Effects of heat treatment on red gemstone spinel: single-crystal X-ray, Raman, and photoluminescence study

被引:21
|
作者
Widmer, Remo [1 ]
Malsy, Anna-Kathrin [2 ]
Armbruster, Thomas [1 ]
机构
[1] Univ Bern, Inst Geol Sci, Mineral Crystallog, CH-3012 Bern, Switzerland
[2] Gubelin Gem Lab Ltd, CH-6006 Luzern, Switzerland
关键词
Spinel; MgAl2O4; Gemstone; Heat treatment; Mg-Al order-disorder; Single-crystal X-ray; Raman spectroscopy; Photoluminescence spectroscopy; ORDER-DISORDER TRANSITION; MGAL2O4; SPINEL; LUMINESCENCE SPECTRA; N-LINES; DISPLACEMENT PARAMETERS; CATION; TEMPERATURE; KINETICS; DIFFRACTION; CHEMISTRY;
D O I
10.1007/s00269-014-0716-7
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A red spinel, MgAl2O4, from Burma (Myanmar) containing as chromophores ca. 0.5 wt% of each Cr2O3 and V2O3, was sequentially heated for at least 72 h at temperatures ranging from 600 A degrees C to 1,100 A degrees C. The untreated and quenched samples were examined with single-crystal X-ray diffraction (XRD), Raman spectroscopy and photoluminescence spectroscopy. XRD results display a linear decrease of the cell parameter a and a continuous shift of the oxygen coordinate u, u, u at 3 m toward lower values with increasing temperature and associated Mg, Al disorder: (T)(Mg1-x Al (x) )(M)(Al2-x Mg (x) )O-4. The natural spinel has x = 0.157(2) and reaches x = 0.286(4) after quenching from 1,100 A degrees C. In its natural state, M-O and T-O distances are 1.9226(2) and 1.9361(4) . With increasing inversion of Mg from the tetrahedrally coordinated T to the octahedrally coordinated M site, M-O distances increase at 1,100 A degrees C to 1.9333(4) and T-O distances decrease to 1.9130(8) . The crossover temperature, at which T-O and M-O distances become equal (i.e., 1.927 ), is found to be at 650 A degrees C and corresponds to an inversion parameter x = 0.208(3). With increasing heat treatment, Raman spectra of quenched samples become significantly broadened and a peak characteristic for Mg, Al disorder at 721 cm(-1) firstly appears for a crystal quenched from 800 A degrees C with x = 0.248(4). At room temperature, photoluminescence spectra are dominated by a strong R line at 684.5 nm accompanied by poorly resolved N lines: N1 (687 nm), N2 (688 nm), and N3 (689 nm). N lines are caused by different Mg, Al environments of Cr3+. With increasing inversion parameter (x), the R line decreases in intensity and the N lines become prominent leading to strongly broadened peaks with a maximum shifted toward higher wave lengths (687.5 nm at 1,100 A degrees C). Criteria for the detection of heat treatment on gemstone spinel applicable to gemological routine examination are provided. Extrapolation of u, a, and bond lengths from heat-treated Burma spinel toward the natural crystal suggests a retrograde "closing temperature" of ca. 400 +/- A 100 A degrees C at which Mg, Al disorder was frozen.
引用
收藏
页码:251 / 260
页数:10
相关论文
共 50 条
  • [21] The dynamic properties of zircon studied by single-crystal X-ray diffraction and Raman spectroscopy
    Kolesov, BA
    Geiger, CA
    Armbruster, T
    EUROPEAN JOURNAL OF MINERALOGY, 2001, 13 (05) : 939 - 948
  • [22] A low temperature X-ray single-crystal diffraction and polarised infra-red study of epidote
    G. Diego Gatta
    Matteo Alvaro
    Geoffrey Bromiley
    Physics and Chemistry of Minerals, 2012, 39 : 1 - 15
  • [23] POLYIODIDES OF TRIETHYLENEDIAMINE - SINGLE-CRYSTAL RESONANCE RAMAN-SPECTRA AND X-RAY STRUCTURES
    BANDRAUK, AD
    TRUONG, KD
    CARLONE, C
    HANSON, AW
    JOURNAL OF PHYSICAL CHEMISTRY, 1987, 91 (08): : 2063 - 2069
  • [24] Average structures of the disordered β-phase of Pigment Red 170: a single-crystal X-ray diffraction study
    Warshamanage, Rangana
    Linden, Anthony
    Schmidt, Martin U.
    Buergi, Hans-Beat
    ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE CRYSTAL ENGINEERING AND MATERIALS, 2014, 70 : 283 - 295
  • [25] X-ray diffraction II: Using single-crystal X-ray diffraction to study polymorphism and solvatomorphism
    Brittain, HG
    SPECTROSCOPY, 2000, 15 (07) : 34 - 39
  • [26] NEUTRON AND X-RAY SINGLE-CRYSTAL STUDY OF THE ALPDMN ICOSAHEDRAL PHASE
    BOUDARD, M
    DEBOISSIEU, M
    JANOT, C
    HEGER, G
    BEELI, C
    NISSEN, HU
    VINCENT, H
    IBBERSON, R
    AUDIER, M
    DUBOIS, JM
    JOURNAL OF PHYSICS-CONDENSED MATTER, 1992, 4 (50) : 10149 - 10168
  • [27] SINGLE-CRYSTAL X-RAY DIFFRACTION STUDY OF BETA-FLUORINE
    JORDAN, TH
    STREIB, WE
    LIPSCOMB, WN
    JOURNAL OF CHEMICAL PHYSICS, 1964, 41 (03): : 760 - +
  • [28] HIGH-TEMPERATURE, SINGLE-CRYSTAL X-RAY STUDY OF NATROLITE
    PEACOR, DR
    AMERICAN MINERALOGIST, 1973, 58 (7-8) : 676 - 680
  • [29] Study of the single-crystal X-ray diffuse scattering in paracetamol polymorphs
    Chan, E. J.
    Goossens, D. J.
    ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE CRYSTAL ENGINEERING AND MATERIALS, 2012, 68 : 80 - 88
  • [30] A SINGLE-CRYSTAL X-RAY STUDY OF ORDER IN BETA-AGCD
    WALKER, CB
    MAREZIO, M
    JOURNAL OF APPLIED PHYSICS, 1963, 34 (05) : 1443 - &