Article ID: 25120
The purpose of this work is to clarify the transformation mechanism from hexacelsian to celsian and the thermal expansion properties of celsian solid solutions (Ba1−xSrxAl2Si2O8, x = 0–1.0) using high-temperature powder X-ray diffraction and dilatometry of sintered polycrystals. Hexacelsian polycrystals were prepared from BaCO3, SrCO3 and finely purified kaolin powder (Al2O3·2SiO2·2H2O) by heat-treatment at 950–1400 °C. Sr-hexacelsian polycrystals transformed to celsian via nucleation and growth from inner to surface to develop cracks at surface at 1100–1200 °C. Single phase of celsian polycrystals in composition of Ba1−xSrxAl2Si2O8 (x = 0–0.8) were prepared by heat-treatment at 1400 °C for 1 h and their dilatometric thermal expansion coefficient (TEC) were almost 4.0–4.2 × 10−6/°C from 25 to 900 °C. On the other hand, average TEC of unit cell of celsian measured by high temperature X-ray diffraction were lower than the values of dilatometry and increased from 3.0 × 10−6/°C to 3.8 × 10−6/°C with the Sr content.