Mechanical and thermal characterization of compression moulded polylactic acid natural fiber composites reinforced with hemp and lyocell fibers

This research evaluates the effects of PLA/PP blend ratio and Lyocell/hemp mixture ratio on the morphology, water absorption, mechanical and thermal properties of PLA‐based composites. The composites were fabricated with 30 mass % hemp using compression moulding. As a reference composites made from PP were also studied. Combining of hemp and Lyocell in PLA composite leads to the reduction of moisture absorption and can improve the impact, tensile, flexural properties when compared with PLA/hemp. Composite based on the PLA/PP blend‐matrix could not improve the tensile and flexural properties compared with PLA/hemp, however; the lighter composite with better impact properties was obtained. The crystallization temperature of the PLA‐PP/hemp increased compared with pure PLA. This result was also confirmed by the SEM micrographs. The moisture absorption of PLA‐PP/hemp was higher than PLA/hemp. Based on theoretical analysis of DMTA data, there was favorable adhesion in all composites. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40534.     

The effect of surface treatment on graphite nanoplatelets used in fiber reinforced composites

Atmospheric plasma treatment (APT) was used to surface‐activate graphite nanoplatelets (GnP) as well as highly graphitic P100 fibers used to manufacture composites. X‐ray photoelectron spectroscopy showed an increase in the O/C ratio of the treated surfaces when using either CO or O₂ as the active gas, whereas CO exhibited less damage to the treated reinforcement carbon material. APT of P100 fibers resulted in a 75% increase in composite tensile strength when compared to composites using untreated fibers. Surface treatment of GnPs also resulted in GnP/epoxy composites with significantly higher glass transition temperatures (Tg's) and 50% higher flexural strengths than those with no surface treatment because of stronger particle‐to‐resin coupling, which was also evidenced by the fracture surfaces. The effect of GnP loading concentration and plasma treatment duration was also evaluated on the tensile strength of fiber‐reinforced composites. The addition of untreated GnP filler resulted in a decrease in strength up to the 1% loading. However, higher loading conditions resulted in a 20% improvement because of GnP orientation effects. Fracture surfaces suggest that the fibers provided a mechanism for the GnPs to orient themselves parallel to the fiber axis, developing an oriented matrix microstructure that contributes to added crack deflection. Incorporating surface‐treated GnPs in these composites resulted in tensile strengths that were as high as 50% stronger than the untreated systems for all loading conditions. Increased GnP‐to‐matrix bonding as well as enhanced orientation of the GnPs resulted in multifunctional composites with improved mechanical performance. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2014 , 131, 39994.     

Char barrier effect of graphene nanoplatelets on the flame retardancy and thermal stability of high‐density polyethylene flame‐retarded by brominated polystyrene

Graphene nanoplatelets (GNPs) with the char barrier effect were combined with brominated polystyrene (BPS) and antimony trioxide (Sb₂O₃) to improve the flame retardancy and thermal stability of high‐density polyethylene. Thermogravimetric analysis, limited oxygen index (LOI) testing, and vertical burning testing (UL‐94) showed that the presence of GNPs led to enhanced thermal oxidation stability and significantly reduced the flammability. The addition of 1 wt % GNPs to polyethylene/BPS–Sb (mass ratio = 92/6/2) led to UL‐94 grades from NG (first burning time > 30 s) to V‐2 (total burning time = 14 s), and the LOI value increased from 23.4 to 24.1%. The results of the pyrolysis products provided evidence that the GNPs restricted volatilization. The morphology of the chars also proved the formation of the char layer, which could act as a barrier to isolate the material from the flame and retard the vaporization of flammable gases via a tortuous pathway. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40520.     

Fabrication and properties of carbon nanotube/styrene–ethylene–butylene–styrene composites via a sequential process of (electrostatic adsorption aided dispersion)‐plus‐(melt mixing)

Carbon nanotube (CNT)/styrene–ethylene–butylene–styrene (SEBS) composites were prepared via a sequential process of (electrostatic adsorption assisted dispersion)‐plus‐(melt mixing). It was found that CNTs were uniformly embedded in SEBS matrix and a low percolation threshold was achieved at the CNT concentration of 0.186 vol %. According to thermal gravimetric analysis, the temperatures of 20% and 50% weight loss were improved from 316°C and 352°C of pure SEBS to 439°C and 463°C of the 3 wt % CNT/SEBS composites, respectively. Meanwhile, the tensile strength and elastic modulus were improved by about 75% and 181.2% from 24 and 1.6 MPa of pure SEBS to 42 and 4.5 MPa of the 3 wt % CNT/SEBS composite based on the tensile tests, respectively. Importantly, this simple and low‐cost method shows the potential for the preparation of CNT/polymer composite materials with enhanced electrical, mechanical properties, and thermal stability for industrial applications. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40227.     

Characterization of rheological and thermophysical properties of HDPE–wood composite

The objective of this study is to develop a new biocomposite material with high deformation ability. In this regard, the thermal, rheological, and thermophysical properties of this new composite were characterized as a function of temperature and filler concentration. High density polyethylene (HDPE) was the matrix of this new composite which was reinforced with six sawdust concentrations 0%, 20%, 30%, 40%, 50%, and 60%. Maleic anhydride grafted polyethylene (PE‐g‐MA) was used as coupling agent. Addition of sawdust with PE‐g‐MA increased significantly the complex viscosity, the storage modulus (G′), and loss modulus (G″) of the matrix. The superposition of the complex viscosity curves using temperature dependent shift factor, allowed the construction of a viscosity master curve covering a wide range of temperatures. Arrhenius law was used for the relationship of the shift factor to temperature. Furthermore, method of Van Gurp and Palmen (tan delta vs. G*) is also used to control the time–temperature superposition. The experimental results can be well fitted with the cross rheological model which allowed the prediction of the thermorheological properties of the composites over a broad frequency range. By increasing wood concentration, both the activation energy and relaxation time for the biocomposites determined using, respectively, the Arrhenius law and the cole–cole rule increased. By contrast, specific heat of the matrix decreased with sawdust addition while its dimensional stability improved. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40495.     

On the mechanism of piezoresistivity of carbon nanotube polymer composites

Carbon nanotube (CNT) polymer composites exhibit strong nonlinear and asymmetric piezoresistivity about zero strain in tensile and compressive strain states. The existing models explain the characteristic qualitatively but not quantitatively. This paper attempts to understand the mechanisms of this piezoresistivity by developing a new 3-dimensional percolation CNT network model, where the effect of CNT deformation (wall indentation and tube bending) is considered for the first time. The predicted electrical conductivity and piezoresistivity agree with experiments quantitatively, which reveals that the CNT deformation is a dominant mechanism for the nonlinearity and asymmetry of piezoresistivity of CNT-polymer composites. Parametric studies have been conducted to show the effects of morphology and electrical properties of CNTs, work functions and Poisson's ratio of polymer on the piezoresistivity of CNT-polymer composites for future application in nanosensing composites.     

Fatigue crack initiation and damage characterization in Brazilian test specimens for adhesive joints

The present study is focused on the fatigue failure initiation at bimaterial corners by means of a configuration based on the Brazilian disc specimens. These specimens were previously used for the generalized fracture toughness determination and prediction of failure in adhesive joints, carried out under static compressive loading. Under static loading, local yielding effects might affect the asymptotic two-dimensional linear elastic stress representation under consideration. Fatigue loading avoids this fact due to the lower load levels used. The present tests were performed using load control; video microscopy and still cameras were used for monitoring initiation and crack growth. The fatigue tests were halted periodically and images of the corner were taken where fatigue damage was anticipated. Damage initiation and subsequent crack growth were observed in some specimens, especially in those which presented brittle failure under static and fatigue tests. These analyses allowed the characterization of damage initiation for a typical bimaterial corner that can be found in composite to aluminium adhesive lap joints.     

Camphor sulfonic acid doped polyaniline-tin oxide hybrid nanocomposites: Synthesis,structural, morphological,optical and electrical transport properties

Camphor sulfonic acid (CSA) doped PANi–SnO₂ hybrid nanocomposites were synthesized by solid-state synthesis route with varying amounts (10–50%) of CSA. X-ray diffraction studies have proven the successful incorporation of CSA into the polyaniline–SnO₂ hybrid nanocomposites and the results are also supported by microstructural analysis. UV–visible and Fourier infrared spectroscopy studies have provided insight into the electronic interaction between the CSA, polyaniline, and SnO₂. The room temperature dc electrical conductivity of CSA-doped PANi–SnO₂ hybrid nanocomposite films were observed to depend on the amount of CSA doping and the morphology.     

Fabrication of cylindrical SiCf/Si/SiC-based composite by electrophoretic deposition and liquid silicon infiltration

Cylindrical SiC-based composites composed of inner Si/SiC reticulated foam and outer Si-infiltrated SiC fiber-reinforced SiC (SiC_f/Si/SiC) skin were fabricated by the electrophoretic deposition of matrix particles into SiC fabrics followed by Si-infiltration for high temperature heat exchanger applications. An electrophoretic deposition combined with ultrasonication was used to fabricate a tubular SiC_f/SiC skin layer, which infiltrated SiC and carbon particles effectively into the voids of SiC fabrics by minimizing the surface sealing effect. After liquid silicon infiltration at 1550 °C, the composite revealed a density of 2.75 g/cm³ along with a well-joined interface between the inside Si/SiC foam and outer SiC_f/Si/SiC skin layer. The results also showed that the skin layer, which was composed of 81.4 wt% β-SiC, 17.2 wt% Si and 1.4 wt% SiO₂, exhibited a gastight dense microstructure and the flexural strength of 192.3 MPa.     

Multiwalled carbon nanotubes–BaTiO3/silica composites with high complex permittivity and improved electromagnetic interference shielding at elevated temperature

Composites with silica matrix and mixed filler of multiwalled carbon nanotubes (MWCNTs) and BaTiO₃ powder were fabricated. Excellent uniform dispersion of MWCNTs can be obtained using a two-step mixing method. Both of the real and imaginary parts of complex permittivity increased with increasing MWCNT content and measured temperature. The electromagnetic interference (EMI) shielding results showed that the absorption mechanism is the main contribution to the total EMI shielding effectiveness (SE). Compared with the EMI SE resulting from reflection, the absorption showed more dependence on the MWCNT content, measured temperature and frequency. The total EMI SE is greater than 20 dB at 25 °C and 50 dB at 600 °C in the whole frequency range of 12.4–18 GHz with a 1.5 mm composite thickness, which suggests that the MWCNT–BaTiO₃/silica composites could be good candidates for the EMI shielding materials in the measured frequency and temperature region.