Structural evolution during the preparation and heating of nanophase zirconia gels

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dc.contributor Southon, Peter David en_AU
dc.date.accessioned 2007-03-14T01:53:11Z
dc.date.accessioned 2012-12-15T03:51:29Z
dc.date.available 2007-03-14T01:53:11Z
dc.date.available 2012-12-15T03:51:29Z
dc.date.issued 2000
dc.identifier.uri http://hdl.handle.net/2100/302
dc.identifier.uri http://hdl.handle.net/10453/20036
dc.description The chemical preparation of ceramic materials has been widely studied over the past few decades, and provides the potential for excellent control over the microstructure and properties of the final product. This control is dependent on a comprehensive understanding of the microstructure and physical/chemical processes that occur at each stage. Aqueous routes have much potential for adoption by industry, but in many cases a comprehensive understanding of the microstructure and chemistry is lacking, partly due to the complicated aqueous chemistry of many transition-metals. This investigation has focussed on a specific inorganic, aqueous, sol-gel route for the preparation of pure zirconia (Zr02). Zirconia is a ceramic with a wide range of current and potential applications, such as catalysis, fuel-cells, coatings and biomaterials. The emphasis has been placed on the characterisation of the structure at each stage of the route, leading to an understanding of the various mechanisms that are at work. This project has also provided an opportunity to investigate broader issues concerning the solution-based processing of zirconia, particularly those involving the 'metastable' tetragonal phase. This phase is frequently observed to be formed by non-equilibrium methods, but the mechanisms of formation and de-stabilisation are not properly understood. The studied route consists of a number of stages: the preparation of an aqueous sol of 'zirconium hydroxide' particles by forced hydrolysis of a zirconyl nitrate solution; the conversion of the sol to a gel by removal of the aqueous phase; the conversion of the gel to a crystalline tetragonal zirconia powder by heating; and transformation of the tetragonal phase to the stable monoclinic phase with further treatment. At each stage of processing a number of aspects of the material structure have been investigated, including the short-range order, crystalline lattice parameters, particle packing, porosity, and speciation of the nitrate anion. This has required a wide range of complementary characterisation techniques, including Raman spectroscopy, XRD, TEM, DTA/TGA, SAXS, dynamic light scattering, EXAFS, NMR, and nitrogen sorption. The importance of techniques that allow changes in structure to be characterised in-situ during heating has been emphasised. The particles in the sol and gel are plate-shaped, approximately 0.5 nm thick and 3 - 4 nm across. They are composed of up to several stacked `sheets' of zirconium hydroxide, each of which is composed of zirconium atoms arranged in a regular square lattice, joined by double hydroxy-bridges. Detailed evidence for this structure has not been previously reported. The stages of decomposition of the precursor have been elucidated, including the stages at which oxolation and loss of nitrate occur. The complex crystallisation process at 450°C has been investigated, and a structural mechanism for crystallisation of the 'metastable' tetragonal phase proposed, based on similarities between the tetragonal crystal structure and the disordered sheet structure in the amorphous material just prior to crystallisation. The crystalline material consists of nano-sized crystals, containing unusual intracrystalline mesopores. The lattice parameters of the tetragonal phase change with increasing heat treatment, with the unit-cell tetragonality (c/a) increasing from 1.017 to 1.020. This is a previously-unreported phenomenon which may be associated with the stability of the phase. The tetragonal phase transforms to the monoclinic phase after heating to a 'critical temperature' between 900 and 950°C; this temperature is associated with the loss of residual surface nitrate species and/or a substantial increase in the mass diffusion rate. The crystal size and surface area has little influence on the tetragonal-to-monoclinic transformation, a result which is contrary to much previously-published work and that has significant implications for certain theories explaining the stability of the tetragonal phase. The transformation itself occurs during cooling, over a range between 400 and 100°C, and has been studied in-situ by time-resolved Raman spectroscopy. The conclusions of this investigation contribute not only to the understanding of this particular route for processing zirconia, but also to a broader understanding of aqueous zirconium systems, the chemical processing of zirconia, and the tetragonal-to-monoclinic zirconia transformation mechanisms. en_AU
dc.format.extent 48139 bytes
dc.format.extent 1188546 bytes
dc.format.extent 1988078 bytes
dc.format.extent 1037316 bytes
dc.format.mimetype application/pdf
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dc.format.mimetype application/pdf
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dc.language en en_AU
dc.language.iso en_AU
dc.publisher University of Technology, Sydney. Department of Chemistry, Materials & Forensic Science en_AU
dc.rights http://www.lib.uts.edu.au/disclaimer.html en_AU
dc.rights Copyright Peter Southon en_AU
dc.subject Zirconium oxide. en_AU
dc.subject Ceramics. en_AU
dc.title Structural evolution during the preparation and heating of nanophase zirconia gels en_AU
dc.type Thesis (PhD)


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