91 research outputs found

    Micro-scale flow on naturally occurring and engineered functional surfaces

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    The deposition and controlled flow of continuous thin liquid film droplets on surfaces containing complex microscale surface patterning (either man-made or naturally occurring) plays a key part in numerous engineering and biologically related fields. For example, in an engineering context, complex surface patterning is present in processes involving printing/photolithography [1] and the application of precision protective coatings [2]; in biological systems they occur in such diverse areas as plant disease control [3], in redistribution of lung linings in respiratory systems [4], and in sustaining life itself, as in the unusual case of the Namibian desert beetle which drinks by harvesting morning mists [5] -- the mist condenses on hydrophilic bumps on its upper surface to form larger droplets which then roll down waxy hydrophobic channels between the bumps to reach the beetle's mouth

    Finite element simulation of three-dimensional free-surface flow problems

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    An adaptive finite element algorithm is described for the stable solution of three-dimensional free-surface-flow problems based primarily on the use of node movement. The algorithm also includes a discrete remeshing procedure which enhances its accuracy and robustness. The spatial discretisation allows an isoparametric piecewise-quadratic approximation of the domain geometry for accurate resolution of the curved free surface. The technique is illustrated through an implementation for surface-tension-dominated viscous flows modelled in terms of the Stokes equations with suitable boundary conditions on the deforming free surface. Two three-dimensional test problems are used to demonstrate the performance of the method: a liquid bridge problem and the formation of a fluid droplet

    Expression of Plet1 controls interstitial migration of murine small intestinal dendritic cells.

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    Under homeostatic conditions, dendritic cells (DCs) continuously patrol the intestinal lamina propria. Upon antigen encounter, DCs initiate C-C motif chemokine receptor 7 (CCR7) expression and migrate into lymph nodes to direct T cell activation and differentiation. The mechanistic underpinnings of DC migration from the tissues to lymph nodes have been largely elucidated, contributing greatly to our understanding of DC functionality and intestinal immunity. In contrast, the molecular mechanisms allowing DCs to efficiently migrate through the complex extracellular matrix of the intestinal lamina propria prior to antigen encounter are still incompletely understood. Here we show that small intestinal murine CD11b <sup>+</sup> CD103 <sup>+</sup> DCs express Placenta-expressed transcript 1 (Plet1), a glycophoshatidylinositol (GPI)-anchored surface protein involved in migration of keratinocytes during wound healing. In the absence of Plet1, CD11b <sup>+</sup> CD103 <sup>+</sup> DCs display aberrant migratory behavior, and accumulate in the small intestine, independent of CCR7 responsiveness. RNA-sequencing indicated involvement of Plet1 in extracellular matrix-interactiveness, and subsequent in-vitro migration assays revealed that Plet1 augments the ability of DCs to migrate through extracellular matrix containing environments. In conclusion, our findings reveal that expression of Plet1 facilitates homeostatic interstitial migration of small intestinal DCs

    Cast Iron Failures in Sulphuric Acid Plant

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    CASE HISTORY: PART 1

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    An experimental technique for measuring the temperature rise during impact testing

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    A fast response radiometer and its associated instrumentation for the measurement of the temperature reached during impact is described in this paper. It is based on a thermoelectrically cooled HgCdTe detector. The sensitivity and time response have been determined by means of static calibration tests, within the range +25 to 500 °C, and a dynamic calibration using an optical chopper at 1.35 kHz. Some results of compression tests are provided
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