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Three‐dimensional ceramic nanofiber‐assembled materials with large specific surface area and excellent thermal insulation properties are attracting increasing interests for their unique structure and promising applications. In this paper, we propose a facile methodology to fabricate three‐dimensional silicon nitride nanofiber‐knitted ceramic foams via in situ reactive synthesis from silicon foams. Silicon particle‐stabilized foams are fabricated for the first time using long‐chain surfactant cetyltrimethyl ammonium bromide as a hydrophobic modifier. First, the fabrication and stability of silicon foams are investigated. Based on the stable silicon foams, silicon nitride‐based nanofiber‐knitted ceramic foams are synthesized via in situ reactive sintering in nitrogen atmosphere. The novel ceramic foam materials consist of three‐dimensional nanofiber‐assembled strut wall and nanofiber‐spheres in the pores. The diameter of obtained silicon nitride nanofibers ranges from 15 to 100 nm. The unique nanofiber‐knitted foams may have potential applications in specific fields, including catalysis, adsorption, separation, and thermal insulation. [ABSTRACT FROM AUTHOR]

Abstract We reveal that zeta potential has a notable effect on properties of foamed suspension, which remains poorly explored. It is demonstrated low zeta potential is beneficial for foam stability, and the experimental results show that absolute value of zeta potential of 30–40 mV is the boundary between stable foams and unstable foams. High zeta potential above 40 mV gives rise to instability of foamed colloidal suspension, owing to strong interparticle repulsion force that prevents particles from forming a closely packed particle network at liquid/air interfaces. Besides, it is found that high zeta potential leads to low foamability of foamed colloidal suspension. It is also demonstrated herein that stable and uniform foams with thin and homogeneous-thickness wall without agglomerates can be prepared at the isoelectric point (IEP) using long-chain surfactant, which generates weak agglomerated particles that can be re-separated to monodisperse particles due to the steric hindrance effect of surfactant. [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 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 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]