Network connectivity in aluminoborosilicate glasses:: A high-resolution 11B, 27Al and 17O NMR study

被引:216
作者
Du, LS [1 ]
Stebbins, JF [1 ]
机构
[1] Stanford Univ, Dept Geog & Environm Sci, Stanford, CA 94305 USA
基金
美国国家科学基金会;
关键词
D O I
10.1016/j.jnoncrysol.2005.08.033
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
O-17 enriched calcium and potassium aluminoborosilicate glasses with compositions similar (or analogous) to commercial E-glass were made and studied by B-11, Al-27 and O-17 NMR in order to explore the network speciation and mixing. Fractions of non-bridging oxygens associated with silicon and boron can be obtained simply from O-17 magic angle spinning (MAS) NMR, while bridging oxygen populations result from complete peak assignment of high-resolution O-17 triple quantum magic angle spinning (3QMAS) NMR spectra. Dramatic differences between the two samples in boron and oxygen speciation demonstrate a large effect of the charge of the modifier cation on mixing behavior and on the stabilization of non-bridging oxygens. The observed oxygen speciation is compared with that calculated from two models: random mixing of Si, B, and Al, and mixing with avoidance of linkages between tetrahedral aluminum and tetrahedral boron groups. Mixing of B and Al in the K-containing glass tends to follow the latter, while the network speciation in the Ca-containing glass is closer to the random model. The effects of Al and Si on boron speciation are discussed, and indicate that the maximum fractions of four-coordinated boron observed in a wide range of glass compositions are closely related to tetrahedral B and Al 'avoidance'. A modified 'Dell and Bray' model is proposed which seems to accurately approximate boron speciation in many alkali aluminoborosilicate glasses. The higher field strength modifier cation (Ca2+ vs. K+) promotes the formation of non-bridging oxygen, trigonal over tetrahedral boron, and at least minor amounts of five-coordinated aluminum. (c) 2005 Elsevier B.V. All rights reserved.
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收藏
页码:3508 / 3520
页数:13
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