TREMBATHITE, (MG,FE)3B7O13CL A NEW BORATE MINERAL FROM THE SALT SPRINGS POTASH DEPOSIT, SUSSEX, NEW-BRUNSWICK

被引:0
|
作者
BURNS, PC [1 ]
HAWTHORNE, FC [1 ]
STIRLING, JAR [1 ]
机构
[1] GEOL SURVEY CANADA,OTTAWA K1A 0E8,ONTARIO,CANADA
来源
CANADIAN MINERALOGIST | 1992年 / 30卷
关键词
TREMBATHITE; BORATE; NEW MINERAL SPECIES; PROPERTIES; X-RAY DATA; CHEMICAL COMPOSITION; SUSSEX; NEW-BRUNSWICK;
D O I
暂无
中图分类号
P57 [矿物学];
学科分类号
070901 ;
摘要
The new mineral species trembathite, ideally (Mg,Fe)3B7O13Cl, from the Salt Springs potash deposit, Sussex, New Brunswick, is the Mg-analogue of congolite and the rhombohedral dimorph of boracite. The mineral occurs as rhombohedra seldom exceeding 2 mm in maximum diameter. Trembathite is associated with halite, hilgardite and clay minerals. It is transparent, colorless to light blue with a vitreous luster and a white streak, it shows no cleavage, and has a conchoidal fracture and a Mohs hardness estimated at 6-8. The measured densities range from 2.84 to 3.34 g/cm 3; the calculated density is 3.14 g/cm 3. Macroscopic twinning was not observed in trembathite, but an optical examination indicates that the crystals are polysynthetically twinned. Trembathite is uniaxial negative, omega-1.684(2), epsilon-1.668(2), and is not pleochroic. It is hexagonal, space group R3c, with a 8.574(2), c 20.99(1) angstrom, V 1336.6(6) angstrom3 and Z = 6. The strongest six lines of the X-ray powder-diffraction pattern [diffractometer; d in angstrom(I)(hkl)] are: 3.497(34)(202,006), 3.028(100)(024), 2.711(66)(122,116), 2.144(37)(220,208), 2.050(73)(131,223,217,119), 1.828(25) (042,226). The electron-microprobe composition based on 0 + Cl = 14 is (Mg2.29Fe0.79 Mn0.03)SIGMA-3.11B6.89012.90Cl1.10. The name honors Lowell T. Trembath, professor at the University of New Brunswick.
引用
收藏
页码:445 / 448
页数:4
相关论文
共 50 条
  • [1] A BORATE MINERAL ASSEMBLAGE FROM THE PENOBSQUIS AND SALT SPRINGS EVAPORITE DEPOSITS OF SOUTHERN NEW BRUNSWICK
    Roulston, B. V.
    Waugh, D. C. E.
    CANADIAN MINERALOGIST, 1981, 19 : 291 - 301
  • [2] PRINGLEITE AND RUITENBERGITE, POLYMORPHS OF CA9B26O34(OH)24CL4.13H2O, 2 NEW MINERAL SPECIES FROM SUSSEX, NEW-BRUNSWICK
    ROBERTS, AC
    STIRLING, JAR
    GRICE, JD
    BURNS, PC
    ROULSTON, BV
    CURTIS, JD
    JAMBOR, JL
    CANADIAN MINERALOGIST, 1993, 31 : 795 - 800
  • [3] Assessment of the molecular structure of the borate mineral boracite Mg3B7O13Cl using vibrational spectroscopy
    Frost, Ray L.
    Xi, Yunfei
    Scholz, Ricardo
    SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 2012, 96 : 946 - 951
  • [4] Boracite Mg3[B7O13Cl] from the Zechstein salt deposits
    Heide, Klaus
    Nolze, Gert
    Voelksch, Guenter
    Heide, Gerhard
    ZEITSCHRIFT FUR KRISTALLOGRAPHIE-CRYSTALLINE MATERIALS, 2013, 228 (09): : 467 - 475
  • [5] The crystal structure of trembathite, (Mg1.55Fe1.43Mn0.02)B7O13Cl, a mineral of the boracite group:: An example of the insertion of a cluster into a three-dimensional net
    Schindler, M
    Hawthorne, FC
    CANADIAN MINERALOGIST, 1998, 36 : 1195 - 1201
  • [6] KARLITE, MG7(BO3)3(OH,CL)5 A NEW BORATE MINERAL AND ASSOCIATED LUDWIGITE FROM THE EASTERN ALPS
    FRANZ, G
    ACKERMAND, D
    KOCH, E
    AMERICAN MINERALOGIST, 1981, 66 (7-8) : 872 - 877
  • [7] Mg3B7O13Cl: A New Quasi-Phase Matching Crystal in the Deep-Ultraviolet Region
    Wang, Zujian
    Qiao, Huimin
    Su, Rongbing
    Hu, Bing
    Yang, Xiaoming
    He, Chao
    Long, Xifa
    ADVANCED FUNCTIONAL MATERIALS, 2018, 28 (41)
  • [8] Mossbauer spectroscopy of the new iron oxide Fe3B7O13(OH)
    Nakamura, Shin
    Tsunoda, Yorihiko
    Nomoto, Ippei
    Sato, Hirohiko
    HYPERFINE INTERACTIONS, 2010, 197 (1-3): : 101 - 104
  • [9] Mössbauer spectroscopy of the new iron oxide Fe3B7O13(OH)
    Nakamura, Shin
    Tsunoda, Yorihiko
    Nomoto, Ippei
    Sato, Hirohiko
    Hyperfine Interactions, 2010, 197 (01): : 101 - 104
  • [10] Mössbauer spectroscopy of the new iron oxide Fe3B7O13(OH)
    Shin Nakamura
    Yorihiko Tsunoda
    Ippei Nomoto
    Hirohiko Sato
    Hyperfine Interactions, 2010, 197 : 101 - 104