Chu, Tien-Min GabrielLien, WenPlatt, Jeffrey A., 1958-Levon, John A.Brown, David T.Xie, Dong2014-05-122014-05-122014https://hdl.handle.net/1805/4414http://dx.doi.org/10.7912/C2/1420Indiana University-Purdue University Indianapolis (IUPUI)Background: Elucidating the lithium disilicate system like the popular IPS e.max® CAD (LS2), made specifically for Computer-Aided Design and Computer-Aided Manufacturing (CAD-CAM), as a function of temperature unravels new ways to enhance material properties and performance. Objective: To study the effect of various thermal processing on the crystallization kinetics, crystallite microstructure, and strength of LS2. Methods: The control group of the LS2 samples was heated using the standard manufacturer heating-schedule. Two experimental groups were tested: (1) an extended temperature range (750-840 °C vs. 820-840 °C) at the segment of 30 °C/min heating rate, and (2) a protracted holding time (14 min vs. 7 min) at the isothermal temperature of 840 °C. Five other groups of different heating schedules with lower-targeted temperatures were evaluated to investigate the microstructural changes. For each group, the crystalline phases and morphologies were measured by X-ray diffraction (XRD) and scanning electron microscope (SEM) respectively. Differential scanning calorimeter (DSC) was used to determine the activation energy of LS2 under non-isothermal conditions. A MTS universal testing machine was used to measure 3-point flexural strength and fracture toughness, and elastic modulus and hardness were measured by the MTS Nanoindenter® XP. A one-way ANOVA/Tukey was performed per property (alpha = 0.05). Results: DSC, XRD, and SEM revealed three distinct microstructures during LS2 crystallization. Significant differences were found between the control group, the two aforementioned experimental groups, and the five lower-targeted-temperature groups per property (p<0.05). The activation energy for lithium disilicate growth was 667.45 (± 28.97) KJ/mole. Conclusions: Groups with the extended temperature range (750-840 °C) and protracted holding time (820-840 °C H14) produced significantly higher elastic-modulus and hardness properties than the control group but showed similar significant flexural-strength and fracture-toughness properties with the control group. In general, explosive growth of lithium disilicates occurred only when maximum formation of lithium metasilicates had ended.en-USAttribution-NonCommercial-ShareAlike 3.0 United StatesGlass-CeramicLithium DisilicateIPS e.max CADHeating ScheduleLithium MetasilicateDental MaterialMicrostructurePhysical PropertiesPhase TransformationTemperature ThresholdNucleation and CrystallizationDifferential Scanning CalorimetryDental Porcelain -- chemistryCeramics -- chemistryDental MaterialsPhysical Properties -- chemistryTransition TemperatureCrystallizationThesis