Effects of copper addition on the sintering behavior and mechanical properties of powder processed Al/SiC<Subscript><Emphasis Type="Bold">p</Emphasis></Subscript> composites

The effect of copper addition on powder processed Al-10 vol% SiC composites was studied in regards to their sintering responses. Copper was mixed with aluminum powder either as elemental powders or as the coated layer on SiC particles. After sintering at 600°C for 1 h, Al-SiC composites with no copper addition showed little densification. It also demonstrated very low bend strengths of 49 and 60 MPa, indicating poor bonding between the powders in the sintered composite. The addition of 8% copper to the Al/SiC system effectively improved the sintering response, producing over 95% theoretical density, a bend strength of 231 MPa with the copper coated SiC, and a 90% density with over 200 MPa bend strength with the admixed copper.The as-sintered microstructures of the Al–SiC composites clearly revealed particle boundaries and sharp pores, indicating that only a limited neck growth occurred during sintering. In the case of Al–Cu–SiC composites, however, a liquid phase was formed and spread through particle boundaries filling the interfaces or voids between SiC particles and the matrix powders. The coated copper on SiC particles produced a somewhat better filling of the interface or voids, resulting in a little more densification and better sintered strength. Since the solubility of copper in aluminum is less than 2% at the sintering temperature, the alloying of copper in the aluminum matrix was limited. Most of the copper added was dissolved in the liquid phase during the sintering and precipitated as CuAl₂ phase upon cooling.     

Preparation, characterisation and processing of carbon fibre/polyamide-12 composites for selective laser sintering

Aiming at developing carbon fibre/polyamide-12 (CF/PA) composite powders for manufacturing high-performance components by selective laser sintering (SLS), the preparation, characteristics and sintering process of the composite powders and mechanical properties of sintered components were studied. Surfaces of the carbon fibres were treated by the oxidation modification and coated with polyamide-12 through the dissolution-precipitation process to provide good interfacial adhesion and homogenous dispersion within the polyamide-12 matrix. The particle size and micro-morphology analyses show that the CF/PA composite powders with 30 wt%, 40 wt% and 50 wt% carbon fibres present the suitable powder sizes and format for SLS. The incorporation of carbon fibres into the polyamide-12 matrix decreases the initial melting temperature and consequently lowers the SLS part bed temperatures, implying lower energy requirement and less thermal degradation in the sintering process. The CF/PA composites also represent higher thermal stability than the pure polyamide-12. The CF/PA sintered components with 30 wt%, 40 wt% and 50 wt% carbon fibres exhibit the greatly enhanced flexural strengths by 44.5%, 83.3%, 114%, and the flexural modulus by 93.4%, 129.4%, 243.4%, respectively, as compared with the pure polyamide-12 sintered parts. Fractured surface analysis shows that the carbon fibres are encapsulated and bonded well with the polyamide matrix. The complex SLS parts with the thinnest wall of 0.6 mm, the density of 1.09 ± 0.02 g/cm³ and the relatively density of 94.13 ± 1.72% were manufactured using the CF/PA composite powder with 30 wt% carbon fibres. This study demonstrates that the CF/PA composite powders prepared by the surface treatment and dissolution-precipitation method represent suitable interfacial adhesion, filler dispersion, particle sizes and sintering behaviours for SLS and enable the manufacture of complex components with high performance.     

An investigation of the effect of SiC particle size on Cu–SiC composites

In this study mechanical properties of copper were enhanced by adding 1 wt.%, 2 wt.%, 3 wt.% and 5 wt.% SiC particles into the matrix. SiC particles of having 1 μm, 5 μm and 30 μm sizes were used as reinforcement. Composite samples were produced by powder metallurgy method and sintering was performed in an open atmospheric furnace at 700 °C for 2 h. Optical and SEM studies showed that the distribution of the reinforced particle was uniform. XRD analysis indicated that the dominant components in the sintered composites were Cu and SiC. Relative density and electrical conductivity of the composites decreased with increasing the amount of SiC and increased with increasing SiC particle size. Hardness of the composites increased with both amount and the particle size of SiC particles. A maximum relative density of 98% and electrical conductivity of 96% IACS were obtained for Cu–1 wt.% SiC with 30 μm particle size.     

Effect of SiC content on the processing, compaction behavior, and properties of Al6061/SiC/Gr hybrid composites

Aluminum matrix composites reinforced with SiC and graphite (Gr) particles are a unique class of advanced engineered materials that have been developed to use in tribological applications. The conventional techniques for producing these composites have some drawbacks. In this study, a new method, namely In situ Powder Metallurgy (IPM), is applied for the preparation of Al6061/SiC/Gr hybrid composites. In this method, the stir casting and the powder metallurgy synthesizing processes are combined into an integrated net shape forming process. 0?C40 vol.% of SiC particles with an average size of 19 ??m, along with 9 vol.% of uncoated Gr particles, were introduced to the molten 6061 aluminum alloy. Then, the slurries were stirred in a specified time?Ctemperature regime resulting in mixtures of the SiC, Gr, and aluminum powder particles. The powder mixtures were cold pressed in six different pressures (between 250 and 750 MPa) and sintered. Finally, the produced composites were heat treated and their hardness and wear properties were investigated. Homogenous distribution of the SiC and Gr particles within the powder mixtures and the hybrid composites is clear from the SEM images. The results also show that the SiC particles decrease the compressibility of the hybrid powders and improve the hardness of composites. The best wear resistance is achieved in the hybrid composite containing 20 vol.% SiC particles.     

Synthesis of β-silicon carbide nanofiber from an exfoliated graphite and amorphous silica

Silicon carbide (SiC) nanofibers were synthesized from exfoliated graphite containing silica particles at 1425 °C in a 25% H₂/Ar atmosphere. Two types of SiC nanofibers with different morphologies were formed depending on the silica content. A higher silica content led to straight nanofibers with a regular diameter size. The SiC nanofibers derived from the exfoliated graphite/40 wt% SiO₂ powder mixture contained a large number of stacking faults and grew along the [1 1 1] direction. A gas–gas reaction mechanism was proposed to explain the formation of SiC nanofibers.     

Development of Al356/SiCp cast composites by injection of SiCp containing composite powders

One of the great challenges of producing cast metal matrix composites is the agglomeration tendency of the reinforcements. This would normally result in poor distribution of the particles, high porosity content, and low mechanical properties. In the present work, a new method for uniform distribution of very fine SiC particles with average size of less than 3 μm was employed. The key idea was to allow for gradual in situ release of properly wetted SiC particles in the liquid metal. For this purpose, SiC particles were injected into the melt in three different forms, i.e., untreated SiC_p, milled particulate Al–SiC_p composite powder, and milled particulate Al–SiC_p–Mg composite powder. The resultant composite slurries were then cast from either fully liquid (stir casting) or semisolid (compocasting) state. Consequently, the effects of the casting method and the type of the injected powder on the microstructural characteristics as well as the mechanical properties of the cast composites were investigated. The results showed that the distribution of SiC particles in the matrix and the porosity content of the composites were greatly improved by injecting milled composite powders instead of untreated-SiC particles into the melt. Casting from semisolid state instead of fully liquid state had similar effects. The average size of SiC particles incorporated into the matrix was also significantly reduced from about 8 to 3 μm by injecting milled composite powders. The ultimate tensile strength, yield strength and elongation of Al356/5 vol.%SiC_p composite manufactured by compocasting of the (Al–SiC_p–Mg)_cp injected melt were increased by 90%, 103% and 135%, respectively, compared to those of the composite manufactured by stir casting of the untreated-SiC_p injected melt.     

Sintered iron-ceramic composites

In order to improve the strength and high-temperature properties of sintered iron, iron-ceramic composites have been studied. In the present investigation, iron powder with 0–8 vol % Al₂O₃ or SiC particles of different sizes were selected for the study. Powders were mixed, compacted and subsequently sintered at 1150°C under an endo gas atmosphere. Various properties of the sintered compacts, such as density and mechanical properties, were evaluated. Fractography, microstructural studies including EDAX, X-Ray image analysis were studied for selected specimens. It was established from the results that 4 vol % Al₂O₃ or SiC are optimum to obtain superior properties of the composites.     

Effects of reinforcement distribution on low and high temperature tensile properties of Al356/SiCp cast composites produced by a novel reinforcement dispersion technique

A major challenge for full utilization of the potentials of SiC_p reinforced metal matrix composites is the uniform dispersion of very fine SiC particles in the matrix alloys. In this study, a novel method for gradual in situ release of properly wetted SiC particles with average size of less than 3 μm in the liquid metal was employed which greatly overcame this challenge. SiC particles were injected into the melt in three different forms, i.e., untreated SiC_p, milled particulate Al-SiC_p composite powder, and milled particulate Al-SiC_p-Mg composite powder. The resultant composite slurries were then cast in either a fully liquid state (stir casting) or semisolid state (compocasting). Subsequently, the effects of the type of the injected powder and the casting method on the microstructural and mechanical characteristics of the cast composites at room temperature and 300 °C were investigated. The results demonstrated that distribution of SiC particles in the matrix were greatly improved by injecting milled composite powders instead of untreated SiC particles into the melt. Also casting the composite slurries in a semisolid state instead of fully liquid state slightly improved the distribution. The ultimate tensile strength, yield strength and elongation at room temperature of Al356/5 vol.% SiC_p composite manufactured by compocasting of the (Al-SiC_p-Mg)_cp-injected melt were increased by 113%, 90% and 135%, respectively, compared to those of the composite manufactured by stir casting of the untreated-SiC_p injected melt. The improvements in these properties at 300 °C were about 100%, 103% and 129%, respectively. Almost all the composite samples retained more than 90% of their strengths at 300 °C, whereas the monolithic samples lost more than 25% of their strength at this temperature. The composites manufactured by compocasting of (Al-SiC_p-Mg)_cp-injected melts exhibited a typical ductile fracture surface with equiaxed dimples at both room temperature and 300 °C.     

石墨烯含量对铜基石墨烯复合材料力学和电学性能的影响

为改进铜基复合材料的力学和电学性能,向铜基体分别加入0.2%、0.3%、0.4%(质量分数)的石墨烯,充分混合后,采用放电等离子烧结技术(SPS)制备了石墨烯/铜(G/Cu)复合材料。通过扫描电镜(SEM)、拉曼(Raman)光谱和XRD等表征了复合材料微观结构,测试了其硬度、屈服强度、抗压强度和导电率等性能,以确定石墨烯在铜基体中的合适掺杂量。结果表明:随着石墨烯含量的降低,其力电性能显著提高。当石墨烯质量分数为0.2%时,G/Cu复合材料的综合性能(力学及电学性能)达到最好匹配,实现了铜基材料的高强度、高导电性:其抗压强度和屈服强度分别为557.23 MPa和256 MPa,相对于用SPS方法制备的纯铜分别提高了59.21%和70.7%;电导率为52.3 MS/m,其IACS高达91.8%。     

Pressureless sintering of AlN-SiC composites

SiC-AlN composites have been successfully pressureless sintered by using commercial SiC and AlN powders with the optimum amount of sintering aid. The important parameters during pressureless sintering, including the amount and type of sintering aids, sintering temperature, sintering period and packing powder have been studied. Yttria was found to be a better sintering aid than alumina or calcia. The yttria sintering aid reacts with AlN and SiC powders and forms a Y-Al-Si-O-N grain-boundary phase to assist densification during pressureless sintering. With 2 wt% yttria, SiC-AlN composites can be pressureless sintered to high density at 2050–2100 °C for 2 h under the firing conditions where alpha-pp packing powder is used during firing. The microstructure and phases of the composites were characterized by using scanning electron microscopy, transmission electron microscopy, energy-dispersive X-ray spectrometry and X-ray diffractometry.     

Sintering and dielectric properties of BaTiO3 prepared by a composite-hydroxide-mediated approach

High purity tetragonal BaTiO₃ powders consisted of uniform particles of ca. 150 nm in diameter were synthesized by a composite-hydroxide-mediated approach at 240 °C using a novel hydrothermal reaction apparatus with a rolling system. The product showed sinterability superior to the commercial powder, i.e., it could be sintered to full theoretical density at 1200 and 1100 °C without an additive and with 0.3 wt% of Li₂CO₃-0.04 wt% of V₂O₅ mixed sintering aid, respectively. The sintered body of the product also showed piezoelectric properties superior to the commercial one.     

Microstructures and improved wear resistance of 3D needled C/SiC composites with graphite filler

Three-dimensional (3D) needled carbon/carbon (C/C) composites with a lowest porosity of 15.6% were achieved after 1 cycle of impregnation by phenolic resin slurry containing graphite filler, hot-pressing curing and pyrolysis. Carbon/silicon carbide (C/SiC) composites were obtained by liquid silicon infiltrating C/C composites. The aim was to incorporate cost effectiveness and excellent performance of C/SiC braking material. Using filler content not exceeding 30 wt% in the slurry promised undamaged C/C segments in C/SiC composites. The linear wear rate of C/SiC using 30 wt% filler was 0.33 μm side⁻¹ cycle⁻¹ and displayed a fourfold decrease; its weight wear rate was 2.46 mg side⁻¹ cycle⁻¹ and minus 171%, compared with the previously reported values of C/SiC without filler, at a braking velocity of 28 m/s. Its friction coefficients and friction stability coefficients appeared relative insensitive to changes in braking velocities and displayed higher values at high braking velocities compared with the previous values.     

Microstructure and mechanical properties of BAS/SiC composites sintered by spark plasma sintering

High-density BAS/SiC composites were obtained from β-SiC starting powder by the spark plasma sintering technique. Various physical properties of the BAS/SiC composites were investigated in detail, such as densification, phase analysis, microstructures and mechanical properties. The results demonstrated that the relative density of the BAS/SiC composites reached over 99.4% at 1900 °C. The SiC grains were uniformly distributed in the continuous BAS matrix which is probably because of complete infiltration of the SiC particles in BAS liquid-phase formed during sintering. The pull-out of SiC particles, crack deflection and bridging were observed as the major toughening mechanism. The flexural strength and fracture toughness of the BAS/SiC composites sintered at 1900 °C were up to 560 MPa and 7.0 MPa·m^1/2, respectively.     

Effects of copper and Al2O3 particles on characteristics of Cu–Al2O3 composites

High-energy milling was used for production of Cu–Al₂O₃ composites. The inert gas-atomized prealloyed copper powder containing 2 wt.%Al and the mixture of the different sized electrolytic copper powders with 4 wt.% commercial Al₂O₃ powders served as starting materials. Milling of prealloyed copper powders promotes formation of nano-sized Al₂O₃ particles by internal oxidation with oxygen from air. Hot-pressed compacts of composites obtained from 5 and 20 h milled powders were additionally subjected to the high-temperature exposure in argon at 800 °C for 1 and 5 h. Characterization of processed material was performed by optical and scanning electron microscopy (SEM), X-ray diffraction analysis (XRD), microhardness, as well as density and electrical conductivity measurements. Due to nano-sized Al₂O₃ particles microhardness and thermal stability of composite processed from milled prealloyed powders are higher than corresponding properties of composites processed from the milled powder mixtures. The results were discussed in terms of the effects of different size of starting copper powders and Al₂O₃ particles on the structure, strengthening of copper matrix, thermal stability and electrical conductivity of Cu–Al₂O₃ composites.     

FABRICATION AND CHARACTERIZATION OF Cu-SiCp COMPOSITES FOR ELECTRICAL DISCHARGE MACHINING APPLICATIONS

Cu-SiC_p composites made by the powder metallurgy method were investigated. To avoid the adverse effect of Cu-SiC_p reaction, sintering was controlled at a reaction temperature less than 1032 K. Electroless plating was employed to deposit a copper film on SiC_p powder before mixing with Cu powder in order to improve the bonding status between Cu and SiC particles during sintering. It was found that a continuous copper film could be deposited on SiC_p by electroless copper plating, and a uniform distribution of SiC_p in Cu matrix could be achieved after the sintering and extrusion process. The mechanical properties of Cu-SiC_p composites with SiC_p contents from 0.6 to 10 wt% were improved evidently, whereas electrical properties remained almost unchanged as compared with that of the pure copper counterpart. In the electrical discharge machining (EDM) test, the as-formed composite electrodes exhibited a character of lower electrode wear ratio, justifying its usage. The optimum conditions for EDM were Cu-2 wt% SiC_p composite electrode operating with a pulse time of 150 μsec.     

Novel silicon carbide/polypyrrole composites; preparation and physicochemical properties

Novel silicon carbide/polypyrrole (SiC/PPy) conducting composites were prepared using silicon carbide as inorganic substrate. The surface modification of SiC was performed in aqueous solution by oxidative polymerization of pyrrole using ferric chloride as oxidant. Elemental analysis was used to determine the mass loading of polypyrrole in the SiC/PPy composites. Scanning electron microscopy showed the surface modification of SiC by PPy. PPy in composites was confirmed by the presence of PPy bands in the infrared spectra of SiC/PPy containing various amounts of conducting polymer. The conductivity of SiC/PPy composites depends on PPy content on the surface. The composite containing 35 wt.% PPy showed conductivity about 2 S cm⁻¹, which is in the same range as the conductivity of pure polypyrrole powder prepared under the same conditions using the same oxidant. PPy in the composites was clearly detected by X-ray photoelectron spectroscopy (XPS) measurements by its N1s and Cl2p peaks. High resolution scans of the C1s regions distinguished between silicon carbide and polypyrrole carbons. The fraction of polypyrrole at the composite surface was estimated from the silicon and nitrogen levels. The combination of XPS and conductivity measurements suggests that the surface of the SiC/PPy composites is polypyrrole-rich for a conducting polymer mass loading of at least 12.6 wt.%.     

Hot-pressed A12O3–SiC(–C) composites with polycarbosilane as the precursor

The processing and mechanical behavior of Al₂O₃–xSiC (–C) (x = 1, 2, 5, 10 wt.%, ASx and ASCx) composites prepared by in situ reaction synthesis SiC from polycarbosilane (PCS) were investigated. The composites were densified by hot pressing. The pyrolysis process of PCS, microstructure, phase structure and mechanical properties of sintered composites were analyzed. Fully dense structure was obtained, and it was found that the fracture toughness and strength were highly improved compared with monolithic Al₂O₃. The fracture toughness reached 5.1 MPa m^1/2 in 1 wt.%SiC composite ASC1. AS1 showed 516 MPa of flexural strength.     

纳米Al_2O_3弥散强化铜复合材料的产业化制备及研究

采用内氧化法以水雾化铜铝粉为原料制备出铝含量(质量分数)分别为0.15%、0.40%、0.60%的Al2O3弥散铜复合材料。研究了Al2O3弥散强化铜材料的组织与性能,结果表明,弥散铜材料的晶粒细小,晶粒大小约为10μm;γ-Al2O3在基体中均匀分布,平均尺寸约为6nm,间距为40nm;挤压态为Al含量0.60%的弥散铜棒材(Φ25mm)不经任何中间热处理,直接冷拉拔即可得到Φ3mm的铜丝,其抗拉强度高达680MPa,电导率达78%IACS。     

Reactive and dense sintering of reinforced-toughened B4C matrix composites

Reactive hot-press (1800-1880 °C, 30 MPa, vacuum) is used to fabricate relatively dense B₄C matrix light composites with the sintering additive of (Al₂O₃ +Y₂O₃). Phase composition, microstructure and mechanical properties are determined by methods of XRD, SEM and SENB, etc. These results show that reactions among original powders B₄C, Si₃N₄ and TiC occur during sintering and new phases as SiC, TiB₂ and BN are produced. The sandwich SiC and claviform TiB₂ play an important role in improving the properties. The composites are ultimately and compactly sintered owing to higher temperature, fine grains and liquid phase sintering, with the highest relative density of 95.6%. The composite sintered at 1880 °C possesses the best general properties with bending strength of 540 MPa and fracture toughness of 5.6 MPa m^1/2, 29 and 80% higher than that of monolithic B₄C, respectively. The fracture mode is the combination of transgranular fracture and intergranular fracture. The toughening mechanism is certified to consist of crack deflection, crack bridging and pulling-out effects of the grains.     

Particle-reinforced aluminum matrix composites produced from powder mixtures via friction stir processing

Particle-reinforced aluminum matrix composites were produced from powder mixtures of aluminum and silicon by using multiple passages of friction stir processing (FSP). In the composites, the Si particles with an average size of ∼1.5 μm are uniformly dispersed in the aluminum matrix which has a fine-grained structure (∼2 μm). The strengthening mechanism of the composites is discussed. It indicates that the fine grain size of aluminum, the Orowan strengthening due to intragranular particles and the dislocations generated by thermal mismatch all contribute significantly to the composite yield strength.