Ayya Bazai

Ayya Bazai

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Ayya Bazai has a total of 35 co-authors. Here are the top co-authors by number of shared publications:


Latest Publications

  • Open Access

    Ion-Selective Properties of Armbrusterite Mineral and the Prospects for Its Laboratory Synthesis

    by Darya Gryaznova, Taras Panikorovskii, Galina Kalashnikova, Ayya Bazai, Margarita Glazunova, Ekaterina Selivanova, Alevtina Gosteva, Victor Yakovenchuk

    In this paper, results of studying the properties of armbrusterite, a natural heterophyllosilicate, are presented. Due to its crystal structure consisting of parallel HOH-type sheets separated by a network of large-diameter (4–6 Å) channels, this mineral is of interest as a prototype for producing novel compounds to be used as sorbents. The studies were conducted by X-ray powder diffraction and X-ray single crystal diffraction analyses, electron microscopy, and IR spectroscopy. The natural sample is shown to be able to selectively extract monovalent cations from the solution of complex composition consisting of mono- and divalent salts. Furthermore, the preliminary results of hydrothermal synthesis of an analog of this mineral are reported. It is demonstrated that the mineral can be produced under milder conditions than the known methods for synthesizing heterophyllosilicates using platinum capsules (Tuttle bombs) at 380–450 °C.

  • Атакамит и йодаргирит рудного поля Пюи де Фоль

    by Ао «Пмгрэ», Легенькова А. М., Центр Наноматериаловедения Фиц Кнц Ран, Базай А. В., Паникоровский Т. Л., Лаборатория Природоподобных Технологий И Техносферной Безопасности Арктики Фиц Кнц Ран

  • Open Access

    Monchegorsk Mafic–Ultramafic Layered PGE-Bearing Complex (2.5 Ga, Kola Region, Russia): On the Problem of Relationships between Magmatic Phases Based on the Study of Cr-Spinels

    by Pavel Pripachkin, Tatiana Rundkvist, Artem Mokrushin, Aiya Bazai

    The composition of Cr-spinels from rocks of the Monchegorsk layered complex (2.5 Ga) basically corresponds to the evolutionary trend that is typical for layered mafic–ultramafic intrusions (late magmatic phases contain Cr-spinels enriched in Fe and depleted in Mg, Cr, and Al). Cr-spinels within the Dunite Body of the Sopcha massif are almost identical to those within the Dunite Block rocks and are close to those from harzburgite of the NKT massif. Cr-spinels within the satellite bodies of the Ore Layer 330 are shown to have zonal structure, which confirms their origin from a new portion of melt, which may have been injected with several pulses. The composition of accessory Cr-spinels may indicate that the layered complex of rocks of the South Sopcha massif was formed from the most evolved portion of magmatic melt (linked with the Monchetundra intrusion), and its vein complex may be considered the one formed at the final stages of the magmatic system evolution. The composition of Cr-spinels from the Pentlandite Gorge mafic–ultramafic rocks may indicate that they are fragments of the NKT massif and not of the Monchetundra massif, as it was believed earlier.


  • Open Access

    Mineral Mimetic Material Sr-Exchanged Sitinakite of Different Crystallinity: Phase Transformations during Heat Treatment and the Strength of SR Fixation in a Ceramic Matrix

    by Igor A. Perovskiy, Dmitry A. Shushkov, Alexey V. Ponaryadov, Galina O. Kalashnikova, Ayya V. Bazai, Vladimir N. Bocharov, Taras L. Panikorovskii

    A simple method for the direct transformation of Sr-exchanged titanosilicate with the sitinakite structure (IONSIV) into ceramic material through cold pressing and subsequent sintering at 1100 °C for 4 h is presented. The temperature transformation of Sr-exchanged sitinakite showed the stages of recrystallization of the material with the formation of Sr-Ti phases matsubaraite (Sr4Ti5[Si2O7]2O8), jeppeite (SrTi6O13), tausonite (SrTiO3), and rutile. Leaching experiments showed the efficiency of fixation of Sr cations in a ceramic matrix; extraction into water does not exceed 0.01% and desorption in 1 M HNO3 solution is only 0.19% within three days. The leaching rates of immobilized Sr demonstrate the structural integrity of the formed phases in the ceramic (2.8 × 10−5–1.0 × 10−5 g/(m2·day). The decrease in the crystallinity of the initial Na-sitinakite, which is achieved by reducing the synthesis temperature from 250 to 210 °C, does not affect the sorption capacity and the fixation of cations in the ceramic matrix. The obtained results confirm the prospect of using inexpensive precursors, titanium ore enrichment waste, for the synthesis of sorption materials.


  • Open Access

    Nb-Ta-Sn Oxides from Lithium-Beryllium-Tantalum Pegmatite Deposits of the Kolmozero–Voronja Belt, NW Russia: Implications for Tracing Ore-Forming Processes and Mineralization Signatures

    by Dmitry Zozulya, Lyudmila N. Morozova, Kåre Kullerud, Ayya Bazai

    In this paper we present textural and compositional data for columbite group minerals (CGMs) and associated Nb-Ta-Sn oxides from lithium-beryllium-tantalum pegmatite deposits of the Kolmozero–Voronja belt, NW Russia, with the aim of deciphering these characteristics for minerals from deposits with different mineral signatures and lithium ore grade. Minerals from four deposits, including two of world-class (Kolmozero and Polmostundra), are examined. The main controlling factors for CGM compositional ranges are the diversity and rate of magmatic fractionation, hydrothermal overprint and mineral paragenesis, following the specific geochemical signature of the different pegmatite deposits. CGM from Kolmozero include several mineral species (columbite-(Fe), columbite-(Mn), tantalite-(Fe), and tantalite-(Mn)), showing large compositional variations, mainly controlled by Nb-Ta fractionation (Ta/(Ta + Nb) = 0.16–0.70; Mn/(Mn + Fe) = 0.45–0.63). Textural patterns are various (oscillatory, homogeneous, and patchy); spongy domains and overgrowing Ta-rich rims are also observed somewhere. This indicates the involvement of numerous magmatic and hydrothermal processes. The Polmostundra CGMs are represented by columbite-(Fe) with Ta/(Ta + Nb), ranging from 0.05 to 0.39; some crystals are homogenous, and others present normal, oscillatory, mottled and reverse-zoning patterns. The Okhmylk CGMs are irregular normal, patchy and homogeneous columbite-(Fe) and columbite-(Mn), with Ta/(Ta + Nb) = 0.09–0.24 and Mn/(Mn + Fe) = 0.29–0.92, indicating the suppressed magmatic fractionation and iron drop due to precipitation of Fe minerals. Columbite-(Fe) and columbite-(Mn) from the Be-Ta Shongui deposit are less evolved, with Ta/(Ta + Nb) = 0.07–0.23 and Mn/(Mn + Fe) = 0.31–0.55. The minerals are characterized by progressive normal, oscillatory, homogeneous and irregular reverse patterns. Associated pyrochlore minerals occur both as early magmatic (Kolmozero) and late hydrothermal (Polmostundra, Okhmylk). Cassiterite is found only in the Okhmylk dykes, and is apparently of hydrothermal origin. CGM from Li pegmatites have impurities of Ti (0.01–0.05 apfu) and W (up to 0.02 apfu), whereas CGM from Be pegmatites contains elevated Ti (up to 0.09 apfu). The mineral system analysis presented here is relevant for exploration.


  • Open Access

    Microwave-Assisted Synthesis of Titanosilicates Using a Precursor Produced from Titanium Ore Concentrate

    by Galina O. Kalashnikova, Darya V. Gryaznova, Alexander E. Baranchikov, Sergey N. Britvin, Victor N. Yakovenchuk, Gleb O. Samburov, Varvara O. Veselova, Aleksandra Y. Pulyalina, Yakov A. Pakhomovsky, Ayya V. Bazai, et al.

    Titanosilicates comprise a broad class of materials with promising technological applications. The typical obstacle that restricts their industrial applicability is the high manufacturing cost due to the use of specific organotitanium precursors. We herein report a new approach to the synthesis of titanosilicates using an inexpensive inorganic precursor, ammonium titanyl sulfate (ATS or STA), (NH4)2TiO(SO4)2∙H2O. The latter is an intermediate in the processing of titanium-bearing concentrates produced from apatite-nepheline ores. In this paper, the new synthetic approach is exemplified by the microwave-assisted synthesis of IONSIVE-911, one of the most effective Cs-ion scavengers. The method can be modified to synthesize various titanosilicate compounds.


  • Open Access

    Nb-Ta-Sn Oxides From Lithium-Beryllium-Tantalum Pegmatite Deposits of the Kolmozero-Voronja Belt, NW Russia: Implica-Tions for Tracing Ore-Forming Processes and Mineralization Signatures

    by Dmitry Zozulya, Lyudmila Morozova, Kåre Kullerud, Ayya Bazai

    In this paper we present textural and compositional data for columbite group minerals (CGM) and associated Nb-Ta-Sn oxides from lithium-beryllium-tantalum pegmatite deposits of the Kolmozero-Voronja belt, NW Russia, with the aim of deciphering the above mentioned features for minerals from deposits with different mineral signatures and lithium ore grade. Minerals from four deposits, including two of world-class (Kolmozero and Polmostundra), are examined. It is shown that the main controlling factors are the diversity and rate of magmatic fractionation, hydrothermal overprint and mineral paragenesis followed from the specific geochemical signature of the different pegmatite deposits. CGM from Kolmozero include several mineral species (columbite-(Fe), columbite-(Mn), tantalite-(Fe), tantalite-(Mn)) showing large compositional variations, mainly controlled by Nb-Ta fractionation (Ta/(Ta+Nb) = 0.16-0.70; Mn/(Mn + Fe) = 0.45-0.63). Textural patterns are extremely various (oscillatory, homogeneous, patchy, spongy, somewhere with over-growing Ta-rich rims) and indicate the involvement of numerous magmatic and hydrothermal processes. The Polmostundra CGM are represented by columbite-(Fe) with Ta/(Ta+Nb) ranging from 0.05 to 0.39 with homogeneous, mottled, oscillatory, patchy and irregular reverse textures. The Okhmylk CGM are irregular normal, patchy and homogeneous columbite-(Fe) and columbite-(Mn) with Ta/(Ta+Nb) = 0.09-0.24 and Mn/(Mn + Fe) = 0.29-0.92, indicating the suppressed magmatic fractionation and iron drop due to precipitation of Fe minerals. Columbite-(Fe) and columbite-(Mn) from the Be-Ta Shongui deposit are less evolved with Ta/(Ta+Nb) = 0.07-0.23 and Mn/(Mn + Fe) = 0.31-0.55. The minerals are characterized by progressive normal, oscillatory, homogeneous and ir-regular reverse patterns. Associated pyrochlore minerals occur both as early magmatic (Kolmozero) and late hydrothermal (Polmostundra, Okhmylk). Cassiterite is found only in the Okhmylk dykes and is apparently of hydrothermal origin. CGM from Li pegmatites have impurities of Ti (0.01-0.05 apfu) and W (up to 0.02 apfu), whereas CGM from Be pegmatites contains elevated Ti (up to 0.09 apfu). The mineral systems analysis presented here is relevant for exploration.


  • Open Access

    The Crystal Structure of Manganotychite, Na6Mn2(CO3)4(SO4), and Structural Relations in the Northupite Group

    by Sergey V. Krivovichev, Taras L. Panikorovskii, Ayya V. Bazai, Mikhail Yu. Sidorov

    The crystal structure of manganotychite has been refined using the holotype specimen from the Alluaiv Mountain, Lovozero massif, Kola peninsula, Russia. The mineral is cubic, Fd3¯, a = 14.0015(3) Å, V = 2744.88(18) Å3, Z = 8, R1 = 0.020 for 388 independently observed reflections. Manganotychite is isotypic to tychite and ferrotychite. Its crystal structure is based upon a three-dimensional infinite framework formed by condensation of MnO6 octahedra and CO3 groups by sharing common O atoms. The sulfate groups and Na+ cations reside in the cavities of the octahedral-triangular metal-carbonate framework. In terms of symmetry and basic construction of the octahedral-triangular framework, the crystal structure of manganotychite is identical to that of northupite, Na3Mg(CO3)2Cl. The transition northupite → tychite can be described as a result of the multiatomic 2Cl− → (SO4)2− substitution, where both chlorine and sulfate ions are the extra-framework constituents. However, the positions occupied by sulfate groups and chlorine ions correspond to different octahedral cavities within the skeletons of Na atoms. The crystal structure of northupite can be considered as an interpenetration of two frameworks: anionic [Mg(CO3)2]2− octahedral-triangular framework and cationic [ClNa3]2− framework with the antipyrochlore topology. Both manganotychite and northupite structure types can be described as a modification of the crystal structure of diamond (or the dia net) via the following steps: (i) replacement of a vertex of the dia net by an M4 tetrahedron (no symmetry reduction); (ii) attachment of (CO3) triangles to the triangular faces of the M4 tetrahedra (accompanied by the Fd3¯m → Fd3¯ symmetry reduction); (iii) filling voids of the resulting framework by Na+ cations (no symmetry reduction); and (iv) filling voids of the Na skeleton by either sulfate groups (in tychite-type structures) or chlorine atoms (in northupite). As a result, the information-based structural complexity of manganotychite and northupite exceeds that of the dia net.