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您的检索式：作者名="Daniel D.Joseph"
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| 1 | Thermoluminescence characteristics and dosimetric aspects of fluoroperovskites (NaMgF_3:Eu^(2+),Ce^(3+))显示文摘The perovskite-like NaMgF3 polycrystalline powder samples, pure and rare earth doped, were synthesized by conventional solid state reaction method. The perovskite material was doped with 0.2 mol.% of EuF3 and CeF3 impurity. Phase purity of synthesized compounds was analyzed by powder X-ray diffraction technique. The thermoluminescence response of polycrystalline samples showed a linear response up to 12 Gy and then became sub linear at higher doses. The order of kinetics(b), activation energy(E) and other trapping parameters were calculated using peak shape method and variable heating rate method. From glow curve analysis the symmetric factor was calculated. The glow curve showed two peaks at 404 and 488 K, and both of them confirmed the thermoluminescence in the phosphor, which obeyed second-order kinetics. The experimental resulted showed that this phosphor could have potential applications in radiation dosimetry. | D.Joseph Daniel O.Annalakshmi U.Madhusoodanan P.Ramasamy | 2014 | Journal of Rare Earths2014，32，6： | 3 |
| 2 | Particles dispersion on fluid-liquid interfaces显示文摘This paper is concerned with the dispersion of particles on the fluid-liquid interface. In a previous study we have shown that when small particles, e.g., flour, pollen, glass beads, etc., contact an air-liquid interface, they disperse rapidly as if they were in an explosion. The rapid dispersion is due to the fact that the capillary force pulls particles into the interface causing them to accelerate to a large velocity. In this paper we show that motion of particles normal to the interface is inertia dominated; they oscillate vertically about their equilibrium position before coming to rest under viscous drag. This vertical motion of a particle causes a radially-outward lateral (secondary) flow on the interface that causes nearby particles to move away. The dispersion on a liquid-liquid interface, which is the primary focus of this study, was relatively weaker than on an air-liquid interface, and occurred over a longer period of time. When falling through an upper liquid the particles have a slower velocity than when falling through air because the liquid has a greater viscosity. Another difference for the liquid-liquid interface is that the separation of particles begins in the upper liquid before the particles reach the interface. The rate of dispersion depended on the size of the particles, the densities of the particle and liquids, the viscosities of the liquids involved, and the contact angle. For small particles, partial pinning and hysteresis of the three-phase contact line on the surface of the particle during adsorption on liquid-liquid interfaces was also important. The frequency of oscillation of particles about their floating equilibrium increased with decreasing particle size on both air-water and liquid-liquid interfaces, and the time to reach equilibrium decreased with decreasing particle size. These results are in agreement with our analysis. | Sathish Gurupatham Bhavin Dalal Md.Shahadat Hossain Ian S.Fischer Pushpendra Singh Daniel D.Joseph | 2011 | Particuology2011，9，1： | 0 |
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