Sound propagation above a porous road surface with extended reaction by boundary element method

Acoustic impedance of an absorbing interface is easily introduced in boundary element codes provided that a local reaction is assumed. But this assumption is not valid in the case of porous road surface. A two-domain approach was developed for the prediction of sound propagation above a porous layer that takes into account the sound propagation inside the porous material. The porous material is modeled by a homogeneous dissipative fluid medium. An alternative to this time consuming two-domain approach is proposed by using the grazing incidence approximate impedance in the traditional single-domain boundary element method (BEM). It can be checked that this value is numerically consistent with the surface impedance calculated at the interface from the pressure and surface velocity solutions of the two-domain approach. The single-domain BEM introducing this grazing incidence impedance is compared in terms of sound attenuation with analytical solutions and two-domain BEM. The comparison is also performed with the single-domain BEM using the normal incidence impedance, and reveals a much better accuracy for the prediction of sound propagation above a porous interface.     

Inertial clustering of particles in high-Reynolds-number turbulence

We report experimental evidence of spatial clustering of dense particles in homogenous, isotropic turbulence at high Reynolds numbers. The dissipation-scale clustering becomes stronger as the Stokes number increases and is found to exhibit similarity with respect to the droplet Stokes number over a range of experimental conditions (particle diameter and turbulent energy dissipation rate). These findings are in qualitative agreement with recent theoretical and computational studies of inertial particle clustering in turbulence. Because of the large Reynolds numbers a broad scaling range of particle clustering due to turbulent mixing is present, and the inertial clustering can clearly be distinguished from that due to mixing of fluid particles.     

Ultrasound promoted the synthesis of N-propargylic β-enaminones

The synthesis of 14 novel N-propargylic β-enaminones from the reaction of β-alkoxy vinyltrihalomethyl[carboxyethyl] ketones [R³C(O)CHC(R¹)OMe, where R³ = CF₃, CCl₃, CO₂Et and R¹ = Me, Et, Pr, Bu, i-Pent, CH₂CH₂CO₂Me] with propargyl amines [R²NHCH₂CCH, where R² = Pr, PhCH₂] is reported. Yields, solvents and reaction times needed for reaction completion, by microwave irradiation (MW), conventional thermal heating (TH) and under ultrasound irradiation (US) are compared. The best results were obtained under US irradiation in good to excellent yields (70-93%).     

Time‐resolved Raman studies on Al2O3: Cr3+: lifetime measurements of the excited‐state transition Ē → 2Ā

A time‐resolved intensified charge coupled device‐based Raman microspectrometer system dedicated to the study of solid samples is described, offering good optical, temporal and spatial resolution. The advantages of this approach are demonstrated on Al₂O₃:Cr³⁺, obtaining for the first time the temporal evolution of the excited state transition Ē → 2Ā. Moreover, the time dependence of the luminescence due to the chromium ion was also determined by the same Raman device. Copyright © 2010 John Wiley & Sons, Ltd.     

Frequency down-conversion using cascading arrays of coupled nonlinear oscillators

A novel coupling scheme using M≥2 arrays of coupled nonlinear elements arranged in a specific configuration can produce multifrequency patterns or a frequency down-converting effect on an external (input) signal. In such a configuration, each array contains N≥3 nonlinear elements with similar dynamics and each element is coupled unidirectionally within the array. The subsequent arrays in the cascade are coupled in a similar fashion except that the coupling direction is arranged in the opposite direction with respect to that of the preceding array. Previous theoretical work and numerical results have already been reported in [P. Longhini, A. Palacios, V. In, J. Neff, A. Kho, A. Bulsara, Exploiting dynamical symmetry in coupled nonlinear elements for efficient frequency down-conversion, Phys. Rev. E 76 (2007) 026201]. This paper is focused on results of experiments implemented on two distinct systems: the first system is fabricated using discrete component circuits to approximate an overdamped bistable Duffing oscillator described by a quartic potential system, and the second system is built in a microcircuit, where the nonlinearity is described by a hyperbolic tangent function, with the option of applying an external signal to investigate resonant effects. In particular, the circuit implementations for each case use M=2 arrays, but their voltage oscillations already demonstrate that the frequency relations between each of the successive arrays decrease by a rational factor, conforming to earlier theoretical and numerical results for the general case containing M arrays. This behavior is important for efficient frequency down-converting applications which are essential in many communication systems where heterodyning is typically used and it involves multi-step processes with complicated circuitry.     

Giant spin splitting through surface alloying

The long-range ordered surface alloy Bi/Ag(111) is found to exhibit a giant spin splitting of its surface electronic structure due to spin-orbit coupling, as is determined by angle-resolved photoelectron spectroscopy. First-principles electronic structure calculations fully confirm the experimental findings. The effect is brought about by a strong in-plane gradient of the crystal potential in the surface layer, in interplay with the structural asymmetry due to the surface-potential barrier. As a result, the spin polarization of the surface states is considerably rotated out of the surface plane.     

A mini-landscape of exact MSSM spectra in heterotic orbifolds

We explore a “fertile patch” of the heterotic landscape based on a Z₆-II${\mathbb{Z}}_6\text{-II}$ orbifold with SO(10) and E₆ local GUT structures. We search for models allowing for the exact MSSM spectrum. Our result is that of order 100 out of a total 3×¹⁰⁴$3\times {10}^4$ inequivalent models satisfy this requirement.     

Intermolecular hybridization governs molecular electrical doping

Current models for molecular electrical doping of organic semiconductors are found to be at odds with other well-established concepts in that field, like polaron formation. Addressing these inconsistencies for prototypical systems, we present experimental and theoretical evidence for intermolecular hybridization of organic semiconductor and dopant frontier molecular orbitals. Common doping-related observations are attributed to this phenomenon, and controlling the degree of hybridization emerges as a strategy for overcoming the present limitations in the yield of doping-induced charge carriers.     

Gold-surface binding of molecular switches studied by M?ssbauer spectroscopy

The nonanuclear coordination compound [Mo^IV{(CN)Fe^III(3-methyl-saldptn)}₈]Cl₄ exhibits multiple spin transitions (3-methyl-saldptn = N,N′-bis(3′′-methyl-2′′-hydroxy-benzyliden)-1,7-diamino-4-azaheptane). This spin crossover cluster is bound via a self-assembled monolayer onto a two dimensional array gold surface. M?ssbauer spectroscopy indicates that the thermally and optically induced spin crossover of the compound is maintained. Thereby, the foundation for its potential practical application (e.g. in the field of information storage) was laid.