Domain Switching During Electromechanical Poling in Lead Zirconate Titanate Ceramics

In many polycrystalline piezoelectric ceramics, domain switching during the poling process leads to the development of a macroscopic polarization and piezoelectric behavior. Traditionally, poling involves the application of electric fields across two parallel electrodes. In the present work, a radial mechanical compressive stress is applied transverse to the electric field, increasing the potential for domain alignment during poling by taking advantage of ferroelasticity. Experiments demonstrate that poling of lead zirconate titanate using a combination of an electric field and a transverse mechanical compressive stress increases the d ₃₃ coefficient from 435 to 489 pC/N. Using neutron diffraction and pole figure inversion methods, the degree of non-180° domain switching is described using pole density distributions of the tetragonal c -axis (002). The degree of 002 domain alignment parallel to the electric field after the electromechanical poling process increases from 1.30 multiples of a random distribution (mrd) to >1.40 mrd at stresses exceeding 40 MPa.     

Comparison of HDTV formats using objective video quality measures

In this paper we compare some of the objective quality measures with subjective, in several HDTV formats, to be able to grade the quality of the objective measures. Also, comparison of objective and subjective measures between progressive and interlaced video signal will be presented to determine which scanning emission format is better, even if it has different resolution format. Several objective quality measures will be tested, to examine the correlation with the subjective test, using various performance measures.     

Wind turbulence used as searching signal for MPPT in variable-speed wind energy conversion systems

The control problem associated to a class of horizontal-axis fixed-pitch variable-speed low-power wind energy conversion systems, working in the partial load region, consisting in the energy conversion maximization, is approached here under the assumption that the wind turbine model and its parameters are poorly known. Using a new approach derived from the optimum seeking methods category, generically called Maximum Power Point Tracking (MPPT), the proposed control solution aims at driving the average position of the operating point near to optimality. Instead of inducing sinusoidal search signals, the wind turbulence is here used as search disturbance. The high-speed shaft's average rotational speed is slowly adjusted using the Fast Fourier Transform processing of some available measures from the system as an estimate of the operating point's position/distance to optimality. Numerical simulations are used for preliminary checking the control law based on this estimation.     

Synthesis and characterization of polyurethane cationomer/MMT hybrid composite

BACKGROUND: The development of polymeric nanocomposites incorporating intercalated or exfoliated layered silicate clays into the organic matrix has been substantially motivated by the significant improvements induced by the presence of the inorganic component. Moreover, understanding and controlling the dispersion of inorganic layers into segmented polyurethane matrices by means of ionic interactions, and exploiting these interactions to enhance physicomechanical behaviour, could be of great interest in the field of polymer nanocomposites. RESULTS: New cationic polyurethane elastomers were prepared starting from poly(butylene adipate)diol (M_n = 1000 g mol^?1), 4,4′‐diphenylmethane diisocyanate, 1,4‐butanediol and N‐methyldiethanolamine or N,N′‐β‐hydroxyethylpiperazine, used as potential quaternizable moieties. The characterization of the polymers was achieved using specific analyses employed for the macromolecular samples (Fourier transform infrared and ¹H NMR spectroscopy, thermogravimetric analysis (TGA), gel permeation chromatography). An extension of our research on polymers reinforced with organically modified montmorillonite (OM‐MMT) in order to prepare hybrid composites with improved properties was performed and the resulting materials were characterized using TGA, X‐ray diffraction, atomic force microscopy and scanning electron microscopy. Also, the mechanical properties of the cationic polyurethane/OM‐MMT composites were investigated in comparison with the pristine ionic/non‐ionic polymers and their composites containing non‐ionic polymer blended with OM‐MMT or ionic polymer and unmodified MMT. CONCLUSION: The insertion of the organically modified clay into the polymeric matrix gave an improvement of the mechanical properties of the polyurethane composites, especially the tensile strength and stiffness of the hybrid materials. Copyright © 2009 Society of Chemical Industry     

Wet air oxidation in a catalytic membrane reactor: Model and industrial wastewaters in single tubes and multichannel contactors

Recent results on catalytic wet air oxidation applied to a membrane contactor are presented that give new insight following a series of previous publications. Model and industrial effluents are treated in both single tube and multichannel catalytic systems. Characterisation of the catalytic material (solid analyses, electron microscopy, EDS and EPMA) is carried out, in order to determine the catalyst distribution. Catalytic results show performances heavily dependent on the nature of the effluent and the operating conditions, and to a lesser extent on the catalytic membrane characteristics. At 80 °C, an industrial effluent is oxidised at a membrane surface related rate of 3.8 mmol/s/m². This result is achieved using a membrane containing about 0.1 wt.% Pt. This allows a revised and improved technico-economical evaluation of the Watercatox process.     

Small Alterations in Cobinamide Structure Considerably Influence sGC Activation

Specially designed B‐ring‐modified cobalamin derivatives were synthesized and tested as potential activators of soluble guanylyl cyclase (sGC). Herein, we disclose the influence of substituents at the c‐ and d‐positions in hydrophilic and hydrophobic cobyrinic acid derivatives on their capacities to activate sGC. The presence of the amide group at c‐/d‐position in cobyrinic acid derivatives strongly influence the level of sGC activation. Removal of the d‐position altogether has a profound effect for hydrophobic compounds. In contrast, little differences were observed in hydrophilic ones.