An oscillatory pressure sintering of zirconia powder: Densification trajectories and mechanical properties

The densification trajectories and mechanical properties of zirconia ceramics obtained by oscillatory pressure sintering (OPS) process were investigated, during the sintering process an oscillatory pressure was applied at three stages. Current results indicated that at intermediate stage the oscillatory pressure revealed a favorable improvement of mechanical properties compared with conventional hot pressing (HP) and pressureless sintering (PS) procedures, while the enhancement was not obvious at initial stage. When the oscillatory pressure was applied at final stage, the OPS specimens exhibited the highest bending strength and hardness of 1455 ± 99MPa and 16.6 ± 0.31GPa compared with the PS and HP specimens. Considering the high elastic modulus and Moiré patterns observed in the OPS specimen, the oscillatory pressure applied at intermediate and final stages was detected to facilitate the sliding of grain boundary, plastic deformation of monolithic grains, the removal of pores and the strengthening of atomic bonds.     

Low‐Temperature Spark Plasma Sintering of Pure Nano WC Powder

For the first time we have demonstrated the densification of high‐purity nanostructured (d_avg ≈ 60 nm) tungsten carbide by High Pressure Spark Plasma Sintering (HPSPS) in the unusually low temperature range of 1200°C–1400°C. The high‐pressure sintering (i.e., 300 MPa) produced dense material at a temperature as low as 1400°C. In comparison with more conventional sintering techniques, such as SPS (80 MPa) or hot isostatic pressing, HPSPS lowered the temperature required for full densification by 400°C–500°C. High Pressure Spark Plasma Sintering, even in absence of any sintering aid or grain growth inhibitor, retained a very fine microstructure resulting in a significant improvement in both hardness (2721 HV₁₀) and fracture toughness (7.2 MPa m^1/2).     

Densification and grain growth behaviour of high-purity MgO ceramics by hot-pressing

High-purity MgO ceramics with a relative density higher than 99.60% and a mean grain size of 8.1 µm were prepared by hot-pressing at 1450 °C and 35 MPa for 120 min. The MgO ceramic was 130 mm in diameter and 10 mm in height. The densification mechanism and grain growth of MgO powder during the sintering process were investigated based on the principles of general deformation and classical phenomenological kinetic theory. The threshold pressure of plastic deformation at the initial sintering stage was also analysed. The results suggest that plastic deformation is the dominant densification mechanism during the initial period and that an applied pressure of 20 MPa is sufficient for the deformation. During the final period, Mg²⁺ diffusion along the grain boundaries controls the densification process, and the grain growth activation energy at the final stage is estimated as 336.38±2.35 kJ mol⁻¹.     

Densification mechanism and microstructure characteristics of nano- and micro- crystalline alumina by high-pressure and low temperature sintering

Fully dense ceramics with retarded grain growth can be attained effectively at relatively low temperatures using a high-pressure sintering method. However, there is a paucity of in-depth research on the densification mechanism, grain growth process, grain boundary characterization, and residual stress. Using a strong, reliable die made from a carbon-fiber-reinforced carbon (C_f/C) composite for spark plasma sintering, two kinds of commercially pure α-Al₂O₃ powders, with average particle sizes of 220 nm and 3 μm, were sintered at relatively low temperatures and under high pressures of up to 200 MPa. The sintering densification temperature and the starting threshold temperature of grain growth (T_sg) were determined by the applied pressure and the surface energy relative to grain size, as they were both observed to increase with grain size and to decrease with applied pressure. Densification with limited grain coarsening occurred under an applied pressure of 200 MPa at 1050 °C for the 220 nm Al₂O₃ powder and 1400 °C for the 3 μm Al₂O₃ powder. The grain boundary energy, residual stress, and dislocation density of the ceramics sintered under high pressure and low temperature were higher than those of the samples sintered without additional pressure. Plastic deformation occurring at the contact area of the adjacent particles was proved to be the dominant mechanism for sintering under high pressure, and a mathematical model based on the plasticity mechanics and close packing of equal spheres was established. Based on the mathematical model, the predicted relative density of an Al₂O₃ compact can reach ～80 % via the plastic deformation mechanism, which fits well with experimental observations. The densification kinetics were investigated from the sintering parameters, i.e., the holding temperature, dwell time, and applied pressure. Diffusion, grain boundary sliding, and dislocation motion were assistant mechanisms in the final stage of sintering, as indicated by the stress exponent and the microstructural evolution. During the sintering of the 220 nm alumina at 1125 °C and 100 MPa, the deformation tends to increase defects and vacancies generation, both of which accelerate lattice diffusion and thus enhance grain growth.     

Modelling of elimination of strength-limiting defects by pressure-assisted sintering at low stress levels

The structural reliability of sintered products depends on large defects introduced during powder processing, which cannot be removed by pressureless sintering. Here, we present a model how a large single ellipsoidal void is deformed, and finally disappears by pressure-assisted sintering. Taya-Seidel’s model is applied to predict the shrinkage of a large void in a compressible linear viscous material by using bulk viscosity, shear viscosity, and sintering stress that are determined experimentally for sintering of alumina powder at low stress levels. The application of mechanical stress promotes the densification rate. Its effect is maximum for hot isostatic pressing (HIP) and minimum for sinter forging. The effect is intermediate for hot pressing (HP) and spark plasma sintering (SPS), because the hydrostatic component of stress varies with densification. While a crack-like defect can be removed during densification, a spherical void must be eliminated by shear deformation in the final stage during dwell time.     

Sintering kinetics and properties of NiFe2O4-based ceramics inert anodes doped with TiN nanoparticles

Sintering kinetics of NiFe₂O₄-based ceramics inert anodes for aluminum electrolysis doped 7 wt% TiN nanoparticles were conducted to investigate densification and grain growth behaviors. The linear shrinkage increased gradually with the increasing sintering temperature between 1000 and 1450°C, whereas the linear shrinkage rate exhibited a broad peak. The maximum linear shrinkage rate was obtained at 1189.4°C, and the highest densification rate was achieved at the relative density of 75.20%. Based on the pressureless sintering kinetics window, the sintering process was divided into the initial stage, the intermediate stage, and the final stage. The grain growth exponent reduced with increased sintering temperature, whereas the grain growth activation energy decreased by increasing sintering temperature and shortening dwelling time. The grain growth was mainly controlled by atomic diffusion. NiFe₂O₄-based ceramics possessed high-temperature semiconductor essential characteristics. The electrical conductivity of NiFe₂O₄-based ceramics first increased and then decreased with increasing sintering temperature, reached their maximum value (960°C) of 33.45 S/cm under 1300°C, mainly attributed to the relatively dense and uniform microstructure. The thermal shock resistance of NiFe₂O₄-based ceramic was improved by a stronger grain boundary bonding strength and lower coefficient of linear thermal expansion.     

Sintering and densification of nanocrystalline ceramic oxide powders: a review

Abstract

Observation of the unconventional properties and material behaviour expected in the nanometre grain size range necessitates the fabrication of fully dense bulk nanostructured ceramics. This is achieved by the application of ceramic nanoparticles and suitable densification conditions, both for the green and sintered compacts. Various sintering and densification strategies were adopted, including pressureless sintering, hot pressing, hot isostatic pressing, microwave sintering, sinter forging, and spark plasma sintering. The theoretical aspects and characteristics of these processing techniques, in conjunction with densification mechanisms in the nanocrystalline oxides, were discussed. Spherical nanoparticles with narrow size distribution are crucial to obtain homogeneous density and low pore-to-particle-size ratio in the green compacts, and to preserve the nanograin size at full densification. High applied pressure is beneficial via the densification mechanisms of nanoparticle rearrangement and sliding, plastic deformation, and pore shrinkage. Low temperature mass transport by surface diffusion during the spark plasma sintering of nanoparticles can lead to rapid densification kinetics with negligible grain growth.     

Fully coupled electromagnetic‐thermal‐mechanical comparative simulation of direct vs hybrid microwave sintering of 3Y‐ZrO2

Direct and hybrid microwave sintering of 3Y‐ZrO₂ are comparatively studied at frequency of 2.45 GHz. Using the continuum theory of sintering, a fully coupled electromagnetic‐thermal‐mechanical (EMTM) finite element simulation is carried out to predict powder samples deformation during their microwave processing. Direct and hybrid heating configurations are computationally tested using advanced heat transfer simulation tools including the surface to surface thermal radiation boundary conditions and a numeric proportional‐integral‐derivative regulation (PID). The developed modeling framework shows a good agreement of the calculation results with the known experimental data on the microwave sintering of 3Y‐ZrO₂ in terms of the densification kinetics. It is shown that the direct heating configuration renders highly hot spot effects resulting in nonhomogenous densification causing processed specimen's final shape distortions. Compared with the direct heating, the hybrid heating configuration provides a reduction of the thermal inhomogeneity along with a densification homogenization. As a result of the hybrid heating, the total densification of the specimen is attained without specimen distortions. It is also shown that the reduction of the sample size has a stabilization effect on the temperature and relative density spatial distributions.     

Sintering highly dense ultra-high temperature ceramics with suppressed grain growth

Grain coarsening normally occurs at the final stage of sintering, resulting in trapped pores within grains, which deteriorates the density and the performance of ceramics, especially for ultra-high temperature ceramics (UHTCs). Here, we propose to sinter this class of ceramics in a specific temperature range and coupled with a relatively high pressure. The retarded grain boundary migration and pressure-enhanced diffusion ensure the proceeding of densification even at final stage. A highly dense TaC ceramic (98.6 %) with the average grain size of 1.48 μm was prepared under 250 MPa via high pressure spark plasma sintering using a C_f/C die at 1850 °C. It was suggested that the final-stage densification is mainly attributed to grain boundary plastic deformation-involved mechanisms. Compared to the usual sintering route using a high temperature (>2000 °C) and normal pressure (<100 MPa), this work provides a useful strategy to acquire highly dense and fine-grained UHTCs.     

Plastic deformation and effects of water in room‐temperature cold sintering of NaCl microwave dielectric ceramics

NaCl ceramics were prepared by room‐temperature cold sintering using moistened NaCl powder with 4 wt% water and dry pressing using dehydrated powder. When the applied uniaxial pressure is low, the relative density of dry‐pressed NaCl ceramic is significantly lower than that of cold‐sintered ceramic, while the former is 98.5%‐99.3% and much higher than the latter (94.3%‐94.6%) for high applied pressure of 200‐300 MPa. The uniaxial pressure‐induced plastic deformation dominates the densification of dry‐pressed NaCl ceramic, and also plays a role during cold sintering as well as the dissolution‐precipitation process. The lower density of cold‐sintered NaCl ceramic under high applied pressure is attributed to the trapped water in ceramic body during cold sintering. Besides, the presence of water always promotes the microstructural homogeneity, which is responsible for the much higher Qf value of cold‐sintered NaCl ceramic. The optimal microwave dielectric properties with ε_r = 5.55, Qf = 49 600 GHz, and τ_f = ?173 ppm/°C are obtained in cold‐sintered NaCl ceramic under the applied pressure of 300 MPa, indicating that it is a promising candidate as a microwave dielectric material.     

Influence of processing atmosphere on the microstructural evolution of submicron alumina powder during sintering

Investigations into the sintering of submicron oxide powders have revealed interesting behavior, particularly insofar as it concerns their microstructural evolution in the early, low temperature transformations during heating. In this work, experiments were conducted on a submicron alumina powder, whose microstructural evolution and densification were characterized after sintering from 900 °C to 1400 °C in air, dry air and high vacuum (10⁻⁸ atm). The results indicated that the processing atmosphere strongly influences the particle size distribution at low temperatures before shrinkage occurs. Shrinkage began concomitantly with grain growth and the sintering atmosphere influenced the sintering kinetics. This factor, which is associated with previous narrowing of the particle size distribution, may affect grain growth and densification during the final stage of sintering.     

DC electric field-assisted hot pressing of zirconia: Methodology,phenomenology, and sintering mechanism

Flash sintering (FS) is an important technique in the field of ceramic sintering. Nevertheless, conventional FS is less attractive for practical applications because of the complex shapes and small sizes of the specimens. In this study, using the novel electric field-assisted hot pressing (FAHP) technique, we successfully achieved FS during the net-shape hot pressing (HP) process for the first time. It was found that the 3 mol% yttria-stabilized zirconia (3YSZ) can be flash sintered at 909°C using a fairly low DC field of 33 V/cm under 30 MPa pressure. The grain sizes of the FAHP-sintered samples were 20% smaller than that of the HP-sintered sample. When the current density limit is ≥240 mA/mm², 3YSZ can be fully densified during the flash events. Careful analysis of the sintering curves suggests that although the carrier type or concentration is changed during flash events, it cannot explain the ultrafast densification. Additionally, we devised a qualitative method to analyze the densification mechanism. The results indicated that the ultrafast densification observed during flash events resulted from the synergistic effects of the rapid heating rate and peak sample temperature. Finally, the atomic force microscopy confirmed the lower grain boundary energy for the FAHP-sintered samples, which accounts for the smaller grain sizes than the HP-sintered sample. We believe that the FAHP technique could create new possibilities for theoretical and applied research on field-assisted sintering techniques.     

Sintering Mechanisms and Kinetics for Reaction Hot‐Pressed ZrB2

Sintering mechanisms and kinetics were investigated for ZrB₂ ceramics produced using reaction hot pressing. Specimens were sintered at temperatures ranging from 1800°C to 2100°C for times up to 120 min. ZrB₂ was the primary phase, although trace amounts of ZrO₂ and C were also detected. Below 2000°C, the densification mechanism was grain‐boundary diffusion with an activation energy of 241 ± 41 kJ/mol. At higher temperatures, the densification mechanism was lattice diffusion with an activation energy of 695 ± 62 kJ/mol. Grain growth exponents were determined to be ~4.5, which indicated that a grain pinning mechanism was active in both temperature regimes. The diffusion coefficients for grain growth were 1.5 × 10^?16 cm⁴/s at 1900°C and 2.1 × 10^?15 cm⁴/s at 2100°C. This study revealed that dense ZrB₂ ceramics can be produced by reactive hot pressing in shorter times and at lower temperatures than conventional hot pressing of commercial powders.     

Theoretical analysis of experimental densification kinetics in final sintering stage of nano-sized zirconia

The experimental densification kinetics of 7.8 mol% Y₂O₃-stabilized zirconia was analyzed theoretically during isothermal sintering in the final stage. By taking concurrent grain growth into account, a possible value of the grain-size exponent n was examined. The Coble’s corner-pore model recognized widely was found not to be applicable for explaining the densification kinetics. The corner-pore model of n = 4 shows a significant divergence in the kinetics at different temperatures. Microstructural observation shows that most pores are not located at grain corners and have a size comparable to the surrounding grains. The observed pore structure is similar to the diffusive model where single pore is surrounded by dense body. The diffusive model combined with theoretical sintering stress predicts n = 1 or n = 2, which shows a good consistence to the measured densification kinetics. During sintering of nano-sized powder, it is found that the densification kinetics can be explained distinctively by the diffusive single-pore model.     

Kinetics and mechanisms for the densification and grain growth of the α-alumina fibers isothermally sintered at elevated temperatures

Understanding the densification and grain growth processes is essential for preparing dense alumina fibers with nanograins. In this study, the alumina fibers were prepared via isothermal sintering at 1200, 1300, 1400, and 1500 °C for 1–30 min. The phase, microstructure, and density of the sintered fibers were investigated using XRD, SEM, and Archimedes methods. It was found that the phase transformation during the isothermal sintering enhances the densification of Al₂O₃ fibers in the initial stage, while the pores generated during the phase transformation retard the densification in the later period. The kinetics and mechanisms for the densification and grain growth of the fibers were discussed based on the sintering and grain growth models. It was revealed that the densification process of the fibers sintered at 1500 °C is dominated by the lattice diffusion mechanism, while the samples sintered at 1200–1400 °C are dominated by the grain boundary diffusion mechanism. The grain growth of the Al₂O₃ fibers sintered at 1200–1300 °C is governed by surface-diffusion-controlled pore drag, and that sintered at 1400 °C is dominated by lattice-diffusion-controlled pore drag.     

Sintering behavior of calcium lanthanum sulfide ceramics in field‐assisted consolidation

In this study, calcium lanthanum sulfide (CaLa₂S₄, CLS) ceramics with the cubic thorium phosphate structure were sintered at different temperatures by field‐assisted sintering technique (FAST). Densification behavior and grain growth kinetics were studied through densification curves and microstructural characterizations. It was determined that the densification in the 850°C‐950°C temperature range was controlled by a mixture of lattice or grain‐boundary diffusion, and grain‐boundary sliding. It was revealed that grain‐boundary diffusion was the main mechanism controlling the grain growth between 950°C and 1100°C. The infrared (IR) transmittance of the FAST‐sintered CLS ceramics was measured and observed to reach a maximum of 48.1% at 9.2 μm in ceramic sintered at 1000°C. In addition, it was observed that the hardness of the CLS ceramics first increased with increasing temperature due to densification, and then decreased due to a decrease in dislocations associated with grain growth.     

Effect of nano CuO addition on the tribo-mechanical behavior of alumina ceramics in non-conformal contact

Sintering of alumina from 1500°C to 1650°C and tribo-mechanical properties at room temperature had been investigated using nano CuO as a sintering aid. Bulk density gradually increases with sintering temperature from 1500°C to 1600°C and is optimized at 1600°C, beyond this, bulk density does not significantly increase at 1650°C. The addition of 2 wt% CuO showed the best result on densification. Densification of about 97.74% was attained at 1600°C with the incorporation of 2 wt% CuO. Nano CuO at grain boundaries forms CuAl₂O₄ liquid which modifies the morphology of the grain and improves mechanical properties. The formation of self-lubricating tribo-film on the wear track results in a low coefficient of friction <0.2 and reduces specific wear rate. 4 wt% CuO addition increases contact tensile stress (σ_max) by 51.2% and high Hertzian contact pressure (P_max≈1.51 GPa) causes plastic deformation of wear track. The re-solidified strengthening bond phase on the wear track simultaneously increases in friction coefficient and wear resistance with CuO addition. The optimizing effect of CuO addition shows that 2 wt% significantly decreases wear rate, and increases hardness and fracture toughness.     

Densification of liquid phase sintered silicon carbide

The densification and phase formation of liquid phase sintered silicon carbide (LPSSiC) with 10 wt.% additives were investigated. The ratio of the Al₂O₃/Y₂O₃-additives was changed between 4:1 and 1:2. Densification was carried out by hot pressing and gas pressure sintering. The different densification routes result in different major grain boundary phases—aluminates in gas pressure sintered materials and silicates in hot pressed samples. Thermodynamic calculations were carried out to determine the amount of liquid phase during densification and for the interpretation of the results.     

Spark plasma sintering and hot pressing of ZTA-NbC materials – A comparison of mechanical and electrical properties

Zirconia toughened alumina can be made electrically conductive and thus electric discharge machinable by addition of a percolating dispersion of niobium carbide. In order to boost the productivity of the sintering process spark plasma sintering was tested at identical temperature and pressure but shorter dwell than in hot pressing. SPS sintering parameters for ZTA-NbC are developed and spark plasma sintered ceramics are compared to the hot pressed benchmark.During SPS a percolating NbC backbone of niobium carbide grains is formed which enhances electrical conductivity but impedes densification. Identical strength at however higher sintering temperature is achieved by SPS but the fracture resistance and hardness were always superior in hot pressed samples. The monoclinic content of zirconia grains in as fired SPS samples is higher despite smaller average grain size and the transformation toughening effect is less pronounced. SPS promises economic benefits due to shorter dwell and cooling cycles.     

Colloidal Processing of Zirconium Diboride Ultra‐High Temperature Ceramics

Colloidal processing of the Ultra‐High Temperature Ceramic (UHTC) zirconium diboride (ZrB₂) to develop near?net‐shaping techniques has been investigated. The use of the colloidal processing technique produces higher particle packing that ultimately enables achieving greater densification at lower temperatures and pressures, even pressureless sintering. ZrB₂ suspension formulations have been optimized in terms of rheological behavior. Suspensions were shaped into green bodies (63% relative density) using slip casting. The densification was carried out at 1900°C, 2000°C, and 2100°C, using both hot pressing at 40 MPa and pressureless sintering. The colloidally processed materials were compared with materials prepared by a conventional dry processing route (cold pressed at 50 MPa) and subjected to the same densification procedures. Sintered densities for samples produced by the colloidal route are higher than produced by the dry route (up to 99.5% relative density by hot pressing), even when pressureless sintering is performed (more than 90% relative density). The promising results are considered as a starting point for the fabrication of complex‐shaped components that can be densified at lower sintering temperatures without pressure.