Coupled swelling and large strain model for hydrogels: application to the nucleus pulposus of the intervertebral disc

The main constituents of the nucleus puposus , the centrl gelatinous part of the intervertebral disc, are water and a solid extracellular matrix of macromolecules. Based on this observation, the nucleus pulposus can be seen as a gel-like material in wich swelling - due to the diffusion of the fluid molecules into the macromolecular network - and large strain elasticity, induced by the macromollecular chains, occur. In recent literature, many autors have been interested in describing such a coupled deformation-diffusion problem for gels. Most of the tim, these works where formulated with respect to the dry configuration of the material. Howevver, for the nucleus pulposus, the dru configuration does not exist. Thus, the formulation of the deformation-diffusion problem should be modified in order to consider a reference configuration, wich is undeformed and unconstrained (but already swollen). The theoretical aspects of the derivation of this coupled deformation-diffusion model is proposed. Then, this model is numerically implemented in the finite element commercial software ABAQUS. The state of equilibrium are investigated on simple homogeneous examples. Finally, the himan nucleus pulposus of the intervertebral disc is chosen as a representative complex crample of application for this approach. The associated annulus fibrosus is modelled using an anisotropic hyperelastic material law

Impact of the capping layers on lateral confinement in InAs/InP quantum dots for 1.55 um laser applications srudied by magneto-photoluminescence.

We have used magnetophotoluminescence to study the impact of different capping layer material combinations (InP, GaInAsP quaternary alloy, or both InP and quaternary alloy) on lateral confinement in InAs/InP quantum dots (QDs) grown on (311)B orientated substrates. Exciton effective masses, Bohr radii, and binding energies are measured for these samples. Conclusions regarding the strength of the lateral confinement in the different samples are supported by photoluminescence at high excitation power. Contrary to theoretical predictions, InAs QDs in quaternary alloy are found to have better confinement properties than InAs/InP QDs. This is attributed to a lack of lateral intermixing with the quaternary alloy, which is present when InP is used to (partially) cap the dots. The implications of the results for reducing the temperature sensitivity of QD lasers are discussed. ©2005 American Institute of Physic

The triangular nasal notch sign in patients with Crohn's disease treated with tumor necrosis factor inhibitors

Tumor necrosis factor (TNF) inhibitors are used to treat a range of chronic inflammatory diseases, such as rheumatoid arthritis, inflammatory bowel disease and psoriasis. Some of the cutaneous side effects of these drugs are well documented, such as infections, skin carcinomas, palmoplantar and skinfold pustulosis, psoriasis-like or eczema-like lesions. We are not aware of TNF inhibitor-induced nasal lesions in the literature. We report a case series demonstrating a specific pattern of cicatricial nasal fissure (triangular nasal notch) following nasal dermatitis episodes in patients treated with TNF inhibitors. This article is protected by copyright. All rights reserved

Olivine or Impact Melt: Nature of the "Orange" Material on Vesta from Dawn

NASA's Dawn mission observed a great variety of colored terrains on asteroid (4) Vesta during its survey with the Framing Camera (FC). Here we present a detailed study of the orange material on Vesta, which was first observed in color ratio images obtained by the FC and presents a red spectral slope. The orange material deposits can be classified into three types, a) diffuse ejecta deposited by recent medium-size impact craters (such as Oppia), b) lobate patches with well-defined edges, and c) ejecta rays from fresh-looking impact craters. The location of the orange diffuse ejecta from Oppia corresponds to the olivine spot nicknamed "Leslie feature" first identified by Gaffey (1997) from ground-based spectral observations. The distribution of the orange material in the FC mosaic is concentrated on the equatorial region and almost exclusively outside the Rheasilvia basin. Our in-depth analysis of the composition of this material uses complementary observations from FC, the visible and infrared spectrometer (VIR), and the Gamma Ray and Neutron Detector (GRaND). Combining the interpretations from the topography, geomorphology, color and spectral parameters, and elemental abundances, the most probable analog for the orange material on Vesta is impact melt

Photostability of Fullerene and Non-Fullerene Polymer Solar Cells:The Role of the Acceptor

Recently, the advent of non-fullerene acceptors (NFAs) made it possible for organic solar cells (OSCs) to break the 10% efficiency barrier hardly attained by fullerene acceptors (FAs). In the past five years alone, more than hundreds of NFAs with applications in organic photovoltaics (OPVs) have been synthesized, enabling a notable current record efficiency of above 15%. Hence, there is a shift in interest towards the use of NFAs in OPVs. However, there has been little work on the stability of these new materials in devices. More importantly, there is very little comparative work on the photo-stability of FAs vs. NFAs solar cells, to ascertain the pros and cons of the two systems. Here, we show the photo-stability of solar cells based on two workhorse acceptors, in both conventional and inverted structures, namely ITIC (as NFA) and [70]PCBM (as FA) blended with either PBDB-T or PTB7-Th polymer. We found that irrespective of the polymer, the cell structure, or the initial efficiency, the [70]PCBM devices are more photo-stable than the ITIC ones. This observation, however, opposes the assumption that NFA solar cells are more photo-chemically stable. These findings suggest that complementary absorption should not take precedence in the design rules for the synthesis of new molecules and there is still work left to be done to achieve stable as well as efficient OSCs

Low-valent homobimetallic Rh complexes: influence of ligands on the structure and the intramolecular reactivity of Rh–H intermediates

Supporting two metal binding sites by a tailored polydentate trop-based (trop - 5H-dibenzo[a,d] cyclohepten-5-yl) ligand yields highly unsymmetric homobimetallic rhodium(I) complexes. Their reaction with hydrogen rapidly forms Rh hydrides that undergo an intramolecular semihydrogenation of two C≡C bonds of the trop ligand. This reaction is chemoselective and converts C≡C bonds to a bridging carbene and an olefinic ligand in the first and the second semihydrogenation steps, respectively. Stabilization by a bridging diphosphine ligand allows characterization of a Rh hydride species by advanced NMR techniques and may provide insight into possible elementary steps of H₂ activation by interfacial sites of heterogeneous Rh/C catalysts

Membrane-assisted reactive crystallisation for the recovery of dissolved phosphorus in vivianite form from liquid effluents

Novel membrane crystallisation processes resolve the mixing challenge on conventional crystallisers, by providing fixed interfacial area over which supersaturation is controlled for nucleation. Moreover, the membrane surface is thought to reduce interfacial energy and encourage micromixing. In this regard, a novel membraneassisted reactive crystallisation (MARC) process was used in this work for the dissolved phosphorous recovery in form of vivianite crystals from a phosphate-rich solution by means of the dosing of iron (II). To characterise the role of the boundary layer in controlling nucleation, a batch lab-scale system was used for the crystallization tests, and different hydraulic conditions (Reynolds ranging from 105 to 395) and polymeric membranes were tested. The crystallisation process was influenced by the hydraulic conditions, in which a low liquid velocity led to a lower induction time and vivianite supersaturation, and therefore, higher nucleation rates. Membrane properties were characterised to establish their role in the modification of the critical free energy requirement for nucleation, and for the promotion of micromixing, as possible factors that can be used to modify nucleation kinetics. As result, the bulk induction time tended to decrease with the increase in membrane hydrophobicity, roughness, pore size and porosity. Spherical vivianite nanoparticles were always synthesised with a mean size around 35 nm and a narrow distribution independently of the hydraulic conditions and membrane used. Finally, the crystallisation kinetic conformed to a diffusion-dependent nucleation mechanism, in which higher residence times for mixing increased the ion collision probability for nucleation. Importantly, this study demonstrated that MARC is an attractive prospect for nutrient recovery from wastewaters where crystal nucleation can be easily controlled by setting the operational conditions and membrane properties, eliciting considerable process intensification over existing conventional crystalliser.European Union funding: 71408

Longitudinal Profile Monitor Using Smith-Purcell Radiation: Recent Results from the E-203 Collaboration

TUPC38 - Work supported by seed funding from the John Fell Fund, University of Oxford, Université Paris-Sud, program "Attractivité" and by the ANR under contract ANR-12-JS05-0003-01International audienceWe report on recent measurements made at FACET by the E-203 collaboration to test a longitudinal bunch profile monitor based on Coherent Smith-Purcell radiation. The capacity of this monitor to resolve sub-picosecond bunches will be shown as well as a comparison of profile reconstructed for different beam compression settings. We will also present recent electromagnetic simulations of the interactions between the beam and the grating as well as the expected resolution of such monitor. Comparison between Coherent Smith-Purcell radiation measurement and those made with other techniques will also be discussed. Finally future upgrades of the experiment and steps toward the construction of a single shot longitudinal profile monitor will be presented