Dehydration of Ca3Al2(SiO4)y(OH)4(3-y) (0<y<0.176) studied by neutron thermodiffractometry

被引:40
作者
Rivas-Mercury, J. M. [2 ]
Pena, P. [1 ]
de Aza, A. H. [1 ]
Turrillas, X. [3 ,4 ]
机构
[1] CSIC, Inst Ceram & Vidrio, E-28049 Madrid, Spain
[2] Ctr Fed Educao Tecnol Maranhao, BR-65025001 Sao Luis, MA, Brazil
[3] CSIC, E Torroja Inst Construct Sci IETcc, Madrid 28033, Spain
[4] European Synchrotron Radiat Facil, F-38043 Grenoble, France
关键词
thermal treatment; neutron powder diffraction; X-ray methods; thermal expansion; calcium aluminates; refractories;
D O I
10.1016/j.jeurceramsoc.2007.12.038
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
Hydrogarnet (Ca12Al2(OH)(12)) and katoite of composition Ca3Al2(SiO4)(0.176)(OH)(11.3) were obtained by hydration of tricalcium aluminium oxide, and for katoite synthesis, by addition of amorphous silica. The thermal dehydration was monitored in situ, by neutron thermodiffractometry, from room temperature to 700 degrees C at atmospheric pressure and at a heating rate of 2 degrees C/min. On heating, powder neutron diffraction patterns were collected every 300 s. Cell parameters were fitted by the Pawley method. Hydrogarnet decomposed to yield Ca12Al14O32 (OH)-mH(2)O and Ca(OH)(2) that eventually transformed to CaO. For katoite, phases of formula Ca12Al14-ySiyO32(O,OH)(1+y/2) related to mayenite were formed. Complementary annealing experiments, for 10 h, at higher temperatures and subsequent quenching lead to the formation of mayenite and traces of Ca3SiO5. Thermogravimetric curves were in agreement with the thermodiffractometry experiments. Also, neutron diffraction data allowed to measure thermal expansion coefficients, at atmospheric pressure, between 25 and 250 degrees C for hydrogarnet and katoite: 1.89 x 10(-5) +/- 0.09 and 1.63 x 10(-5) +/- 0.07 degrees C-1, respectively. (C) 2008 Published by Elsevier Ltd.
引用
收藏
页码:1737 / 1748
页数:12
相关论文
共 23 条
  • [1] *ACC RYS M, 2005, ACC MAT STUD V 4 0
  • [2] THE MULLITE-CORUNDUM BOUNDARY IN THE SYSTEMS MGO-AL2O3-SIO2 AND CAO-AL2O3-SIO2
    ARAMAKI, S
    ROY, R
    [J]. JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 1959, 42 (12) : 644 - 645
  • [3] BARTL H, 1970, NEUES JB MINER MONAT, P547
  • [4] PowderSolve -: a complete package for crystal structure solution from powder diffraction patterns
    Engel, GE
    Wilke, S
    König, O
    Harris, KDM
    Leusen, FJJ
    [J]. JOURNAL OF APPLIED CRYSTALLOGRAPHY, 1999, 32 : 1169 - 1179
  • [5] CHLOROSILICATE WITH THE 12CAO.7AL2O3 STRUCTURE AND ITS RELATIONSHIP TO GARNET
    FENG, QL
    GLASSER, FP
    ALANHOWIE, R
    LACHOWSKI, EE
    [J]. ACTA CRYSTALLOGRAPHICA SECTION C-CRYSTAL STRUCTURE COMMUNICATIONS, 1988, 44 : 589 - 592
  • [6] Controlling the quantity of radical oxygen occluded in a new aluminum silicate with nanopores
    Fujita, S
    Ohkawa, M
    Suzuki, K
    Nakano, H
    Mori, T
    Masuda, H
    [J]. CHEMISTRY OF MATERIALS, 2003, 15 (26) : 4879 - 4881
  • [7] Oxidative destruction of hydrocarbons on a new zeolite-like crystal of Ca12Al10Si4O35 including O2- and O22- radicals
    Fujita, S
    Suzuki, K
    Ohkawa, M
    Mori, T
    Iida, Y
    Miwa, Y
    Masuda, H
    Shimada, S
    [J]. CHEMISTRY OF MATERIALS, 2003, 15 (01) : 255 - 263
  • [8] Reaction of hydrogrossular with hydrogen chloride gas at high temperature
    Fujita, S
    Suzuki, K
    Ohkawa, M
    Shibasaki, Y
    Mori, T
    [J]. CHEMISTRY OF MATERIALS, 2001, 13 (08) : 2523 - 2527
  • [9] OCCURRENCE OF SUPEROXIDE RADICAL ION IN CRYSTALLINE 12CAO.7AL2O3 PREPARED VIA SOLID-STATE REACTIONS
    HOSONO, H
    ABE, Y
    [J]. INORGANIC CHEMISTRY, 1987, 26 (08) : 1192 - 1195
  • [10] Larger G. A., 1987, AM MINERAL, V72, P756