Processing of nanolitre liquid plugs for microfluidic cell-based assays

Plugs, i.e. droplets formed in a microchannel, may revolutionize microfluidic cell-based assays. This study describes a microdevice that handles nanolitre-scale liquid plugs for the preparation of various culture setups and subsequent cellular assays. An important feature of this mode of liquid operation is that the recirculation flow generated inside the plug promotes the rapid mixing of different solutions after plugs are merged, and it keeps cell suspensions homogeneous. Thus, serial dilutions of reagents and cell suspensions with different cell densities and cell types were rapidly performed using nanolitres of solution. Cells seeded through the plug processing grew well in the microdevice, and subsequent plug processing was used to detect the glucose consumption of cells and cellular responses to anticancer agents. The plug-based microdevice may provide a useful platform for cell-based assay systems in various fields, including fundamental cell biology and drug screening applications.     

Single-particle-diagnosis approach: An efficient strategy for discovering new nitride phosphors

Discovery of novel phosphors is extremely important to target the ever change of the solid state lighting technology. In this paper, we present a high-speed way to discover new phosphors, namely single-particle-diagnosis approach. This approach is based on investigating the crystal structure and luminescence of a tiny single crystal, without the necessity of the growth of large-size single crystals or the preparation of single phase powder samples. The concept of the approach and some new nitride phosphors explored by this approach are shown in this paper.     

Polyethylene–Carbon Nanotube Composite Film Deposited by Cold Spray Technique

Carbon nanotubes (CNTs) are high-performance materials because of their superior electrical conductivity, thermal conductivity, and self-lubrication, and they have been studied for application to polymer composite materials as fillers. However, the methods of fabricating polymer composites with CNTs, such as injection molding, are too complicated for industrial applications. We propose a simple cold spray (CS) technique to obtain a polymer composite of polyethylene (PE) and CNTs. The composite films were deposited by CS on polypropylene and nano-porous structured aluminum substrates. The maximum thickness of the composite film was approximately 1 mm. Peaks at G and D bands were observed in the Raman spectra of the films. Scanning electron microscopy images of the film surface revealed that PE particles were melted by the acceleration gas and CNTs were attached with melted PE. The PE particles solidified after contact with the substrate. These results indicate that PE–CNT composite films were successfully deposited on polypropylene and nano-porous structured aluminum substrates by CS.     

东京中心城区的规划历程及其现状——探索迈向成熟都市的阶梯

在梳理东京都城市中心的形成以及城市规划史的基础上,通过选取两大重要的中心街区(丸之内办公街区、银座商业街区)作为案例,进一步剖析近代东京中心城区的形成,以及此后逐步迈向地域主导的规划方式的过程。其中特别着重考察在中心城区形成、发展、更新的过程中将承载了各个历史阶段记忆的街区特征(基因)传承下来并延续到未来的探索和努力。     

Modeling method of fast transient for unsymmetrical stray capacitance to ground

Transient characteristic of power system apparatus in a high‐frequency region should be modeled with stray capacitors. Pi‐type circuit is commonly used to represent the stray capacitors between terminals and those to the ground. A modeling method for the pi‐type circuit with unsymmetrical stray capacitances to ground is proposed in this paper. To obtain the unsymmetrical stray capacitances to ground, a couple of differential‐mode measurements are interchangeably applied. The parameters of the pi‐type circuit can be determined by the measurements with a common‐mode measurement. A nonlinear least‐squares method is used to estimate the capacitances. The method is applied to compose an equivalent circuit of a miniature circuit breaker (MCB), which has unsymmetrical stray capacitances to ground. The application is not only for the MCB but also for a scaled model of a high‐voltage circuit breaker. A gas‐filled arrester is used as a voltage sensor for the test because the voltage across the stray capacitor cannot be directly measured due to the input capacitance of a voltage probe. A transient response of the MCB with the gas‐filled arresters is numerically simulated to show the usefulness of the equivalent circuit. © 2015 Institute of Electrical Engineers of Japan. Published by John Wiley & Sons, Inc.     

Synthesis of thermoresponsive block and graft copolymers via the combination of living cationic polymerization and RAFT polymerization using a vinyl ether-type RAFT agent

A novel vinyl ether-type RAFT agent, benzyl 2-(vinyloxy)ethyl carbonotrithioate (BVCT) was synthesized for various block copolymers via the combination of living cationic polymerization of vinyl ethers and reversible addition−fragmentation chain transfer (RAFT) polymerization. The novel BVCT–trifluoroacetic acid adduct play an important role to produce well-defined block copolymers, which is both as a cationogen under EtAlCl₂ initiation system in the presence of ethyl acetate for living cationic polymerization and a RAFT agent for blocks by RAFT polymerization. The resulting polymer, poly(vinyl ether)s, by living cationic polymerization had a high number average α-end functionality (≥0.9) as determined by both ¹H NMR and MALDI-TOF-MS spectrometry. In addition, this poly(vinyl ether)s worked well as a macromolecular chain transfer agent for RAFT polymerization. The RAFT polymerization of radically polymerizable monomers was conducted in toluene using 2,2′-azobis(isobutyronitrile) at 70 °C. For example, a double thermoresponsive block copolymer (MOVE₆₁-b-NIPAM₁₅₀) consisting of 2-methoxyethyl vinyl ether (MOVE) and N-isopropylacrylamide (NIPAM) was prepared via the combination of living cationic polymerization and RAFT polymerization. The block copolymer reversibly formed and deformed micellar assemblies above the phase separation temperature (T_ps) of poly(NIPAM) block in water. This BVCT is not only functioned as an initiator, but also acted as a monomer. When BVCT was copolymerized with MOVE by living cationic polymerization, followed by graft copolymerization with NIPAM via RAFT polymerization, well-defined graft copolymers (MOVE_n-co-BVCT_m)-g-NIPAM_x (n = 62–73, m = 1–9, x = 19–214) were successfully obtained. However, no micelle formed in water above T_ps of poly(NIPAM) graft chain unlike the case of block copolymers.