Nanocomposite WC-10Co powder produced by spray pyrolysis-continuous reduction & carbonization technology and cubic boron nitride (CBN) plated with titanium by vacuum vapor deposit were used, and this paper adopted...
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Nanocomposite WC-10Co powder produced by spray pyrolysis-continuous reduction & carbonization technology and cubic boron nitride (CBN) plated with titanium by vacuum vapor deposit were used, and this paper adopted spark plasma sintering (SPS) process to prepare CBN enhanced ultrafine WC-10Co cemented carbide cermets composite material. The microstructure and mechanical properties of CBN-WC-10Co composites were investigated. The results show that CBN-WC-10Co composites consolidated by spark plasma sintering can reach 95.0 % relative density, and transverse rupture strength (TRS) is 1050 MPa, the average grain size of cermets matrix is less than 420 nm, and CBN-WC-10Co composites with excellent properties are achieved. The CBN still remains very good crystal shape after 1240°C spark plasma sintering, and there is not obvious clearance between CBN plated with titanium and the cermets matrix, the coated titanium layer can not only improve the thermal stability of CBN, but also increase the properties of CBN-WC-10Co composites.
In this study, SnO2-based ceramics, with 0.5%CuO as sintering aid and Sb2O3 as activator of the electrical conductivity, was obtained by pressureless sintering at 1450°C for 5 h. Densification behavior and micros...
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In this study, SnO2-based ceramics, with 0.5%CuO as sintering aid and Sb2O3 as activator of the electrical conductivity, was obtained by pressureless sintering at 1450°C for 5 h. Densification behavior and microstructure development strongly depend on Sb2O 3. The characteristization of microstructures on Sb2O 3 concentrations are analyzed by SEM. A small amount of CuO improves densification;Sb2O3 retards the densification of SnO 2-based ceramic. The electrical resistivities of SnO 2-based ceramics with different contents of Sb2O 3 are measured by the standard four probe method and varied in a wide range. The electrical resistivity arrives the minimal value of 4.964×10-2 Ω·cm for 99%SnO2+0.5%CuO +0.5%Sb2O3. More content of Sb2O3 than that of CuO causes the degression of density and the increasing of electrical resistivity of ceramics.
MoSi2 is one of the few intermetallics to have potential for farther systems. However, the use of MoSi2 has been hindered due to the brittle nature of the material at low temperatures, inadequate creep resistance at h...
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MoSi2 is one of the few intermetallics to have potential for farther systems. However, the use of MoSi2 has been hindered due to the brittle nature of the material at low temperatures, inadequate creep resistance at high temperatures, accelerated (pest) oxidation at temperatures between 450-550°C. In this investigation Mo(Al,Si2)/Ti 3SiC2 composites has been prepared by reaction hot-pressing from Mo, Si, SiC, Ti, Al powder mixture under different temperatures. XRD results show that the main products are Mo(Si,Al)2 and Ti3SiC2. Part of TiC and SiC also appeared at low treating temperature. With the treating temperature increasing SiC disappeared. No evidence show lattice change of Mo(Si,Al)2. It must be the results of sufficient Al added. The electrical conductivity properties were also investigated. Samples treating under different temperatures showed different changes. Samples under high treating temperature showed a near linear change ranging from 27∼800°C and Samples under low treating temperature showed a nonlinear change.
The reaction mechanism of silicon and iron composite powders was clarified during the fabrication of high silicon iron sheet with the Si-content of 6.5wt% by Direct Powder Rolling (DPR) technique. The changes of phase...
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The reaction mechanism of silicon and iron composite powders was clarified during the fabrication of high silicon iron sheet with the Si-content of 6.5wt% by Direct Powder Rolling (DPR) technique. The changes of phase composition and structure evolvement were mainly studied, It is found that a local graded structure, Fe-Fe(Si)-Fe3Si(Si)-Si, forms when sintering at 950-10007deg;C, which plays an important role in the DPR process. Fe 3Si(Si) phase keeps higher content of Si, and Fe(Si) phase remains the state with much lower Si-content, thus provides good mechanical proprieties of rolling and cutting. Then, the subsequent sintering at about 1200C improves the density and makes the distribution of Si homogeneous in the final high silicon iron sheets.
Translucent AlN ceramics were fabricated using spark plasma sintering (SPS) technique with 3wt% CaF2 as sintering additive. The samples achieved 52.4% maximum transmittance in medium IR region after 10 min holding tim...
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Translucent AlN ceramics were fabricated using spark plasma sintering (SPS) technique with 3wt% CaF2 as sintering additive. The samples achieved 52.4% maximum transmittance in medium IR region after 10 min holding time by spark plasma sintering at 1800°C and 30 MPa pressure in N2. The results from XRD, SEM, TEM and EDX showed that the sintered bodies were densely compacted and highly pure with fine grain size and uniform microstructures. No secondary phases were observed at the grain boundaries and triple grain junctions, which guaranteed good optical property of the sintered bodies.
A novel water-based magnetorheological (MR) suspension is based on the poly(ethy1ene glycol)-coated carbonyl iron particles, which is prepared by the co-sol-gel reaction using carbonyl iron particles as raw materials,...
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ISBN:
(纸本)9812771190
A novel water-based magnetorheological (MR) suspension is based on the poly(ethy1ene glycol)-coated carbonyl iron particles, which is prepared by the co-sol-gel reaction using carbonyl iron particles as raw materials, and water without any other additive. The microshucture, anti-oxidation properties, magnetic and magnetorheological properties of the core-shell particles are characterized by scanning electronic microscopy, transmission electronic microscopy, Fourier transform infrared spectroscopy, thermogravimetric- differential thermal analysis, vibrating sample magnetometer, and ARES2000 rheometer, respectively. The results show that the as prepared particles have core-shell structure with a polymer shell of less than 100 nm and its anti-oxidation property is enhanced due to the compound coating. Both the core-shell particles and its based MR suspension exhibit excellent soft magnetic performance. The based MR suspension shows low zero viscosity and high MR effects, especially greatly improved anti-settlement and redispersibility. The phenomena are attributed to the hydrophilic thin shell of the core-shell particles.
In the present study, α-Si3N4 is prepared by using MgO and Al2O3 as the sintering additives and spark plasma sintering (SPS) technique. The SPS sintering mechanism is discussed. The relationship between the content o...
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In the present study, α-Si3N4 is prepared by using MgO and Al2O3 as the sintering additives and spark plasma sintering (SPS) technique. The SPS sintering mechanism is discussed. The relationship between the content of sintering additives, sintering temperature and relative densities of the samples is analyzed. The results suggest that when the sintering temperature is 1300-1500°C, the content of sintering additives is 6wt.%-10wt.%, the relative density of sintered samples is 64%-96%. When the sintering temperature reaches 1400°C, the content of sintering additives is 10%, the samples can be fully dense sintered and the relative density can be up to 95%. The sintering mechanism is liquid phase sintering. The bending strength of the sintered samples is 50-403MPa and has a close correlation with the relative density.
Novel mesoporous ZnO-SiO2 (MZS) composites with rod-like morphology were synthesized from coprecipitation method, which was the first time to apply this method in the successful synthesis of ordered mesoporous composi...
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Novel mesoporous ZnO-SiO2 (MZS) composites with rod-like morphology were synthesized from coprecipitation method, which was the first time to apply this method in the successful synthesis of ordered mesoporous composites to our knowledge. This direct-synthesis method was more simple, convenient and efficient, compared with the post-synthesis ones. Structural characterization and spectroscopic study were discussed.
This article introduces a process for the growth of one-dimensional oxide nanomaterials that combines rheological phase reaction and hydrothermal self-assembling process. Fundamentals and practical approaches of hydro...
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This article introduces a process for the growth of one-dimensional oxide nanomaterials that combines rheological phase reaction and hydrothermal self-assembling process. Fundamentals and practical approaches of hydrothermal self-assembling process and rheological phase reaction are briefly described. Particular attention is devoted to the rheological self-assembling for the growth of low dimensional oxide nanomaterials. Many examples are shown that the rheological self-assembling is an effective method to prepare one-dimensional nanomaterials, organic-inorganic hybrids and 1-D nanomaterial array for optical-electronic and electrochemical devices and catalysis. Morphologies, microstructures, properties, and application of one-dimensional oxide nanomaterials are reviewed.
Nearly single-phase and polycrystalline charge-density-wave compound K0.3MoO3 have been prepared by using a simple method. In this work, K2CO3 and MoOs were used as starting materials and reacted by hot isostatic pres...
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Nearly single-phase and polycrystalline charge-density-wave compound K0.3MoO3 have been prepared by using a simple method. In this work, K2CO3 and MoOs were used as starting materials and reacted by hot isostatic pressing （HIP） sintering. The product is nearly single phase K0.3MoO3 determined by X-ray powder diffraction （XRD） and energy dispersive spectroscopy （EDS）. Measurement of temperature dependence of resistivity reveals that the transport property of polycrystalline K0.3MoO3 obviously differs from that of single crystal due to the grain boundaries and the anisotropic structure in this kind of compound.
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