Preparation and properties of high-porosity ZrB2-SiC ceramics by water-based freeze casting

The development of novel cermet composites based on porous ceramics with high porosity, interconnected pore structure and good mechanical property has attracted considerable attention in engineering application. In this work, water-based freeze casting process was employed to fabricate ZrB₂-SiC porous ceramic with aligned lamellar-channels structure using PAA-NH₄ as the dispersant. The results revealed that the well-dispersed suspension with best rheological behavior was obtained using 1.0 wt% PAA-NH₄ at pH 9. The crack-free porous ceramic exhibited small volume shrinkage ranging from 2.59 % to 1.87 %. By varying the solid loading, the fabricated samples displayed a tailored porosity ranging from 76.12% to 59.37% and an excellent compressive strength of 7 MPa to 78 MPa. After oxidation, the samples displayed a decreased porosity and an increased compressive strength. The ZrB₂­SiC porous ceramic fabricated in this work will be a promising candidate for the framework of cermet composite.     

Fabrication of porous magnesium spinel with directional pores by unidirectional solidification

A porous magnesium spinel (MgAl₂O₄) with directional pores was fabricated by unidirectional solidification in pressurized argon and hydrogen mixed gases. Two different kinds of pores with large directional and small facet shape were formed in the solidified samples. The former pores were dominant in the porous structure. A small amount of free corundum phase was formed in the solidified porous spinel as a secondary phase by vaporization of MgO component during the solidification process. With increasing total gas pressure, the pore size of the solidified samples decreased while no change in the porosity. The porosity and pore size of the samples increased with increasing hydrogen partial pressure. The porosities of the samples fabricated under 10%H₂–90%Ar and 1%H₂–99%Ar mixed gases were 30 and 10%, respectively, and that under Ar atmosphere was very low, non-porous.     

New multifunctional porous Yb2SiO5 ceramics prepared by freeze casting

New porous Yb₂SiO₅ ceramics were prepared by a water-based freeze casting technique using synthesized Yb₂SiO₅ powders. The prepared porous Yb₂SiO₅ ceramics exhibit multiple pore structures, including lamellar channel pores and small pores, in its skeleton. The effects of the solid content and sintering temperature on the pore structure, porosity, dielectric and mechanical properties of the porous Yb₂SiO₅ ceramics were investigated. The sample with 20 vol% solids content prepared at 1550 °C exhibited an ultra-low linear shrinkage (i.e. 4.5%), a high porosity (i.e. 79.1%), a high compressive strength (i.e. 4.9 MPa), a low dielectric constant (i.e. 2.38) and low thermal conductivity (i.e. 0.168 W/(m K)). These results indicate that porous Yb₂SiO₅ ceramics are good candidates for ultra-high temperature broadband radome structures and thermal insulator materials.     

Fabrication and characterization of cordierite-bonded porous SiC ceramics

A reaction bonding technique was used for the preparation of cordierite-bonded porous SiC ceramics in air from α-SiC, α-Al₂O₃ and MgO, using graphite as the pore-forming agent. Graphite was burned out to produce pores and the surface of SiC was oxidized to SiO₂ at high temperature. With further increasing the temperature, SiO₂ reacted with α-Al₂O₃ and MgO to form cordierite. SiC particles were bonded by the cordierite and oxidation-derived SiO₂. The reaction bonding characteristics, phase composition, open porosity, pore size distribution and mechanical strength as well as microstructure of porous SiC ceramics were investigated. The pore size and porosity were strongly dependent, respectively, on graphite particle size and volume fraction. The porous SiC ceramics sintered at 1350 °C for 2 h exhibited excellent combination properties, the flexural strength of 26.0 MPa was achieved at an open porosity of 44.51%.     

Preparation of self-reinforcement of porous mullite ceramics through in situ synthesis of mullite whisker in flyash body

Self-reinforced porous mullite ceramics were fabricated by a starch consolidation method with flyash, different aluminium sources (Al(OH)₃ and Al₂O₃) and the additive AlF₃ as raw materials. The reinforcement mechanism of needle-like mullite whiskers through in situ synthesis in ceramic body was investigated. The bulk density, apparent porosity and bending strength of the samples were tested. Phase compositions and microstructures of the sintered samples were measured by XRD and SEM, respectively. It showed that AlF₃ as additive was helpful to the formation of mullite whiskers at a low temperature. As the aluminium sources, Al(OH)₃ was more suitable for the preparation of mullite whiskers than Al₂O₃. The in situ synthesized mullite whiskers formed an interlocking structure, which enhanced the mechanical strength of the porous mullite ceramics. Porous mullite ceramics with bending strength of about 100 MPa and apparent porosity of about 55% were made at 1550 °C.     

Mechanical behavior of ferroelastic porous La0.6Sr0.4Co0.2Fe0.8O3−δ prepared with different pore formers

The present work investigated the mechanical behavior of porous La_0.6Sr_0.4Co_0.2 Fe_0.8O_3−δ LSCF under uniaxial compression. The porous (LSCF) samples with the same grain size but different porous structures with 1.5–41% of porosity were prepared using three different pore formers. All the samples had ferroelastic domains and exhibited ferroelastic mechanical behaviors under uniaxial compression. Initial and loading moduli as well as critical stress monotonically decreased and remnant strain increased with increasing the porosity. The initial modulus can be determined by the actual porosity regardless of porous structure or grain size, whereas the other properties were more sensitive to experimental condition such as loading rate and maximum applied stress. Compressive fracture strength could be significantly influenced by porous structure.     

Preparation and properties of porous SiC–Al2O3 ceramics using coal ash

In this paper, we first reported that porous SiC–Al₂O₃ ceramics were prepared from solid waste coal ash, activated carbon, and commercial SiC powder by a carbothermal reduction reaction (CRR) method under Ar atmosphere. The effects of addition amounts of SiC (0, 10, 15, and 20 wt%) on the postsintering properties of as-prepared porous SiC–Al₂O₃ ceramics, such as phase composition, microstructure, apparent porosity, bulk density, pore size distribution, compressive strength, thermal shock resistance, and thermal diffusivity have been investigated. It was found that the final products are β-SiC and α-Al₂O₃. Meanwhile, the SEM shows the pores distribute uniformly and the body gradually contacts closely in the porous SiC–Al₂O₃ ceramics. The properties of as-prepared porous SiC–Al₂O₃ ceramics were found to be remarkably improved by adding proper amounts of SiC (10, 15, and 20 wt%). However, further increasing the amount of SiC leads to a decrease in thermal shock resistance and mechanical properties. Porous SiC–Al₂O₃ ceramics doped with 10 wt% SiC and sintered at 1600°C for 5 hours with the median pore diameter of 4.24 μm, room-temperature compressive strength of 21.70 MPa, apparent porosity of 48%, and thermal diffusivity of 0.0194 cm²/s were successfully obtained.     

High strength porous alumina by spark plasma sintering

High strength porous alumina was fabricated by spark plasma sintering (SPS) at temperatures between 1000 and 1200 °C with nanocrystalline Al(OH)₃ as the starting powder without any seeds, dopants or inclusions. Decomposition of the Al(OH)₃ produced a series of transitional alumina phases depending on sintering temperature and pressure and finally the stable α-alumina phase was obtained. A network of continuous pores with unimodal pore size distribution was estimated by mercury porosimetry and BET surface area measurements, with the porosity ranging between 20% and 60% based on sintering conditions. Predominance of fine grains and extensive necking between them led to better strength in the sintered samples. The bending strength of the sintered compacts rapidly increased with sintering temperature while retaining reasonable porosity suitable for practical applications. The results clearly indicate that in situ phase formation of α-Al₂O₃ and θ-Al₂O₃ provides strength and porosity, respectively. Phase transformation, pore morphology and microstructure evolution were also studied.     

High performance porous silicon nitrides

In structural materials, pores are generally believed to deteriorate the mechanical reliability. This study, however, demonstrates pores can cause improved or unique performance when the porous microstructure is carefully controlled. The first example is a silicon nitride of 14% porosity fabricated by tape-castng whiskers. This material, where the characteristic fibrous grains were aligned uniaxially, shows a high fracture strength in excess of 1 GPa as well as high damage tolerance. The fracture energy obtained by a chevron-noteched beam technique was about seven times larger than that of dense silicon nitride, which was primarily attributable to grain “pull-out” mechanism enhanced by the pores. The other example was a silicon nitride of 24% porosity, fabricated by sinter forging technique which exhibited excellent strain tolerance.     

Structure and properties of Al2O3-bonded porous fibrous YSZ ceramics fabricated by aqueous gel-casting

To meet requirements for high porosity and high strength, novel aqueous gel-casting process has been successfully developed to fabricate Al₂O₃-bonded porous fibrous YSZ ceramics with ρ-Al₂O₃ and YSZ fibers as raw materials. Microstructure, phase composition, apparent porosity, bulk density, thermal conductivity, and compressive strength of fabricated porous ceramics were investigated, and effects of fiber content on properties were discussed. According to results, bird nest 3D mesh with interlaced YSZ fibers and Al₂O₃ binder was formed, ensuring the ability to obtain high performance, lightweight ceramics. An increase in the number of YSZ fibers led to more complex interlaced arrangement of fibers and denser network structure of porous ceramics at retaining their stability. Furthermore, their apparent porosity and bulk density increased, whereas thermal conductivity and compressive strength decreased with increasing the fiber content. In particular, comparatively high porosity (71.1–72.7%), low thermal conductivity (0.209–0.503 W/mK), and relatively high compressive strength (3.45–4.24 MPa) were obtained for as-prepared porous ceramics, making them promising for applications in filters, thermal insulation materials, and separation membranes.     

Mechanical property and gas filtration behavior of porous reaction bonded Si3N4 with monodispersed PMMA as pore former

Porous Si₃N₄ ceramics were prepared by gel casting combined with a reaction bonding route using monodispersed PMMA as the pore former, and Isobam was used as a gel agent. With the PMMA addition varying from 0 to 20 wt.%, the bending strength was degraded from 94.0 to 39.1 MPa owing to the increased porosity and decreased bulk density. The β-Si₃N₄ prismatic grains and round pores introduced by the monodispersed PMMA micro balls would endow the samples with high strength, and the permeability of the resulting samples was increased obviously with the increase of PMMA addition. Flue gas filtration test exhibited that the filtration efficiency of the porous ceramics filter was not degraded with introducing of the PMMA pore former, even though the permeability was increased obviously. The block type of the sample with 20-wt.% PMMA additions during filtration was cake filtration, which indicates that the sample has the characteristic of being reusable after back-blowing in flue gas filtration applications. Porous Si₃N₄ with high strength and permeability fabricated via the reaction bonding route exhibits great potential for low-cost high-performance ceramics filters.     

Synthesis and characterization of mullite-ZrO2 porous fibrous ceramic for highly efficient oil-water separation

This work aimed to proposing a new strategy for preparing the mullite-ZrO₂ porous fibrous ceramic used as alternative matrix material for oil-water separation by the aqueous gel-casting method. The properties of the fabricated porous fibrous ceramics in terms of microstructure, phase composition, apparent porosity, bulk density and compressive strength were investigated and the separation behavior was predicted by analyzing the structural changes. It is demonstrated that the phase composition of green bodies consisted of bayerite, boehmite, ZrSiO₄ and YSZ, and the sintered sample contained mullite, ZrO₂ and YSZ. As the YSZ fibers increased, the porosity of the fabricated porous ceramic increased with the maximum value of 70.65% due to the formation of more pores caused by YSZ fibers. Moreover, a significant increase in compressive strength (up to 9.52–21.86 MPa) was observed with the increase of YSZ fibers. Therefore, the fabricated porous ceramics could be appropriative for advanced applications of separation membranes for oil-water separation.     

Synthesis of chemically bonded porous ceramics from MgO–C refractory bricks waste

Chemically bonded ceramics (CBCs) obtained from industrial waste have attracted great interest in recent years. In the present work, MgO raw material was substituted with refractory MgO–C bricks waste (MgW) for CBCs. Monopotassium phosphate (KDP) and MgW were used as binder systems with varied component ratios (KDP/MgW) of 0.17–0.33 (mass basis) and waste (MgO–C) particles with D50 = 20.5 μm. Bodies containing K-struvite phase (MgKPO₄·6H₂O), with compressive strength ranging from 1 to 1.4 MPa, were obtained. The total porosity ranged between 60 and 74%. Air permeability tests proved the presence of interconnected pores because the coefficients k₁ and k₂ increased with the increasing total porosity of the samples. The leaching test showed that the waste and the samples were nonreactive, nontoxic, and nonhazardous according to the Brazilian standard. The results showed that MgW-based chemically bonded porous ceramics can be produced from MgO–C refractory brick waste via synthesis processes for using as filters.     

In-situ growth of mullite whiskers and their effect on the microstructure and properties of porous mullite ceramics with an open/closed pore structure

Porous mullite ceramics with an open/closed pore structure were prepared by protein foaming method combined with fly ash hollow spheres. Both the open porosity and total porosity of samples were enhanced by increasing the hollow sphere content. Mullite whiskers with a diameter of 0.2–4 μm were grown in-situ in the porous mullite ceramics with an AlF₃ catalyst, conforming to a vapor-solid growth mechanism. The pore structure of the porous mullite ceramics was significantly affected by the mullite whiskers which increased the open porosity and total porosity. Moreover, the median pore size was reduced from 65.05 μm to 36.92 μm after the introduction of mullite whiskers. The flexural strength and the thermal conductivity of the samples decreased with increasing total porosity. The porosity dependence of the thermal conductivity was well described by the universal model, providing a reference for the prediction of thermal conductivity of porous ceramics with open/closed pores.     

Properties of porous zirconia ceramics fabricated by using various pore-forming agents

The present work proposes a new method for fabrication partially stabilized porous zirconia ceramics using monoclinic zirconia as raw material, yttrium nitrate and magnesium compounds as pore-forming agents and stabilizers. Effects of different pore-forming agents, firing temperatures and firing time on properties of samples were investigated. Thermal decomposition of yttrium nitrate and magnesium compounds creates a large number of pores, and thus porous zirconia ceramics were fabricated. ZrO₂ can be partially stabilized by Y₂O₃ and MgO derived from the precursors. The porous ZrO₂ ceramics obtained by using Y(NO₃)₃·6H₂O and 4MgCO₃·Mg(OH)₂·6H₂O as pore-forming agents had relatively high stabilization ratio, uniform pores and high strength. The optimum firing temperature and firing time are 1400 °C and 3 h, and the samples have the stabilization ratio of 45.7%, high cold crushing strength (26 MPa), uniform pores, and apparent porosity is about 40%.     

Investigating the effect of porosity level and pore former type on the mechanical and corrosion resistance properties of agro-waste shaped porous alumina ceramics

The strength integrity and chemical stability of porous alumina ceramics operating under extreme service conditions are of major importance in understanding their service behavior if they are to stand the test of time. In the present study, the effect of porosity and different pore former type on the mechanical strength and corrosion resistance properties of porous alumina ceramics have been studied. Given the potential of agricultural wastes as pore-forming agents (PFAs), a series of porous alumina ceramics (Al₂O₃-xPFA; x=5, 10, 15 and 20 wt%) were successfully prepared from rice husk (RH) and sugarcane bagasse (SCB) through the powder metallurgy technique. Experimental results showed that the porosity (44–67%) and the pore size (70–178 µm) of porous alumina samples maintained a linear relationship with the PFA loading. Comprehensive mechanical strength characterization of the porous alumina samples was conducted not just as a function of porosity but also as a function of the different PFA type used. Overall, the mechanical properties showed an inverse relationship with the porosity as the developed porous alumina samples exhibited tensile and compressive strengths of 20.4–1.5 MPa and 179.5–10.9 MPa respectively. Moreover, higher strengths were observed in the SCB shaped samples up to the 15 wt% PFA mark, while beyond this point, the silica peak observed in the XRD pattern of the RH shaped samples favored their relatively high strength. The corrosion resistance characterization of the porous alumina samples in hot 10 wt% NaOH and 20 wt% H₂SO₄ solutions was also investigated by considering sample formulations with 5–15 wt% PFA addition. With increasing porosity, the mass loss range in RH and SCB shaped samples after corrosion in NaOH solution for 8 h were 1.25–3.6% and 0.44–2.9% respectively; on the other hand, after corrosion in H₂SO₄ solution for 8 h, the mass loss range in RH and SCB shaped samples were 0.62–1.5% and 0.68–3.3% respectively.     

Extrusion of highly porous silicon nitride ceramics with bimodal pore structure and improved gas permeability

Highly porous Si₃N₄ ceramics with bimodal pore structure were prepared by the extrusion processing with petroleum coke of 30 μm as pore‐maker. The microstructure, mechanical strength, and gas permeability were investigated. The microstructure with petroleum coke contained not only numerous fine pores by interlocking the high aspect ratio β‐Si₃N₄ grains, but also some large pores of 15‐25 μm left by the burnout of petroleum coke. The resultant samples obtained an improved gas permeability of 1.2 × 10^?12 m², which is approximately two times that of samples without petroleum coke addition. Furthermore, the mechanical strength is still superior even at a porosity of 67% in comparison with the other porous ceramics used in the current diesel particulate filter.     

Ferroelastic mechanical behaviour of porous La0.6Sr0.4Co0.2Fe0.8O3−δ

The present study investigates the mechanical behaviour of ferroelastic La_0.6Sr_0.4Co_0.2Fe_0.8O_3−δ with porosity ranging from 0.9% to 26.1% under uniaxial compression at room temperature. Both dense and porous samples have ferroelastic domains and exhibit ferroelastic mechanical behaviour. The apparent modulus, compressive strength and critical stress of the material dramatically decrease with increasing porosity, exhibiting exponential relationships. Comparison of the mechanical behaviours of samples with similar porosity but different porous structures reveals that the ferroelastic mechanical behaviour depends not only on porosity but also structural factors such as pore size and distribution.     

Coherency strain induced hardening in bulk polycrystalline ceramics: A case study with MgO-based “ceramic alloys”

The role of coherency strain at the matrix/precipitate interface toward hardening of bulk polycrystalline “ceramic alloys” has been established here. Formation of “near ideal” bulk polycrystalline ceramic microstructure characterized by the presence of uniformly distributed coherent “ultra-fine” MgCr₂O₄ particles (size: ~25 nm) within matrix (MgO) grains was achieved via solid-state precipitation during aging treatment of bulk supersaturated MgO–Cr₂O₃ solid solutions (formed during pressureless sintering in air, followed by fast cooling). The as-aged MgO–MgCr₂O₄ “ceramic alloys” exhibited hardness increment by ~73% over that of phase pure bulk MgO upon aging for just 10 hours at 1000°C in air. Evidences toward the presence of significant coherency strains across the MgO/MgCr₂O₄ coherent interfaces were obtained with transmission electron microscopy. Analysis based on hardening mechanisms and comparisons with MgO–MgFe₂O₄ system, having lesser hardening due to lower misfit strain at MgO/MgFe₂O₄ coherent interfaces (despite greater content of second-phase particles), confirm the dominant role of coherency strains toward hardness enhancement in “ceramic alloys.”     

Preparation,mechanical, dielectric and microwave absorption properties of hierarchical porous SiCnw-Si3N4 composite ceramics

Herein, hierarchical porous SiC_nw-Si₃N₄ composite ceramics with good electromagnetic absorption properties were prepared. A porous Si₃N₄ matrix with different pore structures was first prepared by gelcasting-pressureless sintering (G-PLS) and gelcasting combined with particle stabilized foam-pressureless sintering (G-PSF-PLS). SiC_nw was then introduced by catalytic chemical vapor deposition (CCVD). An increase in solid loading (25–40 vol%) decreased apparent porosity (47.7–41.3%) and improved flexural strength (142.19–240.36 MPa) and fracture toughness (2.25–3.68 MPa·m^1/2). The addition of foam stabilizer propyl gallate (PG, 0.5–1.0 wt%) significantly increased apparent porosity (73.2–86.4%) and realized large-sized spherical pores, reducing flexural strength (58.23–38.56 MPa) and fracture toughness (0.75–0.41 MPa·m^1/2). High apparent porosity and large-sized pores facilitated the introduction of SiC_nw. The 25 vol% sample exhibited a reflection loss of ? 14.67 dB with an effective absorption bandwidth of 3.47 GHz, suggesting a development potential in the electromagnetic wave absorption field.