Limousinite, BaCa[Be4P4O16]·6H2O, a New Beryllophosphate Mineral with a Phillipsite-Type Framework

2020 ◽  
Author(s):  
Frédéric Hatert ◽  
Fabrice Dal Bo ◽  
Yannick Bruni ◽  
Nicolas Meisser ◽  
Pietro Vignola ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Cross Sections ◽  
Natural Zeolite ◽  
Structure Refinement ◽  
Site Occupancy ◽  
New Mineral ◽  
Zeolite Framework ◽  
Calculated Density ◽  
Zeolite Type ◽  
Wavelength Light

Abstract Limousinite, ideally BaCa[Be4P4O16]·6H2O, is a new beryllophosphate mineral discovered in the Vilatte-Haute pegmatite, Chanteloube near Razès, Limousin, Haute-Vienne, France. The new mineral is intimately associated with microcrystalline pale brown greifensteinite, black amorphous vitreous Mn-oxyhydroxide, triplite, and quartz. It forms isolated, partly corroded, colorless to snow-white crystals up to 0.9 mm long, showing rhombic cross sections. Limousinite is transparent with a vitreous luster, non-fluorescent, without cleavage planes; its calculated density is 2.58 g/cm3. Optically, the mineral is biaxial negative, α = 1.532(2), β = 1.553(3), γ = 1.558(2) (measured under 589 nm wavelength light), 2Vcalc. = 18°, non-dispersive, with Z parallel to the elongation of the prismatic crystals. Electron-microprobe analyses indicate an empirical formula of (Ba0.91K0.07)Σ0.98(Ca0.87Na0.05)Σ0.92[(Be3.87Al0.13)Σ4P4O16]·5.56H2O, calculated on the basis of 4 P atoms per formula unit, assuming 4 (Be + Al) pfu and a water content calculated from refined site-occupancy factors. A single-crystal structure refinement was performed to R1 = 4.90%, in the P21/c space group, with a = 9.4958(4), b = 13.6758(4), c = 13.4696(4) Å, β = 90.398(3)°, V = 1749.15(10) Å3, Z = 4. The crystal structure is characterized by a beryllophosphate framework similar to that of phillipsite-group zeolites, based on corner-sharing BeO4 and PO4 tetrahedra forming interconnected four- and eight-membered rings. Large cages within this zeolite framework contain Ba, Ca, and water molecules. Limousinite is the third known natural zeolite-type beryllophosphate, together with pahasapaite and wilancookite; it is also the first phosphate with a framework identical to that of a natural zeolite silicate.

scholarly journals Fluoro-aluminoleakeite, NaNa2(Mg2Al2Li)Si8O22F2, a new mineral of the amphibole group from Norra Kärr, Sweden: description and crystal structure

2009 ◽  
Vol 73 (5) ◽  
pp. 817-824 ◽  
Author(s):  
R. Oberti ◽  
F. Cámaraite ◽  
F. C. Hawthorne ◽  
N. A. Ball
Keyword(s):  
Crystal Structure ◽  
Structure Refinement ◽  
Polarized Light ◽  
Crystal Structure Analysis ◽  
New Mineral ◽  
Monoclinic Space Group ◽  
Calculated Density ◽  
Greenish Blue ◽  
Dark Green ◽  
Pale Green

AbstractFluoro-aluminoleakeite, ideally , is a new mineral of the amphibole group from Norra Kärr, Sweden (IMA-CNMMNC 2009-012). It occurs in a proterozoic alkaline intrusion that mainly comprises a fine-grained schistose agpaitic nepheline-syenite (grennaite). Fluoro- aluminoleakeite occurs as isolated prismatic crystals 0.10–2 mm long in a syenitic matrix. Crystals are light greenish-blue with a greenish-blue streak. It is brittle, has a Mohs hardness of 6 and a splintery fracture; it is non-fluorescent with perfect {110} cleavage, no observable parting, and has a calculated density of 3.14 g cm–3. In plane-polarized light, it is pleochroic, X = pale green, Y = dark green, Z = pale green; X ^ a = 62.9° (in β obtuse), Y || b. Fluoro-aluminoleakeite is biaxial negative, α = 1.632(1), β = 1.638(1), γ = 1.643(1); 2Vobs. = 98.0(4)°, 2Vcalc. = 95.5°.MFluoro-aluminoleakeite is monoclinic, space group C2/m, a = 9.7043(5) Å, b = 17.7341(8) Å, c = 5.2833(3) Å, β = 104.067(4)°, V = 882.0(2) Å3, Z = 2. The eight strongest X-ray diffraction lines in the powder-diffraction pattern are [d in Å, (I), (hkl)]: 2.687, (100), (31, 151); 4.435, (80), (021, 040); 3.377, (80), (131); 2.527, (60), (02); 8.342, (50), (110); 3.096, (40), (310); 2.259, (40), (71, 12) and 2.557, (30), (002, 061). Analysis, by a combination of electron microprobe and crystal-structure refinement, gives SiO2 58.61, Al2O3 7.06, TiO2 0.32, FeO 3.27, Fe2O3 6.05, MgO 8.61, MnO 0.73, ZnO 0.43, CaO 0.05, Na2O 9.90, K2O 2.43, Li2O 1.62, F 3.37, H2Ocalc. 0.50, sum 101.08 wt.%. The formula unit, calculated on the basis of 24 (O,OH,F,Cl) p.f.u. with (OH) + F = 2 a.p.f.u., is A(Na0.65 O22W(F1.47OH0.53)Σ=2.00. Crystal-structure analysis shows CLi to be completely ordered at the M(3) site, and provided reliable site populations. Fluoro-aluminoleakeite is related to the end-member leakeite, , by the substitutions CFe3+ → CAl and WF → W(OH).

Fluoro-sodic-ferropedrizite, NaLi2(Fe22+Al2Li)Si8O22F2, a new mineral of the amphibole group from the Sutlug River, Tuva Republic, Russia: description and crystal structure

2009 ◽  
Vol 73 (3) ◽  
pp. 487-494 ◽  
Author(s):  
R. Oberti ◽  
M. Boiocchi ◽  
N. A. Ball ◽  
F. C. Hawthorne
Keyword(s):  
Crystal Structure ◽  
Country Rock ◽  
Structure Refinement ◽  
Polarized Light ◽  
New Mineral ◽  
Monoclinic Space Group ◽  
Crystal Structure Refinement ◽  
Calculated Density ◽  
Plagioclase Feldspar ◽  
Mohs Hardness

AbstractFluoro-sodic-ferropedrizite, ideally ANaBLi2C()TSi8O22WF2, is a new mineral of the amphibole group from the Sutlug River, Tuva Republic, Russia. It occurs at the endogenic contact of a Li-pegmatite with country rocks near to a diabase dyke and formed by reaction of the pegmatitic melt with the country rock. Fluoro-sodic-ferropedrizite occurs as prismatic to acicular crystals, ranging in length from 0.1–3 cm and widths of up to 50 μm. Crystals occur inparallel to sub-parallel aggregates up to 5 mm across ina matrix of calcite and plagioclase feldspar. Crystals are pale bluish-grey with a greyish-white streak.Fluoro-sodic-ferropedrizite is brittle, has a Mohs hardness of ~6 and a splintery fracture; it is non-fluorescent with perfect {110} cleavage, no observable parting, and has a calculated density of 3.116 g cm–3. In plane-polarized light, it is pleochroic, X = pale purple-grey, Y = light grey, Z = colourless; X ^ a = 71.2º (in β acute), Y || b, Z ^ c = 83.4º (in β obtuse). Fluoro-sodic-ferropedrizite is biaxial positive, α = 1.642(1), β = 1.644(1), γ = 1.652(1); 2V(obs) = 68.0(3)º, 2V(calc) = 56.4º. Fluoro-sodic-ferropedrizite is monoclinic, space group C2/m, a = 9.3720(4) Å, b = 17.6312(8) Å, c = 5.2732(3) Å, β = 102.247(4)º, V = 851.5(2) Å3, Z = 2. The strongest ten X-ray diffraction lines in the powder patternare (d in Å ,(I),(hkl)): 8.146,(10),(110); 2.686,(9),(151); 3.008,(8),(310); 4.430,(7),(021); 2.485,(6),(02); 3.383,(4),(131); 2.876,(3),(51, 11); 2.199,(3),(12); 4.030,(2),(111) and 3.795,(2),(31). Analysis by a combination of electron microprobe and crystal-structure refinement gives SiO2 59.81, Al2O3 12.66, TiO2 0.09, FeO 10.32, MgO 5.56, MnO 0.73, ZnO 0.17, CaO 0.20, Na2O 2.81, Li2O 4.80, F 2.43, H2Ocalc 1.10, sum = 99.65 wt.%. The formula unit, calculated on the basis of 24(O,OH,F) is A(Na0.68)B(Li1.92Na0.05Ca0.03)C() T(Si7.98Al0.02)O22W(F1.03OH0.97). Crystal-structure refinement shows Li to be completely ordered at the M(3) and M(4) sites. Fluoro-sodic-ferropedrizite, ideally ANaBLi2C()TSi8O22WF2, is related to the theoretical end-member ‘sodic-pedrizite’, ANaBLi2C(Mg2Al2Li)TSi8O22W(OH)2, by the substitutions CFe2+ → CMg and WF → W(OH).

scholarly journals Luxembourgite, AgCuPbBi<sub>4</sub>Se<sub>8</sub>, a new mineral species from Bivels, Grand Duchy of Luxembourg

2020 ◽  
Vol 32 (4) ◽  
pp. 449-455
Author(s):  
Simon Philippo ◽  
Frédéric Hatert ◽  
Yannick Bruni ◽  
Pietro Vignola ◽  
Jiří Sejkora
Keyword(s):  
Crystal Structure ◽  
Structure Refinement ◽  
New Mineral ◽  
Tetrahedral Position ◽  
Calculated Density ◽  
Octahedral Sites ◽  
New Mineral Species ◽  
Distorted Octahedral ◽  
Mohs Hardness ◽  
Grand Duchy

Abstract. Luxembourgite, ideally AgCuPbBi4Se8, is a new selenide discovered at Bivels, Grand Duchy of Luxembourg. The mineral forms tiny fibres reaching 200 µm in length and 5 µm in diameter, which are deposited on dolomite crystals. Luxembourgite is grey, with a metallic lustre and without cleavage planes; its Mohs hardness is 3 and its calculated density is 8.00 g cm−3. Electron-microprobe analyses indicate an empirical formula Ag1.00(Cu0.82Ag0.20Fe0.01)Σ1.03Pb1.13Bi4.11(Se7.72S0.01)Σ7.73, calculated on the basis of 15 atoms per formula unit. A single-crystal structure refinement was performed to R1=0.0476, in the P21∕m space group, with a=13.002(1), b=4.1543(3), c=15.312(2) Å, β=108.92(1)∘, V=782.4(2) Å3, Z=2. The crystal structure is similar to that of litochlebite and watkinsonite and can be described as an alternation of two types of anionic layers: a pseudotetragonal layer four atoms thick and a pseudohexagonal layer that is one atom thick. In the pseudotetragonal layers the Bi1, Bi2 ,Bi3, Pb, and Ag1 atoms are localised, while the Cu2 and Bi4 atoms occur between the pseudotetragonal and the pseudohexagonal layers. Bi1, Bi2, and Bi3 atoms occur in weakly distorted octahedral sites, whereas Bi4 occurs in a distorted 7-coordinated site. Ag1 occupies a fairly regular octahedral site, Cu2 a tetrahedral position, and Pb occurs on a very distorted 8-coordinated site.

Fluoroleakeite, NaNa2(Mg2Fe3+2Li)Si8O22F2, a new mineral of the amphibole group from the Verkhnee Espe deposit, Akjailyautas Mountains, Eastern Kazakhstan District, Kazakhstan: description and crystal structure

2010 ◽  
Vol 74 (3) ◽  
pp. 521-528 ◽  
Author(s):  
F. Cámara ◽  
F. C. Hawthorne ◽  
N. A. Ball ◽  
G. Bekenova ◽  
A. V. Stepanov ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Structure Refinement ◽  
Polarized Light ◽  
New Mineral ◽  
Monoclinic Space Group ◽  
Crystal Structure Refinement ◽  
Calculated Density ◽  
Rare Elements ◽  
Host Rocks ◽  
Eastern Kazakhstan

AbstractFluoroleakeite, NaNa2(Mg2Fe3+2Li)Si8O22F2 is a new mineral of the amphibole group from the Verkhnee Espe deposit, Akjailyautas mountains, eastern Kazakhstan district, Kazakhstan. The granites and their host rocks have been intensely reworked by post-magmatic and host-rock fluids, resulting in intense recrystallization, enrichment in F, Li and rare elements, and replacement of primary biotite and sodic-calcic amphiboles by Li-bearing riebeckite, aegirine, astrophyllite and other sodic minerals including fluoroleakeite. Crystals are prismatic parallel to [001] with {100} and {110} faces and cleavage surfaces, and the prism direction is terminated by irregular fractures. Grains are up to 3 mm long, and occur as isolated crystals, as small aggregates, and as inclusions in cámaraite. Crystals are black with a very pale grey to colourless streak. Fluoroleakeite is brittle, has a Mohs hardness of 6 and a splintery fracture; it is non-fluorescent with perfect {110} cleavage, no observable parting, and has a calculated density of 3.245 g cm–3. In plane-polarized light, it is pleochroic, X = pale grey-green, Y = medium grey, Z = grey-brown; X^a = 14.1° (in β obtuse), Y ‖ b, Z^c = 75.9° (in β acute). Fluoroleakeite is biaxial negative, α = 1.663(2), β = 1.673(2), γ = 1.680(2); 2Vobs = 80.9(6)°, 2Vcalc = 79.4°Fluoro-leakeite is monoclinic, space group C2/m, a = 9.8927(3), b = 17.9257(6), c = 5.2969(2) Å, β = 103.990(1)°, V = 905.7(1) Å3, Z = 2. The strongest ten X-ray diffraction lines in the powder pattern are [d in Å(I)(hkl)]: 2.718(100)(151), 8.434(40)(110), 4.464(30)(021), 3.405(30)(131), 3.137(20)(310), 2.541(20)(), 2.166(20)(261), 2.325(15)(), 2.275(15)() and 2.806(10)(330). Analysis by a combination of electron microprobe and crystal-structure refinement gives SiO2 53.34, Al2O3 0.62, TiO2 1.27, V2O3 0.05, Fe2O3 15.10, FeO 6.00, MnO 2.04, ZnO 0.18, MgO 6.40, CaO 0.13, Na2O 9.08, K2O 1.98, Li2O 1.10, F 3.33, H2Ocalc 0.16, sum 99.39 wt.%. The formula unit, calculated on the basis of 23 O, is A(Na0.64K0.38)(Na1.98Ca0.02)(Li0.66Mg1.42Fe0.752+Mn0.262+Zn0.02Fe1.693+V0.013+Ti0.144+Al0.03) (Si7.93Al0.07)O22(F1.57OH0.16O0.27). Crystal-structure refinement shows Li to be completely ordered at the M(3) site. Fluoroleakeite, ideally NaNa2(Mg2Fe23+Li)Si8O22F2, is related to end-member leakeite, NaNa2(Mg2Fe23+Li)Si8O22(OH)2 by the substitution F → (OH).

Oxyplumboroméite, Pb2Sb2O7, a new mineral species of the pyrochlore supergroup from Harstigen mine, Värmland, Sweden

2013 ◽  
Vol 77 (7) ◽  
pp. 2931-2939 ◽  
Author(s):  
U. Hålenius ◽  
F. Bosi
Keyword(s):  
Crystal Structure ◽  
Structure Refinement ◽  
New Mineral ◽  
Crystal Structure Refinement ◽  
Unit Cell Parameters ◽  
Calculated Density ◽  
X Ray ◽  
Cell Parameters ◽  
New Mineral Species ◽  
Mohs Hardness

AbstractOxyplumboroméite, Pb2Sb2O7, is a new mineral of the roméite group of the pyrochlore supergroup (IMA 2013-042). It is found together with calcite and leucophoenicite in fissure fillings in tephroite skarn at the Harstigen mine, Värmland, Sweden. The mineral occurs as yellow to brownish yellow rounded grains or imperfect octahedra. Oxyplumboroméite has a Mohs hardness of ∼5, a calculated density of 6.732 g/cm3 and is isotropic with a calculated refractive index of 2.061. Oxyplumboroméite is cubic, space group Fdm, with the unit-cell parameters a = 10.3783(6) Å, V = 1117.84(11) Å3 and Z = 8. The strongest five X-ray powder-diffraction lines [d in Å(I)(hkl)] are: 2.9915(100)(222), 2.5928(32)(400), 1.8332(48)(440), 1.5638(38)(622) and 1.1900(12)(662). The crystal structure of oxyplumboroméite was refined to an R1 index of 3.02% using 160 unique reflections collected with MoKα radiation. Electron microprobe analyses in combination with crystal-structure refinement, infrared, Mössbauer and electronic absorption spectroscopy resulted in the empirical formula A(Pb0.92Ca0.87Mn0.09Sr0.01Na0.05)Σ1.93B(Sb1.73Fe3+0.27)Σ2.00X+Y[O6.64(OH)0.03]Σ6.67. Oxyplumboroméite is the Pb analogue of oxycalcioroméite, ideally Ca2Sb2O7.

Joanneumite, Cu(C3N3O3H2)2(NH3)2, a new mineral from Pabellón de Pica, Chile and the crystal structure of its synthetic analogue

2017 ◽  
Vol 81 (1) ◽  
pp. 155-166 ◽  
Author(s):  
Hans-Peter Bojar ◽  
Franz Walter ◽  
Judith Baumgartner
Keyword(s):  
Crystal Structure ◽  
Single Crystal ◽  
Structure Refinement ◽  
Structural Formula ◽  
New Mineral ◽  
Synthetic Analogue ◽  
X Ray Diffraction ◽  
Calculated Density ◽  
Cell Parameters ◽  
Mohs Hardness

AbstractThe new mineral joanneumite was found at Pabellón de Pica Mountain, Iquique Province, Tarapacá Region, Chile, where it occurs as violet microcrystalline aggregates up to 2 mm in size in small cracks in a gabbroic rock, which is covered by a guano deposit. Associated minerals are salammoniac, dittmarite, möhnite and gypsum. Joanneumite is non-fluorescent and the Mohs hardness is 1. The calculated density is 2.020 g cm–3. The infrared spectrum of joanneumite shows the frequencies of NH3 and isocyanurate groups and the absence of absorptions of H2O molecules and OH– ions. The chemical composition (electron microprobe data, the hydrogen was calculated from the structural formula, wt.%) is C 20.33, N 31.11, O 28.34, Cu 17.27, Zn 0.24, H 2.82, total 100.11. The empirical formula is Cu0.96Zn0.01N7.84C5.98O6.25H9.96 and the idealized formula is CuN8C6O6H10 with the structural formula Cu(C3N3O3H2)2(NH3)2. Due to the lack of suitable single crystals the synthetic analogue of joanneumite was prepared for the single-crystal structure refinement. The crystal structure was solved and refined to R = 0.025 based upon 1166 unique reflections with I > 2σ (I). Joanneumite is triclinic, space group P1̄, a = 4.982(1), b = 6.896(1), c = 9.115(2) Å, α = 90.53(3), β = 97.85(3), γ = 110.08(3)°, V = 290.8(1) Å3, Z = 1 obtained from single-crystal data at 100 K, which are in good agreement with cell parameters from powder diffraction data of joanneumite at 293 K: a = 5.042(1), b = 6.997(1), c = 9.099(2) Å, α = 90.05(3), β = 98.11(2), γ = 110.95(3)° and V = 296.3(1) Å3. The eight strongest lines of the powder X-ray diffraction pattern are [d, Å (I,%) (hkl)] 6.52 (68) (010), 5.15 (47) (011), 4.66 (21) (100, 110), 4.35 (9) (1̄11), 3.29 (6) (1̄20), 3.22 (7) (1̄1̄1), 3.140 (100) (1̄21), 2.074 (7) (1̄32). The crystal structure of joanneumite is identical with the structure of synthetic bis(isocyanurato) diamminecopper(II).

Description and crystal structure of domerockite, Cu4(AsO4)(AsO3OH)(OH)3·H2O, a new mineral from the Dome Rock Mine, South Australia

2013 ◽  
Vol 77 (4) ◽  
pp. 509-522 ◽  
Author(s):  
P. Elliott ◽  
U. Kolitsch ◽  
A. C. Willis ◽  
E. Libowitzky
Keyword(s):  
Crystal Structure ◽  
Structure Refinement ◽  
South Australia ◽  
Direct Methods ◽  
New Mineral ◽  
Calculated Density ◽  
Bluish Green ◽  
Distorted Octahedra ◽  
Mohs Hardness ◽  
Greenish Blue

AbstractDomerockite, Cu4(AsO4)2(AsO3OH)(OH)3·H2O, is a new mineral from the Dome Rock Mine, South Australia. It occurs as aggregates of bluish green, equant to short prismatic and tabular crystals up to 0.3 mm long and 0.2 mm across. Domerockite is translucent, with a vitreous lustre and pale green streak. It displays no fluorescence under UV irradiation. The mineral is brittle with an uneven fracture, a Mohs hardness of ∼3 and a calculated density of 4.44 g/cm3 (based on the structure refinement). Optically, it is biaxial negative, with α = 1.798(4), β = 1.814(4), γ = 1.817(4), 2Vcalc. = 46°; pleochroism is very weak; X pale greenish yellow, Y greenish blue, Z greenish blue; absorption X < Y = Z; orientation is uncertain. Chemical analysis by electron microprobe gave CuO 52.04, ZnO 0.78, BaO 0.11, As2O537.67, P2O50.32, SiO20.24, H2O 8.84, total 100.00 wt.%, with H2O calculated by difference. The empirical chemical formula is (Cu3.94, Zn0.06)Σ4.00H0.91(As1.97, P0.03, Si0.02)Σ2.02O8(OH)3.00˙H2O based on 12 oxygen atoms.Domerockite is triclinic, space group P, with a = 5.378(11), b = 8.962(18) c = 9.841(2) Å, α = 75.25(3), β = 83.56(3), γ = 79.97(3)°, V = 450.5(16) Å3 and Z = 2. The eight strongest lines in the X-ray powder diffraction pattern are [d (Å), (I)(hkl)]: 4.716 (30)(101, 002, 111), 3.697 (25)(121), 3.605 (30)(120, 12), 3.119 (60)(12), 3.073 (100)(1), 2.856 (40)(02, 030), 2.464 (50)(212, 13), 2.443 (40)(014). The crystal structure of domerockite has been solved by direct methods and refined to an R index of 7.44% using 2635 observed reflections. The structure comprises [Cuφ4] (φ = O, OH) chains of edge-sharing sharing, distorted octahedra that extend along [10] and are decorated by AsO4 tetrahedra to form sheets in the (010) plane. Dimers of edge-sharing [CuO4(OH)(H2O)] octahedra share corners with dimers of edge-sharing [CuO4(OH)] square pyramids to form zigzag chains which extend along [101]. The chains lie between and link to the sheets by sharings corners of octahedra, square pyramids and tetrahedra to form a heteropolyhedral framework.

Gatedalite, Zr(Mn2+2Mn3+4)SiO12, a new mineral species of the braunite group from Långban, Sweden

2015 ◽  
Vol 79 (3) ◽  
pp. 625-634
Author(s):  
Ulf Hålenius ◽  
Ferdinando Bosi
Keyword(s):  
Crystal Structure ◽  
General Formula ◽  
Structure Refinement ◽  
Visible Spectral Range ◽  
New Mineral ◽  
X Ray Diffraction ◽  
Calculated Density ◽  
Cell Parameters ◽  
New Mineral Species ◽  
Oxide Deposit

AbstractGatedalite, Zr(Mn22+Mn43+)SiO12, is a new mineral of the braunite group. It is found in hausmannite-impregnated skarn together with jacobsite, Mn-bearing calcite, tephroite, Mn-bearing phlogopite, långbanite, pinakiolite and oxyplumboroméite at the Långban Mn-Fe oxide deposit, Värmland, central Sweden. The mineral occurs as very rare, small (≤60 μm), grey, submetallic, irregularly rounded anhedral grains. Gatedalite has a calculated density of 4.783 g/cm3. It is opaque and weakly anisotropic with reflectivity in air varying between 17.1 and 20.8% in the visible spectral range. Gatedalite is tetragonal, space groupI41/acd, with the unit-cell parametersa= 9.4668(6) Å,c= 18.8701(14) Å,V= 1691.1(2) Å3andZ= 8. The crystal structure was refined to anR1 index of 5.09% using 1339 unique reflections collected with MoKαX-ray radiation. The five strongest powder X-ray diffraction lines [din Å, (I), (hkl)] are: 2.730(100)(224), 2.367(12)(040), 1.6735(12)(440), 1.6707(29)(048) and 1.4267(16)(264). Electron microprobe analyses in combination with single-crystal structure refinement resulted in the empirical formula: (Zr0.494+Mn0.402+Mg0.07Ca0.02Zn0.01Ce0.013+)Σ1.00(Mn4.443+Fe0.593+Mn0.572+Mg0.41Al0.01)Σ6.02Si0.99O12. Gatedalite is a member of the braunite group (general formula AB6SiO12). It is related to braunite (Mn2+Mn63+SiO12) through the net cation exchange (Zr4++ Mn2+) → 2Mn3+, which results from the substitutions Zr4+→ Mn2+at the 8-fold coordinated site (Ain the general formula) coupled with a 2Mn2+→ 2Mn3+substitution at the 6-fold coordinated sites (Bin the general formula).

Windmountainite, □Fe3+2Mg2□2Si8O20(OH)2(H2O)4·4H2O, a new modulated, layered Fe3+-Mg-silicate-hydrate from Wind Mountain, New Mexico: Characterization and origin, with comments on the classification of palygorskite-group minerals

2020 ◽  
Vol 58 (4) ◽  
pp. 477-509
Author(s):  
Derek D. Leung ◽  
Andrew M. McDonald
Keyword(s):  
Crystal Structure ◽  
New Mexico ◽  
Late Stage ◽  
Structure Refinement ◽  
New Mineral ◽  
X Ray Diffraction ◽  
Calculated Density ◽  
X Ray ◽  
New Mineral Species

ABSTRACT Windmountainite, ideally □Fe3+2Mg2□2Si8O20(OH)2(H2O)4·4H2O, is a new mineral species and member of the palygorskite group discovered as orange-brown, radiating aggregates that commonly fill vesicles (average 1.5 × 2.5 mm) within a phonolite dike at Wind Mountain, Otero County, New Mexico, USA. The mineral develops as tightly bound bundles (up to 0.02 × 6 mm) of acicular to bladed crystals that are elongate on [001] and flattened on the pinacoid {010}. Associated minerals include albite, aegirine, fluorapophyllite-(K), natrolite, neotocite, and montmorillonite, the last of these being observed to replace primary windmountainite. It has a dull luster, silky in aggregates, is translucent and has an orange-brown streak. It does not fluoresce under short-, medium-, or long-wave ultraviolet radiation. Windmountainite is brittle with a splintery fracture and has two good cleavages (predicted) on {110}, an estimated hardness of 2, a calculated density of 2.51 g/cm3, and a calculated navg of 1.593. A total of n = 30 EMPA (WDS) analyses from six grains yielded an average of (wt.%): Na2O 0.08, MgO 3.47, Al2O3 1.15, SiO2 49.76, Cl 0.07, K2O 0.40, CaO 0.68, TiO2 0.30, MnO 5.64, Fe2O3 20.17, H2O (calc.) 16.59, O=Cl –0.02, total 98.29. The empirical formula [based on Σ(T1, T2, M2, M3) = 12 cations pfu, excluding Ca, K, and Na] is: (□0.78Ca0.12K0.08Na0.02)Σ1.00(Fe3+1.93Al0.04Ti0.02)Σ1.99 (Mg0.81Mn2+0.75Fe3+0.44)Σ2.00□2(Si7.81Al0.17Ti0.01Fe3+0.01)Σ8.00O20[(OH)1.98Cl0.02]Σ2.00[(H2O)3.38(OH)0.62]Σ4.00·4H2O, yielding the simplified formula, □Fe3+2Mg2□2Si8O20(OH)2(H2O)4·4H2O. The predominance of Fe3+ is based on color, results from the crystal-structure refinement, the crystal-chemistry of palygorskite-group minerals, the association with Fe3+-dominant minerals, and considerations regarding the late-stage geochemical evolution of agpaitic rocks. The presence of H2O and OH was determined based on results from the refined crystal structure and Fourier-transform infrared spectroscopy. Windmountainite crystallizes in the space group C2/m with a 13.759(3), b 17.911(4), c 5.274(1) Å, β 106.44(3)°, V 1246.6(1) Å3, and Z = 2. The seven strongest powder X-ray diffraction lines are [d in Å (I), (hkl)]: 10.592 (100) (110), 5.453 (16) (130), 4.484 (19) (040), 4.173 (28) , 3.319 (53) (221, 400), 2.652 (30) , 2.530 (27) . The crystal structure was determined from single-crystal X-ray diffraction data and refined to R = 4.01% and wR2 = 10.70% using data from 902 reflections (Fo &gt; 4σFo). It is based on sheets of inverted double chains of SiO4 tetrahedra that sandwich ribbons of Mφ6 octahedra (φ = O, OH, H2O, Cl), giving rise to large channels (∼6.5 × 9 Å) that are occupied by loosely held H2O groups. A modified classification of the palygorskite group [general crystal-chemical formula M1M22M32M42T14T24O20(OH)2(H2O,OH)4·W] is proposed based on the occupants of the four M sites. Within this scheme, windmountainite is the □-Fe3+-Mg-□ member. The palygorskite group includes six members: palygorskite (monoclinic and orthorhombic polytypes), yofortierite, tuperssuatsiaite, raite, windhoekite, and windmountainite. Windmountainite is considered to have formed from late-stage fluids that were alkaline, oxidized, and rich in both Fe3+ and H2O; high aH2O conditions are reflective of abundant, hydrated feldspathoids (natrolite and analcime) forming as primary rock-forming minerals in the phonolite at Wind Mountain.

Wiklundite, ideally Pb2[4](Mn2+,Zn)3(Fe3+,Mn2+)2(Mn2+,Mg)19(As3+O3)2[(Si,As5+)O4]6(OH)18Cl6, a new mineral from Långban, Filipstad, Värmland, Sweden: Description and crystal structure

2017 ◽  
Vol 81 (4) ◽  
pp. 841-855 ◽  
Author(s):  
Mark A. Cooper ◽  
Frank C. Hawthorne ◽  
Jörgen Langhof ◽  
Ulf Hålenius ◽  
Dan Holtstam
Keyword(s):  
Crystal Structure ◽  
Structure Refinement ◽  
Direct Methods ◽  
New Mineral ◽  
Silicate Mineral ◽  
Calculated Density ◽  
International Mineralogical Association ◽  
Perfect Cleavage

AbstractWiklundite, ideally Pb2[4](Mn2+,Zn)3(Fe3+,Mn2+)2(Mn2+,Mg)19(As3+O3)2[(Si,As5+)O4]6(OH)18Cl6, isa new arseno-silicate mineral from Långban, Filipstad, Värmland, Sweden. Both the mineral and the name have been approved by the Commission on New Minerals, Nomenclature and Classification of the International Mineralogical Association (IMA 2015-057). Wiklundite and a disordered wiklundite-like mineral form radiating, sheaf-like aggregates (up to 1 mm long) of thin brownish-red and slightly bent lath-shaped crystals. It occurs in a dolomite-rich skarn in association with tephroite, mimetite, turneaurite, johnbaumite, jacobsite, barite, native lead, filipstadite andparwelite. Wiklundite is reddish brown to dark brown, and the streak is pale yellowish brown. The lustre is resinous to sub-metallic, almost somewhat bronzy, and wiklundite does not fluoresce under ultraviolet light. The calculated density is 4.072 g cm–3. Wiklundite is brittle with an irregular fracture, and has perfect cleavage on {001}; no parting or twinning was observed. Wiklundite is uniaxial (–), orange red and non-pleochroic in transmitted light, but shows incomplete extinction and distorted interference figures, preventing complete determination of optical properties. Electron-microprobe analysis (H2O calculated from the structure) of wiklundite gave SiO2 11.17, Al2O3 0.06, Fe2O3 4.46, As2O5 0.75, As2O3 6.81, MnO 47.89, ZnO 0.78,CaO 0.09, PbO 14.48, Cl 6.65, H2O 5.18, O=Cl2 –1.50, total 97.11 wt.%, As valences and H2O content taken from the crystal-structure refinement, and Fe3+/(Fe2+ + Fe3+) determined by Mössbauer spectroscopy. Wiklundite is hexagonal-rhombohedral, space group R3c, a = 8.257(2), c = 126.59(4) Å, V = 7474(6) Å3, Z = 6. The crystal structure of wiklundite was solved by direct methods and refined to a final R1 index of 3.2%. The structure consists of a stacking of five layers of polyhedra: three layers consist of trimers of edge-sharing Mn2+-dominant octahedra linked by (SiO4) tetrahedra, (Fe3+(OH)6) dominant octahedra and (AsO3) triangular pyramids; one layerof corner-sharing (SiO4) and (Mn2+O4) tetrahedra; and one layer of (Mn2+Cl6) octahedra and (Pb2+(OH)3Cl6) polyhedra. The mineral is named after Markus Wiklund (b. 1969) and Stefan Wiklund (b. 1972), the well-known Swedish mineral collectors who jointly found the specimen containing the mineral.

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