2,797 research outputs found

    A tachyonic extension of the stringy no-go theorem

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    We investigate the tachyon-dilaton-metric system to study the "graceful exit" problem in string theoretic inflation, where tachyon plays the role of the scalar field. From the phase space analysis, we find that the inflationary phase does not smoothly connect to a Friedmann-Robertson-Walker (FRW) expanding universe, thereby providing a simple tachyonic extension of the recently proved stringy no-go theorem.Comment: TeX file (PHYZZX), 10 pages, change in the title, many changes in the text (the version to appear in Phys. Rev. D

    Low-energy excitations of a linearly Jahn-Teller coupled orbital quintet

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    The low-energy spectra of the single-mode h x (G+H) linear Jahn-Teller model is studied by means of exact diagonalization. Both eigenenergies and photoemission spectral intensities are computed. These spectra are useful to understand the vibronic dynamics of icosahedral clusters with partly filled orbital quintet molecular shells, for example C60 positive ions.Comment: 14 pages revte

    Spillover of Peste des Petits Ruminants Virus from Domestic to Wild Ruminants in the Serengeti Ecosystem, Tanzania

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    We tested wildlife inhabiting areas near domestic livestock, pastures, and water sources in the Ngorongoro district in the Serengeti ecosystem of northern Tanzania and found 63% seropositivity for peste des petits ruminants virus. Sequencing of the viral genome from sick sheep in the area confirmed lineage II virus circulation

    Progress on the hybrid gun project at UCLA

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    UCLA/INFN-LNF/Univ. Rome has been developing the hybrid gun which has an RF gun and a short linac for velocity bunching in one structure. After the cavity was manufactured at INFN-LNF in 2012, tests of the gun was carried out at UCLA. The field in the standing wave part was 20 % smaller than the simulation but the phase advance was fine. The cavity was commissioned successfully up to 13 MW. The beam test was performed at 11.5 MW and demonstrated the bunch compression

    ENHANCEMENT OF BIOAVAILABILITY OF GLIPIZIDE USING SOLID DISPERSIONS WITH GUM AEGLE MARMELOS

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    Objective: The aim of the proposed study was formulation and in vitro/ vivo evolution   of solid dispersions of glipizide with gum Aegle marmelos. Methods: The phase solubility of glipizide in 0.1N HCl was investigated in the presence of different concentrations of gum Aegle marmelos. The solid dispersions (SDs) of glipizide with gum Aegle marmelos were formulated using solvent evaporation method at ratios of 1:1, 1:2, and 1:5 (glipizide: gum Aegle marmelos). Dissolution studies were conducted. The physicochemical characterization of the formulations was performed by using Fourier-transform infrared (FTIR) spectroscopy, differential scanning calorimetry (DSC) and X-ray diffraction (XRD). Subsequently, bioavailability of pure glipizide, solid dispersion and marketed product was performed in rat. Results: Glipizide solubility increased as the concentration of gum Aegle marmelos in 0.1N HCl was raised. The solubility study indicates spontaneous drug solubilization, which is supported by negative values of Gibb's free energy (ΔGotr). Glipizide rate of dissolution was increased in SDs containing gum, and the rate increased as the concentration of gum in the SDs increases. After preparing SDs and physical mixtures with gum, the mean dissolution time (MDT) of glipizide decreases considerably. FTIR spectroscopy study revealed that stability and the absence of a well-defined glipizide-gum interaction. The amorphous condition of glipizide in SDs of glipizide with gum was revealed by DSC and XRD studies. Conclusion: The DSC and XRD studies indicate conversion of drug from crystalline to microcrystalline or amorphous form after formulation of solid dispersion with Aegle gum. The solid dispersion of glipizide with Aegle gum (893.04±25.5) showed better therapeutic activity compared to pure glipizide (535.65±11.5) and marketed formulation (767.5±13.6)

    A Multimedia Development Process

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    Effect of textile softeners on BTCA treated cotton fabric

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    96-101The effect of two softeners (Sapamine® OC and Ultratex® ASG) on physical properties of BTCA finished cotton fabric has been studied. Bleached cotton fabrics are treated with 1, 2, 3, 4-butane tetracarboxylic acid (BTCA) followed by finishing with a cationic and a silicone softener by conventional pad-dry-cure method. Properties, such as crease recovery angle, absorbency, whiteness index, tensile strength, moisture regain, surface morphology and crystallinity of the finished fabrics, have been evaluated. The crease recovery angle of the finished fabrics increases from 154° to 257° after treatment with BTCA and further increases to 266° after BTCA+silicone softener based finishing. The absorbency of cationic softener finished fabric is found to be higher than that of silicone softener finished fabrics. Tensile strength reduces after BTCA finishing by more than 50%, and about 17% softeners is recovered. Scanning electron microscope images show smooth ridges and surface characteristics of cotton fibres in BTCA treated samples as well as deposition of softener on the fibre surface in cationic and silicone softener finished fabrics

    Effect of textile softeners on BTCA treated cotton fabric

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    The effect of two softeners (Sapamine® OC and Ultratex® ASG) on physical properties of BTCA finished cotton fabrichas been studied. Bleached cotton fabrics are treated with 1, 2, 3, 4-butane tetracarboxylic acid (BTCA) followed byfinishing with a cationic and a silicone softener by conventional pad-dry-cure method. Properties, such as crease recoveryangle, absorbency, whiteness index, tensile strength, moisture regain, surface morphology and crystallinity of the finishedfabrics, have been evaluated. The crease recovery angle of the finished fabrics increases from 154° to 257° after treatmentwith BTCA and further increases to 266° after BTCA+silicone softener based finishing. The absorbency of cationic softenerfinished fabric is found to be higher than that of silicone softener finished fabrics. Tensile strength reduces after BTCAfinishing by more than 50%, and about 17% softeners is recovered. Scanning electron microscope images show smoothridges and surface characteristics of cotton fibres in BTCA treated samples as well as deposition of softener on the fibresurface in cationic and silicone softener finished fabrics
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