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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: 2015-07-03
    Description: Magnesio-arfvedsonite, the C Fe 3+ -dominant analogue of eckermannite, has been found in a sample of "szechenyite" in the mineral collection of the American Museum of Natural History (AMNH H35024). It comes from the northern part of the Jade Mine Tract near Hpakan, Kachin State, Myanmar. Associated minerals are kosmochlor–jadeite solid-solution pyroxene and clinochlore. The ideal formula of magnesio-arfvedsonite is A Na B Na 2 C (Mg 4 Fe 3+ ) T Si 8 O 22 W (OH) 2 , and the empirical formula derived from electron microprobe analysis and single-crystal structure refinement for the sample of this work is A (Na 0.96 K 0.04 ) =1.00 B (Na 1.57 Ca 0.40 $${\mathrm{Fe}}_{0.02}^{2+}$$ Mn 0.01 ) =2.00 C (Mg 4.26 $${\mathrm{Fe}}_{0.19}^{2+}$$ $${\mathrm{Fe}}_{0.41}^{3+}$$ Al 0.11 $${\mathrm{Ti}}_{0.03}^{4+}$$ ) =5.00 T (Si 7.99 Al 0.01 ) =8.00 O 22 W [F 0.02 (OH) 1.98 ] =2.00 . The unit-cell dimensions are a = 9.867(1), b = 17.928(2), c = 5.284(1) Å, β = 103.80(2)°, V = 907.7 (2) Å 3 , Z = 2. Magnesio-arfvedsonite is biaxial (–), with α = 1.624, β = 1.636, = 1.637, all ± 0.002 and 2V obs = 36(1)°, 2V calc = 32°. The ten strongest reflections in the X-ray powder pattern [ d values (in Å), I , ( hkl )] are: 2.708, 100, (151); 3.399, 68, (131); 3.144, 63, (310); 2.526, 60, (2I02); 8.451, 46, (110); 3.273, 39, (240); 2.167, 37, (261); 2.582, 34, (061); 2.970, 34, (221); 2.326, 33, [(2I51) (4I21)].
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  • 3
    Publication Date: 2015-07-03
    Description: Katophorite has the ideal formula A Na B (NaCa) C (Mg 4 Al) T (Si 7 Al)O 22 W (OH) 2 ( Hawthorne et al. , 2012 ). No published analyses of amphiboles fall in the katophorite compositional field, except that of Harlow and Olds ( 1987 ) for an amphibole from near Hpakan in the Jade Mine Tract, Myanmar. This amphibole was approved by the International Mineralogical Association Commission on New Minerals, Nomenclature and Classification (vote 2013-140) as katophorite, and is reported here. Holotype katophorite is monoclinic, space group C 2/ m, a = 9.8573(8), b = 17.9617(15), c = 5.2833(4) Å, β = 104.707(2)°, V = 904.78(13) Å 3 , Z = 2. The calculated density is 3.091 g cm –3 . In plane-polarized light, katophorite is pleochroic, X = pale blue (medium), Y = light blue-green (strongest), Z = colourless; X ^ a = 30.6° (β obtuse), Y || b, Z ^ c = 15.8 (β acute). It is biaxial negative, α = 1.638, β = 1.642, = 1.644, all ± 0.002; 2V obs = 73(1)°, 2V calc = 70°. The eight strongest lines in the powder X-ray diffraction pattern are [ d in Å ( I )( hkl )]: 2.700 (100)(151), 3.129 (69)(310), 2.536 (65)(2I02), 3.378 (61)(131), 8.421 (55)(110), 2.583 (46)(061), 2.942 (43)(221) and 2.334 (41)(3I51). Electron-microprobe analysis of the refined crystal gave SiO 2 51.74, Al 2 O 3 7.38, TiO 2 0.14, FeO 1.55, Fe 2 O 3 2.82, MgO 18.09, CaO 8.17, Na 2 O 6.02, K 2 O 0.24, F 0.06, H 2 O calc. 1.80, Li 2 O calc. 0.09, sum 100.55 wt.% (Li 2 O and H 2 O based on the results of single-crystal structure refinement). The formula unit, calculated on the basis of 24 (O,OH,F) with (OH + F + O) = 2 is: A (Na 0.85 K 0.04 ) =0.89 B (Ca 1.22 Na 0.78 ) =2.00 C (Mg 3.76 Al 0.43 $${\mathrm{Fe}}_{0.30}^{3+}$$ $${\mathrm{Cr}}_{0.27}^{3+}$$ $${\mathrm{Fe}}_{0.18}^{2+}$$ Li 0.05 $${\mathrm{Ti}}_{0.01}^{4+}$$ ) =5.00 T (Si 7.21 Al 0.79 ) =8.00 O 22 W [(OH) 1.67 O 0.30 F 0.03 )] =2.00 .
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  • 4
    Publication Date: 2011-04-19
    Description: Bavenite is an orthorhombic calcium beryllium aluminosilicate, a {approx} 23.2, b {approx} 5.0, c {approx} 19.4 A, V {approx} 2250 A3, Z = 4, that crystallizes in the space group Cmcm. The crystal structures of 24 bavenite samples from various localities worldwide were refined to R1 values from 2.4 to 7.5% based on [~]1330 unique reflections collected with Mo-K X-radiation on a Bruker P4 CCD single-crystal diffractometer. The composition of each crystal was determined by electron microprobe analysis. There is extensive solid-solution in bavenite according to O(2)OH- + T(4)Si4+ + T(3)Be2+ {rightleftharpoons} O(2)O2- + T(4)Al3+ + T(3)Si4+, such that the general formula may be written Ca4BexSi9Al4-xO28-x(OH)x, where x ranges from 2.00 to [~]3.00 a.p.f.u. Small amounts of additional Be may be incorporated into bavenite via the substitution T(3)Be + O(2)OH- + Na + T(4)Si2 {rightleftharpoons} T(3)Si + O(2)O2- + Ca + T(4)Al2. Local (short-range) bond-valence considerations indicate that Short-Range Order (SRO) should be extensive in the bavenite structure, and this is confirmed by Fourier Transform Infrared (FTIR) spectroscopy in the principal OH-stretching region and by 27Al Magic Angle Spinning Nuclear Magnetic Resonance (MAS NMR) spectroscopy. Short-range bond-valence considerations indicate that the T(3)-T(4)-T(3)-T(4) rings of the framework can incorporate any short-range arrangement of cations consonant with their site populations [T(3) = Be,Si; T(4) = Si,Al], and 27Al MAS NMR spectroscopy confirms this, showing the presence of the local clusters T(3)Be-T(4)Al-T(3)Be, T(3)Si-T(4)Al-T(3)Be and T(3)Si-T(4)Al-T(3)Si. Incorporation of Be at the T(3) site is accompanied by local replacement of O2- by (OH)- at the O(2) site and hydrogen bonding to the adjacent O(3) anion; the latter promotes Be [-〉] Si substitution at the T(3) tetrahedron adjacent in the b direction. T(3)-T(4)-T(3)-T(4) rings link in the c direction through a T(3)-(1)-(3) linkage [T(1) = Si]. Local bond-valence considerations show that occupancy of both T(3) tetrahedra by Be violates the valence-sum rule, and that the linkage T(3)Be-T(1)Si-T(3)Si provides the constraint whereby Be does not exceed 3 a.p.f.u. in bavenite when incorporated via the substitution O(2)OH- + T(4)Si4+ + T(3)Be2+ {rightleftharpoons} O(2)O2- + T(4)Al3+ + T(3)Si4+.
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  • 5
    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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  • 6
    Publication Date: 2011-04-11
    Description: Tourmalines of unusual (mushroom) habit are common in granitic pegmatites of Momeik, northeast of Mogok, Myanmar. Here, we examine a sample of elbaite of significantly different habit, consisting of a series of diverging crystals, resembling a sheaf of wheat and ranging in colour from light purplish-red at the base to dark purplish-red at the tip with a thin green cap at the termination. The crystal structures of eight crystals are refined to R1-indices of [~]2.5% using graphite-monochromated Mo-K X-radiation; the same crystals were analysed by electron microprobe. 11B and 27Al magic angle spinning nuclear magnetic resonance (MAS NMR) spectra were collected on four regions of the wheatsheaf crystal, and show [~]0.3 a.p.f.u. [4]B and
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  • 7
    Publication Date: 2011-01-18
    Description: Fluoro-potassic-magnesio-arfvedsonite, ideally AKBNa2C(Mg4Fe3+)TSi8O22WF2, has been found in a dyke [~]25 km southwest of Monte Metocha, Xixano region, northeastern Mozambique. Fluoro-potassic-magnesio-arfvedsonite and low sanidine form a fine-grained mafic, ultrapotassic, peralkaline igneous rock without visible phenocrysts. The amphibole is brittle, has a Mohs hardness of 6 and a splintery fracture; it is non-fluorescent with perfect {110} cleavage and no observable parting, and has a calculated density of 3.174 gcm-3. In plane-polarized light, it is pleochroic, X = pale grey-green, Y = blue-green, Z = palegrey; X ^ c = 23.6{degrees} (in {beta} obtuse), Y || b, Z ^ c = 66.4{degrees} (in {beta} acute). Fluoro-potassic-magnesio-arfvedsonite is biaxial negative, {alpha} = 1.652(2), {beta} = 1.658(2), {gamma} = 1.660(2); 2Vobs = 22.5(7){degrees}, 2Vcalc = 30.2{degrees}. The unit-cell dimensions are a = 9.9591(4), b = 17.9529(7), c = 5.2867(2) A, {beta} = 104.340(1){degrees}, V = 919.73(10) A3, Z = 2. The nine strongest X-ray diffraction lines in the experimental powder pattern are: [d in A(I)(hkl)]: 2.716(100)(151), 3.410(70)(131), 8.475(50)(110), 3.178(50)(310), 3.309(30)(240), 2.762(20)([IMG]f1.gif" ALT="Formula" BORDER="0"〉31), 2.549(20)(260), 2.351(10)([IMG]f1.gif" ALT="Formula" BORDER="0"〉51), 2.269(10)(331). Electron microprobe analysis gave: SiO2 54.25, Al2O3 0.03, TiO2 1.08, FeO 6.69, Fe2O3 8.07, MgO 13.99, MnO 0.32, ZnO 0.05, CaO 1.16, Na2O 6.33, K2O 5.20, F 2.20, H2Ocalc 0.74, sum 99.18 wt.%. The formula unit, calculated on the basis of 24 (O,OH,F) with (OH+F) = 2-(2 Ti), is AK0.98B(Na1.81Ca0.18){Sigma}1.99C(Mg3.07[IMG]f2.gif" ALT="Formula" BORDER="0"〉Mn0.04[IMG]f3.gif" ALT="Formula" BORDER="0"〉Ti0.12Zn0.01){Sigma}=4.98 TSi8O22W[F1.03(OH)0.73O0.24]{Sigma}2.00 and confirms the usual pattern of cation order in the amphibole structure. The presence of a significant oxo component (locally balanced by Ti at the M(1) site) is related to the crystallization conditions. The presence of Fe3+ at the T sites, originally suggested for the holotype specimen, is discounted for this amphibole composition.
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  • 8
    Publication Date: 2011-01-18
    Description: Fluoro-potassic-pargasite, ideally AKBCa2C(Mg4Al)T(Si6Al2)O22WF2, a new amphibole species, has been found in a skarn in the Tranomaro area, Madgascar. The sample used for the description of the new mineral species is a large single amphibole crystal, 4 mm x 2 mm x 2 cm in size, brownish-black with brownish-yellow phlogopite lamellae adhering to one face of the crystal. Fluoro-potassic-pargasite is brittle, has a Mohs hardness of 6.5 and a splintery fracture; it is non-fluorescent, has perfect {110} cleavage, no observable parting, and has measured and calculated densities of 3.46 and 3.151 g cm-3, respectively. In plane-polarized light, it is pleochroic, X = colourless to very pale grey, Y = very pale grey, Z = colourless; X ^ a = 46.9{degrees} (in {beta} obtuse), Y || b, Z ^ c = 31.4{degrees} (in {beta} acute). It is biaxial positive, {alpha} = 1.638(2), {beta} = 1.641(2), {gamma} = 1.653(2); 2Vobs = 49.6(4){degrees}, 2Vcalc = 53.4{degrees}. Fluoro-potassic-pargasite is monoclinic, space group C2/m, a = 9.9104(2), b = 17.9739(4), c = 5.3205(1) A, {beta} = 105.534(2){degrees}, V = 913.11(6) A3, Z = 2. The eight strongest lines in the X-ray powder-diffraction pattern are [d in A(I)(hkl)]: 3.133(100)(310), 3.270(55)(240), 2.809(47)(330), 8.413(45)(110), 2.698(39)(151), 3.374(31)(131), 2.934(29)(221) and 1.647(29)(461). Electron microprobe analysis gives SiO2 40.20, Al2O3 17.61, TiO2 0.46, FeO 1.96, Fe2O3 2.51, MgO 16.95, MnO 0.05, CaO 13.18, Na2O 0.99, K2O 3.72, F 2.75, H2Ocalc 0.77, sum 99.99 wt.%. The formula unit, calculated on the basis of 24 (O,OH,F) with (OH + F) = 2 - (2 x Ti), is A(K0.69Na0.28Ca0.04){Sigma}=1.01BCa2.00C(Mg3.64[IMG]f1.gif" ALT="Formula" BORDER="0"〉Mn0.01Al0.79[IMG]f2.gif" ALT="Formula" BORDER="0"〉Ti0.05){Sigma}=5.00T(Si5.80Al2.20){Sigma}=8.00O22 W[F1.26(OH)0.74]{Sigma}=2.00. The mineral species and name have been approved by the IMA CMNMC (IMA 2009-091).
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  • 9
    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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  • 10
    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.
    Print ISSN: 0026-461X
    Electronic ISSN: 1471-8022
    Topics: Geosciences
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