Power-controlled flash spark plasma sintering of gadolinia-doped ceria

Electric field-assisted sintering (FAST) is a rapidly growing scientific and engineering domain. In the present paper, we describe the process of flash sintering (FS) in a configuration of classical spark plasma sintering (SPS) (graphite punch and boron nitride (BN) die), also called flash spark plasma sintering (FSPS). The densification process of Gd_0.1Ce_0.9O_2-x powder is studied in detail with a focus on the transition from FAST to FS. We discuss the electrical, geometrical, and thermal evolution of the process and the characteristics of the final compacts. Low electrical fields are sufficient for the onset of FS. Ceria is a material difficult to sinter by FAST techniques due to its known mechanochemical transformations. We observed the disintegration of pellets after experiments with well-pronounced flash event.     

Effect of titanium diboride on the homogeneity of boron carbide ceramic by flash spark plasma sintering

A novel method, namely flash spark plasma sintering (FSPS), combining flash sintering and electric field assisted sintering, was utilized to densify boron carbide/titanium diboride (B₄C/TiB₂) composites. Further, sintering homogeneity of the composites with different contents of TiB₂ was systematically investigated and theoretical model was built. Results indicated that addition of 50?wt% TiB2 led to the densification of B₄C/TiB₂ composite by up to 97.7% with regional range 1.9% at 1872?°C under pressure of 4?MPa in 60?s. The preferential pathway of TiB₂ network proves to disperse the central current and distribute thermal flow throughout the specimen possibly via tunneling, electronic field emission effect at first stage and lower-resistance composite pathway latter, contributing to the increased homogeneity.     

High‐temperature strength and plastic deformation behavior of niobium diboride consolidated by spark plasma sintering

Bulk niobium diboride ceramics were consolidated by spark plasma sintering (SPS) at 1900°C. SPS resulted in dense specimens with a density of 98% of the theoretical density and a mean grain size of 6 μm. During the SPS consolidation, the hexagonal boron nitride (h‐BN) was formed from B₂O₃ on the powder particle surface and residual adsorbed nitrogen in the raw diboride powder. The room‐temperature strength of these NbB₂ bulks was 420 MPa. The flexural strength of the NbB₂ ceramics remained unchanged up to 1600°C. At 1700°C an increase in strength to 450 MPa was observed, which was accompanied by the disappearance of the secondary h‐BN phase. Finally, at 1800°C signs of plastic deformation were observed. Fractographic analysis revealed a number of etching pits and steplike surfaces suggestive of high‐temperature deformation. The temperature dependence of the flexural strength of NbB₂ bulks prepared by SPS was compared with data for monolithic TiB₂, HfB₂ and ZrB₂. Our analysis suggested that the thermal stresses accumulated during SPS consolidation may lead to additional strengthening at elevated temperatures.     

Synthesis of dense NiZn ferrites by spark plasma sintering

Dense NiZn ferrites were fabricated by spark plasma sintering (SPS) at 900 °C and 20 MPa in short periods. The powder was densified to 98% of the theoretical density by the SPS process. The SPS disks exhibited a higher saturation magnetization (Ms), up to 272 emu/cm³, than did the disks sintered by the conventional process. A higher coercivity (Hci) was obtained when the green bodies were sintered by the SPS process for 5 min. A modest holding time is essential to obtain fine grain and uniformity in the SPS process. Secondary crystallization, inhomogeneous microstructure and intragranular pores were found as a result of the rapid sintering and relatively longer holding time in the SPS process. Infrared (IR) spectra were also measured in the range from 350 to 700 cm⁻¹ to study the efforts of the SPS process on NiZn ferrites.     

Consolidation by spark plasma sintering (SPS) of polyetheretherketone

The present study deals with the consolidation of an ultra‐high performance polymer, the poly(ether ether ketone) (PEEK), for structural applications, using the powder metallurgy (PM) way, and more precisely the Spark Plasma Sintering (SPS) processing. The effects of SPS parameters such as temperature, pressure, and dwell time on density and mechanical properties of PEEK were investigated via a Design of Experiments (DoE). A temperature of 250 °C, a pressure of 40 MPa, and a dwell time of 20 min have been identified as the optimal SPS process parameters. In these conditions, a density of 1.31 g / cm³ was reached and homogeneous mechanical properties in the volume determined by means of compression tests were found with a compressive modulus of 2.75 GPa, a yield strength of 134 MPa, and a maximum compressive strain of 43%. These results are better than those of commercial products obtained by injection molding. The pressure appears to be a significant parameter on PEEK properties and plays positive or negative roles according to the responses of DoE studied. To our knowledge, it is one of the first studies based on the application of the PM techniques for PEEK consolidation showing the possibility to process below its melting point. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44911.     

Consolidation by spark plasma sintering of polyimide and polyetheretherketone

This article presents two high‐temperature thermoplastic powders which were sintered by spark plasma sintering in order to get homogeneous mechanical properties. Dense polyimide (PI) and polyetheretherketone (PEEK) specimens were obtained at temperatures as low as 320°C for PI and 200°C for PEEK, respectively. Relative densities higher than 99% were reached for both materials. In order to characterize their properties, in situ measurements with compression and hardness tests were carried out on sintered samples. This method allowed to obtain polymeric materials with improved mechanical properties. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40783.     

Bulk boron carbide nanostructured ceramics by reactive spark plasma sintering

Bulk boron carbide (B₄C) ceramics was fabricated from a boron and carbon mixture by use of one-step reactive spark plasma sintering (RSPS). It was also demonstrated that preliminary high-energy ball milling (HEBM) of the B+C powder mixture leads to the formation of B/C composite particles with enhanced reactivity. Using these reactive composites in RSPS permits tuning of synthesized B₄C ceramic microstructure. Optimization of HEBM + RSPS conditions allows rapid (less than 30 min of SPS) fabrication of B₄C ceramics with porosity less than 2%, hardness of ~35 GPa and fracture toughness of ~ 4.5 MPa m ^1/2     

Densification kinetics of boron carbide with medium entropy alloy as a sintering aid during spark plasma sintering

The high sintering temperature of pure B₄C considerably limits its widespread application, thus searching an effective sintering aid is critical. In this work, B₄C-based ceramic with 1 vol.% nonequiatomic Fe₅₀Mn₃₀Co₁₀Cr₁₀ medium entropy alloy as a sintering aid were fabricated at 1900-2000°C by spark plasma sintering (SPS) under applied pressure, and their mechanical properties were examined and compared with pure B₄C ceramic sintered at same condition. The maximal flexural strength of 255.59 MPa, microhardness of 2297.6 Hv_0.2 and fracture toughness of 3.62 MPa m^1/2 could be obtained at optimized SPS pressure of 50 MPa, which were all higher than those of pure B₄C ceramic. To better understand the densification kinetics mechanisms, the densification ratio as a function of SPS temperature and pressure was theoretically analyzed using steady creep model. It was found that densification controlled by grain-boundary sliding at lower pressure transferred to power law creep regime at higher pressure, which were proved by the dislocation net shown in transmission electron microscopy image.     

Fabrication of translucent AlN ceramics with MgF2 additive by spark plasma sintering

Translucent AlN ceramics with 0‐2 wt.% MgF₂ additive were prepared by spark plasma sintering. AlN powder was heated temporarily up to 2000°C, before holding at 1850°C for 20 minutes in N₂ gas. The sintered ceramics consisted of a single phase of hexagonal AlN, and showed a transgranular fracture mode. The total transmittance was improved remarkably by the additive, to reach 74% at a wavelength of 800 nm for 1 wt.% MgF₂. For 2 wt.% MgF₂, the transmittance was slightly lower than that for 1 wt.% MgF₂, and an absorption band was observed apparently at around 400 nm. The addition of MgF₂ along with the temporary heating at higher temperatures than the sintering temperature contributed to improve the transmittance remarkably.     

Fabrication of ultra-high-temperature nonstoichiometric hafnium carbonitride via combustion synthesis and spark plasma sintering

In this study, nonstoichiometric hafnium carbonitrides (HfC_xN_y) were fabricated via short-term (5 min) high-energy ball milling of Hf and C powders, followed by combustion of mechanically induced Hf/C composite particles in a nitrogen atmosphere (0.8 MPa). The obtained HfC_0.5N_0.35 powder exhibited a rock-salt crystal structure with a lattice parameter of 0.4606 nm. The melting point of this synthesized ceramic material was experimentally shown to be higher than that of binary hafnium carbide (HfC). The nonstoichiometric hafnium carbonitride was then consolidated under a constant pressure of 50 MPa at a temperature of 2000 °C and a dwelling time of 10 min, through spark plasma sintering. The obtained bulk ceramic material had a theoretical material density of 98%, Vickers hardness of 21.3 GPa, and fracture toughness of 4.7 MPa m^1/2.     

Radio‐frequency negative permittivity in the graphene/silicon nitride composites prepared by spark plasma sintering

Graphene/silicon nitride (GR/Si₃N₄) ceramic composites with uniformly dispersed GR sheets were prepared using spark plasma sintering. The effects of GR content on the microstructure and electrical properties of the composites were investigated in detail. With the GR content rising, the conductive GR network was formed in the composites, leading to the appearance of a percolation phenomenon, and the conductive mechanism also changed from hopping conductivity to metal‐like conductivity. When the GR content reached the percolation threshold, the composites showed a negative permittivity behavior, which resulted from the low frequency plasmonic state generated by the formative conducting GR networks. The increasing GR content resulted in a higher plasma frequency and larger magnitude of negative permittivity, which was consistent with the analysis of Drude model. A relatively high dielectric loss was observed in the composites and mainly induced by the high leakage current among GR sheets. Our work is beneficial to expound the regulation mechanism of negative permittivity, and the obtained ceramic composites present some potential applications in microwave absorption, shielding and capacitors.     

Microstructure and properties of WC-8Co cemented carbides prepared by multiple spark plasma sintering

In this study, WC-8Co cemented carbides were prepared by spark plasma sintering. When the samples sintered at 1300℃ were cooled to room temperature, the samples were sintered multiple times at 1250℃. The changes in microstructure and mechanical properties of WC-8Co cemented carbides prepared by multiple spark plasma sintering were studied. The hardness of cemented carbides increased in the first two sintering, reaching 16.5 GPa. However, the hardness decreased seriously in the last two sintering. The attenuation rates of hardness were 6.2% and 2.5% due to the abnormal coarse grains. Furthermore, the crack path along the grain boundary was almost straight, causing a decrease in the indentation fracture toughness of cemented carbides. Additionally, the grains of cemented carbides were abnormally coarsened, and the morphologies of grains became unstable due to multiple sintering.     

Densification behaviour and physico-mechanical properties of porcelains prepared using spark plasma sintering

Porcelain powder was consolidated using spark plasma sintering (SPS) at a constant heating rate of 100°C?min^?1 to peak temperatures ranging from 1000 to 1200°C and was observed to sinter at relatively low temperature ～920°C under the SPS conditions while conventional sintering requires ～1050°C. SPS produced densification rates about 10 times greater than conventional sintering. The dwelling step at the optimal peak temperature was negligible due to rapid flow of the molten glass assisted by applied pressure. SPSed samples exhibited denser microstructures, resulting in improved physico-mechanical properties compared with conventionally sintered samples such as apparent bulk density improved from 2.38 to 2.48?g?cm^?3, Vickers hardness improved from 3–5 to 6–7?GPa, and fracture toughness improved from 2–3 to 4–6?MPa?m^1/2.     

Oxidation effects on spark plasma sintering of molybdenum nanopowders

Surface-oxidized molybdenum nanopowders are compacted by spark plasma sintering (SPS). The oxide impurity behavior is analyzed under various sintering temperatures. The densification mechanism of the nanopowders with a melted oxide phase is identified in situ by regression analysis of the experimental data on the temperature-dependent porosity change and on the SPS multistep pressure dilatometry. To increase the density of the compacted pellets, the nanopowders with the oxide phase are consolidated by SPS using the two in situ oxide removal methods: carbothermic reduction and particle surface cleaning by the electric current flow through the powders. The advantages and disadvantages of these methods in terms of the density, grain size, and mechanical properties of the final products are discussed.     

Preparation of bulk‐nanostructured UO2 pellets using high‐pressure spark plasma sintering for LWR fuel safety assessment

Nuclear fuel undergoes a significant restructuration during its lifetime in the nuclear reactor. Especially at the rim of the pellet, large UO₂ grains disintegrate into a nanosized material. In this paper, we focus on the preparation of bulk UO₂ with grain sizes below 100 nm to investigate the physico‐chemical properties of this so‐called “high burn up structure” (HBS). Preparation of bulk nanocrystalline materials is a challenge that can be overcome using the high‐pressure spark plasma sintering (HP SPS) technique. In‐house developed HP SPS with 500 MPa applied pressure was used for compaction of 11 nm UO₂ powder obtained by oxalate conversion. The procedure yielded dense (>90%) compacts with grain size as low as 34 nm for samples sintered at 800°C.     

Transparent Er2O3 ceramics fabricated by high-pressure spark plasma sintering

Fabrication of transparent Er₂O₃ ceramics was carried out by high-pressure spark plasma sintering (HP-SPS). The color and in-line transmittance of these ceramics was highly sensitive to the sintering parameters. Samples exhibited a strong pink or wine color after sintering at 1150 °C under 600 MPa or 1250 °C under 250 MPa, respectively. This was confirmed to be a result of oxygen vacancies created during the sintering process and high sensitivity of Er₂O₃ to the strong reducing atmosphere in the SPS apparatus. Post-sintering annealing in an air furnace led to elimination of oxygen vacancies and increased transparency. Additionally, the photoluminescence intensity and phosphorescence lifetime of annealed (pink) samples was higher and shorter, respectively, compared to that of the reduced (wine-colored) samples.     

Low-angle twist grain boundary in SrTiO3 fabricated by spark plasma sintering techniques

A SrTiO₃ bicrystal with a low-angle twist grain boundary was fabricated using the spark plasma sintering (SPS) instrument. The atomic and electronic structure of the grain-boundary core was characterized using scanning transmission electron microscopy techniques. It was determined that the boundary is comprised of 2 types of defects with distinct electronic structures: screw dislocations and dislocations with an [001] edge component. The dislocations with an [001] edge component dissociated into 2 partial dislocations, separated by a stacking fault consisting of 2 Ti–O layers. The screw dislocations are attributed to the twist component of the grain boundary, while dislocations with an [001] edge component are attributed to surface steps on the original (100) SrTiO₃ surfaces prior to diffusion bonding. The observed repeat distances between the dislocations with edge components along the grain-boundary plane are smaller than those discovered during traditional diffusion bonding experiments. The higher planar defect density observed in this study results partly from higher heating rates, lower processing temperatures, and shorter holding times during SPS processing.     

Ultraviolet emission transparent Gd:YAG ceramics processed by solid-state reaction spark plasma sintering

Transparent 1% Gd-doped YAG and YAG ceramics were synthesized via solid-state reaction spark plasma sintering using commercially available powder and TESO as a sintering additive. The highest in-line transmission values achieved were 77.1% at 550 nm and 80.6% at 800 nm in the 1% (at.%) Gd-doped YAG transparent ceramic with 99.90% relative density. Ultraviolet emission at 312.5 nm was observed in 1% Gd-doped YAG ceramic via photoluminescence excitation, making it a promising material for applications in solid-state UV devices.     

Electron spin resonance of transparent alumina ceramics fabricated by spark plasma sintering

Transparent α‐alumina ceramics are fabricated using spark plasma sintering. Paramagnetic defects related to the optical properties of the ceramics have been investigated using electron spin resonance (ESR) analyses. An isotropic ESR signal at g = 2.003 (S = 1/2) with a linewidth of 0.5 mT is formed during sintering. The g = 2.003 signal intensity has a weak correlation with the absorbance in the visible region but does not correlate with the real in‐line transmission (RIT) at 650 nm. An ESR signal with a fine structure attributed to Fe³⁺ was detected in both the α‐Al₂O₃ starting powder and the sintered ceramic samples. The degree of c‐axis orientation of the grains has been determined using the Fe³⁺ signal intensity, which depends on the angle between the directions of the c‐axis and the applied magnetic field. The ESR analysis indicated that the c‐axis tends to be oriented in the direction of the sintering pressure. The degree of c‐axis orientation was found to correlate with the RIT in highly densified ceramics.     

Atomic‐scale microstructure of Hf2Al4C5 ceramic synthesized by spark plasma sintering

A layered ternary carbide phase, Hf₂Al₄C₅, was successfully synthesized by spark plasma sintering method. Detailed (atomic‐scale) microstructure of the ternary carbide was investigated by aberration‐corrected scanning transmission electron microscopy and atomic‐resolution energy dispersive X‐ray spectroscopy. Hf₂Al₄C₅ crystal grains have elongated morphologies and are characterized with a high density of stacking faults with the insertion of additional (Al₄C₃) or (HfC) units. Periodic stacking of Hf₂Al₄C₅ and HfAl₄C₄ units along the [0001] direction is frequently observed in the Hf₂Al₄C₅ crystal, and it leads to the formation of Hf₄Al₁₂C₁₃, which consists of 2/3 Hf₂Al₄C₅ unit cell and 1/2 HfAl₄C₄ unit cell. In addition, Z‐shaped planar defects are observed in Hf₂Al₄C₅ grains, and the formation mechanism of the Z‐shaped defects was proposed as blocking effects of the Hf diffusion in Al₄C₃ by pre‐existing {1‐101} pyramidal stacking faults in Al₄C_3.