A method is described wherein a ceramic oxide nanocomposite coating has been produced via a co-precipitation route. The first step in the process consists of forming a solid solution by use of plasma melting, homogenization, and rapid quenching of two ceramics that are normally immiscible. In the best case, the resulting structure is a true solid solution in a new, metastable crystalline structure. The quenched particles can be deposited as a coating or sprayed into water or onto a chill block to form a powder. When the material is sintered via a pressureless process, such as that for a coating, the phase decomposition proceeds quickly, resulting in a homogeneously distributed two-phase structure of micron sized particles. However, when the powders are compacted and sintered at very high pressures (1-8 GPa) and low temperatures (T ~ 0.3 - 0.5 Tm), the increased nucleation of the precipitates results in a composite in which both phases have grain sizes less than 25nm. This paper will review the underlying phenomenon behind the method and the resulting kinetics.

This paper compares the wear properties of HVOF-sprayed WC/12Co hardcoatings produced from different powder feedstock materials, including conventional, nanophase, and mixed powders. The mixed or multimodal feed powder is designed to minimize the amount of material that goes through a high temperature cycle during spraying, thus potentially limiting the extent of decarburization in the resulting coating. As will be shown, decarburization is indeed minimal in a multimodal coating, which translates into exceptional resistance to abrasive and sliding wear. Another favorable factor is the ability to increase the volume fraction of hard WC phase in such a coating, thereby further enhancing its wear resistance.