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  • 1
    In: Mineralogical Magazine, Mineralogical Society, Vol. 78, No. 7 ( 2014-12), p. 1613-1627
    Abstract: A description of the new mineral innsbruckite, Mn 33 (Si 2 O 5 ) 14 (OH) 38 , a hydrous manganese phyllosilicate found in Tyrol, Austria is given. The crystal structure was determined by singlecrystal synchrotron radiation diffraction experiments at the X06DA beamline at the Swiss Light Source (Paul Scherrer Institute, Villigen, Switzerland). The space group is Cm and lattice parameters are a = 17.2760(19), b = 35.957(5), c = 7.2560(8) Å , β = 91.359(7)º, V = 4506.1(10) Å 3 , Z = 2. Innsbruckite belongs to the group of modulated 1:1 layer silicates and is chemically and structurally quite closely related to bementite, Mn 7 (Si 2 O 5 ) 3 (OH) 8 . The chemical analysis revealed a close to ideal composition with only minor amounts of Al, Fe and Mg. Using Liebau’s nomenclature for silicate classification the silicate anion can be described as an unbranched siebener single layer. Innsbruckite shows a complex topology of the silicate sheet, exhibiting 4-, 5-, 6- and 8-membered rings. The silicate sheet is fully characterized using vertex symbols, and its topology is compared to those in other complex sheet silicates. Furthermore, the structural investigation is complemented with Raman spectroscopic studies.
    Type of Medium: Online Resource
    ISSN: 0026-461X , 1471-8022
    RVK:
    Language: English
    Publisher: Mineralogical Society
    Publication Date: 2014
    detail.hit.zdb_id: 2034522-7
    SSG: 13
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  • 2
    In: Mineralogical Magazine, Mineralogical Society
    Abstract: The new mineral mazorite, ideally Ba 3 (PO 4 ) 2 , a P-analogue of gurimite Ba 3 (VO 4 ) 2 , was discovered in rankinite paralava hosted by the massive gehlenite-bearing pyrometamorphic rocks of the Hatrurim Complex in Israel. It has also recently been discovered in xenolith samples from the Bellerberg volcano in Germany. Holotype mazorite usually forms colourless plate-like crystals up to 70–100 μm in length but also occurs in small aggregates in association with other rare Ba-bearing minerals such as zadovite, celsian, hexacelsian, bennesherite, sanbornite, walstromite, fresnoite, gurimite, alforsite and barioferrite. The mineral is transparent, exhibits vitreous lustre and has a good cleavage on (001). Optically, mazorite is uniaxial (+), with ω = 1.760(3) and ɛ = 1.766(3) (λ = 589 nm). The empirical formula of the holotype mazorite calculated on 8O is (Ba 2.69 K 0.22 Na 0.04 Ca 0.02 Sr 0.01 ) Σ2.98 (P 1.16 V 0.57 S 0.24 Al 0.04 Si 0.03 ) Σ2.04 O 8 . Mazorite crystallises in space group R $\bar{3}$ m , with unit-cell parameters a = 5.6617(5) Å, c = 21.1696(17) Å, V = 587.68(9) Å 3 and Z = 3. Its crystal structure consists of BaO 12 , BaO 10 , and PO 4 polyhedra, ordered along the c -axis in PO 4 –BaO 10 –BaO 12 –BaO 10 –PO 4 columnar arrangement characteristic for palmierite-supergroup minerals. A tetrahedrally coordinated site is generally occupied by P 5+ but can be partially substituted by V 5+ and S 6+ . This substitution is shown in the Raman spectrum of mazorite, which reveals bands that can be assigned to the stretching and bending vibrations of (PO 4 ) 3– , (VO 4 ) 3– and (SO 4 ) 2– groups. The Raman spectra of mazorite from two localities (Hatrurim and Bellerberg) and spectra of minerals belonging to the mazorite Ba 3 (PO 4 ) 2 to gurimite Ba 3 (VO 4 ) 2 solid-solution series are presented. The gradual shift of the Raman bands, caused by cation substitutions, is well observed. The high V 5+ → P 5+ substitution is also observed for gurimite, for which the first X-ray structural data are also presented. Mazorite and other Ba-bearing minerals crystallised from a small portion of residual melt enriched in incompatible elements, such as Ba, V, P, U, S, Ti and Nb, at a temperature of ~1000°C.
    Type of Medium: Online Resource
    ISSN: 0026-461X , 1471-8022
    RVK:
    Language: English
    Publisher: Mineralogical Society
    Publication Date: 2023
    detail.hit.zdb_id: 2034522-7
    SSG: 13
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  • 3
    In: Mineralogical Magazine, Mineralogical Society, Vol. 79, No. 1 ( 2015-02), p. 103-120
    Abstract: The high-temperature- and moisture-dependent behaviour of synthetic kanemite (NaSi 2 O 4 (OH)·3H 2 O or SKS-10 ) has been studied by in situ powder X-ray diffraction. Heating experiments in the range between ambient temperatures and 250°C confirm earlier investigations that the dehydration of kanemite occurs in two steps. According to our results the two different reactions start at ∼30 and 75°C. The dehydration products have the following compositions: NaSi 2 O 4 (OH)·H 2 O (monohydrate) and NaSi 2 O 4 (OH), respectively. The crystal structures of both phases have been solved at ambient conditions ab initio from laboratory powder diffraction data using samples that have been carefully dehydrated at 60 and 150°C, respectively, and refined subsequently by the Rietveld method. Basic crystallographic data are as follows: NaSi 2 O 4 (OH)·H 2 O: orthorhombic, space group Pna 2 1 , a = 7.2019(1), b = 15.3252(2), c = 4.8869(1) Å, V = 539.37(1) Å 3 , Z = 4; NaSi 2 O 4 (OH): monoclinic, space group P 2 1 , a = 6.3873(1), b = 4.8876(1), c = 7.1936(1) Å, β = 93.36(1)°, V = 224.19(1) Å 3 , Z = 2. Both compounds belong to the group of single-layer silicates based on Si 2 O 4 (OH) sheets. The sodium cations are located between the tetrahedral sheets and are surrounded by oxygen atoms from silicate anions and/or water molecules. Depending on the dehydration step the coordination numbers of the alkali ions vary between six (kanemite) and five (NaSi 2 O 4 (OH)). Kanemite and its two dehydration products show structural similarities which are discussed in detail. Moisture-dependent diffraction studies at ambient temperatures indicate that kanemite is stable between 10% and at least 90% relative humidity. Below the lower threshold a transformation to the monohydrate phase was observed. Dehydration and rehydration as a function of humidity is reversible. However, this process is combined with a significant loss of crystallinity of the samples.
    Type of Medium: Online Resource
    ISSN: 0026-461X , 1471-8022
    RVK:
    Language: English
    Publisher: Mineralogical Society
    Publication Date: 2015
    detail.hit.zdb_id: 2034522-7
    SSG: 13
    Location Call Number Limitation Availability
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