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In situ coagulation for yttria‐stabilized zirconia (YSZ) suspension via polyvinyl pyrrolidone (PVP) crosslink is reported. PVP is used to prepare sterically stabilized YSZ suspension. Influence of PVP on the dispersion of YSZ suspension was investigated. It indicates that well disperse YSZ suspension with 0.3 wt % PVP can be prepared. Dimethyl sulfate (DMS) was added at 40 °C to coagulate the suspension after degassing. Influence of DMS content and coagulation temperature on coagulation process and properties of green bodies were investigated. It indicates that sufficiently high viscosity to coagulate the suspension is achieved with the addition of 1 vol % DMS at 60~80 °C. The coagulation mechanism is proposed that the YSZ suspension is destabilized by the self‐crosslink of PVP. Coagulated samples with the highest wet compressive strength of 6.34 MPa could be demolded without deformation by treating 50 vol % YSZ suspension at 60 °C. Dense YSZ ceramics with relative density above 99.1% and flexural strength of 920 ± 90 MPa had been prepared by this method sintered at 1450 °C for 3 h. © 2020 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020, 137, 48889. [ABSTRACT FROM AUTHOR]

Hierarchical cellular architectures hold great potential in a vast range of applications due to their superior mechanical properties and multifunctionality. In the present work, hierarchical structures composed of porous struts patterned in the form of quadrangular and triangular honeycombs were fabricated via direct foam writing (DFW) using colloidal particle‐stabilized Al2O3‐MgO‐SiO2 foams as the ink. Hydration process of MgO and subsequent formation of colloidal Mg(OH)2 network endowed the foam ink with viscoelasticity and high storage modulus. The resulting honeycombs with ultrahigh overall porosity (95.3%) and robust compressive strength (2.5 MPa) can be readily fabricated by DFW. The current work exhibits a significant step toward the scalable production of cellular ceramics with hierarchical architecture for various applications, including tissue scaffolds, catalyst supports, thermal insulation, and lightweight structures. [ABSTRACT FROM AUTHOR]

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]

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]

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]

Ultralight ceramics with striking mechanical properties and improved pore connectivity could have wide applications in areas ranging from catalyst support to hot gas filtration. However, creating such materials has proven to be a challenging target. This work demonstrated a novel methodology to prepare porous MgAl 2 O 4 ceramics by calcining gelled MgO–Al 2 O 3 –SiO 2 particle-stabilized foams. The striking green strength of dried foams can be achieved as a consequence of MgO hydration and subsequent formation of gelled Mg(OH) 2 and MgO–SiO 2 –H 2 O skeleton. The decomposition of colloidal substance at elevated temperature resulted in the formation of small pores on the cell wall, thus forming the hierarchical porous architecture and improving the pore connectivity. The highly porous MgAl 2 O 4 ceramics fired at 1600°C possessed the integrated properties of ultrahigh porosity (87.0%), improved pore connectivity and satisfactory compressive strength (7.93 MPa), showing great potential to be used in multiple industrial fields. [ABSTRACT FROM AUTHOR]

Abstract A facile method for preparation of SiC nanofibrous network reinforced hierarchical structured porous Si 3 N 4 based ceramics via annealing Si-Si 3 N 4 binary particle-stabilized foam in coke bed is reported in this work for the first time. The atmosphere created by coke bed enables the fabrication of Si 3 N 4 based porous ceramics at 1450 °C without using sintering additives. As prepared specimens possess a relative high compressive strength due to the partial oxidation of Si 3 N 4 particles. This novel structure with three levels of hierarchy characterized by flexible SiC nanofibrous network, cell walls and unit cells can be characterized. The vaporization of silicon powder results in formation of Si(g), SiO(g) and allows subsequent generation of SiC nanofibrous network, leading to a considerable number of micro-pores on cell walls simultaneously. As-prepared porous ceramics contained 76.7% porosity and had compressive strength of 10.81 MPa. [ABSTRACT FROM AUTHOR]