Blend membranes based on sulfonated poly(ether ether ketone) and poly(vinylidene fluoride) for high performance direct methanol fuel cell

Various polymeric blends based on sulfonated poly(ether ether ketone) (sPEEK)/poly(vinylidene fluoride) (PVdF) were prepared for the membranes of direct methanol fuel cell. The blend membranes showed good compatibility within a limited composition range of less than around 10 wt% of PVdF. The blend membrane containing 2.5 wt% exhibited highest proton conductivity at room temperature among the tested blends. The dimensional stability was enhanced with introducing PVdF into the blend membrane. These could contribute to high performance of the cell based on the blend membrane.     

Highly crosslinked poly(glycidyl methacrylate-co-divinyl benzene) particles by precipitation polymerization

Stable and smooth surface poly(glycidyl metharylate-co-divinylbenzene) (GMA-co-DVB) microspheres composed of various concentrations of DVB from 20 to 90 mol% in acetonitrile medium were prepared without a significant coagulum by precipitation polymerization. The number-average diameter of the microspheres linearly increases from 2.63 to 3.34 μm and the particle size distribution becomes narrower by decreasing the uniformity from 1.10 to 1.02 with the DVB concentration from 20 to 90 mol%. The yield of polymerization increased from 28.9 to 79.7% with the DVB concentration as well. The FT-IR spectrum shows the characteristic peaks at 1725-1650 cm⁻¹ assigned to the confirmation of the polymerization between GMA and DVB. No glass transition temperature and the onset of the thermal degradation temperature at higher temperature indicate that the poly(GMA-co-DVB) is crosslinked; this is evidenced by the swelling ratio measurement relevant to the crosslinking density of the poly(GMA-co-DVB). The swelling test suggested that the poly(GMA-co-DVB) particles would be a core/shell type structure composing of a highly crosslinked DVB rich-phase in the core part and slightly crosslinked GMA rich-phase in the shell part.     

A study on UV-curable coatings for HD-DVD: Primer and top coats

This study relates to the development of coatings for optical discs in high-density digital versatile disc systems (HD-DVD or blue lay disk) that use a high numerical aperture of 0.85 at 405 nm wavelength and have a protective top layer over a primer layer for protection against damage and dust. Ultraviolet-curable raw materials of two acrylic monofunctional monomers ( isobornylacrylate, IBA and tetrahydrofurfurylacrylate, THFA) and two kinds of urethaneacrylate oligomers (OUMD and OUME) have been easily mixed with photoinitiators. Curing rate of these materials was characterized by FT-IR. In case of top coats, VTES (vinyltriethoxysilane) and acrylic acid were added to enhance the abrasion resistance. These two kinds of UV-curable resinous materials having no solvent were synthesized and investigated as means for making a blue ray disk having good optical and mechanical properties. In addition, dynamic characteristics including reflectivity, fluctuation of RF signal and noise level were also investigated.     

Effects of defects generated in ALD TiO<Subscript>2</Subscript> films on electrical properties and interfacial reaction in TiO<Subscript>2</Subscript>/SiO<Subscript>2</Subscript>/Si system upon annealing in vacuum

Thin TiO₂ layers grown at 130°C on SiO₂-coated Si substrates by atomic layer deposition (ALD) using TTIP and H₂O as precursors were annealed, and the effects of the annealing temperature on the resulting electrical properties of TiO₂ and the interface properties between a Pt electrode and TiO₂ were examined using transmission line model (TLM) structures. The as-deposited TiO₂ thin film had an amorphous structure with OH groups and a high resistivity of 6×10³Ω-cm. Vacuum annealing at 700 °C transformed the amorphous film into an anatase structure and reduced its resistivity to 0.04Ω-cm. In addition, the vacuum-annealing of the TiO₂/SiO₂ structure at 700°C produced free silicon at the TiO₂-SiO₂ interface as a result of the reaction between the Ti interstitials and SiO₂. The SiO₂ formed on the TiO₂ surface caused a Schottky contact, which was characterized by the TLM method. The use of the TLM method enabled the accurate measurement of the resistivity of the vacuum-annealed TiO₂ films and the characterization of the Schottky contacts of the metal electrode to the TiO₂.     

Vibration analysis of a planetary gear system based on the transfer matrix method

This study models a 3-dimensional planetary gear system using the transfer matrix method. The local transfer matrices between each component of the planetary gear set were derived with consideration of the tooth width, and the transfer matrix of a planetary gear system corresponding to the inertial transfer matrix was determined. The eigenvalue analysis of the transfer matrix suggested an analysis method in the form of a lambda matrix, instead of the direct search method through a characteristic polynomial. The boundary conditions at the first and the last stations of the entire transfer matrix were partitioned into known and unknown values to generate a concentrated transfer matrix and a latent equation, and the eigenvalue problem in the lambda matrix was solved. The characteristics of the responses according to the phase state of the harmonic component of the transmission error were reviewed through the steady-state response and mode shape type.     

Crack-tip constraints of through-wall cracked pipes and its similarity to curved wide plates

In the present study, the effects of pipe geometries, material properties and loading conditions on crack-tip constraints of pipes with circumferential Through-wall crack (TWC) were investigated via systematic 3-dimensional (3-D) Finite element (FE) analyses. The crack-tip constraints were quantified by Q-stress, and to characterize the elastic-plastic strain hardening material behavior, Ramberg-Osgood (R-O) material was employed. Based on the FE results, it was observed that crack-tip constraints of pipes with TWC were dependent on crack length and thickness of pipe, however, the effects of each variables decreased as either thickness of pipe becomes thinner or crack length becomes longer. Moreover, the effects loading modes on Q-stresses for thin-walled pipes with TWC are negligible. Finally, the present Q-stresses of pipes were compared with those of Curved wide plate (CWP) in tension to address the similarity of crack-tip constraints between pipe and CWP, which could be used to produce the CWP to measure the fracture toughness of pipes accurately.     

Effects of walking speed and age on the directional stride regularity and gait variability in treadmill walking

Journal of Mechanical Science and Technology - In Inertial measurement unit (IMU) based gait analysis systems, the shoe-type sensor is not commonly used, unlike trunk attached sensors. The purpose...     

A study on carbon coating to silicon and electrochemical characteristics of Si-C/Li cells

The aim of this paper is to study the electrochemical behavior of Si-C material synthesized by heating a mixture of silicon and polyvinylidene fluoride (PVDF) in the ratios of 5, 20, and 50 wt%. The particle size of the synthesized material was found to be increased with increase in the PVDF ratio. The coexistence of silicon with carbon was confirmed from the XRD analysis. A field emission scanning electron microscope (FESEM) study performed with the material proved the improvement in coating efficiency with increase in the PVDF ratio. Coin cells of the type 2025 were made by using the synthesized material, and the electrochemical properties were studied. An electrode was prepared by using the developed Si-C material. Si-C|Li cells were made with this electrode. A charge|discharge test was performed for 20 cycles at 0.1 C hour rate. Initial charge and discharge capacities of Si-C material derived from 20 wt% of PVDF was found to be 1,830 and 526 mAh|g, respectively. Initial charge/discharge characteristics of the electrode were analyzed. The level of reversible specific capacity was about 216mAh/g at Si-C material derived from 20 wt% of PVDF, initial intercalation efficiency (IIE), intercalation efficiency at initial charge/discharge, was 68%. Surface irreversible specific capacity was 31 mAh/g, and average specific resistance was 2.6 ohm * g.     

Structures and phase transformations of odd-numbered asymmetric main-chain liquid crystalline polyesters

Two new asymmetric odd-numbered main-chain liquid crystalline (LC) polyesters (BPE-Cn) were synthesized through the condensation polymerization of A-B type asymmetric α,ω-carboxylic acid-hydroxyl terminated monomers with odd-numbers of methylene units in the spacers (BPCA-Cn-PmOH, where n=7 and 9). The phase behaviors and structures of these odd-numbered BPE-Cn samples were characterized using the combined techniques of differential scanning calorimetry (DSC), wide angle X-ray diffraction (WAXD), selected area electron diffraction (SAED) and polarized light microscopy (PLM). One-dimensional (1D) powder WAXD results at different temperatures combined with DSC results revealed that during cooling these two polyesters enter a low-ordered LC phase before developing a crystalline phase at lower temperatures. Based on 2D WAXD of oriented fiber patterns, the low ordered LC phase of odd-numbered BPE-Cn was identified to be a smectic A (SmA) phase, which was constructed by each chemical repeating unit along the fiber drawn direction. The crystalline structures were determined to be monoclinic unit cells (K_M). However, BPE-C7 possessed a γ=87°, while BPE-C9 had a β=100°. These crystalline structure identifications were also confirmed by SAED from single crystals. Two-chain packing models of the K_M phases with four chemical repeating units were proposed on the basis of the experimental diffraction patterns. The different structures were attributed to the interplay between the mesogenic group ordering propensity and the chain constraints dictated by the methylene spacer and the meta-linkage at the end of mesogen. In the ordered phases of these two odd-numbered BPE-Cn polyesters, aromatic mesogenic groups are more or less parallel to each other along the chain with small angles of deviation from the c-axis of the crystal lattice, different from those large zigzag conformation structures in even-numbered BPE-Cn crystals. Crystallographic calculations of these two unit cell structures indicated that the neighboring chains in the crystals are translated along the c-axis (in the case of BPE-C9) or twisted away from the b-axis (in the case of BPE-C7) in order to incorporate both of the bend attributed to the odd-numbered methylene spacers and of the configurational meta-linkage at the end of mesogens. The simulated diffractions based on these calculations qualitatively agreed with the experimental observations. The phase identifications were also supported by the observed texture changes in PLM.     

Poly(trimethylene terephthalate) nanocomposite fibers comprising different organoclays: Thermomechanical properties and morphology

Poly(trimethylene terephthalate) (PTT) nano composites were synthesized by in situ polymerization at high temperature with two thermally stable organoclays: 1,2‐dimethylhexadecylimidazolium‐montmorillonite (IMD‐MMT) and dodecyltriphenyl phosphonium‐MMT (C₁₂PPh‐MMT). PTT hybrid fibers with various organoclay contents were melt‐spun at various draw ratios (DRs) to produce monofilaments. The thermomechanical properties and morphologies of the PTT hybrid fibers were characterized using differential scanning calorimetry, thermogravimetric analysis, wide‐angle X‐ray diffraction, electron microscopy, and mechanical tensile properties analysis. The nanostructure of the hybrid fibers was observed by both scanning and transmission electron microscopy, which showed that the clay layers were well dispersed into the matrix polymer, although some clusters or agglomerated particles were also detected. Unlike the hybrids containing IMD‐MMT, the clay layers of the C₁₂PPh‐MMT hybrid fiber were more dispersed into the matrix polymer. The thermal stability and tensile properties of the hybrid fibers increased with increasing clay content for DR = 1. However, as DR increased from 1 to 9 the ultimate strength and initial modulus of the hybrid fibers with IMD‐MMT increased slightly whereas those of C₁₂PPh‐MMT hybrid fibers decreased slightly. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 4535–4545, 2006