Viscosity, electrical conductivity, shear relaxation time and Raman spectra of aqueous and methanolic sodium thiocyanate solutions

2001 ◽  
Vol 178 (1-2) ◽  
pp. 277-297 ◽  
Author(s):  
Nashiour Rohman ◽  
Abdul Wahab ◽  
Narendra N. Dass ◽  
Sekh Mahiuddin
2005 ◽  
Vol 83 (3) ◽  
pp. 236-243 ◽  
Author(s):  
Mehrdad Bamdad ◽  
Saman Alavi ◽  
Bijan Najafi ◽  
Ezat Keshavarzi

The shear relaxation time, a key quantity in the theory of viscosity, is calculated for the Lennard–Jones fluid and fluid krypton. The shear relaxation time is initially calculated by the Zwanzig–Mountain method, which defines this quantity as the ratio of the shear viscosity coefficient to the infinite shear modulus. The shear modulus is calculated from highly accurate radial distribution functions obtained from molecular dynamics simulations of the Lennard–Jones potential and a realistic potential for krypton. This calculation shows that the density dependence of the shear relaxation time isotherms of the Lennard–Jones fluid and Kr pass through a minimum. The minimum in the shear relaxation times is also obtained from calculations using the different approach originally proposed by van der Gulik. In this approach, the relaxation time is determined as the ratio of shear viscosity coefficient to the thermal pressure. The density of the minimum of the shear relaxation time is about twice the critical density and is equal to the common density, which was previously reported for supercritical gases where the viscosity of the gas becomes independent of temperature. It is shown that this common point occurs in both gas and liquid phases. At densities lower than this common density, even in the liquid state, the viscosity increases with increasing temperature.Key words: dense fluids, radial distribution function, shear modulus, shear relaxation time, shear viscosity.


2017 ◽  
Vol 31 (12) ◽  
pp. 1750134 ◽  
Author(s):  
Oktay Samadov ◽  
Oktay Alakbarov ◽  
Arzu Najafov ◽  
Samir Samadov ◽  
Nizami Mehdiyev ◽  
...  

The dielectric and impedance spectra of TlGaSe2 crystals have been studied at temperatures in the 100–500 K range in the alternating current (AC [Formula: see text]1 V). It has been shown that the conductivity of TlGaSe2 crystals is mainly an ionic characteristic at temperatures above 400 K. The well-defined peak at the frequency dependence of the imaginary part of impedance [Formula: see text] is observed in the 215–500 K temperature range. In a constant field, there occurs a significant decrease in electrical conductivity [Formula: see text] in due course. The ionic contribution to conductivity (76% at [Formula: see text]) has been estimated from a kinetic change in electrical conductivity [Formula: see text] under the influence of a constant electric field. The diagram analysis in a complex plane [Formula: see text] has been conducted by applying the method of an equivalent circuit of the substation. It has been determined that the average relaxation time of the electric module of the sample is [Formula: see text].


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