100 research outputs found

    FE analysis on tube hydroforming of small diametr ZM21 magnesium alloy tube

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    Tube hydroforming (THF) is one of the plasticity processing methods. Tubular parts, for instance automotive components are expanded by forces such as internal pressure and axial compression in order to deform an objective shape. THF has less restriction on shape and size of workpieces owing to adopting the liquid tool. The demand of a small diameter magnesium alloy tubular parts have been increased for applying small medical and electronic devices. In this study, it was investigated that influence of process conditions such as processing temperature, internal pressure and axial feeding amount on formability of small diameter ZM21 magnesium alloy tube with outer diameter of 2.0mm and thickness of 0.20mm. Furthermore, the processing conditions for improving the formability of material in THF were examined. For prior evaluation of deformation characteristics in the warm THF of small diameter ZM21 magnesium alloy tube, a finite element (FE) simulation was conducted. The FE method (FEM) code was used LS-DYNA 3D for analysis of the FE model of the tube and the dies. The material characteristics were obtained by tensile test and fracture test. From FE analysis results, it was elucidated that effect of the processing temperature, the variable internal pressure and the axial feeding amount on deformation behavior. The formability of ZM21 magnesium alloy tube was improved by processing at 250 C. The difference of deformation characteristic between FE results and experimental results was compared. As the results, the processing condition which could improve the formability of ZM21 tube was clarified using this FE model. The effect of adding the straightening stage in the loading path after the preform on formability was investigated. The thinning of the wall thickness of the tube was inhibited by calibration after the axial feeding

    Fano threefolds of large Fano index and large degree

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    We classify Q-Fano threefolds of Fano index > 2 and big degree.Comment: 38 page

    Nanometer scale thermal response of polymers to fast thermal perturbations

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    © 2018 Author(s). Nanometer scale thermal response of polymers to fast thermal perturbations is described by linear integro-differential equations with dynamic heat capacity. The exact analytical solution for the non-equilibrium thermal response of polymers in plane and spherical geometry is obtained in the absence of numerical (finite element) calculations. The solution is different from the iterative method presented in a previous publication. The solution provides analytical relationships for fast thermal response of polymers even at the limit t → 0, when the application of the iterative process is very problematic. However, both methods give the same result. It was found that even fast (ca. 1 ns) components of dynamic heat capacity greatly enhance the thermal response to local thermal perturbations. Non-equilibrium and non-linear thermal response of typical polymers under pulse heating with relaxation parameters corresponding to polystyrene and poly(methyl methacrylate) is determined. The obtained results can be used to analyze the heat transfer process at the early stages of crystallization with fast formation of nanometer scale crystals

    Short-term stability in refractive status despite large fluctuations in glucose levels in diabetes mellitus type 1 and 2

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    Purpose: This work investigates how short-term changes in blood glucose concentration affect the refractive components of the diabetic eye in patients with long-term Type 1 and Type 2 diabetes. Methods: Blood glucose concentration, refractive error components (mean spherical equivalent MSE, J0, J45), central corneal thickness (CCT), anterior chamber depth (ACD), crystalline lens thickness (LT), axial length (AL) and ocular aberrations were monitored at two-hourly intervals over a 12-hour period in: 20 T1DM patients (mean age ± SD) 38±14 years, baseline HbA1c 8.6±1.9%; 21 T2DM patients (mean age ± SD) 56±11 years, HbA1c 7.5±1.8%; and in 20 control subjects (mean age ± SD) 49±23 years, HbA1c 5.5±0.5%. The refractive and biometric results were compared with the corresponding changes in blood glucose concentration. Results: Blood glucose concentration at different times was found to vary significantly within (p0.05). Minor changes of marginal statistical or optical significance were observed in some biometric parameters. Similarly there were some marginally significant differences between the baseline biometric parameters of well-controlled and poorly-controlled diabetic subjects. Conclusion: This work suggests that normal, short-term fluctuations (of up to about 6 mM/l on a timescale of a few hours) in the blood glucose levels of diabetics are not usually associated with acute changes in refractive error or ocular wavefront aberrations. It is therefore possible that factors other than refractive error fluctuations are sometimes responsible for the transient visual problems often reported by diabetic patients

    Effect of multi-step annealing above the glass transition temperature on the crystallization and melting kinetics of semicrystalline polymers

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    © Elsevier Ltd Fast scanning calorimetry (FSC) measurements were carried out for multi-step, isothermal, crystallized poly (butylene terephthalate) to quantify the effect of single-step to triple-step annealing above Tg (40 °C interval below the previous annealing temperature) on the crystallization/melting kinetics. In the case of double-step annealing, two endothermic peaks were observed on the FSC curves due to the melting of the crystal formed during the 1st step (base crystal; BC) and 2nd step (thermal history crystal; THC). The crystallization rate of the THC decreased due to the spatial restriction of the pre-existing BC. The melting kinetics of the THC were not affected by the time of 1st step crystallization. If the sample was re-heated to the 1st step temperature (Tc1) after multiple annealing, the thermal history of the previous annealing was completely erased. Moreover, in the re-annealing process at Tc1, secondary crystallization showed the same behavior as that expected from the result of single-step annealing

    On the crystal stabilization during two-step isothermal crystallization of poly(butylene terephthalate) examined by fast scanning calorimetry

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    Crystallization behaviors on two-step isothermal crystallization at Tc1 and Tc2(<Tc1) were examined by fast scanning calorimetry for poly(butylene terephthalate) in order to identify the dominant process during the secondary stage of crystallization at Tc1 after the completion of spherulitic growth under isothermal condition. From the difference between the melting peaks obtained before and after the low-temperature crystallization step at Tc2, the distinction of the following two processes became realizable: the growth of crystals formed at Tc2 and the stabilization of crystals formed at Tc1. The dependences on Tc2 and the duration of times Δtc1 and Δtc2 revealed the following: The formation and growth of new crystals are controlled by thermodynamic driving force determined by supercooling, and hence are suppressed at Tc1 higher than Tc2. The crystal stabilization is controlled by the mobility of polymer chains, and became more pronounced at Tc1. Therefore, the dominant process of the secondary crystallization under isothermal condition at Tc1 should be the stabilization of crystals formed in the primary stage and the formation of new crystals will only have a secondary effect
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