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Structure Transition in Alkali Silicate Glasses
Author(s) -
LACY E. D.
Publication year - 1968
Publication title -
journal of the american ceramic society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.9
H-Index - 196
eISSN - 1551-2916
pISSN - 0002-7820
DOI - 10.1111/j.1151-2916.1968.tb11858.x
Subject(s) - silicate , thermal expansion , ion , chemical physics , coordination number , glass transition , alkali metal , materials science , transformation (genetics) , configuration entropy , thermodynamics , chemistry , physics , polymer , composite material , biochemistry , organic chemistry , gene
The logarithm of measured high‐temperature fluidities is related to the square of the calculated probability of finding a nonbridging oxygen in a randomly chosen SO4 group. This is interpreted in terms of a flow mechanism (gliding) dependent on juxtaposition of two such oxygens. A theory of the glass transformation is developed. On cooling, the coordination number of nonbridging oxygens increases until, ideally, at T , each touches three oxygens of an external Si04 group (stabilization). Below this temperature, thermal expansion/contraction contains no coordination change component. These changes constitute a second‐order transition. Observed volume data are in agreement with hypothesis. On this view, stabilization creates vacant tetrahedral environments adjacent to existing ones. Migration of glass‐forming ions to these empty sites can unlock the structure and permit the operation of a new set of flow processes. The coordination requirements for stabilization severely restrict the types of local arrangement possible at high silica contents, and therefore reduce the configurational entropy and induce unmixing. The overall transformation is composite in character. Rather extensive bond rearrangement and unmixing (when present) are features of first‐order kind.