Acoustical power amplification and damping by temperature gradients

Ceperley proposed a concept of a traveling wave heat engine ["A pistonless Stirling engine-The traveling wave heat engine," J. Acoust. Soc. Am. 66, 1508-1513 (1979).] that provided a starting point of thermoacoustics today. This paper verifies experimentally his idea through observation of amplification and strong damping of a plane acoustic traveling wave as it passes through axial temperature gradients. The acoustic power gain is shown to obey a universal curve specified by a dimensionless parameter ωτα; ω is the angular frequency and τα is the relaxation time for the gas to thermally equilibrate with channel walls. As an application of his idea, a three-stage acoustic power amplifier is developed, which attains the gain up to 10 with a moderate temperature ratio of 2.3.     

Interquark potential with finite quark mass from lattice QCD

We present an investigation of the interquark potential determined from the q ?q Bethe-Salpeter (BS) amplitude for heavy quarkonia in lattice QCD. The q ?q potential at finite quark mass m(q) can be calculated from the equal-time and Coulomb gauge BS amplitude through the effective Schr?dinger equation. The definition of the potential itself requires information about a kinetic mass of the quark. We then propose a self-consistent determination of the quark kinetic mass on the same footing. To verify the proposed method, we perform quenched lattice QCD simulations with a relativistic heavy-quark action at a lattice cutoff of 1/a≈2.1 GeV in a range 1.0≤m(q)≤3.6 GeV. Our numerical results show that the q ?q potential in the m(q)→∞ limit is fairly consistent with the conventional one obtained from Wilson loops. The quark-mass dependence of the q ?q potential and the spin-spin potential are also examined.     

Fabrication of NdFeB microstructures using a silicon molding technique for NdFeB/Ta multilayered films and NdFeB magnetic powder

The silicon molding technique is described for patterning of NdFeB/Ta multilayered magnetic films and NdFeB magnetic powder at the micron scale. Silicon trenches are seamlessly filled by 12-μm-thick NdFeB/Ta multilayered magnetic films with a magnetic retentivity of 1.3 T. The topography image and magnetic field distribution image are measured using an atomic force microscope and a magnetic force microscope, respectively. Using a silicon molding technique complemented by a lift-off process, NdFeB magnetic powder is utilized to fabricate magnetic microstructures. Silicon trenches as narrow as 20 μm are filled by a mixture of magnetic powder and wax powder. The B-H hysteresis loop of the patterned magnetic powder is characterized using a vibrating sample magnetometer, which shows a magnetic retentivity of approximately 0.37 T.     

Modulation of stimuli-responsiveness toward acid vapor between real-time and write-erase responses based on conjugated polymers containing azobenzene and Schiff base moieties

We developed three types of film-type stimuli-responsive polymers based on aza-substituted conjugated polymers involving azobenzene, N_bith, N_fluo and Schiff base moieties, C_bith. All polymer films showed bathochromic shifts in absorption spectra followed by chromic behaviors by fuming trifluoroacetic acid (TFA). In particular, we disclosed that there were three significant differences on acid detecting ability between azobenzene and Schiff base derivatives in terms of absorption wavelengths, stability, and proton holding time. The azobenzene polymers exhibited real-time responses toward vapor fuming, meanwhile write and erase chromic behaviors were reversibly accomplished with the Schiff base polymer by exposing to acid and amine vapor. Theoretical calculation revealed that red-shifted absorption bands should be induced by protonation on nitrogen atoms in the aza-substituted positions. Diverse responses through dynamic regulation of electronic properties of main-chain conjugation can be accomplished by introducing the aza-substituents in polymers.     

Asymmetric Cyclizative Dimerization of (ortho-Alkynyl Phenyl) (Methoxymethyl) Sulfides with Palladium(II) Bisoxazoline Catalyst

The first example of an asymmetric cyclization–dimerization of (ortho-alkynyl phenyl) (methoxymethyl) sulfides with a palladium(II) bisoxazoline (box) catalyst has been developed. The box ligand enhances the alkynophilicity of benzothienyl palladium(II) intermediate A and thus promotes coordination of the second alkyne substrate, leading to the dimerization. The characteristic properties of the box ligand were supported by density functional theory (DFT) calculations of the intermediate. Axially chiral bibenzothiophenes were obtained in good yields with good enantioselectivities.     

Direct visualization of dewetting of molecularly thin liquid films on solid surfaces

The effect of the surface energy gamma, disjoining pressure, Pi, and roughness on the dewetting of molecularly thin liquid lubricant films on magnetic disks, which have sub-nanometer surface topography, has been investigated by visualizing the dewetting process directly using ellipsometric microscopy. The dewetting process of thin liquids on the rough surface is determined not only by the well-known instability of films, which is determined by the sign of dPi/dh, but also by the sign of Pi and the surface topography of the substrate even if its roughness is of the sub-nanometer order. The dewetting film formed small droplets, which were not along the surface topography of the substrate, when Pi < 0. On the other hand, it formed grooves along the surface topography with a sub-nanometer roughness when Pi > 0. Moreover, the sub-nanometer roughness initiated the dewetting of the metastable liquid thin films.     

Asymmetric Synthesis of Chiral Sulfoximines through the S‐Alkylation of Sulfinamides

Innovation in drug discovery critically depends on the development of new bioisosteric groups. Chiral sulfoximines, which contain a tetrasubstituted sulfur atom that bears one nitrogen, one oxygen, and two different carbon substituents, represent an emerging chiral bioisostere in medicinal chemistry. Chiral sulfoximines are conventionally prepared by a stereospecific nitrene transfer reaction to chiral sulfoxides; however, the number of readily available chiral sulfoxides remains limited. Herein, we report the asymmetric synthesis of a class of hitherto difficult‐to‐access chiral sulfoximines with two structurally similar alkyl chains. Our synthetic approach is based on the sulfur‐selective alkylation of easily accessible chiral sulfinamides with commercially available reagents under simple and safe conditions. This stereospecific S‐alkylation offers a general and scalable approach to the asymmetric synthesis of chiral sulfoximines, which represent important substructures in bioactive molecules.     

Measurements of Rayleigh–Taylor instability growth of laser-shocked iron–silicon alloy

The Rayleigh–Taylor (RT) instability of liquid iron alloys is important for understanding the core formation mechanism in the Earth. Here we first report the measurement of RT instability growth for a liquid iron–silicon (Fe–Si) alloy, which is one of the major candidate for the material of the Earth’s core, using a high power laser. We optimized the measurement setup and analytical technique to observe the growth of perturbation on an Fe–Si sample surface. The growth of perturbation amplitude on the Fe–Si alloy under high pressure and temperature was successfully observed using in situ X-ray radiography. The growth rate of the RT instability for the Fe–Si alloy on about 1000?GPa was estimated to be 0.3 ns^?1.     

Anomalous phase diagram of ferroelectric (Ba,Ca)TiO3 single crystals with giant electromechanical response

We report the anomalous phase evolution in ferroelectric single crystals Ba1-xCaxTiO3 (0.02相似文献