Effect of silicon carbide dispersion on the microwave absorbing properties of silicon carbide-epoxy composites in 2–40 GHz

In this study, silicon carbide powders were manufactured successfully by the method of preheating combustion synthesis in nitrogen atmosphere where it was introduced into an epoxy resin to produce a microwave absorber. The structure of the silicon carbide was characterized by using X-ray diffraction (XRD) and scanning electron microscopy (SEM). Composite based on the various loadings of silicon carbide and epoxy resin specimens were prepared and the reflection losses of these composite samples were studied using the free space method. Based on the microwave measurements, microwave absorber specimens of silicon carbide with thermal plastic resin at frequencies between 2 and 18 and 18–40 GHz could be obtained from a matching thickness of 2.0 mm by controlling the content of silicon carbide.     

Influence of the glass–calcium carbonate mixture's characteristics on the foaming process and the properties of the foam glass

We prepared foam glasses from cathode-ray-tube panel glass and CaCO₃ as a foaming agent. We investigated the influences of powder preparation, CaCO₃ concentration and foaming temperature and time on the density, porosity and homogeneity of the foam glasses. The results show that the decomposition kinetics of CaCO₃ has a strong influence on the foaming process. The decomposition temperature can be modified by varying the milling time of the glass–CaCO₃ mixture and thus for a specific CaCO₃ concentration an optimum milling time exists, at which a minimum in density and a homogeneous closed porosity are obtained. Under the optimum preparation conditions the samples exhibit a density of 260 kg/m³. The thermal conductivity of the foam glass was measured to be 50–53 mW/(m K). The observed dependence of the foaming process on the decomposition kinetics of the foaming agent can be applied as a universal rule for foaming processes based on thermal decomposition.     

Effects of partial substitution of calcium alumino-titanate on the properties and microstructure of mullite–cordierite composites

In order to realize the recycling of calcium alumino-titanate (CAT, a solid waste), the effect of small amounts (3–9% weight ratio) of CAT on the sintering properties of the mullite–cordierite system was investigated. The thermal-shock stability, volume stability, and mechanical properties of samples with different amounts of CAT were characterized and tested. The influence of CAT on the phase composition and microstructure of the mullite–cordierite system was also deduced from thermodynamic calculations. Experimental results, which agreed with the calculations, demonstrate that CAT could promote the close combination and aggregation of matrix materials, thus strengthening the consolidation process and enhancing desirable properties.     

Effect of clay dispersion methods on the mechano-dynamical and electrical properties of epoxy–organoclay nanocomposites

The effect of different clay dispersion methods on the mechano-dynamical and electrical properties of epoxy/clay nanocomposites was investigated. Three different clay dispersion methods (high-speed mechanical shearing, ultrasonication (US), and an optimal combination of high-speed shearing and US) were used for the dispersion of the clay in the epoxy resin. 3 wt% of an organoclay, cloisite 30B, was used as the nanoclay. Wide-angle X-ray diffraction technique and electron microscopic techniques (SEM and TEM) were used to study the morphology of the nanocomposites. Dynamic mechanical analysis was used to study the dynamo-mechanical properties. Studies on the dielectric breakdown strength (EBD) of the nanocomposites show that the EBD strongly depends on the clay dispersion time and clay dispersion method. Pulsed electro-acoustics method measurement shows that the space charge accumulation was considerably reduced in the nanocomposites. In particular, reduction in space charges after polarization depends on the dispersion of the nanofillers, the better the degree of dispersion, the lower the space charges observed.     

Effects of vinyltrimethoxy silane on thermal properties and dynamic mechanical properties of polypropylene–wood flour composites

The viability of vinyltrimethoxy silane was investigated as a coupling agent for the manufacture of wood–plastic composites (WPC). The effect of silane pretreatment of the wood flour on the thermal and the dynamic mechanical properties and thermal degradation properties of the composites were studied. Moreover, the effect of organosilane on the properties of composites was compared with the effect of maleated polypropylene (MAPP). DSC studies indicated that the wood flour acts as a PP-nucleating agent, increasing the PP crystallization rate. In general, pretreatment with small amounts of silane improved this behavior in all the WPCs studied. Thermal degradation studies of the WPCs indicated that the presence of wood flour delayed degradation of the PP. Silane pretreatment of the wood flour augmented this effect, though without significantly affecting cellulose degradation. Studies of dynamic mechanical properties revealed that the wood flour (at up to 30 wt %) increased storage modulus values with respect to those of pure PP; in WPCs with a higher wood flour amount, there was no additional increase in storage modulus. Pretreatment of the wood flour with silane basically had no effect on the dynamic mechanical properties of the WPC. These results show that with small amounts of vinyltrimethoxy silane similar properties to the MAPP are reached. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Adhesion of ethylene–octene copolymers to polypropylene: Interfacial structure and mechanical properties

Four separate ethylene-octene copolymers of differing molecular weight and co-monomer content have been moulded against polypropylene at various temperatures between 120 and 200°C. The adhesion, measured by a 90° peel test, varied with the particular copolymer, but for all of them it varied with moulding temperature, showing a maximum at about 160°C. It is argued that the temperature variation depends on the extent to which interpenetration of chains occurs in the interfacial region. This, in turn, depends on the recrystallization temperature of the polypropylene. The relative magnitudes of peel energy for the different copolymers can be understood in terms of the extent of plastic yielding necessary in order to transmit a critical stress to the interfacial regions during peeling.     

Effect of ZrB2 on the microstructure,mechanical and tribological properties of Mo–Si–B matrix composites

Composites with good mechanical and tribological properties are in high demand for engineering applications. Toward this aim, the Mo–12Si–8.5B alloy with 2.5–10 wt% ZrB₂ ceramic was prepared. The effects of the ZrB₂ content on the microstructure, mechanical properties, and tribological behavior were thoroughly investigated. The composites exhibited reduced density and enhanced hardness and strength owing to the dispersion strengthening of ZrB₂ particles, thus resulting in improved wear resistance. The frictional properties are highly dependent on the ZrB₂ content and counterpart materials. When coupled with GCr15 steel, it shows much slighter abrasive and adhesive wear; therefore, it presents a more preferable anti-wear performance. The wear rate of the composite with 7.5 wt% ZrB₂ showed a minimum value of 2.71 × 10⁻⁷ mm³N⁻¹m⁻¹.     

Improvement of interfacial adhesion between wood and polypropylene in wood–polypropylene composites

N-vinylformamide-grafted polypropylene (VFPP) was successfully synthesized through a free radical grafting reaction. Both polymeric methylene diphenyl diisocyanate (PMDI) and VFPP were effective compatibilizers for increasing both the strength and stiffness of the resulting wood–PP (polypropylene) composites. Both the modulus of rupture (MOR) and the modulus of elasticity (MOE) of the resulting wood–PP composites were further increased when PMDI and VFPP were used together as an integrated compatibilizer system. This new PMDI-VFPP compatibilizer system was comparable to maleic-anhydride-grafted polypropylene in terms of enhancing the strength and stiffness of the wood–PP composites. Study of the fractured surfaces of the wood–PP composites with scanning electron microscopy revealed that this new PMDI-VFPP compatibilizer system greatly improved the interfacial adhesion between wood and PP. This PMDI-VFPP compatibilizer system also greatly reduced the water absorption of the resulting wood–PP composites. In this PMDI-VFPP compatibilizer system, PMDI is proposed to function as a wood-binding domain and VFPP to function as a PP-binding domain. PMDI reacted with the amide group in VFPP, thus forming covalent linkages between PMDI and VFPP.     

Influence of maleation of polypropylene on the interfacial properties between polypropylene and ethylene–vinyl alcohol copolymer

In order to improve the miscibility between the components of a blend, it is possible to modify the chemical structure by functionalizing one or more of the components. This results in better adhesion at the interface between the components and, consequently, in better mechanical properties. In this work, the influence of maleation of polypropylene on the interface between polypropylene and ethylene–vinyl alcohol copolymer was studied using the measurement of interfacial tension, surface analysis with electron spectroscopy for chemical analysis (ESCA), and morphological observation, using scanning electron microscopy (SEM). The interfacial tension between a 0.1-wt % maleated polypropylene and ethylene–vinyl alcohol copolymer was shown to be 25% lower than the interfacial tension between nonmaleated polypropylene and ethylene–vinyl alcohol copolymer. This resulted in better adhesion between maleated polypropylene and ethylene–vinyl alcohol copolymer. The surface analysis indicates that this decrease of interfacial tension is due to migration of the maleic groups of the maleated polypropylene to the interface between the 2 polymers and that, probably, a chemical interaction occurs at the interface between maleated polypropylene and ethylene–vinyl alcohol copolymer. It is also shown in this work that additives, such as SiO₂, found in commercial polymers, can influence the interfacial tension between 2 polymers. © 1998 John Wiley & Sons, Inc. J. Appl. Polym. Sci. 70: 75–87, 1998     

Effect of processing on the stability and electrical properties of pressureless sintered graphene oxide–alumina composites

This paper explores the processing of an alumina matrix composite with a percolating network of graphene oxide (GPO), which exhibits a moderate electric resistivity and a near zero temperature coefficient of resistance. Different formulations of GPO–alumina composites were processed using a water–base blending, and, the pellets were densified by pressureless sintering under Argon flow. Electrical conduction at room temperature was achieved in the 2 wt % GPO–alumina composite sintered at 1400 °C, and, the 3 wt % GPO–alumina composites sintered at 1400, 1550 and 1700 °C. An investigation of the degradation of electrical conductivity was used to identify potential stable operating regimes in which these materials could be used as heaters. Thermogravimetric analysis using the Ozawa–Flynn–Wall method, was used to determine the kinetic parameters of a 3 wt % GPO composite sintered at 1400 °C which, had an activation energy for GPO degradation of 195 ± 68 kJ/mol and, an estimated thermal lifetime of 8.7 ± 0.8 years for a conversion of 0.5 wt % (failure criterion) at an application temperature of 340 °C.     

Effect of titanium–magnesium catalyst morphology on the properties of polypropylene upon propylene polymerization in a liquid monomer

The effect of the particle size of an IK-8-21 domestic titanium-magnesium catalyst on the properties of polypropylene (PP) produced during the polymerization of propylene in a liquid monomer is studied. Catalysts with particle sizes of 20 to 64 μm are shown to have high activity and identical sensitivity to hydrogen and allow PP to be obtained with a narrow distribution of particles over size, high isotacticity, and close values of crystallinity, melting temperature, and physicomechanical properties. A slight decrease in the activity and bulk density of PP powder is observed when the average size of catalyst particles is increased from 20 to 43 μm. A more notable reduction in the activity and bulk density of PP powder is observed for catalyst with particle sizes of 62 to 64 μm. IK-8-21 catalyst is not inferior to its foreign analogues with respect to the properties of the resulting PP.     

Effect of Al addition on the single and cyclic ablation properties of C/C–SiC composites

This article focuses on the damage behavior and mechanism of aluminum addition on reactive melt infiltrated C/C–SiC composites in single and cyclic ablation environments. Plasma ablation tests were performed on C/C–SiC composites containing 20 wt % and 40 wt % aluminum respectively. Coupled with TMA, XRD, SEM and EDS, the results showed that composites with 40 wt % Al had better ablation resistance during the cyclic ablation, while the composites with 20 wt % Al had excellent ablation damage resistance during a single ablation. This difference was due to higher number of microcracks formed inside the composites containing 40 wt % Al than 20 wt % Al, the lower specimen surface temperature during ablation, and the thermal stresses can be released by pore crack expansion during gas reciprocal loading. While in the single continuous loading of gas, the 20 wt % Al composite formed a protective oxide layer with smaller pores and fewer gas and oxygen entry channels, resulting in good resistance to ablation.     

Influence of TiB2 content on the properties of TiC–SiCw composites

The impact of various volume percentages of TiB₂ additive (0, 10, 20, and 30) on the microstructure, relative density (RD), Vickers hardness, flexural strength, and thermal conductivity of as-sintered TiC-10 vol% SiC_w-based composite samples were scrutinized. All four samples were sintered using the SPS method under the following circumstances; sintering temperature of 1900 °C, dwell time of 7 min, and external pressure of 40 MPa. The best relative density of 98.73% was achieved for the sample with no TiB₂ additive, indicating the negative effect of TiB₂ additive on the RD and formation of porosity. The microstructural observations and XRD results confirmed the chemical interaction of TiO₂ and B₂O₃ oxide layers and SiC_w and in-situ formation of the TiSi brittle phase and TiC. The most significant values of flexural strength (511 MPa) and hardness (27.67 GPa) were related to TiC-10 vol% SiC_w and TiC-10 vol% SiC_w-30 vol% TiB₂ samples, respectively. On the contrary, the specimens with 30 vol% and 10 vol% TiB₂ as additive presented the poorest qualities of flexural strength (234 MPa) and Vickers hardness (22.12 GPa). Finally, the influence of the TiB₂ content on the thermal conductivity was evaluated, indicating the positive impact of this secondary phase on this characteristic, so with adding 30 vol% TiB₂ to TiC-10 vol% SiC_w, a thermal conductivity of 30.7 W/m.K was obtained.     

The effects of promoters on catalytic properties and deactivation–regeneration of the catalyst in the synthesis of dimethyl carbonate

The effects of different alkali metal promoters in PdCl₂-CuCl₂/activated carbon (a.c.) catalyst on the reaction performance for synthesizing dimethyl carbonate (DMC) by gas-phase oxidative carbonylation of methanol were studied. The bulk and surface properties of catalyst PdCl₂-CuCl₂-CH₃COOK/a.c. were characterized by XRD, XPS, and AAS techniques. On the basis of catalyst characterization and activity evaluation, the functions of promoters were further investigated, and the deactivation–regeneration of catalyst PdCl₂-CuCl₂-CH₃COOK/a.c. was also discussed. The results show that the space time yield (STY) of DMC on catalysts with different alkali metal promoters ranks in the following order: K>Na>Li. The main reason for catalyst deactivation is the loss of chlorine. Fortunately, during the preparation of the catalyst, the interaction between CH₃COOK and PdCl₂ or CuCl₂ that results in the formation of KCl limits the loss of chlorine. An obvious increase of the catalyst lifetime and catalytic activity is observed by treating fresh catalyst with a methanol solution of methyl chloroacetate. If deactivated catalyst is treated with a methanol solution of methyl chloroacetate in N₂ stream at 200 °C for 4 h and then treated in N₂ stream at 200 °C for 2 h, the catalytic activity can be restored effectively and the regeneration induction period can be shortened. The catalytic activity after two times of regeneration can still be restored to 93% of the fresh catalyst. The run time of this catalyst is up to 300 h.     

Effect of the sintering temperature on microstructure and properties of Al2O3–Cu–Ni hybrid composites obtained by PPS

In the present research, the influence of sintering temperature on the microstructure and properties of Al₂O₃–Cu–Ni hybrid composites prepared by the Pulse Plasma Sintering (PPS) technique were described. In this research, three temperatures have been selected: 1250°C, 1300°C, and 1350°C. SEM observations were carried out to determine the distribution of the metallic phase in the composite depending on the sintering temperature. The conducted experiments and microscopic observations enabled a better understanding of the phenomena occurring between the ceramic matrix and metallic phase in the obtained materials. The mechanical properties like a hardness and fracture toughness were measured. The technology applied allowed us to obtain ceramic-metal composites with a homogeneous microstructure. It was found that the sintering temperature influences the selected physical and mechanical properties of the composites produced. It was found that samples produced at 1300°C are characterized by the highest relative density and the mechanical properties.     

Effects of carbon additives on the properties of ZrB2–based composites: A review

This review presents the recent achievements on carbon additives incorporated in ZrB₂ ceramics, improved properties, and their advancements. Monolithic ZrB₂ ceramics have broad potential applications, but their critical drawbacks such as poor damage tolerance, and weak oxidation and ablation resistance confines their applicability. It is an important issue to resolve these shortages in physiochemical properties by engineering the composite ingredients and process design of the ceramic counterparts for an extensive production and applications, which are especially essential in high–tech industries and products. Carbon additives have exceptional characteristics including low density, low cost, and excellent thermo–mechanical stability. These materials have been incorporated in ZrB₂ ceramics to enhance their efficiency and form practical composite ceramics. Although addition of the secondary carbonaceous phases is generally supposed to improve the mechanical properties of ZrB₂ composites, it may also result in a decrease in other aspects of performance, comparing with monolithic ZrB₂ ceramics. In this work, we reviewed the methods and strategies for the preparation of carbon modulated ZrB₂ ceramic composites. Moreover, the advantages, disadvantages, and the productivity of the introduced composite ceramics have been explored and featured.     

Effect of silica sol on the dispersion–gelation process of concentrated silica suspensions for fibre-reinforced ceramic composites

Sol gel process of silica powders dispersed in silica sol has been used to obtain a suitable suspension for the sol infiltration technique of fibre-reinforced ceramics. Efforts have been focused on analysing the effects of polyelectrolyte content, pH, solid load and concentration of gelling agent on the flow behaviour of silica suspensions. The most adequate suspension to manufacture the matrix of composites is a weak flocculated suspension with negligible thixotropic behaviour at pH ≥ 9.5, which is composed of silica microparticles dispersed in silica sol with 41 vol.% of solid load and 1.8 wt.% of Duramax D3005. This suspension easily undergoes a transition to a gel by a slight alteration of stability conditions adding 0.08 M of NH₄Cl, which reduces both the electrostatic repulsion and the pH to 8. Moreover, silica sol promotes the densification of ceramics up to 70% after sintering at 900 °C, allowing porous matrix processing of the composites.     

Effect of diamond volume fraction on the microstructure and mechanical properties of SPS WC–Co/diamond composites

In this research, the effect of the volume percentage of diamond additive on the sintering behavior, microstructure, and mechanical properties of WC–Co was investigated. WC–Co/diamond composites with different percentages of 0%, 2.5%, 5%, 7.5%, and 10% by volume of diamond were made by spark plasma sintering at 1300°C and 40 MPa for 5 min. A small amount of phase transformation from the diamond phase to the graphite phase was observed. The amount of graphitization was low due to low temperature and short sintering time. The addition of diamond leads to a significant enhancement in both the hardness and fracture toughness of the composites, overcoming the trade-off between hardness and toughness typically observed in WC-based materials. The sample reinforced with 5% by volume of diamond showed simultaneously the highest hardness (22.9 GPa), the highest fracture toughness (22.7 MPa m^1/2), and the highest flexural strength (1896 MPa). The uniform dispersion, good bonding of the superhard diamond phase with the matrix, and the fine microstructure caused the high hardness and toughness of composite. The main effective mechanisms in increasing the fracture toughness of the composite were crack deflection, bridging, and blocking of crack propagation by diamond particles.