Enhanced electrical conductivity of Ag-mercaptosuccinic acid-redoped polyaniline nanoparticles during thermal cycling above 200 °C

Ag-doped polyaniline (PANI) nanoparticles are prepared via doping-dedoping-redoping with the thiol group in mercaptosuccinic acid (MSA) providing the linkage between PANI molecules and Ag atoms. Ag-MSA-doped PANI maintains the electrical conductivity well above the room-temperature value of 3.0 S/cm up to 220 °C, reaching its maximum (9.0 S/cm) at 180 °C. In addition, Ag-MSA-doped PANI nanoparticles show remarkable stability against repeated thermal aging at 120 °C. The room-temperature conductivity, in fact, increases by a factor of ∼3 after 3 cycles of thermal aging. The enhanced stability against repeated thermal aging is attributed to the formation of uniformly distributed Ag nanoparticles within the PANI particles upon heating.     

Effect of the urethane group on treated clay surfaces for high-performance poly(butylene succinate)/montmorillonite nanocomposites

We successfully modified organic clays containing the urethane group by introducing a covalent bond between the silanol group on the clay side and the hydroxyl group of organic modifier in the silicate layer using 1,6-diisocyanatohexane (HDI), namely surface-treated montmorillonite (30BM), to increase both basal spacing and the favorable interaction between clay and polymer. The effect of the surface urethane modification of clay on poly (butylene succinate) (PBS)/30BM nanocomposites was studied. The results of transmission electron microscopy micrographs at a 10-nm resolution and X-ray diffraction measurements allowed us to examine the degree of the high exfoliation and the effect of surface urethane modification on clay dispersibility. As results of high exfoliation, PBS/30BM nanocomposites not only exhibited the high thermal properties, but also showed a remarkable increase in physical properties (e.g., tensile strength, Young's modulus, elongation at break) due to enhanced affinity between the clay and PBS matrix. Over all, the results suggest that wide gallery spacing and the predominant affinity between PBS and clay must be considered simultaneously to increase the degree of exfoliation and physical properties as key factors.     

Simultaneous LC−UV Analysis of Mirodenafil and Its Two Main Metabolites in Rat Plasma and Urine, and in Tissue Homogenates

A simple, rapid, and reproducible isocratic reversed-phase LC method has been established for simultaneous analysis of mirodenafil and its two main metabolites, SK3541 and SK3544, in rat plasma, urine, and tissue homogenates. Samples were deproteinized with acetonitrile containing sildenafil (internal standard). The compounds were separated on a C₁₈ column with 52:48 (v/v) 0.02 m ammonium acetate buffer (pH 6)—acetonitrile as mobile phase at a flow rate of 1.4 mL min^?1. UV detection was at 254 nm and detection limits of mirodenafil, SK3541, and SK3544 in plasma were 0.03, 0.05, and 0.1 μg mL^?1, respectively. The method is applicable to pharmacokinetic studies of mirodenafil and its metabolites in rats.     

Convergence theorems based on hybrid methods for generalized equilibrium problems and fixed point problems

The purpose of this work is to introduce a hybrid projection method for finding a common element of the set of a generalized equilibrium problem, the set of solutions to a variational inequality and the set of fixed points of a strict pseudo-contraction in a real Hilbert space.     

On products of quadratic twists and ranks of elliptic curves over large fields

In this paper, we give examples of elliptic curves E/K overa number field K satisfying the property that there exist P₁,P₂ K[t] such that the twists and are of positiverank over K(t). As a consequence of this result on twists, weshow that for those elliptic curves E/K, and for each , the rank of E over the fixed field (K^ab) under is infinite, where K^ab is the maximal abelian extension ofK.     

Sparse modeling of super-resolution near-field structure read-out signals

In this study, super-RENS disc read-out signals were modeled with various nonlinear models. In the results of modeling the nonlinearity, DC offset, and domain bloom phenomena of the super-RENS channel with a second-order Volterra filter, it was identified that the number of significant quadratic coefficients was relatively small. Therefore, a sparse Volterra model and a truncated Volterra model are applied to effectively model the nonlinear channel. In addition, the Hammerstein-type asymmetric conversion model is employed to model the nonlinear channel for the purpose of comparison. The results demonstrate that the sparse model of a simplified polynomial form achieves good modeling performance for the super-RENS disc read-out signals.     

Unexpected consequences of block polydispersity on the self-assembly of ABA triblock copolymers

Controlled/"living" polymerizations and tandem polymerization methodologies offer enticing opportunities to enchain a wide variety of monomers into new, functional block copolymer materials with unusual physical properties. However, the use of these synthetic methods often introduces nontrivial molecular weight polydispersities, a type of chain length heterogeneity, into one or more of the copolymer blocks. While the self-assembly behavior of monodisperse AB diblock and ABA triblock copolymers is both experimentally and theoretically well understood, the effects of broadening the copolymer molecular weight distribution on block copolymer phase behavior are less well-explored. We report the melt-phase self-assembly behavior of SBS triblock copolymers (S = poly(styrene) and B = poly(1,4-butadiene)) comprised of a broad polydispersity B block (M(w)/M(n) = 1.73-2.00) flanked by relatively narrow dispersity S blocks (M(w)/M(n) = 1.09-1.36), in order to identify the effects of chain length heterogeneity on block copolymer self-assembly. Based on synchrotron small-angle X-ray scattering and transmission electron microscopy analyses of seventeen SBS triblock copolymers with poly(1,4-butadiene) volume fractions 0.27 ≤ f(B) ≤ 0.82, we demonstrate that polydisperse SBS triblock copolymers self-assemble into periodic structures with unexpectedly enhanced stabilities that greatly exceed those of equivalent monodisperse copolymers. The unprecedented stabilities of these polydisperse microphase separated melts are discussed in the context of a complete morphology diagram for this system, which demonstrates that narrow dispersity copolymers are not required for periodic nanoscale assembly.     

Discrete electrostatic charge transfer by the electrophoresis of a charged droplet in a dielectric liquid

We have experimentally investigated the electrostatic charging of a water droplet on an electrified electrode surface to explain the detailed inductive charging processes and use them for the detection of droplet position in a lab-on-a-chip system. The periodic bouncing motion of a droplet between two planar electrodes has been examined by using a high-resolution electrometer and an image analysis method. We have found that this charging process consists of three steps. The first step is inductive charge accumulation on the opposite electrode by the charge of a droplet. This induction process occurs while the droplet approaches the electrode, and it produces an induction current signal at the electrometer. The second step is the discharging of the droplet by the accumulated induced charge at the moment of contact. For this second step, there is no charge-transfer detection at the electrometer. The third step is the charging of the neutralized droplet to a certain charged state while the droplet is in contact with the electrode. The charge transfer of the third step is detected as the pulse-type signal of an electrometer. The second and third steps occur simultaneously and rapidly. We have found that the induction current by the movement of a charged droplet can be accurately used to measure the charge of the droplet and can also be used to monitor the position of a droplet under actuation. The implications of the current findings for understanding and measuring the charging process are discussed.     

The effects of surface modification on the electrical properties of p–n+ junction silicon nanowires grown by an aqueous electroless etching method

Although the aqueous electroless etching (AEE) method has received significant attention for the fabrication of silicon nanowires (SiNWs) due to its simplicity and effectiveness, SiNWs grown via the AEE method have a drawback in that their surface roughness is considerably high. Thus, we fabricated surface-modified p–n ⁺ junction SiNWs grown by AEE, wherein the surface roughness was reduced by a sequential processes of oxide growth using the rapid thermal oxidation (RTO) cycling process and oxide removal with a hydrofluoric acid solution. High-resolution transmission electron microscopy analysis confirmed that the surface roughness of the modified SiNWs was significantly decreased compared with that of the as-fabricated SiNWs. After RTO treatment, the wettability of the SiNWs had dramatically changed from superhydrophilic to superhydrophobic, which can be attributed to the formation of siloxane groups on the native oxide/SiNW surfaces and the effect of the nanoscale structure. Due to the enhancement in surface carrier mobility, the current density of the surface-modified p–n ⁺ junction SiNWs was approximately 6.3-fold greater than that of the as-fabricated sample at a forward bias of 4 V. Meanwhile, the photocurrent density of the surface-modified p–n ⁺ junction SiNWs was considerably decreased as a result of the decreases in the light absorption area, light absorption volume, and light scattering.