70 research outputs found

    Bending Analysis of Folded Laminated Plates by the FSDT Meshfree Method

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    AbstractA meshfree method is developed in this paper to study the flexure behavior of folded laminated plates. A folded laminated plate is considered as an assembly of laminates. Based on the first-order shear deformation theory (FSDT) and the moving-least square approximation, the stiffness equations of the laminates are derived. A treatment is implemented to modify the equations, and the equations are then superposed to obtain the governing equation of the entire folded laminated plate. No mesh is required in the determination of the stiffness equations of the laminates, and therefore the proposed method is more flexible than the finite element methods. The convergence and accuracy of the proposed method are examined by computing several numerical examples, and good agreement is observed between the present results and those given by ANSYS

    Reinforcement of natural rubber with core-shell structure silica-poly(Methyl Methacrylate) nanoparticles

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    A highly performing natural rubber/silica (NR/SiO2) nanocomposite with a SiO2 loading of 2 wt% was prepared by combining similar dissolve mutually theory with latex compounding techniques. Before polymerization, double bonds were introduced onto the surface of the SiO2 particles with the silane-coupling agent. The core-shell structure silica-poly(methyl methacrylate), SiO2-PMMA, nanoparticles were formed by grafting polymerization of MMA on the surface of the modified SiO2 particles via in situ emulsion, and then NR/SiO2 nanocomposite was prepared by blending SiO2-PMMA and PMMA-modified NR (NR-PMMA). The Fourier transform infrared spectroscopy results show that PMMA has been successfully introduced onto the surface of SiO2, which can be well dispersed in NR matrix and present good interfacial adhesion with NR phase. Compared with those of pure NR, the thermal resistance and tensile properties of NR/SiO2 nanocomposite are significantly improved

    Measurements of J/psi Decays into 2(pi+pi-)eta and 3(pi+pi-)eta

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    Based on a sample of 5.8X 10^7 J/psi events taken with the BESII detector, the branching fractions of J/psi--> 2(pi+pi-)eta and J/psi-->3(pi+pi-)eta are measured for the first time to be (2.26+-0.08+-0.27)X10^{-3} and (7.24+-0.96+-1.11)X10^{-4}, respectively.Comment: 11 pages, 6 figure

    BESII Detector Simulation

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    A Monte Carlo program based on Geant3 has been developed for BESII detector simulation. The organization of the program is outlined, and the digitization procedure for simulating the response of various sub-detectors is described. Comparisons with data show that the performance of the program is generally satisfactory.Comment: 17 pages, 14 figures, uses elsart.cls, to be submitted to NIM

    Measurement of branching fractions for the inclusive Cabibbo-favored ~K*0(892) and Cabibbo-suppressed K*0(892) decays of neutral and charged D mesons

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    The branching fractions for the inclusive Cabibbo-favored ~K*0 and Cabibbo-suppressed K*0 decays of D mesons are measured based on a data sample of 33 pb-1 collected at and around the center-of-mass energy of 3.773 GeV with the BES-II detector at the BEPC collider. The branching fractions for the decays D+(0) -> ~K*0(892)X and D0 -> K*0(892)X are determined to be BF(D0 -> \~K*0X) = (8.7 +/- 4.0 +/- 1.2)%, BF(D+ -> ~K*0X) = (23.2 +/- 4.5 +/- 3.0)% and BF(D0 -> K*0X) = (2.8 +/- 1.2 +/- 0.4)%. An upper limit on the branching fraction at 90% C.L. for the decay D+ -> K*0(892)X is set to be BF(D+ -> K*0X) < 6.6%

    Study of J/ψωK+KJ/\psi \to \omega K^+K^-

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    New data are presented on J/ψωK+KJ/\psi \to \omega K^+K^- from a sample of 58M J/ψJ/\psi events in the upgraded BES II detector at the BEPC. There is a conspicuous signal for f0(1710)K+Kf_0(1710) \to K^+K^- and a peak at higher mass which may be fitted with f2(2150)KKˉf_2(2150) \to K\bar K. From a combined analysis with ωπ+π\omega \pi ^+ \pi ^- data, the branching ratio BR(f0(1710)ππ)/BR(f0(1710)KKˉ)BR(f_0(1710)\to\pi\pi)/BR(f_0(1710) \to K\bar K) is <0.11< 0.11 at the 95% confidence level.Comment: 11 pages, 5 figures. Submitted to Phys. Lett.

    Measurements of Cabibbo Suppressed Hadronic Decay Fractions of Charmed D0 and D+ Mesons

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    Using data collected with the BESII detector at e+ee^{+}e^{-} storage ring Beijing Electron Positron Collider, the measurements of relative branching fractions for seven Cabibbo suppressed hadronic weak decays D0KK+D^0 \to K^- K^+, π+π\pi^+ \pi^-, KK+π+πK^- K^+ \pi^+ \pi^- and π+π+ππ\pi^+ \pi^+ \pi^- \pi^-, D+K0ˉK+D^+ \to \bar{K^0} K^+, KK+π+K^- K^+ \pi^+ and ππ+π+\pi^- \pi^+ \pi^+ are presented.Comment: 11 pages, 5 figure

    Direct Measurement of the Pseudoscalar Decay Constant fD+

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    The absolute branching fraction of D+μ+νD^+ \to \mu^+ \nu has been directly measured by an analysis of a data sample of about 33 pb1{\rm pb^{-1}} collected around s=3.773\sqrt{s}=3.773 GeV with the BES-II at the BEPC. At these energies, DD^- meson is produced in pair as e+eD+De^+e^-\to D^{+} D^{-}. A total of 5321±149±1605321 \pm 149 \pm 160 DD^- mesons are reconstructed from this data set. In the recoil side of the tagged DD^- mesons, 2.67±1.742.67\pm1.74 purely leptonic decay events of D+μ+νD^+ \to \mu^+ \nu are observed. This yields a branching fraction of BF(D+μ+νμ)=(0.1220.053+0.111±0.010)BF(D^+ \to \mu^+ \nu_{\mu}) = (0.122^{+0.111}_{-0.053}\pm 0.010)%, and a corresponding pseudoscalar decay constant fD+=(371119+129±25)f_{D^+}=(371^{+129}_{-119}\pm 25) MeV.Comment: 7 pages, 8 figures, Submitted to Physics Letters B in October, 200

    The Pediatric Cell Atlas: defining the growth phase of human development at single-cell resolution

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    Single-cell gene expression analyses of mammalian tissues have uncovered profound stage-specific molecular regulatory phenomena that have changed the understanding of unique cell types and signaling pathways critical for lineage determination, morphogenesis, and growth. We discuss here the case for a Pediatric Cell Atlas as part of the Human Cell Atlas consortium to provide single-cell profiles and spatial characterization of gene expression across human tissues and organs. Such data will complement adult and developmentally focused HCA projects to provide a rich cytogenomic framework for understanding not only pediatric health and disease but also environmental and genetic impacts across the human lifespan
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