Manipulating the microstructure and rheology in polymer‐organoclay composites

A series of nanocomposites prepared by melt‐blending of cloisite‐based organoclays with poly(ethylene‐vinylacetate) (EVA) and neutralized poly (ethylene‐methacrylic acid) (EMA) copolymers were investigated via DSC, small‐angle X‐ray scattering (SAXS), and rheological techniques. SAXS results indicated partial clay exfoliation in all samples. In both EMA and EVA systems, the nominal melting temperature T_m and bulk crystallinity are not significantly affected by the presence of organoclays, suggesting that clay particles are predominantly confined in the amorphous phase. In rheological measurements (above T_m), the EVA‐clay system demonstrated a solid‐like rheological behavior under the small‐strain oscillatory shear, yet it was able to yield and flow under a steady shear, which is the characteristic of physical crosslinking. In contrast, the EMA‐clay system exhibited a melt‐like rheological behavior, where the influence of organoclay on the thermorheological behavior of the EMA composite was quite minimal. We propose that the carbonyl groups of vinylacetate in EVA interact with the clay surface, resulting in a strong physically crosslinking like interaction in the melt. On the other hand, the interaction between EMA and clay is weak because of repulsion between carboxyl anions and negatively charged clay surface.     

Physical Properties of Polyblends of Polyamide 6 Polymer with Cationic Dyeable Polyamide 6 Polymer

Polyamide 6 (PA 6) and cationic dyeable polyamide 6 (CD-PA 6) polymers were blended mechanically in the proportions of 75/25, 50/50, 25/75 in a melt twin-screw extruder to prepare three PA 6/CD-PA 6 polyblended polymers. The molar ratio of dimethyl 5-sulfoisophthalate sodium salt (SIPM) for CD-PA 6 polymer was 2%. This study investigated the physical properties of PA 6/CD-PA 6 polyblended materials using gel permeation chromatograph (GPC), nuclear magnetic resonance (NMR), gas chromatography (GC), potentiometer, thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), the density gradient method, a rheometer, and extension stress–strain measurement. Experimental results of the DSC indicated PA 6 and CD-PA 6 molecules easily formed miscible domains. The surface of PA 6/CD-PA 6 polyblend exhibited a uniform morphology from the scanning electron microscope (SEM). The SEM observations of morphologies were consistent with the DSC results for PA 6/CD-PA 6 polyblends. PA 6 and CD-PA 6 polymers were proven to be a compatible system. Flow behavior of PA 6/CD-PA 6 polyblends exhibited positive-deviation blends (PDB) and the 50/50 blend of PA 6/CD-PA 6 showed a maximum value of the melt viscosity. The crystallinities of PA 6/CD-PA 6 polyblends declined as a SIPM content increased. Moreover, the crystallinity of DSC method was slightly less than that of the density gradient method. The weight loss percentages of the PA 6/CD-PA 6 polyblends increased as the SIPM content increased in aqueous NaOH solution.     

Deformation behaviour during cold drawing of nanocomposites based on single wall carbon nanotubes and poly(ether ester) copolymers

Relationships between the macroscopic deformation behaviour and microstructure of a pure (PBT-b-PTMO) block copolymer and a polymer nanocomposite (PBT-b-PTMO + 0.2 wt% SWCNT) were investigated by simultaneous small- and wide-angle X-ray scattering (SAXS and WAXS) during tensile deformation using synchrotron radiation. The Young's modulus was found to be 15% higher for the nanocomposite than for the pure block copolymer as well as the yield strength, while the elongation-to-break was less than a half. This different behaviour can be explained by taking into account the different structural features revealed by SAXS and WAXS and thus considering that SWCNT act as anchors in the nanocomposite, sharing the applied stress with the PBT crystals and partially preventing the flexible, non-crystallisable PTMO chains to elongate.     

Synthesis and properties of poly(ether imide)s derived from 2,5‐bis(3,4‐dicarboxyphenoxy)biphenyl dianhydride and aromatic ether–diamines

A series of poly(ether imide)s (PEIs) with light colors and good mechanical properties were synthesized from 2,5‐bis(3,4‐dicarboxyphenoxy)biphenyl dianhydride and various aromatic ether–diamines via a conventional two‐step polymerization technique that included ring‐opening polyaddition at room temperature to poly(amic acid)s (PAAs) followed by thermal imidization. The precursor PAAs had inherent viscosities ranging from 0.71 to 1.19 dL/g and were solution‐cast and thermally cyclodehydrated to flexible and tough PEI films. All of the PEI films were essentially colorless, with ultraviolet–visible absorption cutoff wavelengths between 377 and 385 nm and yellowness index values ranging from 10.5 to 19.9. These PEIs showed high thermal stabilities with glass‐transition temperatures of 206–262°C and decomposition temperatures (at 10% weight loss) higher than 478°C. They also showed low dielectric constants of 3.39–3.72 (at 1 MHz) and low water absorptions below 0.85 wt %. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

The significance of telemedicine in a rural emergency department

Telemedicine is evolving into an important tool in delivering services to emergency departments (EDs) in rural areas. However, we do not yet know what kinds of services can be effectively delivered or the degree to which these services might be useful. In this pilot study, a high-speed, high-quality video, 24-hour ATM (asynchronous transfer mode) network linked a rural ED to an ED of a major medical center. The objective was to measure the utilization of telemedical consulting services. Specifically, this one-year study examined the significance of telemedicine in changing diagnosis and treatment and the influence on patient transfers     

Flow and thermal characteristics of cationic dyeable nylon 6/cationic dyeable poly(ethylene terephthalate) polyblended polymers and filaments

Cationic dyeable nylon 6 (CD‐N6) and cationic dyeable poly(ethylene terephthalate) (CD‐PET) polymers were extruded (in the proportions of 75/25, 50/50, 25/75) from one melt twin‐screw extruders to prepare three CD‐N6/CD‐PET polyblended polymers and then spin filaments. The molar ratio of 5‐sodium sulfonate dimethyl isophthalate (5‐SSDMI) for CD‐N6 and CD‐PET polymers were 2.01% and 2.04%, respectively. This study investigated the flow and thermal characteristics of CD‐N6/CD‐PET polyblended polymers and filaments using gel permeation chromatography (GPC), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), potentiometer, a rheometer, the density gradient, wide‐angle X‐ray diffraction (WAXD), and extension stress–strain measurement. Flow behavior of CD‐N6/CD‐PET polyblended polymers exhibited negative‐deviation blends (NDB), and the 50/50 blend of CD‐N6/CD‐PET showed a minimum value of the melt viscosity. Experimental results of the DSC indicated CD‐N6 and CD‐PET molecules formed an immiscible system. Particularly, a double endothermic peak was observed from CD‐N6, CD‐PET and their polyblended filaments. The tenacity of CD‐N6/CD‐PET polyblended filaments decreased initially and then increased as the CD‐PET content increased. Crystallinities and densities of CD‐N6/CD‐PET polyblended filaments were the linear relation with the blend ratio. The miscibility parameter μ values of CD‐N6/CD‐PET all samples were less than zero. It indicated the electrostatic repulsion was evident between CD‐N6 and CD‐PET molecules. From the experimental data, the CD‐N6 and CD‐PET polymers were identified to be immiscible. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 2049–2056, 2007     

Processable and colorless fluorinated poly(ether imide)s based on an isopropylidene‐containing bis(ether anhydride) and various aromatic bis(ether amine)s bearing trifluoromethyl groups

A series of novel organosoluble and light‐colored fluorinated poly(ether imide)s (PEIs) ( IV ) having inherent viscosities of 0.43–0.59 dL/g were prepared from 4,4′‐[1,4‐phenylenbis(isopropylidene‐1,4‐phenyleneoxy)]diphthalic anhydride ( I ) and various trifluoromethyl‐substituted aromatic bis(ether amine)s by a standard two‐step process with thermal and chemical imidization of poly(amic acid) precursors. These PEIs showed excellent solubility in many organic solvents and could be solution‐cast into transparent and tough films. These films were essentially colorless, with an UV–visible absorption edge of 361–375 nm and a very low b* value (a yellowness index) of 15.3–17.0. They also showed good thermal stability with glass‐transition temperature of 191–248°C, 10% weight loss temperature in excess of 494°C, and char yields at 800°C in nitrogen more than 39%. The thermally cured PEI films showed good mechanical properties with tensile strengths of 83–96 MPa, elongations at break of 8–11%, and initial moduli of 1.7–2.0 GPa. They possessed lower dielectric constants of 3.25–3.72 (1 MHz). In comparison with the V series nonfluorinated PEIs, the IV series showed better solubility, lower color intensity, and lower dielectric constants. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 620–628, 2007     

Quadruply coupled linear free vibrations of thin-walled beams with a generic open section

The coupled vibration of thin-walled beams with a generic open section induced by the boundary conditions is investigated using the finite element method. If the axial displacement of the pin end is restrained at another point rather than the centroid of the asymmetric cross section, the axial vibration, two bending vibrations, and torsional vibration may be all coupled. The element developed here has two nodes with seven degrees of freedom per node. The shear center axis is chosen to be the reference axis and the element nodes are chosen to be located at the shear centers of the end cross sections of the beam element. Different sets of element nodal degrees of freedom corresponding to different pin ends are considered here. The relation between element matrices referred to different sets of element nodal degrees of freedom is derived.

Numerical examples are presented to demonstrate the accuracy of the proposed method and to investigate the effects of different pin ends on the coupled vibrations of the thin-wall beam.     

Catalyst layer-free carbon-coated steel—An easy route to bipolar plates of polymer electrolyte membrane fuel cells: Characterization on structure and electrochemistry

Stainless steel coated with carbon by CVD process has been evaluated as a low-cost and small-volume substitute for graphite bipolar plate in polymer electrolyte membrane fuel cell (PEMFC). Carbon film was grown at 690–930 °C under gas-mixture of C₂H₂–H₂. Scanning electron microscopy and X-ray diffractometry were used to characterize surface morphology and crystal structure of resultant carbon films, which were found to depend much on reaction temperature. Interfacial contact resistance (ICR), hydrophobicity and chemical stability of obtained specimens were measured to compare with commercial highly oriented pyrolytic graphite (HOPG). All carbon films investigated in this study show improved ICR and hydrophobicity of SUS304 substrate to the level of HOPG. Amorphous carbon layer with continuous film structure prepared at 810 °C shows the best protection of SUS304 substrate against the attack of H_(aq)⁺ (anodic side) and the best resistance of the coated carbon from gasification (cathodic side) in the simulated PEMFC environment.