complexes. The genetically different PGM accumulations in GPD complexes should be regarded as self-dependent geological objects of local forecasting. In this connection, it is necessary to renew mineralogical and geochemical criteria for prospecting and exploration of PGM genetic types in GPD complexes as well as their mining conditions. 相似文献
14.
Platinum-group Elements and Microstructures of Normal Merensky Reef from Impala Platinum Mines, Bushveld Complex 总被引：11，自引：4，他引：11
The Merensky Reef of the Bushveld Complex contains one of theworld’s largest concentrations of platinum-group elements(PGE). We have investigated ‘normal’ reef, its footwalland its hanging wall at Impala Platinum Mines. The Reef is 46cm thick and consists from bottom to top of leuconorite, anorthosite,chromitite and a very coarse-grained melanorite. The footwallis leuconorite and the hanging wall is melanorite. The onlyhydrous mineral present is biotite, which amounts to 1%, orless, of the rock. All of the rocks contain 0·1–5%interstitial sulphides (pyrrhotite, pentlandite and chalcopyrite),with the Reef rocks containing the most sulphides (1–5%).Lithophile inter-element ratios suggest that the magma fromwhich the rocks formed was a mixture of the two parental magmasof the Bushveld Complex (a high-Mg basaltic andesite and a tholeiiticbasalt). The Reef rocks have low incompatible element contentsindicating that they contain 10% or less melt fraction. Nickel,Cu, Se, Ag, Au and the PGE show good correlations with S inthe silicate rocks, suggesting control of the abundance of thesemetals by sulphides. The concentration of the chalcophile elementsand PGE in the silicate rocks may be modelled by assuming thatthe rocks contain sulphide liquid formed in equilibrium withthe evolving silicate magma. It is, however, difficult to modelthe Os, Ir, Ru, Rh and Pt concentrations in the chromititesby sulphide liquid collection alone, as the rocks contain 3–4times more Os, Ir, Ru, Rh and Pt than the sulphide-collectionmodel would predict. Two possible solutions to this are: (1)platinum-group minerals (PGM) crystallize from the sulphideliquid in the chromitites; (2) PGM crystallize directly fromthe silicate magma. To model the concentrations of Os, Ir, Ru,Rh and Pt in the chromitites it is necessary to postulate thatin addition to the 1% sulphides in the chromitites there isa small quantity (0·005%) of cumulus PGM (laurite, cooperiteand malanite) present. Sulphide liquids do crystallize PGM atlow fS2. Possibly the sulphide liquid that was trapped betweenthe chromite grains lost some Fe and S by reaction with thechromite and this provoked the crystallization of PGM from thesulphide liquid. Alternatively, the PGM could have crystallizeddirectly from the silicate magma when it became saturated inchromite. A weakness of this model is that at present the exactmechanism of how and why the magma becomes saturated in PGMand chromite synchronously is not understood. A third modelfor the concentration of PGE in the Reef is that the PGE arecollected from the underlying cumulus pile by Cl-rich hydrousfluids and concentrated in the Reef at a reaction front. Althoughthere is ample evidence of compaction and intercumulus meltmigration in the Impala rocks, we do not think that the PGEwere introduced into the Reef from below, because the rocksunderlying the Reef are not depleted in PGE, whereas those overlyingthe Reef are depleted. This distribution pattern is inconsistentwith a model that requires introduction of PGE by intercumulusfluid percolation from below. KEY WORDS: Merensky Reef; platinum-group elements; chalcophile elements; microstructures 相似文献
15.
The contents of the platinum-group elements (PGEs: Os, Ir, Ru, Rh, Pt, Pd) in the Abulangdang ultramafic intrusion have been
determined using ICP-MS after nickel sulfide fire assay preconcentration. Different samples show significant differences in
absolute PGE abundance. They display a pronounced negative incline in mantle-normalized patterns which are characterized by
strong enrichment in IPGEs (Os, Ir, Ru) and depleting to slight enrichment in PPGEs (Rh, Pt, Pd). The characteristics of PGE
distribution in the Abulangdang rocks are due to the combined action of sulfide and non-sulfide (spinel/chromite or alloy
or micro-granular aggregation of metals). In comparison with the mafic-ultramafic rocks which host Ni-Cu-PGE deposits in the
Emeishan Large Igneous Province (ELIP), it is assumed that the Abulangdang ultramafic intrusion may be the product of early-stage
magma activity in the ELIP. 相似文献
16.
Prof. Dr. M. Tarkian E. Naidenova Prof. Dr. M. Zhelyaskova-Panayotova 《Mineralogy and Petrology》1991,44(1-2):73-87
Summary The podiform chromitites investigated in the course of this study occur in intensely serpentinized dunites and peridotites of unknown age (paleozoic or older) within a metamorphic complex consisting of gneisses, amphibolites and marbles. Concentrations of platinum group elements (PGE) and the distribution of platinum group minerals (PGM) have been investigated in the chromitite occurrences of Dobromirci and Pletene.PGE concentrations in chromitites vary from 787 to 891 ppb (Dobromirci). The highest value was recorded in chromite ore from Pletene (1274 ppb). The enrichment is due to high contents of Os, Ir and Ru, whereas the contents of Rh, Pt and Pd are relatively low. The Ru-contents (480-600 ppb) are remarkable and correspond to the average content in chondrite Cl. Chondrite-normalized PGE distribution patterns of chromitites of both localities reveal a distinctly negative trend from Ru to Pd, which is typical for chromites from ophiolites.Irrespective of their chemical composition, most chromites carry numerous PGM inclusions which have formed during the magmatic stage at high sulphur fugacity (fs2). In addition to laurite, the main mineral, there are sulpharsenides of Ru-Ir-Os (ruarsite, irarsite, osarsite).Textural aspects and the results of chemical analyses show that the concentration of PGE is not caused by substitution in the lattice of chromite, but by magmatic formation of discrete PGM before or contemporaneously with chromite. All PGM apparently remained unaltered. No evidence for remobilization or redistribution of PGE by serpentinization has been found.
With 7 Figures 相似文献
Minerale der Platinggruppe in Chromititen des Ultramafit-Komplexes des Ost-Rhodopen Massivs, Bulgarien
Zusammenfassung Die untersuchten podiformen Chromite tretey in stark serpentinisierten Duniten und Peridotiten unbekannten Alters (paläozoisch oder älter) innerhalb eines hochmetamorphen Komplexes auf, der aus Gneisen, Amphiboliten und Marmoren besteht. In den Chromitit-Vorkommen von Dobromirci und Pletene wurden Konzentrationen der Elemente der Platingruppe (PGE) und die Verteilung der Minerale der Platingruppe (PGM) untersucht.Die PGE-Konzentration der Chromitite variiert zwischen 787 und 891 ppb (Dobromirci). Die höchste Konzentration wurde im Chromiterz aus Pletene (1274 ppb) gefunden. Die Anreicherung geht auf hohe Beteiligung von Os, Ir und Ru zurück, da die Gehalte an Rh, Pt und Pd relativ niedrig sind. Auffallend hoch sind die Ru-Gehalte (480-600 ppb), die dem mittleren Gehalt im Chondrit Cl entsprechen. Chondritnormalisierte PGE-Verteilungsmuster von Chromititen beider Lokalitäten zeigen einen stark negativen Trend von Ru zu Pd, der für Ophiolith-Chromite typisch ist.Unabhängig von ihrem Chemismus führen die meisten Chromite zahlreiche PGME-Einschlüsse, die sich magmatisch bei hoher Schwefelfugazität (fS2) gebildet haben. Neben dem Hauptmineral Laurit, wurden Sulfarsenide von Ru-Ir-Os (Ruarsit, Irarsit, Osarsit) festgestellt.Texturelle Merkmale der PGM und Ergebnisse der chemischen Analysen führen zu der Schlußfolgerung, daß die Konzentration der PGE nicht auf eine Substitution in Chromit, sondern auf die Frühbildung der selbständigen PGM vor oder gleichzeitig mit den Chromiten zurückzuführen ist. Die PGM zeigen keine Alterationserscheinungen. Es wurden keine Hinweise für eine Remobilisation oder Umsetzung der PGE durch Serpentinisierung gefunden.
With 7 Figures 相似文献
17.
A.V. Kutyrev E.G. Sidorov A.V. Antonov V.M. Chubarov 《Russian Geology and Geophysics》2018,59(8):935-944
In the alluvial deposits of the Prizhlimny Creek (southern part of the Koryak Highland), grains of platinum-group minerals are found along with gold. We have established that the grains are native platinum (Pt, Fe) containing Cu (up to 5 wt.%), Os (up to 8 wt.%), and Rh (up to 2 wt.%). Inclusions in the platinum are native osmium (the content of Ir impurity reaches 12 wt.%, the average content being 0.2–4 wt.%), an unnamed intermetallic compound of composition PtRh, sulfides and arsenides of PGE (cooperite, laurite, malanite, cuproiridsite, cuprorhodsite, sperrylite, hollingworthite, unnamed compounds PdS, (Ir,Ru)S2, (Ir,Pt)S2, Cu, and Fe (bornite, chalcopyrite), chromite, and Cr-magnetite. Replacement of native-osmium crystals by compound IrO2 is described. It has been established that this compound formed during oxidation accompanied by the replacement of isoferroplatinum by native platinum. The data obtained agree with the results of study of platinum-group mineral assemblages from placers localized in weakly eroded Ural–Alaskan-type massifs whose apical parts formed under high oxygen activity conditions. Clinopyroxenites of the Prizhimny massif are considered to be the potential source of PGE. 相似文献
18.
It is of great importance to understand the origin of UG2 chromitite reefs and reasons why some chromitite reefs contain relatively high contents of platinum group elements(PGEs: Os, Ir, Ru, Rh,Pt, Pd) or highly siderophile elements(HSEs: Au, Re, PGE). This paper documents sulphide-silicate assemblages enclosed in chromite grains from the UG2 chromitite. These are formed as a result of crystallisation of sulphide and silicate melts that are trapped during chromite crystallisation. The inclusions display negative crystal shapes ranging from several micrometres to 100 μm in size.Interstitial sulphide assemblages lack pyrrhotite and consist of chalcopyrite, pentlandite and some pyrite. The electron microprobe data of these sulphides show that the pentlandite grains present in some of the sulphide inclusions have a significantly higher iron(Fe) and lower nickel(Ni) content than the pentlandite in the rock matrix. Pyrite and chalcopyrite show no difference. The contrast in composition between inter-cumulus plagioclase(An_(68)) and plagioclase enclosed in chromite(An_(13)), as well as the presence of quartz, is consistent with the existence of a felsic melt at the time of chromite saturation.Detailed studies of HSE distribution in the sulphides and chromite were conducted by LA-ICP-MS(laser ablation-inductively coupled plasma-mass spectrometry), which showed the following.(Ⅰ) Chromite contained no detectable HSE in solid solution.(Ⅱ) HSE distribution in sulphide assemblages interstitial to chromite was variable. In general, Pd, Rh, Ru and Ir occurred dominantly in pentlandite, whereas Os,Pt and Au were detected only in matrix sulphide grains and were clearly associated with Bi and Te.(Ⅲ)In the sulphide inclusions,(a) pyrrhotite did not contain any significant amount of HSE,(b) chalcopyrite contained only some Rh compared to the other sulphides,(c) pentlandite was the main host for Pd,(d)pyrite contained most of the Ru, Os, Ir and Re,(e) Pt and Rh were closely associated with Bi forming a continuous rim between pyrite and pentlandite and(f) no Au was detected. These results show that the use of ArF excimer laser to produce high-resolution trace element maps provides information that cannot be obtained by conventional(spot) LA-ICP-MS analysis or trace element maps that use relatively large beam diameters. 相似文献
19.
Lynnette Pitcher Rosalind T. Helz Richard J. Walker Philip Piccoli 《Chemical Geology》2009,260(3-4):196-210
Kilauea Iki lava lake formed during the 1959 summit eruption of Kilauea Volcano, then crystallized and differentiated over a period of 35 years. It offers an opportunity to evaluate the fractionation behavior of trace elements in a uniquely well-documented basaltic system. A suite of 14 core samples recovered from 1967 to 1981 has been analyzed for 5 platinum-group elements (PGE: Ir, Os, Ru, Pt, Pd), plus Re. These samples have MgO ranging from 2.4 to 26.9 wt.%, with temperatures prior to quench ranging from 1140 °C to ambient (110 °C). Five eruption samples were also analyzed.Osmium and Ru concentrations vary by nearly four orders of magnitude (0.0006–1.40 ppb for Os and 0.0006–2.01 ppb for Ru) and are positively correlated with MgO content. These elements behaved compatibly during crystallization, mostly likely being concentrated in trace phases (alloy or sulfide) present in olivine phenocrysts or included chromite. Iridium also correlates positively with MgO, although less strongly than Os and Ru. The somewhat poorer correlation for Ir, compared with Os and Ru, may reflect variable loss of Ir as volatile IrF6 in some of the most magnesian samples.Rhenium is negatively correlated with MgO, behaving as an incompatible trace element. Its behavior in the lava lake is complicated by apparent volatile loss of Re, as suggested by a decrease in Re concentration with time of quenching for lake samples vs. eruption samples. Platinum and Pd concentrations are negatively, albeit weakly, correlated with MgO, so these elements were modestly incompatible during crystallization of the major silicate phases. Palladium contents peaked before precipitation of immiscible sulfide liquid, however, and decline sharply in the most differentiated samples. In contrast, Pt appears to have been unaffected by sulfide precipitation. Microprobe data confirm that Pd entered the sulfide liquid before Re, and that Pt is not strongly chalcophile in this system. Occasional high Pt values in both eruption and lava lake samples suggest the presence of unevenly distributed, unidentified Pt-rich trace phases in some Kilauea Iki materials.Estimated mineral (olivine + chromite)/melt D values for Os, Ir, Ru and Pt for equilibrium crystallization for samples from ~ 7 to 27 wt.% MgO are 26, 8.2, 19 and 0.55, respectively. These Os, Ir and Ru estimates are somewhat higher than previous estimates for similar systems. If fractional crystallization is instead assumed, D values are much more similar.Results confirm many prior observations in other mafic systems that olivine (together with included phases) has a major effect on absolute and relative abundances of Re and the PGE. The relatively linear correlations between these elements and MgO potentially permit accurate estimation of the concentrations of these elements in the primary melts of comparable systems, especially in instances where the MgO content of the primary melt is well constrained. 相似文献
20.
In order to constrain the highly siderophile elements (HSE: Re and platinum group elements (PGE: Os, Ir, Ru, Pt and Pd)) host mineral(s) in refractory, base metal sulfide-free mantle residues, four very depleted spinel-harzburgites from the Lherz massif (France) have been analyzed for HSE in whole-rock and in major mineral separates (olivine, orthopyroxene, clinopyroxene and spinel) by isotope dilution. In addition, HSE host minerals have been separated and analyzed with a scanning electron microscope. Olivine and spinel show the highest HSE concentration especially for Os, Ir, Ru and Pt (up to 10 ppb) among the modally-major minerals, while the pyroxenes are 1-2 orders of magnitude poorer in HSE. The major minerals account for less than 30% of the whole-rock platinum group element budget. On the other hand, rare, micron to submicron platinum group minerals (PGM), such as Ru-Os ± Ir sulfides and Pt-Ir ± Os alloys, likely located in the intergranular spaces of the refractory depleted harzburgite, account for 50-100% of the HSE budget. The PGM grains are interpreted to be residual, having formed in response to the complete consumption of the base-metal sulfides by the high degree of partial melting (i.e. 23-24%) experienced by these samples. As they sequester the compatible platinum group elements (Os, Ir, Ru and Pt) in the mantle residue, these PGM provide key constraints for the modelling of PGE contents in terrestrial basalts (e.g. the solid/liquid partition coefficients needed to account for the compatible behavior of these elements in the mantle residue) and for understanding the long-lived Os isotope heterogeneities of the upper mantle, especially the old Re-Os ages found in young oceanic mantle. In fact, because of their Os-rich compositions and high melting temperatures, these microphases are likely to preserve their initial Os isotopic compositions unmodified over multiple events of mantle melting and mixing, and therefore generate, through recycling, heterogeneous Os isotopic signatures at different scales in the convecting mantle. 相似文献