Mechanical activation of precursors for nanocrystalline materials

Nanostructured materials win big scientific interest and increasingly economic meaning through their specific exceptional properties. Precursors that were compacted by pressing and sintering are normally used preparation of materials. In present work, the influence of mechanical activation by grindi...

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Veröffentlicht in:Crystal research and technology (1979) 2003-01, Vol.38 (1), p.7-20
Hauptverfasser: Heegn, H., Birkeneder, F., Kamptner, A.
Format: Artikel
Sprache:eng
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Zusammenfassung:Nanostructured materials win big scientific interest and increasingly economic meaning through their specific exceptional properties. Precursors that were compacted by pressing and sintering are normally used preparation of materials. In present work, the influence of mechanical activation by grinding on the structure as well as on compacting and sintering behavior of oxides from magnesium, aluminium and silicon has been investigated. Starting materials for each metal oxide differ in microstructure, dispersity, and porosity. The influence of mechanical activation on the destruction of crystalline structure to nanocrystalline, as well as to the amorphous stage and the compaction of powders with nano‐particles, as well as structures with nanoscale pores have been compared. The possibilities of the consolidation of nanostructured materials were investigated. The mechanical activation took place in a disc vibration mill. The mechanical activated materials as well as their pressing and their sintering products were characterized by density, particle‐sizedistribution, specific surface, pore‐structure, microstructure, and crystallite size by X‐ray powder diffraction (XRD). The mechanical activation of the model‐substances led, in most cases, to an improvement of the compaction properties; thus, this improvement can be achieved with subsequent sintering densities up to 98% of the theoretical density. From these experiments, generalizations transferable to other materials can be made.
ISSN:0232-1300
1521-4079
DOI:10.1002/crat.200310001