氧化铝泡沫陶瓷的制备

采用有机泡沫前驱体浸渍工艺制备氧化铝泡沫陶瓷。通过涂覆处理获得缺陷较少、结构均匀的泡沫陶瓷体。通过TG—DTA，XRD，SEM研究了试样在热处理过程中的物理化学变化，烧结体的物相组成及其显微结构。研究袁明：烧结体以α-Al2O3为主晶相，其次是莫来石；烧结体中宏观孔基本上是连通的。     

Novel fabrication route for porous silicon carbide ceramics through the combination of in situ polymerization and reaction bonding techniques

For the first time, an in situ polymerization technique was applied to produce mullite‐bonded porous SiC ceramics via a reaction bonding technique. In this study, SiC microsized particles and alumina nanopowders were successfully coated by polyethylene (PE), which was synthesized from the particle surface in a slurry phase reactor with a Ziegler–Natta catalyst system. The thermal studies of the resulting samples were performed with differential scanning calorimetry and thermogravimetric analysis. The morphology analysis obtained by transmission electron microscopy and scanning electron microscopy (SEM) confirmed that PE was successfully grafted onto the particle surface. Furthermore, the obtained porous ceramics were characterized in terms of their morphologies, phase composition, open porosity, pore size distribution, and mechanical strength. SEM observations and mercury porosimtery analysis revealed that the quality of the dispersion of nanosized alumina powder into the microsized SiC particles was strongly enhanced when the particles were coated by polymers with in situ polymerization. This resulted in a higher strength and porosity of the formed ceramic porous materials with respect to the traditional process. In addition, the X‐ray diffraction results reveal that the amount of mullite as the binder increased significantly for the samples fabricated by this novel method. The effects of the sintering temperature, forming pressure, and polymer content on the physical and mechanical properties of the final porous ceramic were also evaluated in this study. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40425.     

Novel Method To Optimize the Structure of Reticulated Porous Ceramics

A novel method has been developed for the fabrication of silicon nitride reticulated porous ceramics (RPCs) with regulated structure, using polyurethane sponge as the template. This technique includes two centrifuging steps. In the first stage, the polyurethane sponges are coated with thin slurry through high-speed centrifuging. After the slurry on sponges dried, a high-strength green body without filled cells is obtained. In the second stage, because of improved adhesion between the body and the slurry after the first coating, the body with uniformly thick strut is produced by recoating the as-prepared green body with thixotropic slurry and centrifuging again. The loading content of slurry and the pore diameter of the RPCs body greatly depend on the slurry viscosity in the process of recoating. The strut diameter and pore diameter of the RPCs are effectively optimized by modulating the slurry viscosity.     

Gas permeability and mechanical properties of porous alumina ceramics with unidirectionally aligned pores

Porous alumina ceramics having unidirectionally aligned cylindrical pores were prepared by extrusion method and compared with porous ceramics having randomly distributed pores prepared by conventional method, and their gas permeability and mechanical properties were investigated. SEM micrographs of the porous alumina ceramics prepared by the extrusion method using nylon fibers as the pore former showed excellent orientation of cylindrical pores. The bending strength and Weibull modulus of the extruded porous alumina ceramics with 39% porosity were 156 MPa and 17, respectively. These mechanical properties of extruded samples were higher than those of the conventional porous alumina ceramics. The strength decreased from 156 to 106 MPa with increasing pore size from 8.5 to 38 μm. The gas permeability of the extrusion samples is higher than that of the conventional samples and increased with increasing of porosity and pore size.     

Preparation and properties of porous alumina ceramics with oriented cylindrical pores produced by an extrusion method

Porous alumina ceramics with unidirectionally-oriented pores were prepared by extrusion. Carbon fibers of 14 μm diameter and 600 μm length to be used as the pore-forming agent were kneaded with alumina, binder and dispersing agent. The resulting paste was extruded, dried at 110 °C, degreased at 1000 °C and fired at 1600 °C for 2 h. SEM showed a microstructure of dispersed highly oriented pores in a dense alumina matrix. The pore area in the cross section was 25.3% with about 1700 pores/mm². The pore size distribution of the fired body measured by Hg porosimetry showed a sharp peak corresponding to the diameter of the burnt-out carbon fibers. The resulting porous alumina ceramics with 38% total porosity showed a fracture strength of 171 MPa and a Young's modulus of 132 GPa. This strength is significantly higher than the reported value for other porous alumina ceramics even though the present pore size is much larger.     

Fabrication of mullite-bonded porous SiC ceramics via a sol–gel assisted in situ reaction bonding

In the present work, mullite-bonded porous SiC ceramics were fabricated using reaction bonding techniques. The morphologies, phase composition, open porosity, pore size distribution and mechanical strength of porous ceramics were examined as a function of alumina sources (calcined nano-sized alumina powder and alumina sol prepared from hydrolysis of aluminum isopropoxide) and contents. It was found that the addition of alumina in powder form effectively enhanced the strength and decreased the porosity. In contrast, when alumina was added in sol form, a reverse effect was observed. Moreover, it was revealed that when a portion of calcined alumina was replaced by alumina sol, the mechanical properties improved significantly (more than 30%) as well as porosity compared to the traditional method. Pore size distribution analysis showed that the dispersion of nanosize alumina powder and SiC micro-particles in alumina sol is strongly improved compared to mixing in ethanol.     

Effect of Polystyrene Addition on Freeze Casting of Ceramic/Camphene Slurry for Ultra-High Porosity Ceramics with Aligned Pore Channels

We investigated the effect of polystyrene (PS) addition on the freezing behavior of a very dilute alumina/camphene slurry with an initial solid loading of 5 vol% for the fabrication of ultra-high porosity ceramics with aligned pore channels. To accomplish this, slurries with various PS contents (10, 20, and 30 vol% in relation to the alumina powders) were prepared by ball milling at 60°C and then cast into molds at a constant temperature of 20°C. After removing the frozen camphene, the samples were heat treated to burn out the organic phases and sinter the alumina walls. The addition of the PS binder remarkably enhanced the green strength of the sample, making it possible to handle it without difficulty. All of the sintered samples showed ultra-high porosities of >88% without the collapse of the porous structure, wherein the pore channels were completely interconnected. Three distinctive zones having different pore structures were observed, viz. the outer shell with elongated pores, the inner zone with long aligned pore channels, and the center with equiaxed pores. The content of the PS polymer significantly affected the pore morphologies in the three distinctive zones. In addition, it was found that the addition of the PS polymer was highly beneficial to the alignment of the pore channels.     

Alumina/zirconia ceramic membranes fabricated by temperature induced forming technique

It is well known that the fabrication technique of porous ceramic composites has a significant effect on their microstructure and properties. In the present study, alumina/zirconia ceramic composites doped with magnesia were fabricated by temperature induced forming technique using tri-ammonium citrate and polyacrylic acid (PAA) as dispersant and gelling agents, respectively. The zirconia content was up to 20 wt% and added at the expense of alumina while the magnesia content was up to 2 wt% over the total mass. The optimum amount of ammonium citrate tribasic needed for dispersing the ceramic slurry was determined by measuring zeta potential of slurries. The prepared green alumina/zirconia composites were subjected for solid state sintering at 1550 °C for 1 h. The densification parameters, phase composition, average pore diameter, microstructure and cold crushing strength of sintered alumina/zirconia ceramics were investigated by the suitable techniques. The results revealed that the addition of tri-ammonium citrate to ceramic slurries enhanced the zeta potential which reached ?28.3 mV by adding 1 wt.-%. The bulk density was decreased while the apparent porosity was increased with the increase of zirconia content. The apparent porosities of sintered porous composites were in the range of 38.8–48.5%. The average pore diameter for the composite containing 15% zirconia was 1.79 μm and pore volume was 0.11 ml/g. The obtained microstructure exhibited zirconia grains located on the grain boundaries of Al₂O₃ matrix. The existence of zirconia in addition to magnesia hindered the growth and deformation of the matrix. The cold crushing strength of porous composites was decreased from 16.0 to 8.5 to MPa by increasing the zirconia content from 5 to 20 wt.-%.     

Process control and optimized preparation of porous alumina ceramics by starch consolidation casting

This work concerns details of porosity and pore size control in starch consolidation casting of alumina ceramics using corn starch. In particular, the influence of the solids loading (68-78 wt.% alumina in suspensions with nominal starch contents of 20-50 vol.%) on the porosity, bulk density and shrinkage of alumina ceramics is studied. The results indicate a linear decrease of the linear shrinkage and the bulk density (and a corresponding increase in porosity) as the alumina concentration increases, with slopes that are independent of the starch content. The pore size is characterized via microscopic image analysis, the pore throat size via mercury porosimetry. Relations between the volumetric shrinkage, porosity and the volume fractions of starch and water in the suspensions are discussed, and a new concept, called “affine limit porosity” is proposed to explain the apparently paradoxical finding that the porosity increases with increasing alumina content in the suspension.     

Effect of CTAB as a foaming agent on the properties of alumina ceramic membranes

Alumina-ceramic membranes were prepared by gelcasting process using CTAB as a foaming agent. To increase the fineness, the starting alumina powder was milled for 1 h in a ball mill before the casting process. Particle size distribution and surface area measurements of the as-received and milled alumina powder were examined. The casted alumina membranes were sintered at 1500 °C. Sintering parameters in terms of bulk density (BD) and apparent porosity (AP) were determined by the Archimedes method. Pore size distribution of the sintered porous alumina membranes was measured using mercury porosimeter. Microstructure of sintered membranes was investigated by scanning electron microscope (SEM). Cold crushing strength (CCS) of the sintered specimens was also evaluated. The result revealed that the properties of porous ceramics such as porosity, average pore size, pore size distribution and cold crushing strength could be controlled by adjusting the preparation conditions e.g. solid loading, sintering temperature and foaming agent. The open porosity, cold crushing strength and average pore size of the alumina ceramics sintered at 1500 °C were around 58.35%, 18 MPa and178 nm, respectively.     

Preparation of YSZ porous ceramics with precise porosity control

Conventional preparation of porous ceramics often hard to accurately control the porosity of the samples. In this paper, by improving the foaming method, the foaming process is placed in the limited space of the ball mill tank, and YSZ porous ceramics with different porosity are obtained by changing the amount of slurry. Initial results showed that the porosity of the sample varies linearly with the increasing of addition of slurry. From the microscopic morphology, it can be seen that the increase in slurry content will reduce the number of pore with little changed size, which lead to the decrease in porosity. Therefore, with simple calculation YSZ porous ceramics with 85%, 80%, 75%, 70%, and 65% porosity can be obtained using the method of foaming in limited space by ball milling.     

粒子稳定型泡沫浆料及多孔氧化铝陶瓷的制备

采用短链两亲分子戊酸修饰氧化铝颗粒,使其部分具有的疏水性,在机械搅拌的作用下,形成了粒子稳定型泡沫(particle-stabilized foam),制备了一种新型的超稳定陶瓷泡沫浆料.研究了这种浆料的pH值对发泡率的影响,发现在pH值为4.8附近,戊酸对氧化铝颗粒的表面修饰作用最好,发泡程度最大;通过改变pH值,能够调整浆料的发泡程度,以满足不同应用领域对发泡率的要求.采用凝胶注模成型工艺,利用粒子稳定型泡沫浆料,成功制备了具有相互连通气孔-窗口(cell-window)结构的多孔陶瓷,由于其致密的支架结构使其具有高抗压强度,对于气孔率为85%的多孔氧化铝,其抗压强度在8MPa以上.     

Properties of multiple oxide-bonded porous SiC ceramics prepared by an infiltration technique

Multiple oxide-bonded porous SiC ceramics were fabricated by infiltrating a porous powder compact of SiC and alumina with cordierite sol followed by sintering at 1300-1400°C in air for 3 hours. The microstructures, phase components, mechanical properties, and air permeation behavior of the developed porous ceramics were examined and compared with materials obtained by the traditional powder processing route. The porosity, average pore diameter, and flexural strength of the ceramics varied from 33 to 37 vol%, ~12-14 μm and ~23-39.6 MPa, respectively, with variation in sintering temperature. The X-ray diffraction results reveal that both the amount of cordierite and mullite as the binder increased with increase in sintering temperature. In addition, it was found that the addition of alumina in powder form effectively enhanced the strength due to formation of mullite in the bond phase in contrast to the samples prepared without alumina additive. To determine the suitability of the material in particulate filtration application, particle collection efficiency of the filter material was evaluated theoretically using single collector efficiency model.     

Freeform Gelcasting of Porous Tubular Alumina Substrate

The present work demonstrates a new method for fabrication of thin-walled tubular alumina substrate by combining the principles of gelcasting and freeform fabrication. A tube made up of filter paper or organic preform was filled with 4 N nitric acid and dipped in a 55 vol% alumina (average particle size 0.34 μm) slurry containing methylolurea and urea. A thin layer of alumina slurry was gelled on the filter paper tube by in situ polymerization of methylolurea and urea monomers present in the slurry by delivering the acid through the walls of the filter paper tube. The thickness of the alumina tube obtained depended on the dipping time. Alumina tubes with thicknesses in the range 0.7–2 mm were obtained for dipping times in the range 1–8 min. The tubes obtained had good surface finishes and profiles. These tubes were sintered at 1150°C and microstructural observation indicated uniform grain size and pore morphology. A porosity of 40% and an average pore size of 300 nm were obtained.     

Fabrication of SiC reticulated porous ceramics with multi-layered struts for porous media combustion

Silicon carbide reticulated porous ceramics (SiC RPCs) with multi-layered struts were fabricated at 1450 °C by polymer sponge replica technique, followed by vacuum infiltration. The effect of additives (polycarboxylate, ammonium lignosulfonate and sodium carboxymethyl-cellulose) on the rheological behavior of silicon carbide slurry was firstly investigated, and then the slurry was coated on polyurethane open-cell sponge template. Furthermore, alumina slurry was adopted to fill up the hollow struts in vacuum infiltration process after the coated sponge was pre-treated at 850 °C. The results showed that the coating thickness on the struts and the microstructure in SiC RPCs were closely associated with the solid content of alumina slurry during vacuum infiltration. The typical multi-layered strut of SiC RPCs could be achieved after the infiltration of an alumina slurry containing 77 wt% solid content. The compressive strength and thermal shock resistance of the infiltrated specimens were significantly improved in comparison with those of non-infiltrated ones. The improvement was attributed to the in-situ formation of reaction-bonded multilayer struts in SiC RPCs, which were characterized by the exterior coating of aluminosilicate-corundum, middle part of mullite bonded SiC and interior zone of corundum.     

In-situ growth of mullite whiskers and their effect on the microstructure and properties of porous mullite ceramics with an open/closed pore structure

Porous mullite ceramics with an open/closed pore structure were prepared by protein foaming method combined with fly ash hollow spheres. Both the open porosity and total porosity of samples were enhanced by increasing the hollow sphere content. Mullite whiskers with a diameter of 0.2–4 μm were grown in-situ in the porous mullite ceramics with an AlF₃ catalyst, conforming to a vapor-solid growth mechanism. The pore structure of the porous mullite ceramics was significantly affected by the mullite whiskers which increased the open porosity and total porosity. Moreover, the median pore size was reduced from 65.05 μm to 36.92 μm after the introduction of mullite whiskers. The flexural strength and the thermal conductivity of the samples decreased with increasing total porosity. The porosity dependence of the thermal conductivity was well described by the universal model, providing a reference for the prediction of thermal conductivity of porous ceramics with open/closed pores.     

Preparation of porous Al2O3 ceramics by starch consolidation casting method

Porous alumina ceramics were fabricated by starch consolidation casting using corn starch as a curing agent while their microstructure, mechanical properties, pore size distribution, and corrosion resistance were examined. Results showed that the porous alumina ceramics with the flexural strength of about 44.31MPa, apparent porosity of about 47.67% and pore size distribution in the range of 1‐4 μm could be obtained with 3wt% SiO₂ and 3wt% MgO additives. Corrosion resistance results showed mass losses: hot H₂SO₄ solution and NaOH solution for 10 hours were 0.77% and 2.19%, which showed that these porous alumina ceramics may offer better corrosion resistance in acidic conditions.     

Preparation of high strength lamellar porous calcium silicate ceramics by directional freeze casting

In this study, porous calcium silicate (CS) ceramics with oriented arrangement of lamellar macropore structure were prepared by directional freeze casting method. The lamellar macropores were connected by the micropores on the pore wall, which had good pore interconnectivity. The effects of solid loading of the slurry, freezing temperature, sintering additive content, and sintering temperature on the microstructures and compressive strength of the synthesized porous materials were investigated systematically. The results showed that with the increase of solid loading (≤20 vol%) and sintering additive content, the sizes of lamellar pores and pore walls increased gradually, the open porosity decreased and the compressive strength increased. The sintering temperature had little effect on the pore size of the ceramics, but increasing the sintering temperature (≤1050 °C) promoted the densification of the pore wall, reduced the porosity, and improved the strength. The decrease of freezing temperature had little effect on porosity, but it reduced the size of lamellar pore and pore wall, so as to improve the strength. Finally, porous CS ceramics with lamellar macropores of about 300–600 μm and 2–10 μm micropores on the pore wall were obtained. The porous CS ceramics had high pore interconnectivity, an open porosity of 66.25% and a compressive strength of 5.47 MPa, which was expected to be used in bone tissue engineering.     

Tailored pore structures and mechanical properties of porous alumina ceramics prepared with corn cob pore-forming agent

In this work, the effects of porosity and different particle sizes of pore-forming agent on the mechanical properties of porous alumina ceramics have been reported. Different grades of porous alumina ceramics were developed using corn cob (CC) of different weight contents (5, 10, 15, and 20 wt%) and particle sizes (<63 µm, 63-125 µm and 125-250 µm) as the pore-forming agent. Experimental results showed that total porosity and pore cavity size of the porous alumina ceramics increased with rising addition of CC pore former. Total porosity increased with increasing particle size of CC with the Al₂O₃-^<63CC₅ sample exhibiting the lowest total porosity of 41.3 vol% while the highest total porosity of 68.1 vol% was exhibited by the Al₂O₃-^125-250CC₂₀. The particle size effect of CC on the mechanical properties revealed that diametral tensile strength and hardness of the porous alumina ceramics deteriorated with increasing particle size of CC pore former. The Al₂O₃-^<63CC₅ sample exhibited the highest diametral tensile strength and hardness of 25.1 MPa and 768.2 HV, respectively, while Al₂O₃-^125-250CC₂₀ exhibited the lowest values of 1.1 MPa and 35.9 HV. Overall, porous alumina ceramics with the smallest pore sizes under each particle size category exhibited superior mechanical properties in their respective categories.     

A urea crystal templating method for the preparation of porous alumina ceramics with the aligned pores

A novel process for the preparation of porous alumina ceramics with an aligned pore structure has been reported. The urea dissolved in the aqueous alumina slurry at higher temperature formed rod shaped crystals aligned in the direction of gravity when cooled to room temperature. The gelatin used to set the slurry, controls the crystallization of urea such that the urea crystals produced in the suspension containing the gelatin had much lower width and thickness compared to that produced in the suspension without the gelatin. The alumina powder catalyzed the thermal decomposition of urea that enabled the removal of the majority of the urea crystals from the alumina green body by isothermal heating at temperature much lower than the melting point of urea. The void space created by the removal of the urea crystals remained as pores in the sintered ceramics.