Synergistic Effects of Polybenzimidazole and Aramide on Enhancing Flame-Retardancy and Solubility

Aromatic and functional polymers with processibility derived from biobased starting materials are prerequisite considering sustainable society. Poly(2,5-benzimidazole)s are rigid-rod polymers to show ultrahigh thermal stability such as flame retardance, while usually suffer from poor solubility. Here, poly(benzimidazole-co-amide)s are synthesized from two biobased monomers, 3,4-diaminobenzoic acid and a semirigid comonomer, 4-aminohydrocinnamic acid. The copolymers with an amide composition of 80 mol% and higher are soluble in widely used polar solvents to fabricate the films keeping high flame retardance, which is comparable with popular high-performance polymers such as aromatic polyimides, polyetheretherketone, polyphenylene sulfide, etc.     

Surface treatment of titanium dioxide nanopowder using rotary electrode dielectric barrier discharge reactor

Titanium dioxide (TiO2) nanopowder (P-25;Degussa AG) was treated using dielectric barrier discharge (DBD) in a rotary electrode DBD (RE-DBD) reactor.Its electrical and optical characteristics were investigated during RE-DBD generation.The treated TiO2 nanopowder properties and structures were analyzed using x-ray diffraction (XRD) and Fourier-transform infrared spectroscopy (FTIR).After RE-DBD treatment,XRD measurements indicated that the anatase peak theta positions shifted from 25.3° to 25.1°,which can be attributed to the substitution of new functional groups in the TiO2 lattice.The FTIR results show that hydroxyl groups (OH) at 3400 cm-1 increased considerably.The mechanism used to modify the TiO2 nanopowder surface by air DBD treatment was confirmed from optical emission spectrum measurements.Reactive species,such as OH radical,ozone and atomic oxygen can play key roles in hydroxyl formation on the TiO2 nanopowder surface.     

Neural network-based asymptotic tracking control of unknown nonlinear systems with continuous control command

ABSTRACT

This paper proposes a robust tracking controller for a class of nonlinear second-order systems with time-varying uncertainties. The controller is mainly based on the robust integral of the sign of the error (RISE) control approach to achieve an asymptotic stability result with a continuous control command in the presence of additive uncertainties. An adaptive feedforward neural network control term is blended with a new RISE controller to improve the system's transient performance. The proposed RISE controller is a modified version of the existing saturated RISE controller such that only sign of the derivative of the output is needed. The stability of the closed-loop system is well studied, where a local asymptotic stability is proven. The controller performance is validated through simulations on a two-degree-of-freedom lower limb robotic exoskeleton.     

Improving the photovoltaic performance of co‐evaporated Cu2ZnSnS4 thin‐film solar cells by incorporation of sodium from NaF layers

We have investigated the influence of sodium (Na) on the properties of co‐evaporated Cu₂ZnSnS₄ (CZTS) layer microstructures and solar cells. The photovoltaic performance and diode properties were improved by incorporating Na from NaF layers into the CZTS layers, while Na had a negligible effect on the microstructural properties of the layer. The best cell fabricated by using an optimal CZTS layer (Cu/(Zn + Sn) = 0.70, Zn/Sn = 1.8) yielded an active area efficiency of 5.23%. The analysis of device properties suggests that charge‐carrier recombination at CZTS/CdS interface is suppressed by intentional Na incorporation from NaF layers. Copyright © 2016 John Wiley & Sons, Ltd.     

Synthesis of Succinic Gemini Surfactants and the Effect of Stereochemistry on Their Monolayer Behaviors

In this work, succinic gemini surfactants, dl‐ and meso‐2,3‐bis(alkyl)succinic acids (alkyl: C₆H₁₃–C₁₃H₂₇), were successfully synthesized by oxidative coupling of enolates of fatty acid tert‐butyl esters with copper(II) bromide followed by treatment with CF₃COOH. Focusing on the influence of stereochemistry (dl‐ and meso‐) of succinic geminis, their monolayer behaviors at the air–water interface were explored using surface pressure–area (Π–A) isotherms, the compression modulus of monolayers (ε_s), and Brewster angle microscope (BAM) analysis. meso‐2,3‐Bis(undecyl)succinic acid showed a unique isotherm where the surface pressure drastically decreased at A = ~0.56 nm² (Π = 21.9 mN m^?1) regardless of compression rates and subphase temperatures, while dl‐isomer showed the common isotherm of gas → liquid‐expanded → liquid‐condensed phase transitions. BAM analysis on meso‐2,3‐bis(undecyl)succinic acid films at the air–water interface showed that small islands of aggregates appear just after the maximum pressure (A = ~0.56 nm²), and on further compression needle‐shaped assemblies appear that can grow in size. It was reasonably concluded that hydrophobic interactions can operate more effectively in meso‐isomers than in dl‐isomers, and that meso‐molecules can “jump up” to cause a transition from monolayer to bilayer. This is the first finding of the “jumping‐up” phenomenon of gemini surfactants having meso‐stereochemistry.     

Improved heat and solvent resistance of a pressure‐sensitive adhesive thermally processable by isocyanate dimer dissociation

Methods that do not involve use of an organic solvent are being considered for manufacturing environmental‐friendly pressure‐sensitive adhesive tapes. Among these methods, the hot‐melt method exhibits high productivity but is somewhat limited in terms of performance. Hot‐melt‐fabricated pressure‐sensitive adhesives require heating fluidization and cooling solidification, and it is extremely difficult to improve their heat resistance. We examine thermally processable pressure‐sensitive adhesives with a completely new structure, fabricated based on the thermal dissociation of the isocyanate dimer. This enables thermal processing of materials softened by thermal dissociation. Fabrication of crosslinkable pressure‐sensitive adhesive becomes possible through a reaction of isocyanate caused by dissociation of its dimer. It is found that improving thermal and solvent resistances, which are disadvantages associated with conventional hot‐melt pressure‐sensitive adhesives, is potentially possible with the pressure‐sensitive adhesive reported here. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41444.     

The effect of initial parameters on particle size distribution inverted using the laser diffraction technique and a non-linear iterative method

The Twomey non-linear iteration (NLI) method is known by the simple algorithm. However, the performance of the inversion is strongly depended on parameters of the NLI algorithm. Major parameters in the algorithm are the initial size distribution, weight parameter, and the number of iteration. In the study, we show how values of initial parameters affect to the result of size distribution in the algorithm by the laser diffraction scattering method. Computer simulations and experimental method are carried out to observe the influence of the parameters in the algorithm. Scattering pattern is calculated by Mie scattering model in the range of 5.0 × 10^?4 ? 2.5 rad. Experimental results were measured mono-distribution polystyrene latex (50 μm) and poly-distribution glass beads (3–30 μm, and 10–100 μm). The number of iteration is a most influence parameter in the NLI algorithm. If the number of iteration is too high for calculation, calculated result will lose the smoothness. We also introduced a new parameter C (combination of the sum of residual squares of scattering signals and sum of secondary differentiation of size distribution) to monitor the suitable stop criterion for the NLI method. The parameter C is a useful index for the poly dispersion sample to find the suitable stop criterion.     

Japanese contribution to the DEMO-R&D program under the Broader Approach activities

Several technical R&D activities mainly related to the blanket materials are newly launched as a part of the Broader Approach (BA) activities, which was initiated by the EU and Japan. According to the common interests for these parties in DEMO, R&Ds on reduced activation ferritic/martensitic (RAFM) steels as structural material, SiC_f/SiC composites as a flow channel insert material and/or alternative structural material, advanced tritium breeders and neutron multipliers, and tritium technology are carried out through the BA DEMO R&D program, in order to establish the technical bases on the blanket materials and the tritium technology required for DEMO design. This paper describes overall schedule of those R&D activities and recent progress in Japan carried out by JAEA as the domestic implementing agency on BA, collaborating with Japanese universities and other research institutes.     

Acceleration of the redox kinetics of VO2+/VO2 + and V3+/V2+ couples on carbon paper

The redox kinetics of VO²⁺/VO₂ ⁺ and V³⁺/V²⁺ couples on a carbon paper (CP, HCP030 N, Shanghai Hesen, Ltd., China) electrode were investigated in terms of their standard rate constant (k ₀) and reaction mechanism. The values determined for k ₀ for VO²⁺ ?? VO₂ ⁺ and V³⁺ ?? V²⁺ using the CP electrode are 1.0 × 10^?3 and 1.1 × 10^?3 cm s^?1, respectively. The value of k ₀ increases by one or two order(s) of magnitude compared with values obtained using electrodes composed of pyrolytic graphite and glassy carbon. The acceleration of the redox kinetics of vanadium ions is a result of the large surface area of the CP electrode. An inner-sphere mechanism for the reaction on the surface of the electrode is proposed. The kinetic features of vanadium redox reactions on the CP electrode reveal that CP is suitable for use as the electrodes in vanadium redox-flow batteries.