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residual glass phase
Two compositionally similar but morphologically different glass-ceramics containing about 20% residual glass phase have been creep-tested in tension and compression between 600 and 800°C.
      
The activation energy of the rate-controlling process is the same as that found for secondary creep and is due to viscous flow of the residual glass phase.
      
For the latter, however, compositional changes in the residual glass phase also exert a significant influence.
      
For the latter, however, compositional changes in the residual glass phase also exert a significant influence.
      
It is suggested that grain growth is controlled by precipitate particles rather than by residual glass phase.
      
The mismatch of thermal expansion coefficient between the crystalline phases and the residual glass phase plays an important role in changing the mechanical properties.
      
The crystallization process of the glass phase can be taken almost to completion but a small proportion of residual glass phase is present.
      
A change of composition of the residual glass phase in the glass-ceramic product, in comparison with the parent glass, is considered to explain, in comparative terms, the higher toxic potential of the glass-ceramic over the glass.
      
The microstructure is characterised by fine crystals uniformly distributed arbitrarily oriented throughout the residual glass phase.
      
 

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