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1.
W. Seifert 《Mineralogy and Petrology》2005,84(3-4):129-146
Summary The mineral chemistry of a Variscan lamprophyre (kersantite) from the Frankenwald, Germany, has been investigated by electron
microprobe. This potassic, Si-saturated, mafic rock contains an assemblage of different generations of titanite and allanite-(Ce),
Th-rich zircon, and metamict REE–Ti–Zr–Th silicates. The primary ferroan-ceroan titanite contains unusually high contents
of REE2O3 (max. (ΣLa to Sm)+Y = 36.8 oxide wt.%), ZrO2 (max. 5.4 wt.%), and ThO2 (max. 3.1 wt.%). Its empirical formula averages to (Ca0.31 La0.17 Ce0.30 Pr0.03 Nd0.08 Sm0.01 Y0.01 Fe2+0.06 Th0.02 Mn0.01)Σ1.00 (Ti0.60 Fe2+0.22 Al0.06 Zr0.07 Mg0.04 Nb0.01)Σ1.00 O1.00(Si0.93 Al0.07)Σ1.00 O4. Element correlations reveal operation of the complex substitution Ca2++Ti4++Th4+ ⇔ REE3++Al3++Zr4+. In comparison to allanite-(Ce), ferroan-ceroan titanite preferentially incorporated the LREE and Th. This finding is inconsistent
with previous experimental studies and suggests that both minerals are not cogenetic. High Zr contents in titanite, usually
known only from Si-undersaturated alkaline rocks, and the predominance of Fe2+ suggest that the ferroan-ceroan titanite crystallized from an alkali-rich, low-fO2 residual melt. 相似文献
2.
Christina Yan Wang Hazel M. Prichard Mei-Fu Zhou Peter C. Fisher 《Mineralium Deposita》2008,43(7):791-803
The Jinbaoshan Pt–Pd deposit in Yunnan, SW China, is hosted in a wehrlite body, which is a member of the Permian (∼260 Ma)
Emeishan Large Igneous Province (ELIP). The deposit is reported to contain one million tonnes of Pt–Pd ore grading 0.21% Ni
and 0.16% Cu with 3.0 g/t (Pd + Pt). Platinum-group minerals (PGM) mostly are ∼10 μm in diameter, and are commonly Te-, Sn-
and As-bearing, including moncheite (PtTe2), atokite (Pd3Sn), kotulskite (PdTe), sperrylite (PtAs2), irarsite (IrAsS), cooperite (PtS), sudburyite (PdSb), and Pt–Fe alloy. Primary rock-forming minerals are olivine and clinopyroxene,
with clinopyroxene forming anhedral poikilitic crystals surrounding olivine. Primary chromite occurs either as euhedral grains
enclosed within olivine or as an interstitial phase to the olivine. However, the intrusion has undergone extensive hydrothermal
alteration. Most olivine grains have been altered to serpentine, and interstitial clinopyroxene is often altered to actinolite/tremolite
and locally biotite. Interstitial chromite grains are either partially or totally replaced by secondary magnetite. Base-metal
sulfides (BMS), such as pentlandite and chalcopyrite, are usually interstitial to the altered olivine. PGM are located with
the BMS and are therefore also interstitial to the serpentinized olivine grains, occurring within altered interstitial clinopyroxene
and chromite, or along the edges of these minerals, which predominantly altered to actinolite/tremolite, serpentine and magnetite.
Hydrothermal fluids were responsible for the release of the platinum-group elements (PGE) from the BMS to precipitate the
PGM at low temperature during pervasive alteration. A sequence of alteration of the PGM has been recognized. Initially moncheite
and atokite have been corroded and recrystallized during the formation of actinolite/tremolite, and then, cooperite and moncheite
were altered to Pt–Fe alloy where they are in contact with serpentine. Sudburyite occurs in veins indicating late Pd mobility.
However, textural evidence shows that the PGM are still in close proximity to the BMS. They occur in PGE-rich layers located
at specific igneous horizons in the intrusion, suggesting that PGE were originally magmatic concentrations that, within a
PGE-rich horizon, crystallized with BMS late in the olivine/clinopyroxene crystallization sequence and have not been significantly
transported during serpentinization and alteration. 相似文献
3.
A. V. Mokhov T. A. Gornostaeva P. M. Kartashov A. P. Rybchuk O. A. Bogatikov 《Doklady Earth Sciences》2018,481(1):898-901
The close intergrowth of two native alloys of the compositions Ni0.59Cu0.24Al0.15Fe0.01Mn0.01 and Pd0.55Pt0.36Rh0.09 with a size of 10 μm has been discovered in the regolith from the Mare Crisium. A conclusion on its exhalative origin is made. 相似文献
4.
Nineteen samples from the Kane Fracture Zone have been studied for sulfide mineralogy and analyzed for S, Se, platinum-group elements (PGE), and Au to assess the effect of refertilization processes on the PGE systematics of abyssal peridotites. The lherzolites show broadly chondritic PGE ratios and sulfide modal abundances (0.01 to 0.03 wt%) consistent with partial melting models, although the few pyroxene-hosted sulfide inclusions and in situ LAM-ICPMS analyses provide evidence for in situ mobilization of a Cu-Ni-rich sulfide partial melt. The most refractory harzburgites (spinel Cr# > 29) are almost devoid of magmatic sulfides and show uniformly low PdN/IrN (<0.5) for variable PtN/IrN (0.8 to 1.2). The compatible behavior of Os, Ir, Ru, Rh, and Pt reflects the presence of primary Os-Ru alloys. Some harzburgites displaying petrographic evidence for refertilization by incremental melts en route to the surface are enriched in sulfides (up to 0.1 wt%). Some of these sulfides are concentrated in small veinlets of clinopyroxene and spinel crystallized from these melts. These S-rich harzburgites display superchondritic PdN/IrN (up to 2.04) positively correlated with sulfide modal contents. It is concluded that refertilization processes resulting in precipitation of metasomatic sulfides may significantly enhance Pd concentrations of abyssal peridotites while marginally affecting Pt (PtN/IrN ≤ 1.24) and Rh (RhN/IrN ≤ 1.23) as well. When the effects of such processes are screened out, our database suggests PGE relative abundances in the DMM (Depleted MORB Mantle; MORB: Mid-Ocean Ridge) within the uncertainty range of chondritic meteorites, without evidence of superchondritic Pt/Ir and/or Rh/Ir ratios. 相似文献
5.
P. A. van Aken V. J. Styrsa B. Liebscher A. B. Woodland G. J. Redhammer 《Physics and Chemistry of Minerals》1999,26(7):584-590
The Fe M
2,3-edge spectra of solid solutions of garnets (almandine-skiagite Fe3(Al1–xFex)2[SiO4]3 and andradite-skiagite (Fe1–xCax)3Fe2[SiO4]3), pyroxenes (acmite-hedenbergite (Ca1–xNax)(Fe2+
1−xFe3+
x)Si2O6), and spinels (magnetite-hercynite Fe(Al1–xFex)2O4) have been measured using the technique of parallel electron energy-loss spectroscopy (EELS) conducted in a transmission
electron microscope (TEM). The Fe M
2,3 electron energy-loss near-edge structures (ELNES) of the minerals exhibit a characteristic peak located at 4.2 eV and 2.2 eV
for trivalent and divalent iron, respectively, prior to the main maximum at about 57 eV. The intensity and energy of the pre-edge
feature varies depending on Fe3+/ΣFe. We demonstrate a new quantitative method to extract the ferrous/ferric ratio in minerals. A systematic relationship
between Fe3+/ΣFe and the integral intensity ratio of the main maximum and the pre-edge peak of the Fe M
2,3 edge is observed. Since the partial cross sections of the Fe M
2,3 edges are some orders of magnitude higher than those of the Fe L
2,3 edges, the Fe M
2,3 edges are interesting for valence-specific imaging of Fe. The possibility of iron valence-specific imaging is illustrated
by Fe M
2,3-ELNES investigations with high lateral resolution from a sample of ilmenite containing hematite exsolution lamellae that
shows different edge shapes consistent with variations in the Fe3+/ΣFe ratio over distances on the order of 100 nm.
Received: 14 April 1998 / Revised, accepted: 8 March 1999 相似文献
6.
Argyrios Kapsiotis Tassos A. Grammatikopoulos Basilios Tsikouras Konstantinos Hatzipanagiotou 《Resource Geology》2010,60(2):178-191
The Pindos ophiolite complex, located in the north-western part of continental Greece, hosts various podiform chromite deposits generally characterized by low platinum-group element (PGE) grades. However, a few locally enriched in PPGE + Au (up to 29.3 ppm) chromitites of refractory type are also present, mainly in the area of Korydallos (south-eastern Pindos). The present data reveal that this enrichment is strongly dependant on chromian spinel chemistry and base metal sulfide and/or base metal alloy (BMS and BMA, respectively) content in chromitites. Consequently, we used super-panning to recover PGM from the Al-rich chromitites of the Korydallos area. The concentrate of the composite chromitite sample contained 159 PGM grains, including, in decreasing order of abundance, the following major PGM phases: Pd-Cu alloys (commonly non-stoichiometric, although a few Pd-Cu alloys respond to the chemical formula PdCu4), Pd-bearing tetra-auricupride [(Au,Pd)Cu], nielsenite (PdCu3), sperrylite (PtAs2), skaergaardite (PdCu), Pd-bearing auricupride [(Au,Pd)Cu3], Pt and Pd oxides, Pt-Fe-Ni alloys, hollingworthite (RhAsS) and Pt-Cu alloys. Isomertieite (Pd11Sb2As2), zvyagintsevite (Pd3Pb), native Au, keithconnite (Pd20Te7), naldrettite (Pd2Sb) and Rh-bearing bismuthotelluride (RhBiTe, probably the Rh analogue of michenerite) constitute minor phases. The bulk of PGE-mineralization is dominated by PGM grains that range in size from 5 to 10 µm. The vast majority of the recovered PPGM are associated with secondary BMS and BMA, thus confirming that a sulphur-bearing melt played a very important role in scavenging the PGE + Au content of the silicate magma from which chromian spinel had already started to crystallize. The implemented technique has led to the recovery of more, as well as noble, PGM grains than the in situ mineralogical examination of single chromitite samples. Although, the majority of the PGM occur as free particles and in situ textural information is lost, single grain textural evidence is observed. In summary, this research provides information on the particles, grain size and associations of PGM, which are critical with respect to the petrogenesis and mineral processing. 相似文献
7.
The spin Hamiltonian (SH) parameters (g factors g
x
, g
y
and g
z
and the hyperfine structure constants A
x
, A
y
and A
z
) and local structure for the rhombic Rh4+ and Ir4+ centers in TiO2 (rutile) are theoretically studied from the perturbation formulas of these parameters for a low spin (S = 1/2) d
5 ion under rhombically distorted octahedra. In the calculations, the ligand orbital and spin–orbit coupling contributions
as well as the influence of the local lattice distortions are taken into account using the cluster approach. The local axial
elongation ratios are found to be about 1.7 and 3 times, respectively, larger for the Rh4+ and Ir4+ centers than that (≈0.0075) for the host Ti4+ site in rutile, while the perpendicular distortion angles (≈−0.28° and −0.42°, respectively) are more than one order in magnitude
smaller than the host value (≈−9.12°). This means that the impurity centers exhibit further elongations of the oxygen octahedra
and much smaller perpendicular rhombic distortions as compared with those of the host Ti4+ site in TiO2. The above local lattice distortions can be mainly ascribed to the substitution of the host Ti4+ by the nd
5 impurities, which may induce different physical and chemical properties for the metal–ligand clusters. In addition, the influence
of the Jahn–Teller effect on the local structure may not be completely excluded. The calculated SH parameters show reasonable
agreement with the observed values. 相似文献
8.
Gold and platinum group minerals from the gold placers of the South Urals are studied in order to identify the metal sources. In placers from the Main Uralian fault zone (MUF), the primary gold contains Ag (up to 29 wt.%), Cu (up to 2 wt.%) and Hg (up to 4 wt.%) and its fineness ranges from 538 to 997‰. Tetra-auricupride and cupriferous gold (up to 20 wt.% Cu) are common for the Nizhny Karabash placer of the MUF zone. In the eastern part of the South Urals, the placer gold is mainly characterized by high fineness of 900–1000‰ and low Cu contents (max 1.38 wt.%). Most of the placer gold grains consist of the primary domains, which are rimmed by secondary high-fineness gold with diffuse and clear boundaries. The secondary gold also develops along the shear dislocations of primary gold. Gold contains microinclusions of geerite, balkanite, chalcopyrite, Se-bearing galena, sphalerite, pyrite, pyrrhotite, arsenopyrite and hematite.Twenty four (including five unnamed) platinum group minerals (PGMs) were found in 28 placers; those from the Kialim and Maly Iremel placers of the Miass placer zone were studied in details. In the Kialim placer, ruthenium is most abundant PGM, which hosts microinclusions of isoferroplatinum, ferroan platinum, laurite, cupriferous gold, a mineral similar in composition to tolovkite, heazlewoodite and unnamed RhSbS phase. The osmium contains microinclusions of erlichmanite and laurite. The iridium grains hosts various sulfides and arsenides of platinum group elements (PGEs). The inclusion-free PGMs form Ru compositional trend in contrast to Os–Ru trend of the Ir-depleted inclusion-hosted PGMs. The isoferroplatinum from the Maly Iremel placer hosts laurite, rhodarsenite, bowieite, a mineral similar in composition to miassite and unnamed sulfide of Pt (Pt1.11S2.00) and antimonide of Pd ((Pd2.41Rh0.43Fe0.17)3.01(Sb0.91Te0.09)1.00). Ruthenium is a host to isoferroplatinum, PGE sulfides and arsenides, and heazlewoodite. Osmium contains microinclusions of ferroan platinum; iridium is a host to a mineral similar in composition to hongshiite. Three types of PGM intergrowths were identified in the Maly Iremel samples: (1) the intergrowths of platy grains of ruthenium with isoferroplatinum and a mineral similar in composition to tulameenite; (2) the open-latticework intergrowths of platy crystals of ruthenium with interstitial aggregates made up of gold, isoferroplatinum and a mineral similar in composition to xingzhongite and (3) the intergrowths of osmium and irarsite and iridarsenite, which are developed along cleavage of the osmium grains. Nickel sulfides associated with some PGMs contain Ru (11.32 wt.%) and Rh (2.21 wt.%) in millerite and Ir (31.00 wt.%), Ru (5.81 wt.%) and Rh (2.87 wt.%) in vaesite.The primary metal sources were determined on the basis of the mineral assemblages and composition of minerals, taking into account the nearby mineral deposits and directions of rivers. The rodingite-associated gold, gold-bearing massive sulfide and chromite deposits are major sources of gold and PGMs in placers of the Miass placer zone confined to the MUF structure of the South Urals. In the southern part of this structure, gold was mainly originated from orogenic gold–sulfide deposits associated with volcanic/volcaniclastic rocks and listvenite-associated gold deposits. The placer PGMs were derived from the adjacent ultramafic massifs of ophiolitic origin. The distance between the placers and primary deposits varies from 2 to 5 km (up to 20 km in the extended valley of the Miass River). Usage of ore microinclusions and associated PGMs in study of placer gold is far more advanced than an ordinary consideration of gold composition alone. This approach allowed us to identify the concrete sources for individual placers and to predict some mineralogical findings in already known primary occurrences. 相似文献
9.
N. V. Chukanov A. A. Mukhanova R. K. Rastsvetaeva D. I. Belakovsky S. M?ckel O. V. Karimova S. N. Britvin S. V. Krivovichev 《Geology of Ore Deposits》2011,53(7):583-590
Oxyphlogopite is a new mica-group mineral with the idealized formula K(Mg,Ti,Fe)3[(Si,Al)4O10](O,F)2. The holotype material came from a basalt quarry at Mount Rothenberg near Mendig at the Eifel volcanic complex in Rhineland-Palatinate,
Germany. The mineral occurs as crystals up to 4 × 4 × 0.2 mm in size encrusting cavity walls in alkali basalt. The associated
minerals are nepheline, plagioclase, sanidine, augite, diopside, and magnetite. Its color is dark brown, its streak is brown,
and its luster is vitreous. D
meas = 3.06(1) g/cm3 (flotation in heavy liquids), and D
calc = 3.086 g/cm3. The IR spectrun does not contain bands of OH groups. Oxyphlogopite is biaxial (negative); α = 1.625(3), β = 1.668(1), and
γ = 1.669(1); and 2V
meas = 16(2)° and 2V
calc = 17°. The dispersion is strong; r < ν. The pleochroism is medium; X > Y > Z (brown to dark brown). The chemical composition is as follows (electron microprobe, mean of 5 point analyses, wt %; the ranges
are given in parentheses; the H2O was determined using the Alimarin method; the Fe2+/Fe3+ was determined with X-ray emission spectroscopy): Na2O 0.99 (0.89–1.12), K2O 7.52 (7.44–7.58), MgO 14.65 (14.48–14.80), CaO 0.27 ((0.17–0.51), FeO 4.73, Fe2O3 7.25 (the range of the total iron in the form of FeO is 11.09–11.38), Al2O3 14.32 (14.06–14.64), Cr2O3 0.60 (0.45–0.69), SiO2 34.41 (34.03–34.66), TiO2 12.93 (12.69–13.13), F 3.06 (2.59–3.44), H2O 0.14; O=F2 −1.29; 99/58 in total. The empirical formula is (K0.72Na0.14Ca0.02)(Mg1.64Ti0.73Fe0.302+ Fe0.273+Cr0.04)Σ2.98(Si2.59Al1.27Fe0.143+ O10) O1.20F0.73(OH)0.07. The crystal structure was refined on a single crystal. Oxyphlogopite is monoclinic with space group C2/m; the unit-cell parameters are as follows: a = 5.3165(1), b = 9.2000(2), c = 10.0602(2) ?, β = 100.354(2)°. The presence of Ti results in the strong distortion of octahedron M(2). The strongest lines of the X-ray powder diffraction pattern [d, ? (I, %) [hkl]] are as follows: 9.91(32) [001], 4.53(11) 110], 3.300(100) [003], 3.090(12) [112], 1.895(21) [005], 1.659(12) [−135], 1.527(16)
[−206, 060]. The type specimens of oxyphlogopite are deposited at the Fersman Mineralogical Museum in Moscow, Russia; the
registration numbers are 3884/2 (holotype) and 3884/1 (cotype). 相似文献
10.
This contribution firstly presents particularities of mineral chemistry of platinum-group elements (PGE) mineralization from
placer deposits linked to the Bor-Uryakh massif of the Maimecha-Kotui Province, northern part of the Siberian Craton. The
chemical composition of PGE mineralization has been studied by electron microprobe analysis. At Bor-Uryakh, main platinum-group
minerals (PGM) comprise Os-Ir and Pt-Fe alloys represented by individual crystals, and polyphase PGM assemblages. The majority
(e.g., 12 out of 19) of the Os-rich nuggets are iridian osmium, with subordinate amounts of native osmium (Os) and chengdeite
(Ir3Fe). Pt-Fe alloys have a stoichiometric composition close to Pt2Fe. According to the nomen-clature by L. Cabri and C. Feather [1975] these minerals correspond to ferroan platinum. Based
on geological position and geochemical features of investigated PGE mineralization the particular rock sources have been established.
This study has demonstrated the similarity of chemical characteristics of Os-Ir and Pt-Fe alloys of the Bor-Uryakh massif
to those of PGM from the Guli massif (Maimecha-Kotui Province), platiniferous zoned-type ultramafic massifs (e.g., Kondyor,
Inagli and Chad) of the Aldan Province and Platinum belt of the Urals (Nizhny Tagil, Kytlym, etc.). 相似文献
11.
The mineralogy of the platinum-group elements (PGE), and gold, in the Platreef of the Bushveld Complex, was investigated using an FEI Mineral Liberation Analyser. Polished sections were prepared from 171 samples collected from two boreholes, for the in-situ examination of platinum group minerals (PGM). PGM and gold minerals encountered include maslovite (PtBiTe, 32 area% of total PGM), kotulskite (Pd(BiTe), 17?%), isoferroplatinum (Pt3Fe, 15?%), sperrylite (PtAs2, 11?%), cooperite (PtS, 5?%), moncheite (PtTe2; 5?%), electrum (AuAg; 5?%), michenerite (PdBiTe; 3?%), Pd alloys (Pd, Sb, Sn; 3?%), hollingworthite ((Rh,Pt)AsS; 2?%), as well as minor (all <1 area% of total PGM) merenskyite (PdBiTe2), laurite (RuS2), rustenburgite (Pt0.4Pd0.4Sn0.2), froodite (PdBi2), atokite (Pd0.5Pt0.3Sn0.2), stumpflite (PtSb), plumbopalladinite (Pd3Pb2), and zvyagintsevite (Pd3Pb). An observed association of all PGM with base metal sulfides (BMS), and a pronounced association of PGE tellurides, arsenides and Pd&Pt alloys with secondary silicates, is consistent with the remobilisation and recrystallisation of some of the PGM’s during hydrothermal alteration and serpentinisation subsequent to their initial (primary) crystallisation from BMS (e.g. Godel et al. J Petrol 48:1569–1604, 2007; Hutchinson and McDonald Appl Earth Sci (Trans Inst Min Metall B) 114:B208–224, 2008). 相似文献
12.
A new Cu-Au alloy occurrence is located at the southeastern flank of the Malye Kopty massif of ultramafic rocks in the Vendian-Early
Cambrian Kaa-Khem ophiolitic belt. Lithic clasts with Cu-Au alloy segregations (up to 15 mm in size) intergrown with other
minerals were found in alluvium of the Kara-Oss Creek valley, which extends along the fault zone crosscutting ultramafic rocks.
Cu-Au alloy occupies the main volume of clasts and fills the network of veinlets in grained aggregates consisting of andradite
(2–18% grossular component) and diopside (X
Fe = 0.01–0.05). Cu-Au alloy contains small ingrowths of andradite (up to 43% grossular component), diopside (X
Fe = 0.14–0.19), chlorite (penninite), chalcocite that contains up to 1.5 wt % Au, Cu-bearing greenockite (6.07–13.67 wt % Cu,
0.48–1.56 wt % Zn, and 0.76–1.06 wt % Au), and magnetite. The chemical composition of Cu-Au alloy is nonuniform. The central
parts of large Cu-Au alloy segregations consist of Ag-bearing tetraauricupride (AuCu) blocks (3.2–6.4 wt % Ag). They contain
veinlet-shaped AuCu zones with 13.3–14.5 wt % Ag. The AuCu blocks are cemented by late Cu-Au alloy, whose composition is close
to auricupride (AuCu3). Taking into account the limits of component miscibility in the Au-Ag-Cu system, the temperature of the Cu-Au alloy formation
was estimated at 350–600°C. This temperature corresponds to the formation conditions of garnet-pyroxene rodingite mineral
assemblage (Plyusnina et al., 1993). The studied Cu-Au alloy samples from the Malye Kopty massif are very similar to Cu-Au
alloy minerals hosted in the Alpine-type ultramafic rocks of the Karabash massif in the southern Urals. This similarity is
confirmed by identical chemical compositions of pyroxene, garnet, and chlorite, and similar PT conditions of their formation. The data show that primary ore mineralization of gold-rodingite type occurs in the Kaa-Khem
ophiolitic belt. 相似文献
13.
Summary Batiferrite, ideally Ba[Ti2Fe10]O19, was found in the Quaternary volcanic rocks near üdersdorf, Graulai, and Altburg, western Eifel area, Germany. The new mineral
typically occurs as euhedral platy grains in cavities of melilite- and leucite-nephelinite basalts. Associated minerals are
hematite, magnetite, titanite, g?tzenite, clinopyroxene, nepheline, and biotite. It exhibits a hexagonal tabular habit flattened
on {0001}, diameter 0.5–1 mm, thickness 20–125 μm, and {10&1macr;3}, {10&1macr;0} as observable forms. The mineral is opaque, of black
color with submetallic lustre, and shows a ferrimagnetic behavior. VHN50 is 793 with a range of 710–841 from ten indentations. The quantitative reflectance measurements of Ro/Re on oriented grains in air and oil immersion, respectively, are [%]: for 470 nm 22.1/20.1 and 8.4/7.1, for 546 nm 21.0/19.4
and 7.8/6.6, for 589 nm 20.2/18.8 and 7.4/6.3, and for 650 nm 19.3/18.3 and 6.8/5.9. The bireflectance is distinct (air) to
weak (oil), and parallel (0001) a moderate anisotropy with straight extinction can be observed. Typical microprobe analyses
give [wt%] K2O 0.28–0.33, Na2O 0.17–0.20, SrO 0.46–0.55, BaO 11.80–12.17, MgO 1.27–1.47, Al2O3 0.31–0.33, TiO2 13.11–13.63, MnO 2.38–2.57, Fe2O3 61.36–63.12, FeO 5.49–5.86 (Fe3+/Fe2+ calculated for charge compensation), which is equivalent to (Ba0.84Na0.06K0.06Sr0.05)1.01(Fe8.48
3+Fe0.86
2+Ti1.82Mg0.37Mn0.37Al0.06)11.96O19 as the average composition based on 19 oxygen atoms. Batiferrite is a magnetoplumbite-type mineral with hexagonal symmetry,
space group P6
3
/mmc (no. 194), a = 5.909(1) ?, c = 23.369(4) ?, V = 706.6(2) ?3, Z = 2, and a calculated density of 5.016 gcm−3. The structure was refined to R1 = 0.031 for 278 unique reflections with Fo
2 > 4σ (Fo
2) and R1 = 0.079 for all 452 unique observations using single crystal X-ray data. The strongest reflections of the X-ray powder diffraction
pattern are [d
obs, I/Io, (hkl)]: 2.631, 100, (114); 2.799, 80, (107); 1.478, 70, (220); 2.429, 60, (203); 1.672, 50, (217). The new mineral is comparable to the other Ba containing magnetoplumbite-type minerals haggertyite and
hawthorneite, the iron content, however, is much higher and in the range of magnetoplumbite. The large cation site (A) is
dominated by Ba, and four of the five remaining crystallographic cation sites in the structure are dominated by Fe (M1, 2,
3, 5), the octahedrally coordinated M4-site is dominated by Ti. No oxygen vacancy on the O3-site like in plumboferrite can
be observed. Batiferrite is named for its main chemical composition and the relationship to the M-type hexaferrites (polytype
5H).
Received December 14, 1999; accepted March 2, 2000 相似文献
Zusammenfassung Batiferrit, ein neues ferrimagnetisches Mineral des Magnetoplumbit-Typs aus den quart?ren Vulkaniten der West-Eifel, Deutschland Das neue Mineral Batiferrite, mit der Idealformel Ba[Ti2Fe10]O19, wurde an drei Fundpunkten in den Quart?ren Vulkangesteinen der westlichen Eifel, Deutschland, in der N?he von üdersdorf, Graulai und Altburg gefunden. Das neue Mineral tritt typischerweise bl?ttchenf?rmig in kleinen Hohlr?umen von Melilith- und Leucit-Nephelininit Basalten auf. Vergesellschaftete Minerale sind H?matit, Magnetit, Titanit, G?tzenit, Klinopyroxen, Nephelin und Biotit. Der Habitus ist hexagonal tafelig nach {0001}, mit einem Durchmesser von 0.5–1 mm und einer Dicke von 20–125 μm, zus?tzlich k?nnen die Formen {10&1macr;3} und {10&1macr;0} beobachtet werden. Das Mineral ist opak, hat eine schwarze Farbe mit einem leicht metallischen Glanz, und ist ferromagnetisch. Die H?rte VHN50 ist 793 mit einem Bereich von 710–841 aus 10 Eindruckbestimmungen. Die quantitativen Reflexionsmessungen von Ro/Re an orientierten K?rnern in Luft beziehungsweise ?limmersion, ergaben [%]: für 470 nm 22.1/20.1 und 8.4/7.1, für 546 nm 21.0/19.4 und 7.8/6.6, für 589 nm 20.2/18.8 und 7.4/6.3, und für 650 nm 19.3/18.3 und 6.8/5.9. Die Bireflexion ist deutlich (Luft) bis schwach (?l) und parallel (0001) kann eine mittlere Anisotropie mit gerader Ausl?schung beobachtet werden. Eine typische Mikrosondenanalyse ergibt [wt%] K2O 0.28–0.33, Na2O 0.17–0.20, SrO 0.46–0.55, BaO 11.80–12.17, MgO 1.27–1.47, Al2O3 0.31–0.33, TiO2 13.11–13.63, MnO 2.38–2.57, Fe2O3 61.36–63.12, FeO 5.49–5.86 (Fe3+/Fe2+ berechnet zum Ladungsausgleich), die mittlere chemische Formel auf der Basis von 19 Sauerstoffatomen lautet (Ba0.84Na0.06K0.06Sr0.05)1.01 (Fe8.48 3+Fe0.86 2+Ti1.82Mg0.37Mn0.37Al0.06)11.96O 19. Batiferrit ist ein Mineral der Magnetoplumbitgruppe, hat hexagonale Symmetrie mit der Raumgruppe P63/mmc (Nr. 194), a = 5.909(1) ?, c = 23.369(4) ?, V = 706.6(2) ?3, Z = 2, und einer berechneten Dichte von 5.016 gcm−3. Die Struktur wurde aus Einkristall-R?ntgendaten bis zu einem R1-Wert von 0.031 für 278 Fo 2 > 4σ(Fo 2), und einem R1-Wert von 0.079 für alle 452 Fo 2 verfeinert. Die st?rksten Beugungsreflexe der Pulver-R?ntgendaten sind [dobs, I/Io, (hkl)]: 2.631, 100, (114); 2.799, 80, (107); 1.478, 70, (220); 2.429, 60, (203); 1.672, 50, (217). Das neue Mineral weist deutliche ?hnlichkeiten zu den anderen beiden Ba-reichen Mineralen Haggertyit und Hawthorneit der Magnetoplumbit-Gruppe auf, jedoch ist der Eisengehalt wesentlich h?her und im Bereich des Minerals Magnetoplumbit. Der gro?e Kationenplatz (A) ist von Barium dominiert, vier (M1, 2, 3, 5) der restlichen fünf kristallographischen Kationenpl?tze in der Struktur sind fast ausschlie?lich mit Fe, die oktaedrisch koordinierte M4-Position ist überwiegend mit Ti besetzt. An der O3-Position konnte kein Sauerstoffdefizit wie in Plumboferrit festgestellt werden. Batiferrit ist nach seiner chemischen Beschaffenheit und nach seiner Zugeh?hrigkeit zu den M-Typ Hexaferriten (Polytyp 5H) benannt.
Received December 14, 1999; accepted March 2, 2000 相似文献
14.
Summary ?Results of experimental investigations in the dry system PtS-PdS-NiS at 1100°C, 1000°C, and 900°C are presented. The phases
observed at 1100°C are “cooperite” and a melt, at 1000°C “cooperite”, “braggite”, and a melt and at 900°C “cooperite”, “braggite”,
“vysotskite”, Ni1−xS, and a melt. At 1100°C the maximum solubility of Ni in ideal, Pd-free “cooperite” is 2.7 atomic per cent and the Pd-content
limit in Ni-free “cooperite” is 12.8 atomic per cent. At 1000°C the maximum solubility of Ni in ideal, Pd-free “cooperite”
is 3.3 atomic per cent and the Pd-content in Ni-free “cooperite” is 13.7 atomic per cent. The “braggite” composition ranges
from Pt0.56Pd0.38Ni0.06S and Pt0.59Pd0.41S in a Ni-saturated and Ni-free environment respectively to Pt0.18Pd0.80Ni0.02S and Pt0.14Pd0.86S respectively. At 900°C the maximum Ni-content in ideal Pd-free “cooperite” is 3.1 atomic per cent and the Pd-limit in Ni-free
“cooperite” is 12.5 atomic per cent. The “braggite” composition ranges from Pt0.59Pd0.29Ni0.12S and Pt0.60Pd0.40S for a Ni-saturated and Ni-free environment respectively, to Pd0.91Ni0.09S and PdS respectively. The Ni-content in “braggite” and “vysotskite” increases slightly with increasing Pt/Pd ratios and
is higher at 900°C than at 1000°C. Comparison of experimental trends with cooperite, braggite, and vysotskite analyses from
the literature implies high temperatures of formation for Pt-Pd-Ni sulphides in placers if Ni-saturation is assumed.
Received October 1, 1998;/revised version accepted September 7, 1999 相似文献
Zusammenfassung ?Synthetischer ,,Cooperit”, ,,Braggit” und “Vysotskit” im System PtS-PdS-NiS bei 1100°C, 1000°C und 900°C Ergebnisse experimenteller Untersuchungen im trockenen System PtS-PdS-NiS bei 1100°C, 1000°C und 900°C werden dargestellt. Bei 1100°C sind die Phasen “Cooperit” und Schmelze, bei 1000°C “Cooperit”, “Braggit” und Schmelze und bei 900°C “Cooperit”, “Braggit”, “Vysotskit”, Ni1−xS und Schmelze stabil. Bei 1100°C ist die maximale L?slichkeit von Ni in idealem, Pd-freiem “Cooperit” 2.7 Atomprozent und der Pd-Gehalt in Ni-freien “Cooperit” liegt bei maximal 12.8 Atomprozent. Bei 1000°C ist die maximale L?slichkeit von Ni in idealem, Pd-freien “Cooperit” 3.3 Atomprozent und der Pd-Gehalt in Ni-freien “Cooperit” liegt bei maximal 13.7 Atomprozent. Die Zusammensetzung des “Braggits” variiert zwischen Pt0.56Pd0.38Ni0.06S und Pt0.18Pd0.80Ni0.02S in einem Ni-ges?ttigtem und zwischen Pt0.59Pd0.41S und Pt0.14Pd0.86S in einem Ni-freien Umfeld. Bei 900°C liegt die maximale L?slichkeit von Ni in idealem Pd-freien “Cooperit” bei 3.1 Atomprozent und der Pd-Gehalt in Ni-freien “Cooperit” liegt bei maximal 12.5 Atomprozent. Die Zusammensetzung des “Braggits” variiert zwischen Pt0.59Pd0.29Ni0.12S und Pd0.89Ni0.08S in einem Ni-ges?ttigten und zwischen Pt0.59Pd0.40S und PdS in einem Ni-freien Umfeld. Der Nickelgehalt in “Braggit” und “Vysotskit” nimmt mit zunehmendem Pt/Pd Verh?ltnis zu und ist bei 900°C h?her als bei 1000°C. Ein Vergleich der experimentellen Trends mit Cooperit, Braggit und Vysotskit Analysen aus der Literatur weist auf eine Hochtemperaturbildung der Pt-Pd-Ni Sulfide in Seifenlagerst?tten hin, wenn man von Nickels?ttigung ausgeht.
Received October 1, 1998;/revised version accepted September 7, 1999 相似文献
15.
Mariko Nagashima Takahiro Ishida Masahide Akasaka 《Physics and Chemistry of Minerals》2006,33(3):178-191
Two pumpellyites with the general formula W
8
X
4
Y
8
Z
12O56-n
(OH)
n
were studied using 57Fe Mössbauer spectroscopic and X-ray Rietveld methods to investigate the relationship between the crystal chemical behavior of iron and structural change. The samples are ferrian pumpellyite-(Al) collected from Mitsu and Kouragahana, Shimane Peninsula, Japan. Rietveld refinements gave Fe(X):Fe(Y) ratios (%) of 41.5(4):58.5(4) for the Mitsu pumpellyite and 46(1):54(1) for the Kouragahana pumpellyite, where Fe(X) and Fe(Y) represent Fe content at the X and Y sites, respectively. The Mössbauer spectra consisted of two Fe2+ and two Fe3+ doublets for the Mitsu pumpellyite, and one Fe2+ and two Fe3+ doublets for the Kouragahana pumpellyite. In terms of the area ratios of the Mössbauer doublets and the Fe(X):Fe(Y) ratios determined by the Rietveld refinements, Fe2+(X):Fe3+(X):Fe3+(Y) ratios are determined to be 22:14:64 for the Mitsu pumpellyite and 27:8:65 for the Kouragahana pumpellyite. By applying the Fe2+:Fe3+-ratio determined by the Mössbauer analysis and the site occupancies of Fe at the X and Y sites given by the Rietveld method together with chemical analysis, the resulting formula of the Mitsu and Kouragahana pumpellyites are established as Ca8(Fe
0.88
2+
Mg0.68Fe
0.77
3+
Al1.66)Σ3.99(Al5.67Fe
2.34
3+
)Σ8.01Si12O42.41(OH)13.59 and Ca8(Mg1.24Fe
0.65
2+
Fe
0.46
3+
Al1.66)Σ4.01(Al6.71Fe
1.29
3+
)Σ8.00Si12O42.14(OH)13.86, respectively. Mean Y–O distances and volumes of the YO6 octahedra increase with increasing mean ionic radii, i.e., the Fe3+→Al substitution at the Y site. However, change of the sizes of XO6 octahedra against the mean ionic radii at the X site is not distinct, and tends to depend on the volume change of the YO6 octahedra. Thus, the geometrical change of the YO6 octahedra with Fe3+→Al substitution at the Y site is essential for the structural changes of pumpellyite. The expansion of the YO6 octahedra by the ionic substitution of Fe3+ for Al causes gradual change of the octahedra to more symmetrical and regular forms. 相似文献
16.
The dependence of water concentration in synthetic (Mg, Fe2+)-cordierite on the composition of the solid solution was examined in experiments that lasted for 10 days at = 200–230 MPa,
t = 600–700°C, and oxygen fugacity corresponding to the Fe-FeO buffer. Mass spectrometric data indicate that the dependence
of water concentration in cordierite on its Fe mole fraction Fe2+/(Fe2+ + Mg) has maxima at compositions with F = 0.2–0.3. IR diffuse reflectance spectroscopic data and data on the structural setting
of H2O molecules in the structural channels of alkali-free (Mg, Fe2+)-cordierite indicate that the H-H vector of some H2O molecules (H2O-II) is perpendicular to [001] of the crystal. The dependence of the magnetic properties of synthetic (Mg, Fe2+)-cordierite was studied by static magnetization technique at 5–300 K in an external magnetic field up to 20 kOe in strength. 相似文献
17.
Compositional variations and morphological evolution in platinum beach placers, southern New Zealand
Morphologies of placer platinum group minerals (PGM) are more variable and resistant to modification during transport than placer gold grains. This study documents morphological evolution of PGM placer grains during up to 120 km of transport in beach placers after river transport from inferred sources up to 200 km inland. PGM morphological changes are calibrated with changes in morphology of associated placer gold. Most of the PGM are Pt-Fe alloy and have been fed into the beach placer system from a large river at the western end of the beaches on the south coast of New Zealand. The incoming fluvial PGM suite includes Os, Ir and Ru alloys which may have been derived from distal ophiolitic sources. More proximal sources have Ural-Alaskan affinities and these contributed cooperite and braggite, or sperrylite, locally, as well as Pt-Fe alloy grains. Some PGM may have been recycled through Cretaceous-Quaternary fluvial sediments before entering the modern placer system. Recycled placer PGM grains have also been derived from elevated Quaternary beaches near the coastline. PGM grains entering beach placers have rough surfaces, with remnants of crystal faces, and these evolve to smooth flakes with progressive long-shore transport. PGM flakes have slightly thickened rims caused by impacts by saltating sand on windy beaches, and the most distal beach placers contain flakes with incipient toroidal shapes. These PGM incipient toroids are poorly developed compared to accompanying well-formed toroidal gold that has developed in nearly all beach placers, including those on elevated Quaternary beaches. Typical PGM and gold placer grain size decreases with increasing distance of transport, from fluvial grain size of 400–1,000 to ～200 microns on the most distal beaches, accompanied by eastward loss of equant PGM grains and associated increase in proportion of flakes. Although net transport distance is ～120 km in the beach placer complex, frequent aeolian transport of grains from beach to dunes and subsequent recycling by storm surges substantially increased total transport distance in a dynamic windy tectonic environment. 相似文献
18.
Rodney Grapes Sophia Korzhova Ella Sokol Yurii Seryotkin 《Contributions to Mineralogy and Petrology》2011,162(2):253-273
Sekaninaite (XFe > 0.5)-bearing paralava and clinker are the products of ancient combustion metamorphism in the western part of the Kuznetsk
coal basin, Siberia. The combustion metamorphic rocks typically occur as clinker beds and breccias consisting of vitrified
sandstone–siltstone clinker fragments cemented by paralava, resulting from hanging-wall collapse above burning coal seams
and quenching. Sekaninaite–Fe-cordierite (XFe = 95–45) is associated with tridymite, fayalite, magnetite, ± clinoferrosilite and ±mullite in paralava and with tridymite
and mullite in clinker. Unmelted grains of detrital quartz occur in both rocks (<3 vol% in paralavas and up to 30 vol% in
some clinkers). Compositionally variable siliceous, K-rich peraluminous glass is <30% in paralavas and up to 85% in clinkers.
The paralavas resulted from extensive fusion of sandstone–siltstone (clinker), and sideritic/Fe-hydroxide material contained
within them, with the proportion of clastic sediments ≫ ferruginous component. Calculated dry liquidus temperatures of the
paralavas are 1,120–1,050°C and 920–1,050°C for clinkers, with calculated viscosities at liquidus temperatures of 101.6–7.0 and 107.0–9.8 Pa s, respectively. Dry liquidus temperatures of glass compositions range between 920 and 1,120°C (paralava) and 920–960°C
(clinker), and viscosities at these temperatures are 109.7–5.5 and 108.8–9.7 Pa s, respectively. Compared with worldwide occurrences of cordierite–sekaninaite in pyrometamorphic rocks, sekaninaite occurs
in rocks with XFe (mol% FeO/(FeO + MgO)) > 0.8; sekaninaite and Fe-cordierite occur in rocks with XFe 0.6–0.8, and cordierite (XFe < 0.5) is restricted to rocks with XFe < 0.6. The crystal-chemical formula of an anhydrous sekaninaite based on the refined structure is
| \textK0.02 |(\textFe1.542 + \textMg0.40 \textMn0.06 )\Upsigma 2.00M [(\textAl1.98 \textFe0.022 + \textSi1.00 )\Upsigma 3.00T1 (\textSi3.94 \textAl2.04 \textFe0.022 + )\Upsigma 6.00T2 \textO18 ]. \left| {{\text{K}}_{0.02} } \right|({\text{Fe}}_{1.54}^{2 + } {\text{Mg}}_{0.40} {\text{Mn}}_{0.06} )_{\Upsigma 2.00}^{M} [({\text{Al}}_{1.98} {\text{Fe}}_{0.02}^{2 + } {\text{Si}}_{1.00} )_{\Upsigma 3.00}^{T1} ({\text{Si}}_{3.94} {\text{Al}}_{2.04} {\text{Fe}}_{0.02}^{2 + } )_{\Upsigma 6.00}^{T2} {\text{O}}_{18} ]. 相似文献
19.
V. G. Krivovichev M. V. Charykova O. S. Yakovenko W. Depmeier 《Geology of Ore Deposits》2011,53(7):514-527
The behavior of selenium at the Earth’s surface and nearby at low temperatures and pressures is controlled by variations of
the redox potential and the acidity of solutions. These parameters determine the migration of selenium and its precipitation
as various solid phases. Understanding the mechanism of selenium’s behavior under surface conditions, which is important for
solving environmental problems, is an urgent task of contemporary mineralogy and geochemistry. The activities of components
in natural waters beyond the zones of natural (oxidation zones) and man-made contamination with selenium (a
ΣSe = 10−9, a
ΣFe = 10−5, a
ΣCu = 10−7, a
ΣZn = 5 × 10−7, a
ΣCo = 10−8, a
ΣNi = 6 × 10−8, a
ΣPb = 10−8) and in waters formed in the oxidation zone (a
ΣSe = 10−5–10−4, a
ΣFe = 10−2, a
ΣCu = 10−2, a
ΣZn = 5 × 10−2, a
ΣCo = 10−3, a
ΣNi = 10−2, a
ΣPb = 10−4) have been estimated. Eh-pH diagrams were calculated and plotted using the Geochemist’s Workbench (GMB 7.0) software package.
The database comprises the thermodynamic parameters of 46 elements, 47 main particles, 48 redox pairs, 551 particles in solution,
624 solid phases, and 10 gases. The Eh-pH diagrams of the Me-Se-H2O systems (Me = Co, Ni, Fe, Cu, Zn, Pb) were plotted for the average contents of these elements in underground water and for
their contents in oxidation zones of sulfide deposits. The formation of Co, Ni, Fe, Cu, Zn, and Pb selenites and selenates
at the surface is discussed. 相似文献
20.
Mineralogical studies of the heavy fraction from a Holocene pyrope-rich garnet placer deposit at Vestřev (Krkonoše Piedmont Basin, Bohemian Massif) have identified the presence of very rare grains of platinum group minerals (PGM). Pt–Fe alloy grains are accompanied by Os–Ir–Ru minerals (native osmium, iridium, and ruthenium) with inclusions of Pt–Fe alloy and hongshiite (PtCu). This mineral assemblage is typical for several mantle settings including ophiolites. The chemistry of the Os–Ir–Ru minerals shows an enrichment of the PGM in Ru, which is typical of ophiolites. The grain morphology of PGM and pyrope-rich garnet (mostly rounded with numerous euhedral/subhedral grains) does not exclude a common source. In-situ laser-ablation MC-ICP-MS was used to measure the Re–Os isotopic compositions of single Os-rich grains, which show heterogeneous subchondritic Os isotopic compositions (187Os/188Os = 0.12082–0.12505 ± 0.00003). This precludes their low-temperature origin and indicates derivation of platinum-group elements (PGEs) essentially from mantle-derived rocks without a significant contribution of crustal Os. The mantle model age (TMA) and Re-depletion model age (TRD) model ages range from ~ 0.4 to ~ 1.0 Ga and most likely reflect a long history of melt depletion that affected the mantle sources of PGM. 相似文献