3,379,993 research outputs found

    CVD of CrO2: towards a lower temperature deposition process

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    We report on the synthesis of highly oriented a-axis CrO2 films onto (0001) sapphire by atmospheric pressure CVD from CrO3 precursor, at growth temperatures down to 330 degree Celsius, i.e. close to 70 degrees lower than in published data for the same chemical system. The films keep the high quality magnetic behaviour as those deposited at higher temperature, which can be looked as a promising result in view of their use with thermally sensitive materials, e.g. narrow band gap semiconductors.Comment: 13 pages, 4 figure

    Si/SiC-Ceramic low process shrinkage - high temperature material for the Laser Sinter process

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    Actual RP-systemsare very limited in producing adequate ceramic prototypes. In the presented process, the SiC..green part manufacturing bythe laser sintering process in combination with special postprocessing allows the fast production of SUSiC prototypes. A mixture of SiC powder and a reactive polymer binder system is used in the Laser Sinter process. In the following postprocessing the porous green part has to be .infiltrated with a precursor resin, carbonised and finally infiltrated withimolten silicon.•Incontrast to cold isostatic moulding or slip casting the shrinkage is very low (2-4 0/0).• Experiments with suitable materials/and process conditions were successful. This paper will show the state of and the possible further investigation into process.Mechanical Engineerin

    Fabrication process of a high temperature polymer matrix engine duct

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    The process that was used in the molding of an advanced composite outer by-pass duct planned for the F404 engine is discussed. This duct was developed as a potential replacement for the existing titanium duct in order to reduce both the weight and cost of the duct. The composite duct is now going into the manufacturing technology portion of the program. The duct is fabricated using graphite cloth impregnated with the PMR-15 matrix system

    Slow dynamics near glass transitions in thin polymer films

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    The α\alpha-process (segmental motion) of thin polystyrene films supported on glass substrate has been investigated in a wider frequency range from 103^{-3} Hz to 104^4 Hz using dielectric relaxation spectroscopy and thermal expansion spectroscopy. The relaxation rate of the α\alpha-process increases with decreasing film thickness at a given temperature above the glass transition. This increase in the relaxation rate with decreasing film thickness is much more enhanced near the glass transition temperature. The glass transition temperature determined as the temperature at which the relaxation time of the α\alpha-process becomes a macroscopic time scale shows a distinct molecular weight dependence. It is also found that the Vogel temperature has the thickness dependence, i.e., the Vogel temperature decreases with decreasing film thickness. The expansion coefficient of the free volume αf\alpha_f is extracted from the temperature dependence of the relaxation time within the free volume theory. The fragility index mm is also evaluated as a function of thickness. Both αf\alpha_f and mm are found to decrease with decreasing film thickness.Comment: 9 pages, 7 figures, and 2 table

    NMR Studies on the Temperature-Dependent Dynamics of Confined Water

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    We use 2^2H NMR to study the rotational motion of supercooled water in silica pores of various diameters, specifically, in the MCM-41 materials C10, C12, and C14. Combination of spin-lattice relaxation, line-shape, and stimulated-echo analyses allows us to determine correlation times in very broad time and temperature ranges. For the studied pore diameters, 2.1-2.9 nm, we find two crossovers in the temperature-dependent correlation times of liquid water upon cooling. At 220-230 K, a first kink in the temperature dependence is accompanied by a solidification of a fraction of the confined water, implying that the observed crossover is due to a change from bulk-like to interface-dominated water dynamics, rather than to a liquid-liquid phase transition. Moreover, the results provide evidence that α\alpha process-like dynamics is probed above the crossover temperature, whereas β\beta process-like dynamics is observed below. At 180-190 K, we find a second change of the temperature dependence, which resembles that reported for the β\beta process of supercooled liquids during the glass transition, suggesting a value of Tg ⁣ ⁣185T_g\!\approx\!185 K for interface-affected liquid water. In the high-temperature range, T ⁣> ⁣225T\!>\!225 K, the temperature dependence of water reorientation is weaker in the smaller C10 pores than in the larger C12 and C14 pores, where it is more bulk-like, indicating a significant effect of the silica confinement on the α\alpha process of water in the former 2.1 nm confinement. By contrast, the temperature dependence of water reorientation is largely independent of the confinement size and described by an Arrhenius law with an activation energy of Ea ⁣ ⁣0.5 E_a\!\approx\!0.5\ eV in the low-temperature range, T ⁣< ⁣180T\!<\!180 K, revealing that the confinement size plays a minor role for the β\beta process of water.Comment: 12 pages, 9 figure

    History dependent crystallization of Zr41Ti14Cu12Ni10Be23 melts

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    The crystallization of Zr41Ti14Cu12Ni10Be23 (Vit 1) melts during constant heating is investigated. (Vit 1) melts are cooled with different rates into the amorphous state and the crystallization temperature upon subsequent heating is studied. In addition, Vit 1 melts are cooled using a constant rate to different temperatures and subsequently heated from this temperature with a constant rate. We investigate the influence of the temperature to which the melt was cooled on the crystallization temperature measured upon heating. In both cases the onset temperature of crystallization shows strong history dependence. This can be explained by an accumulating process during cooling and heating. An attempt is made to consider this process in a simple model by steady state nucleation and subsequent growth of the nuclei which results in different crystallization kinetics during cooling or heating. Calculations show qualitative agreement with the experimental results. However, calculated and experimental results differ quantitatively. This difference can be explained by a decomposition process leading to a nonsteady nucleation rate which continuously increases with decreasing temperature

    Features of modelling dynamics for heating processes of cylindrical cast iron products in gas ovens

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    The process of heating the billets of rolling mills from cast iron in gas heating ovens (both in covalent and casting floors) has clear requirements for temperature heating regimes. Compliance with the requirements of technology is possible with the use of automatic control devices. Programmable logic controllers are commonly used as a temperature control device. Correct operation of automation is possible because of a definite model of the heating process dynamics
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