The effects of some variables, namely, ion concentration, matrix tensile strength, matrix yield strength and the matrix tensile modulus on the fiber‐matrix bonding strength were determined for six ionomers (coded PEA‐1 to PEA‐6) bonded to surface‐modified poly(p‐phenylene terephthalamide) (PPTA) fibers. The results obtained show that the mean bonding shear strength of the ionomers correlates well with both their ultimate tensile strengths and their tensile yield stresses. However, correlation of the bonding shear strengths with the matrix yield stresses reveals that the bonding shear strength was about 1.1 times that of the matrix tensile stress. Failure criteria for all the materials predict maximum shear stress to be either 0.5 or 0.577 of the tensile yield stress, hence a value greater than unity cannot be interpreted nor theoretically justified. It was found that the bonding shear strength of the ethylene‐type ionomer PEA‐6 compared to carboxymethyl surface‐modified PPTA is about 20% lower than the bonding shear strength of this resin against sized PPTA fibers. The reduction of entanglements and/or ionic crosslinking across the bound polymer/bulk polymer interface leads to a weak interface with a subsequent decrease in the measured shear strength. 相似文献
Composites of ethylene‐vinyl acetate (EVA) reinforced with graphene platelets are fabricated. Morphological, thermal, mechanical, electrical properties as well as moisture absorption of the composites are characterized. Transmission electron microscopy shows a good dispersion of graphene platelets in the matrix. The unidirectional orientation of graphene platelets parallel to the surface of the composites is revealed by field emission scanning electron microscopy and is validated using the Halpin–Tsai model. Tensile strength and elongation of the composites are respectively improved by 109 and 83%, after the addition of 3 wt% graphene platelets. The incorporation of 5 wt% graphene platelets enhances the char residue of the composites from 0.544% for pure EVA to 6.63% for the composites. The electrical conductivity of the composite with 3 wt% graphene platelets is two orders of magnitude higher than that of pure EVA with 10−13 S cm–1 electrical conductivity.
A blend composition of poly(3‐hydroxybutyrate‐co‐valerate) and polylactide is used as a bioplastic matrix and reinforced with soy hull to engineer novel green composites. A comparative study with soy‐hull‐reinforced polypropylene composite system is performed. A compatibilizer is used to engineer the novel class of green composites with a balanced stiffness and toughness performance with the target to substitute PP‐based composites. The flexural and impact strength along with hydrophobicity of compatibilized composites are improved significantly over the noncompatibilized counterpart. The fiber/matrix interaction is investigated by SEM. These green composites have the potential to substitute PP‐based composites in some applications.
Carbon/carbon(C/C) composites were bonded with a phosphate adhesive prepared from H3PO4 (orthophosphoric acid) and Al(OH)3 as the matrix and Si and CuO as the inorganic fillers. The mechanical properties were tested at room temperature after the bonded specimens were treated from RT to 1500°C. The results showed that the addition of CuO could greatly improve the adhesive's mechanical properties due to the formation of CunSi (copper silicides). The shear strength of bonded specimens could be up to 8.2 MPa without heat treatment and remain above 2 MPa within the whole heat‐treatment temperature range. 相似文献
The insensitive high explosive 1,3,5‐triamino‐2,4,6‐trinitrobenzene (TATB) was selected for coating and desensitization of hexanitrohexaazaisowurtzitane (CL‐20), another high explosive, after surface modification. About 2 wt‐% polymer binder was adopted in the preparation process to further maintain the coating strength and fill the voids among energetic particles. The structure, sensitivity, polymorph properties, and thermal behavior of CL‐20/TATB by coating and physical mixing were studied. Scanning electron microscopy (SEM) and X‐ray photoelectron spectroscopy (XPS) results indicate that submicrometer‐sized TATB was compactly coated onto the CL‐20 surface with coverage close to 100 %. The core‐shell structure of CL‐20/TATB was confirmed by observation of hollow TATB shell from the CL‐20 core dissolved sample. X‐ray diffraction (XRD) analysis revealed that the polymorph of CL‐20 maintained ε form during the whole preparing process. Thermal properties were studied by thermogravimetry (TG) and differential scanning calorimeter (DSC), showing effects of TATB coating on the polymorph thermal stability and exothermic decomposition of CL‐20. Both the impact and friction sensitivities were markedly reduced due to the cushioning and lubricating effects of TATB shell. The preparation of explosive composites with core‐shell structure provides an efficient route for the desensitization of high explosives, such as CL‐20 in this study. 相似文献
Summary: Polyamide‐6 (PA6)/polyarylate of bisphenol A (PAr) blends rich in PA6 and modified with an additional 15% poly[ethylene‐co‐(methacrylic acid)] partially neutralized with zinc (PEMA‐Zn) as a compatibilizer were obtained by melt mixing. Their phase structure, morphology, and mechanical performance were compared with those of the corresponding binary blends. The ternary blends were composed of a PA6 amorphous matrix and a dispersed PAr‐rich phase in which reacted PA6 and PEMA‐Zn were present. Additionally, minor amounts of a crystalline PA6 phase, and a PEMA‐Zn phase were also present. The chemical reactions observed led to a clear decrease in the dispersed particle size when PEMA‐Zn was added, indicating compatibilization. Consequently, the mechanical behavior of the blends with PEMA‐Zn improved, leading, mainly in the case of the blend with 10% PAr, to significant increases in both ductility and impact strength with respect to those of the binary blends. These increases were more remarkable than the slight decrease in stiffness as a consequence of the rubbery nature of the compatibilizer.
Cryogenically fractured surface of the PA6/PAr‐PEMA‐Zn 70/30‐15 ternary blend. 相似文献
High‐strength conductive pristine graphene/epoxy composites are prepared by two simple processing methods – freeze dry/mixing and solution processing. PVP‐stabilized graphene is aggregation‐resistant and allows for excellent dispersion in both the resin and final composite, as confirmed by optical microscopy and SEM images. The superior dispersion quality results in excellent nanofiller/matrix load transfer, with a 38% increase in strength and a 37% improvement in modulus for 0.46 vol% graphene loading. The composites have a very low electrical percolation threshold of 0.088 vol%. Despite the effectiveness of both methods, the freeze‐drying method is more promising and versatile enough to be used for graphene dispersion in a wide range of other composite precursors.
In this study, the use of PLA‐g‐MA is investigated as a potential method for improving interfacial adhesion between agricultural residues and PLA, with the goal of enhancing mechanical properties. Compatibilization was achieved by using PLA‐g‐MA prepared via reactive extrusion. Green renewable and compatibilized PLA/wheat straw composites were extruded and injection‐molded. Addition of 3 and 5 phr PLA‐g‐MA to the composites resulted in significant improvements in tensile strength (20%) and flexural strength (14%) of the composites, matching that of the neat polymer. The observed improvement in strength was attributed to the good interfacial adhesion between the fiber and matrix.
Lead zirconate titanate (PbZr1 ? xTixO3, PZT)/epoxy composites with one‐ dimensional epoxy in PZT matrix (called 3‐1 type piezocomposites) have been fabricated by tert‐butyl alcohol (TBA)‐based directional freeze casting of PZT matrix and afterward infiltration of epoxy. The composites with PZT volume fraction ranging from 0.36 to 0.69 were obtained by adjusting initial solid loading in freeze‐casting slurry. The effect of poling voltage on piezoelectric properties of the composites was studied for various volume fraction of PZT phase. With the increasing of PZT volume fraction, relative permittivity (εr) increased linearly and piezoelectric coefficient (d33 and d31) increased step by step. The resultant composites with 0.57 PZT volume fraction possessed the highest hydrostatic piezoelectric strain coefficient (dh) value (184 pC/N), voltage coefficient (gh) value (13.6 × 10?3 V/m Pa), and hydrostatic figure of merit (HFOM) value (2168 × 10?15 Pa?1). 相似文献
Natural fibre‐biopolymer composites have been prepared from flax and polyhydroxybutyrate (PHB). The flax was modified by drying, followed by plasticiser absorption to replace the water lost to prevent embrittlement. This protects the fibres from problems associated with their water content and changes in water content due to equilibration with the environment. Flax and PHB showed good interfacial adhesion, which was decreased when plasticisers were present. Some plasticiser migrated from the flax to PHB and caused complex changes in the glass transition, crystallisation and crystallinity of the PHB. Morphology of the composites was examined by scanning electron microscopy (SEM) and optical microscopy (OM), SEM provided information on the interfacial adhesion through fractography. OM showed extensive transcrystallinity along the fibre surfaces. Dynamic mechanical analysis was used to measure elastic and damping characteristics and their relation to composition and morphology.
SEM micrograph of the PHB‐plasticiser‐flax system PHB‐PEG‐flax. 相似文献