Melting, crystallization, and the glass transition; toward a unified description for silicate phase transitions

The melting mechanism of Na (sub 2) SiO (sub 3) , a crystal with pyroxene structure, includes three distinct reactions. All are driven by heating with each reaction commencing at a different temperature. The first two reactions proceed within the crystal at temperatures well below the melting point and are expressed by distinctive crystallographic, calorimetric, and Raman spectroscopic changes to the crystal. With the reactions identified and explained for Na (sub 2) SiO (sub 3) (c) and the melting mechanism elucidated, the Na (sub 2) SiO (sub 3) system becomes the "Rosetta Stone" by which to decipher the melting mechanisms of all pyroxenes and other silicate minerals. The first reaction produces itinerant Na (super +) within the crystal. Itinerancy results from dissociation of some NBO-Na bonds due to heating, with dissociation commencing at approximately 770 K. The reaction proceeds according to: Si-O-Na --> Si-O (super -) + Na (super +) . The Si-O (super -) moiety remains attached to its SiO (sub 3) chain and it is charged because one of its NBO atoms has no associated Na ion. The second reaction is characterized by the appearance of a Q (super 3) band in Raman spectra of the crystal at temperatures >770 K. It is produced via a polymerization reaction involving the Si-O (super -) species, a product of the first reaction, and a Q (super 2) species of an adjacent SiO (sub 3) chain according to: 1Na (sub 2) -Q (super 2) + 1(Na (sub 1) -Q (super 2) ) (super -) --> 2Na (sub 1) -Q (super 3) + Na (super +) + O (super 2-) . Na atoms are included with each Q species to preserve mass balances and (Na (sub 1) -Q (super 2) ) (super -) is equivalent to the Si-O (super -) species. The produced Q (super 3) species form cross-chain linkages that affect the crystallographic properties of the crystal. They are responsible for the cessation of thermal expansion of the Na (sub 2) SiO (sub 3) unit cell in the A: - B: axial plane at T >770 K, and the near-constancy of a and b unit-cell parameters between approximately 770 and approximately 1300 K. The presence of Q (super 3) species in Raman spectra and the inhibited expansion in the A: - B: axial plane provide exceedingly strong evidence for this reaction. The third reaction commences at approximately 1200 K where Q (super 1) Raman band first appears. It can be produced only through depolymerization of Q (super 2) chains according to: 2Na (sub 2) -Q (super 2) + 2Na (super +) + O (super 2-) --> 2Na (sub a3) -Q (super 1) where Na (super +) and O (super 2-) are itinerant species produced by the second reaction. With conversion of Q (super 2) to Q (super 1) species, SiO (sub 3) chains are ruptured, long-range order is lost, and melt is produced at 1362 K. The last two reactions proceed by nucleophilic substitution where Si centers are attacked to form fivefold-coordinated activated complexes. Si-O (super -) acts as nucleophile in the second reaction (producing Q (super 3) species), and O (super 2-) acts as nucleophile in the third reaction (producing Q (super 1) ). Taken in reverse, these mechanisms describe the formation of nuclei in crystallizing melts and in addition provide insight into the elusive changes that occur at the glass transition. Elucidation of the melting mechanism could thus provides a unified framework within which melting, crystallization, and the glass transition can be understood.