Quasiparticle approach to the modulational instability of drift waves coupling to zonal flows

The interaction between broadband drift mode turbulence and zonal flows has been studied through the wave-kinetic approach. Simulations have been conducted in which a particle-in-cell representation is used for the quasiparticles, while a fluid model is employed for the plasma. The interactions have been studied in a plasma edge configuration which has applications in both tokamak physics and magnetopause boundary layer studies. Simulation results show the development of a zonal flow through the modulational instability of the drift wave distribution, as well as the existence of solitary zonal flow structures about an ion gyroradius wide, drifting towards steeper relative density gradients.     

Theory of cavitons in complex plasmas

Nonlinear coupling between Langmuir waves with finite amplitude dispersive dust acoustic perturbations is considered. It is shown that the interaction is governed by a pair of coupled nonlinear differential equations. Numerical results reveal the formation of Langmuir envelope solitons composed of the dust density depression created by the ponderomotive force of bell-shaped Langmuir wave envelops. The associated ambipolar potential is positive. The present nonlinear theory should be able to account for the trapping of large amplitude Langmuir waves in finite amplitude dust density holes. This scenario may appear in Saturn's dense rings, and the Cassini spacecraft should be able to observe fully nonlinear cavitons, as presented herein. Furthermore, we propose that new electron-beam plasma experiments should be conducted to verify our theoretical prediction.     

On the electrochemical characterization of ion-selective cellulose acetate membranes with and without stigmasterol liquid membranes

Stigmasterol, a plant product, has been used as a surfactant to generate liquid membranes supported on a cellulose acetate matrix. Electrochemical characterization of the membrane has been attempted with a view to simulating its behavior with natural membranes by measuring membrane potentials and membrane conductance. The selectivity of cellulose acetate membrane kept in contact with magnesium chloride solutions of different mean concentrations has been found to change from anion to cation. Transport numbers have been estimated from membrane potential data. Permselectivity and fixed charge density values for the cellulose acetate membrane with and without stigmasterol have been determined from transport numbers. The variation of these parameters with concentration and pH has also been examined.     

Electroweak interactions between intense neutrino beams and dense electron-positron magnetoplasmas

The electroweak coupling between intense neutrino beams and strongly degenerate relativistic dense electron-positron magnetoplasmas is considered. The intense neutrino bursts interact with the plasma due to the weak Fermi interaction force, and their dynamics is governed by a kinetic equation. Our objective here is to develop a kinetic equation for a degenerate neutrino gas and to use that equation to derive relativistic magnetohydrodynamic equations. The latter are useful for studying numerous collective processes when intense neutrino beams nonlinearly interact with degenerate, relativistic, dense electron-positron plasmas in strong magnetic fields. If the number densities of the plasma particles are of the order of 10³³ cm^-3, the pair plasma becomes ultra-relativistic, which strongly affects the potential energy of the weak Fermi interaction. The new system of equations allows several neutrino-driven streaming instabilities involving new types of relativistic Alfvén-like waves. The relevance of our investigation to the early universe and supernova explosions is discussed. Received 11 September 2002 Published online 4 February 2003 RID="a" ID="a"Permanent address: Department of Physics, Tbilisi State University, Chavchavadze 3, Tbilisi 38028, Georgia. RID="b" ID="b"Also at the Department of Plasma Physics, Ume? University, 90187 Ume?, Sweden; and the Center for Interdisciplinary Plasma Science, Max-Planck Institut für Plasmaphysik und extraterrestrische Physik, Postfach 1312, 85741 Garching, Germany. e-mail: ps@tp4.ruhr-uni-bochum.de RID="c" ID="c"Permanent address: Department of Plasma Physics, Ume?University, 90187 Ume?, Sweden.     

Parametric instability of dust lattice waves in a turbulent plasma sheath

It is shown that dust lattice waves (DLWs) become parametrically unstable in a turbulent dusty plasma sheath that contains random-phase ion plasma waves. Physically, the parametric instability arises because of the nonlinear coupling between ion plasma waves and DLWs. The parametric instability is identified as the possible reason for the observed "sublimation" transition of the plasma crystal from a solid to a gaslike state.     

Anomalous reflection and excitation of surface waves in metamaterials

We consider reflection of electromagnetic waves from layered structures with various dielectric and magnetic properties, including metamaterials. Assuming periodic variations in the permittivity, we find that the reflection is in general anomalous. In particular, we note that the specular reflection vanishes and that the incident energy is totally reflected in the backward direction, when the conditions for resonant excitation of leaking surface waves are fulfilled.     

Density, ultrasonic velocity, surface tension, excess volume and viscosity of quaternary fluid solutions

Density, ultrasonic velocity, surface tension, excess volume and viscosity of quaternary non-electrolyte solution n-pentane+tolune+n-heptane+cyclohexane has been experimentally determined at 25 °C over a wide range of composition. Assuming a quaternary fluid solution to be made of six binaries, a statistical approach of Prigogine–Flory–Patterson (PFP) theory has been extended to develop the expressions for dynamic viscosity, surface tension excess volume and ultrasonic velocity of quaternary fluid system. A reasonable agreement has been achieved between theory and experiment. An attempt has also bee made to explain the nature of molecular interactions involved in the light of excess thermodynamic functions whose sign and magnitude depend upon the chain length and size of the component fluids and also studied the role of order breakers (toluene and cyclohexane) on these properties.     

The kinetics and thermodynamics of a novel efficient mixed water–1,4-dioxan solvent for the effective complexation of a neutral ruthenium complex with carbon monoxide at atmospheric pressure

Kinetic and thermodynamic investigations were performed for a mixed aqueous-organic, 1:1 (v/v) water–1,4-dioxane medium, which was found to be an efficient solvent for the interaction of a neutral dichlorotris(triphenylphosphine) ruthenium(II), RuCl₂(PPh₃)₃ complex with carbon monoxide at atmospheric pressure. During the interaction, RuCl₂(PPh₃)₃ dissociates to a neutral complex dichlorobis(triphenylphosphine) ruthenium(II), RuCl₂(PPh₃)₂, by losing a coordinated PPh₃ ligand and RuCl₂(PPh₃)₂ coordinates with CO to form an in situ carbonyl complex RuCl₂(CO)(PPh₃)₂. The in situ formed carbonyl complex RuCl₂(CO)(PPh₃)₂ was thoroughly characterized by equilibrium, spectrophotometric, IR, and electrochemical techniques. Under equilibrium conditions, the rate and dissociation constants for the dissociation of PPh₃ from RuCl₂(PPh₃)₃ were found to be favorable for the formation of the carbonyl complex RuCl₂(CO)(PPh₃)₂. The rates of complexation for the formation of RuCl₂(CO)(PPh₃)₂ were found to follow an overall second-order kinetics being first order in terms of the concentrations of both carbon monoxide and RuCl₂(PPh₃)₂. The determined activation parameters corresponding to the rate constant (ΔH^# = 35.9 ± 2.5 kJ mol⁻¹ and ΔS^# = −122 ± 6 J K⁻¹ mol⁻¹) and thermodynamic parameters corresponding to the formation constant (ΔH° = −33.5 ± 4.5 kJ mol⁻¹, ΔS° = −25 ± 8 J K⁻¹ mol⁻¹, and ΔG° = −25.7 ± 2.0 kJ mol⁻¹) were found to be highly favorable for the formation of the complex RuCl2(CO)(PPh3)2. © 2008 Wiley Periodicals, Inc. Int J Chem Kinet 40: 359–369, 2008