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  • 1
    Monograph available for loan
    Monograph available for loan
    Leningrad : Gidrometeoizdat
    Call number: MOP 47232/1 / Mitte ; MOP 47232/2 / Mitte
    Type of Medium: Monograph available for loan
    Pages: 553 S.
    Location: MOP - must be ordered
    Location: MOP - must be ordered
    Branch Library: GFZ Library
    Branch Library: GFZ Library
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  • 2
    Publication Date: 1989-07-01
    Print ISSN: 0034-6748
    Electronic ISSN: 1089-7623
    Topics: Electrical Engineering, Measurement and Control Technology , Physics
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  • 3
    Publication Date: 1989-07-01
    Print ISSN: 0034-6748
    Electronic ISSN: 1089-7623
    Topics: Electrical Engineering, Measurement and Control Technology , Physics
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  • 4
    Publication Date: 1975-01-01
    Print ISSN: 0038-0741
    Electronic ISSN: 1573-9279
    Topics: Architecture, Civil Engineering, Surveying , Geosciences
    Published by Springer
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  • 5
    Publication Date: 2004-03-01
    Print ISSN: 1062-7391
    Electronic ISSN: 1573-8736
    Topics: Geosciences , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Published by Springer
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  • 6
    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
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  • 7
    Publication Date: 2013-09-17
    Description: The 2D azimuth and rapidity structure of the two-particle correlations in relativistic A+A collisions is altered significantly by the presence of sharp inhomogeneities in superdense matter formed in such processes. The causality constraints enforce one to associate the long-range longitudinal correlations observed in a narrow angular interval, the so-called (soft) ridge, with peculiarities of the initial conditions of collision process. This study's objective is to analyze whether multiform initial tubular structures, undergoing the subsequent hydrodynamic evolution and gradual decoupling, can form the soft ridges. Motivated by the flux-tube scenarios, the initial energy density distribution contains the different numbers of high density tube-like boost-invariant inclusions that form a bumpy structure in the transverse plane. The influence of various structures of such initial conditions in the most central A+A events on the collective evolution of matter, resulting spectra, angular particle correlations and -coefficients is studied in the framework of the hydrokinetic model (HKM).
    Print ISSN: 1687-7357
    Electronic ISSN: 1687-7365
    Topics: Physics
    Published by Hindawi
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  • 8
    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
    Topics: Geosciences
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  • 9
    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
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  • 10
    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.
    Print ISSN: 0026-461X
    Electronic ISSN: 1471-8022
    Topics: Geosciences
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