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Abstract Persistent luminescence (PersL), also called long-lasting phosphorescence or simply afterglow, is a luminescence characterised by the emission of radiation from a few seconds to several days after the excitation source has been switched off. Over the past two decades, research on PersL materials, both in fundamental and applied physics, has developed rapidly; however, the explanation for the physical processes that cause afterglow still needs to be clarified. Today, PersL materials are used mainly for luminescent paints, safety signs and decorations. At the same time, research into using such materials in medicine, information storage, anti-counterfeiting technology, etc., is underway. Currently, information on the long persistent luminescence materials with emission in the blue and green spectral range is widely available. In contrast, the number of publications on the afterglow in the red and near-infrared spectral range is considerably lower. Within the framework of this research, Mg2SiO4: Mn2+; M3+ (M3+ = B3+; Al3+; Ga3+; In3+) materials were synthesised using solid state reaction synthesis. When excited with X-rays, the materials exhibited a broad Mn2+ PersL band with two maxima at approximately 625 nm and 730 nm. After cessation of irradiation, an afterglow of at least 6 hours could be observed. The research focuses on the trap properties of the materials. It was concluded that at least three discrete trap levels with activation energies approximately between 0.4–1.6 eV were present in the samples. Additionally, co-doping with Al3+; Ga3+; In3+ ions improved PersL longevity of the Mg2SiO4: Mn2+ material.

A membrane assisted process for green hydrogen production from a bioethanol derived feedstock is here developed and evaluated, starting from the conventional Steam Methane Reforming (SMR) process. Such a process is suitable for centralized hydrogen production, and is here analyzed for a large-scale H2 production unit with the capacity of 40.000 Nm3/h. The basic Steam Ethanol Reforming (SER) process scheme is modified in a membrane assisted process by integrating the Pd-membrane separation steps in the most suitable reaction steps. The membrane assisted process, configured in three alternative architectures (Open architecture, Membrane Reactor and Hybrid architecture) was evaluated in terms of efficiencies and hydrogen yields, obtaining a clear indication of improved process performance. The alternative membrane assisted process architectures are compared to the basic SER process and to the benchmark SMR process fed by natural gas, for an overall comparative assessment of the efficiency and specific CO2 emissions and for an economic analysis based on the operating expenditures.

The growth of self-ordered anodic aluminum oxide (AAO) templates with pore diameters in the 140-400 nm range is achieved by anodization in phosphoric acid at low temperatures (-4 °C). The procedure used in this study is able to completely avoid the >burning> of the oxide, highly frequent in anodizations in phosphoric acid solutions at high voltages. The current density measured during the anodizations is rather low, 0.6-0.7 mA/cm2; therefore, low growth rates have been also measured (<2 μm/h). AAO templates present a relatively low porosity value of 8.4%. However, a considerable pore-enlargement-rate (vΔd = 0.636 ± 0.101 nm/h) has been observed as a consequence of the chemical dissolution of the pore walls during the anodization. Thus, the results reported here constitute an exhaustive study on the preparation of large-diameter-pore self-ordered AAO templates that enables both to access to pore diameters up to now inaccessible and to efficiently overcome the difficulties of their fabrication process ascribed to its aggressive reaction conditions. © 2011 Elsevier Inc. All rights reserved. Authors want to thank the ERC 2008 Starting Grant number 240497 for financial support. Peer Reviewed

Abstract Coal gasification is accompanied with formation of tars that cause equipment problems and have to be removed from the raw gas. Our previous studies proved that nickel supported ceria-zirconia catalyst (Ni/CZ) reveals high activity towards decomposition of toluene and 1-methylnaphthalene (1-MN) via steam reforming reaction (SR). However, the components of the raw gas from coal gasification (i.e. H2, CO, CO2 and CH4) may influence the performance of Ni/CZ catalyst. The influence of particular components of the raw gas on catalyst performance during SR of model tar compounds have been studied and discussed in this paper. It has been found that H2 and CO addition to the steam reforming feed drastically decreases the activity of Ni/CZ catalyst, whereas CO2 presence enhances conversion of toluene and 1-MN mixture owing to the occurrence of dry reforming reaction (DR). It has also been observed that methane, which is present in the raw gas from coal gasification consumes partly both the H2O and CO2, causing some decrease in conversion of model tar compounds. The influence of contact time (tc) on hydrocarbons conversion and the participation of (DR) have been examined. As was observed, lower contact times lead to decrease in hydrocarbons conversion in SR, making the same participation of DR more pronounced than for higher tc values. This work proves that Ni/CZ catalyst can be used for removal of tarry compounds via the catalytic hot gas cleaning of the raw gas form coal gasification.

AbstractSmart Grids are electrical grids that require a decentralised way of controlling electric power conditioning and thereby control the production and distribution of energy. Yet, the integration of Distributed Renewable Energy Sources (DRESs) in the Smart Grid introduces new challenges with regards to electrical grid balancing and storing of electrical energy, as well as additional monetary costs. Furthermore, the future smart grid also has to take over the provision of Ancillary Services (ASs). In this paper, a distributed ICT infrastructure to solve such challenges, specifically related to ASs in future Smart Grids, is described. The proposed infrastructure is developed on the basis of the Smart Grid Architecture Model (SGAM) framework, which is defined by the European Commission in Smart Grid Mandate M/490. A testbed that provides a flexible, secure, and low-cost version of this architecture, illustrating the separation of systems and responsibilities, and supporting both emulated DRESs and real hardware has been developed. The resulting system supports the integration of a variety of DRESs with a secure two-way communication channel between the monitoring and controlling components. It assists in the analysis of various inter-operabilities and in the verification of eventual system designs. To validate the system design, the mapping of the proposed architecture to the testbed is presented. Further work will help improve the architecture in two directions; first, by investigating specific-purpose use cases, instantiated using this more generic framework; and second, by investigating the effects a realistic number and variety of connected devices within different grid configurations has on the testbed infrastructure.

Abstract The need to increase energy system flexibility, alongside the need to lower fossil fuel use in the food sector, and the importance of refrigeration infrastructure presents an opportunity for Liquid Air Energy Storage (LAES) integrated with refrigerated warehouses. To quantify this opportunity in Europe we analyse energy scenarios and existing refrigeration infrastructure for four countries with diverse energy systems (UK, Spain, Bulgaria and Germany). We find that with growing levels of electricity generation from variable renewable sources and numerous refrigerated warehouses, LAES has the potential to provide value in many areas of the EU through the 2020s. However, LAES is still pre-commercial, and with the proportion of electricity from variable renewable sources still low in many countries it is likely that LAES will not be deployed widely alongside refrigerated warehouses under current market conditions. Countries such as the UK and Spain, which have the greatest need for additional energy system flexibility and the most refrigerated warehouses are likely to gain the most value initially.

This paper studies the vibrational motion of a dynamical system connected to an electromagnetic device, which is one of the energy harvesting (EH) devices that transform the vibrational motion into electric energy. This system has three degrees-of-freedom (DOF) and consists of two linked parts attached together; one is a nonlinear Duffing oscillator, and the other is a nonlinear damping spring pendulum. The regulating equations of motion (EOM) are achieved utilizing Lagrange’s equations and solved analytically applying the approach of multiple scales (AMS) till the third order of approximation. The accuracy of the attained solutions has been examined by comparing them with the numerical ones of the EOM. The time histories of the solutions and the nonlinear stability analysis of the modulation equations are represented graphically in various plots. The Poincaré maps and phase portraits diagrams displayed the stable behavior of the studied dynamical system. In addition, the different ranges of the stabilities are examined and discussed. In the electromagnetic device, the output power and current time series are depicted as a function of different values of the damping coefficients, excitation amplitudes, and load resistance. It is noted that the output current and power are dropped when the damping coefficient is raised. On the other hand, the increment of the excitation has a positive effect on the electrical generation and produces increment of the output power and current. Furthermore, the output power grows when the total resistance increases to accommodate the applied load. The EH device generates high output current and power at low-frequency values. The significance of this work is limited to the numerous uses of its outcomes in everyday life, such as powering medical devices, serving as a power supply for sensors, and serving as a backup energy source for some electronic devices.