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Porous ceramics are demanded in a wide range of high‐temperature, biological and energy‐related applications, but may show conflicting properties or suffer from poor mechanical properties. Introducing pores at different length scales has been shown to be a promising design strategy to combine antagonistic performance parameters and reach high porosity without severely compromising strength. Herein, a cost‐effective and simple process to create strong, highly porous ceramics via direct ink writing of suspensions of hollow microspheres into cellular architectures with pores at three hierarchical levels is reported. X‐ray diffraction, rheological measurements, scanning electron microscopy, and mechanical tests are conducted to thoroughly study the processing steps and morphology of the printed hierarchical porous ceramics. The presence of pores at multiple length scales increases significantly the mechanical strength of the porous structure, providing a useful platform for the manufacturing of lightweight ceramics from inexpensive and widely available feedstock materials. [ABSTRACT FROM AUTHOR]

Steel fiber foamed concrete (SFFC) combines the impact resistance of steel fiber concrete (SFC) and the energy absorption characteristics of foamed concrete (FC), and it has brought attention to the impact field. Using the mechanical properties of SFFC expanded polystyrene concrete, we prepared (EPSC) specimens with 10%, 20%, 30%, 40%, 50% by volume of expanded polystyrene (Veps), and steel fiber expanded polystyrene concrete (SFEPSC) specimens by adding 1% steel fiber (SF) based on the EPSC in this study. The relationship between compressive strength, the Veps and apparent density was revealed. The relationship between the first crack and the ultimate failure impact of SFEPSC specimens was obtained by a drop-weight test. The impact resistance of SFEPSC and EPSC and the variation law of Veps were studied by mathematical statistics. The log-normal and the two-parameter Weibull distributions were used to fit the probability distribution of impact resistance of the SFEPSC and EPSC specimens. Finally, both types of specimens' destruction modes and mechanisms were analyzed. The mechanism of the EPS particles and the SFs dissipating impact load energy was analyzed from the energy point of view. [ABSTRACT FROM AUTHOR]

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]

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]

In this paper, a new nanomaterial, α-Si 3 N 4 nanobelts assembled by high density nanorods were prepared via the crystallization of amorphous Si 3 N 4 at 1450 °C for 12 h. The as-synthesized nanobelts exhibited a width of ∼900 nm and a thickness of ∼150 nm, and a depressed linear region in the central. α-Si 3 N 4 nanorods on the nanobelts had a width of 8–16 nm and a length of 400–450 nm. The nanorods were single-crystal, growing along (101) plane. The nanobelt appeared to be initiated by α-Si 3 N 4 nanorods constantly growing on the both sides of a nanowire which was caused by secondary nucleation and the growth of Si 3 N 4 microcrystals. Growth mechanism related to the formation of the nanobelts was analyzed in detail on the basis of vapor-solid mechanism and secondary nucleation. The current work would provide new insights into α-Si 3 N 4 nanobelts assembled by nanorods which play an important role in nanoscale devices and show widespread potential applications due to their special morphology. • α-Si 3 N 4 nanobelts assembled by nanorods were prepared from amorphous Si 3 N 4 powders. • The α-Si 3 N 4 nanorods constantly grow on the both sides of a nanowire. • Two emission peaks at 437 nm (2.84 eV) and 462 nm (2.68 eV) was measured in the photoluminescence (PL) spectrum. • The growth mechanisms of the α-Si 3 N 4 nanobelts were vapor-solid mechanism and secondary nucleation. [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]

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]

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]

Graphical abstract Highlights • Aqueous ceramic particle-stabilized foams with UV light response are prepared. • Photocurable particle-stabilized emulsions with controllable structure are achieved. • The colloid foams/emulsions demonstrate excellent stability and photocuring ability. • Rapid and scalable synthesis of ceramic capsules is developed based on the emulsions. Abstract We herein report the design and preparation of ceramic particle-stabilized emulsions/foams with distinct ultraviolet light (UV) response, which can be used for the rapid fabrication of ceramic foams with complex shape, for synthesis of ceramic hollow spheres, and can potentially be used for 3D printing lightweight and hierarchical ceramics with porous skeleton. Photocurable foams/emulsions stabilized by ceramic particles are achieved for the first time using photosensitive oligomer as oil phase and/or using photosensitive aqueous solution containing acrylamide monomer as water phase. Four kinds of photocurable emulsions are demonstrated by adjusting emulsion structure and photosensitive phase. We further synthesize internal multiple-pore structured capsules and lightweight nanoparticle-assembled capsules in micron-scale based on the photocurable particle-stabilized, by separating emulsion into small droplets via diluting and stirring, followed by rapid curing under UV. This new strategy may potentially open opportunities for the rapid and cost-effective synthesis of high-output ceramic capsule materials. The synthesized thin-shell alumina capsules exhibit large specific area surface of 323.18 m2/g as well as uniform mesoporous structure in shell with average pore diameter of 3.4 nm, which has potential application in the fields of adsorption, load and release of materials and thermal insulation. [ABSTRACT FROM AUTHOR]

A novel kind of nanowire sponges, namely Si3N4 nanowire‐weaving microspheres, synthesized from a simple, convenient, high‐efficient approach are proposed here. As the reverse template, three‐dimensional foam skeleton structure with uniform pores and ultrathin pore walls is constructed via the effective particle‐stabilized foam method, where the silica sol and carbon black are chosen as the raw materials, providing the sufficient space for the growth of nanowires during the carbothermal reduction reaction process. The formation mechanism of this novel sponge is studied via multiple characterization methods. Si3N4 nanowires formed microspheres possess uniform and curving morphology due to the stable environment for growing via vapor–solid mechanism, leading to the relatively high specific surface area of 86.77 m2/g. Owing to in‐situ oxidation process, micro‐spherical SiO2 nanowire sponges with similar morphology are synthesized, which present diameter in range of 20‐40 nm and specific surface area of 50.47 m2/g. This work provides insights for the design of high‐performance nanowire sponges with promising applications in the filtration, thermal insulators, and catalyst supports fields. [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 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]

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]

The generation of PVA hydrogel through freeze-thaw technique has been utilized innovatively to complete the forming process of porous Si 3 N 4 ceramics in the present work. In comparison with gelcasting method, green body with comparable strength has been achieved by this novel forming process, which is owing to the strong function of PVA gel caused by the freeze-thaw cycles. Herein, Si 3 N 4 hollow spheres are employed as pore-forming agent in order to achieve closed pores. The morphology of green body illustrates that pores originate from both hollow spheres and the space occupied by ice crystals, and the latter gives rise to the increase of porosity around 10%. Studies on the mechanical, dielectric and thermal properties of porous Si 3 N 4 ceramics dependent on freeze-thaw cycle and freezing time have been performed. It is found that porous ceramics treated for freeze-thaw 2 cycles with freezing time of 24 h present excellent properties, which are promising to be applied as radome materials. [ABSTRACT FROM AUTHOR]

The novel porous diatomite microspheres were prepared by spray drying and subsequent calcination. Effects of calcined temperatures on the microstructure, specific surface area and adsorption properties of the microspheres were investigated systematically. Results showed that the porous microspheres exhibited spherical characteristic with both macropore and mesoporous features. The phases of the microspheres kept amorphous at 800 °C and crystallized into crystobalite at 1000 °C. The microspheres after calcined at 600 °C showed removal efficiency of 95.6% with the dosage of 20 g/L under the starting concentration of 100 mg/L. The adsorption process of methylene blue onto microspheres followed the pseudo-second-order kinetic model and Langmuir equation. The dye solutions could be easily filtrated by the microsphere layers and became colorless. It suggested that the porous diatomite microspheres had potential application in dyeing wastewater filtration and adsorption treatment. [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]

Herein, the preparation of millimeter-sized poly-hollow alumina spheres (PHASs) with high-surface-area is proposed via an innovative and facile ball dropping method based on particle-stabilized emulsions. The PHASs fabricated by this method possess high specific surface area because of their hierarchical pore structures and high porosity, and exhibit remarkable superiority over the commercially available active alumina materials with specific surface areas of 200–300 m2g-1. The resultant millimeter-sized PHASs have diameters in range of 2–6 mm, average mesoporous sizes of 4–8 nm, and excellent specific surface areas of 400–500 m2 g-1, which are achieved with oil-water volume ratio of 3:1, rotation speed of 900 rpm, and sintering temperature of 500 °C. These high-performance PHASs with ultra-high specific areas and hierarchical pore structures can potentially be useful in various applications. [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]

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]

As a copolymer of isobutylene and maleic anhydride, Isobam, a newly-developed gelling agent, plays a significant role in ceramic forming process. However, dispersion and gelation behavior of Isobam has not been discussed in detail yet. To investigate the influence of other dispersants, pH and electrolytes on dispersion and gelation behavior of Isobam, zeta potential, viscosity and modulus curves during gelation were measured from 50 vol% alumina suspensions with 0.1–0.7 wt% Isobam. A two-step bridging mechanism is proposed to explain the gelation behavior of Isobam, providing guidance on usage of Isobam in combination of other additives to achieve suspensions with high solids loading and adjustable gelation characteristic. [ABSTRACT FROM AUTHOR]

In this paper, attapulgite microspheres were prepared by spray drying method and calcination subsequently. The effects of calcining temperature, microsphere dosage, contact time and concentration of dye on the adsorption properties of malachite green were investigated systematically. Results show that the fibrous and fold microstructure could be seen on the surface of the porous microspheres, and was mainly composed of palygorskite. The adsorption capacity of malachite green for microspheres increased firstly (500-700 °C) and then declined (800-1 000 °C ) with the calcination temperature increasing. The adsorption capacity and removal efficiency of malachite green for microspheres treated after 600 °C was 95.45 rng/g and 95.5%, respectively. The ad- sorption capacity of malachite green increased with the amount of microspheres and original concentration of the dye increasing, and the adsorption process could be described by the pseudo-second-order kinetic model. [ABSTRACT FROM AUTHOR]

A novel approach is used for fabricating steel slag foam ceramics based on the particle-stabilized foaming method. In this work, steel slag was used as the raw material and propyl gallate (PG) was used as the surface modifier. For the first time, steel slag ceramic foams were successfully fabricated based on particle-stabilized foams. The results show that the stability of the ceramic foams was closely related to the pH value and PG concentration. The porosity and compressive strength could be controlled by changing the solid loading of steel slag and sintering temperature. The porosity of steel slag foam ceramics ranged from 85.6% to 62.53%, and the compressive strength was from 1.74 MPa to 10.42 MPa. The thermal conductivity of steel slag foam ceramics was only 0.067 W (m·K)−1, which shows that it could be used as a thermal insulation material. [ABSTRACT FROM AUTHOR]

A novel approach is used for fabricating steel slag foam ceramics based on the particle-stabilized foaming method. In this work, steel slag was used as the raw material and propyl gallate (PG) was used as the surface modifier. For the first time, steel slag ceramic foams were successfully fabricated based on particle-stabilized foams. The results show that the stability of the ceramic foams was closely related to the pH value and PG concentration. The porosity and compressive strength could be controlled by changing the solid loading of steel slag and sintering temperature. The porosity of steel slag foam ceramics ranged from 85.6% to 62.53%, and the compressive strength was from 1.74 MPa to 10.42 MPa. The thermal conductivity of steel slag foam ceramics was only 0.067 W (m·K)−1, which shows that it could be used as a thermal insulation material. [ABSTRACT FROM AUTHOR]

In this work, gangue/palygorskite composite microspheres were fabricated through spray drying process and activated by calcination treatment. Its microstructure and adsorption capacity for the removal of dye (MB) were also studied, systematically. Results showed that kaolinite, α‐quartz and palygorskite were the major phases in microspheres after proper calcination (lower than 900°C). BET‐specific surface area of the microspheres reached the maximum value of 62.23 m2/g at 700°C, and then decreased with further increasing the heating temperature. In general, composite microspheres showed the largest adsorption capacity of MB after heat‐treated at 700°C. The qmax of MB onto microspheres was 29.9‐51.9 mg/g. The adsorption process of MB onto microspheres was well described by both the pseudo‐second‐order kinetic and Langmuir isotherm model. The composite microspheres also had extraordinary recyclability. This novel microsphere could be employed as a candidate for novel absorbent and filter medium in the practical application for dye treatment in industrial applications. [ABSTRACT FROM AUTHOR]

Isobam, a copolymer of isobutylene and maleic anhydride, is a newly developed gelling agent for ceramic colloidal forming. However, the Isobam system exposes a weakness of high viscosity when solids loading exceeds 54 vol%. Suitable additives to effectively decrease viscosity and have minimal impact on gelation strength were discovered from various dicarboxylic acids through investigation on zeta potential, viscosity of suspensions, shear modulus during gelation and yield stress and modulus of elasticity of wet green bodies. Alumina ceramics with flexural strength of 442 ± 49 MPa and a Weibull modulus of 10.8 were produced from 54 vol% suspensions with 0.5 wt% Isobam assisted by 0.04 wt% phthalic acid and 0.03 wt% oxalic acid after pressureless sintering. [ABSTRACT FROM AUTHOR]

Mechanically robust alumina ceramics with low shrinkage were successfully prepared via gelcasting using Isobam as the gelling agent and pre-sintered alumina powder as the raw material for the first time. The influence of amount of pre-sintered alumina powder and powder's pre-sintering temperature on the viscosity of suspension and mechanical properties of low-shrinkage alumina ceramics were systematically investigated. The results showed that low-shrinkage alumina ceramics with flexural strength of 294.5 ± 33.0 MPa, linear shrinkage of 7.79% and relative density of 91.5% can be obtained with the addition of 60 wt% alumina powder pre-sintered at 1600 °C. This convenient and facile approach is promising to fabricate low-shrinkage alumina ceramics with large sizes, high dimensional accuracy and complex shapes. [ABSTRACT FROM AUTHOR]

In order to reduce thermal conductivity but to exhibit better mechanical properties of porous alumina ceramics (PACs), a novel approach, based on the modification of pore structures (i.e. mean pore size, micro-pore proportions and pore shape factor) by impregnation of alumina sol, is reported in the present work. The properties of as-impregnated samples were compared with commercial alumina hollowsphere bricks. Results show that impregnation of alumina sol in PACs has a positive influence on pore structures, leading to a superior strength and a lower thermal conductivity. In particular, when 8 wt% alumina sol solid content is impregnated, the crushing strength (35.3 MPa) and thermal conductivity (0.15 W/m K at 200 °C) of sample are much better than that of the commercial alumina hollowsphere bricks. This novel method for excellent PACs provides promising applications as insulating lining materials in the fields of industrial furnace. [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]

In this study, a facile one-step method combining the pore expansion and the enlargement of the hollow cavity of hollow periodic mesoporous organosilica spheres (HPMOSs) into one step was proposed. Moreover, the whole process for the formation just needs 1 h and involves reaction just under normal pressure and temperature. We further investigate the influence of different expanders and the amount of expanders on pore size and hollow cavity size. The obtained HPMOSs using tridecane as expander possess excellent properties, including good spherical morphology, large hollow structures, radially oriented mesochannels (3.44 nm), uniform particle size (115 nm), high BET surface area (1298 m/g), and large pore volume (1.96 cm/g). In addition, the hollow cavity size and the mesoporous size can be controlled via the modulation of tridecane amount. This method also provides a basis for synthesizing both large pore and the hollow cavity of functionalized, monodispersed HPMOSs. [ABSTRACT FROM AUTHOR]

Dense silicon carbide ceramics using chemical treated powder by DCC via dispersant reaction method and liquid phase sintering was reported. Ammonium peroxydisulfate ((NH 4 ) 2 S 2 O 8 ) and ammonium carbonate ((NH 4 ) 2 CO 3 ) were used as acid and base solutions to treat the silicon carbide powder, respectively. Influence of silicon carbide powder with chemical treatment on the preparation of silicon carbide suspension was studied. It was indicated that 50 vol% and 52 vol% silicon carbide suspensions with viscosities of 0.71 Pa s and 0.80 Pa s could be prepared using acid and base treated powders. Influence of silicon carbide powder with chemical treatment on the coagulation process and properties of green bodies and sintered ceramics were studied. It was indicated that silicon carbide green bodies with compressive strength of 1.13 MPa could be prepared using base treated powder. Dense silicon carbide ceramics with relative density above 99.3% and flexural strength of 697 ± 30 MPa had been prepared by DCC via dispersant reaction and liquid phase sintering using Al 2 O 3 and Y 2 O 3 as additives at 1950 °C for 2 h. [ABSTRACT FROM AUTHOR]

The CVD nano-diamond film and Ti-6Al-4V alloy were successfully brazed with AgCuTi active brazing filler. The interfacial microstructure was investigated by SEM, EDS, XRD and TEM. Typical interfacial microstructure of brazed joint was conformed as Ti-6Al-4V/diffusion layer/Ti 2 Cu + TiCu + Ti 3 Cu 4 /Ag(s,s) + Cu(s,s) + Ti 2 Cu 3 /TiCu + TiC/nano-diamond film. The effects of brazing temperature on interfacial microstructure and mechanical properties of the brazed joints were analyzed. With the increasing brazing temperature, the thickness of reaction layers adjacent to Ti-6Al-4V substrate and nano-diamond film increased obviously. Moreover, the Ti 2 Cu 3 phase coarsened and aggregated in brazing seam at higher temperature. The joint was formed by the diffusion and reactions between atoms, and the microstructure evolution of brazed joint was discussed. In addition, a slight graphitization of nano-diamond film occurred during brazing process, and the highest shear strength can reach 25 MPa when the joint was brazed at 880 °C for 10 min. Finally, the fracture positions and fractographs of brazed joints were also discussed. [ABSTRACT FROM AUTHOR]

• A performance-based blast-resistance evaluation framework is proposed for gravity dam. • A modified slip stability coefficient is used to assess the dam foundation stability. • A global damage index is proposed to measure the risk of the dam under explosions. • Safety control criteria for blast-resistance analysis of gravity dams is discussed. In recent years, the blast-resistance of dams under extreme explosion conditions has received more and more concerns by managers and engineers. The blast-resistance evaluation and safety control criteria for concrete gravity dams subjected to explosion loads are still controversial problems. To this end, a fully coupled three-dimensional finite element model of a concrete gravity dam is established to simulate the damage modes of the dam under various explosion scenarios. Then, a performance-based blast-resistance evaluation framework of concrete gravity dams is established in this study to consider the global safety of the dam, including the global crack evolution and the stabilities of dam head and dam foundation. According to the evaluation framework, a blast-vibration-based model for dam head safety, a modified model against sliding for dam foundation stability, and a global damage index with water retaining performance are provided in this study to discuss the global safety of the dam experienced explosions. Finally, safety control criteria of the dam are also proposed as an example, which provide theoretical support for the further protection design of the dam. [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]

A direct coagulation casting method for silicon nitride suspension via dispersant reaction was reported. Tetramethylammonium hydroxide (TMAOH) was used as dispersant to prepare silicon nitride suspension with high solid loading and low viscosity. Influences of TMAOH and pH value on the dispersion of silicon nitride powder were investigated. Glycerol diacetate (GDA) was used to coagulate the silicon nitride suspension. Influences of the concentration of glycerol diacetate on the viscosity and pH value of the suspension were investigated. It was indicated that high viscosity sufficient to coagulate the suspension was achieved by adding 1.0–2.0 vol% glycerol diacetate at 40–70 °C. The coagulation mechanism was proposed that the silicon nitride suspension was destabilized by dispersant reacting with acetic acid which was hydrolyzed from glycerol diacetate at elevated temperature. Coagulated samples could be demolded without deformation by treating 50 vol% silicon nitride suspensions with 0.2 wt% tetramethylammonium hydroxide and 1.0–2.0 vol% glycerol diacetate at different temperatures. Dense silicon nitride ceramics with relative density above 98.8% had been prepared by this method using glycerol diacetate as coagulating agent sintered by different methods. [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]