Dielectric Constant and Dielectric Relaxation Time of Rochelle Salt

1971 ◽  
Vol 31 (6) ◽  
pp. 1748-1753 ◽  
Author(s):  
Ryuji Abe ◽  
Yukuya Tokumaru
2020 ◽  
Vol 17 (3) ◽  
pp. 230-235
Author(s):  
Sampandam Elangovan ◽  
Tilahun Diriba Garbi ◽  
Senbeto Kena Etana

The dielectric relaxation studies are vital in analyzing the strength of the inter molecular interaction between the binary liquid systems [1-4]. Jyostna et al. [5] reported thermodynamic parameters of isoamyl alcohols and mono clinic aromatic liquid mixtures. Shakila et al. [6] studied the dielectric properties of aromatic alcohols and aliphatic amines at different temperatures. In general, dielectric relaxation time varies with the inter molecular forces acting between the molecules in the selected liquid mixtures. Brompheniramine is one of the critical compounds of an amine group with spectacular applications, including pharmaceutical industries [7]. Higher carbon chain length alcohols are having self associated and proton donating ability in the liquid mixtures. The variations in the dielectric constant (є’), dielectric loss (є’’), static dielectric constant (є0) and the dielectric constant at an optical frequency (є∞) with a range of brompheniramine concentrations with 1-butanol,1-pentanol and 1-hexanol systems are useful in the applied research and chemical industries. Moreover, the variations in the dielectric constant and dielectric relaxation time should be useful in the analysis of intermolecular interaction between the functional group of the selected liquid mixtures. This research work attempts to analyse the intermolecular interaction between the brompheniramine and 1-butanol,1-pentanol and 1-hexanol at 303K using time domain reflectometry techniques.


It is shown that polar liquids may be divided into two classes according to whether or not the rotation of the dipoles is prevented by solidification. For liquids belonging to the first class, and having rigid molecules, an equation similar to Debye’s can be used to relate the dielectric relaxation time and the viscosity. This equation does not involve the ‘molecular radius’ which has always made the interpretation of Debye’s equation uncertain, and it can, in consequence, be used to determine from the experimental results how the ratio of the microscopic to the macroscopic relaxation time ( ז/ז ') depends on the static dielectric con­stant. The theory has been applied to a number of organic liquids of rigid molecular struc­ture, and indicates that the dependence of ז/ז ' on the dielectric constant is best expressed by Powles’s equation ז/ז ' = (2∊ 0 + ∊ ∞ )/3∊ 0 . For liquids belonging to the second class no simple relation between dielectric relaxation time and viscosity can be expected, but it may be possible to relate the relaxation time in some way to the transition which occurs in the solid state, in which the freedom of dipole rotation is lost.


1983 ◽  
Vol 26 (2) ◽  
pp. 77-84 ◽  
Author(s):  
S.M. Khameshara ◽  
M.S. Kavadia ◽  
M.S. Lodha ◽  
D.C. Mathur ◽  
V.K. Vaidya

2014 ◽  
Vol 458 (1) ◽  
pp. 56-63 ◽  
Author(s):  
Thanapong Sareein ◽  
Muanjai Unruan ◽  
Athipong Ngamjarurojana ◽  
Supon Ananta ◽  
Rattikorn Yimnirun

1992 ◽  
Vol 47 (11) ◽  
pp. 1127-1134 ◽  
Author(s):  
H. G. Kreul ◽  
R. Waldinger ◽  
A. Würflinger

Abstract Differential thermal analysis (DTA) and dielectric measurements have been performed on 2,2-dimethyl- 1-propanol (neopentanol) up to 200 MPa. Neopentanol exhibits at least one orientationally disordered (ODIC) phase (solid I) that transforms at lower temperatures to a non-plastic phase (solid II). There is evidence of a further ODIC phase denoted as solid I'. The pressure dependence of the phase transitions and the dielectric behaviour up to frequencies of 13 MHz are described. Activation enthalpies and volumes are derived from the dielectric relaxation time and compared with results for other alcohols


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