Structural and morphological characteristics of (Pb<Subscript>1−<Emphasis Type="Italic">x</Emphasis></Subscript>Sr<Subscript><Emphasis Type="Italic">x</Emphasis></Subscript>)TiO<Subscript>3</Subscript> powders obtained by polymeric precursor method

Pb_1−x Sr _x )TiO₃ powders with different compositions (x = 0, 0.10, 0.50, 0.90 and 1) were synthesized by the polymeric precursor method and heat treated at 800 °C for 2 h under air atmosphere. The thermogravimetric and differential scanning calorimetry analyses were performed in the range from 25 to 800 °C in order to estimate the stages corresponding to the water evaporation, organic decomposition and crystallization of these materials. X-ray diffraction patterns and Rietveld analyses showed that the (Pb_1−x Sr _x )TiO₃ phases with strontium content up to x = 0.1 crystallize in a tetragonal structure. The micrographs obtained by scanning electron microscopy and transmission electron microscopy showed that the powders have agglomerated nature, presenting irregular morphologies and polydisperse particle size distribution. The energy dispersive X-ray spectrometry indicated the presence of pure (Pb_0.50Sr_0.50)TiO₃ phase.     

Structure and optical properties of [Ba1–xY2x/3](Zr0.25Ti0.75)O3 powders

[Ba_1–xY_2x/3](Zr_0.25Ti_0.75)O₃ powders with different yttrium concentrations (x = 0, 0.025 and 0.05) were prepared by solid state reaction. These powders were analyzed by X-ray diffraction (XRD), Fourier transform Raman scattering (FT-RS), Fourier transform infrared (FT-IR) and X-ray absorption near-edge (XANES) spectroscopies. The optical properties were investigated by means of ultraviolet–visible (UV–vis) absorption spectroscopy and photoluminescence (PL) measurements. Even with the addition of yttrium, the XRD patterns revealed that all powders crystallize in a perovskite-type cubic structure. FT-RS and FT-IR spectra indicated that the presence of [YO₆] clusters is able to change the interaction forces between the O–Ti–O and O–Zr–O bonds. XANES spectra were used to obtain information on the off-center Ti displacements or distortion effects on the [TiO₆] clusters. The different optical band gap values estimated from UV–vis spectra suggested the existence of intermediary energy levels (shallow or deep holes) within the band gap. The PL measurements carried out with a 350 nm wavelength at room temperature showed that all powders present typical broad band emissions in the blue region.     

Synthesis of niobia nanocrystals with controlled morphology

In this work, TT niobia-phase nanocrystals with controlled morphology were obtained by the hydrothermal treatment of a niobium peroxo complex precursor at very low temperatures. The materials obtained by this route presented a very high surface area (ranging from 79 to 327 m(2)/g), disordered NbO(6), NbO(7), and NbO(8) polyhedra, Nb-O superficial sites, and a superficial OH group, which must have ensured the acidic characteristics of this oxide.     

Structure and Classification of Superconformal Nets

We study the general structure of Fermi conformal nets of von Neumann algebras on S ¹ and consider a class of topological representations, the general representations, that we characterize as Neveu–Schwarz or Ramond representations, in particular a Jones index can be associated with each of them. We then consider a supersymmetric general representation associated with a Fermi modular net and give a formula involving the Fredholm index of the supercharge operator and the Jones index. We then consider the net associated with the super-Virasoro algebra and discuss its structure. If the central charge c belongs to the discrete series, this net is modular by the work of F. Xu and we get an example where our setting is verified by taking the Ramond irreducible representation with lowest weight c/24. We classify all the irreducible Fermi extensions of any super-Virasoro net in the discrete series, thus providing a classification of all superconformal nets with central charge less than 3/2. Sebastino Carpi: Supported by MIUR, GNAMPA-INDAM and EU network “Noncommutative Geometry” MRTN-CT-2006-0031962 Yasuyuki Kawahigashi: Supported in part by the Grants-in-Aid for Scientific Research, JSPS. Submitted: March 3, 2008. Accepted: May 5, 2008.     

Forces, moment, and wave pattern for surface combatant in regular head waves Part I. Measurement systems and uncertainty assessment

A model-scale naval surface combatant, DTMB 5512, is studied experimentally in steady forward speed and regular head waves with the Iowa Institute of Hydraulic Research towing-tank facilities. Unsteady resistance, heave force, pitch moment and free-surface elevations are investigated with different measurement systems for a fairly wide range of test conditions. Test data is procured for validation of RANS computational fluid dynamics codes and for understanding the physics of unsteady ship hydrodynamics. In the first part of the two-part paper, details of data reductions, measurement systems and uncertainty assessment procedures are provided. Received: 4 October 2000 / Accepted: 23 April 2001     

Influence of the precursor salts in the synthesis of CaSnO<Subscript>3</Subscript> by the polymeric precursor method

CaSnO₃ was synthesized by the polymeric precursor method, using different precursor salts as (CH₃COO)₂Ca·H₂O, Ca(NO₃)₂·4H₂O, CaCl₂·2H₂O and CaCO₃, leading to different results. Powder precursor was characterized using thermal analysis. Depending on the precursor different thermal behaviors were obtained. Results also indicate the formation of carbonates, confirmed by IR spectra. After calcination and characterization by XRD, the formation of perovskite as single phase was only identified when calcium acetate was used as precursor. For other precursors, tin oxide was observed as secondary phase.     

A duality for Hopf algebras and for subfactors. I

We provide a duality between subfactors with finite index, or finite dimensional semisimple Hopf algebras, and a class ofC ^*-categories of endomorphisms.Dedicated to Masamichi Takesaki on the occasion of his sixtieth birthdaySupported in part by MURST and CNR-GNAFA     

Structural properties of nonionic cyclodextrin colloids in water

The amphiphilic character in water of a novel class of chemically modified cyclodextrins has been investigated by means of small-angle X-ray scattering and light scattering. The introduction ofhydrophilic oligo(ethylene glycol) onto the secondary side of heptakis[6-alkylthio-6-deoxy-2-oligo(ethylene glycol)]-beta-cyclodextrins produces an enhanced water solubility of these molecules. Shape and dimensions of the generated micellar aggregates, analyzed in terms of a suitable core-shell model, remain stable in the wide concentration range explored. The highly associative behavior of these macromolecules is evidenced by the very low value of the critical micelle concentration (cmc), which is about 2 orders of magnitude smaller than the cmc usually obtained for traditional surfactant. Despite the complex geometry of this novel macromolecule, shape and dimensions of generated micellar aggregates can be properly described according to the thermodynamic approaches generally used for amphiphilic molecules and block copolymers. Results show how the modulation of hydrophobic and hydrophilic components sensitively influence the structural features of the generated aggregates thus offering the possibility to control molecular organization in a manner similar to that for traditional colloids. For all the classes of the investigated systems, the small micelles have been found in equilibrium with polydisperse large aggregates of entangled micelles. These novel nonionic colloidal systems combine inclusion and transport properties of host macrocycles, such as cyclodextrin, together with the increased stability of colloidal aggregates, and may be of interest for their potential application as innovative drug delivery systems.