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.

Sveinbergeite, Ca(Fe2+6 Fe3+)Ti2(Si4O12)2O2(OH)5(H2O)4, a new astrophyllite-group mineral from the Larvik Plutonic Complex, Oslo Region, Norway: description and crystal structure

2011 ◽  
Vol 75 (5) ◽  
pp. 2687-2702 ◽  
Author(s):  
A. P. Khomyakov ◽  
F. Cámara ◽  
E. Sokolova ◽  
Y. Abdu ◽  
F. C. Hawthorne
Keyword(s):  
Crystal Structure ◽  
Manganese Oxides ◽  
Structure Refinement ◽  
Direct Methods ◽  
Calculated Density ◽  
Group Mineral ◽  
Amateur Mineralogist ◽  
Perfect Cleavage ◽  
Mohs Hardness ◽  
Deep Green

AbstractSveinbergeite, Ca(Fe2+6Fe3+)Ti2(Si4O12)2O2(OH)5(H2O)4, is a new astrophyllite-group mineral discovered in a syenite pegmatite at Buer on the Vesteroya peninsula, Sandefjord, Oslo Region, Norway. The mineral occurs in pegmatite cavities as 0.01—0.05 mm thick lamellar (0.2—0.5×5—10 mm) crystals forming rosette-like divergent groups and spherical aggregates, which are covered by brown coatings of iron (and possibly manganese) oxides, associated with magnesiokatophorite, aegirine, microcline, albite. calcite, fluorapatite, molybdenite, galena and a hochelagaite-like mineral. Crystals of sveinbergeite are deep green with a pale green streak and a vitreous and pearly lustre. Sveinbergeite has perfect cleavage on ﹛001﹜ and a Mohs hardness of 3. Its calculated density is 3.152 g/cm3. It is biaxial positive with α 1.745(2), β 1.746(2), γ 1.753(2), 2V(meas.) = 20(3)°. The mineral is pleochroic according to the scheme Z > X ∽ Y : Z is deep green, X and Y are brownish green. Orientation is as follows: X ┴ L (001), Y ᶺ b = 12°, Z = a, elongation positive. Sveinbergeite is triclinic, space group P1̄, a = 5.329(4), b = 11.803(8), c = 11.822(8) Å; α = 101.140(8)°, β = 98.224(8)°, γ = 102.442(8)°; V = 699.0(8) Å3; Z = 1. The nine strongest lines in the X-ray powder diffraction pattern [d in Å(I)(hkl)] are: 11.395(100)(001,010). 2.880(38)(004), 2.640(31)(2̄10,l̄41), 1.643(24)(07̄1,072), 2.492(20)(2l̄l), 1.616(15)(070), 1.573(14)(3̄2̄2), 2.270(13)(1̄3̄4) and 2.757(12)(1̄40,1̄3̄2). Chemical analysis by electron microprobe gave Nb2O5 0.55, TiO2 10.76, ZrO2 0.48, SiO2 34.41, A12O3 0.34, Fe2O3 5.57, FeO 29.39, MnO 1.27, CaO 3.87, MgO 0.52, K2O 0.49, Na2O 0.27, F 0.24, H2O 8.05, O=F -0.10, sum 96.11 wt.%, the amount of H2O was determined from structure refinement, and the valence state of Fe was calculated from structure refinement in accord with Mossbauer spectroscopy. The empirical formula, calculated on the basis of eight (Si + Al) p.f.u., is (Ca0.95Na0.12K0.14)Σ1.21(Fe2+5.65Fe3+0.93Mn0.25Mg0.18)Σ7.01(Ti1.86Nb0.06Zr0.05Fe3+)Σ2 (Si7091Al0.09)Σ8O34.61H12.34F0.17, Z = 1. The infrared spectrum of the mineral contains the following absorption frequencies: 3588, ∽3398 (broad), ∽3204 (broad), 1628, 1069, 1009, 942, 702, 655 and 560 cm–1. The crystal structure of the mineral was solved by direct methods and refined to an R1 index of 21.81%. The main structural unit in the sveinbergeite structure is an HOH layer which is topologically identical to that in the astrophyllite structure. Sveinbergeite differs from all other minerals of the astrophyllite group in the composition and topology of the interstitial A and B sites and linkage of adjacent HOH layers. The mineral is named in honour of Svein Arne Berge (b. 1949), a noted Norwegian amateur mineralogist and collector who was the first to observe and record this mineral from its type locality as a potential new species.

Siwaqaite, Ca6Al2(CrO4)3(OH)12·26H2O, a new mineral of the ettringite group from the pyrometamorphic Daba-Siwaqa complex, Jordan

2020 ◽  
Vol 105 (3) ◽  
pp. 409-421 ◽  
Author(s):  
Rafał Juroszek ◽  
Biljana Krüger ◽  
Irina Galuskina ◽  
Hannes Krüger ◽  
Yevgeny Vapnik ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Direct Methods ◽  
New Mineral ◽  
Calculated Density ◽  
Oh Groups ◽  
The North ◽  
Yellow Color ◽  
Raman And Infrared Spectroscopy ◽  
Ettringite Group ◽  
Perfect Cleavage

Abstract A new mineral, siwaqaite, ideally Ca6Al2(CrO4)3(OH)12·26H2O [P31c, Z = 2, a = 11.3640(2) Å, c = 21.4485(2) Å, V = 2398.78(9) Å3], a member of the ettringite group, was discovered in thin veins and small cavities within the spurrite marble at the North Siwaqa complex, Lisdan-Siwaqa Fault, Hashem region, Jordan. This complex belongs to the widespread pyrometamorphic rock of the Hatrurim Complex. The spurrite marble is mainly composed of calcite, fluorapatite, and brownmillerite. Siwaqaite occurs with calcite and minerals of the baryte-hashemite series. It forms hexagonal prismatic crystals up to 250 μm in size, but most common are grain aggregates. Siwaqaite exhibits a canary yellow color and a yellowish-gray streak. The mineral is transparent and has a vitreous luster. It shows perfect cleavage on (1010). Parting or twinning is not observed. The calculated density of siwaqaite is 1.819 g/cm3. Siwaqaite is optically uniaxial (–) with ω = 1.512(2), ε = 1.502(2) (589 nm), and non-pleochroic. The empirical formula of the holotype siwaqaite calculated on the basis of 8 framework cations and 26 water molecules is Ca6.01(Al1.87Si0.12)Σ1.99[(CrO4)1.71(SO4)1.13(SeO4)0.40]Σ3.24(OH)11.63·26H2O. X-ray diffraction (XRD), Raman, and infrared spectroscopy confirm the presence of OH- groups and H2O molecules and absence of (CO3)2– groups. The crystal structure of this Cr6+-analog of ettringite was solved by direct methods using single-crystal synchrotron XRD data. The structure was refined to an agreement index R1 = 4.54%. The crystal structure of siwaqaite consists of {Ca6[Al(OH)6]2·24H2O}6+ columns with the inter-column space (channels) occupied by (CrO4)2–, (SO4)2–, (SeO4)2–, and (SO3)2– groups and H2O molecules. The tetrahedrally coordinated site occupied by different anion groups is subjected to disordering and rotation of these tetrahedra within the structure. The temperature of siwaqaite formation is not higher than~70–80 °C, as is evident from the mineral association and as inferred from the formation conditions of the natural and synthetic members of the ettringite group minerals, which are stable at conditions of T < 120 °C and pH = 9.5–13. The name siwaqaite is derived from the name of the holotype locality—Siwaqa area, where the mineral was found.

Natrotitanite, ideally (Na0.5Y0.5)Ti(SiO4)O, a new mineral from the Verkhnee Espe deposit, Akjailyautas mountains, Eastern Kazakhstan district, Kazakhstan: description and crystal structure

2012 ◽  
Vol 76 (1) ◽  
pp. 37-44 ◽  
Author(s):  
A. V. Stepanov ◽  
G. K. Bekenova ◽  
V. L. Levin ◽  
F. C. Hawthorne
Keyword(s):  
Crystal Structure ◽  
Incident Beam ◽  
New Mineral ◽  
Mountain Range ◽  
Rare Element ◽  
Calculated Density ◽  
International Mineralogical Association ◽  
The Mean ◽  
Eastern Kazakhstan

AbstractNatrotitanite, ideally (Na0.5Y0.5)Ti(SiO4)O, is a new mineral from the Verkhnee Espe rare-element deposit at the northern exo-contact of the Akjailyautas granite massif in the northern part of the Tarbagatai mountain range, Eastern Kazakhstan. Both the mineral and the name have been approved by the Commission on New Minerals, Nomenclature and Classification of the International Mineralogical Association (IMA 2010-033). Star-shaped aggregates of small short prisms of yellow or yellowish white (Na,Y,REE)-bearing titanite rimmed by thin (∼2 μm) rims of natrotitanite are embedded in yttrium-bearing fluorite and replace narsarsukite. Associated minerals are microcline, albite, quartz, riebeckite, aegirine, biotite, astrophyllite, rutile, zircon and elpidite. Natrotitanite is milky white to yellowish grey, transparent to translucent, and has a white streak and a vitreous lustre. It shows pale orange cathodoluminescence but does not fluoresce under ultraviolet light. It shows no cleavage or parting, and is brittle; the calculated density is 3.833 g cm–3. The indices of refraction, measured with the Bloss spindle stage for the wavelength 590 nm using a gel filter, are α = 1.904, γ = 2.030, and these values are in accord with the mean refractive index, 1.988, calculated from the Gladstone-Dale relation. Natrotitanite is monoclinic, C2/c, a = 6.5691(2), b = 8.6869(3), c = 7.0924(2) Å, β = 114.1269(4)°, V = 369.4(2) Å3, Z = 4, a:b:c = 0.7562:1: 0.8164. The seven strongest lines in the X-ray powder diffraction pattern [in the order d (Å), I, (hkl)] are as follows: 2.597, 10, (130); 3.248, 8, (11); 2.994, 6, (200); 1.641, 4, (330); 4.941, 3, (110); 1.498, 3, (400); 2.273, 3, (11). Chemical analysis by electron microprobe gave Nb2O5 1.28, SiO2 27.83, TiO2 35.00, SnO2 0.57, V2O3 0.36, Fe2O3 0.23, Y2O3 7.87, Ce2O3 0.83, Sm2O3 0.26, Gd2O3 0.46, Tb2O3 0.17, Dy2O3 2.45, Ho2O3 0.16, Er2O3 2.24, Tm2O3 0.50, Yb2O3 2.53, Nd2O3 0.35, Lu2O3 0.28, MnO 0.33, CaO 8.16, Na2O 5.55, F 1.52 O ≡ F –0.64, sum 98.71 wt.%. The resulting empirical formula is (Na0.39Ca0.32Y0.15Dy0.03Yb0.03Er0.03Ce0.01Ho0.01Tm0.01Gd0.01Nd0.01)Σ1.00(Ti0.95Nb0.02Sn0.01Fe3+0.01Mn0.01V0.01)Σ1.01Si1.01O4.00(O0.83F0.17), calculated on the basis of 3 cations per formula unit. The general formula is written as (Na,Ca,Y,REE)TiSiO4(O,F), and the endmember formula is (Na0.5Y0.5)Ti(SiO4)O.The crystal structure of a composite optically continuous crystal of natrotitanite and (Na, Y)-bearing titanite was mounted on a Bruker D8 three-circle diffractometer equipped with a rotating anode generator (MoKα radiation), a multi-layer optics incident-beam path and an APEX-II CCD detector. The crystal structure was refined in space group C2/c to a final R1 index of 1.8%. Natrotitanite is isostructural with titanite, (Na + Y + REE) replacing Ca at the Ca site in the titanite structure.

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.

Schlüterite-(Y), ideally (Y,REE)2Al(Si2O7)(OH)2F, a new mineral species from the Stetind pegmatite, Tysfjord, Nordland, Norway: description and crystal structure

2013 ◽  
Vol 77 (3) ◽  
pp. 353-366 ◽  
Author(s):  
M. A. Cooper ◽  
T. A. Husdal ◽  
N. A. Ball ◽  
Y. A. Abdu ◽  
F. C. Hawthorne
Keyword(s):  
Crystal Structure ◽  
Direct Methods ◽  
Crystal Structure Analysis ◽  
Mineral Species ◽  
New Mineral ◽  
Monoclinic Space Group ◽  
Silicate Mineral ◽  
Dominant Form ◽  
Calculated Density ◽  
New Mineral Species

AbstractSchlüterite-(Y), ideally (Y,REE)2Al(Si2O7)(OH)2F, is a new silicate mineral species from the Stetind pegmatite, Tysfjord, Nordland, Norway. It forms dense, fibrous, radiating aggregates (up to ∼2 mm) diverging to individual needle-like crystals (up to ∼1 mm long) in cavities. Crystals are acicular to bladed, flattened on {001} and elongated along [010], and the dominant form is {001}. Schlüterite-(Y) is transparent, pale pink with a white streak and a vitreous lustre, and does not fluoresce under short-wave ultraviolet light. Mohs hardness is 5½–6, and schlüterite-(Y) is brittle with an irregular fracture, and has no cleavage. The calculated density is 4.644 g/cm3. The indices of refraction are α = 1.755, β = 1.760, γ = 1.770, all ± 0.005, 2Vobs = 71.8 (5)°, 2Vcalc = 71°, non-pleochroic, optic orientation is X ˆ a = 83.1° (β obtuse), Y//b, Z ˆ c = 50.3° (β acute). Schlüterite-(Y) is monoclinic, space group P21/c, a 7.0722(2), b 5.6198(1), c 21.4390(4) Å, β 122.7756(3)°, V 716.43(5) Å3, Z = 4. The seven strongest lines in the X-ray powder-diffraction pattern are as follows: [d (Å), I, (hkl)]: 4.769, 100, (012); 2.972, 55, (14); 3.289, 51, (112); 2.728, 49, (16); 2.810, 37, (020); 3.013, 37, ((16); 4.507, 36, (004). Chemical analysis by electron microprobe gave SiO2 22.64, Al2O3 9.45, Y2O3 15.35, La2O3 3.25, Ce2O3 9.69, Pr2O3 2.05, Nd2O3 9.50, Sm2O3 3.57, Gd2O3 4.65, Dy2O3 4.21, Er2O3 2.31, Yb2O3 1.86, F 2.71, H2Ocalc 3.78, O = F −1.14, sum 93.88 wt%. The H2O content was determined by crystal-structure analysis. On the basis of 10 anions with (OH) + F = 3 a.p.f.u. (atoms per formula unit), the empirical formula is (Y0.73Ce0.32Nd0.30Gd0.14Dy0.12La0.11Sm0.11Pr0.07Er0.06Yb0.05)Σ=2.01Al0.99Si2.01O7(OH)2.24F0.76. The crystal structure of schlüterite-(Y) was solved by direct methods and refined to an R1 index of 1.8% based on 1422 unique observed reflections. In the structure of schlüterite-(Y), Al(OH)4O2 octahedra share (OH)–(OH) edges to form [MΦ4] chains that are decorated by (Si2O7) groups that bridge O vertices of neighbouring octahedra in a staggered fashion on either side of the chain. These [Al(OH)2(Si2O7)] chains extend parallel to b, and are linked into a continuous framework via bonds to interstitial [8](Y,REE) (= <2.400 Å>) and [9](Y,REE) (= <2.548 Å>) atoms.

Cámaraite, Ba3NaTi4(Fe2+,Mn)8(Si2O7)4O4(OH,F)7. I. A new Ti-silicate mineral from the Verkhnee Espe Deposit, Akjailyautas Mountains, Kazakhstan

2009 ◽  
Vol 73 (5) ◽  
pp. 847-854 ◽  
Author(s):  
E. Sokolova ◽  
Y. Abdu ◽  
F. C. Hawthorne ◽  
A. V. Stepanov ◽  
G. K. Bekenova ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Refractive Indices ◽  
New Mineral ◽  
Silicate Mineral ◽  
Calculated Density ◽  
Triclinic Space Group ◽  
X Ray ◽  
International Mineralogical Association ◽  
Mineralogical Association ◽  
Mohs Hardness

AbstractCámaraite, ideally Ba3NaTi4(Fe2+,Mn)8(Si2O7)4O4(OH,F)7, is a new mineral from the Verkhnee Espe deposit, Akjailyautas Mountains, Kazakhstan. It occurs as intergrowths with bafertisite and jinshajiangite in separate platy crystals up to 8 mm × 15 mm × 2 mm in size, or as star-shaped aggregates of crystals with different orientations. Individual crystals are orange-red to brownish-red, and are platy on {001}. Cámaraite is translucent and has a pale-yellow streak, a vitreous lustre, and does not fluoresce under cathode or ultraviolet light. Cleavage is {001} perfect, no parting was observed, and Mohs hardness is <5; the mineral is brittle. The calculated density is 4.018 g cm-3. In transmitted light, camaraite is strongly pleochroic, X = light brown, Y = reddish-brown, Z = yellow- brown, with Z < X < Y. Cámaraite is biaxial +ve and 2Vmeas. = 93(1)°. All refractive indices are greater than 1.80. Cámaraite is triclinic, space group C, a = 10.678(4) Å, b = 13.744(8) Å, c = 21.40(2) Å, α = 99.28(8)°, β = 92.38(5)°, γ = 90.00(6)°, V = 3096(3) Å3, Z = 4, a:b:c = 0.7761:1:1.5565. The seven strongest lines in the X-ray powder-diffraction pattern are as follows: [d (Å), (I), (hkl)]: 2.63, (100), (401); 2.79, (90), (3, 41, 26, 225); 1.721, (70), (11, 49, 02); 3.39, (50), (24, 223); 3.18, (50), (5, 24); 2.101, (50), (2, 40); 1.578, (50), (1, 2, 61, 40). Chemical analysis by electron microprobe gave: Nb2O5 1.57, SiO2 25.25, TiO2 15.69, ZrO2 0.33, Al2O3 0.13, Fe2O3 2.77, FeO 16.54, MnO 9.46, ZnO 0.12, MgO 0.21, CaO 0.56, BaO 21.11, Na2O 1.41, K2O 0.84, H2O 1.84, F 3.11, less O:F 1.31, total 99.63 wt.%, where the valence state of Fe was determined by Mössbauer spectroscopy [Fe3+/(Fe2+ + Fe3+) = 0.13(8)] and the H2O content was derived by crystal-structure determination. The resulting empirical formula on the basis of 39 anions is Ca0.05)Σ7.78Si7.97O35.89H3.88F3.11. Cámaraite is a Group-II TS-block mineral in the structure hierarchy of Sokolova (2006). The mineral is named camaraite after Fernando Cámaraite (born 1967) of Melilla, Spain, in recognition of his contribution to the fields of mineralogy and crystallography. The new mineral and mineral name have been approved by the Commission on New Minerals, Nomenclature and Classification, International Mineralogical Association (IMA 2009-11).

Description and crystal structure of bobkingite, a new mineral from New Cliffe Hill Quarry, Stanton-under-Bardon, Leicestershire, UK

2002 ◽  
Vol 66 (2) ◽  
pp. 301-311 ◽  
Author(s):  
F. C. Hawthorne ◽  
M. A. Cooper ◽  
J. D. Grice ◽  
A. C. Roberts ◽  
N. Hubbard
Keyword(s):  
Crystal Structure ◽  
Direct Methods ◽  
Crystal Structure Analysis ◽  
New Mineral ◽  
Monoclinic Space Group ◽  
X Rays ◽  
Calculated Density ◽  
International Mineralogical Association ◽  
Cell Parameters ◽  
Conchoidal Fracture

AbstractBobkingite, ideally is a new mineral from the New Cliffe Hill Quarry, Stantonunder-Bardon, Leicestershire, England. It occurs as very thin (⩽5 µm) transparent plates up to 0.2 mm across, perched on a compact fibrous crust of malachite and crystalline azurite attached to massive cuprite. Crystals are tabular on {001} with dominant {001} and minor {100} and {110}. Bobkingite is a soft pale blue colour with a pale-blue streak, vitreous lustre and no observable fluorescence under ultraviolet light. It has perfect {001} and fair {100} cleavages, no observable parting, conchoidal fracture, and is brittle. Its Mohs' hardness is 3 and the calculated density is 3.254 g/cm3. Bobkingite is biaxial negative with α = 1.724(2), β = 1.745(2), γ = 1.750(2), 2Vγmeas = 33(6)°, 2Vcalc = 52°, pleochroism distinct, X = very pale blue, Z = pale greenish blue, X^a = 22° (in β obtuse), Y = c, Z = b. Bobkingite is monoclinic, space group C2/m, unit-cell parameters (refined from powder data): a = 10.301(8), b = 6.758(3), c = 8.835(7)Å, β = 111.53(6)°, V = 572.1(7)Å3, Z = 2. The seven strongest lines in the X-ray powder-diffraction pattern are [d (Å), I, (hkl)]: 8.199, 100, (001); 5.502, 100, (110); 5.029, 40, (2̄01); 2.883, 80, (310); 2.693, 40, (1̄13); 2.263, 40, (113), (4̄03); 2.188, 50, (2̄23). Chemical analysis by electron microprobe and crystal-structure solution and refinement gave CuO 70.46, Cl 12.71, H2O 19.19, O≡Cl –2.87, sum 99.49 wt.%, where the amount of H2O was determined by crystal-structure analysis. The resulting empirical formula on the basis of 12 anions (including 8 (OH) and 2H2O) is Cu4.99Cl2.02O10H12. The crystal structure was solved by direct methods and refined to an R index of 2.6% for 638 observed reflections measured with X-rays on a single crystal. Three distinct (Cuϕ6) (ϕ = unspecified anion) octahedra share edges to form a framework that is related to the structures of paratacamite and the Cu2(OH)3Cl polymorphs, atacamite and clinoatacamite. The mineral is named for Robert King, formerly of the Department of Geology, Leicester University, prominent mineral collector and founding member of the Russell Society. The mineral and its name have been approved by the Commission on New Minerals and Mineral Names of the International Mineralogical Association.

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.

scholarly journals As-bearing new mineral species from Valletta mine, Maira Valley, Piedmont, Italy: III. Canosioite, Ba2Fe3+(AsO4)2(OH), description and crystal structure

2017 ◽  
Vol 81 (2) ◽  
pp. 305-317 ◽  
Author(s):  
F. Cámara ◽  
E. Bittarello ◽  
M. E. Ciriotti ◽  
F. Nestola ◽  
F. Radica ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Direct Methods ◽  
Mineral Species ◽  
New Mineral ◽  
X Ray Diffraction ◽  
Calculated Density ◽  
International Mineralogical Association ◽  
New Mineral Species ◽  
Ore Minerals ◽  
Mn Oxides

AbstractThe new mineral species canosioite, ideally Ba2Fe3+(AsO4)2(OH), has been discovered in the dump of Valletta mine, Maira Valley, Cuneo Province, Piedmont, Italy. Its origin is probably related to the reaction between ore minerals and hydrothermal fluids. It occurs in reddish-brown granules, subhedral millimetre-size crystals, with a pale yellow streak and vitreous lustre. Canosioite is associated with aegirine, baryte, calcite, hematite, bronze Mn-bearing muscovite, unidentified Mn oxides and unidentified arsenates. Canosioite is biaxial (+) with a 2Vmeas= 84(2)°. It is weakly pleochroic withX= brownish yellow,Y= brown,Z= reddish brown,Z>Y>X. Canosioite is monoclinic,P21/m, witha= 7.8642(4),b= 6.1083(3),c= 9.1670(5) Å, β = 112.874(6)°,V= 405.73(4) Å3andZ= 2. Calculated density is 4.943 g cm–3. The seven strongest diffraction lines of the observed powder X-ray diffraction pattern are [din Å, (I) (hkl)]: 3.713 (18)(111), 3.304 (100)(211̄), 3.058 (31)(020), 3.047 (59)(103̄), 2.801 (73)(112), 2.337 (24)(220), 2.158 (24)(123̄). Electron microprobe analyses gave (wt.%): Na2O 0.06, MgO 0.43, CaO 0.02, NiO 0.02, CuO 0.03, SrO 0.42, BaO 49.36, PbO 1.69, Al2O31.25, Mn2O33.89, Fe2O36.95, Sb2O30.01, SiO20.03, P2O50.02, V2O510.88, As2O524.64, SO3 0.01, F 0.02, H2O1.61 was calculated on the basis of 1 (OH,F,H2O) group per formula unit. Infrared spectroscopy confirmed the presence of OH. The empirical formula calculated on the basis of 9 O apfu, is (Ba1.92Pb0.05Sr0.02Na0.01)∑2.00(Fe0.523+Mn0.293+Al0.15Mg0.06)∑1.02[(As0.64V0.36)∑1.00O4]2[(OH0.92F0.01)(H2O)0.07]and the ideal formula is Ba2Fe3+(AsO4)2(OH). The crystal structure was solved by direct methods and found to be isostructural to that of arsenbrackebuschite. The structure model was refined (R1= 2.6%) on the basis of 1245 observed reflections. Canosioite is named after the small municipality of Canosio, where the type locality, the Valletta mine, is situated. The new mineral and name were approved by the International Mineralogical Association Commission on New Minerals and Mineral Names (IMA2015-030).

scholarly journals As-bearing new mineral species from Valletta mine, Maira Valley, Piedmont, Italy: II. Braccoite, NaMn2+5 [Si5AsO17(OH)](OH), description and crystal structure

2015 ◽  
Vol 79 (1) ◽  
pp. 171-189 ◽  
Author(s):  
Fernando Cámara ◽  
Erica Bittarello ◽  
Marco E. Ciriotti ◽  
Fabrizio Nestola ◽  
Francesco Radica ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Direct Methods ◽  
Mineral Species ◽  
New Mineral ◽  
Wavelength Dispersive Spectroscopy ◽  
Calculated Density ◽  
Oh Groups ◽  
International Mineralogical Association ◽  
Mine Dumps ◽  
New Mineral Species

AbstractThe new mineral species braccoite, ideally NaMn2+5[Si5AsO17(OH)](OH), has been discovered in the Valletta mine dumps, in Maira Valley, Cuneo province, Piedmont, Italy. Its origin is probably related to the reaction between ore minerals and hydrothermal fluids. It occurs as subhedral crystals in brown-red coloured thin masses, with a pale-yellow streak and vitreous to resinous lustre. Braccoite is associated with tiragalloite, for which new data are provided, as well as gamagarite, hematite, manganberzeliite, palenzonaite, quartz, saneroite, tokyoite, unidentified Mn oxides, organic compounds, and Mn arsenates and silicates under study.Braccoite is biaxial positive with refractive indices α = 1.749(1), β = 1.750(1), γ = 1.760(1). It is triclinic, space group P1̄, with a = 9.7354(4), b = 9.9572(3), c = 9.0657(3) Å, α = 92.691(2), β = 117.057(4), γ = 105.323(3)°, V = 740.37(4) Å3 and Z = 2. Its calculated density is 3.56 g/cm3. The ten strongest diffraction lines of the observed powder X-ray diffraction (XRD) pattern are [d in Å, (I), (hkl)]: 3.055 (69)(22̄1), 3.042 (43)(102), 3.012 (65)(32̄1̄), 2.985 (55)(23̄1̄), 2.825 (100)(213̄), 2.708 (92)(220), 2.627 (43)(23̄2̄), 2.381 (58)(41̄1̄), 2.226 (25)(214̄) and 1.680 (433̄)(36). Chemical analyses by wavelength-dispersive spectroscopy electron microprobe gave (wt.%): Na2O 4.06, CaO 0.05, MnO 41.76, MgO 0.96, Al2O3 0.04, CuO 0.02, SiO239.73, As2O5 6.87, V2O5 1.43, SO3 0.01 and F 0.04. H2O 2.20 was calculated on the basis of 2OH groups p.f.u. Raman spectroscopy confirmed the presence of (SiO4)4–, (AsO4)3– and OH groups. The empirical formula, calculated on the basis of Σ cations-(Na,K) = 11 p.f.u., in agreement with the results of the crystal structure, is Na1.06(Mn2+4.46Mn3+0.32Mg0.19V3+0.01Al0.01Ca0.01)[Si5(As0.48Si0.37V5+0.15)O17(OH)](OH0.98F0.02); the simplified formula is Na(Mn,Mg,Al,Ca)5[Si5(As,V,Si)O17(OH)](OH,F).Single-crystal XRD allowed the structure to be solved by direct methods and revealed that braccoite is the As-dominant analogue of saneroite. The structure model was refined on the basis of 4389 observed reflections to R1 = 3.47%. Braccoite is named in honour of Dr Roberto Bracco (b. 1959), a systematic minerals collector with a special interest in manganese minerals. The new mineral was approved by the International Mineralogical Association Commission on New Minerals, Nomenclature and Classification (IMA 2013-093).

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