Abstract
A model system, composed of powder blends of amorphous isomorphic silica spheres, being 500 nm in diameter, and also monosized crystalline α-Al 2 O 3 powder, was investigated. Two different particle sizes of the corresponding alumina powder were employed: 300 nm and 2 μm. This particular assembly enabled a distinction between amorphous silica and crystalline alumina merely by their difference in particle morphology. The powder blends were sintered at temperatures between 1400 and 1700 C and the microstructure evolution was characterized by scanning (SEM) and transmission electron microscopy (TEM). It is worth noting that upon annealing at 1700°C, both microstructures were indistinguishable. However, depending on the Al 2 O 3 particle size, different conversion mechanisms were monitored. When using the 300 nm Al 2 O 3 powder, fast dissolution of alumina into the coalesced silica glass occurred, followed by homogeneous nucleation and growth of mullite within the glass. Utilizing 2 μm Al 2 O 3 particles, however, resulted in the formation of two Al-containing glasses (phase separation into a Si- and Al-rich glass). In this case, the transformation to mullite can be rationalized by the conversion of the metastable Al-rich transient glass into mullite, which forms an epitaxial, single crystalline coating on the host Al 2 O 3 particle. Therefore, depending on the initial Al 2 O 3 particle size, mullite formation follows either the stable or metastable phase diagram.
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