2,424 research outputs found

    Demonstration of wide band RF photonic transversal phase-shifter

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    A transversal phase-shifter using multiple MZMs is demonstrated. The device exhibits continuously variable phase-shift exceeding 360° at 2 GHz and amplitude uniformity within 3 dB over 0.2-2 GHz. The device stability and practicality are discussed

    Wide-band variable transversal phase-shifter

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    We present a novel broadband phase-shifter based on a transversal filter configuration. This approach allows flexible control of the amplitude response while providing continuous variation of a linear phase slope. Numerical examples, both ideal and using practical RF components are presented and practical challenges in realising the phase-shifter are identified

    Wideband RF photonic vector sum phase-shifter

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    A novel broadband linear phase phase-shifter based on the vector summation method is proposed. A photonic implementation of the phase-shifter with a continuously variable linear phase-shift up to 120° over the frequency range of DC-4 GHz is demonstrated. Good agreement between the measured responses and theoretical predictions is obtained

    Synergistic and Antagonistic Effects of Aromatics on the Agglomeration of Gas Hydrates

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    Surfactants are often used to stabilize aqueous dispersions. For example, surfactants can be used to prevent hydrate particles from forming large plugs that can clog, and sometimes rupture pipelines. Changes in oil composition, however dramatically affect the performance of said surfactants. In this work we demonstrate that aromatic compounds, dissolved in the hydrocarbon phase, can have both synergistic and antagonistic effects, depending on their molecular structure, with respect to surfactants developed to prevent hydrate agglomerations. While monocyclic aromatics such as benzene were found to disrupt the structure of surfactant films at low surfactant density, they are expelled from the interfacial film at high surfactant density. On the other hand, polycyclic aromatics, in particular pyrene, are found to induce order and stabilize the surfactant films both at low and high surfactant density. Based on our simulation results, polycyclic aromatics could behave as natural anti-agglomerants and enhance the performance of the specific surfactants considered here, while monocyclic aromatics could, in some cases, negatively affect performance. Although limited to the conditions chosen for the present simulations, the results, explained in terms of molecular features, could be valuable for better understanding synergistic and antagonistic effects relevant for stabilizing aqueous dispersions used in diverse applications, ranging from foodstuff to processing of nanomaterials and advanced manufacturing

    Wafer scale texturing of LiNbO3

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    We report a novel technique for micro texturing of LiNbO<sub>3</sub>. Well-defined raised ridges and etched trenches are demonstrated. This technique is suitable for the realization of surface relief gratings and photonic crystals

    Etching of lithium niobate using standard Ti indiffusion technique

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    We present evidence of etching LiNbO3 when annealing two wafers in contact with an intermediate Ti strip. Etched features are characterized qualitatively using atomic force microscopy. The impact of the Ti strip thickness on the depth and roughness of the etched surface is quantified. Etched trenches of similar depths to the original Ti film are achieved with very smooth etched surface

    Instantaneous frequency measurement system using optical mixing in highly nonlinear fiber

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    A broadband photonic instantaneous frequency measurement system utilizing four-wave mixing in highly nonlinear fiber is demonstrated. This new approach is highly stable and does not require any high-speed electronics or photodetectors. A first principles model accurately predicts the system response. Frequency measurement responses from 1 to 40 GHz are demonstrated and simple reconfiguration allows the system to operate over multiple bands

    Antineutrino emission and gamma background characteristics from a thermal research reactor

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    The detailed understanding of the antineutrino emission from research reactors is mandatory for any high sensitivity experiments either for fundamental or applied neutrino physics, as well as a good control of the gamma and neutron backgrounds induced by the reactor operation. In this article, the antineutrino emission associated to a thermal research reactor: the OSIRIS reactor located in Saclay, France, is computed in a first part. The calculation is performed with the summation method, which sums all the contributions of the beta decay branches of the fission products, coupled for the first time with a complete core model of the OSIRIS reactor core. The MCNP Utility for Reactor Evolution code was used, allowing to take into account the contributions of all beta decayers in-core. This calculation is representative of the isotopic contributions to the antineutrino flux which can be found at research reactors with a standard 19.75\% enrichment in 235^{235}U. In addition, the required off-equilibrium corrections to be applied to converted antineutrino energy spectra of uranium and plutonium isotopes are provided. In a second part, the gamma energy spectrum emitted at the core level is provided and could be used as an input in the simulation of any reactor antineutrino detector installed at such research facilities. Furthermore, a simulation of the core surrounded by the pool and the concrete shielding of the reactor has been developed in order to propagate the emitted gamma rays and neutrons from the core. The origin of these gamma rays and neutrons is discussed and the associated energy spectrum of the photons transported after the concrete walls is displayed.Comment: 14 pages, 11 figures, Data in Appendix A and B (13 pages

    Modelling Li+ Ion Battery Electrode Properties

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    We formulated two detailed models for an electrolytic cell with particulate electrodes based on a lithium atom concentration dependent Butler-Volmer condition at the interface between electrode particles and the electrolyte. The first was based on a dilute-ion assumption for the electrolyte, while the second assumed that Li ions are present in excess. For the first, we used the method of multiple scales to homogenize this model over the microstructure, formed by the small lithium particles in the electrodes. For the second, we gave rigorous bounds for the effective electrochemical conductivity for a linearized case. We expect similar results and bounds for the "full nonlinear problem" because variational results are generally not adversely affected by a sinh term. Finally we used the asymptotic methods, based on parameters estimated from the literature, to attain a greatly simplified one-dimensional version of the original homogenized model. This simplified model accounts for the fact that diffusion of lithium atoms within individual electrode particles is relatively much faster than that of lithium ions across the whole cell so that lithium ion diffusion is what limits the performance of the battery. However, since most of the potential drop occurs across the Debye layers surrounding each electrode particle, lithium ion diffusion only significantly affects cell performance if there is more or less complete depletion of lithium ions in some region of the electrolyte which causes a break in the current flowing across the cell. This causes catastrophic failure. Providing such failure does not occur the potential drop across the cell is determined by the concentration of lithium atoms in the electrode particles. Within each electrode lithium atom concentration is, to leading order, a function of time only and not of position within the electrode. The depletion of electrode lithium atom concentration is directly proportional to the current being drawn off the cell. This leads one to expect that the potential of the cell gradually drops as current is drawn of it. We would like to emphasize that all the homogenization methods employed in this work give a systematic approach for investigating the effect that changes in the microstructure have on the behaviour of the battery. However, due to lack of time, we have not used this method to investigate particular particle geometries
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