Colloidal processing of ceramics is reviewed with an emphasis on interparticle forces, suspension rheology, consolidation techniques, and drying behavior. Particular attention is given to the scientific concepts that underpin the fabrication of particulate-derived ceramic components. The complex interplay between suspension stability and its structural evolution during colloidal processing is highlighted.

/pdf/colloidal-processing-of-ceramics-1f3f618kn7.pdf

Colloidal Processing of Ceramics

Issues concerning powder consolidation methods compatible with the colloidal approach and issues associated with other powder processing steps, viz., densification and microstructural control, are presented with regard to research directions leading to more reliable ceramics.

Powder Processing Science and Technology for Increased Reliability

Theoretical concepts of sintering were originally based upon ideas of the discrete nature of particulate media. However, the actual sintering kinetics of particulate bodies are determined not only by the properties of the particles themselves and the nature of their local interaction with each other, but also by macroscopic factors. Among them are externally applied forces, kinematic constraints (e.g. adhesion of the sample's end face and furnace surface), and inhomogeneity of properties in the volume under investigation (e.g. inhomogeneity of initial density distribution created during preliminary forming operations). Insufficient treatment of the questions enumerated above was one of the basic reasons hindering the use of sintering theory. A promising approach is connected with the use of continuum mechanics, which has been successfully applied to the analysis of compaction of porous bodies. This approach is based upon the theories of plastic and nonlinear-viscous deformation of porous bodies. Similar ideas have recently been embodied in a continuum theory of sintering. The main results of the application of this theory for the solution of certain technological problems of sintering are introduced including their thermo–mechanical aspects.

Theory of sintering: from discrete to continuum

Superplastic structural ceramics (Y-TZP, A1203, Si3N4, and their composites) that can withstand biaxial stretching to large strains have been developed recently. Microstructural design of these ceramics first requires an ultrafine grain size that is stable against coarsening during sintering and deformation. A low sintering temperature is a necessary, but not a sufficient, condition for achieving the required microstructure. In many cases, the selection of an appropriate phase, such as tetragonal phase in zirconia or a phase in silicon nitride, which is resistant to grain growth, is crucial. The use of sintering aids and grain-growth inhibitors, particularly those that segregate to the grain boundaries, can be beneficial. Second-phase particles are especially effective in suppressing static and dynamic grain growth. Another major concern is to maintain an adequate grain-boundary cohesive strength, relative to the flow stress, to mitigate cavitation or grain-boundary cracking during large strain deformation. Existing evidence suggests that a lower grainboundary energy is instrumental in achieving this objective. The selection of an appropriate phase and the tailoring of the grain boundary or liquid-phase composition can sometimes drastically alter the cavitation resistance. Related observations on forming methods, forming characteristics, and sheet formability are also reviewed. The basic deformation characteristics are similar to diffusional creep and are dominated by R. E. Newnham-contributing editor

/pdf/development-of-superplastic-structural-ceramics-hmamty815f.pdf

Development of Superplastic Structural Ceramics

Monodisperse TiO2 powders were synthesized by the controlled hydrolysis of dilute alcoholic solutions of titanium alkoxides. The state of powder aggregation in dispersions and powder packing in the green bodies strongly affected the sintering behavior. The sintering of uniformly packed powder compacts resulted in finegrained microstructures with >99% of theoretical density nt temperatures much lower than those required to sinter conventional TiO2 powders.

Formation, Packing, and Sintering of Monodisperse TiO2 Powders

The initial-, intermediate-, and final-stage sintering of fine crystallite yttria-stabilized zirconia was studied. Experiments were conducted on powder lots of differing agglomerate size and one specially prepared agglomerate-free powder. Initial-stage sintering kinetics were compared with a sintering study on larger crystallite size calcia-stabilized zirconia to access the Herring scaling law. It was found that agglomerates limit attainable green density, interfere with the development of microstructure, impede initial-stage sintering kinetics, and limit the potential benefit of fine crystallites on final-stage sintering. An gglomerate free powder centrifuge-cast to 74% green density was sintered to 99.5% of theoretical density in a 1 h 1100°C cycle, which is ∼300°C lower than necessary for an agglomerated but equal crystallite size powder.

W. H. Rhodes

Papers

Agglomerate and Particle Size Effects on Sintering Yttria‐Stabilized Zirconia

Agglomerate and particle size effects on sintering yttria‐stabilized zirconia