Feasibility of Using Cordierite Glass-Ceramics as Tile Glazes

2005 ◽  
Vol 80 (7) ◽  
pp. 1757-1766 ◽  
Author(s):  
Anna Maria Ferrari ◽  
Luisa Barbieri ◽  
Cristina Leonelli ◽  
Tiziano Manfredini ◽  
Cristina Siligardi ◽  
...  
2020 ◽  
Vol 547 ◽  
pp. 120298 ◽  
Author(s):  
A. Zandona ◽  
B. Rüdinger ◽  
O. Hochrein ◽  
J. Deubener

Author(s):  
Hitoshi Ohsato ◽  
Jeong-Seog Kim ◽  
Ye-Ji Lee ◽  
Chae-Il Cheon ◽  
Ki-Woong Chae ◽  
...  

2014 ◽  
Vol 0 (s6) ◽  
pp. 45-51 ◽  
Author(s):  
A.S. Chanikova ◽  
◽  
M.V. Voropaeva ◽  
L.A. Alexeeva ◽  
L.A. Orlova ◽  
...  

2009 ◽  
Vol 9 (3) ◽  
pp. 1297-1305 ◽  
Author(s):  
Wim Bras ◽  
Simon M. Clark ◽  
G. Neville Greaves ◽  
Martin Kunz ◽  
Wouter van Beek ◽  
...  

2016 ◽  
Vol 881 ◽  
pp. 83-88 ◽  
Author(s):  
Rafael Bianchini Nuernberg ◽  
Oscar Rubem Klegues Montedo

This work aims to investigate the crystallization kinetics of β-spodumene/cordierite glass-ceramics. Thus, three glasses with compositions based predominantly on cordierite (C), β-spodumene (L) and in a molar ratio 1:1 of both phases (CL) were prepared. The kinetics parameters such as activation energy for crystallization (ranging from 160 to 358 kJ/mol) and Avrami exponent (ranging from 1.4 to 10.7) were determined by means of non-isothermal methods using differential scanning calorimetry (DSC). Additionally, the samples were crystalized according to DSC analyses and characterized by using x-ray diffraction (XRD). The main detected crystalline phases were β-spodumene to the glass L, cordierite to the glass C and β-quartz, mulite and spinel to the glass CL. Considering the thermal and electrical properties of these crystalline phases, these glass-ceramics have potential use for LTCC (Low Thermal Co-fired Ceramics) applications.


1991 ◽  
Vol 8 (3) ◽  
pp. 181-185
Author(s):  
Yu.V. Baschenko ◽  
S.M. Barinov ◽  
V.Ya. Shevchenko ◽  
R.Ya. Hodakovskaya

1997 ◽  
Vol 3 (S2) ◽  
pp. 631-632
Author(s):  
Warren J. MoberlyChan ◽  
T. J. Perham ◽  
L. C. DeJonghe

The crystallization of glass ceramics provides processing advantages for difficult shapes. Machining and sintering are limited to produce complex parts; similarly (superplastic) forming is limited to special ceramics. In theory, however, a liquid (or glass) may be simply poured into any shape, and then crystallized (or partially crystallized) to provide a strong, tough ceramic. In this work, a thin layer of glass ceramic, cordierite (2MgO.2Al2O3.5SiO2), joins SiC [1]. Tailoring secondary phases and percent crystallization provide flexible control of the coefficient of thermal expansion to minimize strain mismatches between the joint components.Three processing steps are involved in crystallization of glass ceramics: first a fast quench produces the initial glass; the second step is a lower temperature “nucleation” anneal, where phase separation and/or precursors and/or the final structure is nucleated and ideally as a fine dispersion; the third step is the higher temperature “crystallization” anneal, where renucleation and/or growth develops a homogeneous (ideally fine grained) final crystalline product [2, 3].


1987 ◽  
Vol 2 (6) ◽  
pp. 801-804 ◽  
Author(s):  
D. R. Clarke ◽  
B. Schwartz

The utilization of transformation toughening has hitherto been restricted to increasing the fracture resistance of polycrystalline ceramic materials. Although a number of investigators have attempted to extend the concept to toughening glasses and glass ceramics with tetragonal zirconia, no successful reports have been published. It is argued that the approaches employed are inevitably limited primarily because they do not take into account the necessity of nucleating the tetragonal-to-monoclinic transformation away from the crack tip itself. By concentrating on the nucleation event and using standard ceramic processing techniques, it has been demonstated that transformation toughening can be used to increase the toughness of glass-ceramic materials, and this approach is illustrated by increasing the fracture toughness of a cordierite glass ceramic.


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