Factors controlling crystallization of miserite glass-ceramic

Dent Mater. 2015 Dec;31(12):1469-73. doi: 10.1016/j.dental.2015.09.017. Epub 2015 Oct 23.

Abstract

Objective: The purpose of this study was to investigate a range of variables affecting the synthesis of a miserite glass-ceramic (GC).

Methods: Miserite glass was synthesized by the melt quench technique. The crystallization kinetics of the glass were determined using Differential Thermal Analysis (DTA). The glasses were ground with dry ball-milling and then sieved to different particle sizes prior to sintering. These particle sizes were submitted to heat treatment regimes in a high temperature furnace to form the GC. The crystal phases of the GC were analyzed by X-ray diffraction (XRD). Scanning electron microscopy (SEM) was used to examine the microstructure of the cerammed glass.

Results: XRD analysis confirmed that the predominant crystalline phase of the GC was miserite along with a minor crystalline phase of cristobalite only when the particle size is <20 μm and the heat treatment at 1000°C was carried out for 4h and slowly cooled at the furnace rate. For larger particle sizes and faster cooling rates, a pseudowollastonite crystalline phase was produced. Short sintering times produced either a pseudowollastonite or xonotolite crystalline phase.

Significance: The current study has shown that particle size and heat treatment schedules are major factors in controlling the synthesis of miserite GC.

Keywords: Cooling rate; DTA; Heat treatment; Miserite glass-ceramic; Particle size; Pseudowollastonite; SEM; XRD; Xonotolite.

MeSH terms

  • Ceramics / chemical synthesis
  • Ceramics / chemistry*
  • Crystallization
  • Differential Thermal Analysis
  • Glass / chemistry*
  • Materials Testing
  • Microscopy, Electron, Scanning
  • Particle Size
  • Silicon Dioxide / chemical synthesis
  • Silicon Dioxide / chemistry
  • X-Ray Diffraction

Substances

  • KCa5(Si2O7)(Si6O15)(OH)F
  • Silicon Dioxide
  • Glass ceramics