Wetting and penetration of cordierite and mullite materials by non-stoichiometric cordierite liquids

被引:13
作者
Camerucci, M. A. [1 ]
Cavalieri, A. L. [1 ]
机构
[1] Univ Nacl Mar del Plata CONICET, Inst Invest Ciencia & Tecnol Mat INTEMA, RA-7600 Mar Del Plata, Argentina
关键词
cordierite; mullite; non-stoichiometric cordierite glass; wetting; penetration;
D O I
10.1016/j.ceramint.2007.06.013
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
The wetting and penetration of two non-stoichiometric cordierite liquids (labelled G1= 25 wt.% Al2O3, 63 wt.% SiO2 and 12 wt.% MgO, and G2 = 20 wt.% Al2O3, 64 wt.% SiO2 and 16 wt.% MgO) on sintered cordierite and mullite substrates were investigated. Their chemical compositions (G1 and G2) correspond to those glasses present in materials sintered from a commercial powder of non-stoichiometric cordierite powder at 1450 or 1400 degrees C, respectively. Sessile drop assemblies for wetting and penetration tests, consisting of cordierite or mullite disks as substrates and pellets of pressed powder glasses positioned above them, were employed. Commercially available cordierite and mullite powders were used to prepare the substrates by uniaxial pressing and sintering at 1450 and 1700 degrees C, 2 h, respectively. The glass pellets were prepared by uniaxial pressing of G1 and G2 glass powders. The assemblies were heating at 25 degrees C/min up to 1450 or 1400 degrees C depending on each glass, soaking at these temperatures for 10, 120 or 360 min and cooling at 25 and 5 degrees C/min down to 1100 degrees C and room temperature, respectively. The contact angles between each glass and both cordierite and mullite substrates according to the temperature, were determined by heating microscopy technique from optical images. Their penetration behavior of both glasses into cordierite or mullite substrates were also studied analyzing by SEM the microstructures of the specimens transversally cut, polished, and chemically etched. (c) 2007 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
引用
收藏
页码:1753 / 1762
页数:10
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