14,034 research outputs found

    Numerical study of solid particle axial mixing in a fixed cylindrical drum with rotating paddles

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    Axial mixture characterization is a wide spread problem in granular particle blending processes such as in an horizontal drum mixer. The homogeneous mixture of particles is obtained by blending the particles via rotating paddles in a fixed cylindrical drum. This problem, common to many technological devices, is crucial in the manufacture of a broad variety of industrial products, such as polypropylene. The granular flow behavior in these systems is still poorly understood and the numerical study of such configurations receives increasing academic and industrial attention. In this paper, a study is conducted to investigate the effects of different aspects of the reactor design on the axial transport of monodisperse, uniform density and spherical polypropylene particles. Results show that principally the shape of the paddles is the important design consideration to enhance the axial transport of particles

    Ciprofloxacin enhances the stimulation of matrix metalloproteinase 3 expression by interleukin-1beta in human tendon-derived cells

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    To determine whether the fluoroquinolone antibiotic ciprofloxacin, which can cause tendon pain and rupture in a proportion of treated patients, affects the expression of matrix metalloproteinases (MMPs) in human tendon-derived cells in culture. Cell cultures were derived from 6 separate tendon explants, and were incubated in 6-well culture plates for 2 periods of 48 hours each, with ciprofloxacin (or DMSO in controls) and interleukin-1ß (IL-1ß), alone and in combination. Samples of supernatant medium from the second 48-hour incubation were assayed for MMPs 1, 2, and 3 by Western blotting. RNA was extracted from the cells and assayed for MMP messenger RNA (mRNA) by semiquantitative reverse transcription–polymerase chain reaction, with normalization for GAPDH mRNA. Unstimulated tendon cells expressed low or undetectable levels of MMP-1 and MMP-3, and substantial levels of MMP-2. IL-1ß induced a substantial output of both MMP-1 and MMP-3 into cell supernatants, reflecting increases (typically 100-fold) in MMP mRNA, but had only minor effects on MMP-2 expression. Ciprofloxacin had no detectable effect on MMP output in unstimulated cells. Preincubation with ciprofloxacin potentiated IL-1ß–stimulated MMP-3 output, reflecting a similar effect on MMP-3 mRNA expression. Ciprofloxacin also potentiated IL-1ß–stimulated MMP-1 mRNA expression, but did not potentiate the output of MMP-1, and had no significant effects on MMP-2 mRNA expression or output. Ciprofloxacin can selectively enhance MMP expression in tendon-derived cells. Such effects might compromise tendon microstructure and integrity

    Scaling of FLIC Fermions

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    Hadron masses are calculated in quenched lattice QCD on a variety of lattices in order to probe the scaling behavior of the Fat-Link Irrelevant Clover (FLIC) fermion action, a fat-link clover fermion action in which the purely irrelevant operators of the fermion action are constructed using APE-smeared links. The scaling analysis indicates FLIC fermions provide a new form of nonperturbative O(a) improvement where near-continuum results are obtained at finite lattice spacing.Comment: 4 pages, 1 figure, 2 tables. Figure updated and references added. Accepted for publication in Phys. Rev.

    Lattice results for the decay constant of heavy-light vector mesons

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    We compute the leptonic decay constants of heavy-light vector mesons in the quenched approximation. The reliability of lattice computations for heavy quarks is checked by comparing the ratio of vector to pseudoscalar decay constant with the prediction of Heavy Quark Effective Theory in the limit of infinitely heavy quark mass. Good agreement is found. We then calculate the decay constant ratio for B mesons: fB/fB=1.01(0.01)(0.01+0.04)f_{B^*}/f_B= 1.01(0.01)(^{+0.04}_{-0.01}). We also quote quenched fB=177(6)(17)f_{B^*}=177(6)(17) MeV.Comment: 11 pages, 3 postscript figs., revtex; two references adde

    Asymmetries in the Value of Existence

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    According to asymmetric comparativism, it is worse for a person to exist with a miserable life than not to exist, but it is not better for a person to exist with a happy life than not to exist. My aim in this paper is to explain how asymmetric comparativism could possibly be true. My account of asymmetric comparativism begins with a different asymmetry, regarding the (dis)value of early death. I offer an account of this early death asymmetry, appealing to the idea of conditional goods, and generalize it to explain how asymmetric comparativism could possibly be true. I also address the objection that asymmetric comparativism has unacceptably antinatalist implications

    Eco Global Evaluation: Cross Benefits of Economic and Ecological Evaluation

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    This paper highlights the complementarities of cost and environmental evaluation in a sustainable approach. Starting with the needs and limits for whole product lifecycle evaluation, this paper begins with the modeling, data capture and performance indicator aspects. In a second step, the information issue, regarding the whole lifecycle of the product is addressed. In order to go further than the economical evaluations/assessment, the value concept (for a product or a service) is discussed. Value could combine functional requirements, cost objectives and environmental impact. Finally, knowledge issues which address the complexity of integrating multi-disciplinary expertise to the whole lifecycle of a product are discussing.EcoSD NetworkEcoSD networ

    Cell-penetrating peptide conjugates of peptide nucleic acids (PNA) as inhibitors of HIV-1 Tat-dependent trans-activation in cells

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    The trans-activation response (TAR) RNA stem–loop that occurs at the 5′ end of HIV RNA transcripts is an important antiviral target and is the site of interaction of the HIV-1 Tat protein together with host cellular factors. Oligonucleotides and their analogues targeted to TAR are potential antiviral candidates. We have investigated a range of cell penetrating peptide (CPP) conjugates of a 16mer peptide nucleic acid (PNA) analogue targeted to the apical stem–loop of TAR and show that disulfide-linked PNA conjugates of two types of CPP (Transportan or a novel chimeric peptide R(6)-Penetratin) exhibit dose-dependent inhibition of Tat-dependent trans-activation in a HeLa cell assay when incubated for 24 h. Activity is reached within 6 h if the lysosomotropic reagent chloroquine is co-administered. Fluorescein-labelled stably-linked conjugates of Tat, Transportan or Transportan TP10 with PNA were inactive when delivered alone, but attained trans-activation inhibition in the presence of chloroquine. Confocal microscopy showed that such fluorescently labelled CPP–PNA conjugates were sequestered in endosomal or membrane-bound compartments of HeLa cells, which varied in appearance depending on the CPP type. Co-administration of chloroquine was seen in some cases to release fluorescence from such compartments into the nucleus, but with different patterns depending on the CPP. The results show that CPP–PNA conjugates of different types can inhibit Tat-dependent trans-activation in HeLa cells and have potential for development as antiviral agents. Endosomal or membrane release is a major factor limiting nuclear delivery and trans-activation inhibition

    Critical coupling for dynamical chiral-symmetry breaking with an infrared finite gluon propagator

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    We compute the critical coupling constant for the dynamical chiral-symmetry breaking in a model of quantum chromodynamics, solving numerically the quark self-energy using infrared finite gluon propagators found as solutions of the Schwinger-Dyson equation for the gluon, and one gluon propagator determined in numerical lattice simulations. The gluon mass scale screens the force responsible for the chiral breaking, and the transition occurs only for a larger critical coupling constant than the one obtained with the perturbative propagator. The critical coupling shows a great sensibility to the gluon mass scale variation, as well as to the functional form of the gluon propagator.Comment: 19 pages, latex, 3 postscript figures, uses epsf.sty and epsf.tex. To be published in Phys. Lett.
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