The obtaining of high-density specimens and analysis of mechanical strength characteristics of a composite based on ZrO2-WC nanopowders
© Gevorkyan et al.; licensee Springer. 2014
Received: 10 December 2013
Accepted: 26 June 2014
Published: 15 July 2014
The structures, processes of shrinkage, and phase composition of the compact system ZrO2-WC, obtained by hot pressing with the transmission of high current, are considered in the article. We found that as a result of compaction, the ZrO2-WC-ceramics have uniform density distribution, with the following optimal mode consolidation values T = 1,350°C, P = 30 MPa and t = 2 min. These conditions allow us to achieve the best combination of ceramic properties by criteria density and strength.
KeywordsElectroconsolidation ZrO2-WC Hardness Fracture toughness
Recently, most binary systems were made based on ZrO2 such as ZrO2-TiB2, ZrO2-TiCN, ZrO2-SiC, ZrO2-TiN, and ZrO2-TiC. Consequently, high mechanical properties of the material can be expected when ZrO2 is hardened by nanoparticles of the second phase (tungsten carbide). It will allow extensive use of obtained ceramics.
It is known that tungsten carbide is widely used in the manufacture of hard alloys based on WC-Co due to its high resistance to wear and low temperatures during use. However, the thermal stability of the cobalt binder greatly limits its use as a structural component, where high heat resistance, resistance to oxidation, and corrosion are very important. Previously, attention was paid to determine the optimum ZrO2 in the composite materials based on WC made by high-energy FAST methods [1, 2]. Also, the authors in  reported that the addition of 30% micron-sized WC to ZrO2-matrix significantly increases the hardness and fracture toughness, but their values were low.
Research on the possibility of compacting ZrO2-WC composites via hot pressing with electric current (electroconsolidation) is the purpose of this work. It is also important to identify optimal regimes to obtain high-density samples having homogeneous microstructure with high mechanical characteristics.
The nanopowders were mixed using a planetary milling plant ‘Pulverisette 6’(Fritsch GmbH, Idar-Oberstein, Germany with isopropyl alcohol for 2 h for a uniform distribution of particles in the sample. The rotation speed of planetary disk is 160 rpm. To break the agglomerates, alumina milling balls were added to the container.
Installation for hot vacuum pressing, designed and patented by the authors, was done to consolidate the powders. This installation, in comparison with the well-known FAST method in Europe, differs mainly because of the possibility that it uses a conventional AC power frequency without special optional equipment pulse generators. This method later in this article will be referred to as electroconsolidation.
The nanopowders were sintered using a hot pressing facility with a direct current under a pressure of 30 MPa and held for 2 min at various temperatures. Further studies were done on molded samples such as tablets of 20 mm in diameter. Sintering curve looks like this: at a pressure of 10 MPa, the temperature was raised at 150°C/min up to a temperature of 600°C; then, at the same pressure, the temperature was adjusted to a holding temperature (1,200°C to 1,400°C). This temperature was held for 2 min. At the same time, the pressure was raised to 30 MPa. After the rise of the holding temperature stopped, the sample cooled and formed. Pressure is removed after the final cooling. Full-time consolidation was 15 min.
The microstructure of the nanoceramic compositions, obtained by electroconsolidation, was examined by scanning electron microscopy; by the same method, the grain sizes of the obtained samples were evaluated. The samples for electron microscopic studies were prepared as shear of sintered tablets.
Using a universal hardness tester, the Vickers hardness (HV10) of the composite is evaluated with a load of 10 kg. The fracture toughness (KIC) calculations were made based on the measurements of the radial crack length produced by Vickers (HV10) indentations, according to Anstis formula . The reported values are the averages of the data obtained from five indentation tests.
Detailed microstructural characterization and phase identification were carried out using a Quanta 200 3D (FEI Co., Hillsboro, OR, USA) scanning electron microscope (SEM) and a Rigaku Ultima IV X-ray diffractometer (Rigaku Europe SE, Ettlingen, Germany) (CuKα radiation, Ni filter).
Results and discussion
The sintering parameters and relative density of the obtained ZrO 2 -WC composites
Sintering temperature (°C)
Holding time (min)
Relative density (%)
Table 1 shows that the holding time is a temperature-independent parameter and slightly influences the densification. The density data reveal that the maximum density of approximately 99.5% ρth can be achieved in composite sintered at 1,350°C and holding time of 2 min with 20 wt.% WC additive.
The microstructure of fracture surfaces of ceramics obtained at 1,350°C. One can distinguish two types of areas: areas of intergranular fracture and the so-called twinning topography (Figure 4b indicated by arrow). The paper  stated that the presence of fracture surface areas with relief twinning can indicated that the structure undergoes a stress-induced martensitic (tetragonal-monoclinic) transformation during fracture. We assume that some of the grains with twin structure are zirconia grains. However, to confirm this hypothesis, the chemical analysis of the samples should be carried out.
where x is the oxygen vacancy concentration in the ZrO2 as a result of the dopant concentration, and y is the additional vacancy concentration created in the ZrO2 due to the reaction with WC.
This reaction contributes to the formation of additional oxygen vacancies and W2C. The occurrence of additional oxygen vacancies leads to an increase of non-stoichiometry ZrO2 phase. This can improve the diffusion coefficient in a certain degree, whereby the mass transfer occurs quickly and, therefore, increases the rate of sintering.
The hardness variation with sintering temperature is closely related to the bulk density and microstructural features. The hardness increased continuously with increasing temperature from 1,200°C to 1,350°C (Figure 5), due to an increased densification, reaching a maximum hardness at full densification when temperature was at 1,350°C. At higher sintering temperatures, the hardness slightly decreased due to the increased WC and ZrO2 grain size, as well as the partial spontaneous transformation of the ZrO2 phase.
The fracture toughness increased rapidly from 5.5 to 8.5 MPa m1/2 with increasing temperature from 1,200°C to 1,350°C (Figure 5), followed by a decreasing trend to 8.1 MPa m1/2 at 1,400°C. The high value of fracture toughness may be due to the fact that a part of the tetragonal phase of ZrO2 transforms to the monoclinic ZrO2 (Figure 4) during electroconsolidation at a temperature of 1,350°C.
Electroconsolidation provides a uniform density distribution, without any plasticizers that are potential sources of impurities and additional porosity in the sintered product. The maximum density of the ZrO2-20 wt.% WC composite was obtained at 1,350°C for 2 min at 30 MPa.
The best combination of mechanical properties was obtained for a 2 mol.% Y2O3-stabilized ZrO2 composite with 20 wt.% WC, obtained by electroconsolidation at 1,350°C, combining a hardness of 16.5 GPa and a fracture toughness of 8.5 MPa m1/2.
We thank the Research Centre of Constructional Ceramics and The Engineering Prototyping (Russia) for research assistance and for providing the ZrO2 nanopowder synthesized from Ukrainian raw materials, using its developed technology.
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