TY - GEN
T1 - Controlled crystallisation of grain boundary-type Y-SiAION glass typical of those found in silicon nitride ceramics
AU - Pomeroy, Michael J.
AU - Hampshire, Stuart
PY - 2010
Y1 - 2010
N2 - Following liquid phase sintering of silicon nitride ceramics with yttria and alumina densification additives, a Y-SiAlON glass remains at the grain boundaries. Crystallisation of such a glass in bulk form has been studied using both differential thermal analysis (DTA) and separate isothermal heat treatments in a tube furnace under nitrogen. The activation energy for the crystallisation process was determined by DTA. The nucleation temperature, Tg + 40°C, which corresponded to the maximum volume fraction of crystalline phases, agreed closely with the optimum nucleation temperature of Tg + 35°C, found from DTA. The optimum crystal growth temperature was observed to be 1210°C and yielded the α- and β-polymorphs of yttrium disilicate. The activation energy for crystallisation was observed to be similar to that for viscous flow of Y-SiAlON glasses. Heat treatments over a range of temperatures resulted in formation of different polymorphs of yttrium disilicate in addition to silicon oxynitride. Careful analysis of DTA crystallisation exothermic peaks were carried out in order to clearly identify polymorphic transformations of yttrium disilicate. Partial substitution of yttrium by lanthanum stabilises the α-polymorph of yttrium disilicate over a wider temperature range.
AB - Following liquid phase sintering of silicon nitride ceramics with yttria and alumina densification additives, a Y-SiAlON glass remains at the grain boundaries. Crystallisation of such a glass in bulk form has been studied using both differential thermal analysis (DTA) and separate isothermal heat treatments in a tube furnace under nitrogen. The activation energy for the crystallisation process was determined by DTA. The nucleation temperature, Tg + 40°C, which corresponded to the maximum volume fraction of crystalline phases, agreed closely with the optimum nucleation temperature of Tg + 35°C, found from DTA. The optimum crystal growth temperature was observed to be 1210°C and yielded the α- and β-polymorphs of yttrium disilicate. The activation energy for crystallisation was observed to be similar to that for viscous flow of Y-SiAlON glasses. Heat treatments over a range of temperatures resulted in formation of different polymorphs of yttrium disilicate in addition to silicon oxynitride. Careful analysis of DTA crystallisation exothermic peaks were carried out in order to clearly identify polymorphic transformations of yttrium disilicate. Partial substitution of yttrium by lanthanum stabilises the α-polymorph of yttrium disilicate over a wider temperature range.
UR - http://www.scopus.com/inward/record.url?scp=77952350763&partnerID=8YFLogxK
M3 - Conference contribution
AN - SCOPUS:77952350763
SN - 9780470408421
T3 - Ceramic Transactions
SP - 279
EP - 284
BT - Ceramic Materials and Components for Energy and Environmental Applications - 9th Int. Symp. on Ceramic Materials for Energy and Environmental Applications and the 4th Laser Ceramics Symp.
T2 - Ceramic Materials and Components for Energy and Environmental Applications - 9th International Symposium on Ceramic Materials for Energy and Environmental Applications and the 4th Laser Ceramics Symposium
Y2 - 10 November 2008 through 14 November 2008
ER -