Phase equilibrium studies at subsolidus temperatures, made in the presence of an aqueous phase at high pressures, are briefly reviewed for the systems eucryptite–silica, Al 2 O 3 –Ga 2 O 3 , MgAl 2 O 4 –Al 2 O 3 , and TiO 2 . Low‐temperature equilibrium relations have been largely clarified for the first three systems because of the greatly increased reaction rate in the presence of a fluid phase. For the system TiO 2 , however, hydrothermal techniques appear to be inadequate for the determination of stability relations. The hydrothermal syntheses of forsterite at 500° to 700°C. from magnesia and silica or from dolomite and silica, and of mullite at 500°C. from clay minerals, are mentioned as reactions of possible industrial significance. A further acceleration of reaction rate at low or moderate temperatures is being achieved by grinding at elevated temperatures and pressures.
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E. F. Osborn (1953) studied this question.
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