journal article·2008-02

Dielectric and thermodynamic studies on a binary mixture of anisole with butyric or caprylic acid

G. Parthipan, G. Arivazhagan, T. Thenappan

Philosophical Magazine Letters· Volume 88· Issue 2
Publisher page

Abstract

The molecular interaction of anisole with fatty acids, such as butyric acid and caprylic acid, has been studied using standard dielectric methods. The permittivity at static and optical frequency (the sodium D-line) of a mixture of anisole + butyric acid and anisole + caprylic acid were measured at three different temperatures. Kirkwood correlation parameters, the excess permittivity, the Bruggeman parameter and excess free-energy were determined for each concentration of the mixture. A positive value of excess permittivity was obtained for the mixture of anisole + butyric acid, whereas for most concentrations of the anisole + caprylic acid mixture, the excess permittivity was negative at all studied temperatures. Negative and positive values of the Bruggeman parameters were obtained for the anisole + butyric acid and anisole + caprylic acid mixtures, respectively. Parallel and anti-parallel alignments of dipoles in the mixtures were identified.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Thermodynamic properties of mixtures · Ionic liquids properties and applications · Liquid Crystal Research Advancements

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

a Department of Physics , Alagappa University , Karaikudi 630003, Tamilnadu, India

References (30)

Show source-provided references
1. 10.1016/j.jct.2004.09.01710.1016/j.jct.2004.09.017 ↗
2. Ghanadzadeh A · J. Mol. Liq. · 2003 · 102 · 36510.1016/S0167-7322(02)00161-7 ↗
3. Thenappan T · J. Pure Appl. Phys. · 2001 · 39 · 694
4. 10.1039/ct905870099810.1039/ct9058700998 ↗
5. Kraubuchi DE · J. Chem. Phys. · 1969 · 5266
6. 10.1016/j.molliq.2003.12.01810.1016/j.molliq.2003.12.018 ↗
7. 10.1016/S0167-7322(01)00239-210.1016/S0167-7322(01)00239-2 ↗
8. Thenappan T · Indian J. Pure Appl. Phys. · 2004 · 42 · 435
9. Thenappan T · 1994
10. 1997
11. Frohilich H · 1949
12. 10.1016/0167-7322(92)80088-Y10.1016/0167-7322(92)80088-Y ↗
13. 10.1016/0167-7322(91)80042-310.1016/0167-7322(91)80042-3 ↗
14. Hasted JB · 1973
15. 10.1080/0950083060074385610.1080/09500830600743856 ↗
16. 10.1016/0167-7322(93)00665-610.1016/0167-7322(93)00665-6 ↗
17. 10.1016/j.molliq.2006.05.01210.1016/j.molliq.2006.05.012 ↗
18. Gupta KK · Indian J. Phys. · 2005 · 79 · 147
19. Kroeger MK · J. Mol. Liq. · 1987 · 36 · 10110.1016/0167-7322(87)80034-X ↗
20. 10.1016/S0167-7322(02)00162-910.1016/S0167-7322(02)00162-9 ↗
21. Bottcher CJF · 1978 · 2
22. Balamurugan D · J. Mol. Liq. · 2005 · 122 · 1110.1016/j.molliq.2004.11.004 ↗
23. Pawar VP · J. Mol. Liq. · 2005 · 121 · 8810.1016/j.molliq.2004.10.038 ↗
24. Chaudhari A · Proc. Natl. Sci. Counc. Roc (a) · 2001 · 25 · 205
25. Buep AH · J. Mol. Liq. · 1990 · 45 · 23710.1016/0167-7322(90)80033-G ↗
26. Chaudhari A · Proc. Natl. Acad. Sci. India A · 2001 · 71 · 75
27. 10.1016/j.molliq.2005.04.01010.1016/j.molliq.2005.04.010 ↗
28. Varadarajan R · Pure Appl. Phys. · 1998 · 36 · 113
29. Thenappan T · J. Mol. Liq. · 2006 · 126 · 2310.1016/j.molliq.2004.09.004 ↗
30. Swain BB · Curr. Sci. · 1985 · 54 · 504