scholarly journals Omariniite, Cu8Fe2ZnGe2S12, the germanium analogue of stannoidite, a new mineral species from Capillitas, Argentina

2017 ◽  
Vol 81 (5) ◽  
pp. 1151-1159 ◽  
Author(s):  
Luca Bindi ◽  
Hubert Putz ◽  
Werner H. Paar ◽  
Christopher J. Stanley
Keyword(s):  
Polarized Light ◽  
New Mineral ◽  
Polished Section ◽  
Orthorhombic Space Group ◽  
X Ray ◽  
Cell Parameters ◽  
New Mineral Species ◽  
Catamarca Province ◽  
Brownish Black ◽  
The University

AbstractOmariniite, ideally Cu8Fe2ZnGe2S12, represents the Ge-analogue of stannoidite and was found in bornite-chalcocite-rich ores near the La Rosario vein of the Capillitas epithermal deposit, Catamarca Province, Argentina. The mineral is associated closely with three other Ge-bearing minerals (putzite, catamarcaite, rarely zincobriartite) and bornite, chalcocite, digenite, covellite, sphalerite, tennantite, luzonite, wittichenite, thalcusite and traces of mawsonite. The width of the seams rarely exceeds 60 μm, their length can attain several 100 μm. The mineral is opaque, orange-brown in polished section, has a metallic lustre and a brownish-black streak. It is brittle, and the fracture is irregular to subconchoidal. Neither cleavage nor parting are observable in the sections. In plane-polarized light omariniite is brownish-orange and has a weak pleochroism. Internal reflections are absent. The mineral is distinctly anisotropic with rotation tints varying between brownish-orange and greenish-brown. The average result of 45 electron-microprobe analyses is Cu 42.18(34), Fe 9.37(26), Zn 5.17(43), In 0.20(6), Ge 11.62(22), S 31.80(20), total 100.34(46) wt.%. The empirical formula, based on Σ(Me + S) = 25, is Cu8.04(Fe2.03In0.02)Σ2.05Zn0.96 Ge1.94S12.01, ideally Cu8+Fe2+Zn2+Ge24+S122-. Omariniite is orthorhombic, space group I222, with unit-cell parameters: a = 10.774(1), b = 5.3921(5), c = 16.085(2) Å, V = 934.5(2) Å3, a:b:c = 1.9981:1:2.9831, Z = 2. X-ray single-crystal studies (R1 = 0.023) revealed the structure to be a sphalerite derivative identical to that of stannoidite. Omariniite is named after Dr. Ricardo Héctor Omarini (1946–2015), Professor at the University of Salta, for his numerous contributions to the geology of Argentina.

Aurivilliusite, Hg2+HgI+OI, a new mineral species from the Clear Creek claim, San Benito County, California, USA

2004 ◽  
Vol 68 (2) ◽  
pp. 241-245 ◽  
Author(s):  
A. C. Roberts ◽  
J. A. R. Stirling ◽  
A. J. Criddle ◽  
G. E. Dunning ◽  
J. Spratt
Keyword(s):  
Inorganic Compounds ◽  
Red Light ◽  
New Mineral ◽  
Polished Section ◽  
Calculated Density ◽  
X Ray ◽  
Cell Parameters ◽  
Surface Patches ◽  
New Mineral Species ◽  
The University

AbstractAurivilliusite, ideally Hg2+Hg1+OI, is monoclinic, C 2/c, with unit-cell parameters refined from X-ray powder data: a= 17.580(6), b= 6.979(1), c= 6.693(3)Å, β = 101.71(4)°, V = 804.0(5)Å3, a:b:c= 2.5190:1:0.9590,Z = 8. The strongest six lines of the X-ray powder-diffraction pattern [din Å (I )(hkl)] are: 8.547(70)(200), 3.275(100)(002), 2.993(80)(2̄21), 2.873(80)(600), 2.404(50b)(6̄02, 421, 2̄22) and 1.878(50)(2̄23). This extremely rare mineral was collected from a small prospect pit near the longabandoned Clear Creek mercury mine, New Idria district, San Benito County, California, USA. It is intimately intermixed with another new undefined Hg-O-I phase (‘CCUK-15’), and is also closely associated with native mercury, cinnabar and edgarbaileyite in a host rock principally composed of quartz and magnesite. Aurivilliusite occurs in a cm-wide quartz vein predominantly as irregular-shaped thin patches ‘splattered’ on the quartz surface; patches vary in size from 10–20 μm up to 0.5 mm. The only known subhedral platy brightly reflecting crystal fragment, with major ﹛100﹜ form and distinct ﹛100﹜ cleavage, did not exceed 0.2 mm in longest dimension. The mineral is dark grey-black with a dark red-brown streak. Physical properties include: metallic lustre; opaque; non-fluorescent; brittle; uneven fracture; calculated density 8.96 g/cm3 (empirical formula), 8.99 g/cm3 (ideal formula). In polished section in plane-polarized reflected light, aurivilliusite resembles cinnabar, is extremely light sensitive, shows twinning and no internal reflections, and exhibits an unusual ‘red light’ coalescing phenomena. Averaged and corrected results of electron-microprobe analyses yielded HgO 40.10, Hg2O 38.62, I 22.76, Br 0.22, Cl 0.06, sum 101.76, less O = I + Br + Cl –1.46, total 100.30 wt.%, corresponding to Hg1.002+Hg1.001+ O1.01(I0.97Br0.01Cl0.01)Σ0.99, based on O + I + Br + Cl = 2 atoms per formula unit (a.p.f.u.). The original value for Hg, 74.27 wt.%, was partitioned in a HgO:Hg2O ratio of 1:1 after the discovery of the crystal-structure paper dealing with the synthetic equivalent of aurivilliusite. The mineral name is in honour of the late Dr Karin Aurivillius (1920 –1982), chemistcrystallographer at the University of Lund, Sweden, for her significant contributions to the crystal chemistry of Hg-bearing inorganic compounds. Aurivilliusite is related chemically to terlinguaite, Hg2+Hg1+OCl, but has a different structure and X-ray characteristics.

Juabite, Cu5(Te6+O4)2(As5+O4)2.3H2O. a new mineral species from the Centennial Eureka mine, Juab County, Utah

1997 ◽  
Vol 61 (404) ◽  
pp. 139-144 ◽  
Author(s):  
Andrew C. Roberts ◽  
Robert A. Gault ◽  
Martin C. Jensen ◽  
Alan J. Criddle ◽  
Elizabeth A. Moffatx
Keyword(s):  
Infrared Absorption Spectrum ◽  
New Mineral ◽  
Polished Section ◽  
Triclinic Space Group ◽  
X Ray ◽  
Cell Parameters ◽  
New Mineral Species ◽  
Reflected Light ◽  
O 19 ◽  
Pale Green

AbstractJuabite, ideally Cu5(Te6+O4)2(As5+O4)2·3H2O, is triclinic, space-group choices P1(1) or P(2), with unit-cell parameters refined from powder data: a = 8.984(5), b = 10.079(7), c = 8.975(5) Å, α = 102.68(7)°, β = 92.45(6)°, γ = 70.45(5)° V = 746.8(8) Å3, a:b:c = 0.8914:1:0.8905, Z = 2. The strongest seven reflections of the X-ray powder-diffraction pattern [d in Å (I)(hkl)] are: 9.28 (70)(010), 4.65 (70)(020), 3.097 (100)(030,11), 3.018 (60)(212), 2.658 (50)(01), 2.468 (50)(2) and 1.740 (50)(1, 521, 5). The mineral is an extremely rare constituent on the dumps of the Centennial Eureka mine, Juab County, Utah, U.S.A., where it occurs as crystalline platy masses that average 0.2–0.3 mm in longest dimension within small interconnected vugs of drusy quartz. Associated minerals are enargite, beudantite, and an undefined, possible Pb-analogue of arsenobismite. Individual crystals are subhedral to euhedral and average 125 × 100 × 1–2 µm in size. Cleavage {010} perfect. Forms are: {010} major; {100}, {01}, and {101} minor. The mineral is translucent (masses) to transparent (crystals), emerald-green, with a pale green streak, and an uneven to subconchoidal fracture. Juabite is vitreous to adamantine (almost gemmy) on cleavage faces, brittle, and nonfluorescent; H (Mohs) 3–4; D (calc.) 4.59 g/cm3 for the idealised formula. In polished section, juabite is white in plane-polarised reflected light in air with ubiquitous turquoise-blue internal reflections; bireflectance and anisotropy are unknown (due to interference from internal reflections). Averaged electronmicroprobe analyses yielded CuO 38.25, PbO 0.57, TeO3 32.58, As2O5 22.81, H2O (calc. assuming 3H2O) [5.19], total [99.40] wt.%, leading to the empirical formula (Cu5.01Pb0.03)Σ5.04(TeO4)l.93(AsO4)2.07·3.00H2O based on O = 19. The infrared absorption spectrum shows definite bands for structural H2O with an O-H stretching frequency centred at 3283 cm−1 and a H-O-H flexing frequency centred at 1642 cm−1. The mineral name is for the county within the state of Utah in which the Centennial Eureka mine is located.

Shannonite, Pb2OCO3, a new mineral from the Grand Reef Mine, Graham County, Arizona, USA

1995 ◽  
Vol 59 (395) ◽  
pp. 305-310 ◽  
Author(s):  
A. C. Roberts ◽  
J. A. R. Stirling ◽  
G. J. C. Carpenter ◽  
A. J. Criddle ◽  
G. C. Jones ◽  
...  
Keyword(s):  
Empirical Formula ◽  
Short Wave ◽  
New Mineral ◽  
Orthorhombic Space Group ◽  
Weak Anisotropy ◽  
Calculated Density ◽  
X Ray ◽  
Cell Parameters ◽  
New Mineral Species ◽  
Transmission Electron

AbstractShannonite, ideally Pb2OCO3, is a new mineral species that occurs as mm-sized white porcellanous crusts, associated with fluorite, at the Grand Reef mine, Graham County, Arizona, USA. Other associated minerals are plumbojarosite, hematite, Mn-oxides, muscovite-2M1, quartz, litharge, massicot, hydrocerussite, minium, and unnamed PbCO3·2PbO. Shannonite is orthorhombic, space group P21221 or P212121, with unit-cell parameters (refined from X-ray powder data): a 9.294(3), b 9.000(3), c 5.133(2) Å, V 429.3(3) Å3, a:b:c 1.0327:1:0.5703, Z = 4. The strongest five lines in the X-ray powder pattern [d in Å (I)(hkl)] are: 4.02(40)(111); 3.215(100)(211); 3.181(90)(121); 2.858(40)(130); 2.564(35)(002). The average of eight electron microprobe analyses is PbO 89.9(5), CO2 (by CHN elemental analyser) 9.70, total 99.60 wt.%. With O = 4, the empirical formula is Pb1.91C1.05O4.00. The calculated density for the empirical formula is 7.31 and for the idealized formula is 7.59 g/cm3. In reflected light, shannonite is colourless-grey to white, with ubiquitous white internal reflections (× 16 objectives), weak anisotropy, barely detectable bireflectance, and no evidence of pleochroism. The calculated refractive index (at 590 nm) is 2.09. Measured reflectance values in air and in oil (× 4 objectives) are tabulated. Transmission electron-microscopy studies reveal that individual crystallites range in size from 10–400 nm, are platy, and are anhedral. Physical properties for cryptocrystalline crusts include: white streak; waxy lustre; opaque; nonfluorescent under both long- and short-wave ultraviolet light; uneven fracture; brittle; VHN100 97 (range 93–100); calculated Mohs’ hardness 3–3½. Shannonite is soluble in concentrated HCl and in dilute HNO3 and H2SO4. The mineral name is for David M. Shannon, who helped collect the samples and who initiated this study.

Fluoro-potassic-pargasite, KCa2(Mg4Al)(Si6Al2)O22F2, from the Tranomaro area, Madagascar: mineral description and crystal chemistry

2010 ◽  
Vol 74 (6) ◽  
pp. 961-967 ◽  
Author(s):  
R. Oberti ◽  
M. Boiocchi ◽  
F. C. Hawthorne ◽  
R. Pagano ◽  
A. Pagano
Keyword(s):  
Polarized Light ◽  
Mineral Species ◽  
New Mineral ◽  
Monoclinic Space Group ◽  
Formula Unit ◽  
X Ray ◽  
New Mineral Species ◽  
Mohs Hardness ◽  
Brownish Black ◽  
Amphibole Crystal

AbstractFluoro-potassic-pargasite, ideally AKBCa2C(Mg4Al) (Si6Al2)O22WF2, a new amphibole species, has been found in a skarn in the Tranomaro area, Madgascar. The sample used for the description of the new mineral species is a large single amphibole crystal, 4 mm × 2 mm × 2 cm in size, brownish-black with brownish-yellow phlogopite lamellae adhering to one face of the crystal. Fluoro-potassic-pargasite is brittle, has a Mohs hardness of 6.5 and a splintery fracture; it is non-fluorescent, has perfect {110} cleavage, no observable parting, and has measured and calculated densities of 3.46 and 3.151 g cm−3, respectively. In plane-polarized light, it is pleochroic, X = colourless to very pale grey, Y = very pale grey, Z = colourless; X ^ a = 46.9° (in β obtuse), Y ‖ b, Z ^ c = 31.4° (in β acute). It is biaxial positive, α = 1.638(2), β = 1.641(2), γ = 1.653(2); 2Vobs = 49.6(4)°, 2Vcalc = 53.4°.Fluoro-potassic-pargasite is monoclinic, space group C2/m, a = 9.9104(2), b = 17.9739(4), c = 5.3205(1) Å, β = 105.534(2)°, V = 913.11(6) Å3, Z = 2. The eight strongest lines in the X-ray powder-diffraction pattern are [d in Å(I)(hkl)]: 3.133(100)(310), 3.270(55)(240), 2.809(47)(330). 8.413(45)(110), 2.698(39)(151), 3.374(31)(131), 2.934(29)(221) and 1.647(29)(461). Electron microp-robe analysis gives SiO2 40.20, Al2O3 17.61, TiO2 0.46, FeO 1.96, Fe2O3 2.51, MgO 16.95, MnO 0.05, CaO 13.18, Na2O 0.99, K2O 3.72, F 2.75, H2Ocalc 0.77, sum 99.99 wt.%. The formula unit, calculated on the basis of 24 (O,OH,F) with (OH + F) = 2 - (2 × Ti), is A(K0.69Na0.28Ca0.04)∑=1.01BCa2.00C(Mg3.64Fe0.242+Mn0.01Al0.79Fe0.273+Ti0.05)∑=5.00T(Si5.80Al2.20)∑=8.00O22W[F1.26(OH)0.74]∑=2.00. The mineral species and name have been approved by the IMA CMNMC (IMA 2009-091).

scholarly journals Isselite, Cu6(SO4)(OH)10(H2O)4⋅H2O, a new mineral species from Eastern Liguria, Italy

2020 ◽  
Vol 84 (5) ◽  
pp. 653-661
Author(s):  
Cristian Biagioni ◽  
Donato Belmonte ◽  
Cristina Carbone ◽  
Roberto Cabella ◽  
Nicola Demitri ◽  
...  
Keyword(s):  
New Mineral ◽  
Optical Orientation ◽  
X Ray Diffraction ◽  
Unit Cell Parameters ◽  
Orthorhombic Space Group ◽  
Light Blue ◽  
X Ray ◽  
Cell Parameters ◽  
New Mineral Species ◽  
Mining Complex

AbstractThe new mineral isselite, Cu6(SO4)(OH)10(H2O)4⋅H2O, has been discovered in the Lagoscuro mine, Monte Ramazzo mining complex, Genoa, Eastern Liguria, Italy. It occurs as sprays of blue acicular crystals, up to 0.1 mm long, associated with brochantite and posnjakite. Streak is light blue and the lustre is vitreous. Isselite is brittle, with irregular fracture and good cleavage on {001} and {100}. Measured density is 3.00(2) g/cm3. Isselite is optically biaxial (–), with α = 1.599(2), β = 1.633(2) and γ = 1.647(2) (determined in white light). The measured 2V is 63.6(5)°. Dispersion is moderate, with r > v. The optical orientation is X = b, Y = c and Z = a. Isselite is pleochroic, with X = light blue, Y = blue, Z = blue; X << Z < Y. Electron microprobe analyses give (wt.%): SO3 11.45(21), MgO 0.31(7), CoO 1.07(14), NiO 9.41(90), CuO 51.29(126), ZnO 1.10(20), H2Ocalc 24.21, total 98.84. The empirical formula of isselite, based on Σ(Mg,Co,Ni,Cu,Zn) = 6 atoms per formula unit, is (Cu4.80Ni0.94Co0.11Zn0.10Mg0.06)Σ6.00(S1.06O4.19)(OH)10⋅5H2O. Isselite is orthorhombic, space group Pmn21, with unit-cell parameters a = 6.8070(14), b = 5.8970(12), c = 20.653(4) Å, V = 829.0(3) Å3 and Z = 2. The crystal structure of isselite was refined from single-crystal X-ray diffraction data to R1 = 0.067 on the basis of 2964 reflections with Fo > 4σ(Fo). It shows a layered structure formed by zig-zag {001} layers of Cu-centred polyhedra. Sulfate groups occur in the interlayer along with one H2O group. Isselite is chemically related to redgillite and montetrisaite.

Hanawaltite, Hg1+6Hg2+[Cl,(OH)]2O3—A new mineral from the Clear Creek claim, San Benito County, California: Description and crystal structure

1996 ◽  
Vol 11 (1) ◽  
pp. 45-50 ◽  
Author(s):  
Andrew C. Roberts ◽  
Joel D. Grice ◽  
Robert A. Gault ◽  
Alan J. Criddle ◽  
Richard C. Erd
Keyword(s):  
Crystal Structure ◽  
Powder Diffraction ◽  
Polarized Light ◽  
Structural Features ◽  
New Mineral ◽  
Single Fracture ◽  
Polished Section ◽  
Calculated Density ◽  
X Ray ◽  
Cell Parameters

Hanawaltite, ideally Hg1+6Hg2+O3Cl2, is orthorhombic, Pbma (57), with unit-cell parameters refined from powder data: a=11.790(3), b=13.881(4), c=6.450(2) Å, V=1055.7(6) Å3, a:b:c =0.8494:1:0.4647, Z=4. The strongest six lines of the X-ray powder-diffraction pattern [d in Å (I)(hkl)] are: 5.25 (80)(111), 3.164 (60)(231), 3.053 (100)(041), 2.954 (70)(141), 2.681 (50)(401), and 2.411 (50)(232,341). The mineral is an extremely rare constituent in a small prospect pit near the long-abandoned Clear Creek mercury mine, New Idria district, San Benito County, California. It was found on a single-fracture surface where it is intimately associated with calomel, native mercury, cinnabar, montroydite, and quartz. Individual crystals are subhedral to anhedral, platy to somewhat bladed, and average about 50 μm in longest dimension. The largest known crystal is approximately 0.3×0.3 mm in size and is striated parallel [001]. Hanawaltite is opaque to translucent (on very thin edges), black to very dark brown–black in color, with a black to dark red–brown streak. Other physical properties include: metallic luster; cleavage {001} good; uneven fracture; brittle; nonfluorescent; H<5; calculated density (for the empirical formula) 9.51 g/cm3.In polished section, hanawaltite is moderately to strongly bireflectant and is pleochroic white (RI) to blue–white (R2). In reflected plane-polarized light, it is white with orange–red internal reflections in very thin grains and at grain margins. The anisotropy is strong with bright metallic blue rotation tints. Measured reflectance values, in air and in oil, are tabulated. Electron-microprobe analysis yielded Hg2O 82.46, HgO 14.27, Cl 3.33, H2O [0.34], sum [100.40], less O=Cl 0.75, total [99.65] wt. %, corresponding to Hg1+6.00Hg2+1.00 [Cl1.43(OH)0.57]Σ2.00O3.00, based on O+Cl=5. After the crystal structure was determined, the original microprobe value for Hg2O, 96.2, was partitioned in a ratio of 6Hg2O:HgO and (OH) was calculated, such that Cl+(OH)=2. The hanawaltite structure consists of undulatory [Hg–Hg]2+ ribbons which roughly parallel (100). The diatomic [Hg–Hg]2+ groups have anion tails which, in turn, serve as cross linkages between dimer ribbons through [Hg2+O2Cl2] planar rhombs. The structure is compared to that of other mercury oxychlorides and each is found to have its own unique structural features. This structural diversity is attributed to the inherent ability of mercury to adopt either metallic or ionic types of bonds. The mineral name honors the late Dr. J. D. (Don) Hanawalt (1903–1987), who was a pioneer in the field of X-ray powder diffraction.

Dalnegroite, Tl5–xPb2x(As,Sb)2l–xS34, a new thallium sulphosalt from Lengenbach quarry, Binntal, Switzerland

2009 ◽  
Vol 73 (6) ◽  
pp. 1027-1032 ◽  
Author(s):  
F. Nestola ◽  
A. Guastoni ◽  
L. Bindi ◽  
L. Secco
Keyword(s):  
Polarized Light ◽  
New Mineral ◽  
X Ray Diffraction ◽  
X Ray ◽  
Elemental Concentrations ◽  
Reflected Light ◽  
Mohs Hardness ◽  
The Mean ◽  
The University ◽  
Probable Space

AbstractDalnegroite, ideally Tl4Pb2(As12Sb8)Σ20S34, is a new mineral from Lengenbach, Binntal, Switzerland. It occurs as anhedral to subhedral grains up to 200 μm across, closely associated with realgar, pyrite, Sb-rich seligmanite in a gangue of dolomite. Dalnegroite is opaque with a submetallic lustre and shows a brownish-red streak. It is brittle; the Vickers hardness (VHN25) is 87 kg mm-2(range: 69—101) (Mohs hardness ∼3—3½). In reflected light, dalnegroite is highly bireflectant and weakly pleochroic, from white to a slightly greenish-grey. In cross-polarized light, it is highly anisotropic with bluish to green rotation tints and red internal reflections.According to chemical and X-ray diffraction data, dalnegroite appears to be isotypic with chabournéite, Tl5-xPb2x(Sb,As)21-xS34. It is triclinic, probable space groupP1, witha= 16.217(7) Å,b= 42.544(9) Å,c= 8.557(4) Å, α = 95.72(4)°, β = 90.25(4)°, γ = 96.78(4)°,V= 5832(4) Å3,Z= 4.The nine strongest powder-diffraction lines [d(Å) (I/I0) (hkl)] are: 3.927 (100) (10 0); 3.775 (45) (22); 3.685 (45) (60); 3.620 (50) (440); 3.124 (50) (2); 2.929 (60) (42); 2.850 (70) (42); 2.579 (45) (02); 2.097 (60) (024). The mean of 11 electron microprobe analyses gave elemental concentrations as follows: Pb 10.09(1) wt.%, Tl 20.36(1), Sb 23.95(1), As 21.33(8), S 26.16(8), totalling 101.95 wt.%, corresponding to Tl4.15Pb2.03(As11.86Sb8.20)S34. The new mineral is named for Alberto Dal Negro, Professor in Mineralogy and Crystallography at the University of Padova since 1976.

Bassoite, SrV3O7·4H2O, a new mineral from Molinello mine, Val Graveglia, eastern Liguria, Italy

2011 ◽  
Vol 75 (5) ◽  
pp. 2677-2686 ◽  
Author(s):  
L. Bindi ◽  
C. Carbone ◽  
R. Cabella ◽  
G. Lucchetti
Keyword(s):  
Structure Refinement ◽  
Full Professor ◽  
New Mineral ◽  
Monoclinic Space Group ◽  
Calculated Density ◽  
X Ray ◽  
Cell Parameters ◽  
Mohs Hardness ◽  
Dark Green ◽  
The University

AbstractBassoite, ideally SrV3O7·4H2O, is a new mineral from the Molinello manganese mine, Val Graveglia. eastern Liguria, northern Apennines, Italy. It occurs as black euhedral to subhedral grains up to 400 urn across, closely associated with rhodonite, quartz and braunite. Bassoite is opaque with a sub-metallic lustre and a black streak. It is brittle and neither fracture nor cleavage was observed; the Vickers micro-hardness (VHN100) is 150 kg/mm (range 142—165; corresponding to a Mohs hardness of 4—41/2). The calculated density is 2.940 g/cm3 (on the basis of the empirical formula and X-ray single-crystal data). Bassoite is weakly bireflectant and very weakly pleochroic from grey to a dark green. Internal reflections are absent. The mineral is anisotropic, without characteristic rotation tints. Reflectance percentages (Rmin and Rmax) for the four standard COM wavelengths are 18.5%, 19.0% (471.1 nm); 17.2%, 17.8% (548.3 nm); 16.8%, 17.5% (586.6 nm) and 16.2%, 16.8% (652.3 nm), respectively.Bassoite is monoclinic, space group P21/m, with unit-cell parameters: a = 5.313(3) Å, b = 10.495(3) Å, c = 8.568(4) Å, β = 91.14(5)°, V= 477.7(4) Å3, a:b:c = 0.506:1:0.816, and Z = 2. The crystal structure was refined to R1 = 0.0209 for 1148 reflections with Fo > 4σ(Fo) and it consists of layers of VO5 pyramids (with vanadium in the tetravalent state) pointing up and down alternately with Sr between the layers (in nine-fold coordination). The nine most intense X-ray powder-diffraction lines [d in Å (I/I0) (hkt)] are: 8.5663 (100) (001); 6.6363 (14) (011); 3.4399 (14) (1̄21); 3.4049 (17) (121); 2.8339 (15) (1̄22); 2.7949 (11) (122); 2.6550 (15) (200); 2.6237 (11) (040) and 1.8666 (15) (240). Electron microprobe analyses produce a chemical formula (Sr0.97Ca0.02Na0.01)V3.00O74H20, on the basis of 2(Sr+Ca+Na) = 1, taking the results of the structure refinement into account. The presence of water molecules was confirmed by micro-Raman spectroscopy. The name honours Riccardo Basso (b. 1947), full professor of Mineralogy and Crystallography at the University of Genova. The new mineral and mineral name have been approved by the Commission on New Minerals, Nomenclature and Classification, IMA (2011-028).

scholarly journals Crystallochemical aspects of two microlite-group new mineral species

2014 ◽  
Vol 70 (a1) ◽  
pp. C1095-C1095
Author(s):  
Marcelo Andrade ◽  
Javier Ellena ◽  
Daniel Atencio
Keyword(s):  
Microprobe Analysis ◽  
Electron Microprobe Analysis ◽  
New Mineral ◽  
X Ray Diffraction ◽  
Unit Cell Parameters ◽  
Space Group ◽  
X Ray ◽  
Cell Parameters ◽  
New Mineral Species ◽  
Group 1

Fluorcalciomicrolite, Ca1.5Ta2O6F, and hydroxycalciomicrolite, Ca1.5Ta2O6(OH), are new microlite-group [1] minerals found in the Volta Grande pegmatite, Nazareno, Minas Gerais, Brazil. Both occur as octahedral and rhombododecahedral crystals. The crystals are colourless, yellow and translucent, with vitreous to resinous luster. The densities calculated for fluorcalciomicrolite [2] and hydroxycalciomicrolite are 6.160 and 6.176 g/cm3, respectively. The empirical formulae obtained from electron microprobe analysis are (Ca1.07Na0.81□0.12)Σ2(Ta1.84Nb0.14Sn0.02)Σ2[O5.93(OH)0.07]Σ6.00[F0.79(OH)0.21] for fluorcalciomicrolite and (Ca1.48Na0.06Mn0.01)Σ1.55(Ta1.88Nb0.11Sn0.01)Σ2O6[(OH)0.76F0.20O0.04] for hydroxycalmicrolite. Fluorcalciomicrolite is cubic, space group Fd-3m, a = 10.4191(6) Å, V = 1131.07(11) Å3, and Z = 8. Hydroxycalciomicrolite is also cubic; however, the presence of P-lattice is confirmed by the large number of weak reflections observed by X-ray diffraction. As a result, the space group is P4332 and unit-cell parameters are a = 10.4211(8) Å, and V = 1131.72(15) Å3.

Leisingite, Cu(Mg,Cu,Fe,Zn)2Te6+O6·6H2O, a new mineral species from the Centennial Eureka mine, Juab County, Utah

1996 ◽  
Vol 60 (401) ◽  
pp. 653-657 ◽  
Author(s):  
Andrew C. Roberts ◽  
Lee A. Groat ◽  
Joel D. Grice ◽  
Robert A. Gault ◽  
Martin C. Jensen ◽  
...  
Keyword(s):  
Absorption Spectrum ◽  
Infrared Absorption Spectrum ◽  
Thin Plates ◽  
New Mineral ◽  
Unit Cell Parameters ◽  
X Ray ◽  
Cell Parameters ◽  
Pale Yellow ◽  
Orange Yellow ◽  
New Mineral Species

AbstractLeisingite, ideally Cu(Mg,Cu,Fe,Zn)2Te6+O6·6H2O, is hexagonal, P3 (143), with unit-cell parameters refined from powder data: a = 5.305(1), c = 9.693(6) Å, V = 236.2(2) Å3, c/a = 1.8271, Z = 1. The strongest six reflections of the X-ray powder-diffraction pattern [d in Å (I) (hkl)] are: 9.70 (100) (001), 4.834 (80) (002), 4.604 (60) (100), 2.655 (60) (110), 2.556 (70) (111) and 2.326 (70) (112). The mineral is found on the dumps of the Centennial Eureka mine, Juab County, Utah U.S.A. where it occurs as isolated, or rarely as clusters of, hexagonal-shaped very thin plates or foliated masses in small vugs of crumbly to drusy white to colourless quartz. Associated minerals are jensenite, cesbronite and hematite. Individual crystals are subhedral to euhedral and average less than 0.1 mm in size. Cleavage {001} perfect. Forms are: {001} major; {100}, {110} minute. The mineral is transparent to somewhat translucent, pale yellow to pale orange-yellow, with a pale yellow streak and an uneven fracture. Leisingite is vitreous with a somewhat satiny to frosted appearance, brittle to somewhat flexible and nonfluorescent; H(Mohs) 3–4; D(calc.) 3.41 for the idealized formula; uniaxial negative, ω = 1.803(3), ɛ = 1.581 (calc.). Averaged electron-microprobe analyses yielded CuO 24.71, FeO 6.86, MgO 6.19, ZnO 0.45, TeO3 36.94, H2O (calc.) [21.55], total [96.70] wt.%, leading to the empirical formula based on O = 12. The infrared absorption spectrum shows definite bands for structural H2O with an O-H stretching frequency centered at 3253 cm−1 and a H-O-H flexing frequency centered at 1670 cm−l. The mineral name honours Joseph F. Leising, Reno, Nevada, who helped collect the discovery specimens.

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