Highly selective PVC-membrane electrodes based on Co(II)-Salen for determination of nitrite ion.

A cobalt(II) derivative was used as a suitable ionophore for the preparation of a polymeric membrane nitrite-selective electrode. The electrode reveals a Nemstian behavior over a very wide NO2- ion concentration range (1.0 x 10(-6)-1.0 x 10(-1) M) and a very low detection limit (5.0 x 10(-7) M). The potentiometric response is independent of the pH of solution in the pH range 4.0-9.5. The electrode shows advantages such as low resistance, fast response and, most importantly, good selectivity relative to a wide variety of inorganic and organic anions. In fact, the selectivity behavior of the proposed NO2- ion-selective electrode shows great improvements compared to the previously reported electrodes for nitrite ion. The proposed electrodes could be used for at least 2 months without any significant changes in potentials. The electrode was successfully applied to the determination of nitrate ion concentrations in sausage and milk samples.     

Iodine‐Catalyzed Friedlander Quinoline Synthesis under Solvent‐Free Conditions

Polyfunctional quinolines were synthesized using Friedlander method catalyzed by molecular iodine in high yields at 60 °C under solvent‐free conditions.     

Spectroscopic investigation of 4f correlations in CeAg; comparison between LDA and many-body descriptions

High resolution photoemission and bremsstrahlung isochromat spectroscopy experiments have been carried out on CeAg and LaAg. From a comparison between these two compounds, we extract the cerium 4f spectral function, we compare it with band structure calculations and with many-body model simulations based on the single-impurity Anderson Hamiltonian. We show that the localized 4f charge estimated from previous band structure calculations cannot be identified with the 4f occupation number deduced from the Anderson model.     

On wave propagation in elastic tubes conducting rotational flows

The propagation of perturbations in liquid filled elastic tubes depends on the stream velocity of the basic flow. This phenomenon is currently analyzed with the method of the characteristics which relies upon a basic flow with a rectangular velocity profile. It seems that this one-dimensional flow approximation has not been convincingly validated, which justifies to consider other, more general velocity profiles.In the present analytical study the velocity profile is a quadratic function of the radial coordinate. Small amplitude perturbations are superposed on this inviscid, basic state in which the mean velocity is arbitrarily large. A normal mode analysis shows that the velocity profile and therefore the vorticity of the basic flow influence the more the phenomenon the larger is. For example, a parabolic profile allows countercurrent wave propagation regardless of.This questions the one-dimensional wave propagation theory in compliant tubes and, consequently, the interpretation of several physiological and medical problems mainly in the respiratory and cardio-vascular systems.

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Resumé La propagation de perturbations dans un tube élastique conduisant un écoulement fluide dépend de la vitesse de l'écoulement de base. Ce phénomène est habituellement étudié avec la méthode des caractéristiques, où l'on suppose que le profil de vitesse de l'écoulement est rectangulaire. Comme cette simplification ne semble pas avoir été bien validée, il paraît indiqué d'étudier l'impact d'autres profils.Dans la présente étude analytique, ce profil de vitesse est une fonction quadratique de la coordonée radiale. A cet écoulement non visqueux, dont la vitesse moyenne est arbitraire, l'on superpose des perturbations de faible amplitude. Une analyse linéarisée montre que le profil de vitesse et donc le rotationel de l'écoulement de base influencent d'autant plus ce phénomène d'ondes que est élévée.Ceci met en question la théorie uni-dimensionelle de la propagation d'ondes dans des tubes compliants et, par là-même, l'interpretation de divers problèmes physiologiques et médicaux, avant tout des systèmes respiratoires et cardio-vasculaires.

     

The Importance of Polarity/Polarizability Interaction on the Acidity Behavior of 9,10-Anthraquinone and 9-Anthrone Derivatives in Methanol-Water Mixed Solvents Using Target Factor Analysis and QSPR Approaches

The influence of solvent properties on acidity constants of some newly synthesized 9,10-anthraquinone and 9-anthrone derivatives was studied in methanol-water mixtures in a composition range of 0.57 to 1.0 methanol mole fraction. The model was established by using both multiple linear regression and target factor analysis. Both methods revealed that the solvent polarity/polarizability parameter ^* is a major factor in controlling the acidity behavior of the anthraquinones and anthrones studied in binary methanol-water mixed solvents. A QSPR study was conducted to drive the relationships between the ^* coefficient s and the polarity/polarizability of molecules. Both dipole moment and polarizability were found to have a linear relationship with s. The results confirm that, in the dipolar protic solvents used, the dipole-dipole interaction (for neutral molecules) and the ion-dipole interaction (for ionized molecules) are the major factors controlling the acidity behavior of these compounds.     

Specific Uphill Transport of Zinc as Zn(SCN)42− Ion using Na+-Dicyclohexyl-18-Crown-6 as Carrier

Sodium-dicyclohexyl- 18-crown-6 complex cation was used as carrier for the uphill transport of zinc as Zn(SCN)₄^2? complex anion. By using L-cysteine as a metal ion acceptor in the receiving phase at the optimized pH of 7.6, the amount of zinc transport through the liquid membrane after 90 min was 97.2 ± 1.0%. The selectivity and efficiency of zinc transport from aqueous solutions containing equimolar mixtures of Ag⁺, Cd²⁺ Co²⁺, Cu²⁺, Fe²⁺, Ni²⁺, Pb²⁺, Pd²⁺, Sr²⁺, Bi³⁺, Cr³⁺ and Fe³⁺ ions was investigated. In the presence of NH₂OH.HCl as a suitable masking agent in the source phase, the interfering effect of Cu²⁺ and Pb²⁺ ions was diminished drastically.     

Separation of peptides and proteins by capillary electrophoresis using acidic buffers containing tetraalkylammonium cations and cyclodextrins

A method for improving separations of peptides and other positively charged species in capillary zone electrophoresis with untreated capillaries using acidic buffers containing tetraalkylammonium cations is described. Tetramethylammonium and tetrabutylammonium cations dynamically modify the capillary surface, leading to a reversal in the direction of the electroosmotic flow. As a result, the adsorption of positively charged peptides and proteins is minimized, and resolution and peak capacity are improved as the migration of cationic analytes is counterbalanced by the electroosmotic flow. The combining effect of reversing electroosmotic flow and cyclodextrin inclusion complexation on separations of closely related peptides and a protein mixture, as well as tryptic digest of hemoglobin is demonstrated.