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  • 1
    Call number: SR 90.1040(16)
    In: Serie geologica
    Type of Medium: Series available for loan
    Pages: 10 S.
    Series Statement: Serie geologica / Instituto de Geologia y Paleontologia, Academia de Ciencias de Cuba 16
    Language: Spanish
    Location: Lower compact magazine
    Branch Library: GFZ Library
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  • 2
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  • 4
    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.
    Print ISSN: 0026-461X
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  • 5
    Publication Date: 2015-12-16
    Description: The crystal structure of betalomonosovite, ideally Na 6 4 Ti 4 (Si 2 O 7 ) 2 [PO 3 (OH)][PO 2 (OH) 2 ]O 2 (OF), a 5.3331(7), b 14.172(2), c 14.509(2) Å, α 103.174(2), β 96.320(2), 90.278(2)°, V 1060.7(4) Å 3 , from the Lovozero alkaline massif, Kola peninsula, Russia, has been refined in the space group P 1{macron} to R = 6.64% using 3379 observed ( F o 〉 4 F ) reflections collected with a single-crystal APEX II ULTRA three-circle diffractometer with a rotating-anode generator (Mo K α), multilayer optics, and an APEX-II 4K CCD detector. Electron-microprobe analysis gave the empirical formula (Na 5.39 Ca 0.36 Mn 0.04 Mg 0.01 ) 5.80 (Ti 2.77 Nb 0.48 Mg 0.29 Fe 3+ 0.23 Mn 0.20 Zr 0.02 Ta 0.01 ) 4 (Si 2.06 O 7 ) 2 [P 1.98 O 5 (OH) 3 ]O 2 [O 0.82 F 0.65 (OH) 0.53 ] 2 , D calc. = 2.969 g cm –3 , Z = 2, calculated on the basis of 26 (O + F) apfu , with H 2 O determined from structure refinement. The crystal structure of betalomonosovite is characterized by extensive cation and anion disorder: more than 50% of cation sites are partly occupied. The crystal structure of betalomonosovite is a combination of a titanium silicate (TS) block and an intermediate ( I ) block. The TS block consists of HOH sheets (H-heteropolyhedral, O-octahedral) and exhibits linkage and stereochemistry typical for Group IV (Ti + Mg + Mn = 4 apfu ) of the TS-block minerals. The I block is a framework of Na polyhedra and P tetrahedra which ideally gives {Na 2 4 [PO 3 (OH)][PO 2 (OH) 2 ]} pfu . Betalomonosovite is an Na-poor OH-bearing analogue of lomonosovite, Na 10 Ti 4 (Si 2 O 7 ) 2 (PO 4 ) 2 O 4 . In the betalomonosovite structure, there is less Na in the I block and in the TS block when compared to the lomonosovite structure. The OH groups occur mainly in the I block where they coordinate P and Na atoms and in the O sheet of the TS block (minor). The presence of OH groups in the I block and in the TS block is supported by IR spectroscopy and bond-valence calculations on anions. High-resolution TEM of lomonosovite shows the presence of pervasive microstructural intergrowths, accounting for the presence of signals from H 2 O in the infrared spectrum of anhydrous lomonosovite. More extensive lamellae in betalomonosovite suggest a topotactic reaction from lomonosovite to betalomonosovite.
    Print ISSN: 0008-4476
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  • 6
    Publication Date: 2015-07-02
    Description: Yusupovite, ideally Na 2 Zr(Si 6 O 15 )(H 2 O) 3 , is a new silicate mineral from the Darai-Pioz alkaline massif in the upper reaches of the Darai-Pioz river, area of the joint Turkestansky, Zeravshansky, and Alaisky ridges, Tajikistan. Yusupovite was found in a pegmatite composed mainly of reedmergnerite, aegirine, microcline, and polylithionite. It occurs as prismatic grains about 2 mm in size embedded in reedmergnerite; associated minerals are quartz, pectolite, zeravshanite, mendeleevite-(Ce), fluorite, leucosphenite, a pyrochlore-group mineral, neptunite, telyushenkoite, moskvinite-(Y), and shibkovite. Yusupovite is colorless, transparent with a white streak, has a vitreous luster, and does not fluoresce under ultraviolet light. Cleavage is perfect on {110}, parting was not observed. Mohs hardness is 5. Yusupovite is brittle with a splintery fracture. The measured and calculated densities are 2.69(2) and 2.713 g/cm 3 , respectively. Yusupovite is optically biaxial (+) with refractive indices ( = 589 nm) α = 1.563(2), β = 1.565(2), = 1.577(2); 2 V meas = 42(3)°, 2 V calc = 45°, strong dispersion: r 〉 v. Yusupovite is monoclinic, C 2/ m , a = 14.5975(4), b = 14.1100(4), c = 14.4394(4) Å, β = 90.0399(4)°, V = 2974.1(3) Å 3 . The six strongest reflections in the X-ray powder diffraction data [ d (Å), I, ( hkl )] are 7.05, 100, (020); 3.24, 96, (420); 3.10, 69, (241, 41); 5.13, 53, (202, 02); 6.51, 42, (201, 01); 3.17, 34, (042). The chemical composition (electron microprobe) is: Nb 2 O 5 0.39, SiO 2 58.84, ZrO 2 16.55, HfO 2 0.30, FeO 0.01, Y 2 O 3 3.05, Cs 2 O 2.58, K 2 O 0.95, Na 2 O 8.91, H 2 O calc 7.40, total 98.98 wt%, with H 2 O calculated from structure refinement. The empirical formula (based on 17.5 O apfu) is (Na 1.76 K 0.12 Cs 0.11 ) 1.99 (Zr 0.82 Y 0.17 Nb 0.02 Hf 0.01 ) 1.02 (Si 6.01 O 14.98 )(H 2 O) 2.52 , Z = 8. The crystal structure of yusupovite was refined to R 1 = 3.46% based on 4428 observed reflections. In the crystal structure, there are six Si sites occupied by Si, two M sites occupied mainly by Zr with minor Y and Hf. Si tetrahedra form an epididymite Si 6 O 15 ribbon along [010]. Epididymite ribbons and Zr-dominant M octahedra share common vertices to form a heteropolyhedral Si-Zr-O framework. There are six interstitial sites partly occupied by alkali cations Na, K, and Cs. The three [7]-coordinated Na sites are occupied by Na at 95, 84, and 78%. The three A sites are occupied by K and Cs at 12, 18, and 16%. There are 10 W sites occupied by H 2 O groups at 18–84%. Due to (K,Cs), Na and H 2 O disorder, the symmetry of yusupovite decreases from orthorhombic, space group Pbcm (elpidite), to monoclinic, space group C 2/ m , and the b unit-cell parameter of yusupovite is doubled compared to the corresponding cell parameter in elpidite, b yus = 2 a elp . Yusupovite, ideally Na 2 Zr(Si 6 O 15 )(H 2 O) 3 , is a dimorph of elpidite, Na 2 Zr(Si 6 O 15 )(H 2 O) 3 .
    Print ISSN: 0003-004X
    Electronic ISSN: 1945-3027
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  • 7
    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.
    Print ISSN: 0026-461X
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  • 8
    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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  • 9
    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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  • 10
    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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