Effect of cup and ball types on alumina–tungsten carbide nanocomposite powder synthesized by mechanical alloying

Alumina-based nanocomposite powders with tungsten carbides particulates were synthesized by ball milling WO₃, Al and graphite powders. X-ray Diffraction (XRD) was used to characterize the milled and annealed powders. Microstructures of milled powders were studied by Transmission Electron Microscopy (TEM). Results showed that Al₂O₃–W₂C composite formed after 5 h of milling with major amount of un-reacted W in stainless steel cup. The remained W was decreased to minor amount by increasing carbon content up to 10 wt.%. When milled with ZrO₂ cup and balls, Al₂O₃–W₂C composite was completely synthesized after 20 h of milling with the major impurity of ZrO₂. In the case of stainless steel cup and balls with 10 wt.% carbon, Fe impurity after 5 h of milling (maximum 0.09 wt.%) was removed from the powder by leaching in 3HCl·HNO₃ solution. The mean grain size of the powder milled for 5 h was less than 60 nm. The powder preserved its nanocrystalline nature after annealing at 800 °C.     

Microstructural evolution of Al–Fe powder mixtures during high-energy ball milling

High-energy ball milling has been performed on FexAl1-x powder mixtures with x=0.75, 0.50, 0.25 and 0.20. X-ray diffraction, Mossbauer spectroscopy and electron microscopy have been used to characterize the samples milled for different times and annealed in a differential scanning calorimeter. It is found that, during milling, there is diffusion of both elements into each other, with a prevalence of iron diffusion into aluminium, at least in the early stages of the process. This behaviour is more pronounced in the aluminium-rich samples. The growth of the Fe(Al) and Al(Fe) solid solutions has been observed for x0.5, different from the lower iron concentrations where the Fe(Al) phase has not been detected. The annealing of pre-milled samples favours the formation, depending on the sample composition and on the annealing temperature, of intermetallic phases such as Fe3Al, FeAl, Fe2Al5 and FeAl3. © 1998 Chapman & Hall     

Effect of calcinations of starting powder on mechanical properties of hydroxyapatite–alumina bioceramic composite

The effect of calcinations of starting powder on the mechanical properties of hydroxyapatite (HA)-based bioceramic composite was investigated. The calcinations of HA powder in air at 900 °C increased the crystallinity as well as the size of the powder. Ball milling after the calcinations was effective in eliminating large agglomerates in the powder. When the powder was mixed with reinforcing Al₂O₃ powder, the mixture became fine and homogeneous. The flexural strength of HA–Al₂O₃ composite was increased by the calcinations processes at all the Al₂O₃ concentration. However, the fracture toughness was not much influenced by the calcinations. These results lead to the conclusion that the calcinations process effectively reduced the critical flaw size in the body by removing the agglomerates in the HA powder.     

Effect of ball milling on the physical and mechanical properties of the nanostructured Co–Cr–Mo powders

In the present study, Co-based machining chips (P1) and Co-based atomized alloy (P2) has been processed through planetary ball mill in order to obtain nanostructured materials and also to comprise some their physical and mechanical properties. The processed powders were investigated by X-ray diffraction technique in order to determine several microstructure parameters including phase fractions, the crystallite size and dislocation density. In addition, hardness and morphological changes of the powders were investigated by scanning electron microscopy and microhardness measurements. The results revealed that with increasing milling time, the FCC phase peaks gradually disappeared indicating the FCC to HCP phase transformation. The P1 powder has a lower value of the crystallite size and higher degree of dislocation density and microhardness than that of the P2 powder. The morphological and particle size investigation showed the role of initial HCP phase and chemical composition on the final processed powders. In addition results showed that in the first step of milling the crystallite size for two powders reach to a nanometer size and after 12 h of milling the crystallite size decreases to approximately 27 and 33 nm for P1 and P2 powders, respectively.     

Synthesis and some properties of Ti3SiC2 by hot pressing of titanium,silicon, and carbon powders Part 1 – Effect of starting composition on formation of Ti3SiC2 and observation of Ti3SiC2 crystal morphology

Abstract

Dense Ti₃SiC₂ bulk ceramic was synthesised by hot pressing of elemental titanium, silicon, and carbon powders. The effects of starting composition of the powders on the synthesis of pure Ti₃SiC₂ were examined. Phase identification was carried out by X-ray diffraction. Silicon content in the starting composition played an important role in formation of the final constituent phases in the composite. It was difficult to obtain the pure phase Ti₃SiC₂ because other thermodynamically stable reaction products such as TiC, TiSi₂, or Ti₅Si₃ were always present together with Ti₃SiC₂. The microstructure of samples was examined using scanning electron microscopy and transmission electron microscopy. Observations showed that the Ti₃SiC₂ matrix was composed of elongated, platelike, and equiaxial grains. It is suggested that the hexagonal crystal Ti₃SiC₂ exhibits anisotropic grain growth behaviour. The relative growth rates on different planes, therefore, endow Ti₃SiC₂ with several morphologies.     

Studies on the mechanism of the structural evolution in Cu–Al–Ni elemental powder mixture during high energy ball milling

The present work is focused on the understanding of the phase and microstructural evolution during mechanical alloying of 82Cu–14Al–4Ni powder mixture. Morphology and phase evolution in the milled powder at different stages of milling were studied and a physical modeling of the mechanical alloying has been proposed. It has been demonstrated that milling process mainly consisted of four stages, i.e., flattening and cold welding of powder particles to form a porous aggregate followed by its fragmentation, plastic deformation of small aggregates to form layered particles, severe plastic deformation of layered particles to form elongated flaky particles, and fragmentation of elongated particles into smaller size flaky powder particles. It was also found that the initial period of milling resulted in rapid grain refining, whereas alloying was accomplished during the later period of milling. TEM study of the 48 h milled powder revealed that the microstructure was equiaxed nanocrystalline in nature. It was found that the grains were either randomly distributed or arranged as banded type. A possible explanation for such a behavior has been presented.     

Effect of high energy ball milling on solid state reactions in Al–25 at.-%Ni powders

Abstract

The effect of high energy ball milling on the solid state reactions between aluminium and nickel in Al–25 at.-%Ni powders has been investigated using scanning electron microscopy, thermal analysis techniques, and X-ray diffractometry. It has been observed that the microstructure of the powder particles evolves in three stages: stage I is the formation of entrapped nickel particles in the aluminium matrix structure; stage II is the formation of an Al–Ni multilayered structure; and stage III is the formation of Al₃Ni single phase. The temperature required to activate the reaction between aluminium and nickel during heating decreases by more than 200 K as the powder particle microstructure evolves from the entrapped particle structure to the multilayered structure, and then it decreases gradually with decreasing nickel layer thickness. The nucleation and lateral growth of Al₃Ni phase at the Al/Ni interfaces occurs at much lower temperatures than those required for the transverse growth of Al₃Ni. The fraction of Al₃Ni formed through nucleation and lateral growth at the interface is almost linearly proportional to the interfacial area. The activation energy for nucleation and lateral growth of Al₃Ni at the Al/Ni interfaces is independent of nickel layer thickness, but the activation energy for transverse growth of Al₃Ni decreases substantially with decreasing nickel layer thickness. The latter is attributed to the observation that the nickel layers are thinned by plastic deformation and thus contain an increasingly higher density of dislocations.     

The effect of ball milling on the melting behavior of Sn–Cu–Ag eutectic alloy

Sn–Ag–Cu (SAC) solder alloys are the best Pb free alternative for electronic industry. Since their introduction, efforts are made to improve their efficacies by tuning the processing and composition to achieve lower melting point and better wettability. Nanostructured alloys with large boundary content are known to depress the melting points of metals and alloys. In this article we explore this possibility by processing prealloyed SAC alloys close to SAC305 composition (Sn-3wt%Ag-0.5wt%Cu) by mechanical milling which results in the formation of nanostructured alloys. Pulverisette ball mill (P7) and Vibratory ball mills are used to carry out the milling of the powders at room temperature and at lower temperatures (−104 °C), respectively. We report a relatively smaller depression of melting point ranging up to 5 °C with respect to original alloys. The minimum grain sizes achieved and the depression of melting point are similar for both room temperature and low-temperature processed samples. An attempt has been made to rationalize the observations in terms of the basic processes occurring during the milling.     

Effect of initial composition on phase selection in Ni–Si powder blends processed by mechanical alloying

The effect of initial powder blend composition on the synthesis and formation mechanism of nickel silicide phases was investigated by mechanical alloying in Ni-60 and Ni-66.7?at.% Si powder blends. It was noted that the equilibrium NiSi phase started to form in the early stages of milling and that the amount of the NiSi phase in the milled powder increased with increasing milling time. Even though, under equilibrium conditions, a mixture of both the NiSi and NiSi₂ phases was expected to be present in the Ni-60?at.% Si composition and the stoichiometric NiSi₂ phase in the Ni-66.7?at.% Si composition, the NiSi phase was present in both the compositions investigated. However, while only the NiSi phase was present homogeneously in the Ni-60?at.% Si powder blend, both the NiSi phase and a very small amount of unreacted Si were present in the powder blend of Ni-66.7?at.% Si composition. This unexpected phase constitution in the milled powders was attributed to a partial loss of Si during mechanical alloying of the powder blends, confirmed by energy dispersive X-ray spectrometer analyses, and explained on a thermodynamic basis.     

Effect of strain rate on the fracture behaviour of epoxy–graphene nanocomposite

In this study, epoxy-based nanocomposite was fabricated by the addition of graphene nanosheet via a solution casting method. To investigate the effect of strain rate on tensile properties of epoxy, tensile tests were done on standard samples at different strain rates (0.05–1 min^?1). The role of strain rate and presence of graphene on fracture behaviour of epoxy were also studied by investigation of the fracture surfaces of some samples by scanning electron microscopy (SEM). Finally, Eyring’s model was performed to clarify the role of strain rate on activation volume and activation enthalpy of epoxy. The results of tensile tests showed a maximum strength of epoxy–graphene nanocomposite at the graphene wt% of 0.1%. Tensile strength of epoxy obviously improved with increasing strain rate, but tensile strength of epoxy/graphene nanocomposite sample was less sensitive. Fracture micrographs showed that the mirror zone of the fracture surface of epoxy diminished by increasing strain rate or addition of graphene; and final fracture zone also became rougher. Finally, by investigation of the activation enthalpies, it was showed that much higher enthalpy was needed to fracture the nanocomposite sample, as the activation enthalpy changed from 41.54 for neat epoxy to 67.34 kJ mol^?1 for EP–0.1% GNS sample.     

Effect of composition on fracture behavior of polypropylene–wollastonite–polyolefin elastomer system

The fracture behavior of polypropylene (PP)–wollastonite–polyolefin elastomer (POE) in the mixed mode region was studied using the essential work of fracture (EWF) method. The relationship between the microstructure and the fracture parameters was analyzed. The effect of wollastonite content on the essential work of fracture and the work of plastic deformation was discussed. The energy dissipation during a double-edge-notched tension (DENT) test was calculated with the EWF method. It was found in the mixed mode region that σ_n increases with shortening of the ligament length region as plastic constraint effect rises and variation of the specific total work of fracture with ligament length was still reasonably linear within the mixed mode region. With increasing wollastonite content, w _e (specific essential work of fracture) increases, while the βw _p (specific non-essential work of fracture) decreases. The measurements of energy dissipation show that improvement in the fracture toughness of PP–wollastonite–POE is mainly due to the increase in crack propagation resistance during the necking and tearing processes after yielding, while the plastic deformation capability of the material depends mainly on the properties of fracture behavior before yielding. It is also found that the impact strength of the material decreases with increasing wollastonite content. However, the composition with high impact strength has lower specific essential energy of fracture and lower long-term fracture resistance, indicating that EWF is a better indicator of long-term fracture properties than the impact strength. DSC results show that the presence of wollastonite hinders crystallization of the PP.     

Structural evolution of an Al–Te mixture during ball milling

An Al–Te mixture was mechanically alloyed with a planetary ball mill, and the structural evolution of the Al–Te mixture during ball milling was characterized by X-ray diffractiometry (XRD), differential scanning calorimetry (DSC), scanning electron microscopy (SEM), and thermodynamic computation. Although crystalline α-Al₂Te₃ was synthesized in the initial stage of milling, but the final product is a metastable Al₂Te_3 ? δ (Space group: Fm 3¯m) with lattice parameter a = 5.925 Å. The metastable Al₂Te_3 ? δ decomposes into Al and Te at about 140 °C.     

Effect of annealing temperature on optical and electrical properties of ZrO2–SnO2 nanocomposite thin films

ZrO₂–SnO₂ nanocomposite thin films were deposited onto quartz substrate by sol–gel dip-coating technique. Films were annealed at 500, 800 and 1,200 °C respectively. X-ray diffraction pattern showed a mixture of three phases: tetragonal ZrO₂ and SnO₂ and orthorhombic ZrSnO₄. ZrSnO₄ phase and grain size increased with annealing temperature. Fourier transform infra-red spectroscopy spectra indicated the reduction of –OH groups and increase in ZrO₂–SnO₂, by increasing the treatment temperature. Scanning electron microscopy observations showed nucleation and particle growth on the films. The electrical conductivity decreased with increase in annealing temperature. An average transmittance greater than 80 % (in UV–visible region) was observed for all the films. The optical constants of the films were calculated. A decrease in optical band gap from 4.79 to 4.59 eV was observed with increase in annealing temperature. Photoluminescence (PL) spectra revealed an emission peak at 424 nm which indicates the presence of oxygen vacancy in ZrSnO₄. PL spectra of the films exhibited an increase in the emission intensity with increase in temperature which substantiates enhancement of ZrSnO₄ phase and reduction in the non-radiative defects in the films. The nanocomposite modifies the structure of the individual metal oxides, accompanied by the crystallite size change and makes it ideal for gas sensor and optical applications.     

Influence of the microstructure evolution of ZrO2 fiber on the fracture toughness of ZrB2–SiC nanocomposite ceramics

ZrB₂–SiC nanocomposite ceramics toughened by ZrO₂ fiber were fabricated by spark plasma sintering (SPS) at 1700 °C. The content of ZrO₂ fiber incorporated into the ZrB₂–SiC nanocomposites ranged from 5 mass% to 20 mass%. The content, microstructure, and phase transformation of ZrO₂ fiber exhibited remarkable effects on the fracture toughness of the ZrO_2(f)/ZrB₂–SiC composites. Fracture toughness of the composites greatly improved to a maximum value of 6.56 MPa m^1/2 ± 0.3 MPa m^1/2 by the addition of 15 mass% of ZrO₂ fiber. The microstructure of the ZrO₂ fiber exhibited certain alterations after the SPS process, which enhanced crack deflection and crack bridging and affected fracture toughness. Some microcracks were induced by the phase transformation from t-ZrO₂ to m-ZrO₂, which was also an important reason behind the improvement in toughness.     

Effect of environment atmosphere on thermal shock resistance of the ZrB2–SiC–graphite composite

The thermal shock resistance of the ZrB₂–SiC–graphite composite was evaluated by measuring the retention of the flexural strength after the electrical resistance heating to the temperature ranging from 1000 °C up to 2500 °C. The experiment was operated in two different environment atmospheres (pure oxygen and low oxygen partial pressure which mixed O₂ and Ar with 1:9) at total pressure 2000 Pa. The residual strength for the specimen decreased gradually as the temperature increased up to 2200 °C, and it was slightly higher when heated in low oxygen partial pressure environment than in pure oxygen. In contrast to the specimen heated in low oxygen partial pressure environment, the residual strength for the specimen in pure oxygen increased steeply as the temperature increased from 1600 °C up to 1800 °C. The analysis of the SEM observations combined with EDS confirmed that the surface oxidation played a positive role in the thermal shock resistance of the ZrB₂–SiC–graphite composite with different environment atmospheres. The results here pointed out a potential method for charactering the effect of environment atmosphere on thermal shock resistance of the ZrB₂–SiC–graphite composite.     

Effect of mechanical milling on Ni–TiH2 powder alloy filler metal for brazing TiAl intermetallic alloy: The microstructure and joint's properties

A TiH₂–50 wt.% Ni powder alloy was mechanically milled in an argon gas atmosphere using milling times up to 480 min. A TiAl intermetallic alloy was joined by vacuum furnace brazing using the TiH₂–50 wt.% Ni powder alloy as the filler metal. The effect of mechanical milling on the microstructure and shear strength of the brazed joints was investigated. The results showed that the grains of TiH₂–50 wt.% Ni powder alloy were refined and the fusion temperature decreased after milling. A sound brazing seam was obtained when the sample was brazed at 1140 °C for 15 min using filler metal powder milled for 120 min. The interfacial zones of the specimens brazed with the milled filler powder were thinner and the shear strength of the joint was increased compared to specimens brazed with non-milled filler powder. A sample brazed at 1180 °C for 15 min using TiH₂–50 wt.% Ni powder alloy milled for 120 min exhibited the highest shear strength at both room and elevated temperatures.     

Effect of B content on thermal stability of nanocomposite Ti–B–N thin films

Abstract

Ti–B–N thin films with different B contents were deposited on Si (100) at room temperature, followed by vacuum annealed at 400, 600, 800 and 1000°C for 1 h respectively. Effect of boron content on thermal stability was investigated using X-ray diffraction, scanning electron microscopy, high resolution transmission electron microscopy and nanoindentation measurements. The results indicated that incorporation of B into TiN produced a nanocomposite structure, which had a positive effect on microstructure stability. A high B content resulted in an elevated recrystallisation temperature. The hardness stability was not consistent with that of microstructure, and depended on phase configuration and composition. The films with a high as deposited hardness showed high hardness stability. Excessive or lack of amorphous phase decreased hardness stability. The residual stress value was decreased with increasing annealing temperature owing to recovery of amorphous matrix, and crystallisation of amorphous phase made its direction transform from compression to tension.     

Effect of extrusion parameters on properties of rapidly solidified Al–Mg powder alloys

Abstract

Three rapidly solidified Al–Mg powder alloys have been consolidated by means of cold compaction followed by hot extrusion. The extrusion conditions of temperature, reduction ratio, and ram speed were varied, and it was observed that the mechanical properties of the extrudates were strongly process related. Relationships between properties and the temperature compensated strain rates during extrusion have been established. These alloys have strength/density properties superior to the strongest conventional ingot cast alloys. Good fracture toughness has been recorded in the Al–7 Mg alloy and all three alloys possess good resistance to stress corrosion cracking.

MST/498     

Explosive consolidation of 316L stainless steel powder – Effect of phase composition

Two stainless steel (SS) AISI 316L powders have been processed by explosive consolidation using a cylindrical configuration. Powders with d₅₀ of 9 and 5 μm and a phasic structure consisting of fcc and bcc are used. After shock processing (3.5 up to 4.9 mm/μs) hardness was evaluated. Powders with the lowest particle size and processed with the highest detonation velocities (4.9 and 4.1 mm/μs) gave rise to a bulk material where in the centre occurred a phase transformation of bcc to fcc phase. Nevertheless, the hardness values were dissimilar along the cross section depending on the macrodefects (centre hole and cracks) produced by detonation. After a pre-heating treatment (900 °C), this powder was full austenitic (fcc) and when submitted to explosive consolidation, it led a monolithic solid without cracks, with a density of 99% TMD (theoretical maximum density) and a hardness of 3.1 GPa. This value is lower than others measured, particularly when a centre hole is not present, revealing hardening by plastic deformation. Concerning powder with higher particle size (d₅₀ = 9 μm), the presence of mainly austenite induces after shock processing function of detonation parameters and localisation hardness values from 3.9 up to 5.0 GPa. The homogeneity of hardness reflex of absence of defects and low stress are almost achieved only for low particle size powders, using the lowest detonation velocities (3.4 GPa).     

On the CVD of MoSi2: an experimental study from the MoCl4–SiCl4–H2–Ar precursor with a view to the preparation of C/MoSi2/SiC and SiC/MoSi2/SiC microcomposites

The chemical vapour deposition of MoSi2 on plane substrates (graphite or sintered-SiC) and ceramic fibres has been studied from MoCl4–SiCl4–H2–Ar gas mixtures at 900相似文献