Ultralight Silicon Nitride Ceramic Foams from Foams Stabilized by Partially Hydrophobic Particles

Ultralight Si₃N₄ ceramic foams have been successfully prepared through particle‐stabilized foams method, which is based on the adsorption of in situ hydrophobized Si₃N₄ particles to the liquid/air interface of the foams. Here, we firstly used a long‐chain surfactant cetyltrimethylammonium chloride to render the Si₃N₄ particles partially hydrophobic. By tailoring the surfactant concentration and pH values of the suspensions, the wet foams were stabilized to avoid coarsening and coalescence. SEM results show that the Si₃N₄ ceramic foams possess single strut walls with elongated β‐Si₃N₄ grains interlocking with each other, and their pores are uniform with an average pore size of 95 μm. The obtained ceramic foams maintain compressive strength of 1.34 ± 0.13 MPa with porosity of 92.0%, when the suspension contains 3 mmol/L surfactant at the pH of 11.0.     

Flame retardancy of ceramic-based rigid polyurethane foam composites

In this work, ceramic fillers zirconia and alumina powder were incorporated in the rigid polyurethane foams derived from modified castor oil and their impact on the mechanical, thermal, and fire performances of composite foams have been analyzed. It was observed that the addition of ceramic filler showed improved mechanical and thermal properties and best properties were shown by 6% zirconia with compressive strength of 6.61 MPa and flexural strength of 5.72 MPa. Zirconia also demonstrated an increase in T_5% up to 260 °C. Cone calorimetry shows a decrease in peak of heat release from 118 to 84 kW m⁻² and 94 kW m⁻² by the incorporation of alumina and zirconia powder, respectively. Furthermore, total heat release (THR), smoke production rate (SPR), and total smoke release (TSR) were also found to decrease remarkably on the incorporation of ceramic fillers. So, these fillers have a great potential as an additive to incorporate good mechanical, thermal, and fire properties in bio-based rigid PU foams. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 48250.     

Processing of Particle-Stabilized Wet Foams Into Porous Ceramics

Direct foaming of colloidal suspensions is a simple and versatile approach for the fabrication of macroporous ceramic materials. Wet foams produced by this method can be stabilized by long-chain surfactants or by colloidal particles. In this work, we investigate the processing of particle-stabilized wet foams into crack-free macroporous ceramics. The processing steps are discussed with particular emphasis on the consolidation and drying process of wet foams. Macroporous alumina ceramics prepared using different consolidation and drying methods are compared in terms of their final microstructure, porosity, and compressive strength. Consolidation of the wet foam by particle coagulation before drying resulted in porous alumina with a closed-cell structure, a porosity of 86.5%, an average cell size of 35 μm, and a remarkable compressive strength of 16.3 MPa. On the other hand, wet foams consolidated via gelation of the liquid within the foam lamella led to porous structures with interconnected cells in the size range from 100 to 150 μm. The tailored microstructure and high mechanical strength of the macroporous ceramics can be of interest for the manufacture of bio-scaffolds, thermal insulators, impact absorbers, separation membranes, and light weight ceramics.     

Hierarchically porous lanthanum zirconate foams with low thermal conductivity from particle-stabilized foams

Lanthanum zirconate (LZO) ceramic foams with hierarchical pore structure were fabricated by particle-stabilized foaming method for the first time, and the as-prepared ceramics have high porosity of 90.7%-94.9%, low thermal conductivity, and relatively high compressive strength. The LZO powder was synthesized by solid-state method. The porosity of the ceramic foams was tailored by suspensions with different solid loadings (20-40 wt%). The sample with porosity of 94.9% has thermal conductivity of 0.073 W/(m·K) and compressive strength of 1.19 MPa, which exhibits outstanding property of thermal insulation and mechanical performance, indicating that LZO ceramic foam is a promising thermal insulation material in high temperature applications.     

Effect of zirconia content and particle size on the properties of 3D-printed alumina-based ceramic cores

Alumina-based ceramic cores are used to manufacture the internal structures of hollow alloy blades, requiring both high precision and moderate properties. In this work, zirconia is regarded as a promoter to improve the mechanical properties of sintered ceramic. The effect of zirconia content and particle size on the microstructure and mechanical properties of ceramics was evaluated. The results indicate that the flexural strength of sintered ceramics reached the maximum of 14.5 ± 0.5 MPa when 20 wt% micron-sized (10 μm) zirconia (agglomerate size, consistent with the alumina particle size) was added, and 26.5±2.5 MPa when 15 wt% 0.3 μm zirconia was added. Zirconia with submicron-sized (0.3 μm) particles effectively filled the pores between alumina particles, thus leading to the maximum flexural strength with a relatively low content. The corresponding sintered ceramics had a bulk density of 2.0 g/cm³ and open porosity of 59.6%.     

Mullite ceramic foams with tunable pores from dual-phase sol nanoparticle-stabilized foams

Particle-stabilized foams employing dual-phase sol of boehmite in combination with silica to prepare mullite ceramic foams has been proposed for the first time. The obtained mullite ceramic foams possess hierarchical pores, that is micropores derived from the air bubble templates and open windows formed by grain growth at thin area of pore wall according to the mullitization reaction. Furthermore, nanoparticles favor the improvement of specific surface area of ceramic foams, and wrinkles caused by drying shrinkage would retain when sintering at low temperature of 900℃-1100℃, leading to high specific surface area of 94.4-219.2 m²/g. The achieved mullite ceramic foams present relatively high compressive strength of 6.6?40.4 MPa at a high open porosity of 64.0 %–87.0 %, and their thermal conductivity could reach as low as 0.10 W/(m·K), which would make them promising lightweight materials applied in broad fields including thermal insulations, filters, bio-scaffolds, catalyst supports and the like.     

Manufacture of Si3N4-SiCN composite bulks with hierarchical pore structure

Si₃N₄-SiCN ceramic foams with hierarchical pore architecture were formed by protein-based gelcasting and precursor infiltration and pyrolysis. The primary pore structure (>100 μm) was generated by protein gelation and precursor ceramization, while the secondary pore structure (10–50 μm) originated from the cell windows after pyrolysis. The network of Si₃N₄ nanowires and the voids among ceramic particles formed the tertiary pore structure (<2 μm). The obtained Si₃N₄-SiCN ceramics had a density of 0.45–0.66 g/cm³ and an open porosity of 72.7–82.8 vol.%. The porous bulks possessed a compressive strength of up to 16.9 ± 1.1 MPa (72.7 vol.% open porosity) at room temperature and 8.6 ± 0.2 MPa at 800 °C. A good gas permeability of the ceramics was indicated with a tested value of 3.27 cm³cm/(cm²·s·kPa). The excellent mechanical property, permeability together with the hierarchical pore structure enabled the Si₃N₄-SiCN composite bulks promising for industrial filtration applications.     

Sintering behaviour and characterisation of low-cost ceramic foams from coal gangue and waste quartz sand

New ceramic foams have been successfully synthesised with coal gangue and waste quartz sand, which supply a feasible way to recycle these hazardous solid wastes. An objective of this research was to investigate the sintering behaviour and effects of sintering conditions on the crystalline phase change, microstructure and main properties of final ceramic foams. Good correlations among porosity, thermal conductivity, water absorption, bulk density, mechanical properties were studied. Results indicated that increasing sintering temperature or time had similar effects on the physical–mechanical properties. Samples sintering at 1140°C for 1 hour exhibited the highest porosity (87.5%), lowest bulk density (0.39?×?10^?3?kg?m^?3), lowest thermal conductivity (0.085?W·(m?K)^?1), moderate water absorption (9.38%) and adequate flexible strength (2.4?MPa). Combined with excellent properties and low-cost characteristics, the new development for ceramic foams preparation will be widely used in building insulation materials for no-load bearing walls.     

Compressive and thermal characterization of syntactic foams containing hollow silicon carbide particles with porous shell

Silicon carbide hollow particle (SiC_HS) reinforced vinyl ester matrix syntactic foams are prepared and characterized for compressive properties and coefficient of thermal expansion (CTE). Two types of SiC_HS were utilized in 60 vol % to prepare syntactic foams. These SiC_HS had ratio of inner to outer radius of 0.91 and 0.84 for the thin and thick walled particles. The specific compressive strength values were 33.4 and 38.8 kPa/kg/m³ and the specific compressive modulus values were 0.8 MPa/kg/m³ and 0.6 MPa/kg/m³ for the thin and thick walled SiC_HS‐filled syntactic foams, respectively. The shell of the hollow particles contained microporous voids, and the porosity was estimated as 16.6% and 24.8% in the walls of the thin and thick walled particles, respectively. The shell porosity adversely affected the specific compressive strength and the modulus of the syntactic foam. However, the SiC_HS‐filled syntactic foams exhibited low CTE values (26.7 and 15.9 × 10^?6/°C). These CTE values were 65.1% and 79.3% lower than the CTE of the neat resin. Such properties can be useful for applications where syntactic foams are exposed to high temperatures and dimensional stability is important. A theoretical model is used to estimate the porosity level in the SiC shells and estimate the effective mechanical properties of the porous SiC material that forms the particle shell. Such analysis can help in using the models as predictive tools to estimate the mechanical properties of syntactic foams. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40689.     

Fabrication of in-situ self-reinforced Si3N4 ceramic foams for high-temperature thermal insulation by protein foaming method

To meet demand for lightweight and high-strength ceramic foams, in-situ self-reinforced Si₃N₄ ceramic foams, with compressive strength of 13.2–45.9 MPa, were fabricated by protein foaming method combined with sintered reaction-bonded method. For comparison, ordinary protein foamed ceramics with irregular block microstructure were fabricated via reaction-bonded method, which had compressive strength of 3.6–20.5 MPa. Physical properties of these two types of samples were systematically compared. When open porosity was about 80%, both types of Si₃N₄ ceramic foams had excellent thermal insulation properties (<0.15 W m^?1 K^?1), while compressive strength of in-situ self-reinforced samples increased by more than 158% compared with ordinary samples. Under high-temperature oxidation conditions, microstructures of both types of samples were deformed with increase in oxidation temperature. Moreover, after oxidation temperature was increased to 1400 °C, oxidation weight gain decreased from 18.07% for ordinary samples to only 2.18% for self-reinforced samples. Thus, high-temperature oxidation resistance of Si₃N₄ ceramic foams was greatly improved.     

A novel way to fabricate fibrous mullite ceramic using sol-gel vacuum impregnation

Inspired by bird's nest structure, fibrous mullite ceramic was fabricated by vacuum impregnation with mullite fibers as raw material and zirconia sol-gel as inorganic binder. The effect of impregnation times on the properties of the fibrous mullite ceramic, such as porosity, microstructure, compressive strength and room-temperature thermal conductivity were investigated. The results showed that low density (0.45–0.66?g/cm³), relative high compressive strength (0.62–3.34?MPa) and low thermal conductivity (0.037–0.125?W/mk) were exhibited for the sample. The toughness of fibrous mullite ceramic was enhanced due to the micro-creaks caused by transformation of zirconia. From the experimental results, it is suggested that it was an optimal method which have the potential use in high-temperature thermal insulation materials to produce fibrous mullite ceramics.     

Highly porous YSZ ceramic foams using hollow spheres with holes in their shell for high-performance thermal insulation

Yttria-stabilized zirconia (YSZ) porous ceramic foams were fabricated using YSZ microspheres with holes on the surface to determine their properties as insulation materials. Highly porous YSZ ceramics with bimodal pore structures, such as internal pores in single hollow spheres and external pores between the spheres, were successfully prepared using YSZ spheres as raw materials. Additionally, holes were added to the shells to reduce continuous thermal pathways and significantly enhance the insulation properties. Furthermore, by adding holes on the surface of the sphere, the porous foams using a hollow sphere exhibit a maximized porosity of 80.69%, remarkably enhanced their insulation properties with low thermal conductivity (0.10 W/m-K), and have sufficient compressive strength to protect the green body (5.7 MPa). The mechanical strength of the YSZ porous foam was maintained owing to the uniform arrangement of the supports.     

New Sintered Li2O–Al2O3–SiO2 Ultra‐Low Expansion Glass‐Ceramic

We developed a new Li₂O–Al₂O₃–SiO₂ (LAS) ultra‐low expansion glass‐ceramic by nonisothermal sintering with concurrent crystallization. The optimum sintering conditions were 30°C/min with a maximum temperature of 1000°C. The best sintered material reached 98% of the theoretical density of the parent glass and has an extremely low linear thermal expansion coefficient (0.02 × 10^?6/°C) in the temperature range of 40°C–500°C, which is even lower than that of the commercial glass‐ceramic Ceran^® that is produced by the traditional ceramization method. The sintered glass‐ceramic presents a four‐point bending strength of 92 ± 15 MPa, which is similar to that of Ceran^® (98 ± 6 MPa), in spite of the 2% porosity. It is white opaque and does not have significant infrared transmission. The maximum use temperature is 600°C. It could thus be used on modern inductively heated cooktops.     

Effects of heating rate on the structure and properties of SiOC ceramic foams derived from silicone resin

Silicon oxycarbide ceramic foams were fabricated in a single step manufacturing process using in situ foaming of SiOC powders loaded silicone resin. The effects of heating rate on the porosity, compressive strength and microstructure of the ceramic foams were investigated. The porosity (total and open) increased firstly and then decreased with increasing heating rate. It was possible to control the total and open porosity of ceramic foams within a range of 81.9–88.2% and 62.4–72.5% respectively, by adjusting the heating rate from 0.25 °C/min to 3 °C/min while keeping the silicone resin content at 90 vol%. However, the compressive strength decreased with increasing the heating rate progressively, and the average compressive strength of the foams was in the range of 1.0–2.3 MPa. Micrographs indicated that the ceramic foams which cross-linked at a heating rate less than 1 °C/min had a well-defined open-cell and regular pore structure.     

High-porosity mullite ceramic foams prepared by selective laser sintering using fly ash hollow spheres as raw materials

A novel method to prepare high-porosity mullite ceramic foams by selective laser sintering (SLS) using fly ash hollow spheres (FAHSs) as raw materials was reported. The complex-shaped FAHS green bodies and ceramic foams without delamination or cracks were prepared by SLS. The influence of sintering temperatures on linear shrinkage, phase composition, porosity and mechanical properties was investigated. With the increase of sintering temperature from 1250?°C to 1400?°C, the compressive strength of ceramic foams increased from 0.2?MPa to 6.7?MPa causing the fracture mechanism change from fracturing along FAHSs to across FAHSs, while the porosity of ceramic foams decreased from 88.7% to 79.9% which was higher than those of ceramic foams prepared by the conventional methods. The relatively high porosity of ceramic foams was resulted from the inner hollow structure of FAHSs, the interspaces between stacking FAHSs, and the gaps between FAHSs directly related to SLS. The results above indicated that the fabrication of high-porosity FAHS ceramic foams by SLS could achieve the advanced utilization of FAHS solid waste.     

Fabrication of novel BPO4 ceramic foams using the combination of the direct foaming method and freeze-drying techniques

In this study, ammonium phosphate monobasic and boric acid were used as the primary starting materials to produce BPO₄ powder by solid-state reaction. Using BPO₄ powders as the main raw material, BPO₄ ceramic foams were prepared for the first time using the direct foaming method and freeze-drying techniques. The effects of the additive content and solid loading on the slurry's rheological behavior were investigated, and the microstructures and properties of the as-prepared BPO₄ ceramic foams were examined. The results reveal that the porosity of the BPO₄ ceramic foams synthesized at 1223 K ranged from 84.2% to 90.4%, the compressive strength ranged from .12 MPa to .72 MPa, and the thermal conductivity ranged from .32 W/(m·K) to .74 W/(m·K) (298 K). The findings of this study have great significance for the development of new thermal insulation ceramic materials.     

Facile processing of oriented macro-porous ceramics with high strength and low thermal conductivity

Unidirectionally oriented architectures demonstrate a notable efficiency in enhancing the properties of macro-porous materials, yet are difficult to construct in a time- and cost-effective fashion. Here a facile approach was exploited for fabricating oriented macro-porous ceramic materials by employing natural graphite flakes as a fugitive material and preferentially aligning the flakes within ceramic matrices using accumulative rolling technique. Flaky to near-ellipsoid shaped pores with a homogeneous distribution were created in macro-porous zirconia ceramics with their porosity and microstructural characteristics adjustable by controlling the additive amounts of graphite flakes. The resulting materials exhibited a good combination of properties with high compressive strength up to over 1.5 GPa, which exceeds those of most other porous zirconia ceramics with similar porosities, along with low thermal conductivity of 0.92–1.85 Wm^?1·K^?1. This study offers a simple means for developing new oriented macro-porous materials with enhanced properties, and may promote their application by allowing for easy mass production.     

Mechanical Properties of Silicon Oxycarbide Ceramic Foams

The mechanical properties of ceramic foams obtained through a novel process that uses the direct foaming and pyrolysis of preceramic polymer/polyurethane solutions were investigated. The elastic modulus, flexural strength, and compressive strengths were obtained for foams in the as-pyrolyzed condition; values up to 7.1 GPa, 13 MPa, and 11 MPa, respectively, were obtained. The strength of the foam was virtually unchanged at temperatures up to 1200°C in air; however, long-term exposure at 1200°C led to a moderate degradation in strength, which was attributed to the evolution of intrastrut porosity during the oxidation of residual free carbon, as well as devitrification of the foams struts.     

Highly porous silica foams prepared via direct foaming with mixed surfactants and their sound absorption characteristics

The highly porous silica ceramics were fabricated by direct foaming with mixed surfactants and the influence of silicon nitride addition and solid content on the microstructures and properties were investigated. The results showed that silicon nitride can impede the formation of cristobalite and facilitates the sintering of silica ceramics. When the addition of silicon nitride powders reached 15 wt%, the highest compressive strength of silica ceramic foams could be obtained. The porosity of silica ceramic foams was tailored in the range of 84.61%–91.35% by adjusting the solid content, and the compressive strength of the obtained ceramic foams ranged from 5.89 MPa to 0.94 MPa. Sound absorption characteristics of silica ceramics foams were investigated. With the porosity of ceramic foams increased from 84.61% to 91.35%, the sound absorption coefficients in the entire sound wave frequency were enhanced due to the reduction of flow resistances, besides, the sound absorption peak varied from 4200 Hz to 2300 Hz, and became more intense and sharper.     

Preparation and characteristics of porous anorthite ceramics with high porosity and high-temperature strength

High-temperature properties including compressive strength, thermal shock behavior, and thermal conductivity of porous anorthite ceramics with high specific strength were tested and analyzed. The results showed that the prepared materials merit high-temperature compressive strength, thermal stability, and conductivity. With the appropriate fabrication parameters, even though containing 0.33 g/cm³ bulk density and 88.2% porosity, its compressive strength could reach 2.03 MPa at 1000°C, 147% of that at room temperature; the residual strength ratio kept as 114.7% after a thermal shock at 1200°C. The X-ray diffraction (XRD), scanning electron microscope (SEM) and transmission electron microscope (TEM) showed that anorthite grains refinement and intergranular voids filling by liquid phase were main factors for the high strength. From room temperature to 1200°C, its thermal conductivity only varied from 0.085 to 0.258 W·(m·K)⁻¹. High porosity, a large number of nanoregions in anorthite grains and amorphous phase in grain boundary were main reasons for low thermal conductivity.