Crystallization study of (TiO2, ZrO2)-rich SiO2-Al2O3-CaO glasses. Part II Surface and internal crystallization processes investigated by differential thermal analysis (DTA)

Abstract

Controlled crystallization of (TiO2-ZrO2)-rich calcium aluminosilicate glasses led to zirconolite in the bulk, and titanite and anorthite on the surface. Such glass-ceramics can be envisaged for minor actinides immobilization. In this study, the crystallization of three glass compositions with increasing TiO2, ZrO2 and CaO amounts was followed by differential thermal analysis (DTA). The effect of glass particle size and of heating rate on DTA curves was studied in order to investigate nucleation mechanisms and to extract the corresponding crystal growth activation energies Ec for the different crystalline phases. Exothermic effects associated with the crystallization of a phase having a defect-fluorite structure in the bulk and its consecutive transformation into zirconolite were only detected for the highly TiO2, ZrO2 and CaO enriched glasses due to their higher crystallization rate. Using an Avrami constant n = 3 and a dimensionality of crystal growth m = 3, the activation energy of defect-fluorite crystal growth was found to be Ec = 440 kJ · mol−1 (modified Kissinger method). Titanite and anorthite grow only from glass surface with activation energies of respectively 493 and 405 kJ · mol−1 (n = m = 1, Kissinger method). DTA study of melt crystallization during cooling showed that baddeleyite (ZrO2) crystals firstly crystallize but become unstable versus zirconolite for higher undercooling.