Temperature-induced boron coordination change in alkali borate glasses and melts -: art. no. 024210

被引:98
作者
Majérus, O
Cormier, L
Calas, G
Beuneu, B
机构
[1] Univ Paris 06, Inst Phys Globe, Lab Mineral Cristallog Paris, CNRS,UMR 7590, F-75252 Paris 05, France
[2] Univ Paris 07, Inst Phys Globe, Lab Mineral Cristallog Paris, CNRS,UMR 7590, F-75252 Paris 05, France
[3] Ctr Etud Saclay, Lab Leon Brillouin, F-91191 Gif Sur Yvette, France
关键词
D O I
10.1103/PhysRevB.67.024210
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Neutron diffraction experiments have been performed on alkali diborate glasses and melts, M2O-2B(2)O(3) with M=Li, Na, K, in order to investigate the structural changes above the glass transition. In the glassy state, the contributions of fourfold- and threefold-coordinated boron could be clearly distinguished on the first peak of the correlation functions, which has been fitted with two Gaussian components. The fraction of boron in fourfold coordination (N-4) is 0.46, 0.43, and 0.40 for the Li-, Na-, and K-bearing glasses, respectively, in agreement with previous NMR studies. In the liquid state at similar to1200 K, a one-component fit of the peak yields an N-4 value of about 0.30, which means that one-third of the BO4 tetrahedra in the glass converts to BO3 triangles in the melt. The estimated change of the mean heat capacity for this conversion is in the range 27-73 J mol(-1)K(-1). This value accounts for the major part of the total heat capacity change at T-g, suggesting that the BO4 to BO3 conversion is mainly responsible for the fragile behavior of the viscosity of alkali borate melts. Indeed it is closely related to the dynamic processes of the viscous flow, which involve both the akali migration and B-O bond breakening and reforming.
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