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Porous materials are useful as lightweight structures, bone substitutes, and thermal insulators, but exhibit poor mechanical properties compared to their dense counterparts. Biological materials such as bone and bamboo are able to circumvent this trade‐off between porosity and mechanical performance by combining pores at multiple length scales. Inspired by these biological architectures, a manufacturing platform that allows for the fabrication of Al2O3 foams and Al2O3/Al composites with hierarchical porosity and enhanced mechanical properties is developed. Macroscale pores are formed through the assembly of aluminum particles around templating air bubbles in wet foams, whereas the thermal oxidation of the metal particles above 800 °C generates porosity at the micrometer scale. After elucidating the mechanism of pore formation under different sintering conditions at the microscale, the mechanical performance of the resulting hierarchical foams using compression experiments and finite element simulations is evaluated. Porous materials manufactured via this simple approach are found to reach unparalleled mechanical properties with near‐zero sintering shrinkage and minimum loss in mechanical strength. The ability to produce macroscopic objects with ultrahigh strength at porosities up to 95% makes this an attractive manufacturing technology for the fabrication of high‐performance lightweight structures or advanced thermal and acoustic insulators. [ABSTRACT FROM AUTHOR]

We herein report a novel hierarchically porous ceramic foams derived from boehmite gel foams, which possess both high porosity and superior strength. The gel foams show excellent printability due to its predominant stability, high yield stress and storage modulus, which endows such foam material ideal ink for 3D printing lightweight and complex-shape materials via direct ink writing approach. The 3D printed ceramic foams possess programmable architecture assembled by porous filaments, uniform macro-pores with tunable size in the range of 4∼70 μm, as well as nanoscale pores in cell wall, after sintering at relatively low temperature of 1200–1300 °C. In this way, ceramic foams with high strength were achieved, attributed to the tiny grains, large amount of grain boundaries, uniform pores and hierarchical pore structure. Notably, the foams sintered below 1200 °C have significant advantage on specific surface area, which could reach up to 300-400 m2/g. [ABSTRACT FROM AUTHOR]

Ultralight ceramic foam materials with high porosity play an important role in increasingly hi‐tech areas due to the combinative merit of ceramic material and highly porous structure. So far, it remains challenging to fabricate alumina ceramic foams with extremely high porosity and high specific surface area that are comparable to aerogel materials by employing a low cost, eco‐friendly and convenient approach. For the first time, we propose the preparation of aerogel‐like ceramic foams with nanoscale cell wall and unprecedentedly high porosity using boehmite sol as both ceramic source and bubble interface stabilizer, based on sol nanoparticles stabilized foams using sodium lauryl sulfate (SDS) as modifier. The obtained ultra‐stable sol foams allow for the achievement of bulk foams with ultrathin cell wall with thickness in the range of 30‐90 nm, super‐high porosity up to 99%, and large specific surface area of 280 m2/g, which is attributed to the well‐organized assembly of nanoparticles at the liquid/air interfaces. This novel foam material demonstrates excellent adsorption ability for polar volatile organic gases (VOCs) due to its extremely high porosity and large specific surface area. Ultralgiht cellular ceramic foams composed of uniformly assembled nanoparticles with nanoscale cell wall. [ABSTRACT FROM AUTHOR]

Hierarchical structured porous ceramics have attracted tremendous research interests because of their numerous excellent properties including robust mechanical strength and large surface area. In this work, silicon carbide (SiC)‐based porous ceramics with three levels of pore hierarchy are fabricated from silicon particle‐stabilized foams and a subsequent one‐step calcination after they were embedded with coke. Three‐dimensional (3D) flexible nanofibrous network is adhered and wrapped on cell walls of porous ceramics, which is readily fine‐tuned and tailored by the temperature to provide optimized pore structure. The resultant SiC‐based porous ceramics present a density of 1.03 g/cm3 at a porosity of 72% with a large quantity of hierarchical micro‐ and macropores. This hierarchical structure leads to robust compressive strength (23.52 MPa) and large surface area (64.32 m2/g). The fabrication method is straightforward and sought‐after, providing a facile technical route for advanced hierarchical porous ceramics used in filtration and catalysis fields. [ABSTRACT FROM AUTHOR]

Herein, the advantage of single-shell hollow microspheres on forming pores has been exploited to acquire porous ceramics with homogeneous microstructure, while the hollow microspheres also acted as reaction source. Dispersant reaction method has been applied to realize the perfect combination between microspheres and Si3N4 particles, which could be attributed to the repulsion between particles is weakened, particles agglomerate together and holding microspheres among them tightly. Owing to the normal distribution of hollow spheres and their single-shell structure, porous Si2N2O-Si3N4 ceramics with uniform pore distribution have been fabricated. The results show that the addition of silica hollow spheres contributes to the decrease in dielectric constant, since their porosity could be increased effectively and Si2N2O phase exhibiting low dielectric constant is generated. High-performance porous Si3N4 ceramics with porosity of 45.7% have been prepared through employing fly ash hollow microspheres, which possess flexural strength of 108.76 ± 6.25 MPa, fracture toughness of 1.78 ± 0.09 MPa m1/2 and dielectric constant of 3.53. This strategy is proved to be a convenient, eco-friendly and effective method to synthesize ideal candidates for radomes. [ABSTRACT FROM AUTHOR]

An innovative approach for fabricating porous alumina ceramics (PACs) with improved mechanical and thermal properties using walnut shell powders as pore-forming agent combined with alumina sol impregnation is reported in the present work. It is demonstrated that uniform distribution of spherical pores can be observed in as-prepared PACs by using above technical route. The decrease of walnut shell powder sizes significantly promotes the enhancement of crushing strength and reduction of thermal conductivity of the PACs. Meanwhile, the impregnated alumina sol is favoring for the formation of spherical micro-pores, then further improves their mechanical and thermal insulation performances. The lowest thermal conductivity and highest crushing strength of resulting sample reach 0.16 W/m K and 29.2 MPa, respectively. This novel method offers new possibilities to fabricate high-quality PACs. [ABSTRACT FROM AUTHOR]

Abstract: In order to investigate the relationship between pore structure and thermal conductivity as well as mechanical strength, porous alumina ceramics (PAC) with various pore structures were fabricated, using starch as the pore‐forming agent. Fractal theory was employed to characterize the pore size distribution more accurately than ever used parameters. The results show that the increase in starch content in PAC leads to an enhanced porosity, a higher mean pore size, and reduced fracture dimension, thermal conductivity and strength. The fractal analysis indicated that the fractal dimension decreases gradually and reaches its minimum value with increasing the starch content up to 25 wt%, but the further incorporation results in an opposite trend. It is suggested from micro‐pore fractographic analysis that the optimization of both thermal insulation performance and mechanical strength are positively correlated with the increase in the mean pore size and proportion of 2‐14 μm pores but negatively corrected with the porosity. These results provide a new perspective and a deeper understanding for fabrication of PAC with both excellent thermal insulation and mechanical performance. [ABSTRACT FROM AUTHOR]

Compressive strength is one of the most important mechanical properties for ceramic foams but the dependence of compressive strength of highly porous ceramic foams on porosity remains unclear up to now, especially for the ceramic foams with porosity above 94%. In this paper, the relationship between compressive strength and porosity of ceramic foams with high porosity in the range of 79–98% was studied for the first time. The alumina ceramic foams and zirconia foams were prepared by particle-stabilized foaming method using sodium dodecyl sulfonate (SDS) as foaming agent. It was found that the function relation between compressive strength and porosity depended on porosity level. Specifically, compressive strength of ceramic foams fitted well with Rice Model when the porosity ranged from 79% to 94%. When the porosity increased above 95%, compressive strength of ceramic foams showed linear relation to porosity, which was probably due to the characteristic of highly porous ceramic foams with thin and lamellate cell wall. [ABSTRACT FROM AUTHOR]

Abstract: A novel method for fabrication of highly porous barium strontium titanate (BST) ceramic foams based on particle‐stabilized foaming method was developed for the first time, in which propyl gallate (PG) was employed as BST particle modifier. The results showed that the stability of wet BST foams closely depends on the pH value and PG concentration, which could be explained by the adsorption behavior of PG on BST particle surface. BST ceramic foams with dense, uniform, and closed pore and defect‐free wall were obtained. The pore size and porosity can be well controlled by adjusting solid loading and sintering temperature. It was revealed that not only sintering temperature but also solid loading significantly influenced the growth of BST grain. The BST ceramic foams exhibited high porosity in the range of 81%‐95%, low dielectric constant in the range of 47‐150, and low dielectric loss below 0.0025. The BST ceramic foams with higher porosity presented a tendency of lower dielectric constant and the fitting results indicated that the natural logarithm of dielectric constant was linear correlated with porosity. [ABSTRACT FROM AUTHOR]

The present work studied a simple direct foaming method for preparation of porous alumina ceramics by expansion of a ceramic suspension based on polyurethane (PU) foam system. The effects of polyurethane formulas including catalyst composition, blowing agent content, NCO index and solid content on the samples properties were investigated. The results showed that the homogeneity, porosity and mechanical properties are various for different formulas. The dried green bodies showed diametrical compressive strength in the range of 0.39-1.25 MPa and were amenable to machining operations such as milling, drilling and lathing. Meanwhile, PU formulas play an important role in the microstructures and mechanical properties of green bodies and sintered ceramic foams. Pyrolytic removal of polyurethane skeleton followed by sintering at 1550 °C produced alumina bodies with open cell porosity 54-75% and diametrical compressive strength 1.39-28.47 MPa. Microstructure showed both large (200-300 μm) and small (50-100 μm) pores all with various sizes of windows. Based on the optimization of polyurethane formulation, the porous alumina foam with porosity of 64% and compressive strength of 25.26 MPa was prepared. This polyurethane foam system is easily available and low-cost, which could be widely applied in preparation of other porous ceramics, such as ZrO2, SiO2, etc. [ABSTRACT FROM AUTHOR]

We prepared porous Si 3 N 4 ceramics with highly ordered and unidirectionally aligned channels by the self-organization method using an alginate template. The obtained samples show uniform pore distribution, high cell density, good mechanical strength and hierarchical pore structure. A great number of long fibrous β-Si 3 N 4 grains protrude into channels, and other short length fibrous β-Si 3 N 4 grains interlock within channel walls forming a peculiar hierarchical pore structure. The pore size, thickness of channel walls, cell density, porosity and mechanical properties of the sintered porous Si 3 N 4 ceramics could be controlled by choosing different solid loadings, whereas β-Si 3 N 4 grains growth could be controlled by adopting different sinter temperatures. [ABSTRACT FROM AUTHOR]