L. Barbieri et al., COLORING INORGANIC OXIDES IN MGO-CAO-AL2O3-SIO2 GLASS-CERAMIC SYSTEMS, Journal of non-crystalline solids, 155(3), 1993, pp. 231-244
Glasses in the system MgO-CaO-Al2O3-SiO2, in which CuO, Fe2O3 and MnO
were substituted for CaO, were prepared and crystallized in absence of
nucleating agents. Surface nucleation dominated for all compositions,
and was followed by growth of only anorthite and diopside. The relati
ve amount of each crystal was influenced by the chemical composition a
nd the nature of the transition metal cation. Cu and Mn segregated at
the grain boundary during crystallization and Fe did not. Changes in t
he coordination symmetry and oxidation states of the transition metal
ions in the glassy and glass-ceramic phases are as follows: Cu(II) is
sixfold coordinated with regularly octahedral symmetry in glass and di
storted in glass-ceramic, while the ratio Cu(II)/Cu(I) is decreased fr
om 5 to 2 during crystallization. Fe(III) is fourfold coordinated with
a symmetry C2v and Fe(II) is present, more in the glass-ceramic than
in the glass, with an octahedral symmetry. Mn(II) is in cubic site sym
metry with a rhombic distortion, more visible in the glass; Mn(III) is
sixfold coordinated with octahedral symmetry in a constant ratio (Mn(
III): Mn(II) is 2:1) during crystallization.