191 research outputs found

    Analytical Formulation of the Jacobian Matrix for Non-linear Calculation of the Forced Response of Turbine Blade Assemblies with Wedge Friction Dampers

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    A fundamental issue in turbomachinery design is the dynamical stress assessment of turbine blades. In order to reduce stress peaks in the turbine blades at engine orders corresponding to blade natural frequencies, friction dampers are employed. Blade response calculation requires the solution of a set of non-linear equations originated by the introduction of friction damping. Such a set of non-linear equations is solved using the iterative numerical Newton-Raphson method. However, calculation of the Jacobian matrix of the system using classical numerical finite difference schemes makes frequency domain solver prohibitively expensive for structures with many contact points. Large computation time results from the evaluation of partial derivatives of the non-linear equations with respect to the displacements. In this work a methodology to compute efficiently the Jacobian matrix of a dynamic system having wedge dampers is presented. It is exact and completely analytical. The proposed methods have been successfully applied to a real intermediate pressure turbine (IPT) blade under cyclic symmetry boundary conditions with underplatform wedge dampers. Its implementation showed to be very effective, and allowed to achieve relevant time savings without loss of precision

    Central obesity as a precursor to the metabolic syndrome in the AusDiab study and Mauritius

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    Evidence from epidemiologic studies that central obesity precedes future metabolic change and does not occur concurrently with the appearance of the blood pressure, glucose, and lipid abnormalities that characterize the metabolic syndrome (MetS) has been lacking. Longitudinal surveys were conducted in Mauritius in 1987, 1992, and 1998, and in Australia in 2000 and 2005 (AusDiab). This analysis included men and women (aged 25 years) in three cohorts: AusDiab 2000&ndash;2005 (n = 5,039), Mauritius 1987&ndash;1992 (n = 2,849), and Mauritius 1987&ndash;1998 (n = 1,999). MetS components included waist circumference, systolic blood pressure, fasting and 2-h postload plasma glucose, high-density lipoprotein (HDL) cholesterol, triglycerides, and homeostasis model assessment of insulin sensitivity (HOMA-S) (representing insulin sensitivity). Linear regression was used to determine which baseline components predicted deterioration in other MetS components over 5 years in AusDiab and 5 and 11 years in Mauritius, adjusted for age, sex, and ethnic group. Baseline waist circumference predicted deterioration (P &lt; 0.01) in four of the other six MetS variables tested in AusDiab, five of six in Mauritius 1987&ndash;1992, and four of six in Mauritius 1987&ndash;1998. In contrast, an increase in waist circumference between baseline and follow-up was only predicted by insulin sensitivity (HOMA-S) at baseline, and only in one of the three cohorts. These results suggest that central obesity plays a central role in the development of the MetS and appears to precede the appearance of the other MetS components.<br /

    On the construction of wear maps for Y-TZP dental ceramics in aqueous environments : pH, exposure time and impact angle effects

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    The purpose of this study was to test in-vitro the micro and nano tribological properties of Y-TZP (Yttria Tetragonal Zirconia Polycrystalline) material used in the construction of artificial teeth or dental crowns. The results showed that the effect of pH was to accelerate the wear rate of the Y-TZP material. However, this phenomenon was more apparent in acid than in alkaline environments. Wear maps were constructed based on the results identifying wastage regimes for the material in the erosion-corrosion conditions at a range of impact angles. In addition, a wear map was generated based on the transition from tetragonal to monoclininc phase for the material and the transition to high wear at various pHs and exposure times

    Modelling and analysis of Markov reward automata

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    Costs and rewards are important ingredients for many types of systems, modelling critical aspects like energy consumption, task completion, repair costs, and memory usage. This paper introduces Markov reward automata, an extension of Markov automata that allows the modelling of systems incorporating rewards (or costs) in addition to nondeterminism, discrete probabilistic choice and continuous stochastic timing. Rewards come in two flavours: action rewards, acquired instantaneously when taking a transition; and state rewards, acquired while residing in a state. We present algorithms to optimise three reward functions: the expected cumulative reward until a goal is reached, the expected cumulative reward until a certain time bound, and the long-run average reward. We have implemented these algorithms in the SCOOP/IMCA tool chain and show their feasibility via several case studies

    Application of a risk-management framework for integration of stromal tumor-infiltrating lymphocytes in clinical trials

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    Stromal tumor-infiltrating lymphocytes (sTILs) are a potential predictive biomarker for immunotherapy response in metastatic triple-negative breast cancer (TNBC). To incorporate sTILs into clinical trials and diagnostics, reliable assessment is essential. In this review, we propose a new concept, namely the implementation of a risk-management framework that enables the use of sTILs as a stratification factor in clinical trials. We present the design of a biomarker risk-mitigation workflow that can be applied to any biomarker incorporation in clinical trials. We demonstrate the implementation of this concept using sTILs as an integral biomarker in a single-center phase II immunotherapy trial for metastatic TNBC (TONIC trial, NCT02499367), using this workflow to mitigate risks of suboptimal inclusion of sTILs in this specific trial. In this review, we demonstrate that a web-based scoring platform can mitigate potential risk factors when including sTILs in clinical trials, and we argue that this framework can be applied for any future biomarker-driven clinical trial setting
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