Cayalsite-(Y), a new rare-earth calcium aluminium fluorosilicate with OD character
- 1. Hamburg Univ. (Germany). Mineralogisch-Petrographisches Inst.
- 2. Hamburg Univ. (Germany). CeNak - Mineralogisches Museum
- 3. Manitoba Univ., Winnipeg, MB (Canada). Dept. of Geological Sciences
- 4. Veslefrikk, Bodoe (Norway)
Description
The crystal structure of cayalsite-(Y), with idealized composition CaY6Al2Si4O18F6, has been determined on the basis of singlecrystal X-ray diffraction data. The mineral occurs in several polytypic modifications arising from the combination of three non-equivalent structural layers. Two maximum degree of order (MDO) polytypes have been identified in cayalsite-(Y). The orthorhombic MDO polytype, cayalsite-(Y)-1O, has lattice parameters a = 15.993(1), b = 5.5306(3) and c = 9.6590(7) Aa. It is described in space group symmetry Pban and refines to Robs = 2.2%. The monoclinic MDO polytype, cayalsite-(Y)-1M, a = 11.0602(7), b = 5.5280(2), c = 16.0195(9) Aa, β = 118.925(3) is described in space group symmetry P2/c and refines to Robs = 3.5% in a two-phase mixture with cayalsite-(Y)-1O. Predominantly heavy lanthanide elements substitute for Y and Ca in cayalsite-(Y), with some Ca also substituting for the rare-earth elements (REE). A typical empirical composition, normalized to 24 anions, is Ca1.03(Y4.73Nd0.02Gd0.34Dy0.43Er0.31Yb0.22)Σ6.05Al1.87Si4.03(F6.08O17.92) Σ24. Cayalsite-(Y) forms colourless to faintly pink, prismatic crystals in cavities of yttrian fluorite in two granitic pegmatites located in Tysfjord, Nordland, Norway. Cayalsite-(Y)-1O crystals are optically biaxial (+), with indices of refraction α = 1.730(5), β = 1.740(5), γ = 1.760(5) and 2Vmeas = 56.5(5). The crystal structure of cayalsite-(Y) is composed of linear chains of edge sharing [AlO6] octahedra with isolated [SiO4] tetrahedra. The REE and Ca-cations occur in eight-fold coordination by O and F anions. Apart from substitutional disorder of REE and Ca atoms, the cayalsite structure is characterized by substitutional and positional disorder affecting the local position of [SiO4] tetrahedra in one of its layers. Avoidance of close Si-F contacts causes the partial splitting of O and F positions. The possible interplay of layer stacking and cation ordering is discussed.
Availability note (English)
Available from: http://dx.doi.org/10.1127/ejm/2015/0027-2465Additional details
Identifiers
Publishing Information
- Journal Title
- European Journal of Mineralogy
- Journal Volume
- 27
- Journal Issue
- 5
- Journal Page Range
- p. 683-694
- ISSN
- 0935-1221
- CODEN
- EJMIER
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- Germany
- INIS RN
- 48044271
- Subject category
- S36: MATERIALS SCIENCE;
- Descriptors DEI
- ALUMINIUM COMPOUNDS; CALCIUM COMPOUNDS; CRYSTAL STRUCTURE; DYSPROSIUM COMPOUNDS; ERBIUM COMPOUNDS; GADOLINIUM COMPOUNDS; LATTICE PARAMETERS; MINERALS; NEODYMIUM COMPOUNDS; NORWAY; OXYFLUORIDES; PEGMATITES; SILICATES; X-RAY DIFFRACTION; YTTERBIUM COMPOUNDS; YTTRIUM COMPOUNDS
- Descriptors DEC
- ALKALINE EARTH METAL COMPOUNDS; COHERENT SCATTERING; DEVELOPED COUNTRIES; DIFFRACTION; EUROPE; FLUORINE COMPOUNDS; HALOGEN COMPOUNDS; IGNEOUS ROCKS; OXYGEN COMPOUNDS; OXYHALIDES; PLUTONIC ROCKS; RARE EARTH COMPOUNDS; ROCKS; SCANDINAVIA; SCATTERING; SILICON COMPOUNDS; TRANSITION ELEMENT COMPOUNDS; WESTERN EUROPE