The influences of particle–particle interaction and viscosity of carrier fluid on characteristics of silica and calcium carbonate suspensions-coated Twaron® composite

The effects of particle–particle interaction and viscosity of carrier fluid on steady and dynamic rheological responses and quasi-static penetration resistance of Twaron® fabrics treated with shear thickening and shear thinning suspensions have been investigated. The suspensions have been made by mechanically dispersing 60 nm silica (SiO₂) and calcium carbonate (CaCO₃) nanoparticles in poly ethylene glycol (PEG) with molecular weights of 200 and 400 g/mol. The CaCO₃ suspensions display shear thinning behaviour along with the total dominance of the elastic state over the viscous state while the SiO₂ suspensions exhibit shear thickening behaviour with the emergence of both the elastic and viscous states. With the increase of molecular weight of PEG, viscosity, viscoelastic modules and instability of the suspensions increase and critical shear rate and frequency of transition to elastic state diminish. The PEG200 and PEG400-contained SiO₂ suspensions-treated Twaron® composites at 35 wt.% have quasi-static penetration resistances which are nearly 2.63 and 2.48 times and maximum absorbed energies which are about 1.54 and 1.55 times higher, respectively, than those of the corresponding CaCO₃ ones. However, the influence of increasing the PEG's molecular weight is not as considerable as the effect of particle–particle interaction on the enhancement of penetration resistance performance.     

Electrolytic deposition of amorphous and crystalline zinc–calcium phosphates

Amorphous Zn–Ca phosphates and crystalline Zn3(PO4)2·4H2O conversion layers on cathode substrates were prepared by electrolysis of mixtures of acidic solutions saturated with metal phosphates. The solutions contained tricalcium phosphate (Ca3(PO4)2) and/or zinc phosphate dihydrate (Zn3(PO4)2·2H2O). The depositions was carried out with constant or pulsating cathode current densities in the range 20–70 mA cm-2 at 20–70 °C. The deposition of the uniform crystalline Zn3(PO4)2·4H2O was performed at a pulsating cathode current density of 70 mA cm-2 at 70 °C for periods up to 10 min. Amorphous deposits of Zn–Ca phosphates containing 20 wt% H2O with variable Zn-to-Ca ratios were deposited at a constant cathodic current of 30 mA cm-2 at 20 °C for 3 min. Surface areas of the amorphous deposits were of the order of 28 m2 g-1. X-ray diffraction, differential thermal analysis and thermogravimetry were used to investigate phase formation and transitions at increasing temperatures. The amorphous Zn–Ca phosphate deposit was after calcination at 900 °C transformed to crystalline phosphates containing the -Ca3(PO4)2 or Ca3-xZnx(PO4)2 and -CaZn2(PO4) phases. © 1998 Kluwer Academic Publishers     

Preparation and properties of cast aluminium alloy–sillimanite particle composite

An attempt has been made to explore the possibility of using natural mineral namely sillimanite for synthesizing aluminium alloy composite through a solidification technique. The sillimanite particles were characterized in terms of X-ray, differential thermal analysis in order to examine their suitability for preparing the composite. An aluminium alloy (BS:LM6) was used as the matrix alloy. The sillimanite particles of mean size 140 μm (major axis) were used as reinforcement. The sillimanite particles were added into the matrix melt by creating a vortex with the help of a mechanical stirrer and the melt temperature was maintained between 750 and 800°C. The cast composite was characterized in terms of microstructural, mechanical and abrasive wear properties. It was noted that the sillimanite particles were reasonably uniformly distributed within the matrix and exhibited good mechanical bonding with the matrix. The strength of the composite was noted to be marginally lower than that of the base alloy but the hardness and the wear resistance of the composite were found to be significantly higher than those of the base alloy.     

Effect of particle size on in vitro cytotoxicity of titania and alumina nanoparticles

Aluminium oxide (Al₂O₃) and titanium dioxide (TiO₂) nanoparticles (NPs) have been widely used in nanotechnology-based products. Recently, researchers and the public have raised concerns about the adverse effects of these NPs in biological systems, particularly in humans. The aim of this study was to investigate the possible adverse effects of these two common metal oxide NPs on human lung epithelium cells (A549) and to investigate NP size-dependent effects on these cells, considering both the primary and hydrodynamic particle size. NPs were found to inhibit cell viability and proliferation at the highest concentration level (10?mg/mL) included in this study, as measured by a clonogenic assay. Moreover, cell viability, proliferation and metabolism were impaired to a greater extent by the smaller NPs (5?nm TiO₂ and 10?nm Al₂O₃) relative to the larger particles (200?nm TiO₂ and 50?nm Al₂O₃) included in this study, as measured by cell proliferation and metabolism. Notably, the observed cytotoxic effects correlated to the primary size, rather than the hydrodynamic size. Similarly, NP cytotoxicity was found to be correlated with the NP surface area. These findings highlight the importance of including primary size and surface area information in NP characterisation in cytotoxicity studies.     

Main and interaction effects of matrix particle size,reinforcement particle size and volume fraction on wear characteristics of Al–SiCp composites using central composite design

The aim of this study was to investigate the effects of matrix particle size, reinforcement particle size, volume fraction, and their interactions on the wear characteristics of Al–SiC_p composites. Central composite design method was used to perform a series of experiments. The statistical analysis of experimental results showed that both main effect and interaction effect of factors investigated were effective on the wear behavior of Al–SiC_p composites. Wear loss decreased as volume fraction increased; however, beyond volume fraction of 17.5%, it increased due to reinforcement particle clustering depending on volume fraction and matrix particle size to reinforcement particle size ratio. With decreasing of matrix particle size and increasing of reinforcement particle size, wear loss also decreased. However, after a certain volume fraction, large sized reinforcement particles had a negative effect on the wear resistance.     

Influence of heat treatment and particle shape on mechanical properties of infiltrated Al2O3 particle reinforced Al–2 wt-% Cu

Abstract

Carbon dioxide (CO₂) generation by ultraviolet irradiation of poly(ethyleneterephthalate) (PET) films in oxygen was monitored by in situ Fourier transform infrared spectroscopy. Typically, the CO₂ absorbance increased by ～100 × 10^?4 in 180 min, with no evidence of hindrance by restricted diffusion of O₂ into, or CO₂ out of, the films. It was concluded that Fourier transform infrared spectrometry monitoring of CO₂ conveniently, reliably and rapidly measures PET films photostability.

Quantitative analysis of the CO₂ evolved from progressively thinner films from successive stages of the biaxial film drawing process indicated that CO₂ was generated within a few microns of the film surface and that the same amounts were generated from the irradiated surface of 540 μm cast, 150 μm uniaxially drawn and 85 μm biaxially drawn films. Although drawing increased film crystallinity, photoreactivity appeared to be unchanged. However, total CO₂ formation followed the pattern PET cast相似文献   

Reactive sintering and particle morphology control of β″-alumina-based water purification filters

This paper reports on the preparation of porous membranes consisting of plate-like β″-alumina grains and the evaluation for microfiltration properties. Porous β″-alumina-based ceramics were prepared by the solid-state reactive sintering of Na₂CO₃ and α-Al₂O₃ at 1100–1300 °C. To study the effect of impurities in the starting powder mixtures, LiF-doped membranes were also prepared. As for the water filtration test, the turbidity before and after the vacuum filtration was measured using sintered porous membranes. To simulate bacteria-contaminated water, a suspension of a commercial boehmite powder (D ₅₀ = 0.7 μm) in distilled water was used. The non-doped samples sintered at 1200 °C were composed of β″-alumina (84 wt%) and β-alumina (16 wt%) grains and showed a good microfiltration performance; the turbidities before and after filtration were 894.4 NTU and 1.46 NTU, respectively.     

Microstructure and mechanical behavior of Mg-5Zn matrix influenced by particle deformation zone

The effect of particle deformation zone(PDZ) on the microstructure and mechanical properties of SiC_p/Mg-5Zn composites was studied.Meanwhile,the work hardening and so ftening behavior of SiC_p/Mg-5Zn composites influenced by PDZ size were analyzed and discussed using neutron diffraction under in-situ tensile deformation.The evolution of FWHM(full width at half maximum) extracted from the diffraction pattern of SiC_p/Mg-5Zn composites was used to interpret the modification of dislocation density during in-situ tension,which discovered the effect of dislocation on the work hardening behavior of SiC_p/Mg-5Zn composites.In addition,the tensile stress reduction(△P_i) values during in-situ tension test were calculated to analyze the effect of PDZ size on the softening behavior of SiC_p/Mg-5Zn composites.The results show that the work hardening rate of SiC_p/Mg-5Zn composites increased with the enlargement of PDZ size,which was attributed to the grain size of SiC_p/Mg-5Zn composites increased with the enlargement of PDZ size.Moreover,the stress reduction(△P_i) values increased continuously during in-situ tensile for SiC_p/Mg-5Zn composites due to the increased stored energy produced during plastic deformation,which provided a driving force for the softening effect.However,the effect of grain size on the softening behavior is greater than that of the stored energy,which led to the tensile stress reduction(△P_i) values of P30(d_PDZ=30 μm)-SiC_p/Mg-5Zn composite were higher than that of P60(d_PDZ=60 μm)-SiC_p/Mg-5Zn composite when the ε_ri were 0.25,0.5,0.75 and 1,respectively.     

Experimental and numerical investigation of effects of particle shape and size distribution on particles’ dispersion in a coaxial jet flow

In this study, an experimental and a numerical investigations are performed to investigate the effect of particle’s shape and size distribution on its dispersion behavior. Firstly, particle dispersion of pulverized coal and spherical polymer particles is observed by Particle Image Velocimetry (PIV) technique in the experiment. Secondly, a simulation is performed to analyze the particle dispersion in detail. Spherical and spheroidal motion models are applied to particle’s movement to investigate the shape effect. Furthermore, monodisperse and polydisperse for particles are applied to investigate the size distribution effect on the dispersion. Experimental results show that in the jet turbulence flow, pulverized coal particles, which have complex shapes and various sizes, have quite different dispersion behavior compared to spherical particles. In terms of the results of the simulation, this difference is mainly caused by the size distribution effect. Although particle’s shape affects the dispersity, it is weakened by the size distribution effect.     

Structural and optical properties of γ-alumina thin films prepared by pulsed laser deposition

Preparation of γ-alumina thin films by pulsed laser deposition from a sintered α-alumina target is investigated. The films were deposited on (100) silicon substrates at 973 K with varying oxygen partial pressures in the range 2.0 × 10⁻⁵-3.5 × 10^− 1 mbar. X-ray diffraction results indicated that the films were polycrystalline γ-Al₂O₃ with cubic structure. The films prepared in the oxygen partial pressure range 2.0 × 10^− 5-3.5 × 10^− 2 mbar contained nanocrystals of sizes in the range 10-16 nm, and became amorphous at pressures > 3.5 × 10^− 1 mbar. Topography of the films was examined by atomic force microscopy using contact mode and it showed the formation of nanostructures. The root-mean square surface roughness of the film prepared at 2.0 × 10^− 5 mbar and 3.5 × 10^− 1 mbar were 1.4 nm and 3.5 nm, respectively. The thickness and optical properties were studied using ellipsometry in the energy range 1.5-5.5 eV for three different angles of incidence. The refractive index was found to decrease from 1.81 to 1.73 with the increase of oxygen partial pressures from 2.0 × 10^− 5 to 3.5 × 10^− 2 mbar. The variation in the refractive index has been found to be influenced by the microstructure of the films obtained as a function of oxygen partial pressure.     

Electrophoretic deposition—mechanisms, myths and materials

Explanations of the deposition process during electrophoretic deposition (EPD) are presented and their boundary conditions discussed. It is suggested increasing resistance during EPD is due to the deposit and not dilution of current carrying species in the suspension. Dialysis membrane experiments demonstrate ions carry significant current. Side-effects of two suspension-conditioning agents are described, i.e., TMAH and PEI. The former can induce aging in suspension as its surface adsorption varies with time and reduces suspension pH. PEI appears to adsorb on all ceramic and metal powders, so may be a universal EPD agent for stoichiometric deposition of ceramic/ceramic and ceramic/metal powder-mixtures. Novel structures produced by EPD are presented.     

Effect of WC particle size and Ag volume fraction on electrical contact resistance and thermal conductivity of Ag–WC contact materials

In this work, theoretically dense (> 99%) composites of Ag and WC have been prepared by press–sintering–infiltration for making electrical contacts used as an arc-resistant material in a model switching device. Composites with varying silver content and WC particle size were investigated to get an insight on their electrical contact resistance (R_c) and their ability to withstand enormous thermal stresses during switching. A break-only model switching sequence was used, where the evolution of R_c was measured over 50 cycles and the post-switching microstructures were investigated for thermal stress induced crack formation. A well-established 2D computational microstructure based model, object-oriented finite element analysis version 2 (OOF2), was used to determine the composite thermal conductivity (k) for various grades as a function of temperature. R_c was observed to be consistently low for the coarser WC containing composite and higher silver content composites. This response was attributed to the ductility of the surface layers formed during switching. Crack formation after switching was found to be a direct consequence of large thermal gradients during 50 cycles, which was minimal for coarser WC grained and higher silver content composites which have a higher thermal shock resistance.     

Laser deposition and study of CuInS2x Se2(1−x) crystals and films

Single-phase films of CuInS_2x Se_2(1−x) solid solutions with a chalcopyrite structure were deposited by laser evaporation of CuInS_2x Se_2(1−x) crystal targets (0≤x≤1). The structural and optical characteristics of the films depend on the chalcogen concentrations.     

Mesoscale analysis of rubber particle effect on young’s modulus and creep behaviour of crumb rubber concrete

International Journal of Mechanics and Materials in Design - This paper presents a mesoscale model to investigate the rubber particle effect on the mechanical properties of crumb rubber concrete...     

Evaluation of stellite coatings by µ-PTA powder,laser, and PTA deposition processes

This article presents comparative evaluation of microplasma-transferred arc powder deposition (µ-PTAPD), laser deposition, and plasma-transferred arc deposition (PTAD) processes for sound quality and cost-effective deposition of Stellite 6 on AISI 4130 steel substrate. Dilution, deposition thickness, microstructure, secondary dendritic arm spacing (SDAS), microhardness, and abrasive wear resistance have been used for comparative evaluation. Analysis of morphology of Stellite deposition revealed that µ-PTAPD process and laser deposition processes could produce a coating of less than 1?mm thickness having good deposition quality, smaller dilution, and SDAS as compared with PTAD process. Analysis of X-ray diffraction patterns revealed that the Stellite coatings manufactured by all three processes had a lamellar structure consisting of Co phases, chromium-rich carbides (Cr₂₃C₆ and Cr₇C₃), and tungsten-containing compounds (W₂C). Analysis of microhardness and abrasive wear resistance found that the Stellite coatings manufactured by µ-PTAPD and laser deposition processes exhibited a lower coefficient of friction, wear volume, and higher microhardness as compared with the coating manufactured by PTAD process, this imparting them with higher abrasive wear resistance. This work proves that µ-PTAPD process has a capability to offer an economical and sustainable solution for good-quality thin coating of Stellite on metallic substrates.     

Effect of alumina particle size and thermal condition of casting on microstructure and mechanical properties of stir cast Al–Al2O3 composites

Abstract

Metal matrix composites are considered as a distinct category of the advanced materials, which have low weight, high strength, high modulus of elasticity, low thermal expansion coefficient and high wear resistance. Among them, Al–Al₂O₃ composites have achieved significant attention due to their desired properties. In the present research, Al–Al₂O₃ composites with 5 vol.-% alumina were produced by stir casting at a temperature of 800°C. Two different particle sizes of alumina were used as 53–63 and 90–105 μm. The microstructure of the samples was evaluated by SEM. In addition, the mechanical properties of the samples were measured, and hence, the optimum temperature and particle size of alumina to be added to the Al matrix were determined. The results demonstrated the positive effect of alumina on improving the properties of Al–Al₂O₃ composites.     

Effect of filler level and particle size on dental caries-inhibiting Ca–PO4 composite

Secondary caries and restoration fracture are common problems in restorative dentistry. The aim of this study was to develop Ca–PO₄ nanocomposite having improved stress-bearing properties and Ca and PO₄ ion release to inhibit caries, and to determine the effects of filler level. Nanoparticles of dicalcium phosphate anhydrous (DCPA), two larger DCPA powders, and reinforcing whiskers were incorporated into a resin. A 6 × 3 design was tested with six filler mass fractions (0, 30, 50, 65, 70, and 75%) and three DCPA particle sizes (112 nm, 0.88 μm, 12.0 μm). The DCPA nanocomposite at 75% fillers had a flexural strength (mean ± SD; n = 6) of 114 ± 23 MPa, matching the 112 ± 22 MPa of a commercial non-releasing, hybrid composite (P > 0.1). This was 2-fold of the 60 ± 6 MPa of a commercial releasing control. Decreasing the particle size increased the ion release. Increasing the filler level increased the ion release at a rate faster than being linear. The amount of ion release from the nanocomposite matched or exceeded those of previous composites that released supersaturating levels of Ca and PO₄ and remineralized tooth lesions. This suggests that the much stronger nanocomposite may also be effective in remineralizing tooth lesion and inhibiting caries. In summary, combining calcium phosphate nanoparticles with reinforcing co-fillers in the composite provided a way to achieving both caries-inhibiting and stress-bearing capabilities. Filler level and particle size can be tailored to achieve optimal composite properties. Disclaimer: Certain commercial materials and equipment are identified to specify the experimental procedure. This does not imply recommendation or endorsement by NIST or ADAF.