Mechanical property analysis of kenaf–glass fibre reinforced polymer composites using finite element analysis

Nowadays, natural fibres are used as a reinforcing material in polymer composites, owing to severe environmental concerns. Among many different types of natural resources, kenaf plants have been extensively exploited over the past few years. In this experimental study, partially eco-friendly hybrid composites were fabricated by using kenaf and glass fibres with two different fibre orientations of 0° and 90°. The mechanical properties such as tensile, flexural and impact strengths of these composites have been evaluated. From the experiment, it was observed that the composites with the 0° fibre orientation can withstand the maximum tensile strength of 49.27 MPa, flexural strength of 164.35 MPa, and impact strength of 6 J. Whereas, the composites with the 90° fibre orientation hold the maximum tensile strength of 69.86 MPa, flexural strength of 162.566 MPa and impact strength of 6.66 J. The finite element analysis was carried out to analyse the elastic behaviour of the composites and to predict the mechanical properties by using NX Nastran 9.0 software. The experimental results were compared with the predicted values and a high correlation between the results was observed. The morphology of the fractured surfaces of the composites was analysed using a scanning electron microscopy analysis. The results indicated that the properties were in the increasing trend and comparable with pure synthetic fibre reinforced composites, which shows the potential for hybridization of kenaf fibre with glass fibre.     

Toughening performance of glass fibre composites with core–shell rubber and silica nanoparticle modified matrices

The fracture energies of glass fibre composites with an anhydride-cured epoxy matrix modified using core–shell rubber (CSR) particles and silica nanoparticles were investigated. The quasi-isotropic laminates with a central 0°/0° ply interface were produced using resin infusion. Mode I fracture tests were performed, and scanning electron microscopy of the fracture surfaces was used to identify the toughening mechanisms.The composite toughness at initiation increased approximately linearly with increasing particle concentration, from 328 J/m² for the control to 842 J/m² with 15 wt% of CSR particles. All of the CSR particles cavitated, giving increased toughness by plastic void growth and shear yielding. However, the toughness of the silica-modified epoxies is lower as the literature shows that only 14% of the silica nanoparticles undergo debonding and void growth. The size of CSR particles had no influence on the composite toughness. The propagation toughness was dominated by the fibre toughening mechanisms, but the composites achieved full toughness transfer from the bulk.     

Damage evolution in glass/epoxy composites engineered using core–shell microparticles under impact loading

The overall objective of the investigation presented in this paper was to study the effect of dispersion of core–shell polymer (CSP) particles within the ply interfaces on damage evolution of glass/epoxy laminates under impact loading. These laminates were fabricated with the CSP particle dispersion controlled to 14 % of the total weight of the used prepreg. A series of impact experiments were done with instrumental drop tower device at all probable impact energies within a practical low velocity impact range. The damage phenomena occurring in the internal microstructure of the laminates were analysed with the help of scanning electron microscope and correlated to the structural response of the laminate. The predominant damage modes were dependent on the magnitude of the applied impact energy. The CSP particle incorporation does not change the sequence of the fracture events but it delays and mitigates the damage creation. The deformation of the CSP particles and the tearing of their outer shells absorb most of the impact energy thereby preventing initiation of matrix cracks at lower impact energies and delaying fibre damage at higher energies. The crushed particles along with their nano-size rubber cores impede crack propagation requiring the cracks to follow torturous paths consequently dissipating additional amount of energy. These particles also promote elastic energy absorption of the laminates minimizing their tendency to fracture easily under impact. The ultimate load bearing capability of the modified laminate showed 60 % improvement and the deflection characteristics indicated lower proneness to impact.     

Characterization of solvent-filled polyurethane/urea–formaldehyde core–shell composites

Encapsulation of liquid phases is a crucial step in many self-healing material systems where a healing agent has to be protected during processing and then released during a damage event. In this work, the mechanical properties of polyurethane (PU) reinforced urea–formaldehyde (UF) shells are characterized. It was found that shell thickness is both a function of PU content in the core phase and of the microcapsule diameter. Furthermore, a saturation thickness was found for high PU contents or high capsule diameters and this phenomenon had direct implications on the bursting force under compression of single microcapsules. With help of an analytical model, the Young's modulus of the hybrid PU/UF was determined and in general, PU-reinforced shells had a lower modulus but higher ductility in terms of elongation at break, leading to more resistant microcapsules overall.     

Preparation and microwave absorbing properties of hollow glass microspheres/Fe3O4/Ag composites with core–shell structure

The low-density, conductive and magnetic hollow glass microspheres (HGM)/Fe₃O₄/Ag composites have been successfully synthesized via co-precipitation and chemical plating method. The morphology, composition, microstructure, magnetic and microwave absorbing properties of the composites were investigated based on the analyses of the results using scanning electron microscope, energy dispersive spectroscopy, X-ray diffraction, vibrating sample magnetometer and vector network analyzer. The results showed that the HGM/Fe₃O₄ composites were successfully prepared, and the coating layers on the surface of HGM are compact and continuous. Moreover, the final composites were completely covered with Ag nanoparticles. With the addition of Ag nanoparticles, the saturation magnetization of the HGM/Fe₃O₄ composites reduces from 32.08 to 14.77 emu/g, whereas its conductivity increases to 0.48 S/cm. The reflection loss (R) of HGM/Fe₃O₄/Ag composites is lower than ?10 dB at 8.2–8.7, 9.6–10.8 and 11.4–11.9 GHz, and the minimum loss value is ?19.1 dB at 9.9 GHz.     

Optical properties of core–shell structured Ag/SiO2 nanocomposites

Silver nanoclusters coated by SiO₂ were synthesized by a reverse micelle technique to obtain a core–shell microstructure with tunable particle size less than 50 nm. The refractive indices of the Ag/SiO₂ nanocomposites were calculated based on a theoretical model for binary composite materials which illustrated a strong correlation to the size of the metallic core and the dielectric shell. Dynamic light scattering analysis of the Ag/SiO₂ nanocomposites revealed that the refractive index of the nanocomposites was about 2.40, which was well in the range predicted by theoretical modeling. Optical absorption spectra and silver quantum dot size induced color change of the Ag/SiO₂ nanocomposites suspension were also investigated.     

Low temperature sintering and properties of Ca–Al–B–Si–O glass/ceramic composites with various ceramic fillers

Low-temperature sintering and properties of low temperature co-fired ceramics materials based on a typical Ca–Al–B–Si–O glass and various ceramic fillers such as (Zr_0.8Sn_0.2)TiO₄, (Ca_0.5Mg_0.5)TiO₃, BaSm₂Ti₄O₁₂ and CaTiO₃ were investigated. Densification, crystallization and dielectric properties are found to strongly depend on the type of filler. The densification process of glass/ceramic composites with different ceramic fillers is mainly from 600 to 925 °C, and the initial compacting temperature of samples is 600 °C. The initial rapid densification of samples starts after glass softening temperature of samples. The XRD patterns of (Ca_0.5Mg_0.5)TiO₃ and CaTiO₃ samples demonstrate crystalline phases, CaTiO(SiO₄) and CaTiSiO₅, respectively, as a result of firing at 875 °C for 15 min. The high dielectric constant fillers produce high ε_r values of the dielectric samples. The maximum dielectric constant of samples for (Zr_0.8Sn_0.2)TiO₄, (Ca_0.5Mg_0.5)TiO₃, BaSm₂Ti₄O₁₂ and CaTiO₃ filler is 14.02, 16.21, 18.64 and 23.78, respectively. Comparing with other samples, the specimens for (Ca_0.5Mg_0.5)TiO₃ and CaTiO₃ ceramic filler have lower dielectric loss. Especially, the sample for (Ca_0.5Mg_0.5)TiO₃ filler exhibits the lowest dielectric loss of 0.00011.     

Mechanical, electrical and electro-mechanical properties of thermoplastic elastomer styrene–butadiene–styrene/multiwall carbon nanotubes composites

Composites of styrene–butadiene–styrene (SBS) block copolymer with multiwall carbon nanotubes were processed by solution casting to investigate the influence of filler content, the different ratios of styrene/butadiene in the copolymer and the architecture of the SBS matrix on the electrical, mechanical and electro-mechanical properties of the composites. It was found that filler content and elastomer matrix architecture influence the percolation threshold and consequently the overall composite electrical conductivity. The mechanical properties are mainly affected by the styrene and filler content. Hopping between nearest fillers is proposed as the main mechanism for the composite conduction. The variation of the electrical resistivity is linear with the deformation. This fact, together with the gauge factor values in the range of 2–18, results in appropriate composites to be used as (large) deformation sensors.     

Preparation and properties of antibacterial TiO2@C/Ag core–shell composite

Abstract

An environment-friendly hydrothermal method was used to prepare TiO₂@C core–shell composite using TiO₂ as core and sucrose as carbon source. TiO₂@C served as a support for the immobilization of Ag by impregnation in silver nitrate aqueous solution. The chemical structures and morphologies of TiO₂@C and TiO₂@C/Ag composite were characterized by x-ray diffraction, transmission electron microscopy, Fourier transform infrared spectroscopy, energy dispersive x-ray spectroscopy and Brunauer–Emmett–Teller (BET) analysis. The antibacterial properties of the TiO₂@C/Ag core–shell composite against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) were examined by the viable cell counting method. The results indicate that silver supported on the surface of TiO₂@C shows excellent antibacterial activity.     

A facile assembly of polyimide/graphene core–shell structured nanocomposites with both high electrical and thermal conductivities

Polyimide/reduced graphene oxide (PI/r-GO) core–shell structured microspheres were fabricated by in-situ reduction of graphene oxide (GO), which was coated on the surface of PI microspheres via hydrogen bonding and π–π stacking interaction. The highly ordered 3D core–shell structure of PI/r-GO microspheres with graphene shell thickness of 3 nm was well characterized by scanning electron microscope (SEM), transmission electron microscopy (TEM) and Raman spectra. The glass transition temperature (T_g) of PI/r-GO microspheres was slightly increased because of the interaction of r-GO and PI matrix while the temperature at 5% weight loss (T_5%) of PI/r-GO microspheres was decreased due to the side effect of reductant hydrazine hydrate. The PI/r-GO nanocomposites exhibited highly electrical conductivity with percolation threshold of 0.15 vol% and ultimate conductivity of 1.4 × 10⁻² S/m. Besides, the thermal conductivity of PI/r-GO nanocomposites with 2% weight content of r-GO could reach up to 0.26 W/m K.     

Structural characterization of CdSe/ZnS core–shell quantum dots (QDs) using TEM/STEM observation

CdSe/ZnS core–shell structured nano-crystal quantum dots (QDs) are ideal candidates for light-emission applications due to their high quantum efficiency, narrow-band, and particle-size-tunable photoluminescence. In particular, their small size results in the quantum confinement of semiconductor nano-crystals, which widens their energy gaps. In general, structural analyses of QDs using a transmission electron microscope (TEM) are very important due to the significantly small size of QDs. We were able to obtain structural information of CdSe/ZnS core–shell QDs using nano-beam diffraction by controlling the nano-probe of the dark field scanning TEM (DF-STEM) mode and strain analysis with high-resolution TEM (HRTEM)/STEM images. Furthermore, we could clearly distinguish the interface between the CdSe core and the ZnS shell from the strain analysis with the HRTEM/STEM images.     

Mechanical behavior and wear prediction of stir cast Al–TiB2 composites using response surface methodology

Al6061 was reinforced with various percentages of TiB₂ particles by using high energy stir casting method. The characterization was performed through X-ray Diffraction, Energy Dispersive Spectrum and Scanning Electron Microscope. The mechanical behaviors such as hardness, tensile strength and tribological behavior were investigated. Wear experiments were conducted by using a pin-on-disc wear tester at varying load. The curve fitting technique was used to develop the respective polynomial and power law equations. The wear mechanism of the specimen was studied through SEM. Response Surface Methodology was used to minimize the number of experimental conditions and develop the mathematical models between the key process parameters namely weight percentage of TiB₂, load and sliding distance. Analysis of Variance technique was applied to check the validity of the developed model. The mathematical model developed for the specific wear rate was predicted at 99.5% confidence level and some useful conclusions were made.     

Fabrication,physiochemical and optoelectronic characterization of SiO2/CdS core–shell nanostructures

Silica/CdS core–shell nanostructures have been developed using a simple wet chemical route. This method utilizes silica spheres formation followed by successive ionic layer adsorption and reaction method assisted CdS shell layer formation. The morphological studies revealed the uniformity in size distribution with core size of 250 nm and shell thickness of 9 nm. The electron microscopic images also indicate the irregular morphology of CdS shell layer. The structural studies indicate the simple cubic system of CdS shell with no other trace for impurities in the crystal structure. This CdS layer exhibit the band gap energy of 2.66 eV, due to weak quantum confinement and numerous defects presence. The studies on room temperature photoluminescence measurement indicate the emission properties and the corresponding electronic energy levels of defect states. Further, the physiochemical understanding of core–shell formation mechanism clearly matches with the motive behind the defects present in the CdS shell layer.     

Synthesis of graphite incorporated core–shell composite of styrene-methylacrylate/polyaniline by surfactant free mini-emulsion polymerization and evaluation of their electrical property

A series of core–shell particles (SMAP/G) having polystyrene-methylacrylate copolymer (styrene-methyl acrylate) as the core and graphite incorporated polyaniline as the shell were prepared by surfactant free mini-emulsion polymerization. Here poly (SMA) copolymer latex particles were first dispersed in water and then coated with polyaniline (PA) by in situ polymerization of aniline in presence of different percentage (0.25, 0.50 and 1.0%) of graphite. The composite particles were characterized by FTIR, XRD and TGA. TEM and SEM analysis confirms the core–shell morphology of the composite particles. DC electrical conductivity values of all the samples were measured by using a standard four-probe method. The effect of temperature and the amount of graphite incorporated into the PA shell on the dc electrical conductivity of the core–shell composites was investigated. The electro chemical behaviour of the core–shell composites was studied by using a cyclic voltammeter. Electro chemical data shows that the core–shell composites are sufficiently stable under redox potential of 50 mV/s to find applications in various electronic devices.     

Effect of heat-treatment on the electrical and dielectric properties of a TiO2-containing lithia–calcia–silica glass and glass ceramics

The glass 65 SiO₂, 20 CaO, 15 Li₂O (mol%) containing 4 g TiO₂/100 g glass was prepared. Samples of this glass were heat treated at temperatures pre-determined by DTA to produce crystalline samples which were characterized by IR, XRD and SEM. The dielectric constant (?′), dielectric loss (?″) and conductivity σ_ac over a wide range of frequency and temperatures were measured. Optical absorption and values of the absorption edge were also determined for the transparent samples. Li–calcium silicate was found to crystallize at 964 °C as the main phase with lithium disilicate and quartz as minor phases. An enhancement in conductivity of about 1–3 orders of magnitude was obtained in the heat treated samples as compared to parent glass. Conduction takes place through an electronic mechanism in the low temperature region. In crystalline samples, the electronic conduction is extended to high temperature regions. Crystallized samples show high ?′ values, particularly at low frequencies. The values of (?′) reached 60–300 at 300 °C. The capacitance results indicated that these materials can be used in capacitors. Dielectric loss bands appeared in the range 0.32–5 MHz and the conduction relaxation times were calculated.     

Maximum SiO2 layer thickness by utilizing polyethylene glycol as the surfactant in synthesis of core/shell structured TiO2–SiO2 nano-composites

TiO₂–SiO₂ nano-composites with the core/shell structure have been prepared by means of a technique based on an extension of well-known Stöber process. In this way, the silica coating of TiO₂ nano-particles in the presence of various commercially available surfactants of cationic, anionic and nonionic has been conducted with the aim to increase barrier properties against UV (UV blocking) radiation, in order to optimize photo-killing ability of the TiO₂ nano-particles and decline of the high photo-catalytic property of titania. The influences of varying coating parameters such as time and temperature on the silica content of nano-composites have been studied and optimum conditions for attaining a thick layer of SiO₂ have been determined. Electro-phoretic mobility measurements indicated that the silica coating shifted the iso-electric point of titania toward that of a typical pure colloidal silica. Surface elemental composition of core/shell structured TiO₂–SiO₂ nano-composites was verified by using energy dispersive X-ray analysis. It was found that maximum silica shell thickness can be obtained in the presence of polyethylene glycol as a nonionic surfactant at 80 °C for 360 min. The photo-catalytic activities were evaluated by the degradation of an aqueous solution of methylene blue under UV light irradiation. In addition, the resultant optimum nano-composites have been characterized by FESEM, TEM, BET, FTIR and UV–Vis spectroscopy.     

High resolution imaging analysis of CdSe/ZnS core–shell quantum dots (QDs) using Cs-corrected HR-TEM/STEM

CdSe/ZnS core–shell structured nano-crystal quantum dots (QDs) are ideal candidates for light-emission applications due to their high quantum efficiency, narrow-band, and particle-size-tunable photoluminescence. In particular, their small size results in the quantum confinement of semiconductor nano-crystals, which widens their energy gaps. In general, high resolution imaging analyses of QDs using a transmission electron microscope are very difficult due to their significantly small size. Successful imaging depends on the capabilities of TEM equipment and the contrast of the QDs sample relative to the supporting film. In this work, all imaging analyses were performed on a TEM equipped with a probe Cs corrector. The samples for observing QDs were prepared by drying each QDs solution on a lacey carbon Cu (300 mesh) grid previously coated with an ultra-thin graphene monolayer (thickness = 0.3 nm), due to the need to minimize the effect of the supported film.     

Combination of chemotherapy and photothermal methods for in vitro ablation of MCF-7 cancer cells using crinkly core–shell structure MoS2/C@SiO2 nanospheres

MoS₂/C@SiO₂ spheres were successfully synthesized by a one-step hydrothermal method using silica as the template, sodium molybdate as the Mo source and glucose as the carbon precursor. In this paper, the antitumor ability of MoS₂/C@SiO₂ and C@SiO₂ nanospheres was evaluated through the photothermal effect induced by near infrared (NIR) spectroscopy and the drug loading and release behaviors of the model drug doxorubicin (DOX). The photothermal conversion efficiency (η) of MoS₂/C@SiO₂ of 42.5% was 1.2 times that of C@SiO₂ (34.7%), which indicated its significant photothermal effect. The drug loading of MoS₂/C@SiO₂ of 46.5% was much higher than that of C@SiO₂ (12.4%); it was 3.75 times that of C@SiO₂. The cumulative drug release of MoS₂/C@SiO₂ and C@SiO₂ under a simulated acidic tumor environment and NIR irradiation was 58.9% and 27.29%, respectively. Moreover, the cell viability assays verified that MoS₂/C@SiO₂-DOX had excellent antitumor ability under the co-stimulation of endogenous (pH) and exogenous (NIR) compared with C@SiO₂-DOX. The experimental results showed that the survival rate of cancer cells in MoS₂/C@SiO₂-DOX under coordinated treatment was only 19.4%, while that of C@SiO₂-DOX was 24.6%.