scholarly journals Hydrotermálny bastnäsit-(Ce) zo štôlne Elisabeth pri Gemerskej Polome (Slovenská republika)

2020 ◽  
Vol 28 (1) ◽  
pp. 1-8
Author(s):  
Martin Števko ◽  
Jiří Sejkora ◽  
Zdeněk Dolníček
Keyword(s):  
Infrared Spectra ◽  
Rare Metal ◽  
Coarse Grained ◽  
Unit Cell Parameters ◽  
Cell Parameters ◽  
Quartz Veins ◽  
Hydrothermal Quartz ◽  
Magmatic Fluids ◽  
Type Granite ◽  
Pale Green

Bastnäsite-(Ce), ideally CeCO3F, was recently found at the dumps of the Elisabeth adit near Gemerská Poloma, Rožňava Co., Košice Region, eastern Slovakia. It forms orange-brown aggregates up to 2 × 1 cm with vitreous to greasy lustre, which occur in the hydrothermal quartz veins crosscutting the coarse-grained, porphyritic rare metal S-type granite. Bastnäsite-(Ce) is closely associated with white, pale-green to purple fluorite, siderite and minor pyrite. It is hexagonal, space group P-62c with refined unit-cell parameters: a 7.1354(1) Å, c 9.7954(2) Å and V 431.90(1) Å3. The empirical formula of bastnäsite-(Ce) from the Gemerská Poloma based on sum of all cations = 1 apfu is (Ce0.49 La0.22Nd0.15Pr0.05Sm0.03Th0.02Ca0.02Gd0.01Y0.01)Σ1.00(CO3)1.00F0.83(OH)0.17. The Raman and infrared spectra of bastnäsite-(Ce) as well as tentative assignment of observed bands are given in this paper. Bastnäsite-(Ce) and associated minerals were formed from the early-hydrothermal post-magmatic fluids related to the adjacent granite.

Brumadoite, a new copper tellurate hydrate, from Brumado, Bahia, Brazil

2008 ◽  
Vol 72 (6) ◽  
pp. 1201-1205 ◽  
Author(s):  
D. Atencio ◽  
A. C. Roberts ◽  
P. A. Matioli ◽  
J. A. R. Stirling ◽  
K. E. Venance ◽  
...  
Keyword(s):  
Powder Diffraction ◽  
Infrared Spectra ◽  
Coarse Grained ◽  
New Mineral ◽  
Unit Cell Parameters ◽  
Quartz Crystals ◽  
X Ray ◽  
Cell Parameters ◽  
New Mineral Species ◽  
Spot Tests

AbstractBrumadoite, ideally Cu3Te6+O4(OH)4-5H2O, is a new mineral from Pedra Preta mine, Serra das Eguas. Brumado, Bahia, Brazil. It occurs as microcrystalline aggregates both on and, rarely, pseudomorphous after coarse-grained magnesite, associated with mottramite and quartz. Crystals are platy, subhedral. 1—2 μm in size. Brumadoite is blue (near RHS 114B), has a pale blue streak and a vitreous lustre. It is transparent to translucent and does not fluoresce. The empirical formula is (Cu2.90Pb0.04Ca0.01)Σ2.95 (Te0.936+Si0.05)Σ0.98O3.92(OH)3.84.5.24H2O. Infrared spectra clearly show both (OH) and H2O. Microchemical spot tests using a KI solution show that brumadoite has tellurium in the 6+ state. The mineral is monoclinic, P2/m or P21. Unit-cell parameters refined from X-ray powder data are a 8.629(2) Å, b 5.805(2) Å, c 7.654(2) Å,β 0 103.17(2)°, F 373.3(2) Å3, Z= 2. The eight strongest X-ray powder-diffraction lines [d in Å,(I),(hkl)] are: 8.432,(100),(100); 3.162,(66),(2̄02); 2.385,(27),(220); 2.291,(12),(l̄22); 1.916,(11),(312); 1.666,(14),(4̄22,114); 1.452,(10),(323,040); 1.450,(10),(422,403). The name is for the type locality, Brumado, Bahia, Brazil. The new mineral species has been approved by the CNMNC (IMA 2008-028).

The occurrence of coarse-grained massive tilleyite in the Redcap Creek magmatic skarn, North Queensland

1985 ◽  
Vol 49 (350) ◽  
pp. 71-75 ◽  
Author(s):  
M. J. Rubenach ◽  
C. Cuff
Keyword(s):  
Experimental Data ◽  
Mass Transfer ◽  
Close Agreement ◽  
Igneous Rocks ◽  
Coarse Grained ◽  
Reverse Direction ◽  
Unit Cell Parameters ◽  
Cell Parameters ◽  
Activity Diagrams ◽  
Grey Colour

AbstractEndoskarns formed where a swarm of diorite dykes have intruded calcite marble at Redcap Creek include an inner melilite-dominated, a wollastonite-dominated, and an outer massive tilleyite zone in contact with marble. The massive tilleyite is unusual in that it is coarse-grained (prisms 2–15 cm in length) and its deep grey colour contrasts with the lighter coloured varieties described elsewhere. A chemical analysis gives a formula close to ideal, with only minor substitution of Al, Ti, and Mg. Refined unit cell parameters are in close agreement with those quoted in the literature. The skarns have clearly formed by transport of Si, Mg, Fe, Al, and Ti from the igneous rocks, and Ca in the reverse direction from the marble. Activity diagrams derived from experimental data are most useful in interpreting the zonal sequence of endoskarns, and preliminary results suggest mass transfer at low Xco2 and temperature of the order of 800°C or higher for the formation of the massive tilleyite.

Kapellasite, Cu3Zn(OH)6CI2, a new mineral from Lavrion, Greece, and its crystal structure

2006 ◽  
Vol 70 (3) ◽  
pp. 329-340 ◽  
Author(s):  
W. Krause ◽  
H.-J. Bernhardt ◽  
R.S.W. Braithwaite ◽  
U. Kolitsch ◽  
R. Pritchard
Keyword(s):  
Crystal Structure ◽  
Electron Microprobe ◽  
Empirical Formula ◽  
New Mineral ◽  
Crystal Data ◽  
Secondary Mineral ◽  
Unit Cell Parameters ◽  
Cell Parameters ◽  
Pale Green ◽  
Light Green

AbstractKapellasite, Cu3Zn(OH)6Cl2, is a new secondary mineral from the Sounion No. 19 mine, Kamariza, Lavrion, Greece. It is a polymorph of herbertsmithite. Kapellasite forms crusts and small aggregates up to 0.5 mm, composed of bladed or needle-like indistinct crystals up to 0.2 mm long. The colour is green-blue, the streak is light green-blue. There is a good cleavage parallel to ﹛0001﹜. Kapellasite is uniaxial negative, ω = 1.80(1), ε = 1.76(1); pleochroism is distinct, with E = pale green, O = green-blue. Dmeas = 3.55(10) g/cm3; Dcalc. = 3.62 g/cm3. Electron microprobe analyses of the type material gave CuO 58.86, ZnO 13.92, NiO 0.03, CoO 0.03, Fe2O3 0.04, Cl 16.70, H2O (calc.) 12.22, total 101.80, less O = Cl 3.77, total 98.03 wt.%. The empirical formula is (Cu3.24Zn0.75)Σ3.99(OH)5.94Cl2.06, based on 8 anions. The five strongest XRD lines are [d in Å (I/I0, hkl)] 5.730 (100, 001), 2.865 (11, 002), 2.730 (4, 200), 2.464 (9, 021/201), 1.976 (5, 022/202). Kapellasite is trigonal, space group Pml, unit-cell parameters (from single-crystal data) a = 6.300(1), c = 5.733(1) Å, V= 197.06(6) Å3, Z = 1. The crystal structure of kapellasite is based on brucite-like sheets parallel to (0001), built from edge-sharing distorted M(OH,Cl)6 (M = Cu, Zn) octahedra. The sheets stack directly on each other (…AAA… stacking). Bonding between adjacent sheets is only due to weak hydrogen and O…C1 bonds. The name is in honour of Christo Kapellas (1938–2004), collector and mineral dealer from Kamariza, Lavrion, Greece.

scholarly journals Bohseit z beryl-columbitového pegmatitu D6e v Maršíkově (silezikum, Česká republika)

2020 ◽  
Vol 28 (1) ◽  
pp. 219-223 ◽  
Author(s):  
Zdeněk Dolníček ◽  
Miroslav Nepejchal ◽  
Jiří Sejkora ◽  
Jana Ulmanová ◽  
Štěpán Chládek
Keyword(s):  
Compositional Data ◽  
Coarse Grained ◽  
Powder Diffraction Data ◽  
Unit Cell Parameters ◽  
Orthorhombic Space Group ◽  
X Ray ◽  
Cell Parameters ◽  
Pegmatite Body ◽  
Small Crystals ◽  
Hydrothermal Stage

Bohseite was found in a lenticular body of D6e beryl-columbite granitic pegmatite near Maršíkov, which is hosted by amphibole gneisses of the Sobotín Amphibolite Massif (Silesicum, northeastern part of Czech Republic). Bohseite forms chalky white aggregates up to 1 cm in size, which are hosted by small vugs in the coarse-grained pegmatite. It is associated with small crystals of quartz, adularia, albite, muscovite and epidote. Bohseite is orthorhombic, space group Cmcm with following unit-cell parameters refined from X-ray powder diffraction data: a 23.210(2), b 4.955(2), c 19.428(3) Å and V 2234.5(1.0) Å3. The electron microprobe compositional data of bohseite are presented. Bohseite from Maršíkov contains 14.3 - 42.5 mol. % of bavenite component, up to 0.06 apfu Na and 0.13 - 0.36 apfu F. The association with other beryllium-rich phases (milarite, bertrandite) points to variable activities of Be and Al during hydrothermal stage of evolution of the pegmatite body. The likely source of Be was beryl, which is sometimes completely dissolved and vugs after its crystals are lined by small crystals of above mentioned hydrothermal phases.

scholarly journals Ion-exchange properties of the natural zeolite amicite

2020 ◽  
Vol 39 (2) ◽  
pp. 207
Author(s):  
Nikita V. Chukanov ◽  
Olga N. Kazheva ◽  
Nadezhda A. Chervonnaya ◽  
Dmitry A. Varlamov ◽  
Vera N. Ermolaeva ◽  
...  
Keyword(s):  
Ion Exchange ◽  
Infrared Spectra ◽  
Natural Zeolite ◽  
Unit Cell Volume ◽  
Cell Parameter ◽  
Direct Methods ◽  
Unit Cell ◽  
Unit Cell Parameters ◽  
Cell Parameters ◽  
Exchange Properties

Crystals of the natural zeolite amicite, ideally K4Na4(Al8Si8O32)·10H2O, were ion-exchanged in the reactions with 0.1 N aqueous solutions of AgNO3, RbNO3, CsNO3 and Pb(NO3)2 at 363 K for 24 h. Under these conditions, Cs+ substitutes K+ whereas the most part of Na+ remains unexchanged; Rb+ partly substitutes both Na+ and K+; Pb2+ and Ag+ completely substitute Na+ and K+. All the compounds are monoclinic. The Cs- and Rb-substituted samples have unit-cell parameters close to those of initial amicite. The exchange of Na+ and K+ for Ag+ is accompanied by a significant decrease of the unit-cell volume. The unit-cell parameter c of Pb-amicite is nearly threefold larger than the c parameter of initial amicite. Infrared spectra show that framework topology is preserved during the ion exchange. The crystal structures of initial and Cs-exchanged amicites have been solved by direct methods.

scholarly journals New data on gersdorffite and associated minerals from the Peloritani Mountains (Sicily, Italy)

2021 ◽  
Vol 33 (6) ◽  
pp. 717-726
Author(s):  
Daniela Mauro ◽  
Cristian Biagioni ◽  
Federica Zaccarini
Keyword(s):  
Crystal Structure ◽  
Microprobe Analysis ◽  
Unit Cell ◽  
X Ray Diffraction ◽  
Unit Cell Parameters ◽  
Space Group ◽  
X Ray ◽  
Cell Parameters ◽  
Quartz Veins ◽  
Group I

Abstract. Gersdorffite, ideally NiAsS, and associated minerals from Contrada Zillì (Peloritani Mountains, Sicily, Italy) have been characterized through electron microprobe analysis and X-ray diffraction. Primary minerals, hosted in quartz veins, are represented by gersdorffite, tetrahedrite-(Fe), and chalcopyrite with minor pyrite and galena. Rare aikinite inclusions were observed in tetrahedrite-(Fe) and chalcopyrite. Gersdorffite occurs as euhedral to subhedral crystals, up to 1 mm in size, with (Sb,Bi)-enriched cores and (Fe,As)-enriched rims. Its chemical composition is (Ni0.79−0.95Fe0.18−0.04Co0.04−0.01)(As0.90−1.03Sb0.10−0.00Bi0.02−0.00)S0.98−0.92. It crystallizes in the space group P213, with unit-cell parameters a=5.6968(7) Å, V=184.88(7) Å3, and Z=4, and its crystal structure was refined down to R1= 0.035. Associated tetrahedrite-(Fe) has chemical formula (Cu5.79Ag0.07)Σ5.86(Cu3.96Fe1.59Zn0.45)Σ6.00(Sb3.95As0.17Bi0.03)Σ4.15S13.06, with unit-cell parameters a= 10.3815(10) Å, V=1118.9(3) Å3, and space group I-43m. Its crystal structure was refined to R1=0.027. Textural and crystallographic data suggest a polyphasic crystallization of gersdorffite under low-temperature conditions.

Olivenite and cornwallite from the Podlipa copper deposit near Ľubietová, Slovakia

2021 ◽  
Vol 29 (2) ◽  
pp. 189-196
Author(s):  
Martin Števko ◽  
Jiří Sejkora ◽  
Zdeněk Dolníček
Keyword(s):  
Copper Deposit ◽  
Unit Cell ◽  
Monoclinic Space Group ◽  
Unit Cell Parameters ◽  
Space Group ◽  
Chemical Zoning ◽  
Cell Parameters ◽  
P Content ◽  
Dark Green ◽  
Pale Green

An interesting occurrence of olivenite and cornwallite was recently discovered in cavities of quartz at the Podlipa copper deposit near Ľubietová, Slovakia. Olivenite occurs as olive to pale green sprays or radial aggregates consisting of individual acicular crystals up to 5 mm long. Its refined unit-cell parameters (for the monoclinic space group P21/n) are: a 8.6192(13) Å, b 8.2300(11) Å, c 5.9349(8) Å, α 90.055(12)° and V 420.99(7) Å3. Studied olivenite shows intense chemical zoning caused by strong variation of As and P contents. Most of the zones are corresponding to olivenite (with P content ranging between 0.02 to 0.39 apfu), but darker zones or domains of As-rich libethenite (with As content ranging between 0.18 to 0.24 apfu) were occasionally observed. Cornwallite forms dark green massive fillings between olivenite crystals or microcrystalline botryoidal crusts. The refined unit-cell parameters (for the monoclinic space group P21/c) of botryoidal cornwallite from the Podlipa deposit are: a 4.6112(2) Å, b 5.7698(3) Å, c 17.4167(11) Å, β 92.009(5)° and V 463.10(3) Å3. The two compositional types of cornwallite were distinguished. The first type is represented by relatively homogenous aggregates with only minor contents of P (from 0.04 to 0.22 apfu). The second type occurs as polycrystalline fillings with strong chemical zoning and has much more significant variation of As and P contents, representing solid-solution series between P-rich cornwallite (with 1.41 apfu of As and 0.59 apfu of P) and As-rich pseudomalachite (with 1.37 apfu of P and 0.63 apfu of As).

Albertiniite, Fe2+(SO3)·3H2O, a new sulfite mineral species from the Monte Falò Pb-Zn mine, Coiromonte, Armeno Municipality, Verbano Cusio Ossola Province, Piedmont, Italy

2016 ◽  
Vol 80 (6) ◽  
pp. 985-994 ◽  
Author(s):  
P. Vignola ◽  
G. D. Gatta ◽  
N. Rotiroti ◽  
P. Gentile ◽  
F. Hatert ◽  
...  
Keyword(s):  
Structure Refinement ◽  
Unit Cell ◽  
Iron Sulfides ◽  
X Ray Diffraction ◽  
Unit Cell Parameters ◽  
Calculated Density ◽  
Cell Parameters ◽  
Quartz Veins ◽  
Crystal Unit Cell ◽  
Brittle Fractures

AbstractAlbertiniite, Fe2+(SO3)·3H2O, is a new Fe2+ sulfite trihydrate, related chemically to gravegliaite. It occurs at the Monte Falò Pb-Zn mine near Coiromonte, in the Armeno Municipality, Verbano–Cusio–Ossola Province, Italy. It is an intermediate product of oxidation between iron sulfides and sulfates, forming monoclinic, colourless to pale yellow, transparent crystals with a vitreous lustre. The mineral occurs associated with stolzite, pyromorphite, hinsdalite, plumbogummite, gibbsite, scheelite and jarosite on brittle fractures of quartz veins or chlorite-schist. Albertiniite is optically biaxial (+) with 2V(meas) ≈ 40° and 2V(calc) = 66°. The measured refractive indices, using sodium light (589 nm) are: α = 1.612(2)°, β = 1.618(2)° and γ = 1.632(2)°. The optical axis plane is parallel to the perfect {010} cleavage plane. It is non-fluorescent under shortwave (254 nm) or longwave (366 nm) ultraviolet light. The calculated density is 2.469 g cm–3 (from the crystal-structure refinement), or 2.458 g cm–3 (from the chemical analysis and the single-crystal unit-cell parameters). The empirical formula is (average of 16 spots and based on 3 anhydrous oxygen apfu) (Ca0.001Mg0.001Na0.003)∑1.061(S0.971O3)·2.84H2O, with the H2O content calculated by difference to 100 wt.%. Albertiniite is monoclinic, with space group P21/n. Its unit-cell parameters are: a = 6.633(1), b = 8.831(1), c = 8.773(1) Å, β = 96.106(8)° and V = 511.0(1) Å3, with Z = 4. The eight strongest measured lines in the powder X-ray diffraction pattern are [d in Å, (I/I0), (hkl)]: 4.072 (100) (1̄11), 3.539 (93) (1̄12), 5.533 (27) (1̄01), 6.167 (14) (011), 2.830 (14) (211), 4.998 (14) (101), 4.353 (12) (111) and 3.897 (12) (012). The mineral, which has been approved by the CNMNC, number IMA2015-004, is named albertiniite in honour of Claudio Albertini, an Italian mineral collector and expert in the systematic mineralogy of the Alps and pegmatites.

scholarly journals Mineralogie křemenných žil ložiska cínových rud Hřebečná u Abertam v Krušných horách (Česká republika)

2021 ◽  
Vol 29 (1) ◽  
pp. 131-163
Author(s):  
Jiří Sejkora ◽  
Petr Pauliš ◽  
Michal Urban ◽  
Zdeněk Dolníček ◽  
Jana Ulmanová ◽  
...  
Keyword(s):  
Coarse Grained ◽  
Powder Diffraction Data ◽  
Vein Quartz ◽  
Unit Cell Parameters ◽  
X Ray ◽  
Cell Parameters ◽  
Fine Grained ◽  
Mineral Phases ◽  
Supergene Processes ◽  
Krušné Hory Mountains

An extraordinary rich mineral assemblage (more than 35 determined mineral species) has been discovered in quartz greisen mineralization found at dump material of the abandoned Mauritius mine. This mine is situated about 1 km N of the Hřebečná village, 16 km N of Karlovy Vary, Krušné hory Mountains, Czech Republic. The studied mineralization with its textural and mineralogical character differs significantly from the usual fine-grained greisens mined in this area. The primary mineralization is represented by coarse-grained quartz and fluorapatite with sporadic zircon, monazite-(Ce), xenotime-(Y) and very rare cassiterite. Besides common sulphides (arsenopyrite, chalcopyrite, pyrite, sphalerite, tetrahedrite-group minerals), Bi-sulphosalts (aikinite, bismuthinite, berryite, cuprobismutite, emplectite, wittichenite) were determined. Members of the tetrahedrite group also contain increased amounts of Bi - in addition to Bi-rich tennantite-(Zn) and tennantite-(Fe), microscopic zones represented by the not approved Bi-dominant analogue of tennantite („annivite-(Zn)“) were also found. The primary mineralization was intensively affected by supergene processes. Chalcopyrite and sphalerite are replaced by Cu sulphides - especially anilite and digenite, and more rarely by geerite, spionkopite and covellite. Some of the fluorapatite grains in the vein quartz were decomposed and mrázekite, mixite, libethenite, pseudomalachite, hydroxylpyromorphite, metatorbernite as well as rare dzhalindite crystallized in the resulting cavities. However, the most abundant supergene phases are the minerals of the alunite supergroup - crandallite, goyazite, plumbogummite, svanbergite and waylandite. The detailed descriptions, X-ray powder diffraction data, refined unit-cell parameters and quantitative chemical composition of individual studied mineral phases are presented.

scholarly journals Kivilompolo Mo mineralization in the Peräpohja belt revisited: Trace element geochemistry and Re-Os dating of molybdenite

2020 ◽  
Vol 92 (2) ◽  
pp. 131-150
Author(s):  
Jukka-Pekka Ranta ◽  
◽  
Eero Hanski ◽  
Holly Stein ◽  
Matthew Goode ◽  
...  
Keyword(s):  
Uranium Mineralization ◽  
Coarse Grained ◽  
Geochemical Data ◽  
Trace Element Geochemistry ◽  
Element Geochemistry ◽  
Zircon Age ◽  
Porphyritic Granite ◽  
Quartz Veins ◽  
Nappe Complex ◽  
Magmatic Fluids

The Kivilompolo molybdenite occurrence is located in the northern part of the Peräpoh jabelt, within the lithodemic Ylitornio nappe complex. It is hosted within a deformed porphyritic granite belonging to the pre-orogenic 1.99 Ga Kierovaara suite. The minerali-zation occurs mostly as coarse-grained molybdenite flakes in boudinaged quartz veins, with minor chalcopyrite, pyrite, magnetite, and ilmenite. In this study, we report new geochemical data from the host-rock granite and Re-Os dating results of molybdenite from the mineralization. For the whole-rock geochemistry, the mineralized granite is similar to the Kierovaara suite granites analyzed in previous studies. Also, the ca. 2.0 Ga Re-Os age for molybdenite is equal, within error, to the U-Pb zircon age of the Kierovaara suite granite. In addition, similar molybdenite and uraninite ages have been reported from the Rompas-Rajapalot Au-Co occurrence located 30 km NE of Kivilompolo. We propose that the magmatism at around 2.0 Ga ago initiated the hydrothermal circulation that was responsible for the formation of the molybdenite mineralization at Kivilompolo and the primary uranium mineralization associated with the Rompas-Rajapalot Au-Co occurrence or at least, the magmas provided heating, and in addition potentially saline magmatic fluids and metals from a large, cooling magmatic-hydrothermal system.

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