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Physical Stabilization of the β → γ Transformation in Dicalcium Silicate
Author(s) -
Chan Chin Jong,
Kriven Waltraud M.,
Young J. Francis
Publication year - 1992
Publication title -
journal of the american ceramic society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.9
H-Index - 196
eISSN - 1551-2916
pISSN - 0002-7820
DOI - 10.1111/j.1151-2916.1992.tb04234.x
Subject(s) - nucleation , materials science , orthorhombic crystal system , crystallization , amorphous solid , annealing (glass) , mineralogy , silicate , chemical engineering , microstructure , monoclinic crystal system , crystallography , metallurgy , crystal structure , chemistry , organic chemistry , engineering
It has been shown that the monoclinic β ‐phase of dicalcium silicate (Ca 2 SiO 4 ) can be stabilized against transformation to the orthorhombic γ ‐phase by physical rather than chemical factors. Stabilization was studied in different types of microstructures fabricated under various processing conditions such as different powder or grain sizes, chemical additives, cooling kinetics, or high‐temperature annealing treatments. The observations can be explained in terms of a critical particle size effect controlling nucleation of the transformation. Rapid quenching through the high‐temperature hexagonal ( α ) to orthorhombic ( a′ H ) transformation at 1425°C, which is accompanied by a −4.7% volume decrease, causes periodic fracture of β ‐twins due to accumulated strains. Chemical doping with K 2 O or Al 2 O 3 promotes the formation of amorphous phases which mold themselves around β ‐Ca 2 SiO 4 grains. Annealing treatments cause crystallization of the glass and subsequent transformation to the γ ‐phase.