Abstract

In several series of lithium, sodium, and potassium borosilicate glasses whose compositions traverse known regions of liquid–liquid phase separation, we have applied triple-quantum magic-angle spinning (3QMAS) 11B and 17O NMR to obtain high-resolution information about short-range structure and connections among various network structural units, and their variation with composition and thermal history. Oxygen-17 3QMAS spectra reveal changes in connectivities between silicate and BO 3 ( [3]B) and BO 4 ( [4]B) units, by quantifying populations of bridging oxygens such as B–O–B, Si–O–B and Si–O–Si, and of non-bridging oxygens. [3]B–O–Si and [4]B–O–Si as well as [3]B–O– [3]B and [4]B–O– [3]B linkages can be distinguished. 11B MAS and 3QMAS at a magnetic field of 14.1 T allow proportions of several borate units to be determined, including [3]B in boroxol ring and non-ring sites and [4]B with 3 versus 4 Si neighbors. By combining the 11B and 17O NMR results, detailed information on Si/B mixing in sodium borosilicates can be derived, showing, for example, that [4]B and non-ring [3]B tend to mix with silicate units, while ring [3]B is mainly connected to borate groups. In a preliminary study of the effects of varying alkali cation, potassium-containing glasses are similar to those in the sodium borosilicate system, but a lithium borosilicate seems to exhibit considerably greater chemical heterogeneity. In annealing experiments that converted an optically clear to obviously phase-separated glasses, the ratio of [3]B to [4]B does not change significantly, but part of the non-ring [3]B converts to ring [3]B as the degree of unmixing increases.

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