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1.
The V-Ti magnetite layers (lodestone) occur within the layered gabbro-anorthosites-ultramafic rocks emplaced into the migmatitic gneisses close to the high grade Archeaen Sargur supracrustal rocks in the Kurihundi area. The ore petrographic studies of the lodestone reveal the presence of primary Ti-magnetite, ilmenite, ulvospinel, pleonaste, hematite and pyrite, chalcopyrite, pyrrhotite and secondary Ti-maghemite, martite and goethite as well as secondary covellite. These layers contain Ti-magnetite (60%) and ilmenite (30%) with silicates (<5%) exhibiting granular mosaic texture with well-defined triple junctions and are classified as adcumulus rocks. The grain-boundary relationships in the ores indicate considerable postcumulus growth and readjustment due to combined effects of sintering and adcumulus growth. Intergrowth textures (ulvospinel, ilmenite and pleonaste in Ti-magnetite and hematite in ilmenite) reflects exsolution features crystallized from solid-solutions compositions under different conditions of oxygen fugacities. Larger bodies of pleonaste and ilmenite in Ti-magnetite become lensoid or rounded in outline and these morphological modifications took place during the regional upper amphibolite to lower granulite facies metamorphism at 2.6 Ga ago. The lodestone contains high TiO2 (20 to 22.59 wt%), with V2O5 (0.85 to 1.15%) and Fe2O3 t (72.03 to 74.25%). Ti-magnetite shows alteration to Ti-maghemite, martite and goethite due to low temperature oxidation and hydration during weathering.  相似文献   

2.
This study describes textures and mineral chemistry of magnetite-ilmenite-bearing pods/pockets in mineralogically diverse feldspathic schist near Pathargora in the Singhbhum Shear Zone, eastern India. The textural and geochemical characteristics of the magnetite-ilmenite assemblage are the results of a protracted geological history involving magmatic crystallization and oxidation-exsolution of titanomagnetite, deformation-induced recrystallization and textural re-equilibration and hydrothermal fluid-induced hematitization of magmatic magnetite. The magnetite grains contain characteristic trellis and sandwich ilmenite lamella, which are interpreted to be the products of oxidation-exsolution of ulvöspinel component of magnetite-ulvöspinel solid solution. The exsolution process was accompanied by preferential partitioning of spinel elements such as Cr, Al and V in magnetite and Ti, Mn, Mg, HFS elements (Nb, Ta), transition elements (Sc, Co, Cu and Zn) and granitophile elements (Mo, Sn and W) in ilmenite. The deformed sandwich lamella is locally recrystallized and transformed into granular ilmenite close to fractures, micro-shear planes and magnetite grain boundaries. Coarse granules of ilmenite, within or associated with magnetite, are of two textural types: one invariably contains Fe-rich exsolved phase and may be of magmatic origin, while the other mostly formed by strain-induced, fluid-mediated expulsion (from the interior of magnetite to its boundary) and dynamic recrystallization of existing ilmenite lamella in magnetite, and dynamic recrystallization of primary ilmenite containing Fe-rich exsolved phases. Magnetite is variably hematitized. The highly porous nature and trace element geochemistry of hematite and mass-balance calculations suggest the hematitization was mostly redox-independent and was caused by infiltration of metal-rich, reduced and acidic fluid. The hematitization process was associated with significant enrichment and immobilization of U, Th, Pb, REEs, Cu, Mo and W and depletion of Ni, Cr, V in hematite.  相似文献   

3.
Oxide–sulphide–Fe–Mg–silicate and titanite–ilmenite textures as well as their mineral compositions have been studied in felsic and intermediate orthogneisses across an amphibolite (north) to granulite facies (south) traverse of lower Archean crust, Tamil Nadu, south India. Titanite is limited to the amphibolite facies terrane where it rims ilmenite or occurs as independent grains. Pyrite is widespread throughout the traverse increasing in abundance with increasing metamorphic grade. Pyrrhotite is confined to the high‐grade granulites. Ilmenite is widespread throughout the traverse increasing in abundance with increasing metamorphic grade and occurring primarily as hemo‐ilmenite in the high‐grade granulite facies rocks. Magnetite is widespread throughout the traverse and is commonly associated with ilmenite. It decreases in abundance with increasing metamorphic grade. In the granulite facies zone, reaction rims of magnetite + quartz occur along Fe–Mg silicate grain boundaries. Magnetite also commonly rims or is associated with pyrite. Both types of reaction rims represent an oxidation effect resulting from the partial subsolidus reduction of the hematite component in ilmenite to magnetite. This is confirmed by the presence of composite three oxide grains consisting of hematite, magnetite and ilmenite. Magnetite and magnetite–pyrite micro‐veins along silicate grain boundaries formed over a wide range of post‐peak metamorphic temperatures and pressures ranging from high‐grade SO2 to low‐grade H2S‐dominated conditions. Oxygen fugacities estimated from the orthopyroxene–magnetite–quartz, orthopyroxene–hematite–quartz, and magnetite–hematite buffers average 2.5 log units above QFM. It is proposed that the trends in mineral assemblages, textures and composition are the result of an external, infiltrating concentrated brine containing an oxidizing component such as CaSO4 during high‐grade metamorphism later acted upon by prograde and retrograde mineral reactions that do not involve an externally derived fluid phase.  相似文献   

4.
Oxygen fugacities have been estimated for a wide distribution of samples from the granulite facies terrane (region C) of the Bamble Sector, SE Norway using both the titaniferous magnetite–ilmenite and orthopyroxene–titaniferous magnetite–quartz oxygen barometers. These oxygen fugacities are estimated using temperatures calculated from the titaniferous magnetite–ilmenite thermometer of Ghiorso and Sack (1991) and are both internally consistent with each other as well with the thermometer. In samples for which the estimated temperature is high, the two oxygen barometers show good agreement whereas agreement is poor for low temperature samples. In these low temperature samples, oxygen fugacities estimated from titaniferous magnetite–ilmenite are considerably less than those estimated from orthopyroxene–titaniferous magnetite–quartz. An increase in this discrepancy with decrease in temperature appears to reflect preferential resetting of the hematite component in the ilmenite grains without significant alteration of the more numerous titaniferous magnetite grains. This is due, in part, to greater re-equilibration of the ilmenite grains during retrograde interoxide resetting between the ilmenite grains and the titaniferous magnetite grains. The mean temperature for the non-reset samples, 791?±?17?°C (1σ), is in good agreement with temperatures obtained from garnet–orthopyroxene KD exchange thermometry in the same region, 785–795?°C (1σ) (Harlov 1992, 2000a). Most non-reset oxygen fugacities range from log10?f?O2=?14 to ?11.8 or approximately 0.5–1.5?log units above quartz–fayalite–magnetite at 7.5?kbar. Both these temperatures and the range of oxygen fugacities are in good agreement with those estimated using the titaniferous magnetite–ilmenite thermometer/oxygen barometer of Andersen et?al. (1991). The QUIlP equilibrium (quartz–ulvöspinel–ilmenite–pyroxene) is used to project self-consistent equilibrium temperatures and oxygen fugacities for samples reset due to hematite loss from the ilmenite grains. These projected temperatures and oxygen fugacities agree reasonably well with the non-reset samples. The mean projected QUIlP temperature is 823?±?6?°C (1σ). This result supports the conclusion that low titaniferous magnetite–ilmenite temperatures (down to 489?°C) and accompanying low oxygen fugacities are the result of hematite loss from the ilmenite grains. Non-reset oxygen fugacities lie approximately 1.5?log10 units above the upper graphite stability curve indicating that the stable C–O–H fluid phase interacting with these gneisses, whether regionally or locally, was CO2. This is borne out by the presence of numerous CO2-rich fluid inclusions in these rocks.  相似文献   

5.
The iron titanium oxide phases ulvite, ilmenite and ferropseudobrookite were synthesized in equilibrium with metallic iron at 1000 ° C, 1130 ° C and 1300 ° C in CO2/H2 gas mixtures.The composition of the phases were determined by wet chemical and electron microprobe analyses and by direct oxygen determination.The chemical composition of the Fe-Ti oxide phases in equilibrium with metallic iron is sensitively influenced by temperature and by bulk composition.Ulvite in equilibrium with wüstite does not contrivalent titanium in the whole temperature range up to the eutectic temperature at 1312 °C.Ulvite+ilmenite phase assemblages contain trivalent titanium only at temperatures above 1200 ° C.A ferropseudobrookite phase is stable under the given conditions at temperatures above 1068 °C (Ender and Woermann, 1977).Ferropseudobrookite in equilibrium with metallic iron always contains trivalent titanium.Deviations from stoichiometric compositions of the solid solution phases are generally small. Thus recalculation of microprobe data to stoichiometric solid solutions does not involve a major error.From: Bruno Simons, Diplomarbeit Aachen, October 1974  相似文献   

6.
峨眉山玄武岩中钛以什么矿物形式存在一直以来很少有学者提及。本文通过镜下观察、全岩化学分析、X-衍射、能谱、扫描电镜、电子探针、阴极发光对川西南部周公山-汉王场地区钻井岩心中峨眉山玄武岩进行了详细的分析,讨论了其主要赋钛矿物及成因。(1)SiO2含量46.4%~48.3%和TiO2>3%显示区内峨眉山玄武岩属于高钛峨眉山玄武岩系列。但多个层段榍石含量>5%,而极少见磁铁矿、钛铁矿;(2)榍石主要以隐晶质的云雾状、雪花状、芝麻点状、枝状等形态分布于微晶长石之间和溶孔、溶洞边缘及裂缝中,少量呈显晶质粒状分布于微晶长石、绿泥石之间。(3)电子探针分析显示:所有含钛矿物中,钛铁矿中TiO2含量最高,为39.069%,榍石中TiO2次之,TiO2含量为17.143%~38.648%,磁铁矿中TiO2含量最高为12.293%,平均在5%~10%左右,其他矿物基本上都少于1%。(4)扫描电镜及其能谱分析显示:榍石中的Ti含量(2.49%~24.97%)明显高于含钛磁铁矿(2.68%~9.21%)、含钛赤铁矿(3.64%)中Ti含量,与钛铁矿(19.51%)含量相当。分析结果认为:峨眉山玄武岩中大量出现的隐晶榍石可能是岩浆后期产物或期后蚀变的产物。在峨眉山玄武岩中首次鉴别出的大量隐晶质榍石是高钛峨眉山玄武岩中最主要的赋钛矿物。隐晶榍石在玄武岩中的含量是区分"高钛"和"低钛"玄武岩的主要标志之一。  相似文献   

7.
The development of Fe-Ti oxide assemblages in basic rocks from the Penninic series of the southern Venediger rea, Austria, during polyphase Alpine metamorphism has been studied. Textural and compositional relations indicate thorough reequilibration of the opaque mineral assemblages during late Barrovian metamorphism at essentially static conditions of lower amphibolite to greenschist facies. In contrast, silicate mineralogy of the preceeding blueschist to eclogite facies metamorphism might still be preserved to a large extent. Chemical adjustment of the Fe-Ti oxide minerals to decreasing P-T conditions is characterized by (1) formation of complex intergrowths of ilmenite and hematite solid solutions (<550° C), (2) the decomposition of hemo-ilmenite 1 to ferrianilmenite2+magnetite+rutile and of ilmeno-hematite1 to titanhematite2+rutile±magnetite (<450° C), and (3) low-grade oxidation of ferrianilmenite2 to magnetite+hematite-rutile intergrowths or hematite +rutile and of titanhematite2 to hematite-rutile intergrowths (≦400° C). Chemical equilibrium is suggested by the regular partitioning of Cr, V, Mg and Mn between coexisting hemo-ilmenite, ilmeno-hematite, and magnetite. The hematite-ilmenite miscibility gap has been delimited on the basis of the bulk compositions of the exsolved phases and the temperature estimates obtained from Fe-Ti oxide thermometry.  相似文献   

8.
Summary ?Detailed petrographic studies and microchemical analyses of titanomagnetite from igneous and metamorphic rocks and ore deposits form the basis of this investigation. Its aim is to compare the data obtained and their interpretations with the experimentally deduced subsolidus oxidation-exsolution model of Buddington and Lindsley (1964). The results are also considered relevant for the interpretation of compositional variations in black sands which are recovered for titanium production. The arrangement of the samples investigated is in accordance with textural stages C1 to C5 caused by subsolidus exsolution with increasing degrees of oxidation (Haggerty, 1991). Stage 1 is represented by two types of optically homogeneous TiO2-rich magnetite: a. An isotropic type considered to represent solid solutions of magnetite and ulvite containing between 5.2 to 27.5 wt% TiO2 corresponding to about 14.7 to 77.7 mol% Fe2TiO4 in solid solution with magnetite. The general formula of this type is Fe2+ 1+x Fe3+ 2−2x Ti x O4 (x = 0.0–1.0). b. The second type which has not been reported so far is anisotropic and shows complex internal twinning resembling inversion textures. It is thus attributed to inversion of a high-temperature ilmenite modification (with statistical distribution of the cations) which forms solid solutions with magnetite. TiO2 varies between 9.3 and 24.5 wt% corresponding to about 17.2 to 43.6 mol% ilmenite in solid solution with magnetite. This type is interpreted as a cation-deficient spinel with the general formula Fe2+ 12/12 + 1/4xFe3+ 24/12 − 3/2x □ 0 + 1/4x Ti x O4 (x = 0.0–16/12). Isotropic and anisotropic homogeneous magnetites occur in volcanic rocks only; the homogeneity of the solid solutions was explained by fast cooling which prevented the development of exsolution textures. Stages 2 and 3 are represented by magnetite with or without ulvite. The magnetite host contains ilmenite lamellae forming trellis and sandwich textures. In contrast to the requirement of the oxidation-exsolution model, the ilmenite lamellae are concentrated exclusively in the cores of the host crystals. The reverse host-guest relationship may also occur. Stages 4 and 5 are identical with thermally generated martite (= martite due to heating). The textures are characterized by very broad lamellae of ferrian ilmenite or titanohematite dominantly concentrated along the margins of the host crystals. Thermally generated martite is restricted to subsolidus-oxidation reactions. The ilmenite lamellae of trellis and sandwich textures contain low Fe2O3-concentrations (average 4.8 mol%; to a maximum of 8.3), whereas the Fe2O3-content of thermally generated martite is between 32 to 71 mol%. With respect to the Fe2O3-concentrations in the ilmenite lamellae, no transition between the two types was observed. The results of this paper show that the widely accepted oxy-exsolution model of Buddington and Lindsley (1964) which is based on experimental results can – with the exception of thermally generated martite – not explain the tremendous variety of magnetite–ilmenite–ulvite relationships in natural rocks and ore deposits. Received October 16, 2001; accepted May 2, 2002  相似文献   

9.
The south-eastern part of Kunene Intrusive Complex (KIC), Namibia/Angola, is host to volumetrically significant, and economically important, concentrations of sodalite in the area around Swartbooisdrif, north-west Namibia. The mineralisation was formed by metasomatic exchange with carbonatites of the Epembe–Swartbooisdrif Alkaline Province. This process led to the breakdown of ore minerals initially present in various rock types of the KIC and caused the formation of new opaque phases in the sodalite-bearing metasomatites. A detailed investigation of textures and chemical compositions of the Fe–Ti oxides and sulphides has allowed evaluation of the complex ore-forming processes related to the polyphase magmatic and metasomatic history of the sodalite deposit. The predominant opaque phases in the various rock types of the KIC are ilmenite and (titano)magnetite, which are highly concentrated in the so-called magnetite plugs. It is clear from the textural evidence that most of the ilmenite and (titano)magnetite, although of orthomagmatic origin, recrystallised under subsolidus conditions. Conformably, their respective chemical compositions and phase relations represented in the system FeO–1/2Fe2O3–TiO2 point to re-equilibration at temperatures below 600 °C. Ilmenite and (titano)magnetite were affected by later deformation and decomposed by various reactions, related to, or outlasting, the metasomatic process. Oxidation of ilmenite led to the formation of symplectitic aggregates of rutile and secondary magnetite. Carbonatisation of the Fe–Ti oxides produced rutile and the siderite and rhodochrosite components in ankerite. Pyrite, in part together with rutile and secondary magnetite, was formed by sulphidation of the Fe–Ti oxides. Conspicuous aggregates of granular or lamellar intergrowths of pyrite with hematite and/or magnetite are interpreted as products of contemporaneous sulphidation and oxidation of former igneous pyrrhotite. Rarely observed pyrrhotite with pentlandite lamellae is probably not an igneous relic, but was formed during the metasomatic event. Smaller amounts of chalcopyrite, bornite, digenite–chalcocite, galena, ferroan siegenite, millerite and polydymite testify to different cooling stages during or after metasomatism. Applying the phase relations in the simplified system Fe–Co–Ni–S–O, we were able to reconstruct a semi-quantitative T–f(S2)–f(O2) path for the ore-forming processes. Received: 22 October 1998 / Accepted: 27 October 1999  相似文献   

10.
Qara-aghaj and Skandian as hard rock titanium deposit and Kahnooj one as a placer deposit were investigated from applied mineralogical point of view. The mineralogical studies were carried out using XRD, XRF, optical microscopy, scanning electron microscopy and microprobe analysis. These studies indicated that ilmenite and magnetite are main valuable minerals in the studied ores. Pyroxene, olivine and plagioclase are the main gangue minerals in Qara-aghaj ore while chlorite and plagioclase are the major gangue minerals in Skandian ore. Plagioclase, clinopyroxene, amphibole, feldspate and some quartz are the important gangue minerals in kahnooj deposit. In all three ores ilmenite is mainly in the form of ilmenite grains but some lamellae of ilmenite with thickness between 0.1 to 20 μm have been occurred as exsolution textures inside magnetite grains, where the magnetite here can be referred to as ilmenomagnetite. In the hard rock ores some fine ilmenites have been disseminated in silicate minerals. The liberation degree of granular ilmenite was determined 150, 140 and 200 μm for Qara-aghaj, Skandian and Kahnooj, respectively. So, only the granular form of ilmenite is recoverable by physical methods. Some sphene and rutile as titanium containing minerals were observed mainly inside ilmenite phase in kahnooj ore. Some fine rutile was also found inside Skandian ilmenite while there were not any other titanium minerals inside Qara-aghaj ilmenite. Apatite is another valuable mineral which was found only in Qara-aghaj ore. Using SEM and microprobe analysis it was found that there are different amounts of exsolved fine lamellae of hematite inside ilmenite in Qara-aghaj and Kahnooj ores while it was not observed in Sckandian one. The average contents of TiO2 in the lattice of Qara-aghaj, Skandian and Kahnooj ilmenite were determined 51.13, 50.9% and 52.02%, respectively. FeO content of ilmenite lattice for all three samples is clearly lower than the theoretical content. This is due to the substitution of Mg and Mn for some Fe2+ ions in the ilmenite lattice. V2O3 content of magnetite lattice is up to 1%. So, magnetite can be a suitable source for production of vanadium as a by-product in all three deposits.  相似文献   

11.
Sapphirine and spinel can accommodate significant ferric iron and therefore the mineral equilibria involving these phases must be sensitive to a(O2). In this paper we examine the theoretical phase relationships involving sapphirine and spinel in addition to sillimanite, garnet, cordierite, rutile, hematite-ilmenite solid solution (henceforth ilmenite), and magnetite-ulvospinel solid solution (henceforth magnetite), in the presence of quartz and hypersthene in the system FeO-MgO-Al2O3-SiO2-TiO2-O2 (FMASTO), with particular reference to the topological inversion in P-T postulated by Hensen (Hensen 1986). Documented natural associations suggest that the appropriate topology for assemblages involving magnetite and ilmenite is Hensen's higher a(O2) one, while, in contrast, the topology for assemblages involving ilmenite and rutile is the lower a(O2) one. The exact configuration of the inversion between these two topologies remains uncertain because of uncertainties in the ferric/ferrous iron partitioning between sapphirine and spinel-cordierite at high temperatures. By comparison with experimental data and natural occurences, the sillimanite-sapphirine-cordierite-garnet-hypersthene-quartz assemblage is in equilibrium at about 1000°–1020° C and 7–8 kbars, while sapphirine-cordierite-spinel-garnet-hypersthene-quartz occurs at temperatures in excess of those attainable during crustal metamorphism, for ilmenite-rutile buffered assemblages. This implies that sapphirine-rutil-ehypersthene-quartz assemblages, as found in the Napier Complex, Antarctica, can only occur at > 1000° C. Also, spinel-rutile-hypersthene-quartz assemblages should not be found in rocks because temperatures in excess of 1100° C are expected to be involved in their formation. The temperatures of formation of spinel-sillimanite-sapphirine-garnethypersthene-quartz, sapphirine-spinel-cordierite-sillimanite-hypersthene-quartz, and sillimanite-spinel-cordieritegarnet-hypersthene-quartz in assemblages buffered by magnetite and ilmenite are less well constrained, but are likely to be in the range 900°–1000° C. These conclusions apply to rocks with compositions close to FMASTO; the perturbing effects of substantial concentrations of additional components, in particular Ca, mainly in garnet, and Zn and Cr, mainly in spinel, may invalidate these conclusions.  相似文献   

12.
The effect of mineralogy and texture of Qara-aghaj ilmenite concentrate on titanium dioxide prepared via reduction-slagging acid leaching process as a raw material in chloride route was investigated. The concentrate contains 44.5 % TiO2 and its content in ilmenite lattice varies from 41.6–48 %. Hematite exsolved lamellae inside ilmenite which affect the reduction process positively are host of the most of the Cr and V as pigment colorizer metals. Apatite fine inclusions inside ilmenite as the source of Ca and P could have negative effects on synthetic rutile. Spinel ultrafine particles inside ilmenite containing Al and Si could also affect the synthetic rutile negatively. The other important elements which have been substituted in ilmenite lattice are Mg and Mn. The prepared titanium dioxide concentrate containing 91 % TiO2 and 0.6 % Fe2O3 is mainly formed by rutile and small amount of anatase and Ti2O3 phases. The solid solution of rutile inside Ti2O3 was also observed. The content of Cr, V, Mn, and Al are decreased to permissible amount during slagging and leaching process while the quantity of other impurities such as Mg, Si, and Ca are relatively high in the product, and they cause some difficulties in pigment production via chloride route. The Mg and Ca sourced from ilmenite lattice and apatite inclusions, respectively, can affect the precipitation process. So, it is predicted that Qara-aghaj ilmenite concentrate will be suitable for sulfate route, but it is necessary to investigate comprehensively.  相似文献   

13.
利用高分辨电子显微镜及微区X射线能谱成分测定的方法,对含钒的天然磁铁矿的精细结构进行了研究。结果表明,[110]方向的高分辨像清楚地显示钒钛磁铁矿在磁铁矿基体中以共(110)面紧密连生的方式与基体共生,形成波状连生体。这种成份调制波结构表明它们是出溶产物。  相似文献   

14.
The Paleoproterozoic Kauhajärvi gabbro is one of several Fe-, Ti-, and P-rich mafic intrusions associated with granitoids in the Fennoscandian shield in western Finland. The gabbro is cut by the late-orogenic Lauhanvuori granite (ca.1870?Ma), whereas the surrounding area is composed of synorogenic, collision-related granitoids and calc-alkaline volcanic rocks (ca. 1890?Ma) belonging to the Mid Finland Granitoid Complex. The mafic intrusions were probably emplaced into a Svecofennian rift zone. They are characterized by a high phosphorus content; the common occurrence of ilmenite as separate grains; and the coeval crystallization of apatite, Fe-Ti oxides, and Fe-Mg silicates. The Kauhajärvi gabbro is composed of two geochemically and structurally distinct zones. The basal zone is composed of poorly-layered, fine- to medium-grained gabbro, which represents an early intrusion of tholeiitic magma, and has rather high concentrations of chromium, magnesium and silica. Typically, the concentrations of iron, titanium and phosphorus are low, except for the top that is enriched in apatite and ilmenite. During most of the crystal-liquid fractionation of the basal zone magma, low f O2 limited the crystallization of Fe-Ti-oxides. Instead, titanium became enriched in the uppermost layer of the basal zone. The main zone represents a later injection of more evolved tholeiitic magma and makes up 80 to 90%of the total intrusion volume. Peridotite is common, along with gabbro and gabbronorite, in the lower and middle parts of the main zone, and anorthosite is common near the top of the main zone. The Mg:Fe ratio in mafic minerals and vanadium concentrations in magnetite decrease upwards. The variation within the main zone can be explained by crystal-liquid fractionation of a single batch of a parental magma under conditions of relatively high f O2. Titanium is not progressively enriched. The ratio of titanium to iron (TiO2/Fe2O3 = 0.16 to 0.20; Fe total as Fe2O3) is constant in the main zone and normal for mafic intrusions. Titanium is sited in separate ilmenite grains and in lamella within ilmenomagnetite (Ti-bearing magnetite). The high phosphorus content in the main zone is interpreted to result in crystallization of ilmenite and ilmenomagnetite instead of Ti-rich magnetite under relatively high f O2 conditions. High concentrations of titanium, iron and phosphorus in rocks of the main zone can be explained by pre-emplacement crystal-melt fractionation in a deep magma reservoir and/or contamination of mantle-derived mafic magmas by granitic magmas from partial melting of crustal rocks. A low-grade Fe-Ti-P resource at Kauhajärvi consists of layers with as much as 20 wt. % combined ilmenite (usually 8 to 11 wt. %), apatite (1 to 8 wt. %) and magnetite (1 to 9 wt. %). Mineralized layers are of variable thickness (2?m to 30?m) and occur in variable host rocks (peridotite or gabbro). The Fe-Ti oxides are most abundant in peridotite and pyroxene- or olivine-rich gabbronorite within the main zone. The contact between mineralized rocks (4%TiO2) and non- or slightly-mineralized rocks is gradual. The deposit as a whole consists of three to five mineralized layers with maximum combined thickness of 70?m. Apatite is most abundant in the oxide-rich layers, but is locally also concentrated in anorthosite with low Fe-Ti oxide contents. The weight ratio of ilmenite to magnetite is 3:2. The ratio of total Ti-Fe-oxides to apatite averages 4.0, with the range of 1.5 to >15.  相似文献   

15.
Geochemical and iron isotopic compositions of magnetite, ilmenite and pyrite separates from the FeTi oxide ores hosted in the Damiao anorthosite-type FeTi ore deposit were analyzed to investigate sub-solidus cooling history of the titanomagnetite. The FeTi oxides form two series of solid solutions, namely, ulvöspinel-magnetite (Usp-Mtss) and hematite-ilmenite (Hem-Ilmss) solid solutions. The magnetite separates have 14–27 mol% ulvöspinel, while the ilmenite separates have 5–8 mol% hematite. Major element compositions of the mineral separates suggest that the ilmenites were mainly exsolved from the Usp-Mtss by oxidation of ulvöspinel in the temperature range of ~820–600 °C and experienced inter-oxide re-equilibration with the magnetites. Associated with the exsolution is the substantial inter-mineral iron isotope fractionation. The magnetite separates are characterized by high δ57Fe (+0.27 − +0.65‰), whereas the ilmenite separates have lower δ57Fe (−0.65 to −0.28‰). Two types of pyrite are petrographically observed, each of which has a distinctive iron isotope fingerprint. Type I pyrite (pyriteI) with higher δ57Fe (δ57Fe = +0.63 − +0.95‰) is consistent with magmatic origin, and type II pyrite (pyriteII) with lower δ57Fe (δ57Fe = −0.90 to −0.11‰) was likely to have precipitated from fluids. Iron isotopic fingerprints of the pyriteI probably indicate variations of oxygen fugacity, whereas those of the pyriteII may result from fluid activities. The iron isotopic fractionation between the magnetite and ilmenite is the net result of sub-solidus processes (including ulvöspinel oxidation and inter-oxide re-equilibration) without needing varying oxygen fugacity albeit its presence. Although varying composition of magnetite-ilmenite pairs reflects variations of oxygen fugacity, inter-oxide iron isotopic fractionation does not.  相似文献   

16.
Mineral equilibria calculations in the system K2O–FeO–MgO–Al2O3–SiO2–H2O–TiO2–Fe2O3 (KFMASHTO) using thermocalc and its internally consistent thermodynamic dataset constrain the effect of TiO2 and Fe2O3 on greenschist and amphibolite facies mineral equilibria in metapelites. The end‐member data and activity–composition relationships for biotite and chloritoid, calibrated with natural rock data, and activity–composition data for garnet, calibrated using experimental data, provide new constraints on the effects of TiO2 and Fe2O3 on the stability of these minerals. Thermodynamic models for ilmenite–hematite and magnetite–ulvospinel solid solutions accounting for order–disorder in these phases allow the distribution of TiO2 and Fe2O3 between oxide minerals and silicate minerals to be calculated. The calculations indicate that small to moderate amounts of TiO2 and Fe2O3 in typical metapelitic bulk compositions have little effect on silicate mineral equilibria in metapelites at greenschist to amphibolite facies, compared with those calculated in KFMASH. The addition of large amounts of TiO2 to typical pelitic bulk compositions has little effect on the stability of silicate assemblages; in contrast, rocks rich in Fe2O3 develop a markedly different metamorphic succession from that of common Barrovian sequences. In particular, Fe2O3‐rich metapelites show a marked reduction in the stability fields of staurolite and garnet to higher pressures, in comparison to those predicted by KFMASH grids.  相似文献   

17.
Retrograde textural and chemical changes in oxide minerals from the Proterozoic Serrote da Laje deposit, northeastern Brazil, have been investigated. The deposit is situated in a mafic-ultramafic layered sill. Oxidation and cooling leading to successively decreasing diffusion rates resulted in disequilibrium on the microscale. Pleonaste in particular shows a rapid change in composition between (a) coarse grains in a granoblastic magnetite host, indicating metamorphic peak conditions, (b) coarse lamellae in magnetite, indicating commencement of exsolution, and (c) composite pleonaste — ilmenite lamellae in magnetite, which indicate oxidation exsolution. Barren rock layers cooled under more oxidized conditions compared with oxide-rich layers. Formation of pleonaste- and ilmenite lamellae in magnetite and ilmenite — hematite relations are discussed.  相似文献   

18.
Magnetite-ilmenite oxidation-exsolution intergrowths from an original titanomagnetite microphenocryst from an ash flow tuff unit have been studied using conventional transmission electron microscopy and analytical electron microscopy. Silicon has been found to be in solid solution in all of the magnetite studied and in some of the coexisting ilmenite. The average value in magnetite is 1.2 wt.% Si, equivalent to solid solution of 9 mole % Fe2SiO4. Silicon is also present in very small silicate inclusions and as unusual Si-rich domains of uncertain origin in magnetite. The inclusions and domains may be irregularly distributed through the magnetite in sizes well below those resolvable with the electron microprobe. Microprobe analyses for Si in magnetite generally reflect these heterogeneities in addition to a component presumably in solid solution. The petrologic implications of the data can be assessed only when relevant thermochemical data become available and the distribution of Si in magnetite is better understood.Contribution No. 376 from the Mineralogical Laboratory, Department of Geological Sciences, The University of Michigan  相似文献   

19.
产于层状镁铁质-超镁铁质岩体中的太和岩浆型Fe-Ti氧化物矿床是峨眉山大火成岩省内带几个超大型Fe-Ti氧化物矿床之一。太和岩体长超过3km,宽2km,厚约1.2km。根据矿物含量和结构等特征,整个岩体从下向上可划分为下部岩相带、中部岩相带、上部岩相带。下部岩相带主要以(橄榄)辉长岩和厚层不含磷灰石的块状Fe-Ti氧化物矿层组成。中部岩相带韵律旋回发育,(磷灰石)磁铁辉石岩主要位于旋回的底部,旋回上部为(磷灰石)辉长岩。上部岩相带主要是贫Fe-Ti氧化物的磷灰石辉长岩。太和中部岩相带磷灰石磁铁辉石岩含有5%~12%磷灰石、20%~35%Fe-Ti氧化物、50%~60%硅酸盐矿物,且硅酸盐矿物与磷灰石呈堆积结构。磷灰石磁铁辉石岩中磁铁矿显示高TiO2、FeO、MnO、MgO,且变化范围与趋势接近于攀枝花岩体。钛铁矿FeO分别与TiO2、MgO显示负相关,而FeO分别与Fe2O3、MnO显示正的相关,且TiO2、FeO、MnO、MgO含量变化较大,这些特征都暗示磁铁矿和钛铁矿是从富Fe-Ti-P岩浆中分离结晶。因此,可以推断太和磷灰石磁铁矿辉石岩形成于矿物重力分选和堆积。太和下部岩相带包裹在橄榄石中磁铁矿含有相对较高Cr2O3(0.07%~0.21%),而中部岩相带包裹在橄榄石中磁铁矿Cr2O3(0.00%~0.03%)显著降低,且这些磁铁矿Cr2O3含量变化与单斜辉石Cr含量和斜长石An牌号呈正相关。这些特征印证了形成中部岩相带的相对演化的富Fe-Ti-P母岩浆可能是源自中部岩浆房的混合岩浆。上部岩相带磁铁矿和中部岩相带顶部少量磁铁矿显示较低Ti+V可能是由于岩浆房中累积的岩浆热液对磁铁矿成分进行了改造。  相似文献   

20.
金红石高-超高压变质成矿作用的几个问题   总被引：4，自引：0，他引：4  
通过岩石及矿物晶体化学特征的计算,试图解决“为什么高-超高压变质作用利于金红石形成”的三方面内容:在高-超高压变质基性岩中,金红石普遍出现(即使在岩石全钛含量很低情况下)、基本不出现(或很少出现)钛铁矿、榍石、磁铁矿及赤铁矿等非金红石钛矿物及铁质矿物;石榴石和绿辉石“分流”的钛是极其有限的;以及从低压到高压,形成金红石粒度有逐渐变粗的趋势等问题。  相似文献   

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