Microstructural control of CaO–Al2O3–SiO2 (CAS) glass ceramics (GCs) was achieved by oxidation and mixing with nucleation agents. CAS GCs were precipitated with hexagonal platy particles of metastable CaAl2Si2O8 layered crystals… Click to show full abstract
Microstructural control of CaO–Al2O3–SiO2 (CAS) glass ceramics (GCs) was achieved by oxidation and mixing with nucleation agents. CAS GCs were precipitated with hexagonal platy particles of metastable CaAl2Si2O8 layered crystals (CAS GC-H), which are typically prepared under a reductive atmosphere that forms metallic Mo or W particles as nucleation agents. The average particle size of crystals decreased significantly from 50 to 11 μm when the CAS GC-H containing metallic W particles was prepared under an oxidative atmosphere. Compared to this CAS-GC-H, the crystal particle size increased from 8–20 to 10–30 μm when the CAS GC-H was prepared by mixing glass cullet containing metallic Mo and that containing metallic W particles. These results indicate that one microstructure of CAS GC-H is controlled on the micrometer scale from a parent glass with one composition by varying the experimental conditions related to the glass melting state.
               
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