Effects of introducing silica particles on the rheological properties and crystallization behavior of poly(ethylene terephthalate)

Poly(ethylene terephthalate) (PET)/silica composites were prepared by melt compounding, and their rheological properties and isothermal crystallization were discussed. Introduction of silica particles (0.5–2 wt.%) increased the storage modulus (G′) and decreased loss tangent (tanδ). However, the effect of the particles on rheological properties became negligible at a high frequency more than ca. 70 rad/s. In the Cole–Cole plot, the PET/silica composites showed little deviation from the master curve regardless of the presence of silica particles. The particles increased the relaxation time of PET at particularly low frequency. The isothermal crystallization kinetics of PET/silica was examined using a differential scanning calorimeter (DSC). The half-time of crystallization was decreased with increasing the silica content. The incorporation of silica particles decreased the equilibrium melting temperature by ca. 5.5 °C. In addition, the composites exhibited higher average value of Avrami exponent (2.7–2.9) in comparison with that of pure PET (2.2).     

Solid-state spun fibers and yarns from 1-mm long carbon nanotube forests synthesized by water-assisted chemical vapor deposition

We report continuous carbon nanotube (CNT) fibers and yarns dry-drawn directly from water-assisted chemical vapor deposition (CVD) grown forests with about 1-mm height. As-drawn CNT fibers exist as aerogel and can be transformed into more compact fibers through twisting or densification with a volatile organic liquid. CNT fibers are characterized by scanning electron microscopy, X-ray photoelectron spectroscopy, Raman microscopy, and wide-angle X-ray diffraction. Mechanical properties and electrical conductivity of the post-treated CNT fibers are investigated. The resulting fibers show the work of rupture of 30 J/g and DC electrical conductivity of 5.0 × 10⁴ S/m.     

Deoxycholate‐Based Glycosides (DCGs) for Membrane Protein Stabilisation

Detergents are an absolute requirement for studying the structure of membrane proteins. However, many conventional detergents fail to stabilise denaturation‐sensitive membrane proteins, such as eukaryotic proteins and membrane protein complexes. New amphipathic agents with enhanced efficacy in stabilising membrane proteins will be helpful in overcoming the barriers to studying membrane protein structures. We have prepared a number of deoxycholate‐based amphiphiles with carbohydrate head groups, designated deoxycholate‐based glycosides (DCGs). These DCGs are the hydrophilic variants of previously reported deoxycholate‐based N‐oxides (DCAOs). Membrane proteins in these agents, particularly the branched diglucoside‐bearing amphiphiles DCG‐1 and DCG‐2, displayed favourable behaviour compared to previously reported parent compounds (DCAOs) and conventional detergents (LDAO and DDM). Given their excellent properties, these agents should have significant potential for membrane protein studies.     

Enhanced efficiency of white polymer light-emitting diodes with inorganic nanodots

Enhanced efficiency of white polymer light-emitting diodes (PLEDs) was observed by incorporating polysilicic acid (PSA) nanodots into the hole-injection layer (HIL). The PLEDs employed three different phosphorescent dyes in a single emissive layer with a host polymer of poly(vinylcarbazole) (PVK). The optimal composition of the phosphorescent dyes has been found to accomplish the white emission. By incorporating 1.5 wt% of PSA nanodots into the HIL, the maximum efficiency has been found to increase about 65%, from 13.7 cd/A to 22.9 cd/A. This remarkable improvement in efficiency may be attributed to the introduction of the PSA nanodots, which leads to the better carrier balance in the PLEDs.     

Synthesis and characterization of multiferroic BiFeO3 powders fabricated by hydrothermal method

The influence of processing parameters on phase formation and particle size of hydrothermally synthesized BiFeO₃ powders was investigated. BiFeO₃ powder was synthesized by dissolving bismuth nitrate and iron nitrate in KOH solution at temperatures ranging from 150 to 225 °C. X-ray diffraction patterns and scanning electron microscopy observation indicated that rod-like α-Bi₂O₃ phase was formed at initial stage of reaction and dissolved into ions to form thermodynamically stable BiFeO₃ phase. Single-phase perovskite BiFeO₃ has been formed using a KOH concentration of 8 M at a temperature of ≥175 °C in a 6 h reaction period. BiFeO₃ particle growth was promoted by lowering the KOH concentration, or increasing the duration time or reaction temperature. The effects of processing conditions on the formation of crystalline BiFeO₃ powders were discussed in terms of a dissolution–precipitation mechanism. The magnetization of the BiFeO₃ powders at room temperature showed a weak a ferromagnetic nature.     

Processing,Structure, and Properties of PAN/MWNT Composite Fibers

Conventional dry‐jet wet fiber spinning techniques were used to fabricate continuous PAN/MWNT composite fibers with up to 20 wt.‐% nanotube loading. PAN at the MWNT interface exhibited lower solubility under thermodynamically favorable conditions than in bulk PAN, indicating good interfacial interaction. Due to the PAN/MWNT interaction at the interface, thermal shrinkage decreases with increasing MWNT loading (5 to 20 wt.‐%). For high MWNT loadings, PAN/MWNT composite fiber at 15 wt.‐% MWNT loading showed an axial electrical conductivity of 1.24 S · m^?1. For all loadings, PAN/MWNT composite fibers exhibited higher tensile moduli than theoretically predicted by rule‐of‐mixture calculations, suggesting good reinforcement of the PAN by MWNT.

     

Fluorine geochemistry in bedrock groundwater of South Korea

High fluoride concentrations (median=4.4 mg/L) in deep bedrock groundwater of South Korea prevent the usage of it as a drinking water source. The hydrogeochemistry of deep thermal groundwaters (N=377) in diverse bedrocks has been studied in order to evaluate the geologic and geochemical controls on fluoride concentrations in groundwater. The groundwater samples were clustered geologically, and the average and median concentrations of fluoride were compared by the Mann-Whitney U test. The order of median fluoride concentration with respect to geology is as follows: metamorphic rocks> or =granitoids > or =complex rock>volcanic rocks> or =sedimentary rocks. This result indicates that the geological source of fluoride in groundwater is related to the mineral composition of metamorphic rocks and granitoids. With respect to groundwater chemistry, the fluoride concentration was highest in Na-HCO3 type groundwater and lowest in Ca-HCO3 type groundwater. Ionic relationships also imply that the geochemical behavior of fluoride in groundwater is related to the geochemical process releasing Na and removing Ca ions. The thermodynamic relationship between the activities of Ca and F indicates that fluoride concentration is controlled by the equilibrium of fluorite (CaF2). In other words, the upper limits of fluoride concentration are determined by the Ca ion; i.e., Ca concentrations play a crucial role in fluoride behavior in deep thermal groundwater. The result of this study suggests that the high fluoride in groundwater originates from geological sources and fluoride can be removed by fluorite precipitation when high Ca concentration is maintained. This provides a basis for a proper management plan to develop the deep thermal groundwater and for treatment of high fluoride groundwater frequently found in South Korea.     

Transition in fouling mechanism in microfiltration of a surface water

The main disadvantage of membrane filtration is membrane fouling, which remains as the major obstacle for more efficient use of this technology. Information about the constituents that cause fouling is indispensable for more efficient operation. We examined the changes in both foulant characteristics and membrane morphology by performing the pilot-scale filtration test using one microfiltration membrane. During the operation, we cut the membrane fibers three times, and the components that caused irreversible fouling were extracted by acid or alkaline solution. We found that the characteristic of inorganic matter extracted by acid solution completely differed depending on the filtration period. A large amount of iron was extracted in the second chemical cleaning, while manganese was the dominant component of the extracted inorganic matter in the third chemical cleaning. The analysis of Fourier transform infrared (FTIR) and cross polarization magic angle spinning carbon-13 (CPMAS (13)C) nuclear magnetic resonance (NMR) demonstrated that the contribution of humic substances and carbohydrate in the organic foulant had increased as fouling developed. The changes in the major foulant have no relation with the fluctuation in feed water. The analysis of membrane morphology illustrated that the cake layer started to build up after the blockage of membrane pores. Based on the above results, we hypothesized the following fouling mechanism: the pores were covered or narrowed with relatively large particles such as iron, carbohydrate or protein; small particles such as manganese or humic substances blocked the narrowed pores; and finally an irreversible cake layer started to build up on the membrane surface.     

High-power piezoelectric energy harvester produced using [0 0 1]-textured (Na,K)NbO3-based lead-free piezoceramics

High-power piezoelectric energy harvesters (PEHs) require piezoceramics with a large k_p and d₃₃ but small ε^T₃₃/ε₀ values. The [0 0 1]-textured 0.96(Na, K)(Nb_1−xSb_x)–0.04SrZrO₃ piezoceramics (x = 0.025 and 0.045) exhibited the improved electromechanical coupling factor (k_p) and piezoelectric charge constant (d₃₃); however, the increase of dielectric constant (ε^T₃₃/ε₀) was not significant. Further, the textured piezoceramic with x = 0.045 shows the large d₃₃ × g₃₃ value of 21.5 pm²/N, where g₃₃ is piezoelectric voltage constant, indicating that texturing is a good technique to fabricate the piezoceramics for PEH. The impedance curve of the PEH consisting of the metal substrate and textured piezoceramic shows a piezoelectric resonance peak at a low frequency, which is the same as the mechanical resonance frequency of the PEH. Hence, the PEH can be considered a piezoelectric material. The figure of merit of the PEH was determined using the mechanical quality and electromechanical coupling factor calculated from the impedance curve of the PEH. A large power output of 1.7 mW was obtained from the type-1 PEH at the resonance frequency produced using the textured thick film (x = 0.045). Hence, this PEH can be used as a permanent power source for microelectronic devices in the Internet of Things.