Electrochemical curing of epoxy resins

An electrochemical method has been developed for bonding electrically-conductive adherends. The procedure is based on the electrochemical generation of a curing agent from an otherwise chemically-unreactive precursor mixed with an epoxy resin sandwiched between the bonding members. The one-part epoxy resin is storage stable and cured rapidly on passage of current.     

Cell cycle analysis of Chinese hamster ovary cells stimulated by phosphatidic acid in serum-free culture

When recombinant Chinese hamster ovary cells were treated with pertussis toxin or genistein, not only lysophosphatidic acid (LPA) but also phosphatidic acid (PA) failed to stimulate progression through the cell cycle in serum-free culture, suggesting that PA and LPA induce cell growth through the same signal transduction pathway. Cell cycle analysis also indicates that cell growth promoted by PA results in enhanced protein production.     

A torsional transducer through in-plane shearing of paired planar piezoelectric elements

A torsional microtransducer for high-power applications was developed using standard bulk lead zirconium titantate (PZT) placed upon a small rectangular prism made from phosphor bronze, with a tapered conical end serving as a horn and a machined interior to improve the actuator's response. Torsion was obtained from a prototype at the design frequency of 192 kHz as well as over a wide range of frequencies from 136 kHz to 1.02 MHz. Torsional vibration velocities of 335 mm/s at 192 kHz were measured at 27.3 V(RMS) on the 1.5-mm diameter output tip, amounting to 25,600 degree/s vibration velocity along the outer circumference of the tip. At 1.02 MHz, a torsional vibration velocity of 1750 mm/s (134,000 degree/s) at 17.8 V(RMS) was obtained through use of the thickness mode of the PZT elements. Using the design described in this study, high-power torsional transducers with diameters of 5 mm and below are now possible.     

Post-densification behavior of reaction-bonded silicon nitride (RBSN): Effect of various characteristics of RBSN

The effects of the various characteristics of reaction-bonded silicon nitride (RBSN), such as crystalline secondary phases, residual Si, pore size distribution, and agglomerates developed during nitridation on the post-densification behavior, were investigated in detail. A model experiment was carried out to study the effect of crystalline secondary phases in RBSN on the post-densification. The result clearly indicates that the pre-formation of crystalline secondary phases does not influence the sintering of Si₃N₄-powder compacts, which is further demonstrated in the post-densification of RBSN, because the formation of a liquid, including its composition and properties, is dependent on the composition of the system and sintering temperature, but independent of the presence of crystalline secondary phases. In particular, the complete melt of crystalline secondary phases is not related to their melting points and only relies on the composition of the system. The residual Si and pore size distribution in RBSN show no significant effect on the post-densification. Some large pores of 5 m in size could be eliminated by liquid filling and grain growth during post-sintering. The residual Si in RBSN could change into -Si₃N₄ by nitridation of liquid Si and contribute to the weight gain during the early stage of post-sintering. However, it is shown that the agglomerates in RBSN play an important role in the post-densification. The effect of agglomerates on the post-densification strongly depends on their size and amounts in RBSN. Nearly complete densification of RBSN could be reached through lowering of the nitriding temperature or adding Si₃N₄ powder to green bodies, which leads to the formation of more uniform microstructure during nitridation. A mechanism that explains how the agglomerates affect the post-densification of RBSN was discussed based on the theories of liquid phase sintering.     

An aqueous suspension system for phospholipase D-mediated synthesis of PS without toxic organic solvent

Enzymatic synthesis of PS by phospholipase D (PLD)-mediated transphosphatidylation in an aqueous media was investigated. The purpose of this study was to establish a novel synthetic method where no toxic organic solvents were used. An attempt to react soybean lecithin (simply dispersed in an aqueous buffer) with an aqueous solution of l-serine and PLD was unsuccessful, giving only 20% of PS. By contrast, a suspension of lecithin adsorbed on fine powders such as silica was effectively converted into PS in an aqueous solution of l-serine and PLD. After screening various powders for use as the lecithin adsorbent, calcium sulfate was found to be the best with respect to lecithin conversion. In addition, calcium sulfate did not require prior adsorption of lecithin (i.e., the reaction proceeded effectively simply by adding the powder to an aqueous mixture of lecithin, l-serine, and PLD). With this “aqueous suspension system” of calcium sulfate, up to 180 mg/mL lecithin was completely converted, resulting in more than 80% PS in 24 h. The synthesized PS could easily be recovered from the powder by extracting with a mixture of n-hexane, ethanol, and diluted HCl.     

A single-element tuning fork piezoelectric linear actuator

This paper describes the design of a piezoelectric tuning-fork, dual-mode motor. The motor uses a single multilayer piezoelectric element in combination with tuning fork and shearing motion to form an actuator using a single drive signal. Finite-element analysis was used in the design of the motor, and the process is described along with the selection of the device's materials and its performance. Swaging was used to mount the multilayer piezoelectric element within the stator. Prototypes of the 25-mm long bidirectional actuator achieved a maximum linear no-load speed of 16.5 cm/s, a maximum linear force of 1.86 N, and maximum efficiency of 18.9%.     

EACLE : Energy-Aware Clustering Scheme with Transmission Power Control for Sensor Networks

In this paper, we propose a new energy efficient clustering scheme with transmission power control named “EACLE” (Energy-Aware CLustering scheme with transmission power control for sEnsor networks) for wireless sensor networks, which are composed of the following three components; “EACLE clustering” is a distributed clustering method by means of transmission power control, “EACLE routing” builds a tree rooted at a sink node and sets the paths from sensor nodes taking energy saving into consideration, and “EACLE transmission timing control” changes the transmission timing with different levels of transmission power to avoid packet collisions and facilitates packet binding. With an indoor wireless channel model which we obtained from channel measurement campaigns in rooms and corridors and an energy consumption model which we obtained from a measurement of a chipset, we performed computer simulations to investigate the performance of EACLE in a realistic environment. Our simulation results indicate that EACLE outperforms a conventional scheme such as EAD (Energy-Aware Data-centric routing) in terms of communication success rate and energy consumption. Furthermore, we fully discuss the impact of transmission power and timing control on the performance of EACLE.     

State difference feedback for stabilizing uncertain steady states of non-linear systems

Supposing a non-linear system is subjected to parametric uncertainties, the present paper aims at stabilizing its unstable steady states. A distinctive feature of the problem is that exact information about the steady state is unavailable. To cope with the difficulty, we have examined the applicability of the state difference feedback which uses the difference between the present state x(t) and the past state x(t-T). A rigorous stability analysis has been executed for the case where state deviations are controllable by a single input variable. The stability analysis has led to a favourable conclusion that if the number of unstable modes is just two, and if they are not associated with the origin in the complex plane, we are always able to find a controller which stabilizes the deviations from the unknown steady state. Design process is illustrated by using two kinds of pendulum systems.     

Metal-Induced Structural Switching of a Folded Quinone-Sandwiched Porphyrin

We report the synthesis of a novel quinone-sandwiched porphyrin in which two benzoquinones are connected oppositely at the meso positions of a porphyrin through rigid 3-amido 2,2′-bipyridine linkers. ¹H-NMR and single crystal X-ray analyses revealed that the quinone-sandwiched porphyrin has a folded structure in which the porphyrin unit was inserted into the two quinone moieties via π-stacking. Insertion of a Zn(II) ion into the porphyrin center induced a drastic conformational change which is resulted in coordination of the oxygen atoms of both benzoquinone moieties to the Zn-porphyrin to afford a 6-coordinated structure.     

Microstructural Design of Silicon Nitride with Improved Fracture Toughness: II, Effects of Yttria and Alumina Additives

Significant improvements in the fracture resistance of self-reinforced silicon nitride ceramics have been obtained by tailoring the chemistry of the intergranular amorphous phase. First, the overall microstructure of the material was controlled by incorporation of a fixed amount of elongated ß-Si₃N₄ seeds into the starting powder to regulate the size and fraction of the large reinforcing grains. With controlled microstructures, the interfacial debond strength between the reinforcement and the intergranular glass was optimized by varying the yttria-to-alumina ratio in the sintering additives. It was found that the steady-state fracture toughness value of these silicon nitrides increased with the Y:Al ratio of the oxide additives. The increased toughness was accompanied by a steeply rising R -curve and extensive interfacial debonding between the elongated ß-Si₃N₄ grains and the intergranular glassy phase. Microstructural analyses indicate that the different fracture behavior is related to the Al (and O) content in the ß´-SiAlON growth layer formed on the elongated ß-Si₃N₄ grains during densification. The results imply that the interfacial bond strength is a function of the extent of Al and Si bonding with N and O in the adjoining phases with an abrupt structural/chemical interface achieved by reducing the Al concentration in both the intergranular phase and the ß´-SiAlON growth layer. Analytical modeling revealed that the residual thermal expansion mismatch stress is not a dominant influence on the interfacial fracture behavior when a distinct ß´-SiAlON growth layer forms. It is concluded that the fracture resistance of self-reinforced silicon nitrides can be improved by optimizing the sintering additives employed.