Thin layer chromatography of 57 metal ions on an inorganic ion-exchanger in mixed solvent systems

Summary Thin layers of stannic arsenate have been used to study the chromatographic behaviour of 57 metal ions in different mixed solvents. Au³⁺, Hg²⁺, UO ₂ ²⁺ , Be²⁺ and Al³⁺ and others can be easily separated from numerous metal ions. Fast quaternary, ternary and binary separations have been also achieved. Important separations are discussed. The effect of pH, duration of heating of ionexchanger plates and layer thickness on the R_f values has been studied and discussed. It is shown that Lederer's equation is also obeyed by thin layers of stannic arsenate, if instead of concentration of Na⁺ ion its activity is taken into consideration.     

Dispersion and deposition mechanisms of particles suspended in a turbulent plane Couette flow

Inertial particle transfer in a turbulent plane Couette flow (C flow) was studied using Direct Numerical Simulation (DNS) of the flow combined with a Lagrangian particle tracking approach for particles with Stokes numbers (St) 5, 25 and 125. The particle concentration was assumed low enough, so that the simulations were done under one-way coupling condition.     

Development of a new synthesis approach for S-pregabalin by optimizing the preparation stages

Journal of the Iranian Chemical Society - In the present study, we aimed to optimize the synthesis stages of S-pregabalin ((S)-3-(aminomethyl)-5-methylhexanoic acid), a well-known anticonvulsant...     

Guaranteed cost nonlinear sampled-data control: applications to a class of chaotic systems

Nonlinear Dynamics - This paper addresses the guaranteed cost sampled-data controller synthesis and analysis problems with application to nonlinear chaotic systems. A linear parameter-varying (LPV)...     

Electrochemically induced oxidative cyclization of 2,3‐dihydroxypyridine. Synthesis of a novel highly oxygenated heterocyclic compound

Electrochemical oxidation of 2,3‐dihydroxypyridine in aqueous phosphate buffer solution at a glassy carbon electrode has been studied using cyclic voltammetry and controlled potential coulometry. The results indicate that oxidation of 2,3‐dihydroxypyridine on glassy carbon electrode shows an irreversible feature in aqueous solution. This data indicates that the electrochemically generated pyridindione is unstable and via an oxidative conversion pathway converts to a novel highly oxygenated heterocyclic compound. By means of the obtained electrochemical data, an efficient, one‐pot method for the synthesis of this heterocyclic compound based on the oxidative cyclization of 2,3‐dihydroxypyridine under green conditions, and in a good yield and purity is described. Copyright © 2011 John Wiley & Sons, Ltd.     

Al(HSO4)3 and Al2O3-SO3H as Efficient Catalysts for Modified Preparation of 3,4-Dihydropyrimidin-2 (1H)-ones/thiones

An environmentally friendly procedure for the preparation of dihydropyrimidinone derivatives or their sulfur analogues under thermal solvent-free conditions in the presence of aluminium hydrogen sulfate [Al(HSO₄)₃] and alumina sulfuric acid (Al₂O₃-SO₃H) as heterogeneous catalysts was developed.     

Kinetic study of electrochemically induced Michael reaction of1,4-dihydroxyanthraquinone with acetylacetone and benzoylacetone

The electrochemical oxidation of 1,4-dihydroxyanthraquinone has been studied in the presence of acetylacetone and benzoylacetone as nucleophiles in a mixture of ethanol/water by means of cyclic voltammetry as a diagnostic technique.The results indicate the participation of electrochemically produced anthraquinone in the Michael addition reaction with acetylacetone and benzoylacetone to form the corresponding new anthraquinone derivatives.On the basis of the EC mechanism,the observed homogeneous rate constants（kobs）of the reaction of anthraquinone with acetylacetone and benzoylacetone were estimated by comparing the experimental cyclic voltammograms with the digitally simulated results.     

Synthesis,crystal structure,and electrochemical properties of Ni(II) and Cu(II) complexes with two unsymmetrical N2O2 Schiff base ligands

Nickel(II) and copper(II) complexes of two unsymmetrical tetradentate Schiff base ligands [Ni(Me-salabza)] (1), [Cu(Me-salabza)] (2) and [Ni(salabza)] (3), {H₂salabza = N,N′-bis[(salicylidene)-2-aminobenzylamine] and H₂Me-salabza = N,N′-bis[(methylsalicylidene)-2-aminobenzylamine]}, have been synthesized and characterized by elemental analysis and spectroscopic methods. The crystal structures of 2 and 3 complexes have been determined by single crystal X-ray diffraction. Both copper(II) and nickel(II) ions adopt a distorted square planar geometry in [Cu(Me-salabza)] and [Ni(salabza)] complexes. The cyclic voltammetric studies of these complexes in dichloromethane indicate the electronic effects of the methyl groups on redox potential.     

On the existence of chaotic circumferential waves in spinning disks

We use a third-order perturbation theory and Melnikov's method to prove the existence of chaos in spinning circular disks subject to a lateral point load. We show that the emergence of transverse homoclinic and heteroclinic points lead, respectively, to a random reversal in the traveling direction of circumferential waves and a random phase shift of magnitude pi for both forward and backward wave components. These long-term phenomena occur in imperfect low-speed disks sufficiently far from fundamental resonances.