Markeyite, a new calcium uranyl carbonate mineral from the Markey mine, San Juan County, Utah, USA

2018 ◽  
Vol 82 (5) ◽  
pp. 1089-1100 ◽  
Author(s):  
Anthony R. Kampf ◽  
Jakub Plášil ◽  
Anatoly V. Kasatkin ◽  
Joe Marty ◽  
Jiří Čejka
Keyword(s):  
Secondary Phase ◽  
New Mineral ◽  
San Juan ◽  
X Ray Diffraction ◽  
X Ray ◽  
Light Yellow ◽  
Uranyl Carbonate ◽  
Laser Crystals ◽  
Mohs Hardness ◽  
San Juan County

ABSTRACTThe new mineral markeyite (IMA2016-090), Ca9(UO2)4(CO3)13·28H2O, was found in the Markey mine, San Juan County, Utah, USA, where it occurs as a secondary phase on asphaltum in association with calcite, gypsum and natrozippeite. The mineral is pale yellowish-green with white streak and fluoresces bright bluish white under a 405 nm laser. Crystals are transparent and have vitreous to pearly lustre. It is brittle, with Mohs hardness 1½ to 2, irregular fracture and three cleavages: perfect on {001}; good on {100} and {010}. The measured density is 2.68 g cm–3. Crystals are blades, flattened on {001} and elongate on [010], exhibiting the forms {100}, {010}, {001}, {110}, {101}, {011} and {111}. Markeyite is optically biaxial (–) with α = 1.538(2), β = 1.542(2) and γ = 1.545(2) (white light); the measured 2V is 81(2)°; the dispersion isr<v(weak); the optical orientation isX=c,Y=b,Z=a; and pleochroism isX= light greenish yellow,YandZ= light yellow (X>Y≈Z). Electron microprobe analyses (energy-dispersive spectroscopy mode) yielded CaO 18.60, UO342.90, CO221.30 (calc.) and H2O 18.78 (calc.), total 101.58 wt.% and the empirical formula Ca8.91(U1.01O2)4(CO3)13·28H2O. The six strongest powder X-ray diffraction lines are [dobsÅ(I)(hkl)]: 10.12(69)(001), 6.41(91)(220,121), 5.43(100)(221), 5.07(33)(301,002,131), 4.104(37)(401,141) and 3.984(34)(222). Markeyite is orthorhombic,Pmmn,a= 17.9688(13),b= 18.4705(6),c= 10.1136(4) Å,V= 3356.6(3) Å3andZ= 2. The structure of markeyite (R1= 0.0435 for 3427Fo> 4σF) contains uranyl tricarbonate clusters (UTC) that are linked by Ca–O polyhedra forming thick corrugated heteropolyhedral layers. Included within the layers is an additional disordered CO3group linking the Ca–O polyhedra. The layers are linked to one another and to interlayer H2O groups only via hydrogen bonds. The structure bears some similarities to that of liebigite.

Pseudomeisserite-(NH4), a new mineral with a novel uranyl-sulfate linkage from the Blue Lizard mine, San Juan County, Utah, USA

2020 ◽  
Vol 84 (3) ◽  
pp. 435-443
Author(s):  
Anthony R. Kampf ◽  
Travis A. Olds ◽  
Jakub Plášil ◽  
Barbara P. Nash ◽  
Joe Marty
Keyword(s):  
New Mineral ◽  
San Juan ◽  
Optical Orientation ◽  
Uranyl Sulfate ◽  
X Ray ◽  
Pale Yellow ◽  
Light Yellow ◽  
Perfect Cleavage ◽  
Mohs Hardness ◽  
San Juan County

AbstractThe new mineral pseudomeisserite-(NH4) (IMA2018-166), (NH4,K)2Na4[(UO2)2(SO4)5]⋅4H2O, was found in the Blue Lizard mine, San Juan County, Utah, USA, where it occurs as light yellow prisms in a secondary assemblage with belakovskiite, blödite, changoite, ferrinatrite, gypsum, ivsite, metavoltine and tamarugite. The streak is very pale yellow and the fluorescence is bright lime green under 405 nm ultraviolet light. Crystals are transparent with vitreous lustre. The tenacity is brittle, the Mohs hardness is 2½, the fracture is curved or conchoidal and there is one perfect cleavage on {100}. The mineral is easily soluble in H2O and has a measured density of 3.22(2) g⋅cm–3. Pseudomeisserite-(NH4) is optically biaxial (–) with α = 1.536(2), β = 1.559(2) and γ = 1.565(2) (white light); 2Vmeas. = 53(1)°; dispersion is r > v, distinct; pleochroism: X colourless, Y light yellow and Z pale yellow (X < Z < Y); optical orientation: Z = b, Y ∧ c = 33° in obtuse β). Electron microprobe analyses (WDS mode) provided (NH4)1.49K0.60Na3.87U2.00S5.04O28H7.78. The five strongest X-ray powder diffraction lines are [dobs, Å(I)(hkl)]: 12.69(76)(100), 6.83(84)(012,102), 6.01(100)($\bar{2}$02), 3.959(67)($\bar{2}$21,$\bar{2}$14,$\bar{1}$23) and 3.135(76)($\bar{2}$06,223,$\bar{1}$16). Pseudomeisserite-(NH4) is monoclinic, P21/c, a = 13.1010(3), b = 10.0948(2), c = 19.4945(14) Å, β = 104.285(7)°, V = 2498.5(2) Å3 and Z = 4. The structural unit in the structure (R1 = 0.0254 for 3837 I > 2σI reflections) is a novel [(UO2)2(SO4)5]6– uranyl-sulfate band.

Feynmanite, a new sodium uranyl sulfate mineral from Red Canyon, San Juan County, Utah, USA

2018 ◽  
Vol 83 (02) ◽  
pp. 153-160 ◽  
Author(s):  
Anthony R. Kampf ◽  
Travis A. Olds ◽  
Jakub Plášil ◽  
Joe Marty ◽  
Samuel N. Perry
Keyword(s):  
Secondary Phase ◽  
New Mineral ◽  
San Juan ◽  
Uranyl Sulfate ◽  
Calculated Density ◽  
Laser Crystals ◽  
Perfect Cleavage ◽  
Mohs Hardness ◽  
San Juan County ◽  
Pale Green

AbstractThe new mineral feynmanite, Na(UO2)(SO4)(OH)·3.5H2O, was found in both the Blue Lizard and Markey mines, San Juan County, Utah, USA, where it occurs as a secondary phase on pyrite-rich asphaltum in association with chinleite-(Y), gypsum, goethite, natrojarosite, natrozippeite, plášilite, shumwayite (Blue Lizard) and wetherillite (Markey). The mineral is pale greenish yellow with a white streak and fluoresces bright greenish white under a 405 nm laser. Crystals are transparent with a vitreous lustre. It is brittle, with a Mohs hardness of ~2, irregular fracture and one perfect cleavage on {010}. The calculated density is 3.324 g cm–3. Crystals are thin needles or blades, flattened on {010} and elongate on [100], exhibiting the forms {010}, {001}, {101} and {10$\bar{1}$}, and are up to ~0.1 mm in length. Feynmanite is optically biaxial (–), with α = 1.534(2), β = 1.561(2) and γ = 1.571(2) (white light); 2Vmeas.= 62(2)°; no dispersion; and optical orientation:X=b,Y≈a,Z≈c. It is weakly pleochroic:X= colourless,Y= very pale green yellow andZ= pale green yellow (X&lt;Y&lt;Z). Electron microprobe analyses (WDS mode) provided (Na0.84Fe0.01)(U1.01O2)(S1.01O4)(OH)·3.5H2O. The five strongest powder X-ray diffraction lines are [dobsÅ(I)(hkl)]: 8.37(100)(010), 6.37(33)($\bar{1}$01,101), 5.07(27)($\bar{1}$11,111), 4.053(46)(004,021) and 3.578(34)(120). Feynmanite is monoclinic, has space groupP2/n,a= 6.927(3),b= 8.355(4),c= 16.210(7) Å, β = 90.543(4)°,V= 938.1(7) Å3andZ= 4. The structure of feynmanite (R1= 0.0371 for 1879Io&gt; 2σI) contains edge-sharing pairs of pentagonal bipyramids that are linked by sharing corners with SO4groups, yielding a [(UO2)2(SO4)2(OH)2]2–sheet based on the phosphuranylite anion topology. The sheet is topologically identical to those in deliensite, johannite and plášilite. The dehydration of feynmanite to plášilite results in interlayer collapse involving geometric reconfiguration of the sheets and the ordering of Na.

Alwilkinsite-(Y), a new rare-earth uranyl sulfate mineral from the Blue Lizard mine, San Juan County, Utah, USA

2017 ◽  
Vol 81 (4) ◽  
pp. 895-907 ◽  
Author(s):  
Anthony R. Kampf ◽  
Jakub Plášil ◽  
Jiří Čejka ◽  
Joe Marty ◽  
Radek Škoda ◽  
...  
Keyword(s):  
New Mineral ◽  
San Juan ◽  
X Ray Diffraction ◽  
Uranyl Sulfate ◽  
Calculated Density ◽  
Secondary Alteration ◽  
X Ray ◽  
Perfect Cleavage ◽  
Mohs Hardness ◽  
San Juan County

AbstractThe new mineral alwilkinsite-(Y) (IMA2015-097), Y(H2O)7[(UO2)3(SO4)2O(OH)3]·7H2O, was found in the Blue Lizard mine, San Juan County, Utah, USA, where it occurs as a secondary alteration phase.The mineral is slightly flexible before brittle failure with splintery fracture and perfect cleavage parallel to [010], has Mohs hardness of ∼2–2½, exhibits dull greenish-grey fluorescence and has a calculated density of 3.371 g cm–3. Alwilkinsite-(Y) occursas yellowish-green needles, elongate on [010], with domatic terminations and exhibits the forms {102}, {301} and {124}. It is optically biaxial (+) with α = 1.573(1), β = 1.581(1), γ = 1.601(1) (white light), the measured 2V is 65.3(1)°, the dispersion is r<v (weak), the optical orientation is X = c, Y = a, Z = b and there is no pleochroism. Electron microprobe analyses yielded the empirical formula (Y0.66Dy0.08Gd0.06Er0.05Nd0.03Yb0.03Sm0.02Ce0.01)∑0.94(H2O)7[(UO2)3(S1.01O4)2O(OH)3]·7H2O.The eight strongest powder X-ray diffraction lines are [dobs Å(I)(hkl)]: 9.88(100)(101,002), 7.47(13)(102), 5.621(17)(103,201), 4.483(18)(104), 3.886(14)(130,222), 3.322(46)(multiple), 3.223(13)(multiple) and 3.145(16)(034). Alwilkinsite-(Y) is orthorhombic,P212121, a = 11.6194(5), b = 12.4250(6), c = 19.4495(14) Å, V = 2807.9(3) Å3 and Z = 4. The structure of alwilkinsite-(Y) (R1 = 0.042 for 4244 Fo > 4σF)contains edge-sharing chains of uranyl bipyramids with outlying sulfate tetrahedra that are similar to the chain linkages within the uranyl sulfate sheets of the zippeite structure. Short segments of the uranyl sulfate chains in the alwilkinsite-(Y) structure have the same topology as portionsof the uranyl sulfate linkages in uranopilite. Alwilkinsite-(Y) is named for Alan (Al) J. Wilkins, MD (born 1955), the discoverer of the mineral.

Lussierite, a new sodium uranyl sulfate mineral with bidentate UO7–SO4linkage from the Blue Lizard mine, San Juan County, Utah, USA

2019 ◽  
Vol 83 (6) ◽  
pp. 799-808 ◽  
Author(s):  
Anthony R. Kampf ◽  
Travis A. Olds ◽  
Jakub Plášil ◽  
Barbara P. Nash ◽  
Joe Marty
Keyword(s):  
Pentagonal Bipyramid ◽  
New Mineral ◽  
San Juan ◽  
Charge Balance ◽  
Uranyl Sulfate ◽  
Wavelength Dispersive Spectroscopy ◽  
X Ray ◽  
Mohs Hardness ◽  
San Juan County ◽  
Pale Green

AbstractThe new mineral lussierite (IMA2018-101), Na10[(UO2)(SO4)4](SO4)2(H2O)3, was found in the Blue Lizard mine, San Juan County, Utah, USA, where it occurs as pale green–yellow prisms or blades in a secondary assemblage with belakovskiite, ferrinatrite, halite, ivsite, metavoltine and thénardite. The streak is white and the fluorescence is bright cyan under 365 nm ultraviolet light. Crystals are transparent with vitreous lustre. The tenacity is brittle, the Mohs hardness is 2½, the fracture is irregular and no cleavage was observed. The mineral is easily soluble in H2O and has a measured density of 2.87(2) g cm–3. Lussierite is optically biaxial (+), with α = 1.493(1), β = 1.505(1) and γ = 1.518(1) (white light); 2Vmeas.= 88(1)°; dispersion isr>v, moderate; pleochroism:X= colourless,YandZ= green yellow (X<Y≈Z); optical orientation:X=b,Z∧a= 44° in obtuse β. Electron microprobe analyses (wavelength-dispersive spectroscopy mode) provided Na10(U0.99O2)(S1.00O4)6·3H2O (+0.06 H for charge balance). The five strongest X-ray powder diffraction lines are [dobsÅ(I)(hkl)]: 6.69(95)($\bar{1}$11,130), 4.814(100)(150,002,060), 3.461(83)(171,$\bar{2}$02), 2.955(81)(113,330) and 2.882(74)($\bar{1}$91,311,191,0·10·0). Lussierite is monoclinic,Cc,a= 9.3134(4),b= 28.7501(11),c= 9.6346(7) Å, β = 93.442(7)°,V= 2575.1(2) Å3andZ= 4. The structure (R1= 0.0298 for 5202I> 2σI) contains a [(UO2)(SO4)4]6–uranyl sulfate cluster in which one SO4tetrahedron shares an edge (bidentate linkage) with the UO7pentagonal bipyramid. The uranyl sulfate clusters occur in layers and are linked through a complex network of bonds involving Na+cations, isolated SO4tetrahedra and isolated H2O groups.

Leószilárdite, the first Na,Mg-containing uranyl carbonate from the Markey Mine, San Juan County, Utah, USA

2017 ◽  
Vol 81 (5) ◽  
pp. 1039-1050 ◽  
Author(s):  
Travis A. Olds ◽  
Luke R. Sadergaski ◽  
Jakub Plášil ◽  
Anthony R. Kampf ◽  
Peter C. Burns ◽  
...  
Keyword(s):  
New Mineral ◽  
San Juan ◽  
Pale Yellow ◽  
Light Yellow ◽  
Spectroscopic Analyses ◽  
Uranyl Carbonate ◽  
Anion Clusters ◽  
Perfect Cleavage ◽  
San Juan County ◽  
American Physicist

AbstractLeószilárdite (IMA2015-128), Na6Mg(UO2)2(CO3)6·6H2O, was found in the Markey Mine, Red Canyon, White Canyon District, San Juan County, Utah, USA, in areas with abundant andersonite, natrozippeite, gypsum, anhydrite, and probable hydromagnesite along with other secondary uranium minerals bayleyite, čejkaite and johannite. The new mineral occurs as aggregates of pale yellow bladed crystals flattened on ﹛001﹜ and elongated along [010], individually reaching up to 0.2 mmlong. More commonly it occurs as pale yellow pearlescent masses to 2 mm consisting of very small plates. Leószilárdite fluoresces green under both longwave and shortwave ultraviolet light, and is translucent with a white streak, hardness of 2 (Mohs), and brittle tenacity with uneven fracture. The new mineral is readily soluble in room temperature H2O. Crystals have perfect cleavage along ﹛001﹜, and exhibit the forms ﹛110﹜,﹛001﹜,﹛100﹜,﹛101﹜ and ﹛101﹜. Optically, leószilárdite is biaxial (-), α= 1.504(1), β= 1.597(1), γ= 1.628(1) (white light); 2V (meas.) = 57(1)°, 2V (calc.) = 57.1°; dispersion r > v, slight. Pleochroism: X= colourless, Y and Z= light yellow; X<Y ≈ Z The average of six wavelength dispersive spectroscopic analyses provided Na2O 14.54, MgO 3.05, UO3 47.95, CO2 22.13, H2O 9.51, total 97.18 wt.%. The empirical formula is Na5.60Mg0.90U2O28C6H12.60, based on 28 O apfu. Leószilárdite is monoclinic, C2/m, a = 11.6093(21), b = 6.7843(13), c = 15.1058(28) Å, β = 91.378(3)°, V= 1189.4(4) Å3 and Z = 2. The crystal structure (R1 = 0.0387 for 1394 reflections with Iobs > 4σI), consists of uranyl tricarbonate anion clusters [(UO2)(CO3)3]4- held together in part by irregular chains of NaO5(H2O) polyhedra sub parallel to [010]. Individual uranyl tricarbonate clusters are also linked together by three-octahedron units consisting of two Na-centred octahedra that share the opposite faces of a Mg-centred octahedron at the centre (Na–Mg–Na), and have the composition Na2MgO12(H2O)4. The name of the new mineral honours the Hungarian-American physicist, inventor and biologist Dr. Leó Szilárd (1898–1964).

New arsenate minerals from the Arsenatnaya fumarole, Tolbachik volcano, Kamchatka, Russia. VIII. Arsenowagnerite, Mg2(AsO4)F

2018 ◽  
Vol 82 (4) ◽  
pp. 877-888 ◽  
Author(s):  
Igor V. Pekov ◽  
Natalia V. Zubkova ◽  
Atali A. Agakhanov ◽  
Vasiliy O. Yapaskurt ◽  
Nikita V. Chukanov ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Scoria Cone ◽  
New Mineral ◽  
Lemon Yellow ◽  
X Ray Diffraction ◽  
Absorption Bands ◽  
X Ray ◽  
Light Yellow ◽  
Tolbachik Volcano ◽  
Mohs Hardness

ABSTRACTA new mineral arsenowagnerite, Mg2(AsO4)F, the arsenate analogue of wagnerite, was found in sublimates of the Arsenatnaya fumarole at the Second scoria cone of the Northern Breakthrough of the Great Tolbachik Fissure Eruption, Tolbachik volcano, Kamchatka, Russia. It is associated closely with johillerite, tilasite, anhydrite, hematite, fluorophlogopite, cassiterite, calciojohillerite, aphthitalite and fluoborite. Arsenowagnerite occurs as equant to tabular crystals up to 1 mm across combined in interrupted crusts up to 0.1 cm × 1.5 cm × 3 cm. The mineral is transparent, light yellow, lemon-yellow, greenish-yellow or colourless and has a vitreous lustre. Arsenowagnerite is brittle, with Mohs hardness of ~5. Cleavage is distinct, the fracture is uneven. Dcalc = 3.70 g cm–3. Arsenowagnerite is optically biaxial (+), α = 1.614(2), β = 1.615(2), γ = 1.640(2) and 2Vmeas = 25(5)°. Wavenumbers of the strongest absorption bands in the IR spectrum (cm–1) are: 874, 861, 507, 491 and 470. The chemical composition (average of six electron-microprobe analyses, wt.%) is: MgO 38.72, CaO 0.23, MnO 0.32, CuO 0.60, ZnO 0.05, Fe2O3 0.11, TiO2 0.03, SiO2 0.08, P2O5 0.18, V2O5 0.03, As2O5 54.96, SO3 0.10, F 8.91 and –O=F –3.75, total 100.57. The empirical formula calculated on the basis of 5 (O + F) apfu is: (Mg1.98Cu0.02Mn0.01Ca0.01)Σ2.02(As0.99P0.01)Σ1.00O4.03F0.97. Arsenowagnerite is monoclinic, P21/c, a = 9.8638(3), b = 12.9830(3), c = 12.3284(3) Å, β = 109.291(3)°, V = 1490.15(7) Å3 and Z = 16. The strongest reflections of the powder X-ray diffraction pattern [d,Å(I)(hkl)] are: 5.80(41)(002), 5.31(35)(120), 3.916(37)($\bar 2$21), 3.339(98)(221, 023), 3.155(65)(202), 3.043(100)($\bar 1$41), 2.940(72)($\bar 2$04), 2.879(34)($\bar 3$22) and 2.787(51)(320, $\bar 1$24). The crystal structure was solved from single-crystal X-ray diffraction data, R = 0.0485. Arsenowagnerite is isostructural to wagnerite-Ma2bc. The crystal structure is built by almost regular AsO4 tetrahedra, distorted MgO4F2 octahedra and distorted MgO4F trigonal bipyramids.

Chinleite-(Y), NaY(SO4)2·H2O, a new rare-earth sulfate mineral structurally related to bassanite

2017 ◽  
Vol 81 (4) ◽  
pp. 909-916 ◽  
Author(s):  
Anthony R. Kampf ◽  
Barbara P. Nash ◽  
Joe Marty
Keyword(s):  
Room Temperature ◽  
Three Dimensional ◽  
New Mineral ◽  
X Ray Diffraction ◽  
Calculated Density ◽  
Secondary Alteration ◽  
X Ray ◽  
Mohs Hardness ◽  
San Juan County ◽  
Bow Tie

AbstractThe new mineral chinleite-(Y) (IMA2016-017), NaY(SO4)2·H2O, was found in the Blue Lizard mine, San Juan County, Utah, USA, where it occurs as a secondary alteration phase. Chinleite-(Y) crystals are thin hexagonal {100} prisms (up to 0.3 mm long) with pyramidal terminations consisting of the forms {101} and {011}. Prisms are typically intergrown in divergent sprays, bow-tie aggregates or subparallel intergrowths. Crystals are colourless and transparent with a vitreous lustre. The streak is white and the mineral is nonfluorescent. The Mohs hardness is between 2½ and 3. Crystals are brittle with at least one good cleavage parallel to [001], probably {100}, and have splintery fracture. The mineral is slowly soluble in H2O at room temperature. The calculated density is 3.385 g cm–3. The mineralis optically uniaxial (+), with ω = 1.565(1) and ε = 1.603(1) (white light). Electron microprobe analyses yielded the empirical formula (Na0.507Ca0.285Y0.176)∑0.968(Y0.724Dy0.110Er0.053Gd0.037Ho0.021Yb0.013Nd0.014Eu0.005Sm0.008Ce0.010Pr0.003La0.002)∑1.000(SO4)2·H1.401O.The eight strongest powder X-ray diffraction lines are [dobs Å(I)(hkl)]: 6.01(59)(100), 5.43(63)(011), 3.457(46)(110), 3.010(100)(200), 2.826(95)(014), 2.1365(39)(006,122), 1.8493(67)(214) and 1.6901(28)(125,034). Chinleite-(Y) is trigonal, P3221,a = 6.890(2), c = 12.767(2) Å, V = 524.9(3) Å3 and Z = 3. The structure of chinleite-(Y) (R1 = 0.0444 for 303 Fo > 4σF), a three-dimensional framework, consisting of SO4 groups, irregular NaO8 polyhedra and YO9 distorted tricapped trigonal prisms, is similar to the structure of bassanite.

Belakovskiite, Na7(UO2)(SO4)4(SO3OH)(H2O)3, a new uranyl sulfate mineral from the Blue Lizard mine, San Juan County, Utah, USA

2014 ◽  
Vol 78 (3) ◽  
pp. 639-649 ◽  
Author(s):  
A. R. Kampf ◽  
J. Plášil ◽  
A. V. Kasatkin ◽  
J. Marty
Keyword(s):  
Microprobe Analysis ◽  
Electron Microprobe Analysis ◽  
New Mineral ◽  
San Juan ◽  
Uranyl Sulfate ◽  
Calculated Density ◽  
Secondary Alteration ◽  
X Ray ◽  
Mohs Hardness ◽  
San Juan County

AbstractThe new mineral belakovskiite (IMA2013-075), Na7(UO2)(SO4)4(SO3OH)(H2O)3, was found in the Blue Lizard mine, Red Canyon, White Canyon district, San Juan County, Utah, USA, where it occurs as a secondary alteration phase in association with blödite, ferrinatrite, kröhnkite, meisserite and metavoltine. Crystals of belakovskiite are very pale yellowish-green hair-like fibres up to 2 mm long and usually no more than a few mm in diameter. The fibres are elongated on [100] and slightly flattened on {021}. Crystals are transparent with a vitreous lustre. The mineral has a white streak and a probable Mohs hardness of ∼2. Fibres are flexible and elastic, with brittle failure and irregular fracture. No cleavage was observed. The mineral is readily soluble in cold H2O. The calculated density is 2.953 g cm−3. Optically, belakovskiite is biaxial (+) with α = 1.500(1), β = 1.511(1) and γ = 1.523(1) (measured in white light). The measured 2V is 87.1(6)° and the calculated 2V is 88°. The mineral is non-pleochroic. The partially determined optical orientation is X ≈ a. Electron-microprobe analysis provided Na2O 21.67, UO3 30.48, SO3 40.86, H2O 6.45 (structure), total 99.46 wt.% yielding the empirical formula Na6.83(U1.04O2)(SO4)4(S0.99O3OH)(H2O)3 based on 25 O a.p.f.u. Belakovskiite is triclinic, P, with a = 5.4581(3), b = 11.3288(6), c = 18.4163(13) Å, α = 104.786(7)°, β = 90.092(6)°, γ = 96.767(7)°, V = 1092.76(11) Å3 and Z = 2. The eight strongest X-ray powder diffraction lines are [dobs Å(I)(hkl)]: 8.96(35)(002), 8.46(29)(011), 5.19(100)(01,101,10), 4.66(58)(013,02,0,110), 3.568(37)(120,023,005,03), 3.057(59)(06,15,31), 2.930(27)(multiple) and 1.8320(29)(multiple). The structure, refined to R1 = 5.39% for 3163 Fo > 4σF reflections, contains [(UO2)(SO4)4(H2O)]6− polyhedral clusters connected via an extensive network of Na−O bonds and H bonds involving eight Na sites, three other H2O sites and an SO3OH (hydrosulfate) group. The 3-D framework, thus defined, is unique among known uranyl sulfate structures. The mineral is named for Dmitry Ilych Belakovskiy, a prominent Russian mineralogist and Curator of the Fersman Mineralogical Museum.

Magnesiocanutite, NaMnMg2[AsO4]2[AsO2(OH)2], a new protonated alluaudite-group mineral from the Torrecillas mine, Iquique Province, Chile

2017 ◽  
Vol 81 (6) ◽  
pp. 1523-1531 ◽  
Author(s):  
Anthony R. Kampf ◽  
Barbara P. Nash ◽  
Dini Maurizio ◽  
Arturo A. Molina Donoso
Keyword(s):  
Structure Refinement ◽  
Secondary Phase ◽  
Obtuse Angle ◽  
New Mineral ◽  
X Ray Diffraction ◽  
Calculated Density ◽  
Crystal Forms ◽  
X Ray ◽  
Temperature Electron ◽  
Mohs Hardness

AbstractThe new mineral magnesiocanutite (IMA2016-057), NaMnMg2[AsO4]2[AsO2(OH)2], was found at the Torrecillas mine, Iquique Province, Chile, where it occurs as a secondary phase in association with anhydrite, canutite, halite, lavendulan and magnesiokoritnigite. Magnesiocanutite occurs as pale brownish-pink to rose-pink, lozenge-shaped tablets that are often grouped in tightly intergrown aggregates. The crystal forms are {110} and {102}. Crystals are transparent, with vitreous lustre and white to very pale pink streak. The Mohs hardness is 2½, tenacity is brittle, and the fracture is splintery. Crystals exhibit two perfect cleavages: {010} and {101}. The calculated density is 3.957 g/cm3. Optically, magnesiocanutite is biaxial (+), with α = 1.689(2), β = 1.700(2), γ = 1.730(2) (measured in white light); 2Vmeas. = 64.3(4)°; slight dispersion, r <v; orientation Z = b; X ∧ a = 15° in obtuse angle β. The mineral is slowly soluble in dilute HCl at room temperature. Electron-microprobe analyses, provided Na2O 5.44, CaO 0.26, MgO 8.84, MnO 18.45, CoO 1.47, CuO 2.13, As2O5 59.51, H2O(calc) 2.86, total 98.96 wt.%. Magnesiocanutite is monoclinic, C2/c, a = 12.2514(8), b = 12.4980(9), c = 6.8345(5) Å, β = 113.167(8)°, V = 962.10(13) Å3 and Z = 4. The eight strongest powder X-ray diffraction lines are [dobs Å(I )(hkl)]: 6.25(42)(020), 3.566(43)(310,1̄31), 3.262(96)(1̄12), 3.120(59)(002,131,040,221), 2.787(93)(400,022,041,330), 2.718(100) (4̄21,240,112,402), 2.641(42)(1̄32) and 1.5026(43)(multiple). Magnesiocanutite has a protonated alluaudite-type structure (R1 = 2.59% for 789 Fo > 4σF reflections) and is the Mg analogue of canutite. Using the results of both the microprobe analyses and structure refinement, the structurally based empirical formula is Na(Mn0.78Mg0.22)Σ1.00(Mg1.04Mn0.70Cu0.15Co0.11)Σ2.00[AsO4]2[AsO2(OH)2].

Crimsonite, PbFe3+2(PO4)2(OH)2, the phosphate analogue of carminite from the Silver Coin mine, Valmy, Nevada, USA

2016 ◽  
Vol 80 (6) ◽  
pp. 925-935 ◽  
Author(s):  
A. R. Kampf ◽  
P. M. Adams ◽  
S. J. Mills ◽  
B. P. Nash
Keyword(s):  
New Mineral ◽  
X Ray Diffraction ◽  
Maximum Dimension ◽  
Calculated Density ◽  
Electron Pairs ◽  
X Ray ◽  
Silver Coin ◽  
Humboldt County ◽  
Light Yellow ◽  
Mohs Hardness

AbstractCrimsonite (IMA2014-095), PbFe3+2(PO 4)2(OH)2, the phosphate analogue of carminite, is a new mineral from the Silver Coin mine, Valmy, Iron Point district, Humboldt County, Nevada, USA, where it occurs as a low-temperature secondary mineral in association with fluorwavellite, goethite, hematite, hentschelite, plumbogummite and variscite on quartz. Crimsonite occurs in subparallel aggregates of deep red blades or plates flattened on {100} and up to 0.1 mm in maximum dimension. The streak is light purplish orange. Crystals are transparent and have adamantine lustre. The Mohs hardness is ∼3½, the tenacity is brittle, the fracture is irregular to splintery and an imperfect cleavage is likely on {101}. The calculated density is 5.180 g/cm3. Crimsonite is optically biaxial (+), with 2V = 85.5(5)° and γ – α = 0.011. Using the Gladstone-Dale relationship, the calculated indices of refraction are α = 2.021, β = 2.026 and γ = 2.032. The optical orientation is X = b; Y = a; Z = c and the pleochroism is X light orange, Y light yellow, Z red brown; Y < X < Z. Electron microprobe analyses provided PbO 40.69, CaO 0.60, ZnO 0.72, CuO 0.13, Fe2O3 23.36, Al2O3 0.34, V2O5 0.70, As2O5 12.05, P2O5 16.03, SO3 0.33 and H2O 3.64 (structure), total 98.59 wt.%. The empirical formula (based on 10 O apfu) is (Pb1.06Ca0.06)∑1.12(Fe1.71Zn0.05Al0.04Cu0.01)∑1.81(P1.32As0.61V0.05S0.02)∑2.00O8[(OH)1.64(H2O)0.36]∑2.00. Crimsonite is orthorhombic, Cccm, a = 16.2535(13), b = 7.4724(4), c = 12.1533(9) Å, V = 1476.04(17) Å3 and Z = 8. The eight strongest lines in the powder X-ray diffraction pattern are [dobs in Å(I)(hkl)]: 5.86(42)(111); 4.53(45)(112); 3.485(64)(113); 3.190(100) (022); 3.026(40)(004); 2.902(54)(511); 2.502(77)(422) and 2.268(54)(224). The structure of crimsonite (R1 = 3.57% for 740 Fo > 4σF) contains FeO6 octahedra that share edges to form dimers, which are then linked to other dimers by corner sharing to form chains along [010]. These chains are linked by PO4 tetrahedra yielding sheets parallel to {001}. The sheets are linked to one another via bonds to 8-coordinated Pb2+ atoms with non-stereoactive 6s2 lone-electron pairs.

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