Manufacturing of Al/SiCp composite foams using calcium carbonate as foaming agent

Abstract

The aluminium composite foams reinforced by different volume fractions of SiC particles were manufactured with the direct foaming route of melt using different contents of CaCO₃ foaming agent. The density of produced foams changed from 0·43 to 0·76 g cm^?3. The microstructural features and compressive properties of the Al/SiC_p composite foams were investigated. Compressive stress–strain curve of Al/SiC_p composite foams is not smooth and exhibits some serrations. At the same relative density of composite foams, the plateau stress of the composite foams increases with increasing volume fraction of SiCp and decreasing weight percentage of CaCO₃. The relation between plateau stress, relative density, weight percentage of CaCO₃ and SiCp volume fraction of Al/SiCp composite foams with a given particle size was investigated.     

Fabrication of pure SiC ceramic foams using SiO2 as a foaming agent via high-temperature recrystallization

A novel method was developed to produce the pure silicon carbide foams via the high-temperature recrystallization with the presence of a novel foaming agent-SiO₂. In this method, SiO₂ reacts with SiC to produce the gases in the silica liquid at high temperature, which leads to the formation of foams. The foams consist of the directional and interconnecting SiC crystals, and numerous intercommunicating pores that are located between them. The phase of foams was identified as 6H-SiC without the presence of SiO₂ since SiO₂ particles could react completely with SiC particles and vaporize from the sample at high temperature. The total porosity, weight loss and volume expansion rate can be increased with increasing SiO₂ contents while the three-point bending strength decreasing. The porosity of SiC foam with 25 wt.% SiO₂ as a foaming agent exhibits the maximum value while the three-point bending strength shows minimum value correspondingly. The sintered samples presented the porosities of 61-81%, the bending strength from 1.5 MPa to 4.8 MPa, and the volume expansion rate from 17.4% to 65%. This research can develop the theory for the preparation of SiC ceramics foams with controlled structure.     

Closed cell ZA27–SiC foam made through stir-casting technique

Closed cell zinc aluminum alloy (ZA27)–SiC composite foam has been synthesized using conventional stir-casting technique and CaH₂ as foaming agent. The synthesized foams are characterized in terms of its micro-architectural characteristics and deformation responses under compressive loading. It is observed that ZA27–SiC foams could be easily foamed without any difficulty. The density of the developed foam ranges from 0.25 gm/cc to 0.45 gm/cc due to the variation of CaH₂ percentage. The plateau stress and energy absorption of these foams follow power law relationship with relative density. Wherein, the densification strain follows a linear relationship with the relative density.     

Effect of nano-Calcium Carbonate on microcellular foaming of polypropylene

Using supercritical carbon dioxide as the physical foaming agent, a new batch process was carried out to prepare microcellular polypropylene (PP) and polypropylene/nano-Calcium Carbonate (PP/nano-CaCO₃) foams. Four concentrations of nano-CaCO₃, 3, 5, 7, and 10 wt% were used. The cell structure of foams and advantages of this new process were investigated and explained by thermal properties. Results showed that the foamed PP/5 wt% nano-CaCO₃ produced a microcellular foam with the minimum mean cell diameter (9.55 μm) and maximum cell density (1.50 × 10⁹ cells/cm³) among the four blends. Some unfoamed regions were observed in nanocomposite foams because nano-CaCO₃ could accelerate crystallization in cooling and cryostat stage. The new process took much less time (2.5 h) to foam and had much broader foaming temperature range (about 55 °C). But the foaming temperature range decreased after blending nano-CaCO₃ into PP matrix because nano-CaCO₃-induced isothermal and non-isothermal crystallization at higher temperature. In addition, the cell growth effect on variations of volume expansion ratio in PP/nano-CaCO₃ nanocomposites could be neglected comparing with the heterogeneous cell nucleation effect.     

Experimental Investigation on Steel Foams Fabricated by Sintering-Dissolution Process

This article describes a new process to manufacture open-cell steel foams. Calcium chloride anhydrous is used as a space holder. By changing the values of the main manufacturing parameters such as volume percentage, and the size and shape of the space holder, we produce different steel foam samples which cover a wide range of solid fraction, pore size, and shape. The effects of space-holder content and sintering condition such as temperature and time on the porosity of steel foam samples are discussed. The microstructure and composition of steel foam samples are observed and analyzed by scanning electron microscope and X-ray diffraction. The compressive curves of steel foams are measured by a universal testing machine. The experiment results show the compressive strength of steel foam samples with porosities between 65% and 85% is in the range of 66.4 ～ 12.9 MPa. The compressive strength depends mainly on the porosity and pore shape. The absorbed energy per unit volume (W) of steel foams with porosities between 85% and 65% is in range of 6.8 ～ 31.2 MJ/m³. Under the condition of identical porosity, the absorbed energy per unit volume (W) of steel foam is about three times of aluminum foam. In compression, steel foam specimens show heterogeneous macroscopic deformation.     

镀铜碳纤维增强铝基泡沫材料结构的特性表征

以纯铝为基体材料,TiH2为发泡剂,镀铜碳纤维为添加剂,制备了不同孔隙率的泡沫铝材料。研究了发泡时间、镀铜碳纤维掺杂量对泡沫铝相对密度、孔径和微观结构的影响。结果表明,在碳纤维含量相同情况下,发泡时间越短,泡沫铝试样的相对密度越大,孔径越小。发泡时间相同时,碳纤维含量越多,泡沫铝的相对密度越大。SEM检测表明,碳纤维在Plateau边界内随机分布,而在气泡壁中和气泡壁表面基本呈平行分布,未发生团聚现象。     

Formulation optimization of unreinforced and lignin nanoparticle-reinforced phenolic foams using an analysis of variance approach

Formulations of unreinforced and lignin nanoparticle-reinforced phenolic foams were optimized using an analysis of variance approach. The variables studied in the formulation of phenolic foams were stirring speed (650–850 rpm) and blowing agent amount (1.5–3.5 wt.%). For lignin nanoparticle-reinforced phenolic foams, the variables were lignin nanoparticle weight fraction (1.5–8.5 wt.%) and blowing agent amount (1.5–3.5 wt.%). The responses measured for both foams were density, compressive modulus, and compressive strength. In addition, the morphology of the foams was observed using scanning electron microscopy (SEM) to determine cell size distributions. The results showed that the variables studied exhibited a strong influence on the responses and the cell size distribution of the foams. Statistical models allowed for prediction of the properties of the foams and for comparison of the properties of unreinforced and lignin nanoparticle-reinforced phenolic foams. The incorporation of lignin nanoparticles in phenolic foams results in a compressive modulus and compressive strength that has up to 128% and 174%, respectively, of the values for unreinforced foams. The amount of blowing agent saved to produce a reinforced foam was up to 31% of the amount necessary to produce an unreinforced foam of the same density.     

泡沫SiC颗粒增强铝基复合材料的制备工艺和拉伸强度

介绍了一种新的泡沫金属材料－泡沫SiC颗粒增强铝基复合,泡沫的孔隙率为60％－85％。用TiH2作发泡剂,采用直接发泡工艺制备。由于复合材料熔体自身粘度较大,不需要采用任何增粘措施,发泡工艺简单,易于操作,该泡沫材料比普通泡沫铝或铝合金具有更高的抗拉、抗压强度。     

Effects of Electromagnetic Stirring,Shearing, and Extrusion on TiB2 and TiAl3 Particles in Al–5Ti–1B(wt.%) Alloy

Electromagnetic stirring induced metal flow and led to homogenous dispersion of TiAl₃ particles. Fragmentation mechanism induced by electromagnetic stirring also contributed to TiAl₃ particle refining. TiAl₃ particle size decreased with the increases of stirring temperature and time. Shearing force among different melt layers under the shear action of roll in the roll-shoe gap increased with the decrease of casting temperature and the increase of melt viscosity, and the fragmentation of TiAl₃ phase became obvious correspondingly. Under the optimal process parameters, Al–5Ti–1B(wt.%) alloy wire with excellent inner microstructure and high surface quality was produced. The average sizes of TiAl₃ are less than 20 µm, and TiB₂ phases are less than 0.5 µm, respectively. Al–5Ti–1B(wt.%) alloy wire manufactured by present method has a high refining ability on pure aluminum and an excellent ability of refining effectiveness.     

SiC-particulate aluminum composite foams produced from powder compacts: foaming and compression behavior

The foaming behavior of SiC-particulate (SiC_p) aluminum composite powder compacts containing titanium hydride blowing agent was investigated by heating to 750°C in a pre-heated furnace. Aluminum powder compacts were also prepared and foamed using similar compaction and foaming parameters in order to determine the effect of SiC_p-addition on the foaming and compression behavior. The SiC_p-addition (10 wt%) was found to increase the linear expansion of the Al powder compacts presumably by increasing the surface as well as the bulk viscosities. The compression tests conducted on Al and 10 and 20% SiC_p foams further showed a more brittle compression behavior of SiC_p/Al foams as compared with Al foams. The collapse stresses of Al and 10% SiC_p/Al foams were also predicted using the equations developed for the open and closed cell foams. Predictions have shown that Al foam samples behaved similar to open cell foams, while 10% SiC_p/Al foam collapse stress values were found between those of open and closed cell foams, biasing towards those of the open cell foams.     

基于常温干燥法的纤维素基泡沫制备及性能分析

传统的石油基泡沫难以降解,因而带来环境污染和安全问题。纤维素基泡沫借助其可生物降解的天然特性,逐渐成为研究热点。然而,目前的成型技术在很大程度上依赖于干燥条件（如冷冻干燥和超临界干燥）,存在干燥耗时长、成本高的问题,因而难以实现泡沫的规模化生产。为解决此问题,提出一种常温干燥制备可再生纤维素基泡沫的新方法。以纸浆纤维为主料、纳米纤维素为黏结剂、聚乙烯醇作为纤维分散剂和泡沫助剂,经过充分混合、发泡、排水和干燥后,制成纤维素基泡沫。最后,测试泡沫密度、孔隙率,分析导热性能、力学性能。结果表明：制备的纤维素基泡沫具有密度低（(0.015±0.002)~(0.028±0.004) g/cm3）、孔隙率高（>98%）、热导率低（(0.060±0.003)~(0.069±0.003) W/(m·K)）等特点。纤维素基泡沫在80%应变下的最大应力值为59.366 kPa,比其他文献报道的类似纳米纤维素基泡沫高37.1%。未来,纤维素基泡沫有望替代石油基泡沫,在冷链运输过程中对产品进行缓冲保护和隔热保温。     

Pretreatment process of SiC particles and fabrication technology of SiC particulate reinforced Zn–Al alloy matrix composite

Abstract

In the present paper, a novel pretreatment process for SiC particulate and a new mechanical–electromagnetic combination stirring process for fabricating Zn–Al(ZA27)/SiC_p composites are described. The optimal pretreatment route and the most appropriate SiC particle parameters were experimentally determined. The pretreated SiC particles were easily incorporated and dispersed in the ZA27 alloy melt and were not agglomerated before addition to the melt. The surface status of the SiC particles before and after pretreatment was observed and analysed by scanning electron microscopy, energy dispersive spectroscopy, X-ray diffraction, and transmission electron microscopy. It was found that gas existing on the SiC particle surfaces by physical and chemical absorption was a significant hindrance to the incorporation and dispersion of SiC particles in the alloy melt. The gas absorption was induced by ultrafine SiC powders, fracture steps, and ions existing on the SiC particle surfaces. The carbon, silicon, and oxygen contents on the SiC surface were varied with different pretreatment techniques. Moreover, a dense layer of amorphous SiO₂, which improves wetting of SiC particles in the ZA27 melt, was formed owing to calcination of SiC particles in air. The new combined stirring process exploits the advantages of both mechanical and electromagnetic stirring of the melt at the different processing stages during fabrication. The microstructural characteristics of the resulting composites are: homogeneously distributed SiC particles, fewer macro gas blows and inclusions, and little shrinkage porosity in comparison to composites fabricated by a mechanical stirring process. Finally, the mechanisms of degassing and reducing the porosity and the number of oxide inclusions are discussed.     

Microstructure and thermal decomposition property of Ni-P/Cr2N composite powder by electroless plating

Cr₂N is the most promising blowing agent for the preparation of steel foam using melt foaming method. In this work, to obtain a blowing agent with suitable density and gas decomposition characteristics for steel melt foaming, Ni-P/Cr₂N composite powder was prepared by electroless plating. The surface morphology, phase, coating thickness, density and decomposition characteristics of Ni-P/Cr₂N composite powder were analyzed. The results indicate that the surface of Ni-P/Cr₂N composite coating powder is covered by the high nickel and low phosphorus layer which has a dense and uniform cell structure. The decomposition rate of the Ni-P/Cr₂N composite powder is 7.46?mW/mg slower than that of the uncoated Cr₂N powder at 1107.4?°C. When the plating time is 30?min, the thickness of Ni-P layer reaches 2.86?μm, the density of the Ni-P/Cr₂N composite powder is 7.45?g/cm³, and maximal decomposition rate temperature reaches 1500?°C. These findings suggested that Ni-P/Cr₂N composite powder meets the requirements of decomposition temperature and density of the blowing agent used to produce steel foam with a uniform pore structure by the melt foaming method.     

应用于包装领域的明胶泡沫性能研究

目的 制作和表征基于明胶的生物基可堆肥降解泡沫材料,并应用于包装领域。方法 明胶泡沫通过机械发泡和在周围环境中干燥制成。研究明胶含量、表面活性剂含量以及发泡温度对泡沫最大发泡倍率(MER)、收缩、密度、结构以及压缩性能的影响。此外,研究不同明胶含量样品的导热率。结果 研究的3个因素对泡沫性能和结构有显著影响。MER值和收缩是黏度相关,并极大地影响泡沫密度、力学性能以及热导率。增加明胶含量制造出了密度和压缩强度更高的泡沫(由于MER值更低)。表面活性剂质量分数从0.75%增加到1.5%由于发泡性提升造成泡沫密度轻微下降。然而,进一步将表面活性剂质量分数提升至3%造成黏度显著增加、MER值下降,从而导致泡沫密度增加。更高的发泡温度可以得到更高的MER,但是由于液态泡沫稳定时间更长,收缩程度更大,泡沫密度更大。结论 明胶泡沫展现出作为低密度传统塑料泡沫(密度小于30 kg/m³)环保替代品极具潜力的性能。研究成功实现了明胶泡沫的低热导率〔0.038～0.039 W/(m.K)〕和相对较低的收缩程度。     

Processing of heat-treated silicon carbide-reinforced aluminum alloy composites

The present study investigates the processing of heat-treated silicon carbide (SiC) particle-reinforced 6061 aluminum alloy (AA) composites. As-received SiC powders were heat treated at 1300ºC, 1400ºC, and 1500ºC in nitrogen atmosphere for 2 h, and the 6061 AA–SiC composites were developed by spark plasma sintering at 560ºC and 60 MPa for 5 min in argon atmosphere. The amorphous silicon nitride is found to form in SiC particles as a result of heating at 1400ºC. The microstructure of the composites exhibited uniform distribution of SiC or SiC/Si₃N₄ particles in 6061 AA matrix. Further, the heat-treated SiC-reinforced 6061AA composites exhibited improved mechanical properties. A typical combination of UTS of 240 MPa and elongation of 21% is obtained for the 6061 AA composites prepared using SiC powders heated at 1400ºC.     

Fabrication of Near Net Shape Metallic Foam via Plaster Mould

Fabrication characteristics are unstable in direct foaming method. Therefore, most of near net-shape metallic foams are produced, and investigated by powder metallurgy. Direct foaming method, however, has many benefits （i.e. reduce the unit cost of goods and fabrication process etc.） to fabrication of metallic foams. In this article, the fabrication characteristic of near net-shape metallic foams by direct foaming method was evaluated. Al and Plaster was used for base material and mould material respectively. Ca and TiH2 were added to molten Al as thickening and blowing agent for stable condition of bubbles. Thickening time was about 10 min with a stirring speed of 600 r/min. Foaming time was 30-120 s for evaluation of the optimum foaming condition. Amount of agent was selected by pre-experimental data. Porosity of near net-shape goods was measured by Archimedes method. On the other hand, it seems that increasing poring time and thickening agent make the poor porosity     

Rapid sintering of silicon nitride foams decorated with one-dimensional nanostructures by intense thermal radiation

Silicon nitride foams were prepared by direct foaming and subsequent rapid sintering at 1600 °C. The intense thermal radiation generated under the pressureless spark plasma sintering condition facilitated necking of Si₃N₄ grains. The prepared foams possessed a porosity of ～80 vol% and a compressive strength of ～10 MPa, which required only ～30 min for the entire sintering processes. Rapid growth of one-dimensional SiC nanowires from the cell walls was also observed. Thermodynamic calculations indicated that the vapor–liquid–solid model is applicable to the formation of SiC nanowires under vacuum.     

Production and characterization of AA6082-(Si3N4 + Gr) stir cast hybrid composites

The present research work emphasizes the development of hybrid aluminum (AA6082) matrix composites (HAMCs) reinforced with different weight percentages (wt.%) of ball-milled (silicon nitride (Si₃N₄) + graphite (Gr)) ceramic particulates by conventional stir casting process. Si₃N₄ and Gr are ball milled to obtain a definite density of combined powder. The weight percentage of ball-milled ceramic powder is varied from 0 to 12 wt.% in a stage of 3%. The microstructures as well as mechanical properties of the fabricated hybrid composites are analyzed. The scanning electron micrograph reveals the uniform distribution of ball-milled (Si₃N₄ + Gr) ceramic particulates in the aluminum matrix. The distribution of ball-milled (Si₃N₄ + Gr) ceramic particulates has also been analyzed with x-ray diffraction (XRD) technique. Both the hardness and ultimate tensile strength have enhanced with a reduction in percentage elongation with increase in weight percentage of ball-milled (Si₃N₄ + Gr) ceramic particulates in the aluminum matrix.     

Closed-cell Al alloy composite foams: Production and characterization

Foamy Al alloy SiCp composites of different densities ranging from 0.4 to 0.7 g/cm³ were manufactured by melt-foaming process, which consisted of direct CaCO₃ addition into the molten A356 aluminum bath. Mechanical properties and morphological observations indicated that the three-stage deformation mechanism of typical cellular foams is dominant in the produced A356 aluminum foams. Middle-stage stress plateau shrinkage plus compressive strength and bending stress enhancements were observed in denser foams. With the same Al/SiCp ratio, energy absorption ability and plastic collapse strength of the closed-cell foams were increased with the foam density. Doubling cell-face bending effects resulted in larger compressive than bending strengths in the closed-cell foams; while stiffness lowering was due to the cell-face stretching conditions.     

Effect of sintering on TiO2-impregnated alumina foams

The effect of sintering on the bulk properties, morphology and phase composition of ultralight Al₂O₃ foams impregnated with TiO₂ was investigated in comparison with pure alumina foam in the temperature range of 900–1600°C in air. Impregnation was carried out by immersion of pre-sintered alumina foam in a sol of titanium isopropoxide-acetylacetone complex. The changes of the foam linear shrinkage, effective density and porosity were studied along with morphological evolution and relationship between these properties was demonstrated. Titania impregnation increased the linear shrinkage (LS) during sintering by a maximum of 5% relative to pure alumina foams. The change of LS and weight loss of TiO₂/Al₂O₃ foams lead to a final density of 0.19 g/cm³ and porosity of 95%. The initial coating was found to develop a mosaic structure due to early shrinkage of the coating. After sintering at 1600°C the coating reacted with the underlying Al₂O₃ surface and became uniformly distributed. Finally, it was shown that the reacting TiO₂ layer formed the tialite (Al₂TiO₅) phase below 1400°C. This Tialite coating remained intact under 1200°C without stabilizers.