Mechanical properties of composite heterogeneous gels

Composites with a matrix of poly(2-hydroxyethyl methacrylate) (PHEMA) and 10% by volume of various crosslinked PHEMA polymer fillers (prepared by copolymerization with 0.1, 0.4, 1.0, and 20.0% by weight of ethylenedimethacrylate) of particle size about 1 μm were prepared. Some polymer matrixes were prepared from soluble branched PHEMA (Hydron S), and others by copolymerization, in the presence of the filler with 0.4 and 1.0% of ethylenedimethacrylate as a crosslinking agent. In the case of the uncrosslinked matrix, a linear polymer–crosslinked polymer system, resulted; in the case of the crosslinked matrix, a composite heterogeneous network was formed (in the latter case, the particles of the filler were swollen with monomer during the crosslinking polymerization). Stress–strain, equilibrium, and ultimate characteristics were measured at 3, 10, 25, 40, 60, and 80°C on samples swollen to equilibrium in water (T_g ≈ ?50°C) and at 80, 110, and 140°C on dry samples (T_g ≈ 100°C). Depending on experimental conditions, above all on the distance from the main transition region and on whether the polymer is dry or swollen, it was found that the measured hydrophilic composite systems behaves as a filled system (with the polymer filler acting mostly as solid particles, irrespective of the crosslink density) or as a system with crosslink density fluctuations (where both networks, the matrix and the filler, contribute roughly additively to the properties of the system), or finally as defect heterogeneous systems (where the properties depend primarily on the character of the polymer–filler interface).     

Mechanical properties of composite polymer microstructures fabricated by interference lithography

We demonstrate that organized, porous, polymer microstructures with continuous open nanoscale pores and a sub-micron spacing obtained via interference lithography can be successfully utilized in a non-traditional field of ordered polymer microcomposites. The examples presented here include porous matrices for the fabrication of binary, glassy-rubbery microcomposites with intriguing mechanical properties with large energy dissipation and lattice-controlled fracturing.     

Mechanical properties of polyimide/multi-walled carbon nanotube composite fibers

A series of polyimide (PI)/multi-walled carbon nanotube (MWCNT) composite fibers were prepared by copolymerizing a mixture of monomers and carboxylic-functionalized MWCNTs, followed by dry-jet wet spinning, thermal imidization, and hot-drawing process. The content of the carboxylic groups of MWCNTs significantly increased when treated with mixed acid, whereas their length decreased with treatment time. Both the carboxylic content and length of MWCNTs influenced the mechanical properties of the composite fibers. Fiber added with 0.1 wt% MWCNTs treated for 4 h exhibited the best mechanical properties, i.e., 1.4 GPa tensile strength and 14.30% elongation at break, which were 51% and 32% higher than those of pure PI fibers, respectively. These results indicated that a suitable MWCNT content strengthened and toughened the resultant PI composite fibers, simultaneously. Moreover, raising draw ratio resulted in the increase of tensile strength and tensile modulus of the composite fibers.     

Moisture barrier,wetting and mechanical properties of shellac/agar or shellac/cassava starch bilayer bio-membrane for food applications

Edible bilayer membrane composed of agar (AG) or cassava starch (CAS) as a cohesive structural layer and ethanol-cast shellac layer as a moisture barrier are investigated for their potential use in food preservation as bio-packaging film, membrane or coating. Bilayer membranes containing non-plasticized shellac exhibit low water vapor permeability (WVP), from 0.89 to 1.03 × 10⁻¹¹ g m⁻¹ s⁻¹ Pa⁻¹. A high value of contact angle (≈92°) and a low liquid water adsorption rate (26 × 10⁻³ μL s⁻¹) indicate that these barrier layers have a quite hydrophobic surface. However, the rigid and brittle characteristics of shellac induce a lack of integrity for this layer. It tends to be cracked and scaled off. The incorporation of PEG 200 (plasticizer) into shellac improves the flexibility that prevents the defects in structure and reinforces the adhesion between the shellac and the cohesive-structural layer. The use of plasticizer weakly affects the WVP of bilayer membranes; however, the surface hydrophobicity as well as the liquid water adsorption rate is comparable to that of non-plasticized shellac layer. Furthermore, PEG increases the stretchability of bilayer membranes. Either being plasticized or not, shellac layer could improve significantly the functional properties of bilayer barriers and give a promising use as biopackaging.     

Mechanical properties and morphological structures of short glass fiber reinforced PP/EPDM composite

The mechanical properties and crystal morphological structures of short glass fiber (SGF) reinforced dynamically photo-irradiated polypropylene (PP)/ethylene-propylene-diene terpolymer (EPDM) composites were studied by mechanical tests, wide-angle X-ray diffraction (WAXD), optical microscopy, scanning electron microscopy (SEM), differential scanning calorimetry (DSC), and thermogravimetric analyzer (TGA). The mechanical properties of PP/EPDM composites, especially the tensile strength were greatly strengthened by dynamically photo-irradiation and the incorporation of SGF. The results from the WAXD, SEM, DSC, and TGA measurements reveal: (i) the formation of β-type crystal of PP in the PP/EPDM/SGF composite; (ii) the fiber length in dynamically photo-irradiated PP/EPDM/SGF composites are general longer than that in corresponding unirradiated samples. The size of EPDM phase in the photo-irradiated composites reduces obviously whereas the droplet number increases; (iii) photo-irradiation improves the interface adhesion between SGF and polymer matrix; (iv) the melting and crystallization temperatures of the photo-irradiated composites are not affected greatly by increasing the SGF content; (v) the thermal analysis results show that the incorporation of SGF into PP/EPDM plays an important role for increasing its thermal stability.     

Mechanical behaviour of nano composite aerogels

In order to improve the mechanical properties of silica aerogels, we propose the synthesis of nano composite aerogels. Silica particles (20–100 nm) are added in the monomer solution, just before gelling and supercritical drying. The silica particles addition increases the mechanical properties, but also affects the aggregation process, the aerogel structure and the pore sizes. We discuss the different parameters which infer in the mechanical behaviour of silica aerogel such as: brittle behaviour, load bearing fraction of solid (pore volume), internal stresses (shrinkage), size and distribution of flaws, subcritical flaws propagation (chemical susceptibility). With silica particles addition, the mechanical properties rapidly increase, stiffening and strengthening the structure by a factor 4–8. Moreover, the mechanical strength distribution and the Weibull modulus characterizing the statistical nature of flaws size in brittle materials show a more homogeneous strength distribution. The composite structure is made of two imbricate networks, the polymeric silica and the particles silica networks. Ultra Small Angle X-ray Scattering experiments show that besides the fractal network usually built up by the organosiloxane, the silica particles is forming another fractal structure at a higher scale. The fractal structure could be related to the low Weibull parameter characteristic of a large flaws size distribution, pores being the critical flaws.     

Synthesis of binary polyelectrolyte/inorganic composite capsules of micron size

Different approaches for the synthesis of binary polyelectrolyte/inorganic layered composite capsules of micron size are described. As the polyelectrolyte part of the composite, a poly(styrene sulfonate)/poly(allylamine hydrochloride) complex was taken; the inorganic component was composed of magnetic nanoparticles (Fe₃O₄, CoFe₂O₄, MnFe₂O₄, ZnFe₂O₄), insulator nanoparticles (rare-earth fluorides) or metal nanoparticles (Ag). An inner inorganic layer was formed inside the hollow polyelectrolyte capsule via chemical or photochemical reaction in a spatially restricted capsule volume. The inorganic nanophase synthesized was characterized by transmission electron microscopy, scanning electron microscopy, and wide angle X-ray scattering techniques and weakly crystallized particles 6–9 nm in diameter were detected, presumably attached to the inner side of the capsule shell. Polyelectrolyte capsules filled with ferrite (magnetite) particles possess substantial magnetic activity and are easily manipulated in water solution by an external magnetic field.     

Controlling ionic conductivity in lipid polyelectrolyte composite capsules by cholesterol

The effect of cholesterol on the formation and properties of bilayer lipid membranes deposited on polyelectrolyte multilayered capsules was studied. The permeability of lipid/cholesterol coated capsules for NaCl was derived from osmotic response experiments and ranged from 1.45 x 10(-8) to 2.9 x 10(-8) m.s(-1), which corresponds to a lipid layer conductivity of (0.7-1.4) x 10(-8) S.m(-1). These conductivity values were in good agreement with the value of 0.8 x 10(-8) S.m(-1) obtained by electrorotation and were by 3 orders of magnitude lower than those found earlier for lipid layers on polyelectrolyte capsules in the absence of cholesterol.     

Mechanical properties of interlayer hybrid textile composite materials based on modified aramid and UHMWPE fabrics

Aramid fibers and ultra-high molecular weight polyethylene (UHMWPE) fibers lack active surface functional groups, and the surface is smooth, limiting their practical application in textile composite materials. In this study, zinc oxide nanorods were used to grow on aramid fibers surfaces, and oxygen plasma followed by treatment with a silane coupling agent was used to modify UHMWPE fibers. The effects of surface modification on the surface morphology and composition, and mechanical properties of fibers and composites were investigated. The mechanical response of interlayer hybrid textile composite materials based on modified aramid and UHMWPE fabrics was examined. The results reveal that surface roughness, active surface functional groups, and wettability that can be controlled by treatment conditions and parameters are important for improving interface adhesion. In addition, the interlayer hybridization pattern as a result of using dissimilar layer materials and altering stacking sequence has a great impact on the mechanical behavior of hybrid textile composite materials.     

Waterborne polyurethane-coated polyamide/fullerene composite films: Mechanical,thermal, and flammability properties

Novel waterborne polyurethane (WPU) was prepared and coated on nylon 12 (Ny12) and fullerene-C60 (Full-C60, 1–10 wt%) composite films using simple dip coating technique. In Ny12/Full-C60 composite, fullerene nanoparticles were dispersed in a wavy layered pattern, whereas coated WPU/Ny12/Full-C60 films depicted uniform pattern of non-overlapping scales. WPU/Ny12/Full-C60 1–10 showed higher values of tensile strength and modulus, 91.4–98.1 MPa and 52.2–57.9 GPa, respectively. In WPU/Ny12/Full-C60 1–10, maximum degradation temperature was increased to 598°C and char yield to 35%. Increasing fullerene content from 1 to 10 wt% decreased maximum peak heat release rate from 209 to 132 kW m^?2, i.e., 53% reduction in flammability compared to WPU.     

Mechanical properties of Nafion and titania/Nafion composite membranes for polymer electrolyte membrane fuel cells

Measurements of the mechanical and electrical properties of Nafion and Nafion/titania composite membranes in constrained environments are reported. The elastic and plastic deformation of Nafion‐based materials decreases with both the temperature and water content. Nafion/titania composites have slightly higher elastic moduli. Thecomposite membranes exhibit less strain hardening than Nafion. Composite membranes also show a reduction in the long‐time creep of ～40% in comparison with Nafion. Water uptake is faster in Nafion membranes recast from solution in comparison with extruded Nafion. The addition of 3–20 wt % titania particles has minimal effect on the rate of water uptake. Water sorption by Nafion membranes generates a swelling pressure of ～0.55 MPa in 125‐μm membranes. The resistivity of Nafion increases when the membrane is placed under a load. At 23 °C and 100% relative humidity, the resistivity of Nafion increases by ～15% under an applied stress of 7.5 MPa. There is a substantial hysteresis in the membrane resistivity as a function of the applied stress depending on whether the pressure is increasing or decreasing. The results demonstrate how the dynamics of water uptake and loss from membranes are dependent on physical constraints, and these constraints can impact fuel cell performance. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 2327–2345, 2006     

Mechanical,low-velocity impact,and hydrothermal aging properties of flax/carbon hybrid composite plates

A hybrid of flax and carbon fibers was considered as an effective way to enhance the mechanical and hydrothermal resistance of flax-reinforced polymer composites. In this study, hybrid composites based on three layers of cross-ply flax fabrics, two layers of unidirectional carbon fabrics, and an epoxy resin were investigated in terms of the tensile, three-point bending, impact, and water absorption properties. The flax fabric reinforcement of the hybrid composites contributed to an improvement in the toughness, whereas the carbon fabric contributed to an improvement in their hydrothermal resistance and overall strength and stiffness. The hybrid composites with carbon fibers on the surface (CFFFC) exhibited brittle failure in the tensile test, whereas those with alternating layers (FCFCF) exhibited greater plastic deformation. In addition, the failure strain of the CFFFC samples showed a negative hybrid effect, whereas that of the FCFCF samples improved 63.5% compared with that of carbon-fiber-reinforced polymer composites. A positive hybrid effect on the impact performance of hybrid reinforced epoxy composites containing the unidirectional carbon fabric and cross-ply flax fabric was observed. At 40 °C and 80% relative humidity, the diffusion rate of water molecules in the FCFCF samples was 16 times that in the CFFFC samples.     

Mechanical properties of ormosils

Many organically modified silicates (ormosils) can be prepared by the sol-gel method with very different mechanical properties by varying the ratio of polydimethylsiloxane (PDMS) to tetraethoxysilane (TEOS) contents and processing conditions. With a low PDMS concentration, the ormosils are harder, stiffer and stronger than those with higher concentration of PDMS. Even harder ormosils are possible when ultrasonic irradiation is used during synthesis. As the PDMS concentration is increased, the ormosils take on a more flexible nature, and over a critical concentration actually become rubbery. These new rubbery materials can contain as much as 75% inorganic components, and have more stable mechanical properties than commercial rubbers at elevated temperatures. Effects of PDMS addition to the network structure and mechanical properties of the ormosils were investigated.     

Water-soluble molecular capsules: self-assembly and binding properties

The self-assembly and characterization of water-soluble calix[4]arene-based molecular capsules (12) is reported. The assemblies are the result of ionic interactions between negatively charged calix[4]arenes 1 a and 1 b, functionalized at the upper rim with amino acid moieties, and a positively charged tetraamidiniumcalix[4]arene 2. The formation of the molecular capsules is studied by (1)H NMR spectroscopy, ESI mass spectrometry (ESI-MS), and isothermal titration calorimetry (ITC). A molecular docking protocol was used to identify potential guest molecules for the self-assembled capsule 1 a2. Experimental guest encapsulation studies indicate that capsule 1 a2 is an effective host for both charged (N-methylquinuclidinium cation) and neutral molecules (6-amino-2-methylquinoline) in water.     

Structure and binding properties of water-soluble cavitands and capsules

Synthetic receptors are modern tools for investigations into the forces involved in recognition. A widely exploited class of receptors are the resorcin[4]arene-based cavitands and capsules. This critical review (71 references) describes the evolution of water-soluble versions of these structures, along with insights the resulting host-ndash complexes have provided with regard to complexation driving forces in water. An emphasis has been placed on the influence of host structure on guest affinity and dynamics.     

Mechanical properties of ultra-oriented polyethylene

Semicrystalline polymers generally exhibit moduli well below their theoretical limit due to chain folding and to lack of crystal alignment. Modulus increases attainable through standard drawing procedures are limited by sample fracture before large draw ratios are reached. Using an Instron capillary rheometer which allowed a draw ratio of > 300, transparent polyethylene strands of unusually high c-axis orientation have been produced by a combination of pressure and shear. The virtually perfect crystalline orientation and evidence for extended chains confirm that a significant improvement in modulus can be realized by this technique. The dynamic tensile storage modulus was measured by Vibron over the temperature range ?160°C to +120°C. Room-temperature moduli were 7 × 10¹¹ dyne/cm², higher than any reported values for drawn polyethylene. Values also remained above 10¹¹ dyne/cm² even at 120°C. The moduli and morphological data have been related by a model consisting of an extended-chain component in paralled with a conventional drawn morphology. Experimental and calculated moduli are compared and related to available theory.     

Mechanical properties of recycled polymers

Modifications of structure and morphology of the polymers induced by the thermomechanical stress (or by the presence of water for some polymers) during reprocessing can cause a drastic deterioration of mechanical properties of the recycled material. The property - reprocessing relationships are an important tool to determine not only the properties of the recycled polymers but also the strategies to use (processing conditions, stabilizers, fillers, compatibilizers, etc) in order to obtain recycled polymers with good mechanical properties. In this work, typical behaviour of some mechanical properties as a function of the number of reprocessing operations is discussed and correlated with their structure and morphology. The influences of the type of apparatus and of the processing conditions are also considered.     

Mechanical properties of metal hydrides

The role of metal hydrides in the hydrogen embrittlement of a number of metal-hydrogen systems is reviewed. The stress-induced formation and cleavage of hydrides at crack tips and the thermodynamics of the hydrides in the stress field of the crack tip are discussed.The mechanical response of the hydrides to applied stresses is described. Many of the hydrides exhibit some plastic deformation under favorable stress systems with the amount of this deformation increasing as the temperature of testing is increased. Phonon properties and the elastic moduli of the hydrides are briefly discussed and it is suggested that these parameters do not provide a basis for understanding the mechanical properties of the hydrides. The deformation response of the hydrides is consistent with the expected behavior of dislocations in the ordered hydride structures.