The identification of tyre induced vehicle interior noise

Sound transmission into a vehicle is classified as either airborne or structure borne sound. From the point view of noise control, the reduction of noise transferred by different paths requires different solutions. Coherence function analysis is often used to identify transmission paths. However it can be difficult to separate the airborne from structure borne components. The principle of acoustic reciprocity offers a convenient method for overcoming this difficulty. The principal states that the transfer function between an acoustic volume velocity source and an acoustic receiver is independent of a reversal of the position of source and receiver. The work done on this study involves exciting a stationary tyre and measuring the surface velocity of the tyre at a number of discrete points. The acoustic transfer functions between each point on the tyre and a receiver point are measured reciprocally. Two sets of measurements are then combined to yield a measure of the sound pressure due to a point force on the tyre via the acoustic transmission path only. This technique also provides information on the relative contributions of various regions of the tyre wall to the resultant noise. Also the sound radiation characteristics, the horn effect, and resonance at the wheel housing are identified through the reciprocal measurement.     

Fine competition and control among argentophilic,electrostatic, and π···π interactions in a molecular chair structure

The reaction of AgX (X⁻ = NO₃ ⁻, ClO₄ ⁻, or CF₃SO₃ ⁻) with 1,3-bis(3-pyridyl)tetramethyldisiloxane (L) at room temperature affords 20-membered metallacyclodimers, [Ag(L)]₂(X)₂. For the macrocyclodimer, fine competition among argentophilic, electrostatic, and π···π interaction exists. The macrocyclodimer is a unique molecular chair that tunes a transannular argentophilic interaction via the bite size of the counteranions. In order to reversibly control the argentophilic interaction, anion exchange has been accomplished. The anion exchangeability depends on the water solubility rather than the electrostatic interaction between silver(I) and anions.     

The impact of investment lags on investment decision

This paper suggests a valuation framework for an investment project through the concept of real options. Generally, in real asset world, decision time and its payment time are not identical. This so-called investment lag problem should be considered when valuing real assets. When investment lags exist, firms’ accommodation capacities play important roles. In this paper, the real effect of investment lag on investment value is tested upon various conditions. We show the valuation process of real assets under the risk-neutral world. The closed-form formula is also provided for valuing real assets, including R&D project.     

Synthesis and characterization of a novel polymer based on anthracene moiety for organic thin film transistor

We have designed and synthesized a new polymer, which could be used in the organic thin film transistor (OTFT). Poly[2,6‐bis(3′‐dodecythiophene‐2′‐yl)anthracene] (PDTAn), which is composed with anthracene moiety and dodecyl alkyl thiophene, was synthesized by oxidative polymerization using iron (III) chloride. The mole ratio of FeCl₃ and monomer (4.2:1), keeping low temperature during the initiation reaction, amount of solvent, and dropping order were very important for oxidative polymerization without crosslinking. The molecular weight of the polymer (M_w) was measured to be 40,000 with 2.85 of polydispersity index by GPC. The physical and optical properties of the polymer were characterized by differential scanning calorimetry (DSC), cyclic voltammetry (CV), and optical absorption and photoluminescence (PL) spectroscopy. A field‐effect mobility of 1.1 × 10^?4 cm² V^?1 S^?1, a current on/off ratio of 10⁵, and the V_th at ?15.2 V had been obtained for OTFTs using this polymer semiconductor by solution coating. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 5115–5122, 2008     

Temperature driven morphological changes of hydrothermally prepared copper oxide nanoparticles

The size and shape of nanocrystals have a strong effect on the optical, electrical and catalytic properties. Therefore, controlling the size, shape and structure of nanocrystals is technically important. The controlled synthesis of CuO nanostructures was achieved using a hydrothermal process by simply controlling the precipitation reaction temperature between copper nitrate trihydrate and sodium hydroxide. The Scanning Electron Microscopy (SEM), EDS, XRD, and FTIR analysis revealed that the synthesized product at 200 °C is of pure copper oxide particles. From Scherrer formula, the prepared CuO particles varied approximately 3–7 nm in size simply by varying the reaction temperature. The synthesized particles exhibited a regular flake like morphology and had a uniform size distribution. The morphology and size depend on the reaction conditions. Copyright © 2008 John Wiley & Sons, Ltd.