5,293 research outputs found
Couple stress effects in a thin film bonded to a half-space
This study investigates the contact mechanics of a thin film laying on an elastic substrate within the context of couple-stress elasticity. It aims to introduce the effects of material internal length scale, which has proven an effective way of modeling structures at micro to nano-scales, allowing to capture their size dependent behavior. Specifically, stress analysis for a thin film bonded to a couple stress elastic half-space is considered under plane strain loading conditions by assuming that both shear stress and couple tractions are exchanged between the thin film and the substrate. The problem is converted to a singular integral equation, which is solved by expanding the shear stress tractions as a Chebyshev series. The results show that the introduction of couple tractions decreases the shear stress tractions and the axial load in the thin film. When the characteristic length is sufficiently small, but still finite, the results for classical elastic behavior are approached
High precision determination of the -evolution of the Bjorken Sum
We present a significantly improved determination of the Bjorken Sum for
0.64.8 GeV using precise new and
data taken with the CLAS detector at Jefferson Lab. A higher-twist analysis of
the -dependence of the Bjorken Sum yields the twist-4 coefficient
. This leads to the color
polarizabilities and
. The strong force coupling is determined to be
\alpha_{s}^{\overline{\mbox{ MS}}}(M_{Z}^{2})=0.1124\pm0.0061, which has an
uncertainty a factor of 1.5 smaller than earlier estimates using polarized DIS
data. This improvement makes the comparison between extracted from
polarized DIS and other techniques a valuable test of QCD.Comment: Published in Phys. Rev. D. V1: 8 pages, 3 figures. V2: Updated
references; Included threshold matching in \alpha_s evolution. Corrected a
typo on the uncertainty for \Lambda_QCD. V3: Published versio
Interfiber interactions alter the stiffness of gels formed by supramolecular self-assembled nanofibers
Cataloged from PDF version of article.Molecular self-assembly is a powerful technique for developing novel nanostructures by using noncovalent interactions such as hydrogen bonding, hydrophobic, electrostatic, metal-ligand, p-p and van der Waals interactions. These interactions are highly dynamic and are often delicate due to their relatively weak nature. However, a sufficient number of these weak interactions can yield a stable assembly. In this work, we studied the mechanical properties of self-assembled peptide amphiphile nanostructures in the nanometre and micrometre scale. Hydrogen bonding, hydrophobic and electrostatic interactions promote self-assembly of peptide amphiphile molecules into nanofibers. Bundles of nanofibers form a three-dimensional network resulting in gel formation. The effect of the nanofiber network on the mechanical properties of the gels was analyzed by AFM, rheology and CD. Concentration and temperature dependent measurements of gel stiffness suggest that the mechanical properties of the gels are determined by a number of factors including the interfiber interactions and mechanical properties of individual nanofibers. We point out that the divergence in gel stiffness may arise from the difference in strength of interfiber bonds based on an energetic model of elastic rod networks, along with continuum mechanical models of bundles of rods. This finding differs from the results observed with traditional polymeric materials. Understanding the mechanisms behind the viscoelastic properties of the gels formed by self-assembling molecules can lead to development of new materials with controlled stiffness. Tissue engineering applications can especially benefit from these materials, where the mechanical properties of the extracellular matrix are crucial for cell fate determination. © The Royal Society of Chemistry 2011
Nanomechanical characterization by double-pass force-distance mapping
Cataloged from PDF version of article.We demonstrate high speed force–distance mapping using a double-pass scheme. The topography is measured in tapping mode in the first pass and this information is used in the second pass to move the tip over the sample. In the second pass, the cantilever dither signal is turned off and the sample is vibrated. Rapid (few kHz frequency) force–distance curves can be recorded with small peak interaction force, and can be processed into an image. Such a double-pass measurement eliminates the need for feedback during force–distance measurements. The method is demonstrated on self-assembled peptidic nanofibers
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Precise determination of the deuteron spin structure at low to moderate Q(2) with CLAS and extraction of the neutron contribution
We present the final results for the deuteron spin structure functions obtained from the full data set collected in 2000-2001 with Jefferson Lab\u27s continuous electron beam accelerator facility (CEBAF) using the CEBAF large acceptance spectrometer (CLAS). Polarized electrons with energies of 1.6, 2.5, 4.2, and 5.8 GeV were scattered from deuteron ((ND3)-N-15) targets, dynamically polarized along the beam direction, and detected with CLAS. From the measured double-spin asymmetry, the virtual photon absorption asymmetry A(1)(d) and the polarized structure function g(1)(d) were extracted over a wide kinematic range (0.05 GeV2 \u3c Q(2) \u3c 5 GeV2 and 0.9 GeV \u3c W \u3c 3 GeV). We use an unfolding procedure and a parametrization of the corresponding proton results to extract from these data the polarized structure functions A(1)(n) and g(1)(n) of the (bound) neutron, which are so far unknown in the resonance region, W \u3c 2 GeV. We compare our final results, including several moments of the deuteron and neutron spin structure functions, with various theoretical models and expectations, as well as parametrizations of the world data. The unprecedented precision and dense kinematic coverage of these data can aid in future extractions of polarized parton distributions, tests of perturbative QCD predictions for the quark polarization at large x, a better understanding of quark-hadron duality, and more precise values for higher-twist matrix elements in the framework of the operator product expansion
Neutrino physics at accelerators
Present and future neutrino experiments at accelerators are mainly concerned
with understanding the neutrino oscillation phenomenon and its implications.
Here a brief account of neutrino oscillations is given together with a
description of the supporting data. Some current and planned accelerator
neutrino experiments are also explained.Comment: 23 pages, 24 figures. Talk given at the Corfu Summer Institute on
Elementary Particle Physics 200
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