Kummerite, Mn2+Fe3+Al(PO4)2(OH)2·8H2O, a new laueite-group mineral from the Hagendorf Süd pegmatite, Bavaria, with ordering of Al and Fe3+

2016 ◽  
Vol 80 (7) ◽  
pp. 1243-1254 ◽  
Author(s):  
I. E. Grey ◽  
E. Keck ◽  
W. G. Mumme ◽  
A. Pring ◽  
C. M. Macrae ◽  
...  

AbstractKummerite, ideally Mn2+Fe3+A1(PO4)2(OH)2.8H2O, is a new secondary phosphate mineral belonging to the laueite group, from the Hagendorf-Süd pegmatite, Hagendorf, Oberpfalz, Bavaria, Germany. Kummerite occurs as sprays or rounded aggregates of very thin, typically deformed, amber yellow laths. Cleavage is good parallel to ﹛010﹜. The mineral is associated closely with green Zn- and Al-bearing beraunite needles. Other associated minerals are jahnsite-(CaMnMn) and Al-bearing frondelite. The calculated density of kummerite is 2.34 g cm 3. It is optically biaxial (-), α= 1.565(5), β = 1.600(5) and y = 1.630(5), with weak dispersion. Pleochroism is weak, with amber yellow tones. Electron microprobe analyses (average of 13 grains) with H2O and FeO/Fe2O3 calculated on structural grounds and normalized to 100%, gave Fe2O3 17.2, FeO 4.8, MnO 5.4, MgO 2.2, ZnO 0.5, Al2O3 9.8, P2O5 27.6, H2O 32.5, total 100 wt.%. The empirical formula, based on 3 metal apfu is (Mn2+0.37Mg0.27Zn0.03Fe2+0.33)Σ1.00(Fe3+1.06Al0. 94)Σ2.00PO4)1.91(OH)2.27(H2O)7.73. Kummerite is triclinic, P1̄, with the unit-cell parameters of a = 5.316(1) Å, b =10.620(3) Å , c = 7.118(1) Å, α = 107.33(3)°, β= 111.22(3)°, γ = 72.22(2)° and V= 348.4(2) Å3. The strongest lines in the powder X-ray diffraction pattern are [dobs in Å(I) (hkl)] 9.885 (100) (010); 6.476 (20) (001); 4.942 (30) (020); 3.988 (9) (̄110); 3.116 (18) (1̄20); 2.873 (11) (1̄21). Kummerite is isostructural with laueite, but differs in having Al and Fe3+ ordered into alternate octahedral sites in the 7.1 Å trans-connected octahedral chains.

2017 ◽  
Vol 81 (2) ◽  
pp. 287-296 ◽  
Author(s):  
I. E. Grey ◽  
E. Keck ◽  
A. R. Kampf ◽  
C. M. Macrae ◽  
A. M. Glenn ◽  
...  

AbstractWilhelmgümbelite, ideally [ZnFe2+Fe33+(PO4)3(OH)4(H2O)5]·2H2O, is a new secondary phosphate mineral related closely to schoonerite, [ZnMnFe22+Fe3+(PO4)3(OH)2(H2O)7]·2H2O, from oxidized zones of the Hagendorf-Süd pegmatite, Hagendorf, Oberpfalz, Bavaria, Germany. Wilhelmgümbelite occurs as radiating sprays of needle-like rectangular laths, up to 0.2 mm long and with colour varying from light yellow brown to orange red. Cleavage is perfect parallel to {010}. The mineral is associated closely with an oxidized pseudomorph of phosphophyllite, recently named steinmetzite. Other associated minerals are albite, apatite, chalcophanite, jahnsite, mitridatite, muscovite and quartz. The calculated density of wilhelmgümbelite is 2.82 g cm–3. It is optically biaxial (+) with α = 1.560(2), β = 1.669(2), γ = 1.718(2), 2V(meas) = 63(1)° and 2V(calc.) = 65°. Dispersion is weak with r > v, orientation X = b, Y = c, Z = a. Pleochroism is weak, with coloursZ = orange brown, Y = yellow brown, X = light yellow brown, Z >> Y > X. Electron microprobe analyses (average of seven analyses, seven crystals) with H2O and FeO/Fe2O3 calculated on structural grounds, gave FeO 5.8, Fe2O3 25.0, MnO 2.6, ZnO 16.4, P2O5 28.7, H2O 23.4, total 101.9 wt.%. The empirical formula, scaled to 3 P and OH– adjusted for charge balance is Zn1.50Mn0.272+Fe0.602+Fe2.333+(PO4)3·(OH)2.73(H2O)8.27. The structural formula is [Zn(Mn0.27Fe0.733+)∑1.0(Zn0.25Fe0.152+Fe0.603+)∑1.0(Zn0.25Fe0.452+)∑0.7Fe3+(PO4)3(OH,H2O)9]·2H2O.Wilhelmgümbelite has orthorhombic symmetry, Pmab, Z = 4, with the unit-cell parameters of a = 10.987(7) Å, b = 25.378(13) Å, c = 6.387(6) Å and V = 1781(2) Å3. The strongest lines in the powder X-ray diffraction pattern are [dobs in Å(Iobs) (hkl)] 12.65 (100) (020); 8.339 (5) (120); 6.421 (14) (001); 6.228 (8) (011); 4.223 (30) (120) and 2.111 (7) (0 12 0). Wilhelmgümbelite is an oxidized form of schoonerite, with the Mn2+ replaced principally by Fe3+. Its structure differs from that of schoonerite in having the Zn partitioned between two different sites, one five-coordinated as in schoonerite and the other tetrahedrally coordinated. Wilhelmgümbelite also differs structurally from schoonerite in having partial occupation of one of the Fe sites, which appears to be correlated with the Zn partitioning.


2021 ◽  
Vol 59 (6) ◽  
pp. 1865-1886
Author(s):  
Andrew M. McDonald ◽  
Doreen E. Ames ◽  
Ingrid M. Kjarsgaard ◽  
Louis J. Cabri ◽  
William Zhe ◽  
...  

ABSTRACT Marathonite, Pd25Ge9, and palladogermanide, Pd2Ge, are two new platinum-group minerals discovered in the Marathon deposit, Coldwell Complex, Ontario, Canada. Marathonite is trigonal, space group P3, with a 7.391(1), c 10.477(2) Å, V 495.6(1) Å3, Z = 1. The six strongest lines of the X-ray powder-diffraction pattern [d in Å (I)(hkl)] are: 2.436(10)(014,104,120,210), 2.374(29)(023,203,121,211), 2.148(100)(114,030), 1.759(10)(025,205,131,311), 1.3605(13)(233,323,036,306), and 1.2395(14)(144,414,330). Associated minerals include: vysotskite, Au-Ag alloy, isoferroplatinum, Ge-bearing keithconnite, majakite, coldwellite, ferhodsite-series minerals (cuprorhodsite-ferhodsite), kotulskite and mertieite-II, the base-metal sulfides, chalcopyrite, bornite, millerite and Rh-bearing pentlandite, oberthürite and torryweiserite, and silicates including a clinoamphibole and a Fe-rich chlorite-group mineral. Rounded, elongated grains of marathonite are up to 33 × 48 μm. Marathonite is white, but pinkish brown compared to palladogermanide and bornite. No streak or microhardness could be measured. The mineral shows no discernible pleochroism, bireflectance, or anisotropy. The reflectance values (%) in air for the standard COM wavelengths are: 40.8 (470 nm), 44.1 (546 nm), 45.3 (589 nm), and 47.4 (650 nm). The calculated density is 10.933 g/cm3, determined using the empirical formula and the unit-cell parameters from the refined crystal structure. The average result (n = 19) using energy-dispersive spectrometry is: Si 0.11, S 0.39, Cu 2.32, Ge 18.46, Pd 77.83, Pt 1.10, total 100.22 wt.%, corresponding to the empirical formula (based on 34 apfu): (Pd23.82Cu1.19Pt0.18)Σ25.19(Ge8.28S0.40Si0.13)∑8.81 and the simplified formula is Pd25Ge9. The name is for the town of Marathon, Ontario, Canada, after which the Marathon deposit (Coldwell complex) is named. Results from electron backscattered diffraction show that palladogermanide is isostructural with synthetic Pd2Ge. Based on this, palladogermanide is considered to be hexagonal, space group , with a 6.712(1), c 3.408(1) Å, V 133.0(1), Z = 3. The seven strongest lines of the X-ray powder-diffraction pattern calculated for the synthetic analogue [d in Å (I)(hkl)] are: 2.392(100)(111), 2.211(58)(201), 2.197(43)(210), 1.937(34)(300), 1.846(16)(211), 1.7037(16)(002), and 1.2418(18)(321). Associated minerals are the same as for marathonite. Palladogermanide occurs as an angular, anhedral grain measuring 29 × 35 μm. It is white, but grayish-white when compared to marathonite, bornite, and chalcopyrite. Compared to zvyagintsevite, palladogermanide is a dull gray. No streak or microhardness could be measured. The mineral shows no discernible pleochroism, bireflectance, or anisotropy. The reflectance values (%) in air for the standard COM wavelengths for Ro and Ro' are: 46.8, 53.4 (470 nm), 49.5, 55.4 (546 nm), 50.1, 55.7 (589 nm), and 51.2, 56.5 (650 nm). The calculated density is 10.74 g/cm3, determined using the empirical formula and the unit-cell parameters from synthetic Pd2Ge. The average result (n = 14) using wavelength-dispersive spectrometry is: Si 0.04, Fe 0.14, Cu 0.06, Ge 25.21, Te 0.30, Pd 73.10, Pt 0.95, Pb 0.08, total 99.88 wt.%, corresponding (based on 3 apfu) to: (Pd1.97Pt0.01Fe0.01)Σ1.99(Ge1.00Te0.01)∑1.01 or ideally, Pd2Ge. The name is for its chemistry and relationship to palladosilicide. The crystal structure of marathonite was solved by single-crystal X-ray diffraction methods (R = 7.55, wR2 = 19.96 %). It is based on two basic modules, one ordered and one disordered, that alternate along [001]. The ordered module, ∼7.6 Å in thickness, is based on a simple Pd4Ge3 unit cross-linked by Pd atoms to form a six-membered trigonal ring that in turn gives rise to a layered module containing fully occupied Pd and Ge sites. This alternates along [001] with a highly disordered module, ∼3 Å in thickness, composed of a number of partially occupied Pd and Ge sites. The combination of sites in the ordered and disordered modules give the stoichiometric formula Pd25Ge9. The observed paragenetic sequence is: bornite → marathonite → palladogermanide. Phase equilibria studies in the Pd-Ge system show Pd25Ge9 (marathonite) to be stable over the range of 550–970 °C and that Pd2Ge (palladogermanide) is stable down to 200 °C. Both minerals are observed in an assemblage of clinoamphibole, a Fe-rich, chlorite-group mineral, and fragmented chalcopyrite, suggesting physical or chemical alteration, possibly both. Palladogermanide is also found associated with a magnetite of near end-member composition, potentially indicating a relative increase in fO2. Both minerals are considered to have developed at temperatures of 500–600 °C, under conditions of low fS2 and fO2, given the requirements needed to fractionate, concentrate, and form minerals with Ge-dominant chemistries.


2015 ◽  
Vol 79 (2) ◽  
pp. 345-354 ◽  
Author(s):  
Anthony R. Kampf ◽  
Stuart J. Mills ◽  
Barbara P. Nash ◽  
Maurizio Dini ◽  
Arturo A. Molina Donoso

AbstractTapiaite (IMA2014-024), Ca5Al2(AsO4)4(OH)4·12H2O, is a new mineral from the Jote mine, Tierra Amarilla, Copiapó Province, Atacama, Chile. The mineral is a late-stage, low-temperature, secondary mineral occurring with conichalcite, joteite, mansfieldite, pharmacoalumite, pharmacosiderite and scorodite in narrow seams and vughs in the oxidized upper portion of a hydrothermal sulfide vein hosted by volcanoclastic rocks. Crystals occur as colourless blades, flattened on {101} and elongated and striated along [010], up to ∼0.5 mm long, and exhibiting the forms {101}, {101} and {111}. The blades are commonly intergrown in subparallel bundles and less commonly in sprays. The mineral is transparent and has a white streak and vitreous lustre. The Mohs hardness is estimated to be between 2 and 3, the tenacity is brittle, and the fracture is splintery. It has two perfect cleavages on {101} and {101}. The calculated density based on the empirical formula is 2.681 g cm–3. It is optically biaxial (+) with α = 1.579(1), β = 1.588(1), γ = 1.610(1) (white light), 2Vmeas = 66(2)° and 2Vcalc = 66°. The mineral exhibits no dispersion. The optical orientation is X ≈ [101]; Y = b, Z ≈ [101]. The electron-microprobe analyses (average of five) provided: Na2O 0.09, CaO 24.96, CuO 0.73, Al2O3 10.08, Fe2O3 0.19, As2O5 40.98, Sb2O5 0.09, H2 O 23.46 (structure), total 100.58 wt.%. In terms of the structure, the empirical formula (based on 32 O a.p.f.u.) is (Ca4.83Cu0.102+Na0.03)Σ4.96(Al2.14Fe0.033+)Σ2.17[(As3.875+Sb0.015+)Σ3.88O16][(OH)3.76(H2O)0.24]Σ4(H2O)10·2H2O. The mineral is easily soluble in RT dilute HCl. Tapiaite is monoclinic, P21/n, with unit-cell parameters a = 16.016(1), b = 5.7781(3), c = 16.341(1) Å, β = 116.704(8)°, V = 1350.9(2) Å3 and Z = 2. The eight strongest lines in the powder X-ray diffraction pattern are [dobs Å(I)(hkl)]: 13.91(100)(101), 7.23(17)(200,002), 5.39(22)(110,011), 4.64(33)(112,211,303), 3.952(42)(113,311,213), 3.290(35)(214,412,114,411), 2.823(39)(303,315) and 2.753(15)(513,115,121,511). The structure of tapiaite (R1 = 5.37% for 1733 Fo > 4σF) contains Al(AsO4)(OH)2 chains of octahedra and tetrahedra that are topologically identical to the chain in the structure of linarite. CaO8 polyhedra condense to the chains, forming columns, which are decorated with additional peripheral AsO4 tetrahedra. The CaO8 polyhedra in adjacent columns link to one another by corner-sharing to form thick layers parallel to {101} and the peripheral AsO4 tetrahedra link to CaO6 octahedra in the interlayer region, resulting in a framework structure.


2017 ◽  
Vol 81 (4) ◽  
pp. 917-922
Author(s):  
Peter Elliott

AbstractThe crystal structure of the copper aluminium phosphate mineral sieleckiite, Cu3Al4(PO4)2 (OH)12·2H2O, from the Mt Oxide copper mine, Queensland, Australia was solved from single-crystal X-ray diffraction data utilizing synchrotron radiation. Sieleckiite has monoclinic rather than triclinic symmetry as previously reported and is space group C2/m with unit-cell parameters a = 11.711(2), b = 6.9233(14), c = 9.828(2) Å, β = 92.88(3)°, V = 795.8(3) Å3and Z = 2. The crystal structure, which has been refined to R1 = 0.0456 on the basis of 1186 unique reflections with Fo > 4σF, is a framework of corner-, edge- and face- sharing Cu and Al octahedra and PO4 tetrahedra.


Author(s):  
Dan Holtstam ◽  
Luca Bindi ◽  
Paola Bonazzi ◽  
Hans-Jürgen Förster ◽  
Ulf B. Andersson

ABSTRACT Arrheniusite-(Ce) is a new mineral (IMA 2019-086) from the Östanmossa mine, one of the Bastnäs-type deposits in the Bergslagen ore region, Sweden. It occurs in a metasomatic F-rich skarn, associated with dolomite, tremolite, talc, magnetite, calcite, pyrite, dollaseite-(Ce), parisite-(Ce), bastnäsite-(Ce), fluorbritholite-(Ce), and gadolinite-(Nd). Arrheniusite-(Ce) forms anhedral, greenish-yellow translucent grains, exceptionally up to 0.8 mm in diameter. It is optically uniaxial (–), with ω = 1.750(5), ε = 1.725(5), and non-pleochroic in thin section. The calculated density is 4.78(1) g/cm3. Arrheniusite-(Ce) is trigonal, space group R3m, with unit-cell parameters a = 10.8082(3) Å, c = 27.5196(9) Å, and V = 2784.07(14) Å3 for Z = 3. The crystal structure was refined from X-ray diffraction data to R1 = 3.85% for 2286 observed reflections [Fo > 4σ(Fo)]. The empirical formula for the fragment used for the structural study, based on EPMA data and results from the structure refinement, is: (Ca0.65As3+0.35)Σ1(Mg0.57Fe2+0.30As5+0.10Al0.03)Σ1[(Ce2.24Nd2.13La0.86Gd0.74Sm0.71Pr0.37)Σ7.05(Y2.76Dy0.26Er0.11Tb0.08Tm0.01Ho0.04Yb0.01)Σ3.27Ca4.14]Σ14.46(SiO4)3[(Si3.26B2.74)Σ6O17.31F0.69][(As5+0.65Si0.22P0.13)Σ1O4](B0.77O3)F11; the ideal formula obtained is CaMg[(Ce7Y3)Ca5](SiO4)3(Si3B3O18)(AsO4)(BO3)F11. Arrheniusite-(Ce) belongs to the vicanite group of minerals and is distinct from other isostructural members mainly by having a Mg-dominant, octahedrally coordinated site (M6); it can be considered a Mg-As analog to hundholmenite-(Y). The threefold coordinated T5 site is partly occupied by B, like in laptevite-(Ce) and vicanite-(Ce). The mineral name honors C.A. Arrhenius (1757–1824), a Swedish officer and chemist, who first discovered gadolinite-(Y) from the famous Ytterby pegmatite quarry.


2020 ◽  
pp. 1-8
Author(s):  
Koichi Momma ◽  
Takuji Ikeda ◽  
Toshiro Nagase ◽  
Takahiro Kuribayashi ◽  
Chibune Honma ◽  
...  

Abstract Bosoite (IMA2014-023) is a new silica clathrate mineral containing hydrocarbon molecules in its crystal structure. Bosoite can be considered structurally as a silica analogue of the structure-H gas hydrate, where guest molecules are trapped in cage-like voids constructed of the host framework. The mineral occurs in the Miocene tuffaceous sedimentary rocks at Arakawa, Minami-boso City, Chiba Prefecture, Japan. Bosoite is hexagonal, and it crystallises as an epitaxial intergrowth on chibaite crystals, with the {0001} of bosoite parallel to octahedral {111} form of chibaite. Crystals are colourless and transparent with vitreous lustre. The calculated density is 2.04 g/cm3. The empirical formula (based on 2 O apfu and guest molecules assumed as CH4) is Na0.01(Si0.98Al0.02)Σ1.00O2⋅0.50CH4; the end-member formula is SiO2⋅nC x H2x+2. Bosoite has the space group P6/mmm, with the unit-cell parameters a = 13.9020(3) Å, c = 11.2802(2) Å, V = 1887.99(6) Å3 and Z = 34. The crystal structure of bosoite was refined by single-crystal X-ray diffraction and converged to R1 = 4.26% for the average model and R1 = 2.96% for the model where all oxygen sites are split.


2005 ◽  
Vol 69 (2) ◽  
pp. 145-153 ◽  
Author(s):  
R. S. W. Braithwaite ◽  
R. G. Pritchard ◽  
W. H. Paar ◽  
R. A. D. Pattrick

AbstractTiny green crystals from Kabwe, Zambia, associated with hopeite and tarbuttite (and probably first recorded in 1908 but never adequately characterized because of their scarcity) have been studied by X-ray diffraction, microchemical and electron probe microanalysis, infrared spectroscopy, and synthesis experiments. They are shown to be orthorhombic, stoichiometric CuZnPO4OH, of species rank, forming the end-member of a solid-solution series to libethenite, Cu2PO4OH, and are named zincolibethenite. The libethenite structure is unwilling to accommodate any more Zn substituting for Cu at atmospheric pressure, syntheses using Zn-rich solutions precipitating a mixture of zincolibethenite with hopeite, Zn3(PO4)2.4H2O. Single-crystal X-ray data confirm that the Cu(II) occupies the Jahn-Teller distorted 6-coordinate cation site in the libethenite lattice, and the Zn(II) occupies the 5-coordinate site. The space group of zincolibethenite is Pnnm, the same as that of libethenite, with unit-cell parameters a = 8.326, b = 8.260, c = 5.877 Å , V = 404.5 Å 3, Z = 4, calculated density = 3.972 g/cm3 (libethenite has a = 8.076, b = 8.407, c = 5.898 Å , V = 400.44 Å 3, Z = 4, calculated density = 3.965 g/cm3). Zincolibethenite is biaxial negative, with 2Vα(calc.) of 49°, r<v, and α = 1.660, β = 1.705, and γ = 1.715 The mineral is named for its relationship to libethenite.


2010 ◽  
Vol 74 (3) ◽  
pp. 463-468 ◽  
Author(s):  
V. A. Kovalenker ◽  
O. Yu. Plotinskaya ◽  
C. J. Stanley ◽  
A. C. Roberts ◽  
A. M. McDonald ◽  
...  

AbstractKurilite, with the simplified formula, Ag8Te3Se, is a new mineral from the Prasolovskoe epithermal Au-Ag deposit, Kunashir Island, Kuril arc, Russian Federation. It occurs as aggregates up to 2 mm in size, composed of brittle xenomorphic grains, up to several μm in size, in quartz, associated with tetrahedrite, hessite, sylvanite and petzite. Kurilite is opaque, grey, with a metallic lustre and a black streak. Under plane-polarized light, kurilite is white with no observed bireflectance, cleavage, or parting observed. Under crossed polars it appears isotropic without internal reflections. Reflectance values in air and in oil, are tabulated. It has a mean VHN (25 g load) of 99.9 kg/mm2 which equates roughly to a Mohs hardness of 3. Electron microprobe analyses yield a mean composition of Ag 63.71, Au 0.29, Te 29.48, Se 5.04, S 0.07, total 98.71 wt.%. The empirical formula (based on 12 atoms) is (Ag7.97Au0.02)Σ7.99Te3.00(Se0.86Te0.12S0.03)Σ1.01. The calculated density is 7.799 g/cm3 (based on the empirical formula and unit-cell parameters refined from single-crystal data). Kurilite is rhombohedral, R3 or , a 15.80(1), c 19.57(6) Å, V 4231(12)Å3, c:a 1.2386, Z = 15. Its crystal structure remains unsolved. The seven strongest lines of the X-ray powder-diffraction pattern [d in Å (I)(hkl)] are: 3.727(20)(131), 2.996(50)(232), 2.510(30)(226,422), 2.201(100)(128,416,342), 2.152(20)(603), 2.079(30)(253), 2.046(20)(336,434). The mineral is named after the locality.


Author(s):  
Dan Holtstam ◽  
Cristian Biagioni ◽  
Ulf Hålenius

AbstractBrattforsite is an approved mineral (IMA2019-127), with ideal formula Mn19(AsO3)12Cl2. Associated minerals in the type specimen from the Brattfors mine, Nordmark (Värmland, Sweden) include jacobsite, alleghanyite, phlogopite, calcite and dolomite. Brattforsite, forming subhedral, mostly equant crystals up to 0.5 mm across, is orange to reddish-brown with a white streak, and translucent with a resinous to vitreous lustre. The fracture is uneven to subconchoidal, and no cleavage is observed. It is very weakly pleochroic in yellow, optically biaxial (–) with 2V = 44(5)° and has calculated mean refractive index of 1.981. Measured and calculated density values are 4.49(1) and 4.54(1) g·cm− 3, respectively. Chemical analyses yields (in wt%): MgO 0.62, CaO 1.26, MnO 48.66, FeO 0.13, As2O3 46.72, Cl 2.61, H2Ocalc 0.07, O ≡ Cl –0.59, sum 99.49, corresponding to the empirical formula (Mn17.67Ca0.58Mg0.40Fe0.05)∑18.70As12.17O35.90Cl1.90(OH)0.20, based on 38 (O + Cl + OH) atoms per formula unit. The five strongest Bragg peaks in the powder X-ray diffraction pattern are [d (Å), I (%), (hkl)]: 2.843,100, ($$ \overline{4} $$ 4 - 44); 2.828, 99, (444); 1.731, 32, (880); 2.448, 28, (800); 1.739, 25, (088). Brattforsite is monoclinic and pseudotetragonal, space group I2/a, with unit-cell parameters a = 19.5806(7), b = 19.5763(7), c = 19.7595(7) Å, β = 90.393(3)°, V = 7573.9(5) Å3 and Z = 8. The crystal structure was solved and refined to an R1 index of 3.4 % for 7445 reflections [Fo > 4σ(Fo)]. Brattforsite has the same overall structural topology as magnussonite (i.e., the species can be considered as homeotypic), but with 12 independent tetrahedrally coordinated As sites and 21 Mn sites with varying (4–8) coordination. The Mn-centered polyhedra, bonded through edge- and face-sharing, give rise to a three-dimensional framework. The (AsO3)3− groups are bonded to this framework through corner- and edge-sharing. Spectroscopic measurements (optical absorption, Raman, FTIR) carried out support the interpretation of the compositional and structural data.


2018 ◽  
Vol 233 (7) ◽  
pp. 469-477
Author(s):  
Sergey M. Aksenov ◽  
Nikita V. Chukanov ◽  
Jörg Göttlicher ◽  
Rupert Hochleitner ◽  
Ekaterina S. Zarubina ◽  
...  

Abstract Mn2+-bearing eleonorite from the Hagendorf South pegmatite situated south of Waidhaus, Upper Palatinate, Bavaria, Germany was study based on single crystal X-ray analysis, Mn and Fe K-edge XANES spectroscopy, as well as IR spectroscopy. According to spectroscopic data, all Mn is bivalent, and all Fe is trivalent. The empirical formula of the mineral is (Mn2+0.58Zn0.13Mg0.04 Fe3+5.24)Σ5.98(PO4)4(H2O,OH,O)11. The monoclinic unit-cell parameters are: a=20.832(3) Å, b=5.1569(3) Å, c=19.200(2) Å, β=93.01(1)°; space group C2/c. The structure was refined to R1=5.20% in anisotropic approximation using 1994 reflections with I>3σ(I). Despite in most beraunite-group minerals M1-site demonstrates selective accumulation of bivalent cations, in Mn-bearing eleonorite Mn2+-cations are disordered between octahedral sites without statistical predominance anywhere; all octahedral M(1–4)-sites are predominantly occupied by Fe3+. M1-site is half-occupied by Fe3+ and contains subordinate Mn2+ and minor Zn2+ and Mg2+. Based on the new data we suppose that Mn-bearing eleonorite was formed as a secondary phase as a result of oxidation of a primary Mn-bearing beraunite-group mineral in with Mn2+ was initially distributed between different M sites.


Sign in / Sign up

Export Citation Format

Share Document