Platinum-group Minerals Research Articles

Trace precious metals in major sulfide minerals from the Federova Tundra platinum group element deposit in the Fedorova-Pana layered intrusion, central Kola Peninsula, Russia

ABSTRACTDrill-core samples from the basal Cu-Ni-platinum-group element mineralization of the Early Proterozoic Fedorova Tundra intrusion in the Fedorova-Pana layered intrusion, central Kola Peninsula, Russia, were studied in two separate projects in Canada and Russia. In Canada, trace precious metal analyses by laser ablation inductively coupled mass spectrometry of 323 base metal sulfide particles [pentlandite (101), pyrrhotite (98), chalcopyrite (25), and pyrite (99)] show that Pd is highly concentrated in pentlandite. Most of the analyses (71%) were done using two master composite samples of comminuted drill core representative of the West Pit and East Pit mineralization, FWMC and FEMC, respectively. Fewer analyses were made of three other comminuted drill core samples from the West Pit referred to as “lithology” samples: OLFW (olivine-bearing rocks), ANFW (leucocratic rocks), and GNFW (gabbronorite). In Russia, 120 polished sections sliced from drill core from the West and East Pits and from four other Fedorova Tundra intrusion deposits (Kievey, Northern Kamennik, Eastern Chuarvy, and Southern Kievey) were studied mineralogically. Platinum group mineral characterization and trace Pd electron probe microanalyses of pentlandite were done using polished sections from all six locations (n = 95). The trace electron probe microanalysis data for Pd in pentlandite from the West (n = 35) and East (n = 19) Pit samples, though at much higher detection levels, are considered to be comparable to the laser ablation inductively coupled mass spectrometry data. The Eastern Chuarvy samples show particularly high Pd concentrations averaging 0.49 wt.% Pd (n = 11) and as high as 1.64 wt.% Pd. The combined data from these studies guides our estimate that pentlandite accounts for 30 to 50% of the Pd in these ores and that Rh solid solution in sulfides may account for >98% of the total Rh.

Atypical Mineralization Involving Pd-Pt, Au-Ag, REE, Y, Zr, Th, U, and Cl-F in the Oktyabrsky Deposit, Norilsk Complex, Russia

Highly atypical mineralization involving Pd-Pt, Au-Ag, REE, Y, Zr, U, Th, and Cl-F-enriched minerals is found in zones with base metal sulfides (BMS; ~5 vol.% to 20 vol.%) in the eastern portion of the Oktyabrsky deposit in the Norilsk complex (Russia). The overall variations in Mg# index, 100 Mg/(Mg + Fe2+ + Mn), in host-rock minerals are 79.8 → 74.1 in olivine, 77.7 → 65.3 in orthopyroxene, 79.9 → 9.2 in clinopyroxene, and An79.0 → An3.7. The span of clinopyroxene and plagioclase compositions reflects their protracted crystallization from early magmatic to late interstitial associations. The magnesian chromite (Mg# 43.9) trends towards Cr-bearing magnetite with progressive buildups in oxygen fugacity; ilmenite varies from early Mg-rich to late Mn-rich variants. The main BMS are chalcopyrite, pyrrhotite, troilite, and Co-bearing pentlandite, with less abundant cubanite (or isocubanite), rare bornite, Co-bearing pyrite, Cd-bearing sphalerite (or wurtzite), altaite, members of the galena-clausthalite series and nickeline. A full series of Au-Ag alloy compositions is found with minor hessite, acanthite and argentopentlandite. The uncommon assemblage includes monazite-(Ce), thorite-coffinite, thorianite, uraninite, zirconolite, baddeleyite, zircon, bastnäsite-(La), and an unnamed metamict Y-dominant zirconolite-related mineral. About 20 species of PGM (platinum group minerals) were analyzed, including Pd-Pt tellurides, bismuthotellurides, bismuthides and stannides, Pd antimonides and plumbides, a Pd-Ag telluride, a Pt arsenide, a Pd-Ni arsenide, and unnamed Pd stannide-arsenide, Pd germanide-arsenide and Pt-Cu arseno-oxysulfide. The atypical assemblages are associated with Cl-rich annite with up to 7.54 wt.% Cl, Cl-rich hastingsite with up 4.06 wt.% Cl, ferro-hornblende (2.53 wt.% Cl), chlorapatite (>6 wt.% Cl) and extensive solid solutions of chlorapatite, fluorapatite and hydroxylapatite, Cl-bearing members of the chlorite group (chamosite; up to 0.96 wt.% Cl), and a Cl-bearing serpentine (up to 0.79 wt.% Cl). A decoupling of Cl and F in the geochemically evolved system is evident. The complex assemblages formed late from Cl-enriched fluids under subsolidus conditions of crystallization following extensive magmatic differentiation in the ore-bearing sequences.

Open System Re-Os Isotope Behavior in Platinum-Group Minerals during Laterization?

In this short communication, we present preliminary data on the Re-Os isotopic systematics of platinum-group minerals (PGM) recovered from different horizons in the Falcondo Ni-laterite in the Dominican Republic. The results show differences in the Os-isotope composition in different populations of PGM: (i) pre-lateritic PGM yield 187Os/188Os varying from 0.11973 ± 0.00134 to 0.12215 ± 0.00005 (2σ uncertainty) whereas (ii) lateritic PGM are more radiogenic in terms of 187Os/188Os (from 0.12390 ± 0.00001 to 0.12645 ± 0.00005; 2σ uncertainty). We suggest that these differences reflect the opening of the Re-Os system in individual grains of PGM during lateritic weathering. The implications of these results are twofold as they will help to (1) elucidate the small-scale mobility of noble metals in the supergene setting and therefore the possible formation of PGM at these very low temperatures, (2) better refine the Os-isotopic datasets of PGM that are currently being used for defining dynamic models of core–mantle separation, crustal generation, and fundamental plate-tectonic processes such as the opening of oceans.

Ore mineralogy of podiform-type chromite deposit in Tedubara area and its vicinity, Kabaena Island, Indonesia

Kabaena Island is one of the areas in Southeast Sulawesi that has the potential for chromite deposits. This paper is aimed to provide information on the mineralogical aspects of chromitite from the research area. Back-scattered electron (BSE) imaging and chemical analysis of chromite were performed using an electron microprobe. Chromite deposits in the study area are of podiform-type. Chromite is massive and brecciated. Based on the content of Cr # = Cr/(Cr + Fe3+) of the chromite, comprised between 0.61 and 0.74, the studied chromitite can be classified as Cr-rich. The only PGM (Platinum Group Minerals) found in several chromitite samples is laurite (RuS2). PGM occurs enclosed in chromite crystals and in the contact with microfractures of chromite crystals.

Metallogenic fingerprint of a metasomatized lithospheric mantle feeding gold endowment in the western Mediterranean basin

AbstractSpinel peridotite xenoliths (one plagioclase-bearing) hosted in alkaline basalts from Tallante (southeast Spain) record the mineralogical and geochemical fingerprint of the subcontinental lithospheric mantle (SCLM) evolution beneath the southern Iberian margin. Mantle metasomatism in fertile lherzolites caused the crystallization of clinopyroxene + orthopyroxene + spinel clusters through the percolation of Miocene subalkaline melts during the westward migration of the subduction front in the western Mediterranean. In the Pliocene, heat and volatiles provided by alkaline host-magmas triggered very low melting degrees of metasomatic pyroxene-spinel assemblages, producing melt quenched to silicate glass and reactive spongy coronae around clinopyroxene and spinel. Refertilization of the Tallante peridotites induced the precipitation of base-metal sulfides (BMS) included in metasomatic clino- and orthopyroxene. These sulfides consist of pentlandite ± chalcopyrite ± bornite aggregates with homogeneous composition in terms of major elements (Ni, Fe, Cu) and semi-metals (Se, As, Te, Sb, Bi), but with wide variability of platinum-group elements (PGE) fractionation (0.14 < PdN/IrN < 30.74). Heterogeneous PGE signatures, as well as the presence of euhedral Pt-Pd-Sn-rich platinum-group minerals (PGM) and/or Au-particles within BMS, cannot be explained by conventional models of chalcophile partitioning from sulfide melt. Alternatively, we suggest that they reflect the incorporation of distinct populations of BMS, PGM, and metal nanoparticles (especially of Pt, Pd, and Au) during mantle melting and/or melt percolation. Therefore, we conclude that Miocene subalkaline melts released by asthenosphere upwelling upon slab tearing of the Iberian continental margin effectively stored metals in metasomatized domains of this sector of the SCLM. Remarkably high Au concentrations in Tallante BMS (median 1.78 ppm) support that these metasomatized domains provided a fertile source of metals, especially gold, for the ore-productive Miocene magmatism of the westernmost Mediterranean.

Decoupling the effects of alteration on the mineralogy and flotation performance of Great Dyke PGE ores

Ores from a single deposit may exhibit extensive variability in their mineralogy and texture. The ability to quantify this variability and link it to mineral processing performance is one of the primary goals of process mineralogy. This study focuses on the effect of alteration in three platinum group element ore samples from the Great Dyke in Zimbabwe - two of which were more pristine compared to the third, which was locally classified as 'oxidized' ore. These ores are known to be characterized by varying degrees of alteration, resulting in numerous challenges in flotation and affecting both grade and recovery. Alteration, by near-surface oxidation, of the valuable base metal sulphides and platinum group minerals resulted in lower flotation recoveries of Cu, Ni, Pt, and Pd. Evidence of incipient oxidation was more readily observed in the base metal sulphide assemblage than the platinum group mineral assemblage, even though the loss in recovery (because of oxidation) was most significant for Pd. Alteration through hydration resulted in a significant increase in mass pull and dilution of concentrate grade through the inadvertent recovery of naturally floating gangue comprising composite orthopyroxene and talc particles. In this study, the amount of naturally floating gangue was more strongly correlated with the talc grain size distribution than the grade of talc in the flotation feed. The oxidation and hydration alteration reactions are not necessarily mutually exclusive, although one may be more dominant than the other, giving rise to ore variability.

The Troia–Pedra Branca mafic–ultramafic complex, Borborema Province, Brazil: Record of 2.04 Ga post–collisional Alaskan–type magmatism and PGE mineralization

The Troia–Pedra Branca complex is the most extensive exposure of mafic–ultramafic rocks in the Borborema Province, northeastern Brazil. These rocks have been known for a long time, particularly because of their platinum group element (PGE) mineralization associated with chromitites. The Troia–Pedra Branca complex consists of a succession of serpentinites (after dunite), metachromitites, metaperidotites, hornblendites and metagabbros. PGE–bearing metachromitites are hosted by the serpentinite–peridotite unit, occurring as dispersed blocks, well preserved from weathering. However, host metadunites are poorly preserved, and are only accessed by drill core samples. Scanning Electron Microscopy (SEM) analysis in thin sections of selected metachromitite samples revealed that most of the platinum group minerals (PGM) occur in the chlorite–serpentine matrix, generally in contact with chromite grains. The main PGM are sperrylite (PtAs2), cooperite (PtS), irarsite ((Ir,Pt,Rh)AsS) and hollingworthite ((Rh,Pd,Pt,Ru)AsS). Within chromite grains, very few PGM were found, and sulfide inclusions are mainly chalcopyrite (CuFeS2), pentlandite ((Fe,Ni)9S8) and bornite (Cu5FeS4). Whole–rock geochemical data reveal that metagabbros are LILE–enriched and show subduction–related signature similar to that of Alaskan–type intrusions. Mineral chemistry of chromite and olivine is also compatible with arc–related Alaskan–type complexes. The U–Pb SHRIMP zircon age for a metachromitite sample yielded an upper intercept age of 2036 ± 27 Ma, which we interpret as the crystallization age. However, dispersion in the data implies that zircons lost variable amounts of radiogenic Pb at around 749 ± 54 Ma (lower intercept), which may be related to Neoproterozoic metamorphism. The age obtained for the Troia–Pedra Branca metachromitites (2036 Ma) is younger than the 2190–2130 Ma arc–related plutons of the area, and it is closely related in age to the 2.10–2.04 Ga syn– to late–collisional plutonism and high–temperature metamorphism. Therefore, this Alaskan–type mafic–ultramafic magmatism may be related to the post–collisional setting of the 2.2–2.0 Ga Eburnean/Transamazonian orogeny.

The distribution of platinum-group elements and Te, As, Bi, Sb and Se (TABS+) in the Paraná Magmatic Province: Effects of crystal fractionation, sulfide segregation and magma degassing

The concentrations of Te, As, Bi, Sb and Se (TABS+) in magmas from large igneous provinces (LIPs) are of interest because these elements are important in the formation of platinum-group minerals (PGM) found in magmatic NiCu platinum-group element (PGE) deposits. Furthermore, the TABS+ are volatile and hence they may be lost in degassing and have a role to play in the mass extinctions associated with LIPs events because these are mostly toxic elements. However, the concentrations of TABS+ in magmas from LIPs are not well documented due in part to the analytical difficulties and in part to the numerous processes that affect their distribution. We have determined the concentration of TABS+ and PGE in rocks from the Paraná Magmatic Province (PMP) in order to assess the effects of fractional crystallization, sulfide segregation and magma degassing. Decrease in the Rh, Ru and Ir concentrations with Mg and Cr indicate that these elements behaved as compatible elements during crystal fractionation. Based on changes in the Cu/Pd sulfide saturation occurred in some cases resulting into a decrease in Pd and Pt. Arsenic and Sb behave as incompatible elements, whereas Se, Te and Bi show variable behaviour. Most lavas from the PMP display negative As, Se and Te anomalies on mantle-normalized patters coupled with Te/Cu, Se/Cu and As/Th and Sb/Th ratios lower than mantle values, which we attribute to loss of the TABS+ during degassing.

Placer mineral deposits of Russian Arctic zone: Genetic prerequisites of formation and prospect of development of mineral resources

Placer deposits are an accumulation of valuable minerals both dense and resistant to weathering processes, formed by gravity separation during sedimentary processes. Placer deposits of the Russian Arctic zone (RAZ) include gold, platinum group minerals (PGM), tin, diamonds, rare metals, zircon-titanium mineral deposits and a specific type of related to placer deposits - fossil ivory. There are an insufficient number of scientific geological articles on placer deposits of RAZ in the English-language literature at present, especially of an overview nature. This review paper attempts to fill the gap and marshal on the regional scale all available data aiming to provide a framework for generating and testing new ideas on the placer deposits of RAZ. The focus is on main factors and conditions of generation of the placer deposits of industrial importance, details of key placer deposits, and perspectives of development of placer mineral resources in the region. Localization and scales of placer deposits are controlled by metallogenic, tectonic, climatic and geomorphological factors which have regional and local characters. The metallogenic factor specifies the primary sources of the placer minerals, especially for proximal (retained and partly transient) placers that have moderate transportation. Tectonics have a dual role: on the regional level it determines rate of the erosion and disintegration of the host rocks due to weathering process; while on the local level, tectonic dislocation forms structural traps of placer deposits. Climatic factor is determinative for the character of supergene processes: warm humid conditions (especially combined with stable tectonics) result in deep chemical weathering and disintegration of the host rocks containing primary mineralization which is favorable for the placer forming process; in frozen (periglacial) climate conditions, mechanical weathering processes are prevalent. Geomorphological factors are closely connected with the dynamic state of the placer forming area, from the source location to the final sedimentary accumulations. Industrial placer deposits are formed when an optimal ratio of the main factors of placer forming processes occurs. A special type of anthropogenic (technogenic) placers are formed as result of human mining activities.It is impossible to distinguish only one or two of the main universal factors which are responsible for the formation of placer deposits, as all types of placers will have one or more of these. However, the formation of placers of economic importance are always the result of an optimal combination of the metallogenic, tectonic, climatic and geomorphological factors, and the absence of even one of these may result in placers of weak or non-economic ore concentrations.As evidenced by the extensive historical mining of placer deposits and the presence of undeveloped inferred placer mineral resources, the Arctic region is a large polymineral and polygenic megaprovince with considerable placer potential.

Ni-Cu sulfide mineralization and PGM from the Samapleu mafic-ultramafic intrusion, Yacouba complex, western Ivory Coast

ABSTRACT The mafic-ultramafic Samapleu deposits of the Yacouba complex, which host nickel, copper sulfides, and platinum-group minerals, are located in the Biankouma-Silipou region, western Ivory Coast. These intrusions originate from the mantle and would have been established during the Proterozoic (2.09 Ga) around 22 km deep within the Archean granulites (3.6–2.7 Ga) which at least partially contaminated them. Platinum-group and sulfide minerals from the Samapleu deposits were studied using optical microscopy, scanning electron microscopy, the electronic microprobe, X-ray fluorescence, fire assay, and a Thermo Fisher Scientific Delta S isotope ratio mass spectrometer system. The sulfide mineralization (mainly pyrrhotite, pentlandite, chalcopyrite ± pyrite) is mainly disseminated with, in places, semi-massive to massive sulfide veins. It is especially abundant in pyroxenite horizons with net or breccia textures. The isotopic ratios of sulfur measured from the sulfides (an average of 0.1‰), the R factor (between 1500 and 10,000), and the Cu/Pd ratios indicate a mantle source. Thus, the sulfides would have formed from sulfide liquids produced by immiscibility from the silicate mantle magma under mafic-ultramafic intrusion emplacement conditions and with possible geochemical modification of the magmas by assimilation of the surrounding continental crust. The platinum-group minerals (michenerite, merenskyite, moncheite, Co-rich gersdorffite, irarsite, and hollingworthite) are mainly associated with the sulfide phases. The nature of the platinum-group minerals is indicative of the probable role of late-magmatic hydrothermal fluids during the mineralizing process.

Platinum and gold placer from Tugidak Island, Alaska: Platinum-group minerals and their inclusions, gold, and chromite mineralogy

ABSTRACT Black sand beach placers from Kodiak, Sitkinak, and Tugidak Islands, Alaska, have been mined intermittently for gold and minor platinum-group alloys for more than 100 years. High-grade platinum-rich magnetic separate and accompanying black sand from the southern beach placer of Tugidak Island were studied using electron microprobe WDS and scanning electron microscope EDS; mineral classification and identification were based on these techniques. The major platinum mineral is isoferroplatinum, followed by minor tetraferroplatinum and tulameenite, and rare ferronickelplatinum. Two types of alteration were identified in about 3–4% of the alloy grains: rim formation involving Pt loss and increased Fe, Ni, and/or Cu, and fracturing and vein filling by Cu-rich alloy. Ruthenium-Ir-Os-Pt alloys occur as inclusions and veins as well as form part of composite grains. Ten percent of the alloy grains contain a large variety of platinum-group minerals (PGM). Inclusions of cuprorhodsite, malanite, cuproiridsite, laurite, erlichmanite, cooperite, braggite, bowieite, kashinite, miassite, hollingworthite, irarsite, sperrylite, stillwaterite, genkinite, stibiopalladinite, keithconnite, zvyagintsevite, and probable palladodymite and vincentite were identified. Two unidentified inclusion phases also occur. Most of the PGM inclusions are primary and were trapped by a growing crystal from a melt; some inclusions exhibit textures that suggest trapping of an As,Te,S-rich immiscible melt. Secondary inclusions and evidence of deformation were observed in a few alloy grains. Associated with PGM inclusions or as separate inclusions are various base-metal sulfides. Two silicate-melt inclusions in one isoferroplatinum grain have an andesite–shoshonite composition. Minor gold and Ag-rich gold in the high-grade magnetic separate contain magnetite, pyrrhotite, and chromite inclusions. The gold composition suggests that their sources are the numerous quartz veins and apophyses related to granitoids on Kodiak Island. The composition of the placer chromite is similar to chromite from the Border Ranges mélange fault system and suggests that the Uyak Complex ultramafic and mafic rocks are part of a supra-subduction-zone ophiolite and are the source of the platinum-group minerals.

PLATINUM METAL MINERALIZATION OF THE SOUTH URALS MAGMATIC COMPLEXES: GEOLOGICAL AND GEODYNAMIC CHARACTERISTICS OF FORMATIONS, PROBLEMS OF THEIR GENESIS, AND PROSPECTS

In the South Urals, we have identified and investigated two platinum-bearing formations – ophiolite chromitebearing complexes, and the Khudolaz differentiated mafic-ultramafic complex with sulfide Cu-Ni mineralization. The ophiolite chromite-bearing complexes include fragments of the upper mantle and lower crust of the Paleouralian Ocean, which were induced by collision onto the edge of the East European platform. The origin of the Khudolaz complex is related a mantle plume activity. Here, we review and compare the main features of platinum-metal mineralization (PMM) in these two formations.The article presents the results of mineralogical and geochemical studies of PMM associated with chromite and sulfide Cu-Ni ores. In association with chromitites, two types of PMM are distinguished: (1) predominating refractory platinoids in chromitites of the mantle unit of the section, and (2) predominating platinum and palladium in chromitites of the transitional wehrlite-clinopyroxenite complex. Compositions of platinum group minerals (PGM) and relations between their elements and host minerals suggest that the minerals of the ophiolite chromite-bearing complexes are of a restite origin, while the Khudolaz complex results from a combination of magmatic processes and solid-phase redistribution of material. Palladium (michenerite, froodite, merenskyite, borovskite, sudburyite) and platinum (sperrylite, moncheite) minerals are found in magmatic sulfide ores of the Khudolaz complex, which were subjected to hydrothermal metasomatization. Texture observations using electron microscope and optical (reflected light) images, as well as LA ICP MS analyses of sulfides suggest late- and post-magmatic crystallization of PMM in three phases: (1) immiscible metalloid or highly fractionated residual sulfide melts trapped in sulfides; (2) segregation of isomorphic impurities of platinum group elements (PGE) and chalcogenide elements from sulfide solid solutions; and (3) interaction of hydrothermal fluids with soluble sulfides.Prospective for PMM are extended bodies of disseminated chromitites in marginal dunites of the Kraka and Nurali massifs, and wehrlite-clinopyroxenite complexes of the same massifs containing PGE (above 500 ppb). In the Khudolaz complex, promising PMM bodies are low-metasomatized parts of sulfide ore bodies (1 ppm of ΣPGE and above) located in the largest massifs, Severny Buskun and Zapadny Karasaz. Exocontact zones of these intrusions are also promising for PMM.

Mineralogical and isotopic peculiarities of high-Cr chromitites: Implications for a mantle convection genesis of the Bulqiza ophiolite

Submicroscopic to micro-diamonds, silicates, wüstite, platinum group minerals (PGM), sulfides and ultra-high pressure (UHP) mineral inclusions have been recovered from podiform and banded chromitites of the Bulqiza ophiolite in Albania. The alignment of acicular silicate inclusions with crystallographic planes of magnesiochromite suggests an exsolution origin. Positive and negative-crystal faces of cubic silicate inclusions are consistent withs a high-temperature paragenesis.Micro-inclusions and nanoparticles (<500 nm) of RuOs bisulfides (laurite; RuS2), OsIr, and Os-Ir-Ru alloys, tolovike, irarsite, IrNi sulfides, and millerite (NiS) are also common in the Bulqiza chromitites. Dispersed spherical, nano-inclusions of IrPt and OsIr may reflect formation of the IrPt and OsIr particles by sulfide liquid immiscibility. The high Cr# of the chromitites, their evolved whole-rock PGE abundances, and IPGE/PPGE ratios (≥ 10) suggest extensive partial melting, likely in a supra-subduction zone (SSZ) environment. This interpretation is supported by the variable 187Re/188Os (0.0103–0.0271) and 187Os/188Os (0.12600–0.13014) ratios and the low γOs isotope values (mean + 0.01) of the chromitites, reflecting derivation from heterogeneously depleted mantle materials. The presence of remarkably zoned zircons with UPb ages (164–3354 Ma) represents the addition of crustal materials.Discrete micro-diamonds, PGM, and sulfide inclusions point to a super-reducing (SuR), ultra-high pressure (UHP) origin. We propose a genetic model that involves incorporation of crustal and UHP phases into the mantle by convection or subduction. The UHP and crustal silicates are consistent with a subduction-related origin, but the presence of super-reduced (SuR) inclusions suggests equilibration under subduction-disparate mantle conditions.

Platinum group elements in lamprophyre, picrobasalt, gabbro and basalts of the Phenai Mata and nearby areas: implications for Fe–Ni–Cu–PGE mineralization in the Deccan Large Igneous Province

Abstract Among the basaltic large igneous provinces (LIPs) world over, the Deccan Large Igneous Province (DLIP) is considered barren of metalliferous sulfide deposits, and especially platinum group minerals (PGMs). The tholeiitic basaltic magmas of the DLIP were found to lack sulfur saturation at all stages of its evolution. However, we found some incidences of Fe–Ni–platinum group element (PGE) mineralization in the cumulate gabbros of the Phenai Mata Igneous Complex (PMIC), as well as intrusive dykes of lamprophyre, picrobasalt and basalt in adjoining areas. To examine the metal potential of the gabbros, we adopted the following approach: (a) whole-rock PGE analysis of selected rocks; (b) preconcentration of the samples by communition, sieving and gravity-magnetic separation, followed by froth floatation, Ni-sulfide fire assay and geochemical analysis of the concentrates; and (c) direct scanning of samples using an electron probe microanalyser (EPMA). The geochemical proxies – namely, Pd/Ir, Cu/Ir, Ni/Pd and Ni/Cu – indicate that PMIC has distinct geochemical signatures compared to other parts of the DLIP. The results have further indicated an interesting suite of minerals comprising metal sulfides of Fe–Cu–Zn–Pb–Co–Ni. This metal-rich suite in the otherwise ‘barren’ Deccan Trap tholeiites is a result of accidental fertilization of metals into their sulfides due to the mixing of crustal sulfur.

Chromitites from the Vavdos ophiolite (Chalkidiki, Greece): Petrogenesis and geotectonic settings; constrains from spinel, olivine composition, PGE mineralogy and geochemistry

Podiform chromitites of the Vavdos ophiolite are associated with dunite bodies hosted within residual mantle harzburgite. The mantle source is highly depleted and apparently developed at fore-arc settings as inferred from the presence of boninitic melts. The ascendance of these melts through dunite pathways and their subsequent interaction with the depleted harzburgite instigated chromitite mineralization within dunite. Spinel occurs in a) massive accumulations (Mg# = 0.56–0.68 and Cr# = 0.69–0.77), b) in non-massive disseminated textures (Mg# = 0.52–0.61 and Cr# = 0.80–0.81) and c) in schlieren chromitite deposits within dunite bodies (Mg# = 0.43–0.48 and Cr# = 0.79–0.82). Olivine is the main silicate inclusion in chromitites, whereas the absence of hydrous mineral phases is linked with crystallization at relatively deeper parts of the mantle.Olivine inclusions in spinel are enriched in Fo, Ni and Ca compared to the interstitial olivine grains. No compositional gaps were noted between the mineral analyses of chromitites and dunites; the calculated parental melts are also homogeneous, reinforcing the view for production of melt batches by similar processes. Platinum-group elements (PGE) concentrations and platinum-group minerals (PGM) demonstrate high (Os + Ir + Ru)/ (Rh + Pt + Pd) ratios, typical of many Tethyan ophiolitic chromitites. The main PGM phase is laurite that forms an extended solid solution series with substitution of Ru for Os + Ir, linked to the cooling of the system. Massive chromitites contain Ru-rich laurite and Os-Ir alloys whereas non-massive ores contain Ru-poor laurite. The PGM were included in fresh magnesiochromite favoring their magmatic origin and initial entrapment at ~ 1200 °C and low sulfur fugacity.

Tamuraite, Ir5Fe10S16, a New Species of Platinum-Group Mineral from the Sisim Placer Zone, Eastern Sayans, Russia

Tamuraite, ideally Ir5Fe10S16, occurs as discrete phases (≤20 μm) in composite inclusions hosted by grains of osmium (≤0.5 mm across) rich in Ir, in association with other platinum-group minerals in the River Ko deposit of the Sisim Placer Zone, southern Krasnoyarskiy Kray, Russia. In droplet-like inclusions, tamuraite is typically intergrown with Rh-rich pentlandite and Ir-bearing members of the laurite–erlichmanite series (up to ~20 mol.% “IrS2”). Tamuraite is gray to brownish gray in reflected light. It is opaque, with a metallic luster. Its bireflectance is very weak to absent. It is nonpleochroic to slightly pleochroic (grayish to light brown tints). It appears to be very weakly anisotropic. The calculated density is 6.30 g·cm−3. The results of six WDS analyses are Ir 29.30 (27.75–30.68), Rh 9.57 (8.46–10.71), Pt 1.85 (1.43–2.10), Ru 0.05 (0.02–0.07), Os 0.06 (0.03–0.13), Fe 13.09 (12.38–13.74), Ni 12.18 (11.78–13.12), Cu 6.30 (6.06–6.56), Co 0.06 (0.04–0.07), S 27.23 (26.14–27.89), for a total of 99.69 wt %. This composition corresponds to (Ir2.87Rh1.75Pt0.18Ru0.01Os0.01)Σ4.82(Fe4.41Ni3.90Cu1.87Co0.02)Σ10.20S15.98, calculated based on a total of 31 atoms per formula unit. The general formula is (Ir,Rh)5(Fe,Ni,Cu)10S16. Results of synchrotron micro-Laue diffraction studies indicate that tamuraite is trigonal. Its probable space group is R3m (#166), and the unit-cell parameters are a = 7.073(1) Å, c = 34.277(8) Å, V = 1485(1) Å3, and Z = 3. The c:a ratio is 4.8462. The strongest eight peaks in the X-ray diffraction pattern [d in Å(hkl)(I)] are: 3.0106(216)(100), 1.7699(420)(71), 1.7583(2016)(65), 2.7994(205)(56), 2.9963(1010)(50), 5.7740(102)(45), 3.0534(201)(43) and 2.4948(208)(38). The crystal structure is derivative of pentlandite and related to that of oberthürite and torryweiserite. Tamuraite crystallized from a residual melt enriched in S, Fe, Ni, Cu, and Rh; these elements were incompatible in the Os–Ir alloy that nucleated in lode zones of chromitites in the Lysanskiy layered complex, Eastern Sayans, Russia. The name honors Nobumichi Tamura, senior scientist at the Advanced Light Source of the Lawrence Berkeley National Laboratory, Berkeley, California.

Challenges Related to the Processing of Fines in the Recovery of Platinum Group Minerals (PGMs)

In order to increase the recovery of PGMs by flotation, it is necessary to optimise the liberation of the key minerals in which the platinum group elements (PGEs) are contained which include sulphides, arsenides, tellurides, and ferroalloys among others, while at the same time ensuring the optimal depression of gangue minerals. In order to achieve this, comminution circuits usually consist of two or three stages of milling, in which the first stage is autogeneous, followed by ball milling. Further liberation is achieved in subsequent stages using ultra-fine grinding. Each comminution stage is followed by flotation in the so-called MF2 or MF3 circuits. While this staged process increases overall recoveries, overgrinding may occur, hence creating problems associated with fine particle flotation. This paper presents an overview of the mineralogy of most of the more significant PGM ores processed in South Africa and the various technologies used in comminution circuits. The paper then summarises the methodology used in flotation circuits to optimise recovery of fine particles in terms of the collectors, depressants, and frothers used. The effect of entrainment, slimes coating, changes in rheology caused by the presence of a significant amount of fines and of chromite recovery is addressed.

Characteristics and implications of podiform-chromite hosted silicate inclusions in the Zedang ophiolite, Southern Tibet

The Zedang ophiolite, containing pods of massive chromitite, crops out in the eastern segment of the Yarlung-Zangbo suture zone, Southern Tibet. Chromite grains in the Zedang chromitite bodies have high Cr# [Cr/(Cr + Al)] (0.73–0.82) and Mg# [Mg/(Mg + Fe)] (0.73–0.79), and low TiO2 content (0.13–0.25 wt%); they contain diopside (Di) exsolution lamellae and abundant inclusions of diopside, enstatite, hydrous silicates (e.q., Cr-bearing amphibole), and serpentine. The inclusions occur as isolated single-phase or multiphase (clinopyroxene + amphibole ± platinum group mineral) grains. Diopside lamellae-bearing chromite was probably a precursor CaFe2O4-phase (CF phase) forming at >12.5 GPa. Individual octahedral serpentine inclusions are likely pseudomorphs after isometric ringwoodite. Both the CF phase and ringwoodite crystallized within the mantle transition zone (MTZ). Equilibrium pressure-temperature (P-T) conditions of coexisting clinopyroxene-orthopyroxene (Cpx-Opx) inclusions are 8.5–21.5 ± 1.5 kbar, and 996–1097 ± 30 °C. These P-T conditions suggest that the inferred parental melts of the Zedang chromitites were boninitic. The boninitic liquid in turn was generated from depleted, metasomatized mantle in a supra-subduction zone (SSZ) environment. Linear alignment of hydrous silicate inclusions in chromitites imply fluid infiltration along fracture zones at shallow depths during consolidation of the ophiolite. Based on our new data, we propose a new three-stage model to explain the formation and evolution of the Zedang chromitites. It experienced a long journey from (i) the MTZ forming high-P chromite (containing ultrahigh-pressure minerals), (ii) to the upper mantle attending to the formation of the major part of the chromite, whereas it's host chromitites formed at melt-rock reaction process, and (iii) where high-P chromite was incorporated in low-P neoblastic chromite during subducting slab rollback-induced channel return flow to shallow depths (involving fluid input and alteration).

The Application of a Nitrile-based Collector in the Flotation of a Platreef PGM Ore

ABSTRACT Declining ore grades, coupled with the increasing mineralogical complexity of ores, have forced the platinum group mineral (PGM) industry to search for collectors that outperform the conventional options. One such potential alternative is Nouryon’s Tecflote™ family of nitrile-based collectors for sulfide flotation; whilst notable success has been reported in the copper industry, the potential value of these in the PGM industry has not yet been evaluated. This study employed batch rougher flotation tests coupled with mineralogical analysis of tailings samples to investigate the application of Tecflote S11 as a partial or complete replacement of thiol collectors in the flotation of a PGM bearing Platreef ore. Tecflote S11 as sole collector and in combination with different thiol collectors were investigated. At low dosages of 80 g/t, the Tecflote and PAX as single collectors achieved similar 3E (Pt, Pd and Au), Ni, and Fe recoveries, with Tecflote proving to be the more powerful Cu collector. At higher dosages of 160 g/t, PAX outperformed Tecflote in terms of 3E, Cu, Ni and Fe recoveries. A 50:50 mass% combination of the Tecflote with either DTP, DTC or PAX showed improved recoveries without a loss in 3E grade. The Tecflote-PAX combination achieved the highest 3E, Cu and Ni recoveries. Under these conditions, fully liberated PGMs and those associated with liberated base metal sulfides (BMS) were recovered. Overall, the study demonstrated that the Tecflote requires the backing of a strong thiol-based collector to achieve an improved flotation response for the Platreef ore.

Characterizing the behaviour of platinum group minerals in a grinding circuit

This paper introduces a methodology to determine the gravity-recoverable platinum group minerals (GRPGMs) of a stream, and behaviour of platinum group minerals (PGMs) in a ball mill-cyclone circuit. The GRPGM is determined by a modification of the method developed for gravity-recoverable gold (GRG). Mineral behaviour in the circuit employs element and GRPGM cyclone partition curves and cumulative element selection functions. The methodology is illustrated on the grinding circuit at Vale’s Clarabelle mill (Sudbury, Canada). As an example, GRPGM for platinum (Pt) in the ball mill-cyclone circulating load was about 80%. The cumulative selection functions of Pt and palladium (Pd) were ca. 1.3 times higher than the solids for size fractions above 212 μm, which moderated their buildup in the closed circuit, but were ca. 60% that of the solids below 212 μm which contributed to buildup of these sizes. The partition curves showed more than 90% of the Pt and Pd above ca 50 μm reported to the cyclone underflow. The buildup of PGMs in the circulating load and the high GRPGM offers an opportunity for gravity recovery.