scholarly journals A Fractional Complex Permittivity Model of Media with Dielectric Relaxation

2017 ◽  
Vol 1 (1) ◽  
pp. 4 ◽  
Author(s):  
Armando Ciancio ◽  
Bruno Flora
1984 ◽  
Vol 39 (7) ◽  
pp. 646-650
Author(s):  
M. Stockhausen ◽  
E. Dachwitz

The complex permittivity of methanol + acetonitrile at 20 °C was measured over the whole composition range at frequencies up to 36 GHz. It can be described by superposition of two Debye type components, one of them being due to associated methanol. This component is discussed with respect to two simple models, considering relaxation as governed by rotational tumbling of associates or by fluctuation of hydrogen bonds. The latter description appears to be the more suitable one.


1981 ◽  
Vol 59 (7) ◽  
pp. 1051-1060 ◽  
Author(s):  
Hubert Cachet ◽  
Mohamed Fekir ◽  
Jean-Claude Lestrade

The complex permittivity of LiClO4 and NaClO4 solutions in 1,2-dimethoxyethane (DME) has been measured in the frequency range 0.140–123.2 GHz. The data have been analysed according to a model for the reorientation of ion pairs given in a previous paper. The dielectric data are supplemented by conductivity measurements in a broad concentration range (10−4–1 mol/L) which evidence the large extent of salt association. The main result is that the solvation of Li+ and Na+ by DME cannot be described as simply as in the case of other solvents, such as tetrahydrofuran or ethyl acetate, as far as the dielectric properties are concerned: while the assumption of rigidly bound solvating molecules was acceptable for the latter solvents, some freedom in the reorientation of these molecules has to be taken into account for the case of DME. LiClO4 solutions in propylene carbonate (PC) + benzene and PC + DME mixtures have also been studied. The data, for the latter, can be qualitatively interpreted under the assumption that PC molecules take the place of DME molecules in the solvation sheath, even at low PC concentration.


1985 ◽  
Vol 40 (6) ◽  
pp. 588-595 ◽  
Author(s):  
H. Utzel ◽  
M. Stockhausen

The complex permittivity of the partially miscible systems ethanol-water-benzene and ethanol-water- n-hexane has been measured in the frequency range from 20 MHz to 36 GHz at 20 °C. The results are described as superposition of Debye-terms, which are considered as physically significant and are ascribed to (i) higher, ill-defined, fluctuating self- and hetero-associates (main term), (ii) associates of lower order, relaxing by rotational tumbling, (iii) free molecules. The demultimerization by benzene appears to be more effective than by hexane.


1991 ◽  
Vol 46 (10) ◽  
pp. 920-922
Author(s):  
◽  
A. Steffen ◽  
M. Stockhausen

AbstractThe complex permittivity of the title solution system (c≤1.5 mol/1) was measured at frequencies ranging up to 72 GHz at 20 °C. Apart from the conductivity contribution there are two distinguishable relaxation regions, which are ascribed to the solvent (at higher frequencies) and to solvated ionic species (at lower frequencies).


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