Energy management of a hybrid photovoltaic system

This work describes a new control strategy for active energy flow in a hybrid photovoltaic (PV) system. The method introduces an online energy management by a hierarchical fuzzy controller between energy sources that consist of a photovoltaic panel (PVP), the battery and the load. The fuzzy logic controller has been developed for power splitting between PVP and battery, and it makes decision to choose the switching chain rules and corresponding controller. Simulation test results illustrate improvement in the operation's efficiency of online state of the switches and the battery's state of charge (SOC) has been maintained at a reasonable level. Copyright © 2010 John Wiley & Sons, Ltd.     

Synthesis,structure and optical properties of x(CuO)/(1−x)Ni(OH)2 [x=0, 0.1 and 0.3] nanocomposites

The x(CuO)/(1−x)Ni(OH)₂ [x=0, 0.1 and 0.3] nanocomposites were prepared by the hydrothermal method in the presence of the surfactant polyethylenglycol-10000 (PEG-10000). X-ray diffraction (XRD), infrared (IR) spectroscopy, scanning electron microscopy (SEM) and transmission electron microscopy (TEM) were used to characterize the as-prepared samples. The increase of the CuO content led to the increase of the crystallite size of both, the β-Ni(OH)₂ and the CuO. The increase in the crystallite size greatly affects the band gap energy of the as-prepared nanocomposites. The band gap energies of the x(CuO)/(1−x)Ni(OH)₂ nanocomposites were estimated by UV–vis spectroscopic method. UV–vis spectroscopic results showed an apparent decrease in the direct band gap energies. The x(CuO)/(1−x)Ni(OH)₂ [x=0, 0.1 and 0.3] nanocomposites show low band gap energies compared to the Ni(OH)₂ bulk materials. The enhanced optical properties lead to their possible use in photocatalytic and photovoltaic applications.     

An advanced VHDL‐AMS PiN diode model: towards simulation‐based design of power converters

This paper focuses on the modeling of a power PiN diode. The focal point basis is the dependence on temperature. The PiN diode remains a difficult device to model mainly during switching transients. An advanced PiN diode temperature‐dependent model is developed and implemented in VHDL‐AMS. Heterogeneous simulation scheme including the circuit wiring parasitic components, the probe effects and the dependent diode models is successfully simulated using SIMPLORER simulator. Experimental data of several commercial PiN diodes are compared to simulation results at different temperature levels. A good rate of consistency is found. Copyright © 2014 John Wiley & Sons, Ltd.     

Experimentally validated analytical modeling of diesel engine power and in-cylinder gas speed dynamics

Supercharged diesel engines are a key element in diesel powertrains that have been extensively modelled yet often without explainable mathematical trends. The present paper demonstrates the analytical modelling of in-cylinder gas speed dynamics and engine brake power. These analytical models provide explainable mathematical trends. In addition, they provide gear-shifting-based modeling because the model parameters can be adjusted to reflect different driving conditions without the need for gathering field data. An unprecedented sensitivity analysis was conducted on these developed models for simplifying them. They were validated using experimental data and the relative error of the developed model of the in-cylinder gas speed dynamics was 9.8%. The study demonstrates with 73% coefficient of determination that the average percentage of deviation of the simulated results from the corresponding field data on the engine brake power is 6.9%. The relative error of the developed model of the engine brake power is 7%. These values of relative error are an order of magnitude of deviation that is less than that of widely recognized models in the field of vehicle powertrain modeling such as the CMEM and GT-Power. These analytically developed models serve as widely valid models. Having addressed and corrected flaws in the corresponding models, such as the model of the in-cylinder gas speed dynamics presented in a key reference in this research area, these developed models can help in better analyzing and assessing the performance of diesel engines.

     

Photoinitiierte Polymerisation mit Dialkoxythiocarbonyldisulfiden – eine Polymerisationsreaktion mit Primärradikalabbruch

Photoinitiated Polymerization with Dialkoxy Thiocarbonyl Disulfides – a Polymerization Reaction with Primary Radical Termination The photoinduced free radical polymerization of methyl methacrylate (MMA) and some other vinyl monomers using dialkoxy thiocarbonyl disulfides ( 1 – 4 ) as photoinitiators was studied. The photolysis of these initiators leads to cleavage of the S S bond, which was determined by spin trapping experiments with phenyl tert-butyl nitrone. No evidence was found for a further thermal decomposition of the primary alkoxy thiocarbonyl sulfide radicals (R·) at room temperature. In the absence of scavengers the primary radicals react back exclusively to the initial compounds, due to a strong cage effect. By means of UV spectroscopic measurements and in the presence of MMA the quantum yields of the initiator decomposition were detected to be 0.8. The polymerization of acrylic and methacrylic derivatives can be initiated by the R·, contrary to the situation with fumarates and maleates. The mechanism of MMA polymerization depends on the light intensity absorbed by the initiators. At high intensities the combination of primary and polymer radicals terminates the chain reaction. This follows from the measured monomer exponent of α = 2, the light intensity exponent of β = 0,2 and the number of thiocarbonyl end groups of 2 in the polymers isolated. Contrary to this, in the low intensity region the experimental data obey the ideal kinetic equation. Kinetic modelling gives evidence for an interaction of the monomer with the cage radicals.     

Dielectric analysis of α‐relaxation process of chlorinated poly(vinyl chloride) stabilized with nitro‐phenyl maleimide

Nitro‐phenyl maleimide (NPM), is the organic stabilizer for poly (vinyl chloride) (PVC), has been investigated as thermal plasticization for rigid chlorinated poly (vinyl chloride) (CPVC). Dielectric relaxation of CPVC stabilized with 10 wt% of NPM has been studied in temperature and frequency ranges of 300–450 K and 10 kHz–1 MHz, respectively. An analysis of the dielectric constant, ε′ and dielectric loss index, ε″, was performed assuming a plasticization effect of NPM molecules. The plasticization effect of NPM molecules was confirmed by the behavior of the dielectric modulus M′ and M″ spectra. A clear dielectric α‐relaxation process has been obtained in the studied temperature range. The results showed that NPM reduce the glass transition temperature, T_g, of CPVC by about 20 K. This effect has been assigned to the plasticization effect of NPM. At lower temperatures, dielectric modulus spectra reveal that there is a role of the effect of the electrode polarization in the relaxation process. The behavior AC conductivity, σ_ac, indicated that the conduction mechanism in all CPVC samples is hopping type conduction. POLYM. ENG. SCI., 2013. © 2012 Society of Plastics Engineers     

Copper activated LiF nanorods as TLD material for high exposures of gamma-rays

Lithium fluoride (LiF) doped with proper activators is a highly sensitive phosphor commonly used for radiation dosimetry using thermoluminescence (TL) technique. Nanorods of this material activated with Cu, Mg and P as single dopants are synthesized in our laboratory and exposed to gamma-rays for their thermoluminescence (TL) properties. The induced TL glow curves of the Cu, Mg and P doped samples are similar with a single peak at 410 K. Copper doped sample is found to be the most sensitive sample with TL intensity around 65, 7 and 8 times of those of LiF:Mg, LiF:P and LiF:Mg,Cu,P, respectively, indicating that Cu is the luminescence center in the host of LiF nanorods, while Mg and P act as TL quencher particularly when used as codopants. These observations on the nanostructured form of LiF doped with these activators are entirely different from those of the widely studied LiF:Mg,Cu,P and LiF:Mg,Ti single crystals. The nanorods of LiF:Cu might be used for heavy doses measurement as they are sensitive to gamma-rays and have a linear TL response curve in a long span of exposures.     

Can lanthanum doping enhance catalytic performance of silver in direct propylene epoxidation over NaMoAg/SiO_2?

In the attempt to reduce surface free energy of silica to improve interaction of silica with silver, silica was doped by different amounts of low surface energy lanthanum, La_2O_3, through impregnation. The doped and undoped silica were used as supports for preparation of Na/Ag/Mo/La_2O_3-SiO_2 catalysts. Catalytic performances of the catalysts were evaluated in direct epoxidation of propylene(DPO) using molecular oxygen under atmospheric pressure and without adding hydrogen. Adding 5 wt%La to the Na/Ag/Mo/SiO_2 catalyst improves both the catalysts electivity in DPO and its stability over 20h of time-on-stream.The characterization results show that La_2O_3 species interact strongly with silver particles on the silica surface which result in significant improvement in the dispersion profile of silver and marked decrease in the size of silver nanoparticles(AgNPs). The estimated mean diameter of AgNPs is ca. 4.0 nm in Na/Ag/Mo/5 wt%La_2O_3-SiO_2, which is smaller than that(53.9 nm) found in Na/Ag/SiO_2. The presence of subnanometer AgNPs on Ag/La_2O_3-SiO_2 prior addition of MoO_3 and NaCl to the sample can enhance the mutual electronic synergism between Ag, MoO_3 and Na for selective production of propylene oxide.     

Electrodeposition of lead dioxide on Fe electrode: application to the degradation of Indigo Carmine dye

Journal of Applied Electrochemistry - The modification of an iron electrode was carried out according to the following two steps. In a first step, a cathodic reduction is performed to form a film...