Time Domain Reflectometric and spectroscopic studies on toluene plus butyronitrile solution

被引:25
|
作者
Karthick, N. K. [1 ]
Arivazhagan, G. [1 ]
Kumbharkhane, A. C. [2 ]
Joshi, Y. S. [3 ]
Kannan, P. P. [1 ]
机构
[1] Thiagarajar Coll, Dept Phys, Madurai 625009, Tamil Nadu, India
[2] SRTM Univ, Sch Phys Sci, Nanded 431606, MS, India
[3] Lal Bahadur Shastri Mahavidyalaya, Dept Elect, Nanded 431809, MS, India
关键词
Weak intermolecular forces; Relaxation time; Time domain reflectometry; DIELECTRIC-RELAXATION; BINARY-MIXTURES; MOLECULAR INTERACTION; AQUEOUS-SOLUTIONS; ELECTROLYTE-SOLUTIONS; BINDING PROTEIN; PROPIONIC-ACID; DYNAMICS; 1,4-DIOXANE; WATER;
D O I
10.1016/j.molstruc.2015.12.009
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The dielectric parameters of toluene + butyronitrile solution have been obtained by time domain reflectometry (TDR) technique in the frequency range from 10 MHz to 30 GHz at 298 K. Spectroscopic (FTIR and 13C NMR) studies have also been carried out on the solution and the results of the studies show that neat butyronitrile is self-associative through C-H center dot center dot center dot N contacts and weak intermolecular forces of C-H center dot center dot center dot N and C-H center dot center dot center dot pi type are operative in the solution. The obtained dielectric parameters such as Kirkwood correlation factor g, relaxation time tau etc. have been analyzed in view of these weak intermolecular forces. The weak non-covalent interactions between heteromolecules appear to have no influence on the ideality of epsilon(m) vs X-2 curve of the solution. Heteromolecular entities with weak intermolecular forces experience larger hindrance leading to longer relaxation time tau. Crown Copyright (C) 2015 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:203 / 208
页数:6
相关论文
共 50 条
  • [1] Time domain reflectometric study on toluene plus propionitrile binary mixture
    Karthick, N. K.
    Arivazhagan, G.
    Kumbharkhane, A. C.
    Joshi, Y. S.
    Kannan, P. P.
    PHYSICS AND CHEMISTRY OF LIQUIDS, 2016, 54 (06) : 779 - 785
  • [2] Time Domain Reflectometric Studies on Methylcellosolve-acetylacetone Binary Solutions
    Pandi, Dineshkumar
    Paramasivam, Naganandhini
    Tiruchithan, Sangeetha
    Ganesan, Arivazhagan
    ORIENTAL JOURNAL OF CHEMISTRY, 2021, 37 (03) : 717 - 721
  • [3] Dielectric and hydrogen bonding studies of butyronitrile with 1,4-dioxane using a time-domain reflectometry
    Dongre, D. G.
    Deshmukh, A. R.
    Garad, N. P.
    Gubre, A. G.
    Saknure, S. H.
    Kumbharkhane, A. C.
    CANADIAN JOURNAL OF PHYSICS, 2024, 102 (06) : 352 - 357
  • [4] Time Domain Dielectric Spectroscopic Studies of Potassium Oleate and Cetyl Pyridinium Chloride in Acetate Buffer Solution
    Gopalakrishnan, D.
    Kumbharkhane, A. C.
    Sampathkumar, R.
    MACROMOLECULAR SYMPOSIA, 2017, 376 (01)
  • [5] THz time-domain spectroscopic studies on magnetoresistive manganites
    Kida, N
    Tonouchi, M
    PHYSICS IN LOCAL LATTICE DISTORTIONS: FUNDAMENTALS AND NOVEL CONCEPTS LLD2K, 2001, 554 : 366 - 370
  • [6] TIME DOMAIN SPECTROSCOPIC STUDIES OF MIXED-VALENT PEROVSKITES
    DRAGO, RS
    DOAN, PE
    KROEGER, MK
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1988, 110 (13) : 4423 - 4424
  • [7] Quantitative analysis on toluene contents in hexane solution using terahertz time domain spectroscopy
    Nashima, S.
    Nishimura, R.
    Hosoda, M.
    2012 37TH INTERNATIONAL CONFERENCE ON INFRARED, MILLIMETER, AND TERAHERTZ WAVES (IRMMW-THZ), 2012,
  • [8] SPECTROSCOPIC STUDIES OF TOLUENE IN SIMPLE MOLECULAR LIQUIDS
    LEE, J
    LI, F
    BERNSTEIN, ER
    JOURNAL OF PHYSICAL CHEMISTRY, 1983, 87 (07): : 1180 - 1183
  • [9] Time domain dielectric relaxation studies of amphiphilics in solution state
    Sylvester, M. Maria
    Ganesh, T.
    Karunakaran, D. J. S. Anand
    Hudge, Praveen
    Kumbharkhane, A. C.
    JOURNAL OF MOLECULAR LIQUIDS, 2014, 194 : 57 - 61
  • [10] SOLUTION STUDIES OF ALIQUAT 336 USING TIME DOMAIN REFLECTOMETRY
    WONG, NM
    DRAGO, RS
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1989, 198 : 59 - INOR