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.     

Editorial

In this study the Taguchi method is used to find the optimal process parameters for aluminium foam manufacturing. Porous metals are the unique materials used for light weight structural components, for filters and electrodes and for shock or sound absorbing products. Recently, interesting foaming technology developments have proposed metallic foams as a valid commercial chance. Metallic foam manufacturing techniques include solid state powder methods, gas blowing processes, metal deposition onto a polymer precursor and liquid state processing. The aluminium foams presented in this study are produced by the powder metallurgy route starting from aluminium powders with titanium hydride as the foaming agent. During the experimental work, many samples are made by utilizing the combination of process parameters based on Taguchi orthogonal design. Three manufacturing parameters are studied: the silicon carbide content in powder mixture, the compaction pressure and the foaming temperature. The Taguchi method is applied to design an orthogonal experimental array and a multi-objective optimization approach is then proposed by simultaneously minimizing the relative density and maximizing the absorbed energy. Verification test is also performed to prove the effectiveness of the presented technique.     

Effects of aluminium powder content and cold rolling on foaming behaviour of xAlp/Al5Si4Cu4Mg/0.8TiH2 composites

Abstract

Aluminium foams were produced by applying powder metallurgy technology. The process began by making aluminium powder and mixing it with alloy powder (Al5Si4Cu4Mg) and foaming agent (TiH₂). The mix was compacted to the form of a billet by cold pressing and then it was hot extruded to a dense foamable strip, which was cold rolled to give 40% thickness reduction. The resulting precursor composites of both the extruded strip and the extruded plus rolled strip were then freely foamed without a mould at a constant temperature of 700°C for different foaming times. The effects of aluminium powder content and cold rolling on the foaming characteristics of the foamable composite strip were studied. It is noted that aluminium powder fibre in the extruded composite strip acts as a barrier to pore initiation and evolution due to the higher melting point of pure aluminium fibre than that of the alloy matrix. Cold rolling promotes foaming of the composite strip due to the TiH₂ cracking and debonding between TiH₂ particles and metal matrix. The morphological and microstructural evolution of composite foams was also investigated. The foaming mechanism can be described by the following sequence: cracklike pore nucleation between elongated powder fibres; ellipsoidal, spherical, and polygonal pore growth; and the collapse of pores as a result of coalescence.     

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 and investigation of influence of CaCO3 as foaming agent on Al-SiCp foam

Closed cell aluminum foams have been used in various disciplines of engineering. Aluminum foams provide high strength with the advantage of low weight. In the current research, CaCO₃ is used as a foaming agent for producing closed-cell aluminum foams. For the fabrication of homogenous foam, optimization of process parameters was done. The effect of SiC as a thickening agent on structural property of foams viz. density and porosity have been inspected. Foams with density 0.40–0.86 g/cm³ were produced. The produced foams were studied under axial compression tests for evaluating mechanical properties. It can be inferred from the results that by adding 3 wt.% CaCO₃, the uniform viscosity of melt was achieved and a homogeneous foam structure is achieved with optimum porosity. Also, 5 wt.% addition of CaCO₃ in melt and stirring speed at 1400 rpm tend to increase porosity and decrease cell wall thickness. The optimum values for thickening agent SiC, foaming agent CaCO₃ at stirring speed 1400 rpm were found out to be 15 wt.%, 3 wt.%. The effect of relative density, the addition of thickening and foaming agent is studied.     

Dynamic Collapse Mechanisms in Metal Foam Expansion

The study provides insight into decomposition of titanium hydride as foaming agent for powder metallurgically produced aluminum foams. Decomposition is characterized using thermal and kinetic analysis, allowing prediction of decomposition reactions. Such predictions are made for various time–temperature cycles, which are experimentally evaluated in parallel foaming experiments. A new explanation of foam collapse is derived from the results, which interprets hints at a maximum gas release rate, limiting maximum expansion, in terms of the existence of a maximum cell wall stretching rate and expanding foam can sustain. Thus a dynamic collapse criterion is added to existing static ones.     

The relationship between thermal decomposition properties of titanium hydride and the Al alloy melt foaming process

Using a new temperature programmed decomposition (TPD) theory and related experimental technique, a set of thermal decomposition kinetics equations of titanium hydride can be acquired by separating and simulating its TPD spectrum. According to these equations, the relation curve of decomposition quantity and time for titanium hydride at temperature of 940 K is obtained and the result coincides well with the Al alloy melt foaming process, which provides a scientific basis for controlling the Al alloy melt foam and then the Al alloy foams with different pore structure are successfully prepared.     

The influence of the stabilizing agent SDS on porosity development in alkali-activated fly-ash based foams

Alkali activated foams (known also as “geopolymer foams”) are formed by the adding of a foaming agent, such as Al powder or H₂O₂, to an alkali activated matrix which can be based on, for example, fly ash, slag or meta-kaolin. The foaming agent decomposes and reacts inside the matrix, resulting in the release of gasses which form pores within the structure. Such pores have to be created before the alkali activated foams harden. In order to prevent the escape of these gasses from the foam, a stabilizing agent can be added to the foam mixture. This paper presents the results of tests involving the pore-foaming process in the case of highly porous, alkali activated, fly-ash based foams. Between 0.5 and 1.5 mass % of H₂O₂ was added to the fly ash precursor as a foaming agent, as well as different amounts (varying from 0.1 to 4.0 mass %) of the selected stabilizing agent, which is known as SDS - sodium dodecyl sulfate. The physical, mechanical, and microstructural properties of the hardened alkali-activated foams were determined. Their pore structures were characterised by SEM, as well as by a three-dimensional (3D) technique, X-ray computed micro-tomography. The advantage of the latter method is that a better insight can be obtained into the characteristics of the hardened pore structure, including information about its homogeneity and the pore size distribution. The influence of the amount of the added foaming agent, as well as that of the amount of the stabilization agent, was evaluated, and optimal addition mass percentages were determined. In the case of the best mixtures, the investigated hardened pore structures showed relatively good mechanical properties, and could therefore be used for various applications in the building industry.     

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.     

The FOAMCARP process: foaming of aluminium MMCs by the chalk-aluminium reaction in precursors

A brief outline is presented of the factors involved in the search for gas-generating agents offering superior performance for foaming of liquid aluminium alloys. These include kinetic and thermodynamic characteristics of decomposition reactions, the ease of dispersion of the powdered foaming agent in the melt, the nature and likely effect of decomposition products on melt flow, potential reactions between the foaming gas and the melt and the availability, cost and ease of handling of the powder concerned. There is one very promising candidate material, calcium carbonate, which offers advantages compared to currently-employed hydride powders in virtually all aspects of their performance. It is shown that foams can be produced having appreciably finer cells (<1 mm diameter) and more uniform cell structures than currently-available melt route foams, a potentially lower ceramic content in the cell walls and dramatically reduced raw material costs. The presence of an oxidising foaming gas in the cells leads to reaction with the liquid cell surface, forming a continuous oxide film. The presence of this film has a significant effect on foam stabilisation, slowing down cell coalescence and melt drainage.     

In situ fabrication of titanium carbide reinforced copper MMC

Abstract

The in situ fabrication of titanium carbide reinforced copper and aluminium bronze (AB2) composites by carbothermal reduction of titanium in an induction furnace has been investigated. An inert atmosphere was maintained with carbon monoxide created as a byproduct from the heat of reaction between the induction field, graphite crucible and graphite lid. Titanium carbide particles of the order 1–3 μm were formed in aluminium bronze at approximately 1250°C and, in copper, particles of order 1–6 μm were produced at approximately 1330°C. Dispersion concentrations of titanium carbide of 20% and 6.5% were obtained for copper and aluminium bronze respectively. In addition, evidence is presented indicating that iron could be used as a dispersion medium for titanium carbide particulates in aluminium bronze alloys.     

SiOC ceramic foams synthesized from electron beam irradiated methylsilicone resin

A new method to prepare silicon oxycarbide (SiOC) foams has been developed and it consists of electron beam irradiation of a methylsilicone preceramic polymer followed by pyrolysis in an inert atmosphere. Methylsilicone resin foams were prepared by simultaneous curing and foaming, without the addition of calalysts or blowing agents. The polymer precursor was irradiated with 1.5 MeV EB up to a dose of 7.0 MGy and at a dose rate of 2.8 kG/s, in air. During irradiation the polymer melted, due to rapid increase in temperature, and simultaneously crosslinked by interaction with the ionizing radiation. Crosslinking occurred mainly by poly-condensation reactions and gaseous condensation products were released. The latter acted as an intrinsic foaming agent in the molten polymer. Foams obtained with radiation doses higher than 3.5 MGy showed a high degree of crosslinking with a ceramic yield of over 89% at 1,000 °C. Pyrolysis at 1,200–1,500 °C resulted in SiOC ceramic foams with dense struts and walls, with bulk density around 0.3 g/cm³ and total porosity of 84%. Foams pyrolyzed at 1,200 °C revealed compression strength of 6.8 MPa.     

Compressive properties of closed cell Al alloy–fly ash particle composite foams

Abstract

The closed cell aluminium alloy–fly ash particle composite (Al/FA) foams containing 1·5 wt-% fly ash were manufactured by molten body transitional foaming process. The quasi-static compressive properties of Al/FA have been investigated. Results show the compressive stress–strain curves of Al/FA foams exhibit three regions, i.e. the elastic region, the plastic plateau region and the densification region. A linear relationship between the densification strain and the relative density was obtained. The relation between the plastic collapse stress and the relative density can be described with Gibson and Ashby’s model. The energy absorption capacities of the Al/FA foams gradually increase with increasing strain and relative density.     

A study of fabricating and compressive properties of cellular Al–Si (355.0) foam using TiH2

Al–Si (355.0) alloy foam has been produced by Alporas method (in which foam alloy melts, and titanium hydride is used as a blowing agent). Mechanical behavior such as quasi-static compression (strain–stress curves, energy absorption capacity), also the effects of thermal properties on the macroscopic structure of the produced foam were investigated. In addition, the effect of energy absorption capacity on percentage porosity has also been studied. The research shows that the produced foam with an average cell size and proper distribution has a more mechanical stability compared to the foams with no such characteristics. It was found that yield strength tends to increase from 12.51 MPa for porosity 74.0% to 22.32 MPa for porosity 54.0%. This foam has also been compared with other foams such as Al-pure foam and Mg foam. It can be stated that Al–Si (355.0) foam has a higher yield strength in comparison to Al-pure foam and Mg foam.     

Deformation characteristics of metal foams

The deformation behaviour of a series of aluminium and zinc foams was investigated by uniaxial testing. Because the deformation behaviour of metal foams is expected to be anisotropic owing to the existence of a closed outer skin and with respect to the foaming direction, a series of measurements was carried out where the orientation of the outer skin and the foaming direction were varied. Stress–strain diagrams and corresponding compression strengths were determined for aluminium- and zinc-based foams. The influence of an age-hardening heat treatment was investigated. Finally, the axial deformation behaviour of aluminium tubes filled with aluminium foam was tested under uniaxial loading conditions. The results of the measurements are discussed in the context of possible applications of metal foams as energy absorbers. © 1998 Chapman & Hall     

Improvement of the foaming process for 4045 and 6061 aluminium foams by using the Taguchi methodology

Taguchi methodology has been applied to the production process of aluminium foams to investigate the variability detected in several properties (including bulk density, outward appearance and density homogeneity along foaming direction), for foaming tests carried out under identical conditions. The analysis of the process has been performed separately for two different alloys, the 4045 and 6061. The results have allowed finding the main factors that influence those properties. In addition, it has been possible to establish those foaming conditions able to minimize the variability in density, to improve the outward appearance and to obtain a higher homogeneity in density, all at the same time. Different final factors have been found for the two alloys; such differences have been explained in terms of the different viscosity of the aluminium melts as well as the different content of foaming agent.     

双马来酰亚胺泡沫的微观形貌与结构控制研究

以偶氮二甲酰胺(AC)为发泡剂制备了改性双马来酰亚胺(BMI)泡沫,用扫描电镜(SEM)对泡沫的微观形貌进行观察,研究泡沫的发泡过程及不同条件下泡沫的泡孔结构,包括密度、孔径、单位体积的泡孔数目、发泡倍率等。结果表明:改性的BMI泡沫是一种闭孔结构泡沫,其构型为排泄型十二面体。可通过发泡体系的黏度、温度和发泡剂含量控制BMI泡沫的结构,随发泡体系黏度的增加,泡沫密度,成核密度N0和单位体积的泡孔数目Nf增加,泡孔直径减小,均匀性变好。泡沫密度随发泡剂AC含量提高而降低,当AC含量超过7%(质量分数)时,泡沫密度反而上升。随发泡温度提高,泡沫密度降低,孔径增大,泡沫成型稳定性变差。     

Moulded polypropylene foams produced using chemical or physical blowing agents: structure–properties relationship

Polypropylene (PP) foams have become essential items due to their excellent properties. Nevertheless, obtaining net-shaped PP foams with medium relative densities is a complicated issue. In this article, two processes able to produce moulded PP foams in this density range are presented. One of them is based on a modification of the pressure quench foaming method and therefore uses a physical blowing agent (CO₂). The second one is the improved compression moulding technique which uses a chemical blowing agent (azodicarbonamide). PP foams with relative densities in the range between 0.25 and 0.6 and cylindrical shape were prepared using these foaming techniques. A common PP grade (instead a highly branched one) was used to obtain the samples, showing, that by combining the appropriate foaming technique, the adequate moulds, suitable blowing agent and proper foaming parameters, net-shaped PP foams with excellent properties can be produced starting from a conventional PP grade. Samples were characterized by analyzing their cellular structure and their mechanical properties. Results have showed that depending on the chosen foaming route isotropic or anisotropic structures with cell sizes ranging from 40 to 350 μm and open cell content in the range between 0 and 65% can be obtained. Moreover, mechanical properties are highly influenced by the production route and chemical composition of the foams. For instance, the stiffer materials at relative densities higher than 0.4 are the ones produced using the chemical blowing agent while at relative densities lower than 0.4 are the ones produced using the physical blowing agent.     

Fracture of open- and closed-cell metal foams

Two closed cell aluminium foams and one open cell nickel-chromium foam were subjected to microstructural characterization, in situ fracture tests and fractography. The failure process of the open cell foam was observed to be rather ductile, while that of the closed cell foams was found to be brittle. The ductility was related to the purity of the nickel chromium alloy, resulting in necking to be the dominant source of energy dissipation during failure. The brittleness of the closed cell foams was related to the presence of precipitates and particles in the cell wall microstructure, limiting the amount of plastic dissipation. The embrittling phases were traced back to the alloy composition, viscosity enhancing additions and foaming agent.