Porous yttria-stabilized zirconia ceramics with ultra-low thermal conductivity

Porous yttria-stabilized zirconia (ZrO₂-8 mol% Y₂O₃, YSZ) ceramics with ultra-low thermal conductivity (as low as 0.06 W/mK) could be fabricated by tert-butyl alcohol (TBA)-based gel-casting process with low solid loadings of 10 and 15 vol%. High porosity (52–76%) and fine pores with average pore size of 0.7–1.8 μm formed after sintering at 1350–1550 °C. These air-containing pores were believed to affect the through-thickness heat transfer propagation, resulting in low thermal conductivity. The thermal conductivity of porous YSZ ceramics with different porosities fits well with computed values derived from Effective Medium Theory (EMT).     

Effects of weak boundary phases (WBP) on the microstructure and mechanical properties of pressureless sintered Al2O3/h-BN machinable composites

Al₂O₃/h-BN machinable composites were fabricated by pressureless sintering at 1750 °C for 2 h in nitrogen atmosphere. The relative density of the sintered composites decreased, while the porosity increased with increasing h-BN content. By adding 20 vol.% h-BN to the composites, the porosity increased up to 16.7%. The effects of weak boundary phases (WBP), including h-BN and pores, on the microstructure, mechanical properties and machinability of the composites were investigated. The flexural strength, fracture toughness, Young's modulus and hardness of the composites decreased with increasing WBP content. When WBP content increased up to 18.8 vol.%, the composites can be machined easily by cemented carbide drills. Furthermore, the machining mechanisms of the composites were investigated using Hertzian contact tests.     

Differential Sintering and Self-Stress Effects on YSZ Ionic Conductivity

Thermomechanical stress simulations are combined with experimental tests to assess the effects of rigid inclusions on the sintering of 8 mol% yttria-stabilized zirconia (8YSZ) green compacts and the phenomena of restricted and differential sintering on microstructure development and electrical properties are investigated. Rigid inclusions of sintered ceramic particles with different shapes (spherical and jagged) and compositions (alumina, 3YSZ, and 8YSZ) are added in different volume fractions (1, 5, and 15 vol%) to 8YSZ commercial powders, which are formed by isostatic pressing and sintered by conventional method. Restricted and differential sintering effects are observed in the development of the microstructure varying in function of volume fraction, shape, structural composition, and thermomechanical properties of the inclusions, resulting in different combinations of tensile and compressive strain states in the matrix, and varying electrical behaviors. The addition of 1 vol% of 8YSZ irregular rigid inclusions leads to an increase of 36% in total electrical conductivity and a 33% increase in power density under solid oxide fuel cells operation conditions compared to samples without inclusions.     

Abnormal grain growth enhanced densification of liquid phase-sintered WC–Co in support of the pore filling theory

This study examines the effect of grain growth on densification during liquid phase sintering of compacts with faceted grains. Two kinds of WC powders with different sizes were used to produce WC–Co alloys. Large pores of ~5 μm size were generated in 95WC–5Co (wt%) using spherical Co particles of the same size. The overall sintering behavior was observed by measuring grain growth and densification as a function of sintering time at a sintering temperature of 1350 °C. When the WC powder was fine (0.4 μm), large pores disappeared upon filling of pores by liquid with the formation of abnormal grains. On the contrary, when the WC powder was large (4.2 μm), grain growth is not observed, and large pores remained intact even after a long period of sintering (24 h). These observations confirm that densification during final stage liquid phase sintering occurs via filling of pores by liquid as a result of grain growth. This finding is consistent with the model of densification predicted by the pore filling theory.     

Processing and compression testing of Ti6Al4V foams for biomedical applications

Open cell Ti6Al4V foams (60% porosity) were prepared at sintering temperatures between 1,200 and 1,350 °C using ammonium bicarbonate particles (315–500 μm) as space holder. The resulting cellular structure of the foams showed bimodal pore size distribution, comprising macropores (300–500 μm) and micropores (1–30 μm). Compression tests have shown that increasing sintering temperature increased the elastic modulus, yield and compressive strength, and failure strain of foams. The improvements in the mechanical properties of foams prepared using smaller size Ti64 powder with bimodal particle distribution were attributed to the increased number of sintering necks and contact areas between the particles. Finally, the strength of foams sintered at 1,350 °C was found to satisfy the strength requirement for cancellous bone replacement.     

Microstructure and abrasive wear behaviour of B<Subscript>4</Subscript>C particle reinforced 2014 Al matrix composites

In this study, the microstructure and abrasive wear properties of varying volume fraction of particles up to 12% B₄C particle reinforced 2014 aluminium alloy metal matrix composites produced by stircasting method was investigated. The density, porosity and hardness of composites were also examined. Wear behaviour of B₄C particle reinforced aluminium alloy composites was investigated by a block-on-disc abrasion test apparatus where the samples slid against the abrasive suspension mixture (contained 10 vol.% SiC particles and 90 vol.% oil) at room conditions. Wear tests performed under 92 N against the abrasive suspension mixture with a novel three body abrasive. For wear behaviour, the volume loss and specific rate of the samples have been measured and the effects of sliding time and the content of B₄C particles on the abrasive wear properties of the composites have been evaluated. The dominant wear mechanisms were identified using SEM. Microscopic observation of the microstructures revealed that dispersion of B₄C particles was generally uniform while increasing volume fraction led to agglomeration of the particles and porosity. The density of the composite decreased with increasing reinforcement volume fraction but the porosity and hardness increased with increasing particle content. Moreover, the specific wear rate of composite decreased with increasing particle volume fraction. The wear resistance of the composite was found to be considerably higher than that of the matrix alloy and increased with increasing particle content.     

Reaction-sintered porous mineral-based mullite ceramic membrane supports made from recycled materials

Bulk porous mullite supports for ceramic membranes were prepared directly using a mixture of industrial waste fly ash and bauxite by dry-pressing, followed by sintering between 1200 and 1550 °C. The effects of sintering temperature on the phase composition and shrinkage percent of porous mullite were studied. The XRD results indicate that secondary mullitization reaction took place above 1200 °C, and completed at 1450 °C. During sintering, the mixture samples first shrunk, then expanded abnormally between 1326 and 1477 °C, and finally shrunk again above 1477 °C. This unique volume self-expansion is ascribed to the secondary mullitization reaction between bauxite and fly ash. More especially, the micro-structural variations induced by this self-expansion sintering were verified by SEM, porosity, pore size distribution and nitrogen gas permeation flux. During self-expansion sintering, with increasing temperature, an abnormal increase in both open porosity and pore size is observed, which also results in the increase of nitrogen gas flux. The mineral-based mullite supports with increased open porosity were obtained. Furthermore, the sintered porous mullite membrane supports were characterized in terms of thermal expansion co-efficient and mechanical strength.     

Formation of porosity in ferritic ODS alloys on high temperature exposure

In order to investigate the formation, distribution, growth behavior and volume fraction of porosity at high temperatures in ferritic Oxide Dispersion Strengthened (ODS) superalloys MA 956, ODM 751 and PM 2000 were exposed at 1100 and 1200C in air and in 2% oxygen containing nitrogen atmospheres for up to 8760 h. All samples exhibited small amounts of porosity (% < 0.1) in the as-received condition. During the early stages of exposure (up to 10 h) pores were generally located close to the surface of the samples. Later they were found in the central region of the samples and the volume fraction of porosity and the mean pore size increased. After exposure for 240–1000 h, mainly depending on sample thickness, the size and volume fraction of porosity reached a maximum value and then decreased. SEM and EDS analysis results showed that some pores contained small amounts of Ti, Al and Y rich particles which were distributed over the internal surface of pores. It was noted that when the volume fraction of porosity and the size of pores began to decrease the pores had filled with the matrix material. A relation was established between the production environment of the materials and the growth behavior of the pores.     

WCCo/cBN composites produced by pulse plasma sintering method

WCCo/cBN composites have been considered as a next-generation material for use in cutting-tool edges, being characterized by an optimal combination of hardness and toughness. They can be used instead of WCCo/diamond composites in machining of iron-based materials. The major challenge in sintering these composites is to produce a well-bonded interface between the WCCo matrix and cBN particles. In this study, WCCo/cBN composites were fabricated by the pulse plasma sintering technique. The aim of this work is to obtain sintered parts with density near the theoretical value and with very good contact between the cBN particles and WCCo matrix. cBN/cemented carbide containing 30 vol.% of cBN particles was produced using a mixture of 6 and 12 wt.% Co-added WC powder, with WC grain size of 0.4 μm and cBN powder with grain size ranging from 4 to 40 μm. Scanning electron microscopy (SEM) observations of the microstructure and diffraction phase examinations did not show the presence of hBN phase. The specific heating conditions used to consolidate the material using high-current pulses hamper the transformation of cBN into hBN and ensure a strong bond between the cBN particles and the cemented carbide matrix. Fractures through the WCCo/cBN composite showed that only few cBN particles were torn out from the cemented carbide matrix, with most of them having been cleaved along the fracture plane. This provides evidence that the bond at the WCCo/cBN interface is mechanically strong. Composites sintered at temperature of 1,200 °C under pressure of 100 MPa for 5 min had density near the theoretical value. Increase of the sintering temperature to 1,200 °C resulted in an increase of the hardness to 2,330 HK1 for the WC6Co/cBN(1/3) composite and to 2,160 HK1 for the WC6Co/cBN(37/44) composite.     

Fabrication and mechanical properties of oriented SiC short-fiber-reinforced SiC composite by tape casting

SiC fiber-reinforced SiC composites with nearly unidirectionally and randomly aligned SiC short fiber were prepared by tape-casting and hot-pressing (HP). Volume fractions of fibers were 10 and 20 vol.%. Three-point bending test was carried out at room temperature. The SiC short-fiber-reinforced SiC composites showed completely brittle fracture for any fiber volume fraction and orientation. The maximum strength increased with increasing sintering temperature regardless of orientation of short fiber. In the unidirectionally and randomly aligned composites sintered at 1700 °C containing 20 vol.% fiber, the maximum bending strength was about 390 and 280 MPa, respectively.     

Mechanically alloyed Ni/8YSZ powder mixtures: preparation, powder characterization and sintering behavior

A state of the art anode for the solid oxide fuel cell (SOFC)consists of a mixture of 8 mol % Y2O3-stabilized zirconia (8YSZ) andnickel particles, which form an interconnected porous structure after sintering. Coarsening of the Ni particles under SOFC workingconditions has to be avoided, hence it leads to a deterioration of the anode's performance. In the present work the aim was to improve thestability of the Ni particles by a reduction of the sinteringactivity of nickel. For this purpose between 10 and 50 % by volume of nano-sized zirconia particleshave been dispersed in the nickel matrix by dry ball milling in a planetary mill.Forpressed samples made of mechanically alloyed Ni with 10 vol % of 8YSZ,a homogeneous dispersion of 8YSZ particles in the Ni matrix wasconfirmed by transmission electron microscopy. It was confirmed bymercury porosity penetration and optical microscopy that thisdispersoid structure leads to a retardation of recrystallization.Also, an essentially lowered densification during sintering was found, compared to samples made of the pure Ni powder. Samples made of mechanically alloyed Ni with a higher zirconia amountshowed a higher densification during sintering and annealing thansamples containing 10 vol % 8YSZ. It is assumed that this results frominsufficient dispersion in these systems. The results show that mechanically alloyed nickel,with a homogeneous dispersion of 8YSZ crystallites, is a promising candidate for high temperature catalysts.     

Sintering of fibrous barium titanate powder compacts with preferred orientation

The sintering of fibrous BaTiO₃ powder particles was investigated. Special emphasis was given to the role of particle orientation in the compact on densification and microstructure development. Compacts were made by dry-pressing. During the initial stage of sintering, the fibrous particles rearranged and bundles of particles were formed. The volume of pores between bundles of particles decreased on further heating. Grain growth started when the sintered density reached ca. 56% of the theoretical density. Higher temperatures of sintering increased the degree of the crystal axis orientation. Thus, highly orientated sintered bodies with high densities were prepared by heating at 1500 °C.     

Fabrication of PZT-polymer composite materials having 3-3 connectivity for hydrophone applications

Lanthanum-modified lead zirconate titanate (PZT) powder and volatilisable polymethylmethacrylate (PMM) polymer particles have been used for fabrication of porous sintered ceramics of interconnected porosity varying from 25% to 59%. Sintered ceramics are converted into piezoelectric PZT-polymer composites by incorporating silicone rubber elastomer followed by electroding and poling. Influence of the variation of PZT-PMM ratio and sintering temperatures on the open and closed porosity of the sintered ceramics as well as volume fraction PZT in the composites has been studied and correlated for the optimization of piezoelectric properties. The PZT-polymer composites possess low density, considerably high piezoelectric voltage coefficient and considerably lower ageing characteristics and are therefore considered suitable for designing highly sensitive hydrophone systems.     

Effect of sintering on thermally sprayed carbon nanotube reinforced aluminum nanocomposite

Reconsolidation of thermally spray formed (plasma and high velocity oxyfuel spraying) hypereutectic Al–Si nanocomposites with multiwalled carbon nanotube (MWCNT) reinforcement was carried out by inert atmosphere sintering for prolonged time periods. The sintering treatment resulted in the removal of porosity and residual stress, and increase in size and volume fraction of primary Si particles in the Al–Si matrix. The morphology of multiwalled carbon nanotubes in sintered nanocomposites remained unchanged after sintering. The interfacial ultrathin product layer of silicon carbide between MWCNT reinforcement and Al–Si matrix was unaltered. Microhardness and elastic modulus of the sintered nanocomposites were influenced by combined effect of multiple factors, i.e. reduction in porosity, residual stress removal and MWCNT distribution. Overall improvement of microhardness and elastic modulus of the sintered nanocomposites was observed. The experimentally measured elastic modulus values were compared with theoretically estimated values using micromechanics models.     

Aqueous tape casting of yttria stabilized zirconia

Tape casting process was used to produce yttria stabilized zirconia (YSZ) substrates in an aqueous system with poly(vinylalcohol) (PVA) and glycerine as binder and plasticizer, respectively. Various compositions of YSZ slips with different amounts of PVA and glycerine and consequently different solid/liquid ratios were prepared. The influence of the slip composition on the rheological properties of the slips was studied. In addition, the effect of the slip composition on the properties of the green and sintered tapes was investigated. PVA and glycerine did not affect the dispersion properties of the YSZ powder. Glycerine additions enhanced the flexibility of the green tapes but also produced a decrease in the tensile strength. The increase in the PVA content increased the tensile strength but resulted in a markedly decrease in the green density of the tapes. A correlation between the green and sintered density was found. The anisotropic sintering shrinkage parallel and perpendicular to the casting direction increased with increasing the PVA content. The slip compositions with 5 wt% PVA produced green tapes with satisfactory tensile strength. They had the highest sintered density, the lower sintering shrinkage and the lesser shrinkage anisotropy.     

Investigation of microstructure and mechanical properties of nano MgO reinforced Al composites manufactured by stir casting and powder metallurgy methods: A comparative study

In the present work, Al–nano MgO composites using A356 aluminum alloy and MgO nanoparticles (1.5, 2.5, and 5 vol.%) have been fabricated via stir casting and powder metallurgy (PM) methods. Different processing temperatures of 800, 850, and 950 °C for stir casting and 575, 600, and 625 °C for powder metallurgy were considered. Powder metallurgy samples showed more porosity portions compare to the casting samples which results in higher density values of casting composites (close to the theoretical density) compare to the sintering samples. Introduction of MgO nanoparticles to the Al matrix caused increasing of the hardness values which was more considerable in casting samples. The highest hardness value for casting and sintering samples have been obtained at 850 and 625 °C respectively, in 5 vol.% of MgO. Compressive strength values of casting composites were higher than sintered samples which were majorly due to the more homogeneity of Al matrix, less porosity portions, and better wettability of MgO nanoparticles in casting method. The highest compressive strength values for casting and sintered composites have been obtained at 850 and 625 °C, respectively. Scanning electron microscopy images showed higher porosity portions in sintered composites and more agglomeration and aggregation of MgO nanoparticles in casting samples which was due to the fundamental difference of two methods. Generally, the optimum processing temperatures to achieve better mechanical properties were 625 and 850 °C for powder metallurgy and stir-casting, respectively. Moreover, casting method represented more homogeneous data and higher values of mechanical properties compare to the powder metallurgy method.     

Fabrication of bimodal porous alumina ceramics

An alumina foam with two kinds of pores was prepared by combining the sponge method and the pore-former method. The large pores were provided by the sponge method, and their sizes were in the range of 1-2 mm. The small pores were produced by the pore-former method with size in the micrometer range. The large pores offered a high porosity while the small pores offered a large surface area. The strength of samples sintered at different temperatures was measured, and the effect of sintering temperature on foam strength was analyzed by discussing porosity and grain bonding area. The sample sintered at 1550 °C has a compressive strength of 1.3 MPa and a porosity of 86%.     

Al/SiC composite coatings of steels by thermal spraying

Thermal spraying has been used to coat carbon steels (F112) and austenitic stainless steels (AISI 304) with aluminium matrix composites. Mixtures of aluminium powder and SiC particles were used as spraying material. A sol-gel silica coating was laid on SiC particles to reduce the porosity of the composite coatings and to inhibit the formation of aluminium carbide. The sol-gel silica coating acts as an active barrier enhancing the wettability of the reinforcement by molten aluminium. Coatings with a reinforcement volume fraction up to 30 vol.% were obtained with porosities of about 1.0 vol.%. The incorporation of sol-gel silica coated SiC particles reduces the coefficient of thermal expansion of the composite coating and enhances its adhesion to the substrates more than when uncoated SiC particles were used.     

La2O3-Y2O3-ZrO2纳米陶瓷粉末的制备及高温相稳定性

用化学共沉淀法制备4.5%Y2O3-ZrO2(YSZ)和0.6%La2O3-YSZ、0.8%La2O3-YSZ、1.2%La2O3-YSZ(0.6La、0.8La、1.2La)(摩尔分数)纳米复合陶瓷粉末,研究了四组粉末的高温相稳定性.结果表明:采用正向滴淀方法制备的0.6La粉末(粒径～50 nm)团聚严重,而用反向...     

Selective laser sintering of gas atomized M2 high speed steel powder

Selective laser sintering of the gas atomized M2 high speed steel powder was performed using laser powers of 2.5–100 W, scan rates of 1–30 mm/s and scan line spacings of 0.15–0.75 mm. With increasing laser power, the sintered surface varied from open/closed pores to a fully dense structure. Large lateral pores were found in the sintered surface of samples using high scan rates. For fully dense samples, smooth surfaces could be achieved using large scan line spacing. The as-supplied and sieved M2 powder particles with size ranging from 0.04 to 400 m and 53 to 150 m, respectively, were found to give better laser sinterability as compared with those powder particles with finer (<38 m) or coarser (>150 m) sizes.