Novel design of elongated mullite reinforced highly porous alumina ceramics using carbonized rice husk as pore-forming agent

A facile strategy for the fabrication of elongated mullite reinforced porous alumina ceramics (PACs) using carbonized rice husk (CRH) as pore-forming agent and silica source is reported for the first time. A large amount of elongated mullite is synthesized in pores due to the reaction of amorphous silica in CRH skeleton and alumina ceramic powder. Elongated mullite acts as the bridges between pore walls, enhancing the compressive strength of PACs. Furthermore, secondary pores from the intersection of elongated mullite is favor of decreasing of the thermal conductivity. High performance PAC with porosity of 74.3% has been fabricated by employing 25 wt% CRH, which possesses relatively low thermal conductivity of 0.189 W/(m•K) and ultra-high compressive strength of 45 MPa. Its comprehensive performance is much better than that of existing ceramic materials. Our findings present a facile, eco-friendly and effective approach to fabricate high performance PACs as the high-temperature thermal insulation materials.     

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.     

Effects of pore structure on thermal conductivity and strength of alumina porous ceramics using carbon black as pore-forming agent

In the present work, carbon black (CB) works as a pore-forming agent in the preparation of alumina porous ceramics. The pore structures (i.e. mean pore size, pore size distribution and various pores size proportions) were characterized by means of Micro-image Analysis and Process System (MIAPS) software and mercury intrusion porosimetry. Then their correlation and thermal conductivity as well as strength were determined using grey relation theory. The results showed that the porosity and mean pore size increased against the amount of CB, whereas the thermal conductivity, cold crushing strength and cold modulus of rupture reduced. The <2 μm pores were helpful for enhancing the strength and decreasing the thermal conductivity whereas the >14 μm pores had the opposite effects.     

A novel approach to fabricate porous alumina ceramics with excellent properties via pore-forming agent combined with sol impregnation technique

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.     

Thermal conductivity of porous alumina ceramics prepared using starch as a pore-forming agent

The thermal conductivity of porous alumina ceramics prepared using different types of starch (potato, wheat, corn, and rice starch) as pore-forming agents is investigated from room temperature up to 500 °C. The temperature dependence measured for alumina ceramics of different porosity (in the range 6–47%) is fitted with second-order polynomials and 1/T-type relations, and compared to available literature data for dense alumina. It is found that the porosity dependence of the relative thermal conductivity k_r = k/k₀ is well described by a modified exponential relation of the form k_r = exp(?1.5?/(1 ? ?)), where ? is the porosity. This finding is in agreement with other literature data and seems to indicate a common feature of all porous materials with microstructures resulting from fugitive pore-forming agents.     

多孔陶瓷材料的制备研究进展

介绍了多孔陶瓷材料的分类、性能和应用,综述了多孔陶瓷的制备方法,并分析了不同制备方法的特点。     

Preparation of near net size porous alumina-calcium aluminate ceramics by gelcasting-pore-forming agent processs

In the processing of porous ceramics, shrinkage from green body to sintered compact during drying and sintering is one of the key concerns which affect microstructure and properties of porous ceramics. Through releasing gases from the burning of the pore forming agents, and volume expansion from the formation of low density resultants during sintering, the sintering shrinkage can be effectively compensated and near net size preparation can be achieved. Herein, near net size porous alumina-calcium aluminate ceramics with controllable shrinkage have been prepared using a combination of gelcasting and pore-forming agent process by adjusting the amount of CaCO₃ and polymethyl methacrylate (PMMA) microspheres added. Al₂O₃ and CaCO₃ were used as raw materials, PMMA microspheres were used as pore-forming agent, isobutylene/maleic anhydride copolymer (Isobam104) was used as gelling agent and dispersing agent. The effects of the addition amounts of CaCO₃ and PMMA in the slurry on the phase composition, shrinkage, porosity, and strength of porous alumina-calcium aluminate ceramics were investigated. The results show that as the CaCO₃ addition amount increases from 0 to 20 wt%, the shrinkage of the samples gradually decreases from 7.3% to −1.4%, and the consequent porosity increases from 58% to 66%, while the compressive strength increases from 5.9 to 15.5 MPa. When PMMA content increases from 10 to 50 wt%, the shrinkage of the samples decreases first and then increases, the porosity increases from 51% to 74%, and the compressive strength decreases from 12.5 to 5.3 MPa. The mechanisms for controlling shrinkages during preparation of porous alumina-calcium aluminate ceramics can be attributed to the following aspects: on one hand, gas release from burning of PMMA and decomposition of CaCO₃ during sintering; on the other hand, volume expansion due to the formation of lower density calcium aluminates which come from the reactions between CaO and Al₂O₃. The near net size preparation technique is of great significance for the manufacture of porous ceramics since the subsequent machining cost can be effectively reduced.     

Sintering of porous alumina using an alumina slurry containing aluminum and polysiloxane

We herein describe the sintering of a slurry containing alumina, aluminum, and polysiloxane. After sintering, porous alumina was obtained with an increased bulk density but without any remarkable change in volume. In addition, necking was found to occur between the alumina and aluminum particles due to the formation of an aluminum silicate layer by polysiloxane upon sintering at 800°C, and this necking resulted in volume expansion upon further heating. Furthermore, the bulk density of the sample increased due to aluminum filling the spaces between particles during aluminum oxidation when sintering at temperatures ≥1200°C.     

Optimal design on the mechanical and thermal properties of porous alumina ceramics based on fractal dimension analysis

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.     

Porous ceramics derived from steel slag/coal gangue mixtures using cigarette butts as the pore-forming agent

Fabrication of ceramic materials with interconnected pores is necessary to improve thermal energy storage efficiency in high-temperature infiltration technology. In the present study, industrial wastes such as coal gangue, steel slag, etc., were selected as the raw materials to prepare ceramics with interconnected pores. By adopting 50% cigarette butts as the pore-forming agent, steel slag–coal gangue mixtures with a mass ratio of steel slag to coal gangue of 1:9 were sintered at 1100°C, and ceramics with interconnected elongated pores were prepared successfully. The highest apparent porosity and lowest volume density of the as-prepared ceramics were ca. 73% and .74 g/cm³, respectively. Further measurements of the thermophysical properties indicated that no obvious mass loss was observed in the temperature range from ambient temperature to 800°C. The maximum values of specific heat and thermal conductivity were 1.38 J/(g K) and 1.661 W/(m K), respectively, and meanwhile the minimum compressive strength could exceed 3.5 MPa. These research results implied that the as-prepared steel slag–coal gangue ceramics can provide long-term service and offer excellent thermal stability over a wide temperature range. Therefore, they should have potential applications in high-temperature infiltration technology.     

Properties of porous zirconia ceramics fabricated by using various pore-forming agents

The present work proposes a new method for fabrication partially stabilized porous zirconia ceramics using monoclinic zirconia as raw material, yttrium nitrate and magnesium compounds as pore-forming agents and stabilizers. Effects of different pore-forming agents, firing temperatures and firing time on properties of samples were investigated. Thermal decomposition of yttrium nitrate and magnesium compounds creates a large number of pores, and thus porous zirconia ceramics were fabricated. ZrO₂ can be partially stabilized by Y₂O₃ and MgO derived from the precursors. The porous ZrO₂ ceramics obtained by using Y(NO₃)₃·6H₂O and 4MgCO₃·Mg(OH)₂·6H₂O as pore-forming agents had relatively high stabilization ratio, uniform pores and high strength. The optimum firing temperature and firing time are 1400 °C and 3 h, and the samples have the stabilization ratio of 45.7%, high cold crushing strength (26 MPa), uniform pores, and apparent porosity is about 40%.     

Low-temperature preparation of porous SiC ceramics using phosphoric acid as a pore-forming agent and a binder

Porous SiC ceramics combine the properties of both SiC ceramics and porous materials. Herein, we design a facile method via pressureless sintering at relatively low temperatures for the synthesis of porous SiC ceramics. In the synthesis process, phosphoric acid was used as the sintering additive that reacted with SiO₂ on the surface of SiC to form phosphates. The formed phosphates acted as a binder to connect the SiC particles. At a fixed temperature, the phosphates were partially decomposed and released a large amount of gas. This changed the pore structure of the ceramics and greatly improved their porosity. Finally, we obtained the porous SiC ceramics with high porosity and high strength. We investigate the effects of H₃PO₄ content on the phase composition, microstructure, porosity, mechanical properties and thermal expansion coefficient of the prepared porous SiC ceramics. It was shown that at the sintering temperature of 1200 °C, the highest porosity of the samples can reach 70.42% when the H₃PO₄ content is 25 wt%, and their bending strength reaches 36.11 MPa at room temperature when the H₃PO₄ content is 15 wt%. In addition, the porous SiC ceramics show good high-temperature stability with a bending strength of 42.05 MPa at 1000 °C and the thermal expansion coefficient of 3.966 × 10⁻⁶/°C.     

Foam-gelcasting preparation of high-strength self-reinforced porous mullite ceramics

High-strength self-reinforced porous mullite ceramics were prepared via foam-gelcasting using mullite powder as a main raw material, AlF₃·3H₂O (0–8 wt%) as an additive, Isobam-104 as a dispersing and gelling agent, sodium carboxymethyl cellulose as a foam stabilizing agent, and triethanolamine lauryl sulfate as a foaming agent. The effects of AlF₃·3H₂O content on rheological and gelling behaviors of the slurries, and porosity and mechanical properties of self-reinforced porous mullite samples were examined. Addition of AlF₃·3H₂O promoted the in-situ formation of elongated mullite in the fired porous samples, which improved considerably their mechanical properties. Compressive strength and flexural strength of 67.0% porous mullite ceramics prepared with addition of 6 wt% AlF₃·3H₂O was as high as 41.3 and 13.9 MPa, respectively. Its hot modulus rupture (HMOR) increased initially with the testing temperature, and peaked (with a maximum value of 16.6 MPa) at 800 °C above which it started to decrease with the testing temperature. Nevertheless, it was still retained as high as 6.7 and 2.8 MPa at 1200 and 1400 °C, respectively.     

Effect of alumina fiber content on pore structure and properties of porous ceramics

Porous Al₂O₃ ceramics with different contents of alumina fibers were prepared by gel-casting process. The effects of Al₂O₃ fiber content on pore size distribution, porosity, compressive strength, and load-displacement behavior of the ceramic materials were investigated. Initial results showed that with the increase of Al₂O₃ fiber content, the pore size and porosity of the material is increased, and the compressive strength is decreased. However, upon increasing the fiber content from 50 wt% to 67 wt%, the performance of the samples changed greatly. The compressive strength of the material increased, while the porosity remained unchanged, the pore size increased greatly, and the shape of the load displacement curve changed. It showed that when the fiber content increased from 50 wt% to 67 wt%, the loading body in the fiber-reinforced porous ceramics changed from particles to fibers.     

堇青石多孔陶瓷制备及其性能优化研究进展

堇青石多孔陶瓷因具有高的孔隙率,优异的力学强度和良好的抗热震性能而被用作汽车尾气催化剂的载体材料.为此,综述了堇青石多孔陶瓷的制备方法和掺杂元素与其性能(孔结构、抗热震性和力学强度等)的相关性,同时指出了堇青石多孔陶瓷在制备过程中存在的问题,并展望了作为汽车尾气催化剂载体的堇青石多孔陶瓷未来的发展方向.     

氧化铝陶瓷低温烧结的研究现状和发展前景

本文综述了氧化铝陶瓷低温烧结的研究现状,包括粉体的制备,处理,成型及烧结工艺,并对此领域做了相应的设想和展望。     

叔丁醇基凝胶注模成型制备氧化铝多孔陶瓷

以微米级Al2O3粉料为原料,叔丁醇为溶剂,采用凝胶注模成型工艺制备了氧化铝多孔陶瓷,并研究了Al2O3浆料的固相体积分数(分别为8%、10%、13%和15%)对1 500℃保温2 h烧后氧化铝多孔陶瓷的气孔率、气孔孔径分布、耐压强度、热导率和显微结构的影响.结果表明:当Al2O3浆料的固相体积分数从8%增加到15%时,氧化铝多孔陶瓷烧结体的总气孔率从71.2%逐渐降低至61.2%,气孔平均孔径从1.0 μm逐渐减小至0.78 μm,耐压强度从16.0 MPa逐渐增大至45.6 MPa,而热导率从1.03 W·(m·K)-1逐渐增大至1.83W·(m·K)-1.     

Novel camphene/photopolymer solution as pore-forming agent for photocuring-assisted additive manufacturing of porous ceramics

This study proposes camphene/photopolymer solutions as a novel pore-forming agent for the photocuring-assisted additive manufacturing of porous ceramics. Unlike conventional techniques using molten camphene, solid camphene can be directly dissolved in the photocurable monomer hexanediol diacrylate (HDDA) at room temperature, which can then crystallize with a dendrite-like morphology based on phase separation at lower temperatures. This unique approach allows alumina suspensions to solidify at ―2 °C and then effectively be photopolymerized using a digital light processing engine, resulting in camphene-rich crystals surrounded by photopolymerized alumina/HDDA walls. Sintered samples exhibited a highly porous structure, with the pores created after the removal of the camphene-rich crystals. Two different pore sizes were obtained in the lower and upper regions of a single layer, due to a decrease in the solidification rate along the building direction, although their porosities were similar (～ 52 vol%). The porous samples exhibited a compressive strength of ～ 265 MPa.     

Preparation of calcium hexaluminate porous ceramics by gel-casting method with polymethyl methacrylate as pore-forming agent

Calcium hexaluminate (CA₆) porous ceramics were prepared by gel-casting method, with α-Al₂O₃ and CaCO₃ as raw materials and polymethyl methacrylate (PMMA) microspheres as pore-forming agent. The effects of the amount of pore-forming agent PMMA microspheres on the phase composition, bulk density, apparent porosity, flexural strength, microstructure, thermal shock stability and thermal conductivity of CA₆ porous ceramics were systematically studied. The pores of CA₆ porous ceramics are mainly formed by the burning loss of PMMA microspheres and the decomposition of organic matter. Adding an appropriate amount of PMMA microspheres as pore-forming agent has a positive effect on the thermal shock stability of CA₆ porous ceramics. When the amount of pore-forming agent is 15 wt%, the volume density of CA₆ porous ceramics is 1.33 g/cm³, the porosity is 63%, the flexural strength is 13.9 MPa, the thermal shock times can reach 9 times, and the thermal conductivity is 0.293 W/(m·K), which can meet the application in refractory, ceramics or high temperature cement industries.     

Preparation and characterization of eco-friendly and low-cost mullite-corundum foamed ceramics with low thermal conductivity

Mullite-corundum foamed ceramics were prepared by direct-foaming method using white clay and industrial alumina as raw materials, and calcium aluminate cement (CAC) as the binder. Effects of the calcium aluminate cement content on the phase compositions, microstructures and properties of the foamed ceramics were investigated through X-ray diffractometer (XRD), scanning electron microscopy (SEM) and energy dispersive spectrometer (EDS), etc. The results showed that with increasing the calcium aluminate cement content from 0 wt% to 8 wt%, the viscosities of the initial slurries decreased, the porosities of the samples improved, the thermal conductivities decreased, and the compressive strengths increased first and then decreased. The optimized sample with 4.0 wt% CAC content had a high porosity of 80.8%, a low bulk density of 0.56 g/cm³ and a low thermal conductivity of 0.232 W/(m·K) (800 °C). On the foundation of research results, the Gong equation (GE model) and a modified GE model were used to predict the thermal conductivity at 200 °C and 800 °C of the mullite-corundum foamed ceramics with different pore characteristics and phase compositions, respectively.