1,210 research outputs found

    Making internal fixation work with limited bone stock

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    Fractures are common in small animal practice and there are many options for managing them. Plates and screws remain a popular means to manage many fractures; however, some fractures are sufficiently close to a joint (juxta-articular), that they limit the amount of bone available to achieve a standard stable plate and screw fixation. This article discusses the options to achieve a stable internal fixation when there is limited bone stock

    Comparison Of Quasi-Phase-Matching Geometries For Second-Harmonic Generation In Poled Polymer Channel Waveguides At 1.5 Mu M

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    We have investigated three different quasi-phase-matching approaches to second-harmonic generation (SHG) in DANS (4-dimethylamino-4\u27-nitrostilbene) poled polymer channel waveguides at 1.5 mu m. Periodic photobleaching and periodically poled electrodes deposited directly on the film produced unacceptably high propagation losses. However, periodic electrodes on the substrate gave low losses and useful SHG

    Fluctuating Bond Aggregation: a Model for Chemical Gel Formation

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    The Diffusion-Limited Cluster-Cluster Aggregation (DLCA) model is modified by including cluster deformations using the {\it bond fluctuation} algorithm. From 3dd computer simulations, it is shown that, below a given threshold value cgc_g of the volumic fraction cc, the realization of all intra-aggregate bonding possibilities prevents the formation of a gelling network. For c>cgc>c_g, the sol-gel transition occurs at a time tgt_g which, in contrast to DLCA, doesnot diverge with the box size. Several results are reported including small angle scattering curves and possible applications are discussed.Comment: RevTex, 9 pages + 3 postscript figures appended using "uufiles". To appear in Phys. Rev. Let

    Interface energies of (100)_{YSZ} and (111)_{YSZ} epitaxial islands on (0001)_{alpha-Al_2O_3} substrates from first principles

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    We present an ab initio study of the interface energies of cubic yttria-stabilized zirconia (YSZ) epitaxial layers on a (0001)_{alpha-Al_2O_3} substrate. The interfaces are modelled using a supercell geometry and the calculations are carried out in the framework of density-functional theory (DFT) and the local-density approximation (LDA) using the projector-augmented-wave (PAW) pseudopotential approach. Our calculations clearly demonstrate that the (111)_{YSZ} || (0001)_{alpha-Al_2O_3} interface energy is lower than that of (100)_{YSZ} || (0001)_{alpha-Al_2O_3}. This result is central to understanding the behaviour of YSZ thin solid film islanding on (0001)_{alpha-Al_2O_3} substrates, either flat or in presence of defects.Comment: 25 pages, 5 figures, 10 tables, submitted to Physical Review

    Band Formation during Gaseous Diffusion in Aerogels

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    We study experimentally how gaseous HCl and NH_3 diffuse from opposite sides of and react in silica aerogel rods with porosity of 92 % and average pore size of about 50 nm. The reaction leads to solid NH_4Cl, which is deposited in thin sheet-like structures. We present a numerical study of the phenomenon. Due to the difference in boundary conditions between this system and those usually studied, we find the sheet-like structures in the aerogel to differ significantly from older studies. The influence of random nucleation centers and inhomogeneities in the aerogel is studied numerically.Comment: 7 pages RevTex and 8 figures. Figs. 4-8 in Postscript, Figs. 1-3 on request from author

    Three-dimensional coherent X-ray diffraction imaging of a ceramic nanofoam: determination of structural deformation mechanisms

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    Ultra-low density polymers, metals, and ceramic nanofoams are valued for their high strength-to-weight ratio, high surface area and insulating properties ascribed to their structural geometry. We obtain the labrynthine internal structure of a tantalum oxide nanofoam by X-ray diffractive imaging. Finite element analysis from the structure reveals mechanical properties consistent with bulk samples and with a diffusion limited cluster aggregation model, while excess mass on the nodes discounts the dangling fragments hypothesis of percolation theory.Comment: 8 pages, 5 figures, 30 reference

    Tunable anisotropy in inverse opals and emerging optical properties

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    Using self-assembly, nanoscale materials can be fabricated from the bottom up. Opals and inverse opals are examples of self-assembled nanomaterials made from crystallizing colloidal particles. As self-assembly requires a high level of control, it is challenging to use building blocks with anisotropic geometry to form complex opals, which limits the realizable structures. Typically, spherical colloids are employed as building blocks, leading to symmetric, isotropic superstructures. However, a significantly richer palette of directionally dependent properties are expected if less symmetric, anisotropic structures can be created, especially originating from the assembly of regular, spherical particles. Here we show a simple method to introduce anisotropy into inverse opals by subjecting them to a post-assembly thermal treatment that results in directional shrinkage of the silica matrix caused by condensation of partially hydrated sol-gel silica structures. In this way, we can tailor the shape of the pores, and the anisotropy of the final inverse opal preserves the order and uniformity of the self-assembled structure, while completely avoiding the need to synthesize complex oval-shaped particles and crystallize them into such target geometries. Detailed X-ray photoelectron spectroscopy (XPS) and infrared (IR) spectroscopy studies clearly identify increasing degrees of sol-gel condensation in confinement as a mechanism for the structure change. A computer simulation of structure changes resulting from the condensation-induced shrinkage further confirmed this mechanism. As an example of property changes induced by the introduction of anisotropy, we characterized the optical spectra of the anisotropic inverse opals and found that the optical properties can be controlled in a precise way using calcination temperature

    Permeability reduction in porous materials by in situ

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    The effect of in situ formed silica gel on the permeability of a porous material was investigated experimentally. Gelling solutions of tetra-methyl-ortho-silicate (TMOS) and methanol in water were imbibed into dry sandstone plates and cured for several days. The permeability of the untreated sandstone is on the order of 1 ”m^2, whereas the intrinsic permeability of the silica alcogel is 5–6 orders of magnitude lower. The method of beam bending was employed to measure concurrently the permeability D and Young’s modulus Ep of cylindrical gel rods, prepared from the TMOS-based sol-gel solutions. Second, the permeabilities and moduli of the treated sandstones were measured. For both types of samples the gel structure was varied by varying the concentration of the TMOS in a solution and the pH of the water used. The parameters D and Ep follow from a detailed analysis of the measured relaxation of the load that is applied to the sample under constant deflection. In case of the gels, the relaxation was interpreted using common expressions for hydrodynamic relaxation and viscoelastic (VE) relaxation. It was found that the permeability of the gels decreases with increasing silica content and that acid-catalyzed gels exhibit a significantly lower permeability than base-catalyzed gels. The modulus Ep increases with increasing silica content and aging time. The relaxation data of the sandstone—treated with gel—exhibited a more complex behavior. The normalized load curves showed hydrodynamic relaxation as well as strong and fast VE relaxation. The relaxation data for the rock samples treated with the lowest concentration gel was fitted successfully with the predictions. For higher concentrations the fit was less accurate, but the permeability estimates were within an order of magnitude. The overall permeability of the treated rock is higher than the intrinsic permeability of the gels; this indicates that the gel does not completely fill the pore space. Nevertheless, the permeability is reduced by a factor 10^4 with respect to untreated sandstone, and therefore the gel adequately blocks the pores

    Influence of the initial chemical conditions on the rational design of silica particles

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    The influence of the water content in the initial composition on the size of silica particles produced using the Stöber process is well known. We have shown that there are three morphological regimes defined by compositional boundaries. At low water levels (below stoichiometric ratio of water:tetraethoxysilane), very high surface area and aggregated structures are formed; at high water content (>40 wt%) similar structures are also seen. Between these two boundary conditions, discrete particles are formed whose size are dictated by the water content. Within the compositional regime that enables the classical Stöber silica, the structural evolution shows a more rapid attainment of final particle size than the rate of formation of silica supporting the monomer addition hypothesis. The clearer understanding of the role of the initial composition on the output of this synthesis method will be of considerable use for the establishment of reliable reproducible silica production for future industrial adoption
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