Structural and Crystal Chemical Investigation of Intermediate Phases in the System Ca2SiO4-Ca3(PO4)2-CaNaPO4

被引:15
|
作者
Widmer, Remo [1 ]
Gfeller, Frank [1 ]
Armbruster, Thomas [1 ]
机构
[1] Univ Bern, Inst Geol Sci, Mineral Crystallog, CH-3012 Bern, Switzerland
关键词
POWDER DIFFRACTION DATA; STRUCTURE REFINEMENTS; HIGH-TEMPERATURE; CA3(PO4)2-CANAPO4; TRANSITIONS; POLYMORPHS;
D O I
10.1111/jace.13850
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Two intermediate compounds of the system Ca2SiO4-Ca-3(PO4)(2)-CaNaPO4 were synthesized by reaction sintering at 1600 degrees C and analyzed structurally, chemically, and optically. The structure of Ca-7(PO4)(2)(SiO4)(2) nagelschmidtite (space group P6(1), a = 10.7754(1) angstrom, c = 21.4166(3) angstrom) was determined by single crystal X-ray analysis. Its unit cell can be interpreted as a supercell (approximate to 2 x a, 3 x c) of the high-temperature polymorph alpha-Ca2SiO4. Evidence for pseudo-hexagonal symmetry is shown. Using electron microprobe, the solid solution Ca7 - xNax(PO4)(2)+ x(SiO4)(2 - x), (x <= 2), of nagelschmidtite was confirmed. Volume thermal expansion coefficients of Ca6.8Na0.2(PO4)(2.2)(SiO4)(1.8) and Ca5.4Na1.5(PO4)(3.7)(SiO4)(0.3) were determined using high-temperature X-ray powder diffraction, yielding mean alpha(V) = 3.95 and 5.21 [x10 (5)/degrees C], respectively. Ca-15(PO4)(2)(SiO4)(6) is a distinct phase in the binary section Ca2SiO4-Ca-3(PO4)(2) and was found to extend into the ternary space according to Ca15 - xNax(PO4)(2 + x)(SiO4)(6 - x), (x <= 0.1). Quenching experiments of the latter allowed for structural analysis of a strongly disordered, defective high-temperature polymorph of the alpha-Ca2SiO4-alpha-Ca-3(PO4)(2) solid solution. Structural relations between nagelschmidtite, Ca-15(PO4)(2)(SiO4)(6) and the end-member compounds of the system are discussed.
引用
收藏
页码:3956 / 3965
页数:10
相关论文
共 50 条
  • [1] HYDRATION IN THE SYSTEM CA2SIO4-CA3(PO4)2 AT 90-DEGREES-C
    BARNES, MW
    KLIMKIEWICZ, M
    BROWN, PW
    JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 1992, 75 (06) : 1423 - 1429
  • [2] Synthesis and stability of α-tricalcium phosphate doped with dicalcium silicate in the system Ca3(PO4)2-Ca2SiO4
    Martinez, I. M.
    Velasquez, P. A.
    De Aza, P. N.
    MATERIALS CHARACTERIZATION, 2010, 61 (07) : 761 - 767
  • [3] Single-phase silicocarnotite synthesis in the subsystem Ca3(PO4)2-Ca2SiO4
    Serena, S.
    Sainz, M. A.
    Caballero, A.
    CERAMICS INTERNATIONAL, 2014, 40 (06) : 8245 - 8252
  • [4] Thermodynamic investigation on β- and γ-Ca3(PO4)2 and the phase equilibria
    Zhai, Shuangmeng
    Akaogi, Masaki
    Kojitani, Hiroshi
    Xue, Weihong
    Ito, Eiji
    PHYSICS OF THE EARTH AND PLANETARY INTERIORS, 2014, 228 : 144 - 149
  • [5] Equation of state of γ-tricalcium phosphate, γ-Ca3(PO4)2, to lower mantle pressures
    Zhai, Shuangmeng
    Liu, Xi
    Shieh, Sean R.
    Zhang, Lifei
    Ito, Eiji
    AMERICAN MINERALOGIST, 2009, 94 (10) : 1388 - 1391
  • [6] Raman spectra of Sr3(PO4)2 and Ba3(PO4)2 orthophosphates at various temperatures
    Zhai, Shuangmeng
    Lin, Chung-Cherng
    Xue, Weihong
    VIBRATIONAL SPECTROSCOPY, 2014, 70 : 6 - 11
  • [7] Synthesis and characterization of strontium-calcium phosphate γ-Ca3-xSrx(PO4)2 (0 ≤ x ≤ 2)
    Zhai, Shuangmeng
    Kanzaki, Masami
    Katsura, Tomoo
    Ito, Eiji
    MATERIALS CHEMISTRY AND PHYSICS, 2010, 120 (2-3) : 348 - 350
  • [8] High-pressure Raman spectra of Sr-substituted γ-Ca3-xSrx(PO4)2
    Xue, Weihong
    Liu, Ang
    Song, Yang
    Zhai, Shuangmeng
    HIGH PRESSURE RESEARCH, 2012, 32 (02) : 213 - 219
  • [9] Activators lattice migration strategy customized for tunable luminescence of Ce3+ doped β-Ca3(PO4)2
    Pan, Xin
    Mei, Lefu
    Wang, Yuhua
    Seto, Takatoshi
    Zhuang, Yixi
    Guo, Qingfeng
    Plyaskin, Mikhail
    Xi, Wei
    Li, Chao
    Guo, YueShuai
    Liao, Libing
    CHEMICAL ENGINEERING JOURNAL, 2022, 446
  • [10] Crystal structure of larnite β-Ca2SiO4 and specific features of polymorphic transitions in dicalcium orthosilicate
    Yamnova, N. A.
    Zubkova, N. V.
    Eremin, N. N.
    Zadov, A. E.
    Gazeev, V. M.
    CRYSTALLOGRAPHY REPORTS, 2011, 56 (02) : 210 - 220