Polymer electrolyte membrane with nanomatrix channel prepared by sulfonation of natural rubber grafted with polystyrene

High‐proton‐conductive polymer electrolyte with a nanomatrix channel was prepared by graft copolymerization of styrene onto deproteinized natural rubber followed by sulfonation with chlorosulfonic acid. First, natural rubber latex was purified with urea in the presence of surfactant to remove almost all proteins present in the rubber. Second, graft copolymerization of styrene onto deproteinized natural rubber was carried out with tert‐butyl hydroperoxide/tetraethylenepentamine as an initiator at 30°C in latex stage. The graft‐copolymerized natural rubber (DPNR‐graft‐PS) was sulfonated with chlorosulfonic acid in chloroform solution at an ambient temperature. The resulting sulfonated DPNR‐graft‐PS was characterized by FTIR spectroscopy, solid state ¹³C CP/MAS NMR spectroscopy, elemental analysis, and transmission electron microscopy. High proton conductivity of about 0.1 S/cm, less water uptake of 24 wt % and comparatively good stress at break of 9 MPa were accomplished at suitable contents of styrene units and sulfur, i.e., 32 wt % and 75 mol %, respectively. The high proton conductivity, excellent stability, and good mechanical properties were associated with not only the formation of the nanomatrix channel but also a specific concentration of sulfuric acid group. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011.     

Phase Relations and Volume Changes of Hafnia under High Pressure and High Temperature

Using multi-anvil high-pressure devices and synchrotron radiation, X-ray in situ observations of HfO₂ under high pressure and high temperature have been performed to investigate its phase relations and compression behavior. An orthorhombic phase (orthoI) is stable from 4 to 14.5 GPa below 1250°–1400°C and transforms to a tetragonal phase, which is one of the high-temperature forms of HfO₂, above these temperatures. Another orthorhombic phase (orthoII) with a cotunnite-type structure appears above 14.5 GPa. OrthoII is stable up to 1800°C at 21 GPa. OrthoII is quenchable to ambient conditions. The orthoI-to-orthoII transition is accompanied by ∼8 vol% decrease. The bulk moduli of orthoI and orthoII at room temperature are 220 and 312 GPa, respectively. This low compressibility of orthoII indicates that it is a potential candidate for very hard materials.     

Effect of Talc Size on Surface Roughness and Glossiness of Polypropylene Injection Molding Application to Automotive Plastics

Talc-containing polypropylene (PP) resin is extensively employed in automobiles. Herein, considering the microstructure transfer process in injection molding, the effect of the talc's dispersibility and particle size on this process and its impact on the gloss level of the product were investigated. Results show that a fine unevenness of about several micrometers was self-formed by the shrinkage of PP in nontransferred areas due to the blending of talc. Additionally, the amount of self-formed unevenness tended with an increase in the average particle size of talc. Furthermore, due to PP shrinkage and different densities of talc, it was observed that a fine tiger-stripe pattern was self-formed using special molds with modified microstructure. This self-formed fine unevenness changes the gloss level owing to the diffused light reflection effect. This study proposes controlling this change by controlling the average particle size of talc and structure of the mold. POLYM. ENG. SCI., 60:132–139, 2020. © 2019 Society of Plastics Engineers     

Insights from ab initio molecular dynamics simulations for a multicomponent oxide glass

It remains a challenge to establish structural models of multicomponent oxide glass systems. In this study, we have investigated 68.3SiO₂–16.1B₂O₃–4.2Al₂O₃–11.4Na₂O glass and melt structures by ab initio molecular dynamics (AIMD) simulations. The atomic configurations obtained from AIMD simulations were validated against ¹⁷O solid‐state NMR spectrum under 24.0 T and neutron diffraction data, and excellent agreement was achieved. The bond lengths, angles, and coordination geometries were statistically analyzed for each atomic species. Here we particularly address the role of minor atomic species such as five‐coordinate Si (Si^V) and Al (Al^V). The Si^V–O bond lengths and O–Si^V–O angle distribution in the glass indicated 1.718 Å and three peaks at 90°, 120°, and 175°, which are assigned to a coordination geometry of the trigonal bipyramidal structure. Ring statistic analysis revealed that Si^V and Al^V were found to preferentially contribute to the formation of small ring sizes.     

Modified tensile adhesion test for evaluation of interfacial toughness of HVOF sprayed coatings

Tensile adhesion test is widely used to evaluate the adhesion strength of coatings sprayed by High Velocity Oxy-Fuel (HVOF) technique. But there are two issues to be improved. Firstly, when the coatings have high adhesion strength, failure occurs in an adhesive layer, and secondary, the edge of a substrate is heavily deformed and rounded due to the high impact energy of sprayed particles. This deformation causes large scatter of adhesion test results. In this paper, a new technique to evaluate the interfacial fracture toughness has been proposed by introducing pre-crack at the interface of a conventional tensile adhesion test specimen. The asymptotic analytical formula was derived for interfacial toughness evaluation. Numerical analysis was also carried out for comparison. The difference between the numerical and the theoretical data was less than 5%. The developed procedure was applied for the SUS316 L steel coatings and the significant effects of the surface roughness and preheating temperature on adhesion strength were reconfirmed quantitatively.     

Effects of Some Light Alloying Elements on the Oxidation Behavior of Fe and Ni-Cr Based Alloys During Air Plasma Spraying

The oxidation behavior of iron binary powders with addition of Si (1, 4 wt.%) and B (1, 3 wt.%) and that of a Ni-Cr based alloy powder with Si (4.3 wt.%), B (3.0 wt.%), and C (0.8 wt.%) additions during atmosphere plasma spray (APS) have been investigated. Analysis of the chemical composition and phases of oxides in the captured in-flight particles and deposited coatings was carried out. The results show that the addition of Si and B to iron effectively reduced the oxygen contents in the coatings, especially during the in-flight period at higher particles temperature. Ni-Cr based alloy powder with Si, B, and C additions reduced the oxidation of the base alloys significantly. Preferential oxidation and subsequent vaporization of Si, B, and C from the surface of the sprayed particles are believed to play a major role in controlling oxidation in the APS process.     

Electrical resistivity and thermopower of (La1−xSrx)MnO3 and (La1−xSrx)CoO3 at elevated temperatures

Electrical resistivity and Seebeck (S) measurements were performed on (La_1−xSr_x)MnO₃ (0.02x0.50) and (La_1−xSr_x)CoO₃ (0x0.15) in air up to 1073 K. (La_1−xSr_x)MnO₃ (x0.35) showed a metal-to-semiconductor transition; the transition temperature almost linearly increased from 250 to 390 K with increasing Sr content. The semiconductor phase above the transition temperature showed negative values of S. (La_1−xSr_x)CoO₃ (0x0.10) showed a semiconductor-to-metal transition at 500 K. Dominant carriers were holes for the samples of x0.02 above room temperature. LaCoO₃ showed large negative values of S below ca. 400 K, indicative of the electron conduction in the semiconductor phase.     

An edible oil deodorizer with a direct-fired heater

Engineers have long believed a direct-fired heater (DFH) for deodorization is always in danger of over-heating. Commercial tests done in recent years have proved this danger can be avoided by proper furnace design. At least ten commercial deodorizers with this system are now used in Asia. A new deodorizer with a DFH was designed and built in 1986 in Taiwan. It features a single-shell design and steam-stripping of deep oil layers. It has been operated successfully for several years. The deodorized oil was compared with oil produced by conventional deodorizers. The new deodorizer with a DFH revealed several advantages.     

Synthesis and properties of poly(phenylacetylene)s having dialkylamino groups

Summary Poly(phenylacetylene)s bearing dialkylamino groups were prepared by the polymerization of p-(N,N-dialkylamino)phenylacetylenes with [Rh(nbd)Cl]₂, and their electrochemical behavior was examined. Rh-catalyzed polymerization of p-(N,N-diethylamino)phenylacetylene (DEAPA) and p-(N,N-di-n-butylamino)phenylacetylene (DBAPA) in toluene in the presence of triethylamine gave good yields of the polymers (86 and 90%, respectively). Poly(DEAPA) was soluble in chloroform and dichloromethane, and poly(DBAPA) dissolved in various solvents such as toluene, THF, dichloromethane and chloroform. Poly(DEAPA) and poly(DBAPA) showed onset temperatures at 248 and 190°C, respectively, and absorptions around 300–400 nm. Electrochemical doping of the polymer films resulted in the shift of the absorptions to a region around 680 nm, which accompanied a color change of the polymer films from green ocher to deep blue. Received: 26 October 1998/Revised version: 6 November 1998/Accepted: 12 November 1998     

Surface Relief Associated with Isothermal Martensite in Zirconia–3-mol%-Yttria Ceramics Observed by Atomic Force Microscopy

Surface relief associated with martensitic transformation—tetragonal-to-monoclinic phase transformation—that occurred during isothermal aging at temperatures of 400 and 473 K was observed via atomic force microscopy, using prepolished and thermally etched surfaces of zirconia–3 mol% yttria that was sintered at a temperature of 1923 K for 5 h. The isothermal martensitic transformation occurred first at grain boundaries and advanced into grain interiors as the aging time increased and then spread successively into the surrounding grains. The transformation area, which had an approximately round shape, increased as the aging time increased. The fine structure of the surface relief was composed of many tent shapes that were several nanometers high with an angle of ∼165°.