ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Mineralogical Association of Canada  (64)
  • Mineralogical Society of Great Britain and Ireland  (43)
  • 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.
    Print ISSN: 0026-461X
    Electronic ISSN: 1471-8022
    Topics: Geosciences
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    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
    Topics: Geosciences
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    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
    Electronic ISSN: 1471-8022
    Topics: Geosciences
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    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.
    Print ISSN: 0026-461X
    Electronic ISSN: 1471-8022
    Topics: Geosciences
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    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
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    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.
    Print ISSN: 0026-461X
    Electronic ISSN: 1471-8022
    Topics: Geosciences
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    Publication Date: 2019
    Description: 〈span〉〈div〉Abstract〈/div〉The crystal structure of polylithionite-1〈span〉M〈/span〉 from Darai-Pioz, (K〈sub〉0.97〈/sub〉Na〈sub〉0.03〈/sub〉Rb〈sub〉0.01〈/sub〉)〈sub〉Σ1.01〈/sub〉(Li〈sub〉2.04〈/sub〉Al〈sub〉0.84〈/sub〉 Ti〈sup〉4+〈/sup〉〈sub〉0.09〈/sub〉Fe〈sup〉3+〈/sup〉〈sub〉0.03〈/sub〉)〈sub〉Σ3.00〈/sub〉(Si〈sub〉3.98〈/sub〉Al〈sub〉0.02〈/sub〉)O〈sub〉10〈/sub〉[F〈sub〉1.68〈/sub〉(OH)〈sub〉0.33〈/sub〉]〈sub〉Σ2〈/sub〉, 〈span〉a〈/span〉 5.1974(4), 〈span〉b〈/span〉 8.9753(6), 〈span〉c〈/span〉 10.0556(7) Å, β 100.454(1)°, 〈span〉V〈/span〉 461.30(6) Å〈sup〉3〈/sup〉, space group 〈span〉C〈/span〉2, 〈span〉Z〈/span〉 = 2, was refined to 〈span〉R〈/span〉〈sub〉1〈/sub〉 = 1.99% using Mo〈span〉K〈/span〉α X-radiation. In the space group 〈span〉C〈/span〉2, there are three octahedrally coordinated 〈span〉M〈/span〉 sites in the 1〈span〉M〈/span〉 mica structure: the 〈span〉M〈/span〉(1) site is occupied by Li〈sup〉+〈/sup〉 and minor vacancy that is likely locally associated with Ti〈sup〉4+〈/sup〉 at the 〈span〉M〈/span〉(2) site; the 〈span〉M〈/span〉(2) site is occupied dominantly by Al〈sup〉3+〈/sup〉, with other minor divalent to tetravalent cations; the 〈span〉M〈/span〉(3) site is completely occupied by Li〈sup〉+〈/sup〉. In the space group 〈span〉C〈/span〉2, the structure is completely ordered. Each non-bridging O〈sup〉2–〈/sup〉 ion is surrounded by an ordered arrangement of 2Li〈sup〉+〈/sup〉 + Al〈sup〉3+〈/sup〉 + Si〈sup〉4+〈/sup〉 with an incident bond-valence sum of 1.95 〈span〉vu〈/span〉 (valence units). The F〈sup〉–〈/sup〉 ion is coordinated by Li〈sup〉+〈/sup〉 + Li〈sup〉+〈/sup〉 + Al〈sup〉3+〈/sup〉 with an incident bond-valence sum of 0.84 〈span〉vu〈/span〉 (values around F〈sup〉–〈/sup〉 generally tend to be lower than ideal). Thus, the valence-sum rule is satisfied, both long range and short range. In the space group 〈span〉C〈/span〉2/〈span〉m〈/span〉, there is long-range order but not short-range order. There are three different short-range arrangements, one of which has bond-valence deficiencies of 0.38 and 0.49 〈span〉vu〈/span〉 around the non-bridging O〈sup〉2–〈/sup〉 ion and the F〈sup〉–〈/sup〉 ion, destabilizing the structure relative to the more ordered arrangement of the 〈span〉C〈/span〉2 structure, which conforms more closely to the valence-sum rule. The drive to lower the symmetry in polylithionite-1〈span〉M〈/span〉 from 〈span〉C〈/span〉2/〈span〉m〈/span〉 to 〈span〉C〈/span〉2 comes from the short-range bond-valence requirements of the structure.〈/span〉
    Print ISSN: 0008-4476
    Electronic ISSN: 1499-1276
    Topics: Geosciences
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    Publication Date: 2014-02-12
    Description: The crystal structure of schüllerite, ideally Na 2 Ba 2 Mg 2 Ti 2 (Si 2 O 7 ) 2 O 2 F 2 , a 5.396(1), b 7.071(1), c 10.226(2) Å, α 99.73(3), β 99.55(3), 90.09(3)°, V 379.1(2) Å 3 , Z = 1, from the Eifel volcanic region, Germany, has been refined in the space group P 1 to R = 1.33% using 2247 observed ( F o 〉 4 F ) reflections collected with a single-crystal Bruker D8 three-circle diffractometer equipped with a rotating-anode generator (Mo K α radiation), multilayer optics and an APEX-II detector. The empirical formula for schüllerite was calculated on the basis of 18 (O + F) anions: (Na 1.10 Ca 0.43 Mn 0.30 Fe 2+ 0.17 ) 2 (Ba 1.57 Sr 0.14 K 0.14 0.15 ) 2 (Mg 0.79 Fe 2+ 0.71 Na 0.33 Fe 3+ 0.17 ) 2 (Ti 1.67 Fe 3+ 0.21 Nb 0.09 Zr 0.02 Al 0.01 ) 2 Si 3.95 O 15.93 F 2.07 , D calc. = 3.879 g/cm 3 , Z = 1, with Fe 3+ / (Fe 2+ +Fe 3+ ) ratio determined by Mössbauer spectroscopy. Schüllerite is a Group-IV TS-block mineral: Ti + Mg = 4 apfu . The crystal structure of schüllerite is an alternation of TS (Titanium Silicate) and I (intermediate) blocks of the ideal composition [Na 2 Mg 2 Ti 2 (Si 2 O 7 ) 2 O 2 F 2 ] 4– and [Ba 2 ] 4+ , respectively. The TS block is composed of the central O (octahedral) sheet and two adjacent H (heteropolyhedral) sheets. In the O sheet, there are two brookite-like chains of M O octahedra of the following ideal compositions: [Mg 2 O 8 ] 12– [M O (1)] and [Na 2 O 8 ] 14– [M O (2)]; the ideal composition of the O sheet is [Na 2 Mg 2 O 2 F 2 ] 0. The H sheet is composed of the [5]-coordinated Ti-dominant M H polyhedra and Si 2 O 7 groups; the composition of the two H sheets is [Ti 2 (Si 2 O 7 ) 2 ] 4–. In schüllerite, the TS block has a topology characteristic of Group IV of TS-block minerals: two H sheets connect to the O sheet such that two Si 2 O 7 groups link to the Mg-dominant octahedra of the O sheet adjacent along t 1 . In the O sheet, occurrence of divalent cations at the M O (1) site results in the presence of monovalent anions, F – , at the X O A site. The A P site of the H sheet is occupied mainly by Ba; the A P site is shifted from the plane of the H sheet, and Ba atoms constitute the I block of the composition [Ba 2 ] 4+ . Schüllerite is the only mineral of Group IV that has (1) a brookite-like [Mg 2 O 8 ] 12– chain of octahedra in the O sheet; (2) [5]-coordinated Ti in the H sheet; (3) Ba atoms in the I block. The ideal structural formula of schüllerite is of the form A P 2 M H 2 M O 4 (Si 2 O 7 ) 2 (X O M ) 2 (X O A ) 2 : Ba 2 Ti 2 Na 2 Mg 2 Ti 2 (Si 2 O 7 ) 2 O 2 F 2 , Z = 1.
    Print ISSN: 0008-4476
    Topics: Geosciences
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    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.
    Print ISSN: 0026-461X
    Electronic ISSN: 1471-8022
    Topics: Geosciences
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Publication Date: 2014-10-22
    Description: The HOH layer is the main structural unit in the crystal structures of Fe 3+ -disilicates ericssonite-2 O , ideally Ba 2 Fe 3+ 2 Mn 4 (Si 2 O 7 ) 2 O 2 (OH) 2 , ferroericssonite, ideally Ba 2 Fe 3+ 2 Fe 2+ 4 (Si 2 O 7 ) 2 O 2 (OH) 2 , and yoshimuraite, ideally Ba 4 Ti 2 Mn 4 (Si 2 O 7 ) 2 (PO 4 ) 2 O 2 (OH) 2 , a TS-block mineral of Group II. The chemical compositions of the core part of the HOH layer in ericssonite-2 O and ferroericssonite, [5] Fe 3+ 2 Mn 4 (Si 2 O 7 ) 2 O 2 (OH) 2 and [5] Fe 3+ 2 Fe 2+ 4 (Si 2 O 7 ) 2 O 2 (OH) 2 , are similar to the chemical composition of the core part of the HOH layer in yoshimuraite, [5] Ti 4+ 2 Mn 4 (Si 2 O 7 ) 2 O 2 (OH) 2 , except for the cation species at the [5]-coordinated M H site in the H sheets: [5] Fe 3+ and [5] Ti 4+ , respectively. Despite this similarity, the topology of the HOH layer in ericssonite-2 O and ferroericssonite is different from that in yoshimuraite. In TS-block minerals, different distortions of M O octahedra correspond to specific types of linkage of H and O sheets. Topological consideration of Fe 3+ -disilicates ericssonite-2 O and ferroericssonite and yoshimuraite, a TS-block mineral of Group II, shows that different topologies of the chemically identical HOH layer are due to a difference in the bond-valence contributions of Fe 3+ and Ti 4+ at the M H site in the H sheet ( i.e. , inability of Fe 3+ to contribute sufficient bond-valence to the X O M anion) and subsequent different distortions of M O octahedra in the O sheet, where M O = Mn 2+ , Fe 2+ .
    Print ISSN: 0008-4476
    Topics: Geosciences
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...