共查询到20条相似文献，搜索用时 31 毫秒
1.
The Ni-Co-Cu ores of Pevkos and Lakxia tou Mavrou, Limassol Forest, Cyprus, have been investigated microscopically and by electron microprobe analysis. At Pevkos, the mineral association consists of pyrrhotite, pentlandite, maucherite, chalcopyrite, cubanite, magnetite, chromite and valleriite with minor amounts of westerveldite, bornite, neodigenite, covellite and cobaltite. The mineralization at Lakxia tou Mavrou comprises pyrrhotite, pentlandite, löllingite, chalcopyrite, cubanite and chromite with traces of magnetite, pyrite, maucherite and valleriite. Paragenetic, compositional and textural features suggest a nonmagmatic origin for the sulfides and arsenides; they were deposited during serpentinization of the ultramafic host rocks. A conceptual model for mineralization linked to decreasing temperatures in a hydrothermal system is presented. 相似文献
2.
Ore mineralization and wall rock alteration of Crater Mountain gold deposit, Papua New Guinea, were investigated using ore and host rock samples from drill holes for ore and alteration mineralogical study. The host rocks of the deposit are quartz‐feldspar porphyry, feldspar‐hornblende porphyry, andesitic volcanics and pyroclastics, and basaltic‐andesitic tuff. The main ore minerals are pyrite, sphalerite, galena, chalcopyrite and moderate amounts of tetrahedrite, tennantite, pyrrhotite, bornite and enargite. Small amounts of enargite, tetradymite, altaite, heyrovskyite, bismuthinite, bornite, idaite, cubanite, native gold, CuPbS2, an unidentified Bi‐Te‐S mineral and argentopyrite occur as inclusions mainly in pyrite veins and grains. Native gold occurs significantly in the As‐rich pyrite veins in volcanic units, and coexists with Bi‐Te‐S mineral species and rarely with chalcopyrite and cubanite relics. Four mineralization stages were recognized based on the observations of ore textures. Stage I is characterized by quartz‐sericite‐calcite alteration with trace pyrite and chalcopyrite in the monomict diatreme breccias; Stage II is defined by the crystallization of pyrite and by weak quartz‐chlorite‐sericite‐calcite alteration; Stage III is a major ore formation episode where sulfides deposited as disseminated grains and veins that host native gold, and is divided into three sub‐stages; Stage IV is characterized by predominant carbonitization. Gold mineralization occurred in the sub‐stages 2 and 3 in Stage III. The fS2 is considered to have decreased from ～10?2 to 10?14 atm with decreasing temperature of fluid. 相似文献
3.
Calculation of sulfur isotope fractionation in sulfides 总被引：3，自引：0，他引：3
The increment method has been successfully applied to calculate thermodynamic isotope fractionation factors of oxygen in silicates, oxides, carbonates, and sulfates. In this paper, we modified the increment method to calculate thermodynamic isotope fractionation factors of sulfur in sulfides, based on chemical features of sulfur-metal bonds and crystal features of sulfide minerals. To approximate the bond strength of sulfides, a new constant, known as the Madelung constant, was introduced. The increment method was then extended to calculate the reduced partition function ratios of sphalerite, chalcopyrite, galena, pyrrhotite, greenockite, bornite, cubanite, sulvanite, and violarite, as well as the isotope fractionation factors between them over the temperature range from 0 to 1000 °C. The order of 34S enrichment in these nine minerals is pyrrhotite > greenockite > sphalerite > chalcopyrite > cubanite > sulvanite > bornite > violarite > galena. Our improved method constitutes another model for calculating the thermodynamic isotope fractionation factors of sulfur in sulfides of geochemical interest. 相似文献
4.
5.
In the Ospin–Kitoi ultramafic massif of the Eastern Sayan, accessory and ore Cr-spinel are mainly represented by alumochromite and chromite. Copper–nickel mineralization hosted in serpentinized ultramafic rocks occurs as separate grains of pentlandite and pyrrhotite, as well as assemblages of (i) hexagonal pyrrhotite + pentlandite + chalcopyrite and (ii) monoclinal pyrrhotite + pentlandite + chalcopyrite. Copper mineralization in rodingite is presented by bornite, chalcopyrite, and covellite. Talc–breunnerite–quartz and muscovite–breunnerite–quartz listvenite contains abundant sulfide and sulfoarsenide mineralization: pyrite, gersdorffite, sphalerite, Ag–Bi and Bi-galena, millerite, and kuestelite. Noble metal mineralization is represented by Ru–Ir–Os alloy, sulfides, and sulfoarsenides of these metals, Au–Cu–Ag alloys in chromitite, laurite intergrowth, an unnamed mineral with a composition of Cu3Pt, orcelite in carbonized serpentinite, and sperrylite and electrum in serpentinite. Sulfide mineralization formed at the late magmatic stage of the origination of intrusion and due to fluid–metamorphic and retrograde metasomatism of primary rocks. 相似文献
6.
《International Geology Review》2012,54(9):1377-1381
Reactions between sulfides of heavy metals and solutions of hexavalent uranium sulfate at pH about 2, in the range of 200-360°C, led to replacement of pyrrhotite by marcasite-pyrite aggregate, development of bornite and pyrite after chalcopyrite, growth of regenerated chalcopyrite on the periphery of uranium oxides, replacement of chalcopyrite by bornite (with the accompanying complications, fig. 3), redepositions of chalcocite and native copper, and, in experiments with pyrite-galena and galena-marmatite pairs, redepositions of the minerals with the corresponding growth of pyrite. —V.P. Sokoloff. 相似文献
7.
The mattes resulting from lead smelting have been studied in order to determine the distribution of heavy metals and metalloids in primary phases. The chemical analysis (EPMA) revealed the presence of various metals (Pb, Sb, Cu), sulphides (galena, wurtzite, pyrrhotite, bornite, digenite, cubanite), arsenides (koutekite, löllingite) and other complex intermetallic compounds. Extreme saturation of the initial matte melt in heavy metals and metalloids as well as a relatively rapid cooling regime are responsible for numerous elemental substitutions in the crystal structures of all the involved phases. To cite this article: V. Ettler, Z. Johan, C. R. Geoscience 335 (2003). 相似文献
8.
Studies of Metallic and Trace Minerals of the Tiegelongnan Cu‐Au Deposit,Central Tibet,China 总被引：1，自引：0，他引：1
Electron probe micro-analysis(EPMA) and scanning electron microscopy(SEM) equipped with energy dispersive spectrometry(EDS) have been used to investigate the principal ore minerals and coexisting metallic mineral inclusions in polished thin sections from the Tiegelongnan deposit, which consists of a high-sulfidation epithermal system(HSES) and a porphyry system(PS). Molybdenite,chalcopyrite, bornite, tennantite, enargite, digenite, anilite, covellite, and tetrahedrite have been identified by EPMA. Intergrowth, cross-cutting and replacement relationships between the metallic minerals suggest that molybdenite formed first(stage 1),followed by chalcopyrite ± bornite ± hematite(stage 2),then bornite ± Cu-sulfides ± Cu-Fe-sulfoarsenides(stage 3),and lastly Cu-Fe-sulfoarsenides ±Cu-sulfides(stage 4). Pyrite is developed throughout all the stages. Droplet-like inclusions of Au-Te minerals commonly occur in tennantite but not in the other major sulfides(molybdenite, chalcopyrite and bornite),implying that tennantite is the most important Au telluride carrier. The pervasive binary equilibrium phases of calaverite and altaite constrain f_(Te2) in the range from ～-6.5 to ～-8 and f_(S2)-11.The intergrowth of bornite and chalcopyrite and the conversion from bornite to digenite suggest fluctuated and relatively low precipitation temperature conditions in the HSES relative to the PS.Contrastingly, the dominance of chalcopyrite in the PS, with minor bornite, suggests relatively high temperature conditions. These new results are important for further understanding the mineral formation processes superimposed by HSES and PS systems. 相似文献
9.
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
10.
The mineralogy of the Istala deposit, Gümüşhane, northeastern Turkey, was studied in detail, and a geochemical investigation was carried out using electron probe micro-analysis (EPMA). Sphalerite, galena, chalcopyrite and pyrite are the major sulfide minerals found in the Istala deposit, with minor amounts of bornite, idaite, tetrahedrite–tennantite, anilite, yarrowite, mckinstryite, covellite and chalcocite. In addition to these, barite and a small quantity of quartz occur as gangue minerals. Based on the textural relations and mineral assemblages, five different stages of crystallization have been recognized. Mineral paragenesis of the first four stages has been found to be similar, whereas clear enrichment has been observed in the modal abundance of the copper sulfide mineral assemblage at the fifth-stage ore formation. Whole-rock geochemical analyses of the Istala ore show an enrichment of Ag content up to 3328 ppm. Optical observations and EPMA study indicated that abundant silver mineralization was found in the Istala ore, especially during the later-stage ore deposition. Repetition to the presence of native silver in the samples, a significant amount of silver was incorporated in bornite, idaite, tetrahedrite–tennantite, anilite, yarrowite, mckinstryite, covellite and chalcocite, whereas a trace amount of silver has been detected in sphalerite, galena, chalcopyrite and pyrite. The homogenization temperatures (Th) of the primary fluid inclusions were measured between 98 and 284 °C, with frequency peaks around 140 °C, 190 °C and 240 °C. All data obtained support the theory that later stage copper-rich sulfides, formed under the low temperature conditions, are responsible for the large amounts of silver content in the Istala mine. 相似文献
11.
Ibrahim M. Shalaby Eugen Stumpfl Hassan M. Helmy Mahmoud M. El Mahallawi Omar A. Kamel 《Mineralium Deposita》2004,39(5-6):608-621
The Um Samiuki Zn–Cu–Pb–Ag mineralisation, south Eastern Desert, Egypt is hosted by felsic volcanic rocks which form part of the 712-Ma-old, east-west-trending Shadli Volcanic Belt. Two major occurrences of massive sulphides are present at the top of rhyolitic breccia in the Western and Eastern mine areas. In each occurrence, a bornite-bearing zone is overlain by a pyrite-chalcopyrite-bearing zone and underlain by a disseminated, Cu-depleted zone. In the massive sulphide ore, sphalerite, chalcopyrite, pyrite, galena, bornite and tetrahedrite–tennantite are major minerals, whereas arsenopyrite, pyrrhotite, molybdenite and magnetite are accessory phases. Covellite and digenite are common secondary minerals. Bornite, tetrahedrite–tennantite and covellite contain high amounts of silver (averages of 1.97, 1.39 and 1.82 wt% respectively). Based on mineralogical balance calculations, bornite and covellite accommodate 80% of silver in the Um Samiuki deposit. Ag was incorporated in the crystal structure of the early-crystallised copper sulphides and sulphosalts and silver minerals. The temperature, sequential precipitation of the fluids and the structure of the crystallising phases control the distribution of silver. Post-depositional deformation and metamorphic processes caused liberation, remobilisation and redeposition of silver within the massive sulphides.Editorial handling: D. Lentz 相似文献
12.
Metal L2,3, sulfur K and oxygen K near-edge X-ray absorption fine structure (NEXAFS) spectra for chalcopyrite, bornite, chalcocite, covellite, pyrrhotite and pyrite have been determined from single-piece natural mineral specimens in order to assess claims that chalcopyrite should be regarded as CuIIFeIIS2 rather than CuIFeIIIS2, and that copper oxide species are the principal initial oxidation products on chalcopyrite and bornite exposed to air. Spectra were obtained using both fluorescence and electron yields to obtain information representative of the bulk as well as the surface. Where appropriate, NEXAFS spectra have been interpreted by comparison with the densities of unfilled states and simulated spectra derived from ab initio calculations using primarily the FEFF8 code and to a lesser extent WIEN2k. Metal 2p and S 2p photoelectron spectra excited by monochromatised Al Kα X-rays were determined for each of the surfaces characterised by NEXAFS spectroscopy. The X-ray excited Cu LMM Auger spectrum was also determined for each copper-containing sulfide. FEFF8 calculations were able to simulate the experimental NEXAFS spectra quite well in most cases. For covellite and chalcocite, it was found that FEFF8 did not provide a good simulation of the Cu L3-edge spectra, but WIEN2k simulations were in close agreement with the experimental spectra. Largely on the basis of these simulations, it was concluded that there was no convincing evidence for chalcopyrite to be represented as CuIIFeIIS2, and no strong argument for some of the Cu in either bornite or covellite to be regarded as Cu(II). The ab initio calculations for chalcopyrite and bornite indicated that the density of Cu d-states immediately above the Fermi level was sufficient to account for the Cu L3-edge absorption spectrum, however these incompletely filled Cu d-states should not be interpreted as indicating some Cu(II) in the sulfide structure. It was also concluded that the X-ray absorption spectra were quite consistent with the initial oxidation products on chalcopyrite and bornite surfaces being iron oxide species, and inconsistent with the concomitant formation of copper-oxygen species. 相似文献
13.
Primary Ore Mineral Assemblage and Fluid Inclusion Study of the Batu Hijau Porphyry Cu-Au Deposit, Sumbawa, Indonesia 总被引：3，自引：0，他引：3
Abstract. The Batu Hijau porphyry Cu‐Au deposit, Sumbawa Island, Indonesia, is associated with a tonalitic intrusive complex. The temperature‐pressure condition of mineralization at the Batu Hijau deposit is discussed on the basis of fluid inclusion microthermometry. Then, the initial Cu‐Fe sulfide mineral assemblage is discussed. Bornite and chalcopyrite are major copper ore minerals associated with quartz veinlets. The quartz veinlets have been classified into ‘A’ veinlets associated with bornite, digenite, chalcocite and chalcopyrite, ‘B’ veinlets having chalcopyrite bornite along vuggy center‐line, rare ‘C’ chalcopyrite‐quartz veinlets, and late ‘D’ veinlets consisting of massive pyrite and quartz (Clode et al., 1999). Copper and gold mineralization is associated with abundant ‘A’ quartz veinlets. Abundant fluid inclusions are found in veinlet quartz consisting mainly of gas‐rich inclusions and polyphase inclusions throughout the veinlet types. The hydrothermal activity occurred in temperature‐pressure conditions of aqueous fluid immiscibility into hypersaline brine and dilute vapor. The halite dissolution (Tm[halite]) and liquid‐vapor homogenization (Th) temperatures of the polyphase inclusions in veinlet quartz range from 270 to 472d?C and from 280 to 454d?C, respectively. The estimated salinity ranges from 36 to 47 wt% (NaCl equiv.). The apparent pressures lower than 300 bars are estimated to have been along the liquid‐vapor‐halite curve for the fluid inclusions having the Th lower than the Tm that trapped the brine saturated with halite, or at slightly higher pressure relative to liquid‐vapor‐halite curve for the fluid inclusions having the Th higher than the Tm that trapped the brine unsaturated with halite. The actual temperature and pressure during the hydrothermal activity at the Batu Hijau deposit are estimated to have been around 300d?C and 50 bars. At such temperature‐pressure conditions, the principal and initial Cu‐Fe sulfide mineral assemblages are thought to be chalcopyrite + bornite solid solution (bnss) for the chalcopyrite‐bearing assemblage, and chalcocite‐digenite solid solution and bnss for the chalcopyrite‐free assemblage. 相似文献
14.
Abstract: Ore specimens collected by the late Professor Takeo Watanabe from the Hol Kol and the Tul Mi Chung deposits, Suan mining district, Korean peninsula, were examined. In addition, measurements of sulfur isotopic ratio of ores and preliminary fluid inclusion microthermometry were carried out. Ores from the New orebody of the Hol Kol deposit consist mainly of bornite, wittichenite and chalcopyrite presently, which exhibit lamellae intergrowth texture, associated with native bismuth and electrum. Bismuthian bornite solid solution is considered to be a principal initial phases, while native bismuth was nucleated as molten bismuth melt initially. The occurrence of cubanite, miharaite, carrollite, siegenite, hessite and geikielite are recognized from the New orebody. Ores from the Eastern orebody of the Hol Kol deposit consist chiefly of chalcopyrite, occasionally associated with trace amounts of pyrrhotite, pyrite, bismuthinite and rare tellurobismuthite, while an ore specimen from the Western orebody consists mainly of sphalerite associated with chalcopyrite, pyrite and galena. Ores from the Tul Mi Chung deposit consist mainly of chalcopyrite and pyrite, occasionally associated with magnetite, sphalerite, galena and rare molybdenite. Some portions of magnetite are revealed to be silician magnetite. Sulfur fugacity is supposed to be below the stability field of bismuthinite in the New orebody. A reducing condition is suggested by the occurrence of geikielite without Fe3+ content. The sulfur and oxygen fugacities for the Eastern and Western orebodies of the Hol Kol deposit and for the Tul Mi Chung deposit were higher than the New orebody of the Hol Kol deposit. On the other hand, the Suan granite (porphyritic granodiorite) and the Chil Sing Dai granite (biotite granite porphyry) from the Hol Kol area can be classified as weakly magnetic magnetite‐series. Polyphase fluid inclusions are observed in gangue diopside associated with Cu ore of two specimens. The dissolution temperatures of daughter crystals are 394±26°C and 442±45°C, while the disappearing temperatures of vapor bubble were 475±25°C and > 500°C. Highly saline fluids were responsible for the mineralization at the Hol Kol deposit. The δ34S values of ore sulfides of the Hol Kol and the Tul Mi Chung deposit range from +11. 5% to +16. 1%, having anomalous lower values mainly from the Tul Mi Chung deposit. Such anomalous lower 634S values can be caused by isotopic fractionation against oxidized sulfur species. The δ34S value of bulk sulfur in the ore solutions responsible for the Hol Kol and the Tul Mi Chung deposit is estimated to be +13.5±2.5‰. 相似文献
15.
Ö. Amcoff 《Mineralium Deposita》1988,23(4):286-292
Chalcopyrite was reacted with covellite and with chalcocite, respectively, between 200°C and 500°C. The ensuing solid-state replacement of chalcopyrite by bornite was studied both texturally and chemically. The relatively oxidizing conditions of the reaction chalcopyrite+covellite result in massive replacement, lacking structural control, where bornite and pyrite form complex intergrowth textures in chalcopyrite. Bornite nucleates around growing pyrite aggregates because of the release of copper and a decrease in volume. Diffusion of sulphur along grain boundaries and fractures largely controls the textural development. Reaction under the relatively reducing conditions involving chalcopyrite+chalcocite results in replacement of chalcopyrite in the sequence where chalcopyrite is replaced by bornite, below about 355°C, and by intermediate solid solution (ISS) and later bornite, above 355°C. The textural development, changing from replacement, apparently uninfluenced by directional properties in the host, to semioriented replacement, is structurally controlled. This suggests that the process is governed by diffusion of copper and iron through a sulphur framework. It is suggested that the observed formation of oriented bornite lamellae in chalcopyrite and in ISS during the chalcopyrite+chalcocite reaction may be explained by replacement exsolution at constant temperature. 相似文献
16.
Abstract. A detail investigation of ore and gangue minerals was performed on the Doyashiki Kuroko deposits, Hokuroku basin, Japan for the first time. Main ore minerals are sphalerite, galena, pyrite, chalcopyrite, tetrahedrite-tennantite and digen-ite. Small amounts of enargite, wittichenite, electrum, covellite, bornite, marcasite and hematite are also observed. Quartz, barite and gypsum are common gangue minerals. Homogenization temperatures and salinities of fluid inclusions in quartz, sphalerite and barite range from 190 to 240C and 3.0 to 5.5 wt% NaCl equivalent, respectively. The FeS contents of sphalerite and Ag contents of electrum were 0.12 to 0.18 mol %, 39.0 to 39.6 atom %, respectively. The chemical composition of digenite as a primary mineral shows high sulfur contents.
These data indicate that ore fluid responsible for digenite and associated ore minerals was characterized by a range of high sulfur fugacity with a moderate formation temperature. This is concordant with the mineral assemblage of bornite-pyrite and chalcopyrite, which shows high sulfur fugacity conditions. It seems that the mineralization closely associated with acidic volcanism has occurred around 13 Ma of Middle Miocene on the seafloor at the depth of about 1500 m. 相似文献
These data indicate that ore fluid responsible for digenite and associated ore minerals was characterized by a range of high sulfur fugacity with a moderate formation temperature. This is concordant with the mineral assemblage of bornite-pyrite and chalcopyrite, which shows high sulfur fugacity conditions. It seems that the mineralization closely associated with acidic volcanism has occurred around 13 Ma of Middle Miocene on the seafloor at the depth of about 1500 m. 相似文献
17.
Tolga Oyman 《Ore Geology Reviews》2010,37(3-4):175-201
The Ayazmant Fe–Cu skarn deposit is located approximately 20 km SE of Ayval?k or 140 km N of Izmir in western Turkey. The skarn occurs at the contact between metapelites and the metabasites of the Early Triassic K?n?k Formation and the porphyritic hypabyssal intrusive rocks of the Late Oligocene Kozak Intrusive Complex. The major, trace, and rare earth-element geochemical analysis of the igneous rocks indicate that they are I-type, subalkaline, calc-alkaline, metaluminous, I-type products of a high-level magma chamber, generated in a continental arc setting. The 40Ar–39Ar isochron age obtained from biotite of hornfels is 20.3 ± 0.1 Ma, probably reflecting the age of metamorphic–bimetasomatic alteration which commenced shortly after intrusion into impure carbonates. Three stages of skarn formation and ore development are recognized: (1) Early skarn stage (Stage I) consisting mainly of garnet with grossular-rich (Gr75–79) cores and andradite-rich (Gr36–38) rims, diopside (Di94–97), scapolite and magnetite; (2) sulfide-rich skarn (Stage II), dominated by chalcopyrite with magnetite, andraditic garnet (Ad84–89), diopside (Di65–75) and actinolite; and (3) retrograde alteration (Stage III) dominated by actinolite, epidote, orthoclase, phlogopite and chlorite in which sulfides are the main ore phases. 40Ar–39Ar age data indicate that potassic alteration, synchronous or postdating magnetite–pyroxene–amphibole skarn, occurred at 20.0 ± 0.1 Ma. The high pyroxene/garnet ratio, plus the presence of scapolite in calc-silicate and associated ore paragenesis characterized by magnetite (± hematite), chalcopyrite and bornite, suggests that the bulk of the Ayazmant skarns were formed under oxidized conditions. Oxygen isotope compositions of pyroxene, magnetite and garnet of prograde skarn alteration indicate a magmatic fluid with δ18O values between 5.4 and 9.5‰. On the basis of oxygen isotope data from mineral pairs, the early stage of prograde skarn formation is characterized by pyroxene (Di94–97)-magnetite assemblage formed at an upper temperature limit of 576 °C. The lower temperature limit for magnetite precipitation is estimated below 300 °C, on the basis of magnetite–calcite pairs either as fracture-fillings or massive ore in recrystallized limestone-marble. The sulfide assemblage is dominated by chalcopyrite with subordinate molybdenite, pyrite, cubanite, bornite, pyrrhotite, galena, sphalerite and idaite. Gold–copper mineralization formed adjacent to andradite-dominated skarn which occurs in close proximity to the intrusion contacts. Native gold and electrum are most abundant in sulfides, as fine-grained inclusions; grain size with varying from 5 to 20 µm. Sulfur isotope compositions obtained from pyrrhotite, pyrite, chalcopyrite, sphalerite and galena form a narrow range between ? 4.8 and 1.6‰, suggesting the sulfur was probably mantle-derived or leached from magmatic rocks. Geochemical data from Ayazmant shows that Cu is strongly associated with Au, Bi, Te, Se, Cd, Zn, Pb, Ni and Co. The Ayazmant mineralizing system possesses all the ingredients of a skarn system either cogenetic with, or formed prior to a porphyry Cu(Au–Mo) system. The results of this study indicate that the Aegean Region of Turkey has considerable exploration potential for both porphyry-related skarns and porphyry Cu and Au mineralization. 相似文献
18.
To characterize the hydrothermal processes of East Pacific rise at 9o-10oN, sulfide mineral compositions, textural, and geochemical features of chimney ores were studied using ore microscope, scanning electron microscope, X-ray diffraction analysis, and electron microprobe techniques. Results show that there are three mineral assemblages for the hydrothermal chimney ores, namely: (i) anhydrite marcasite pyrite, (ii) pyrite sphalerite chalcopyrite, and (iii) chalcopyrite bornite digenite covellite. Mineral assemblages, zonational features, and geochemical characteristics of the ore minerals indicate that ore fluid temperature changed from low to high then to low with a maximum temperature up to 400 ℃. The chimney is a typical black smoker. The initial structure of the chimney was formed by the precipitation of anhydrites, and later the sulfides began to precipitate in the inner wall. 相似文献
19.
P.S. Minyuk E.E. Tyukova T.V. Subbotnikova A.Yu. Kazansky A.P. Fedotov 《Russian Geology and Geophysics》2013,54(4):464-474
Dependences of magnetic susceptibility (MS) on the temperature of natural iron sulfide samples (pyrite, marcasite, greigite, chalcopyrite, arsenopyrite, pyrrhotite) from the deposits of northeastern Russia were studied. The thermal MS curves for pyrite and marcasite are the same: On heating, MS increases at 420–450 °C, and unstable magnetite (maghemite) and monoclinic pyrrhotite with a well-defined Hopkinson peak are produced. In oxygen-free media with carbon or nitrogen, magnetite formation is weak, whereas pyrrhotite generation is more significant. The heating curves for chalcopyrite are similar to those for pyrite. They show an increase in MS at the same temperatures (420–450 °C). However, stable magnetite is produced, whereas monoclinic pyrrhotite is absent. In contrast to that in pyrite, marcasite, and chalcopyrite, magnetite formation in arsenopyrite begins at > 500 °C. Arsenopyrite cooling is accompanied by the formation of magnetite (S-rich arsenopyrite) or maghemite (As-rich arsenopyrite) with a dramatic increase in MS. Arsenopyrite with an increased S content is characterized by insignificant pyrrhotite formation. Greigite is marked by a decrease in MS on the heating curves at 360–420 °C with the formation of unstable cation-deficient magnetite.Monoclinic pyrrhotite is characterized by a decrease in MS at ～ 320 °C, and hexagonal pyrrhotite, by a transition to a ferrimagnetic state at 210–260 °C. The addition of organic matter to monoclinic pyrrhotite stimulates the formation of hexagonal pyrrhotite, which transforms back into monoclinic pyrrhotite on repeated heating. The oxidation products of sulfides (greigite, chalcopyrite) show an increase in MS at 240–250 °C owing to lepidocrocite. 相似文献
20.
Pyrite, chalcopyrite, and gold occur in quartz veins in granitic rocks and as scattered and disseminated impregnations in shear zones of the highly altered metavolcanics in the Hamash area, Southeastern Desert, Egypt. The minerals are associated in part with pyrrhotite, digenite, tetrahedrite, chalcocite, bornite, and covellite. Pyrite occurs in two forms: (1) idio- to hypidiomorphic coarse crystals with inclusions of preexisting sulfides, and (2) fine-crystalline aggregates. Chalcopyrite occurs in three forms: (1) idiomorphic coarse crystals, (2) fine-crystalline microinclusions, and (3) xenomorphic relicts. Three genetic phases of sulfide mineralization were identified. They are related to the successive cooling of the crystallizing solutions. Gold was hosted in the older sulfide minerals during a high-temperature disorder phase. Native gold was formed during the latest, decreasing-temperature phase through remobilization of auriferous pyrite. Microprobe analysis confirmed that gold and copper are relatively enriched in the late pyrite. Identified surface-alteration products include goethite, limonite, gold, carbonates, and sulfates of iron and copper. 相似文献