Abstract
Nanometre-sized particles of transition (t)-aluminas are important for the fabrication of high-quality alumina ceramics. Multiple tons are produced each year using a variety of gas-phase processes1,2,3,4. The nanoparticles produced by these methods consist mainly of the undesired δ phase with some γ- and θ-Al2O3. Nano-t-aluminas should provide access to dense nano/submicrometre-grained α-Al2O3 shapes offering significant advantages over micrometre-grained shapes5,6,7,8,9,10,11. Unfortunately, polymorphism coupled with the high activation energy for nucleating α-Al2O3 greatly impedes efforts to process dense α-Al2O3 with controlled grain sizes, especially for submicrometre materials. Typically α-Al2O3 nucleation within t-aluminas is sporadic rather than uniform, leading to exaggerated grain growth and vermicular microstructures without full densification5. Thus, production of quantities of nano-α-Al2O3 from multiple nano-t-aluminas for seeding or direct processing of α-Al2O3 monoliths could greatly change how α-Al2O3 components are processed. We report here that liquid-feed flame spray pyrolysis3 of nano-t-aluminas converts them to dispersible 30–80 nm α-Al2O3 powders (50–85% phase transformed). Surprisingly, the powder surfaces are fully dehydrated. These powders pressureless sinter to more than 99.5% dense α-Al2O3 with final grain sizes ≤500 nm without sintering aids.
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Acknowledgements
This work was supported by the Air Force Office of Scientific Research on Contract F49620-03-1-0389. We thank G. Varga of Degussa and R. Brotzman of Nanophase for providing samples of nano-t-aluminas and M. Solomon and M. Kogan for help with the dynamic light scattering experiments.
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J.C.M. and R.M.L. were responsible for the experimental work, planning and the majority of the data analysis. X.P. and H.P. were responsible for the design and execution of weeks of extensive transmission electron microscopy work.
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Laine, R., Marchal, J., Sun, H. et al. Nano-α-Al2O3 by liquid-feed flame spray pyrolysis. Nature Mater 5, 710–712 (2006). https://doi.org/10.1038/nmat1711
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DOI: https://doi.org/10.1038/nmat1711
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