Polyethylene multiwalled carbon nanotube composites

Polyethylene (PE) multiwalled carbon nanotubes (MWCNTs) with weight fractions ranging from 0.1 to 10 wt% were prepared by melt blending using a mini-twin screw extruder. The morphology and degree of dispersion of the MWCNTs in the PE matrix at different length scales was investigated using scanning electron microscopy (SEM), transmission electron microscopy (TEM), atomic force microscopy (AFM) and wide-angle X-ray diffraction (WAXD). Both individual and agglomerations of MWCNTs were evident. An up-shift of 17 cm⁻¹ for the G band and the evolution of a shoulder to this peak were obtained in the Raman spectra of the nanocomposites, probably due to compressive forces exerted on the MWCNTs by PE chains and indicating intercalation of PE into the MWCNT bundles. The electrical conductivity and linear viscoelastic behaviour of these nanocomposites were investigated. A percolation threshold of about 7.5 wt% was obtained and the electrical conductivity of PE was increased significantly, by 16 orders of magnitude, from 10⁻²⁰ to 10⁻⁴ S/cm. The storage modulus (G′) versus frequency curves approached a plateau above the percolation threshold with the formation of an interconnected nanotube structure, indicative of ‘pseudo-solid-like’ behaviour. The ultimate tensile strength and elongation at break of the nanocomposites decreased with addition of MWCNTs. The diminution of mechanical properties of the nanocomposites, though concomitant with a significant increase in electrical conductivity, implies the mechanism for mechanical reinforcement for PE/MWCNT composites is filler-matrix interfacial interactions and not filler percolation. The temperature of crystallisation (T_c) and fraction of PE that was crystalline (F_c) were modified by incorporating MWCNTs. The thermal decomposition temperature of PE was enhanced by 20 K on addition of 10 wt% MWCNT.     

Synthesis and cryogenic properties of polyimide-silica hybrid films by sol-gel process

Polyimide-silica hybrid films were prepared from tetraethoxysilane (TEOS) and polyamic acid (PAA) via sol-gel process in the solution of N,N-dimethylacetamide (DMAc). The cryogenic mechanical and electrical properties of polyimide-silica hybrid films were studied taking into account the effects of silica content. The results indicated that the cryogenic modulus increased with the increase of silica content while the tensile strength and failure strain had a maximum value at proper silica contents. Moreover, the tensile strength and modulus of the hybrid films at cryogenic temperature (77 K) were obviously higher than those at room temperature, while the failure strain of the hybrid films was much lower at cryogenic temperature (77 K) than that at room temperature. The mean electrical breakdown strength of the hybrid films was shown to range from 151 to 225 kV/mm at cryogenic temperature (77 K).     

Effects of Excess Bi2O3 on the Ferroelectric Behavior of Nd-Doped Bi4Ti3O12 Thin Films

Effects of excess Bi₂O₃ content on formation of (Bi_3.15Nd_0.85)Ti₃O₁₂ (BNT) films deposited by RF sputtering were investigated. The microstructures and electrical properties of BNT thin films are strongly dependent on the excess Bi₂O₃ content and post-sputtering annealing temperature, as examined by XRD, SEM, and P – E hysteresis loops. A small amount of excess bismuth improves the crystallinity and therefore polarization of BNT films, while too much excess bismuth leads to a reduction in polarization and an increase in coercive field. P – E loops of well-established squareness were observed for the BNT films derived from a moderate amount of Bi₂O₃ excess (5 mol%), where a remanent polarization 2P _r of 25.2 μC/cm² and 2E _c of 161.5 kV/cm were shown. A similar change in dielectric constant with increasing excess Bi₂O₃ content was also observed, with the highest dielectric constant of 304.1 being measured for the BNT film derived from 5 mol% excess Bi₂O₃.     

The Mechanics of Indentation Induced Lateral Cracking

The mechanics governing the lateral cracks that form when a hard object plastically penetrates a ceramic is presented. The roles of indentation load, penetration depth, and work of indentation are all highlighted, as are the influences of the mechanical properties of the material. A closed form solution for cracking induced by expansion of a two-dimensional cavity is used to bring out essential features related to parametric dependence and scaling. The three-dimensional axisymmetric problem for an annular crack driven by a rigid spherical or conical indenter is solved using numerical methods. The region of highest tensile stress is identified corresponding to the location where a crack is most likely to nucleate. This location coincides with the depth below the surface where the crack will expand parallel to the surface under mode I conditions. The solutions have been substantiated by comparison with measurements of the cracks that form upon Vickers indentation. The basic formula for the crack radius has been used to predict trends in cracking upon static penetration and impact by a projectile. In both cases, the extent of the cracking is substantially diminished by increasing the toughness of the material. The yield strength has a much smaller effect. The cracks caused by penetration and the volume removed per impact both decrease marginally at higher yield strength.     

Mechanically Activated Synthesis and Magnetoresistance of Nanocrystalline Double Perovskite Sr2FeMoO6

Nanocrystalline Sr₂FeMoO₆ (SFMO) of double perovskite structure has been successfully synthesized by mechanical activation (MA) in air using SrO, Fe₂O₃, and MoO₂ as the starting materials. Magnetization of the polycrystalline SFMO derived from MA increases with increasing MA time. Similarly, the magnetoresistance (MR) effect also increases with increasing MA time up to 25 h, which is ascribed to the elimination of SrMoO₄ impurity phase and the refinement in grain size of the polycrystalline double perovskite phase. Prolonged MA adversely affects the MR effect, where Fe contamination was evidenced.     

Solvent and oxygen effects on the free radical polymerization of 6-O-vinyladipoyl-d-glucopyranose

The vinyl ester-type glycomonomer 6-O-vinyladipoyl-d-glucopyranose was polymerized in water and alcohol solutions. In all cases, long polymerization times were necessary to achieve reasonable conversions. Depending on the nature of the solvent, polydisperse glycopolymers were obtained possessing a molecular weight ranging between 10,000 and 122,000 Da (PS equivalent). Higher alcohols appeared to act as chain transfer agents and oligomers with DP_n between 2 and 6 were indeed obtained when 2-propanol was the solvent. Also, thorough oxygen removal from the reaction mixture proved to be essential for the success of the experiment, plain nitrogen sparging being ineffective in most cases.     

Fluorination of pressure-polymerized C60 phases

The reactivity of O-, T- and R-phases of the high pressure-high temperature (HPHT) polymerized C₆₀ towards gaseous fluorine in the temperature range of 50-250 °C was investigated. The reaction products were characterized by FTIR, powder X-ray diffraction, SEM, EDX, and VTP-EIMS to determine the bulk stoichiometries, bonding patterns, phase compositions, crystalline structures and thermal decomposition behavior of the fluorinated polymers. At 1 h isothermal treatment duration, fluorinated products with various bulk stoichiometries were obtained from different polymer phases with the R-phase showing the highest fluorine uptake. At 250 °C, all C₆₀ polymers showed partial decomposition to unfluorinated C₆₀ monomer under fluorine atmosphere. At 200 °C, the fluorination of R-phase yielded a pure fluoropolymer most likely having a {C₆₀F_x}_n (x = 36-44) composition. The same fluoropolymer was presumably obtained from O- and T-phases in lower yields. The linear chain structure was suggested for this new fluorocarbon polymer in agreement with the molecular mechanics modeling calculations.     

Evidence of anomalous thermal expansion of water in cement paste

A comparative study of permeability measurement by thermopermeametry (TPA) and beam bending was performed on cement paste. To bring the two measurements into agreement, it is necessary to recognize that the pore solution has a thermal expansion coefficient about one and a half times that of bulk liquid and to account for viscoelastic stress relaxation during TPA experiments. The anomalous thermal expansion is not accounted for by the presence of ions in the cement paste pore solution.