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Ceramic foams with significant porosity and robust mechanical properties have received extensive attentions. However, it is still difficult to achieve excellent compressive strength at high porosity levels. In this work, a gelation of foamed boehmite sol method is proposed to settle this issue. The technological parameters during preparation process are systematically investigated. As‐prepared alumina ceramic foams possess unprecedentedly high compressive strength of 34.1‐89.1 MPa at high porosity levels of 66.0%‐87.2%, which is attributed to the present of hierarchical pore structure, small grain size and pore size. This work demonstrates a facile and novel method for the fabrication of high‐performance alumina ceramic foams toward practical applications. [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]

Abstract The mechanical strength of highly porous ceramic foams shows significant attenuation with the increase of porosity, especially for ceramic foams with very high porosity level above 95%. Ultra-light bulk composite ceramic foams were fabricated via introducing 20 wt% zirconia in alumina-based cell wall, aiming at improving mechanical strength of alumina based ceramic foams. The preparation and stability of alumina and zirconia particles synergistically stabilized foams were investigated. The obtained bulk ceramic foams manifested an exciting combination of both high porosity above 96% and excellent specific compressive strength, due to their closed pore structure, defect-free cell wall with uniform thickness, and uniformly distributed zirconia grains in alumina matrix. The alumina/zirconia composite ceramic foams with porosity of 96.7% exhibited compressive strength of 1.11 ± 0.07 MPa, which was much higher than that of alumina ceramic foams in the case of same porosity. [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]

A novel approach to fabricate mullite ceramic foams with high porosity and mechanical strength using fly ash hollow spheres (FAHSs) as the only raw material was reported for the first time, in which FAHSs served as both matrix and pore-forming agent. It was demonstrated that uniform FAHS ceramic foams without cracks could be fabricated by both direct stack sintering method and gel-casting route. The effect of sintering temperature on linear shrinkage, porosity, phase composition and mechanical properties was investigated. With the increase of sintering temperature from 1200 °C to 1350 °C, the fracture mechanism changed from fracturing along FAHSs to fracturing across FAHSs, and the compressive strength of the FAHS ceramic foams increased from 4.4 MPa to 33.4 MPa. The FAHS ceramic foams exhibited high porosity in the range of 73–81% and high mechanical strength, which benefited from the dense assembling of small FAHSs with natural diameter distribution and excellent wall-thickness uniformity. [ABSTRACT FROM AUTHOR]

The weak compressive strength of dried ceramic foams is a disadvantage of fabricating ultralight ceramic foams, especially for the ceramic foams with porosity exceeding 95%. In this study, dried alumina foams were enhanced by agar and PVA-freezing-thawing using sodium dodecyl sulfate as surfactant. It is found that the two additives have no negative influence on adsorption of sodium dodecyl sulfate on alumina particles as well as the hydrophobic character of alumina particles. Stable alumina particle-stabilized foams were prepared with less than 0.5 wt% agar and 1.0 wt% PVA. High additive concentration above the critical values weakens stability of wet foams, which is probably due to the aggregate of alumina particles caused by long-chain molecules connecting. The compressive strength of dried alumina foams has a significant improvement with the employment of agar and PVA-freezing-thawing. The dried foams prepared with 1wt% PVA assisted by freezing-thawing has porosity of 97.1% and compressive strength of 0.16 MPa, which could maintain integrity of dried foams without destruction in the fabricating process. [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]