Vanadia-based coatings of self-repairing functionality for advanced magnesium Elektron ZE41 Mg–Zn–rare earth alloy

A smart vanadia protective coating of self-repairing functionality that has proven to provide superior corrosion resistance for several magnesium and aluminum alloys has successfully been designed by our group. A newly developed series of magnesium alloys, namely ZE41 alloy, has recently been proposed for automotive, electronics and aerospace applications. The advanced ZE41 alloy possesses very low density, high specific strength, and good castability and weldability characteristics compared to aluminum and steel based alloys. However, the corrosion resistance of ZE41 alloy in the presence of corrosive chloride environment is relatively low. The possibility of utilizing such coatings to add self-repairing functionalities to ZE41 alloy was discussed in this paper. The electrochemical corrosion behavior of the vanadia coatings over ZE41 alloy was investigated in 3.5% NaCl solution using EIS, linear polarization and cyclic voltammetry techniques. The optimum conditions for obtaining protective vanadia coatings of self-repairing abilities and improved localized corrosion resistance were determined. Surface examination of the coatings was investigated using SEM-EDS and macroscopic imaging.     

A kinetic study of nickel complexation in model systems by adsorptive cathodic stripping voltammetry

Adsorptive cathodic stripping voltammetry (AdCSV) in conjunction with the competing ligand-exchange method (CLEM) was investigated as a tool for measuring dissociation rate coefficients of nickel complexes in model systems. Dimethylglyoxime (DMG) was used as the competing ligand. Citric acid (CA) and a well-characterized fulvic acid (FA) were used as model ligands. The rate coefficients were calculated, and the consistency of equilibrium and kinetic data was discussed. The contributions of the disjunctive pathway (proceeding by the dissociation of the initial complex) and the adjunctive pathway (proceeding by the formation of an intermediate complex as a result of direct attack of the competing ligand on the initial complex) on the overall reactions were investigated. The reactions of Ni-CA or Ni-FA complexes with DMG were demonstrated to proceed by both disjunctive and adjunctive pathways. The predominant pathway for the overall reaction depends on the nickel-to-initial ligand and the DMG-to-initial ligand ratios. The reactions follow predominantly the disjunctive pathway for [DMG] > or = 3 mM and Ni-to-dissolved organic carbon (DOC) ratios greater than 10 nM Ni 2+/g of DOC. Since free nickel ion in freshwaters is reported to be toxic, its rate and pathway of formation are of environmental concern.     

Integration of PV system with SMES based on model predictive control for utility grid reliability improvement.

This paper describes the integration of a photovoltaic (PV) renewable energy source with a superconducting magnetic energy storage (SMES) system. The integrated system can improve the voltage stability of the utility grid and achieve power leveling. The control schemes employ model predictive control (MPC), which has gained significant attention in recent years because of its advantages such as fast response and simple implementation. The PV system provides maximum power at various irradiation levels using the incremental conductance technique (INC). The interfaced grid side converter of the SMES can control the grid voltage by regulating its injected reactive power to the grid, while the charge and discharge operation of the SMES coil can be managed by the system operator to inject/absorb active power to/from the grid to achieve the power leveling strategy. Simulation results based on MATLAB/Simulink® software prove the fast response of the system control objectives in tracking the setpoints at different loading scenarios and PV irradiance levels, while the SMES injects/absorbs active and reactive power to/from the grid during various events to improve the voltage response and achieve power leveling strategy.     

An implantable closedloop asynchronous drug delivery system for the treatment of refractory epilepsy

In this paper, we present an implantable device for intra-cerebral electroencephalography (icEEG) data acquisition and real-time epileptic seizure detection with simultaneous focal antiepileptic drug injection feedback. This implantable device includes a neural signal amplifier, an asynchronous seizure detector, a drug delivery system (DDS) including a micropump, and a hybrid subdural electrode (HSE). The asynchronous detection algorithm is based on data-dependent analysis and validated with Matlab tools. The detector and DDS have a power saving mode. The HSE contacts are made of Platinum (Pt) encapsulated with polydimethylsiloxane (PDMS). Given the heterogeneity of electrographic seizure signals and seizure suppression threshold, the implantable device provides tunable parameters facility through an external transmitter to adapt to each individual's neurophysiology prior to clinical deployment. The proposed detector and DDS were assembled in ? 50 mm and ? 30 mm circular printed circuit boards, respectively. The detector was validated using icEEG recordings of seven patients who had previously undergone an intracranial investigation for epilepsy surgery. The triggering of the DDS was tested and a predefined seizure suppression dose was delivered ~16 s after electrographical seizure onsets. The device's power consumption was reduced by 12% in active mode and 49% in power saving mode compared to similar seizure detection algorithms implemented with synchronous architecture.     

One-Pot Multicomponent Synthesis of Pyrazolo[3,4-d]pyrimidine-6-one Derivatives

An environmentally benign, simple, and efficient procedure has been developed for the one-pot multicomponent synthesis of pyrazolo[3,4-d]pyrimidine-6-one derivatives by the reaction of the variety of aryl-aldehydes, 5-methyl-2-phenyl-2,4-dihydro-3H-pyrazol-3-one, and urea in the presence of catalytic amount of poly(N-vinylpyridinium) hydrogen sulfate in glycerol. The present method affords non-toxic and non-corrosive medium, short reaction times, high yield of the products, mild reaction conditions as well as simple experimental and isolation procedures. The catalyst can be recycled by simple filtration and reused without any significant reduction in its activity.     

Liquid-Phase Catalytic Hydroxylation of Phenol Using Cu(II), Ni(II) and Zn(II) Complexes of Amidate Ligand Encapsulated in Zeolite-Y as Catalysts

Copper(II), nickel(II) and zinc(II) complexes of amidate ligand 1,2-bis(2-hydroxybenzamido)ethane(H₂hybe) encapsulated in the super cages of zeolite-Y have been prepared and characterized by spectroscopic studies and thermal as well as X-ray diffraction (XRD) patterns. These complexes catalyze the liquid-phase hydroxylation of phenol with H₂O₂ to catechol as a major product and hydroquinone as a minor product. Considering the concentration of substrate and oxidant, amount of catalyst, temperature of the reaction and volume of solvent, a best-suited reaction condition has been optimized to get maximum hydroxylation. Under the optimized reaction conditions, [Cu(hybe)]-Y has shown the highest conversion of 40% after 6h, which is followed by [Ni(hybe)]-Y with 37% conversion and [Zn(hybe)]-Y has shown the poorest performance with 33% conversion. All these catalysts are more selective towards catechol formation (90%), irrespective of their catalytic performance.     

Oxidation and Oxidative Bromination Reactions Catalyzed By a Reusable Polymer-Anchored Iron(III) Complex in Water at Room Temperature

A polymer-anchored iron(III) catalyst was synthesized and characterized. Its catalytic activity was evaluated for the oxidation of various alkenes, sulfides, aromatic alcohols and ethylbenzene with 30 % H₂O₂ as the oxidizing agent. The catalyst was also effective for the oxidative bromination reaction with 80–100 % selectivity of monobrominated products with H₂O₂/KBr at room temperature. The above reactions require a minimum amount of H₂O₂ and short reaction time. Most importantly, all the above reactions occur in aqueous medium. The catalyst can be facilely recovered and reused six-atimes without significant decrease in its activity and selectivity.     

Performance analysis of switch‐and‐examine diversity systems with interference and Rayleigh fading channels

This paper studies the behavior of the low‐complexity switch‐and‐examine diversity combining (SEC) and switch‐and‐examine diversity combining with post‐examine selection (SECps) antenna selection schemes with interference. In this paper, we first derive the cumulative distribution function (CDF) of the end‐to‐end (e2e) signal‐to‐interference plus noise ratio at the selection scheme combiner output. This CDF is then used to derive closed‐form expressions for the e2e outage and symbol error probabilities for the independent nonidentically distributed and independent identically distributed cases of diversity branches. In the analysis, the channels of the desired user and the interferers are assumed to follow Rayleigh distribution. Furthermore, to have more details about the system insights, the performance is evaluated at the high signal‐to‐noise ratio (SNR) values where the diversity order and coding gain are derived and analyzed. The derived analytical and asymptotic results are validated via a comparison with Monte‐Carlo simulations. Main findings show that with interference power does not scale with average SNR; the system can still achieve performance gain when more receive antennas are used. This happens at the values of switching threshold that are close to average SNR. Also, results illustrate that the interference is noticeably affecting the gain achieved in system performance when more antennas are used. Furthermore, findings show that the SECps selection scheme outperforms the conventional SEC scheme when more antennas are added with the switching threshold is much larger than the average SNR. Finally, findings show that the SEC and SECps antenna selection schemes are efficient for systems which operate at the range of low SNR values and this makes them attractive candidates to be implemented in the emerging mobile broadband communication systems. Copyright © 2015 John Wiley & Sons, Ltd.