Nanocrystalline Al/Al12(Fe,V)3Si alloy prepared by mechanical alloying: Synthesis and thermodynamic analysis

Al–Al₁₂(Fe,V)₃Si nanocrystalline alloy was fabricated by mechanical alloying (MA) of Al–11.6Fe–1.3V–2.3Si (wt.%) powder mixture followed by a suitable subsequent annealing process. Structural changes of powder particles during the MA were investigated by X-ray diffraction (XRD). Microstructure of powder particles were characterized using scanning electron microscopy (SEM). Differential scanning calorimeter (DSC) was used to study thermal behavior of the as-milled product. A thermodynamic analysis of the process was performed using the extended Miedema model. This analysis showed that in the Al–11.6Fe–1.3V–2.3Si powder mixture, the thermodynamic driving force for solid solution formation is greater than that for amorphous phase formation. XRD results showed that no intermetallic phase is formed by MA alone. Microstructure of the powder after 60 h of MA consisted of a nanostructured Al-based solid solution, with a crystallite size of 19 nm. After annealing of the as-milled powder at 550 °C for 30 min, the Al₁₂(Fe,V)₃Si intermetallic phase precipitated in the Al matrix. The final alloy obtained by MA and subsequent annealing had a crystallite size of 49 nm and showed a high microhardness value of 249 HV which is higher than that reported for similar alloy obtained by melt spinning and subsequent milling.     

Al3Ni2–Al composites with nanocrystalline intermetallic matrix produced by consolidation of milled powders

Mechanically alloyed nanocrystalline Al₆₃Ni₃₇ powder with a metastable structure of NiAl phase was mixed with 20, 30 and 40 vol.% of Al powder. The powder mixtures as well as pure powder of Al₆₃Ni₃₇ alloy were consolidated at 600 °C under the pressure of 7.7 GPa. The bulk materials were characterised by structural investigations (X-ray diffraction, light and scanning electron microscopy, energy dispersive spectroscopy), compression and hardness tests and measurements of density and open porosity. During the consolidation, the metastable NiAl phase transformed into the equilibrium Al₃Ni₂ intermetallic. The mean crystallite size of the Al₃Ni₂ intermetallic in the bulk materials is below 40 nm. The microstructure of the composite samples consists of Al₃Ni₂ intermetallic areas surrounded by lamellae-like Al regions. The hardness of the produced Al₃Ni₂–Al composites is in the range of 5–6.5 GPa (514–663 HV1), while that of the Al₃Ni₂ intermetallic is 9.18 GPa (936 HV1). The compressive strength of the composites increases with the decrease of Al content, ranging from 567 MPa to 876 MPa. The plastic elongation of the composites was increasing with the increase of Al content, while the Al₃Ni₂ intermetallic failed in the elastic region.     

Synthesis of an Al2O3/Al co-continuous composite by reactive melt infiltration

The route for the fabrication of an Al₂O₃/Al co-continuous composite by reactive melt infiltration was investigated using scanning electron microscopy, energy dispersive X-ray microanalysis and X-ray diffraction analysis. It was found that in the process of molten aluminium infiltration into the SiO₂ preform, the chemical reaction of 3SiO₂ + 4Al → 2Al₂O₃ + 3Si occurred at the infiltration front, and generated a transition zone containing a new type of continuous porosity about 100 μm in width. The reaction continued with further infiltration of molten aluminium alloy into this porosity which reacted with the residual SiO₂ until all the SiO₂ was transformed into Al₂O₃. A comparison was made between this route and that by direct infiltration of molten aluminium alloy into the open porosity of an Al₂O₃ preform. As a result of the increased wetting ability of the molten aluminium alloy by the chemical reaction, reactive melt infiltration took place at a higher rate for the SiO₂ preform than that for the direct infiltration of the Al₂O₃ preform. A fracture surface examination demonstrated a toughening effect provided by the continuous aluminium alloy in the composite.     

Microstructure and mechanical properties of hot extruded 6016 aluminum alloy/graphite composites

The incorporation of graphite particles into AA6016 aluminum alloy matrix to fabricate metal/ceramic composites is still a great challenge and various parameters should be considered. In this study, dense AA6016 aluminum alloy/(0-20 wt%) graphite composites have successfully been fabricated by powder metallurgy process. At first, the mixed aluminum and graphite powders were cold compacted at 200 MPa and then sintered at 500 ℃ for 1 h followed by hot extrusion at 450 ℃. The influence of ceramic phases(free graphite and in-situ formed carbides) on microstructure, physical and mechanical properties of the produced composites were finally investigated. The results show that the fabricated composites have a relative density of over 98%. SEM observations indicate that the graphite has a good dispersion in the alloy matrix even at high graphite content. Hardness of all the produced composites was higher than that of aluminum alloy matrix. No cracks were observed at strain less than 23% for all hot extruded materials.Compressive strength, reduction in height, ultimate tensile stress, fracture stress, yield stress, and fracture strain of all Al/graphite composites were determined by high precision second order equations. Both compressive and ultimate tensile strengths have been correlated to microstructure constituents with focusing on the in-situ formed ceramic phases, silicon carbide(SiC) and aluminum carbide(Al_4 C_3). The ductile fracture mode of the produced composites became less dominant with increasing free graphite content and in-situ formed carbides. Wear resistance of Al/graphite composites was increased with increasing graphite content. Aluminum/20 wt% graphite composite exhibited superior wear resistance over that of AA6016 aluminum alloy.     

Infiltrated Cu8Al–Ti alumina composites

The effect of titanium additions on the interface and mechanical properties of infiltrated Cu8 wt%Al–Al₂O₃ composites containing 57 ± 2 vol% ceramic are investigated, exploring two different Al₂O₃ particle types and four different Ti concentrations (0, 0.2, 1, 2 wt%Ti). Addition of 0.2 wt%Ti leads to the development of a thin (5–10 nm) layer enriched in Ti at the interface between Cu alloy and Al₂O₃ particles; this Ti concentration produces the best mechanical properties. With higher Ti-contents Ti₃(Cu, Al)₃O appears; this decreases both the interface and composite strength. Composites reinforced with vapor-grown polygonal alumina particles show superior mechanical properties compared to those reinforced by angular comminuted alumina particles, as has been previously documented for aluminum-based matrices. Micromechanical analysis shows that damage accumulation is more extensive, as is matrix hardening by dislocation emission during composite cooldown, in the present Cu8 wt%Al matrix composites compared with similarly reinforced and processed Al-matrix composites.     

Influence of B4C on the tribological and mechanical properties of Al 7075–B4C composites

In the present investigation, the influence of B₄C on the mechanical and Tribological behavior of Al 7075 composites is identified. Al 7075 particle reinforced composites were produced through casting, K₂TiF₆ added as the flux, to overcome the wetting problem between B₄C and liquid aluminium metal. The aluminium B₄C composites thus produced were subsequently subjected to T6 heat treatment. The samples of Al 7075 composites were tested for hardness, tensile, compression, flexural strengths and wear behavior. The test results showed increasing hardness of composites compared with the base alloy because of the presence of the increased ceramic phase. The wear resistance of the composites increased with increasing content of B₄C particles, and the wear rate was significantly less for the composite material compared to the matrix alloy. A mechanically mixed layer containing oxygen and iron was observed on the surface, and this acted as an effective insulation layer preventing metal to metal contact. The coefficient of friction decreased with increased B₄C content and reached its minimum at 10 vol% B₄C.     

Production and properties of SiCp-reinforced aluminium alloy composites

A vacuum infiltration process was developed to produce aluminium alloy composites containing various volume fractions of ceramic particles. The matrix composites of aluminium with 9.42 wt%Si and 0.36 wt%Mg containing up to 55 vol% SiCp were successfully infiltrated and the effect of infiltration temperature and volume fraction of particle on infiltration behaviour was investigated. In addition to aluminium powder, magnesium was used to improve the wetting of SiC particles by the molten aluminium alloy. The infiltration rate increased with increasing infiltration time, temperature and volume fraction of particle, but full infiltration appeared at the optimum process parameters for the various volumes of fraction composite compacts. In addition, the microstructure, hardness, density, porosity and wear resistance of the composites were also examined. It is observed that the distribution of SiC particles was uniform. The hardness and density of the composite increased with increasing reinforcement volume fraction and porosity decreased with increasing particle content. Moreover, the wear rate of the composite increased with increasing load and decreased with increasing particle content.     

Al2O3–FeCrAl composites and functionally graded materials fabricated by reactive hot pressing

Al₂O₃–FeCrAl composites were fabricated by mixing Fe₂O₃, Al and Cr powders and then reactive hot pressing. The high temperature alloy FeCrAl was formed by the reaction of extra Al, Cr and the Fe reduced from Fe₂O₃. The Al₂O₃–FeCrAl composites with various Al₂O₃ fractions were successfully fabricated by the proper addition of extra Fe, Cr, Al or Al₂O₃ powders. A five-layer functionally graded material of YSZ–FeCrAl was fabricated using the Al₂O₃–FeCrAl composites with compositions of 25, 53.2 and 75 vol.% Al₂O₃ as interlayer. The results from XRD analysis, optical microscope observation and thermal cycling test show that the composites fabricated by this method consist of α-Al₂O₃ phase and (Fe, Cr, Al) solid solution. The α-Al₂O₃ grain formed by this in-situ reaction between Fe₂O₃ and Fe is ultrafine and uniform distribution. The three-point bending strength is 305.0 MPa for the composite with 53.2 vol.% Al₂O₃ prepared by the reactive hot pressing, about 20% higher than that of the composite with same composition prepared by ex situ hot pressing method (252.0 MPa). No cracking was found in the functionally graded materials after 10 thermal cycles up to 1000 °C due to the better metal–ceramic bond, continuous in microstructure at interface of FGM and good oxidation resistance component FeCrAl alloy formed in the FGM.     

Mechanical properties of rolled A356 based composites reinforced by Cu-coated bimodal ceramic particles

Three kinds of A356 based composites reinforced with 3 wt.% Al₂O₃ (average particle size: 170 μm), 3 wt.% SiC (average particle size: 15 μm), and 3 wt.% of mixed Al₂O₃–SiC powders (a novel composite with equal weights of reinforcement) were fabricated in this study via a two-step approach. This first process step was semi-solid stir casting, which was followed by rolling as the second process step. Electroless deposition of a copper coating onto the reinforcement was used to improve the wettability of the ceramic particles by the molten A356 alloy. From microstructural characterization, it was found that coarse alumina particles were most effective as obstacles for grain growth during solidification. The rolling process broke the otherwise present fine silicon platelets, which were mostly present around the Al₂O₃ particles. The rolling process was also found to cause fracture of silicon particles, improve the distribution of fine SiC particles, and eliminate porosity remaining after the first casting process step. Examination of the mechanical properties of the obtained composites revealed that samples which contained a bimodal ceramic reinforecment of fine SiC and coarse Al₂O₃ particles had the highest strength and hardness.     

Fabrication,interface characterization and modeling of oriented graphite flakes/Si/Al composites for thermal management applications

Highly thermally conductive graphite flakes (G_f)/Si/Al composites have been fabricated using G_f, Si powder and an AlSi₇Mg_0.3 alloy by an optimized pressure infiltration process for thermal management applications. In the composites, the layers of G_f were spaced apart by Si particles and oriented perpendicular to the pressing direction, which offered the opportunity to tailor the thermal conductivity (TC) and coefficient of thermal expansion (CTE) of the composites. Microstructural characterization revealed that the formation of a clean and tightly-adhered interface at the nanoscale between the side surface of the G_f and Al matrix, devoid of a detrimental Al₄C₃ phase and a reacted amorphous Al–Si–O–C layer, contributed to excellent thermal performance along the alignment direction. With increasing volume fraction of G_f from 13.7 to 71.1 vol.%, the longitudinal (i.e. parallel to the graphite layers) TC of the composites increased from 179 to 526 W/m K, while the longitudinal CTE decreased from 12.1 to 7.3 ppm/K (matching the values of electronic components). Furthermore, the modified layers-in-parallel model better fitted the longitudinal TC data than the layers-in-parallel model and confirmed that the clean and tightly-adhered interface is favorable for the enhanced longitudinal TC.     

Investigation on in situ Al0.5FeSi0.5/Al composites prepared by transient liquid phase sintering

In situ Al_0.5FeSi_0.5/Al composites were prepared by transient liquid-phase sintering. The hardness and wear resistance of the composites were investigated with an XHV-1000 microhardness tester and an M-2000 wear tester. Results show that with increased sintering temperature and holding time, the in situ needle-like reinforcement is transformed into short, bar-like, massive particles. At a sintering temperature of 510 °C and holding time of 4 h, the reinforcement consists of short, bar-like Al_0.5FeSi_0.5; moreover, the hardness of the in situ Al_0.5FeSi_0.5/Al composites peaks to a value eight times that of pure aluminum and 2.5 times that of Al–Si alloy. Accordingly, the wear resistance of the composites is the highest, i.e., 6.6 that of pure Al and 4.5 times that of Al–Si alloy.     

In situ TiB2 particulate reinforced near eutectic Al–Si alloy composites

In situ TiB₂ particulate reinforced near eutectic Al–Si alloy composites fabricated by the melt reaction composing (MRC) methods have been investigated. It has been shown that minute TiB₂ particles (less than 1 μm) uniformly distribute in the eutectic structure and they are interlaced with the coralline-like eutectic Si, while there are very few TiB₂ particles in α-Al. It has been also shown that in situ TiB₂ particles can enhance the tensile strength of the Al–Si alloy matrix. The strengthening effect increases with increasing TiB₂ content. The ultimate tensile strength (UTS) at room temperature of as-cast 6%TiB₂/Al–Si–Mg composite is 296 MPa, that is a 14.7% increase over the matrix, and its elongation at fracture is 5.5%. After heat-treatment (T6), the UTS of the composites reaches 384 MPa. The strengthening mechanism has been discussed.     

Properties of near- and sub-micrometre Al matrix composites strengthened with nano-scale in-situ Al2O3 aimed for low temperature applications

Mechanical and electrical properties of in-situ Al–Al₂O₃ metal matrix composites (MMCs) fabricated by powder metallurgy approach using different aluminium powders of particle size 0.8–21 µm and purity 99.8–99.996% were examined. Hot working powder consolidation by vacuum hot pressing at 270 °C and direct extrusion at 425 °C and reduction ratio of 7:1 were applied. Subsequently, extruded composite rods with the diameter of 7.5 mm were cold worked by groove rolling and rotary swaging to the wires with the diameter of 1.1 mm. Detailed microstructural characterization of composite materials was carried out. Stress-strain characteristics of composite wires were measured at 77 and 300 K. In addition, resistivity of all wires were measured by four-probe method between 25 and 300 K and eddy current losses at frequency 72 Hz and temperatures between 18 and 77 K. Obtained results clearly showed that properly designed Al–Al₂O₃ MMC materials can be utilized at low temperatures e.g., for the thermal stabilization of superconducting wires.     

Improvement of yield strength of LM24 alloy

In this study, Al₂O₃ particles were employed to improve the microstructure of LM24 and therefore, to increase the yield strength and tensile strength of this kind of alloy. In situ Al₂O₃ particles were obtained by direct reaction between oxygen and Al melt at 750–800 °C. Microstructure examination shows that the size of in situ formed Al₂O₃ particles was about 1–2 μm, and interestingly, with addition of in situ Al₂O₃ particles, the coarse primary Si phase was disappeared completely. More important, the yield strength and the tensile strength of Al₂O₃/LM24 are increased by 52 MPa, 16 MPa than that of LM24 alloy with 0.1% Sb addition. The value of 181 MPa and 315 MPa is for yield strength and tensile strength of Al₂O₃/LM24 respectively. Besides, the yield strength and tensile strength are 180 MPa and 314 MPa respectively for Al₂O₃/LM24 alloy after remelting and casting. This verifies that the improvement of mechanical properties of such kind of material possesses stability and reliability.     

Synthesis of Cu–Zr–Al/Al2O3 amorphous nanocomposite by mechanical alloying

Two routes were used to produce Cu–Zr–Al/Al₂O₃ amorphous nanocomposite. First route included mechanical alloying of elemental powders mixture. In second route Cu₆₀Zr₄₀ alloy was synthesized by melting of Cu and Zr. Cu₆₀Zr₄₀ alloy was then ball milled with Al and CuO powder. It was not possible to obtain a fully amorphous structure via first route. The mechanical alloying of Cu₆₀Zr₄₀, Al and CuO powder mixture for 10 h led to the reaction of CuO with Al, forming Al₂O₃ particulate, and concurrent formation of Cu₆₂Zr₃₂Al₄ amorphous matrix. The thermodynamical investigations on the basis of extended Miedema’s model illustrated that there is a strong thermodynamic driving force for formation of amorphous phase in this system. Lack of amorphization in first route appeared to be related to the oxidation of free Zr during ball milling.     

Microstructure and mechanical properties of an Al–TiC metal matrix composite obtained by reactive synthesis

A metal matrix composite has been obtained by a novel synthesis route, reacting Al₃Ti and graphite at 1000 °C for about 1 min after ball-milling and compaction. The resulting composite is made of an aluminium matrix reinforced by nanometer sized TiC particles (average diameter 70 nm). The average TiC/Al ratio is 34.6 wt.% (22.3 vol.%). The microstructure consists of an intimate mixture of two domains, an unreinforced domain made of the Al solid solution with a low TiC reinforcement content, and a reinforced domain. This composite exhibits uncommon mechanical properties with regard to previous micrometer sized Al–TiC composites and to its high reinforcement volume fraction, with a Young’s modulus of ∼110 GPa, an ultimate tensile strength of about 500 MPa and a maximum elongation of 6%.     

Preparation of Al matrix nanocomposites by diluting the composite granules containing nano-SiCp under ultrasonic vibaration

In this work, an efficient process by diluting the nano-SiCp/Al composite granules in the molten matrix under ultrasonic vibration(UV) was developed to prepare metal matrix nano-composites(MMNCs).Millimeter-sized composite granules with high content of SiC particle(8 wt%) were specially fabricated by dry high-energy ball milling(HBM) without process control agent, and then remelted and diluted in molten Al alloy under UV. The MMNCs melt was finally squeeze cast under a squeeze pressure of 200 MPa, Microstructure of the composite granules during dry HBM was investigated, and the effect of UV on microstructure and mechanical properties of the MMNCs was discussed. The results indicate that nano-SiC particles are uniformly distributed in the nano-SiCp/Al composite granules, which are covered by vestures of pure Al. During diluting, nano-SiC particles released from the composite granules are quickly dispersed in the molten matrix by UV within 4 min. Microstructure of MMNCs is significantly refined under UV and squeeze casting, eutectic Si phase modified to fine islands with an average length of 1.4 μm. Tensile strength of the squeeze cast MMNCs with 1 wt% of nano-SiC particles is 269 MPa, which is improved by 25% compared with the A356 alloy matrix.     

Ti particle-reinforced surface layers in Al: Effect of particle size on microstructure,hardness and wear

Two types of Ti particles are used in an ultrasonic impact peening (UIP) process to modify sub-surface layers of cp aluminium atomized, with an average size of approx. 20 μm and milled (0.3–0.5 μm). They are introduced into a zone of severe plastic deformation induced by UIP. The effect of Ti particles of different sizes on microstructure, phase composition, microhardness and wear resistance of sub-surface composite layers in aluminium is studied in this paper. The formed layers of a composite reinforced with smaller particles have a highly misoriented fine-grain microstructure of its matrix with a mean grain size of 200–400 nm, while reinforcement with larger particles results in relatively large Al grains (1–2 μm). XRD, SEM, EDX and TEM studies confirm significantly higher particle/matrix bonding in the former case due to formation of a Ti₃Al interlayer around Ti particles with rough surface caused by milling. Different microstructures determine hardness and wear resistance of reinforced aluminium layers: while higher magnitudes of microhardness are observed for both composites (when compared with those of annealed and UIP-treated aluminium), the wear resistance is improved only in the case of reinforcement with small particles.     

In situ fabrication of α-Al2O3 and Ni2Al3 reinforced aluminum matrix composites in an Al–Ni2O3 system

α-Al₂O₃ ceramic particles and Ni₂Al₃ intermetallic compound reinforced aluminum matrix composites were successfully fabricated via exothermic dispersion (XD) reaction in an Al–Ni₂O₃ system. Thermodynamic analysis indicated that the reaction between Al and Ni₂O₃ could occur spontaneously due to its negative Gibbs free energy. The reaction characteristic was discussed by using X-ray diffraction (XRD) method and differential scanning calorimetry (DSC) analysis. The results showed that the reactions of the Al–Ni₂O₃ system consisted of two steps as following: (1) the Al firstly reacted with Ni₂O₃ to form the stable α-Al₂O₃ particles and active Ni atoms; (2) the active Ni atoms further reacted with Al to form Ni₂Al₃. The values of activation energy of the two step reactions were around 457.3 and 282.4 kJ/mol, respectively. The scanning electron microscopy (SEM) and energy dispersive spectrometer (EDS) revealed that the Ni₂Al₃ blocks were uniformly distributed throughout the matrix, while the α-Al₂O₃ particles were slightly segregated in the matrix. The strength of the composite is controlled by the strength of Ni₂Al₃ phase, and the tensile strength and the elongation rate of the composite with 30 vol.% reinforcement volume fraction are 210 MPa and 8%, respectively.     

Production of TiC reinforced-aluminum composites with the addition of elemental carbon

TiC reinforced Al matrix composites were produced by the additions of elemental carbon to both Al + 4%Ti and Al + 5%Ti alloys. It is shown that the microstructure, phase composition as well as fracture behavior of the composites produced are controlled by the processing parameters, such as temperature, amount of excess carbon and duration. Composite microstructure subjected to 1300 °C for 15 min includes only TiC particles where the fracture occurs in a ductile manner whilst composites subjected to 1200 °C for 30 min contain Al₃Ti and TiC particles which show mixed mode of fracture behavior where Al₃Ti particles resulted in brittle fracture due to their coarser size.