Reducing the undesirable effects of wind farms＇ high-penetration on frequency

This paper reviews the effects caused by a high penetration of wind farms on network frequency. Energy generation in wind farms that use induction generators （as installed in Manjil Power Plant） is simulated, and, assuming that wind farm units provide 10% of the network power, the effect on frequency is studied, and it is shown that such a high penetration of the wind farms has a destructive effect on network frequency. It will be shown that the negative effects can be compensated for by using stored energy, but in the absence of energy storage equipments like SMES （Super Magnetic Energy Storage）, this solution is beyond reach. An alternative method is presented that is based on Rotary Frequency Converter （RFC）, and, as can be seen in the simulations, the wind farm output creates fewer disturbances, and frequency variations can be controlled considerably.     

Non‐linear behavior of yielding damped braced frames

Since the nature of an earthquake is the energy which is released due to tectonic events, improvements of behaviour of structures based on energy concepts have been a matter of great concern. Input energy must be dissipated by structures in order to decrease earthquake damage. For this purpose the YDBF (yielding damped braced frame) system is presented, which acts as a fuse when an earthquake occurs. Because of the high ductility of this system, damage to the main structural elements such as columns is prevented, and because of the non‐linear behaviour of such a system, which is based on the yielding of ductile steel, YDBF increases hysteretic dissipated energy. This class of dampers often yields in high or intermediate earthquake shakes and their hysteretic loops are relatively thick and stable. In this research seven YDBF system are modelled. These models are tested with various percentages of opening and the results of structural behaviour due to variation of opening percentages are compared. Copyright © 2004 John Wiley & Sons, Ltd.     

Hydrogen separation and purification in membranes of miscible polymer blends with interpenetration networks

This study demonstrates the successful implications of blending technique cum chemical modification for the fabrication of high performance polymeric membranes for gas separation applications. The effect of variation in composition on miscibility and microstructure, gas permeability and selectivity of blend membranes is investigated. It is found that augmentation in PBI composition results in enhancement in gas separation performance of membranes which is attributed mainly to the effect of diffusivity selectivity. Analysis of the microstructure of membranes confirms the variations in chain packing density, d-spacing and segmental mobility of polymer chains as a result of blending. Separation performance of membranes is further ameliorated through chemical modification of blend constituents. Modification of PBI phase with p-xylene dichloride brings about slight improvements in selectivity performance, especially for H₂/CO₂ and H₂/N₂. In contrast, the selectivity of membranes is improved significantly after cross-linking of Matrimid phase with p-xylene diamine. The results indicate that higher tendency of Matrimid toward cross-linking reaction contributes more in controlling the transport properties of membranes through diffusion coefficient by increase in chain packing density and diminishing the excess free volumes. Results obtained in this study reveal the promising features of developed membranes for gas separation applications with great potential for hydrogen separation and purification on industrial scale.     

Boehmite nanopetals self assembled to form rosette-like nanostructures

Rosette-like boehmite nanostructures were prepared successfully via a simple hydrothermal process. The obtained material was characterized with X-ray powder diffractometry (XRD), transmission electron microscopy (TEM) and scanning electron microscopy (SEM). Using Scherrer formula, the average crystallite size of the obtained boehmite rosettes was measured to be about 8 nm. It was shown that boehmite nanopetals with average width of about 41 nm determined by TEM, were formed during the hydrothermal process and then self assembled due to weak hydrogen bonds to fabricate boehmite rosettes. The specific surface area of the obtained rosette-like nanostructures was calculated through BET N₂-adsorption technique to be about 143.08 m²/g.     

Investigation of styrene/1‐hexene copolymerization by homogeneous and heterogeneous bisindenyl ethane zirconium dichloride catalyst system

Homogeneous copolymerization of styrene and 1‐hexene was carried out in toluene at room temperature using bisindenyl ethane zirconium dichloride/methylaluminoxane (MAO). The supported catalyst was prepared with immobilization of Et(Ind)₂ZrCl₂/MAO on silica (calcinated at 500°C) with premixed method. Heterogeneous copolymerization of styrene/1‐hexene with different mole ratios was carried out in the presence of supported catalyst system. The copolymers obtained from homogeneous and heterogeneous catalyst system were characterized by ¹H NMR and ¹³C NMR. Composition of the resulting copolymers was determined by ¹H NMR data. Analysis of ¹³C NMR spectra of obtained copolymers by homogeneous and heterogeneous catalyst systems present isotactic olefin‐enriched copolymers. Molecular weight and thermal behavior of resulting copolymers was investigated. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 4008–4014, 2007     

Molecular dynamics simulation for investigating and assessing reaction conditions between carboxylated polyethersulfone and polyethyleneimine

Recently, nano-filtration membranes are made by the reaction between a reactive functional group on the surface of a tight ultrafiltration membrane and a charged branched polymer. This reaction makes the selective layer of the nanofiltration membrane, which plays an essential role in membrane performance. A molecular dynamics simulation with a reactive force field was used to investigate the reaction of carboxylated polyethersulfone as the functional group of the ultrafiltration membrane with polyethyleneimine. Experimental elucidation of the reaction between the PEI amine and carboxyl groups is challenging, and an MD simulation was thus employed. Furthermore, the simulation results show that the PEI and carboxylated polyethersulfone polymers react with each other in a temperature-dependent manner. While no reaction occurs at 298 K, carboxylated polyethersulfone and PEI begin to react when the temperature is increased from 298 to 323 K. Furthermore, a reversible reaction was observed with a subsequent increase in temperature to 353 K.