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  • 1
    Publication Date: 2015-09-17
    Description: Khvorovite, ideally $${\mathrm{Pb}}_{4}^{2+}$$ Ca 2 [Si 8 B 2 (SiB)O 28 ]F, is a new borosilicate mineral of the hyalotekite group from the Darai-Pioz alkaline massif in the upper reaches of the Darai-Pioz river, Tajikistan. Khvorovite was found in a pectolite aggregate in silexites (quartz-rich rocks). The pectolite aggregate consists mainly of pectolite, quartz and fluorite, with minor aegirine, polylithionite, turkestanite and baratovite; accessory minerals are calcite, pyrochlore-group minerals, reedmergnerite, stillwellite-(Ce), pekovite, zeravshanite, senkevichite, sokolovaite, mendeleevite-(Ce), alamosite, orlovite, leucosphenite and several unknown Cs-silicates. Khvorovite occurs as irregular grains, rarely with square or rectangular sections up to 150 μm, and grain aggregates up to 0.5 mm. Khvorovite is colourless, rarely white, transparent with a white streak, has a vitreous lustre and does not fluoresce under ultraviolet light. Cleavage and parting were not observed. Mohs hardness is 5–5.5, and khvorovite is brittle with an uneven fracture. The measured and calculated densities are 3.96(2) and 3.968 g/cm 3 , respectively. Khvorovite is biaxial (+) with refractive indices ( = 589 nm) α = 1.659(3), β calc. = 1.671(2), = 1.676(3); 2V meas. = 64(3)°, medium dispersion: r 〈 v . Khvorovite is triclinic, space group I 1I, a = 11.354(2), b = 10.960(2), c = 10.271(2) Å, α = 90.32(3), β = 90.00(3), = 90.00(3)°, V = 1278(1) Å 3 , Z = 2. The six strongest lines in the powder X-ray diffraction pattern [ d (Å), I, ( hkl )] are: 7.86, 100, (110); 7.65, 90, (1I01); 7.55, 90, (011); 3.81, 90, (202); 3.55, 90, (301); 2.934, 90, (3I12, 312). Chemical analysis by electron microprobe gave SiO 2 36.98, B 2 O 3 6.01, Y 2 O 3 0.26, PbO 40.08, BaO 6.18, SrO 0.43, CaO 6.77, K 2 O 1.72, Na 2 O 0.41, F 0.88, O=F –0.37, sum 99.35 wt.%. The empirical formula based on 29 (O+F) a.p.f.u. is ( $${\mathrm{Pb}}_{2.76}^{2+}$$ Ba 0.62 K 0.56 Na 0.16 ) 4.10 (Ca 1.86 Sr 0.06 Y 0.04 Na 0.04 ) 2 [Si 8 B 2 (Si 1.46 B 0.65 ) 2.11 O 28 ](F 0.71 O 0.29 ), Z = 2, and the simplified formula is (Pb 2+ ,Ba,K) 4 Ca 2 [Si 8 B 2 (Si,B) 2 O 28 ]F. The crystal structure of khvorovite was refined to R 1 = 2.89% based on 3680 observed reflections collected on a four-circle diffractometer with Mo K α radiation. In the crystal structure of khvorovite, there are four [4]-coordinated Si sites occupied solely by Si with 〈Si–O〉 = 1.617 Å. The [4]-coordinated B site is occupied solely by B, with 〈B–O〉 = 1.478 Å. The [4]-coordinated T site is occupied by Si and B (Si 1.46 B 0.54 ), with 〈T–O〉 = 1.605 Å; it ideally gives (SiB) a.p.f.u. The Si, B and T tetrahedra form an interrupted framework of ideal composition [Si 8 B 2 (SiB)O 28 ] 11– . The interstitial cations are Pb 2+ , Ba and K (minor Na) [ A (11–22) sites] and Ca [ M site]. The two A sites are each split into two subsites ~0.5 Å apart and occupied by Pb 2+ and Ba + K. The [8]-coordinated M site is occupied mainly by Ca, with minor Sr, Y and Na. Khvorovite is a Pb 2+ -analogue of hyalotekite, (Ba,Pb 2+ ,K) 4 (Ca,Y) 2 [Si 8 (B,Be) 2 (Si,B) 2 O 28 ]F and a Pb 2+ -, Ca-analogue of kapitsaite-(Y), (Ba,K) 4 (Y,Ca) 2 [Si 8 B 2 (B,Si) 2 O 28 ]F. It is named after Pavel V. Khvorov (b. 1965), a Russian mineralogist, to honour his contribution to the study of the mineralogy of the Darai-Pioz massif.
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  • 2
    Publication Date: 2011-10-10
    Description: The crystal structure of mendeleevite-(Ce), (Cs,{square})6({square},Cs)6({square},K)6(REE,Ca,{square})30(Si70O175) (H2O,OH,F,{square})35, a new mineral from the moraine of the Darai-Pioz glacier, the Alai mountain ridge, Tien-Shan mountains, northern Tajikistan, was solved by direct methods and refined to R1 = 4.15% based on 2274 observed [Fo 〉 4{sigma}|F|] unique reflections measured with Mo-K radiation on a Bruker P4 diffractometer equipped with a CCD detector. Mendeleevite-(Ce) is cubic, space group Pm[IMG]f1.gif" ALT="Formula" BORDER="0"〉, a 21.9148(4) A, V 10525(1) A3, Z = 2, Dcalc = 3.066 g/cm3. The empirical formula (electron microprobe) is Cs5.94 K2.22 [(Ce11.35La5.86Nd3.23 Pr1.54 Sm0.32Gd0.20){Sigma}22.50(Ca4.68Sr1.00){Sigma}5.68]{Sigma}28.18Si70.12O203.17H45.67F6.83, Z = 2, calculated on the basis of 210 (O + F) a.p.f.u., with H2O and OH calculated from structure refinement (OH + F = 17 p.f.u.; H2O = 17.75 p.f.u.). The structural formula is (Cs4.65{square}1.35){Sigma}6({square}4.71Cs1.29){Sigma}6({square}3.78K2.22){Sigma}6{[(Ce11.35La5.86Nd3.23 Pr1.54Sm0.32Gd0.20){Sigma}22.50(Ca4.68Sr1.00){Sigma}5.68]{Sigma}28.18{square}1.82}{Sigma}30(Si70O175)[(OH)10.17F6.83]{Sigma}17(H2O)17.75. Simplified and endmember formulae are as follows: (Cs,{square})6({square},Cs)6({square},K)6(REE,Ca,{square})30(Si70O175) (H2O,OH,F,{square})35 and Cs6(REE22Ca6)(Si70O175)(OH,F)14(H2O)21. The crystal structure of mendeleevite-(Ce) is an intercalation of two independent Si-O radicals and an M framework of (REE,Ca) polyhedra. The Si-O radicals are an (Si104O260)104- framework and an (Si36O90)36-cluster which do not link directly. The M framework is located between the Si-O framework and the Si-O clusters. Interstitial cations occupy two types of cages and channels. Cages I and II are 78 and 22% occupied by Cs. Channels along [100[IMG]/medium/Curve_arrow.gif" ALT="Formula "〉] contain K atoms and H2O groups. Mendeleevite-(Ce) has no natural or synthetic structural analogues. Mendeleevite-(Ce) is a framework mineral with large cavities and it has the potential to be used as a model for the synthesis of microporous materials of industrial interest.
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  • 3
    Publication Date: 2011-12-01
    Description: Rinkite, ideally Na2Ca4REETi(Si2O7)2OF3, is a common mineral in alkaline and peralkaline rocks. The crystal structures of five rinkite crystals from three alkaline massifs: Ilimaussaq, Greenland; Khibiny, Kola Peninsula, Russia and Mont Saint-Hilaire, Canada, have been refined as two components related by the TWIN matrix (-1 0 0, 0 -1 0, 1 0 1) (Mo-Ka radiation). The crystals, a = 7.4132–7.4414, b = 5.6595–5.6816, c = 18.8181–18.9431 Å, ß = 101.353–101.424(2)°, V = 776.1–786.7 Å3, space group P21/c, Z = 2, Dcalc = 3.376–3.502 g cm-3, were analysed using an electron microprobe subsequent to collection of the X-ray intensity data. Transmission electron microscopy confirmed the presence of pseudomerohedral twinning in rinkite crystals. The crystal structure of rinkite is a framework of TS (titanium silicate) blocks. The TS block consists of HOH sheets (H-heteropolyhedral, O-octahedral). The TS block in rinkite exhibits linkage and stereochemistry typical for Group I (Ti = 1 a.p.f.u.) of Ti disilicate minerals: two H sheets connect to the O sheet such that two (Si2O7) groups link to the trans edges of a Na polyhedron of the O sheet. The crystal chemistry of rinkite and nacareniobsite-(Ce) is discussed.
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  • 4
    Publication Date: 2012-06-01
    Description: Kazanskyite, Ba□TiNbNa3Ti(Si2O7)2O2(OH)2(H2O)4, is a Group-III TS-block mineral from the Kirovskii mine, Mount Kukisvumchorr, Khibiny alkaline massif, Kola Peninsula, Russia. The mineral occurs as flexible and commonly bent flakes 2–15 μm thick and up to 330 μm across. It is colourless to pale tan, with a white streak and a vitreous lustre. The mineral formed in a pegmatite as a result of hydrothermal activity. Associated minerals are natrolite, barytolamprophyllite, nechelyustovite, hydroxylapatite, belovite-(La), belovite-(Ce), gaidonnayite, nenadkevichite, epididymite, apophyllite-(KF) and sphalerite. Kazanskyite has perfect cleavage on {001}, splintery fracture and a Mohs hardness of 3. Its calculated density is 2.930 g cm−3. Kazanskyite is biaxial positive with α 1.695, β 1.703, γ 1.733 (λ 590 nm), 2Vmeas = 64.8(7)°, 2Vcalc = 55.4°, with no discernible dispersion. It is not pleochroic. Kazanskyite is triclinic, space group P1İ, a 5.4260(9), b 7.135(1), c 25.514(4) Å, α 90.172(4), β 90.916(4), γ 89.964(3)°, V 977.61(3) Å3. The strongest lines in the X-ray powder-diffraction pattern [d(Å)(I)(hkl)] are: 2.813(100)(124İ,12İ2İ), 2.149(82)(222İ,22İ0,207,220,22İ2), 3.938(70)(11İ 3,112), 4.288(44)(111İ,11İ0,110,11İ1), 2.128(44)(223İ,22İ1İ,13İ4,221,13İ4,221,22İ3), 3.127(39)(11İ6,115), 3.690(36)(11İ4), 2.895(33)(12İ3,121) and 2.955(32)(12İ0,120,12İ2). Chemical analysis by electron microprobe gave Nb2O5 9.70, TiO2 19.41, SiO2 28.21, Al2O3 0.13, FeO 0.28, MnO 4.65, BaO 12.50, SrO 3.41, CaO 0.89, K2O 1.12, Na2O 9.15, H2O 9.87, F 1.29, O = F – 0.54, sum 100.07 wt.%; H2O was determined from structure refinement. The empirical formula is (Na2.55Mn0.31Ca0.11 )Σ3(Ba0.70Sr0.28K0.21Ca0.03)Σ1.22*Ti2.09Nb0.63Mn0.26Al0.02)Σ3Si4.05O21.42H9.45F0.59, calculated on 22 (O + F) a.p.f.u., Z = 2. The structural formula of the form is (Ba0.56Sr0.22K0.15Ca0.03□0.04)Σ1(□0.74Ba0.14Sr0.06K0.06)Σ1(Ti0.98Al0.02)Σ1(Nb0.63Ti0.37)Σ1(Na2.55Mn0.31Ca0.11 )Σ3(Ti0.74Mn0.26)Σ(Si2O7)2O2(OH1.41F0.59)Σ2(H2O)(□0.74H2O0.26)Σ(H2O)2.74. Simplified and ideal formulae are as follows: Ba(□,Ba)Ti(Nb,Ti)(Na,Mn)3(Ti,Mn)(Si2O7)2O2(OH,F)2(H2O)4 and Ba□TiNbNa3Ti (Si2O7)2O2(OH)2(H2O)4. The Raman spectrum of the mineral contains the following bands: 3462 cm−1 (broad) and 3545 and 3628 cm−1 (sharp). The crystal structure was solved by direct methods and refined to an R1 index of 8.09%. The crystal structure of kazanskyite is a combination of a TS (titanium silicate) block and an I (intermediate) block. The TS block consists of HOH sheets (H is heteropolyhedral and O is octahedral). The TS block exhibits linkage and stereochemistry typical for Group-III (Ti = 3 a.p.f.u.) Ti-disilicate minerals. The TS block has two different H sheets where (Si2O7) groups link to [5]-coordinated Ti and [6]-coordinated Nb polyhedra, respectively. There are two peripheral sites, AP(1,2), occupied mainly by Ba (less Sr and K) at 96% and 26%. There are two I blocks: the I1 block is a layer of Ba atoms; the I2 block consists of H2O groups and AP (2) atoms. The TS and I blocks are topologically identical to those in the nechelyustovite structure. The mineral is named in honour of Professor Vadim Ivanovich Kazansky (), a prominent Russian ore geologist and an expert in Precambrian metallogeny.
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  • 5
    Publication Date: 2011-08-30
    Description: The crystal structures of two polytypes of innelite, ideally Ba4Ti2Na2M2+Ti(Si2O7)2[(SO4)(PO4)]O2[O(OH)] where M2+ = Mn, Fe2+, Mg, Ca: innelite-1T, a 5.4234(9), b 7.131(1), c 14.785(3) A, 98.442(4), {beta} 94.579(3), {gamma} 90.009(4){degrees}, V 563.7(3) A3, space group P[IMG]f1.gif" ALT="Formula" BORDER="0"〉, Dcalc. = 4.028 g/cm3, Z = 1; and innelite-2M, a 5.4206(8), b 7.125(1), c 29.314(4) A, {beta} 94.698(3){degrees}, V 1128.3(2) A3, space group P2/c, Dcalc. = 4.024 g/cm3, Z = 2, from the Inagli massif, Yakutia, Russia, have been refined to R values of 8.99 and 7.60%, respectively. Electron-microprobe analysis gave the empirical formula for innelite as (Ba3.94Sr0.06){Sigma}4.00(Na2.16[IMG]f2.gif" ALT="Formula" BORDER="0"〉[IMG]f3.gif" ALT="Formula" BORDER="0"〉Mg0.15Ca0.10{square}0.04){Sigma}3(Ti2.97Nb0.02Al0.02){Sigma}3.01Si4.01(S1.02P0.81{square}0.17){Sigma}2H1.84O25.79F0.21 which is equivalent to (Ba3.94Sr0.06){Sigma}4.00(Ti1.97Nb0.02Al0.02){Sigma}2.01(Na2.16[IMG]f2.gif" ALT="Formula" BORDER="0"〉[IMG]f3.gif" ALT="Formula" BORDER="0"〉Mg0.15Ca0.10{square}0.04){Sigma}3Ti(Si4.01O14)[(SO4)1.02(PO4)0.81(OH)0.51H2O0.17]O2[(OH0.99F0.21){Sigma}1.20O0.80], calculated on the basis of 26 (O + F) anions, with H2O calculated from structure refinement. The crystal structure of innelite is a combination of a TS (titanium silicate) block and an I (intermediate) block. The TS block consists of HOH sheets (H-heteropolyhedral, O-octahedral) and exhibits linkage and stereochemistry typical for Ti-disilicate minerals of Group III (Ti = 3 a.p.f.u.): two H sheets connect to the O sheet such that two (Si2O7) groups link to the trans edges of a Ti octahedron of the O sheet. The I block contains T sites, statistically occupied by S and P, and Ba atoms. In the structures of innelite-1T and innelite-2M, TS blocks are related by an inversion centre and a cy glide plane, respectively. HRTEM images show a coherent intergrowth of the two polytypes, together with an as-yet unidentified [~]10 A phase.
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  • 6
    Publication Date: 2011-10-13
    Description: Sveinbergeite, Ca(Fe2+ 6 Fe3+)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 x 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 1.745(2), {beta} 1.746(2), {gamma} 1.753(2), 2V(meas.) = 20(3){degrees}. 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 {perp} (001), Y ^ b = 12{degrees}, Z = a, elongation positive. Sveinbergeite is triclinic, space group P1, a = 5.329(4), b = 11.803(8), c = 11.822(8) A; = 101.140(8){degrees}, {beta} = 98.224(8){degrees}, {gamma} = 102.442(8){degrees}; V = 699.0(8) A3; Z = 1. The nine strongest lines in the X-ray powder diffraction pattern [d in A(I)(hkl)] are: 11.395(100)(001,010), 2.880(38)(004), 2.640(31)(210,141), 1.643(24)(071,072), 2.492(20)(211), 1.616(15)(070), 1.573(14)(322), 2.270(13)(134) and 2.757(12)(140,132). Chemical analysis by electron microprobe gave Nb2O5 0.55, TiO2 10.76, ZrO2 0.48, SiO2 34.41, Al2O3 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){Sigma}1.21(Fe2+ 5.65 Fe3+ 0.93 Mn0.25Mg0.18){Sigma}7.01(Ti1.86Nb0.06Zr0.05 Fe3+ 0.03){Sigma}2(Si7.91Al0.09){Sigma}8O34.61H12.34F0.17, 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.
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  • 7
    Publication Date: 2016-09-24
    Description: Berezanskite, ideally Ti 2 2 KLi 3 (Si 12 O 30 ), is hexagonal, space group P 6/ mcc , a = 9.898(4), c = 14.276(6) Å, V = 1211.2(9) Å 3 , Z = 2. The crystal structure was refined to an R 1 index of 2.08% based on 392 unique observed reflections. Berezanskite is isostructural with milarite, ideally A Ca 2 B o C K T (2) (Be 2 Al)( T (1) Si 12 O 30 )(H 2 O) 0–2 . The structural unit is of the form [ T (2) 3 T (1) 12 O 30 ] with T (1) = Si and T (2) = Li, in which (LiO 4 ) tetrahedra link [Si 12 O 30 ] six-membered double-rings into a framework. The A , B and C sites occur in the interstices of the framework with the following site populations: A = Ti 4+ 2 , 〈 A –O〉 = 1.938(2) Å; B = 2 ; C = K, 〈 C –O〉 = 3.058(2) Å. In the T (2) = Li 3 milarite-group minerals, the 〈 C –O〉 distance is inversely related to the occupancy of the B site.
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  • 8
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    Unknown
    Mineralogical Society of Great Britain and Ireland
    Publication Date: 2012-08-01
    Description: The structure topology and crystal chemistry have been considered for ten astrophyllite-group minerals that contain the HOH layer, a central trioctahedral (O) sheet and two adjacent (H) sheets of [5]- and [6]-coordinated D polyhedra and the astrophyllite (T4O12) ribbons. The HOH layer is characterized by a planar cell with a ~5.4, b ~11.9 Å and a^b ~103°. The ideal composition of the O sheet is (astrophyllite) or (kupletskite). All structures consist of an HOH layer and an I (intermediate) block that consists of atoms between two HOH layers. In the astrophyllite group, there are two types of structures based on the type of linkage of HOH layers: (1) HOH layers link directly where they share common vertices of D octahedra, and (2) HOH layers do not link directly via polyhedra of the H sheets. The type-1 structure occurs in astrophyllite, niobophyllite, nalivkinite, tarbagataite, kupletskite, niobokupletskite and kupletskite-(Cs); the type-2 structure occurs in magnesioastrophyllite, sveinbergeite and devitoite. The general formulae for the eight astrophyllite-group minerals (astrophyllite, niobophyllite, nalivkinite, tarbagataite, kupletskite, niobokupletskite, kupletskite-(Cs), magnesioastrophyllite) and for the extended astrophyllite group including devitoite and sveinbergeite are A2BC7D2T8O26(OH)4X0– and A2pBrC7D2(T4O12)2 , respectively, where C and D are cations of the O and H sheets, C = [6](Fe2+, Mn, Fe3+, Na, Mg, Zn) at the M(1–4) sites; D = [6,5](Ti, Nb, Zr, Fe3+); T = Si, minor Al; A2pBrI is the composition of the I block where p = 1,2; r = 1,2; A = K, Cs, Li, Ba, H2O, □; B = Na, Ca, Ba, H2O, □; I represents the composition of the central part of the I block, excluding peripheral layers of the form A2B; X = O, OH, F and H2O; n = 0, 1, 2. Two topological issues have been considered: (1) the pattern of sizes of the M octahedra in the O sheet, M(1) 〉 M(2) 〉 M(3) 〉 M(4) and (2) different topologies of the HOH layer in magnesioastrophyllite and all other structures of the astrophyllite group.
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  • 9
    Publication Date: 2013-08-22
    Description: The crystal structure of mosandrite, ideally (Ca 3 REE )[(H 2 O) 2 Ca 0.5 0.5 ]Ti(Si 2 O 7 ) 2 (OH) 2 (H 2 O) 2 , from the Saga mine, Morje, Porsgrunn, Norway, has been refined as two components related by the TWIN matrix (1I 0 0, 0 1I 0, 1 0 1): a 7.4222(3), b 5.6178(2), c 18.7232(7) Å , β 101.4226(6)°, V = 765.23(9) Å 3 , space group P 2 1 / c , D calc. = 3.361 g.cm –3 , R 1 = 3.69% using 1347 observed ( F o 〉 4 F ) reflections. The empirical formula of mosandrite (EMPA) was calculated on the basis of 4 Si a.p.f.u., with H 2 O determined from structure refinement: [(Ca 2.89 Ba 0.01 ) 2.90 (Ce 0.39 La 0.18 Nd 0.14 Sm 0.02 Gd 0.03 Y 0.16 Th 0.03 ) 1.01 Zr 0.09 ] 4 [(H 2 O) 2.00 Ca 0.32 Na 0.17 Al 0.10 Mn 0.04 $${\mathrm{Fe}}_{0.02}^{2+}$$ 0.35 ] 3 (Ti 0.87 Nb 0.09 Zr 0.04 ) 1 (Si 2 O 7 ) 2 [(OH) 1.54 F 0.46 ] 2 [(H 2 O) 1.50 F 0.50 ] 2 , Z = 2. The crystal structure of mosandrite is a framework of TS (titanium silicate) blocks; each TS block consists of HOH sheets (H-heteropolyhedral, O-octahedral). In the TS block, there are five fully occupied cation sites, two [4]-coordinated Si sites with 〈Si–O〉 1.623 Å , [7]-coordinated M H and A P sites occupied by Ca and REE in the ratio ~ 3:1, and one [6]-coordinated Ti-dominant M O (1) site. There are two H 2 O-dominant H 2 O-alkali-cation sites. The partly occupied M O (2) site has composition [(H 2 O) 0.5 0.33 Na 0.17 ], ideally [(H 2 O) 0.5 0.5 ] p.f.u. The M O (3) site has ideal composition [(H 2 O) 1.5 Ca 0.5 ] p.f.u. In the O sheet, the $${X}_{\mathrm{M}}^{\mathrm{O}}$$ and $${X}_{\mathrm{A}}^{\mathrm{O}}$$ anion sites have compositions [(OH) 1.54 F 0.46 ] ( $${X}_{\mathrm{M}}^{\mathrm{O}}$$ ) and [(H 2 O) 1.50 F 0.50 ] ( $${X}_{\mathrm{A}}^{\mathrm{O}}$$ ), ideally (OH) 2 and (H 2 O) 2 p.f.u. The M H and A P polyhedra and Si 2 O 7 groups constitute the H sheet that is completely ordered. In the O sheet, M O (1) octahedra are long-range ordered whereas H 2 O and OH groups and alkali cations Na and Ca are long-range disordered. Two SRO (short-range ordered) arrangements have been proposed for the O sheet: (1) Na [ M O (2)], Ca [ M O (3)] and F 4 [ $${X}_{\mathrm{M}}^{\mathrm{O}}$$ and $${X}_{\mathrm{A}}^{\mathrm{O}}$$ anion sites]; (2) 2 H 2 O [ M O (2)] and M O (3)] and (OH) 2 and (H 2 O) 2 [ $${X}_{\mathrm{M}}^{\mathrm{O}}$$ and $${X}_{\mathrm{A}}^{\mathrm{O}}$$ ]. Linkage of H and O sheets occurs mainly via common vertices of M H polyhedra and Si 2 O 7 groups and M O (1) octahedra. Two adjacent TS blocks are related by the glide plane c y . Mosandrite is an H 2 O- and OH-bearing Na- and Ca-depleted analogue of rinkite, ideally (Ca 3 REE )Na(NaCa) Ti(Si 2 O 7 ) 2 (OF)F 2 . Mosandrite and rinkite are related by the following substitution at the M O (2,3) and $${X}_{(\mathrm{M},\mathrm{A})}^{\mathrm{O}}$$ sites in the O sheet: M [(H 2 O) + 0.5 ] + X [ $${\left(\mathrm{OH}\right)}_{2}^{-}$$ + (H 2 O) 2 ] -〉 M [ $${\mathrm{Na}}_{2}^{+}$$ + $${\mathrm{Ca}}_{0.5}^{2+}$$ ] + X [(OF) 3– + (F 2 ) 2– ].
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    Electronic ISSN: 1471-8022
    Topics: Geosciences
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  • 10
    Publication Date: 2013-10-26
    Description: Veblenite, ideally K 2 2 Na( $${\mathrm{Fe}}_{5}^{2+}$$ $${\mathrm{Fe}}_{4}^{3+}$$ $${\mathrm{Mn}}_{7}^{2+}$$ )Nb 3 Ti(Si 2 O 7 ) 2 (Si 8 O 22 ) 2 O 6 (OH) 10 (H 2 O) 3 , is a new mineral with no natural or synthetic analogues. The mineral occurs at Ten Mile Lake, Seal Lake area, Newfoundland and Labrador (Canada), in a band of paragneiss consisting chiefly of albite and arfvedsonite. Veblenite occurs as red brown single laths and fibres included in feldspar. Associated minerals are niobophyllite, albite, arfvedsonite, aegirine-augite, barylite, eudidymite, neptunite, Mn-rich pectolite, pyrochlore, sphalerite and galena. Veblenite has perfect cleavage on {001} and splintery fracture. Its calculated density is 3.046 g cm –3 . Veblenite is biaxial negative with α 1.676(2), β 1.688(2), 1.692(2) ( 590 nm), 2V meas = 65(1)°, 2V calc = 59.6°, with no discernible dispersion. It is pleochroic in the following pattern: X = black, Y = black, Z = orange-brown. The mineral is red-brown with a vitreous, translucent lustre and very pale brown streak. It does not fluoresce under short and long-wave UV-light. Veblenite is triclicnic, space group P 1I, a 5.3761(3), b 27.5062(11), c 18.6972(9) Å, α 140.301(3), β 93.033(3), 95.664(3)°, V = 1720.96(14) Å 3 . The strongest lines in the X-ray powder diffraction pattern [ d (Å)(I)( hkl )] are: 16.894(100)(010), 18.204(23)(01I1), 4.271(9)(14I1, 040, 120), 11.661(8)(001), 2.721(3)(19I5), 4.404(3)(1I3I2, 14I2), 4.056(3)(031, 11I2; 15I2, 1I4I3), 3.891(2)(003). The chemical composition of veblenite from a combination of electron microprobe analysis and structural determination for H 2 O and the Fe 2+ /Fe 3+ ratio is Nb 2 O 5 11.69, TiO 2 2.26, SiO 2 35.71, Al 2 O 3 0.60, Fe 2 O 3 10.40, FeO 11.58, MnO 12.84, ZnO 0.36, MgO 0.08, BaO 1.31, SrO 0.09, CaO 1.49, Cs 2 O 0.30, K 2 O 1.78, Na 2 O 0.68, H 2 O 4.39, F 0.22, O = F –0.09, sum 95.69 wt.%. The empirical formula [based on 20 (Al+Si) p.f.u. is (K 0.53 Ba 0.28 Sr 0.03 0.16 ) 1 (K 0.72 Cs 0.07 1.21 ) 2 (Na 0.72 Ca 0.17 1.11 ) 2 ( $${\mathrm{Fe}}_{5.32}^{2+}$$ $${\mathrm{Fe}}_{4.13}^{3+}$$ $${\mathrm{Mn}}_{5.97}^{2+}$$ Ca 0.70 Zn 0.15 Mg 0.07 0.66 ) 17 (Nb 2.90 Ti 0.93 $${\mathrm{Fe}}_{0.17}^{3+}$$ ) 4 (Si 19.61 Al 0.39 ) 20 O 77.01 H 16.08 F 0.38 . The simplified formula is (K,Ba,) 3 (,Na) 2 (Fe 2+ ,Fe 3+ ,Mn 2+ ) 17 (Nb,Ti) 4 (Si 2 O 7 ) 2 (Si 8 O 22 ) 2 O 6 (OH) 10 (H 2 O) 3 . The infrared spectrum of the mineral contains the following bands (cm –1 ): 453, 531, 550, 654 and 958, with shoulders at 1070, 1031 and 908. A broad absorption was observed between ~3610 and 3300 with a maximum at ~3525. The crystal structure was solved by direct methods and refined to an R 1 index of 9.1%. In veblenite, the main structural unit is an HOH layer, which consists of the octahedral (O) and two heteropolyhedral (H) sheets. The H sheet is composed of Si 2 O 7 groups, veblenite Si 8 O 22 ribbons and Nb-dominant D octahedra. This is the first occurrence of an eight-membered Si 8 O 22 ribbon in a mineral crystal structure. In the O sheet, (Fe 2+ , Fe 3+ , Mn 2+ ) octahedra share common edges to form a modulated O sheet parallel to (001). HOH layers connect via common vertices of D octahedra and cations at the interstitial A (1,2) and B sites. In the intermediate space between two adjacent HOH layers, the A (1) site is occupied mainly by K; the A (2) site is partly occupied by K and H 2 O groups, the B site is partly occupied by Na. The crystal structure of veblenite is related to several HOH structures: jinshanjiangite, niobophyllite (astrophyllite group) and nafertisite. The mineral is named in honour of David R. Veblen in recognition of his outstanding contributions to the fields of mineralogy and crystallography.
    Print ISSN: 0026-461X
    Electronic ISSN: 1471-8022
    Topics: Geosciences
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