DIELECTRIC RELAXATION IN HYDROGEN-BONDED LIQUIDS

Abstract

The temperature dependence of the dielectric relaxation time was investigated from -5 to 50 C for ethanol-cyclohexane solutions from 1.0 to 0.25 mole fraction ethanol. T e previously observed maximum in the relaxation time around equimolar composition is explained by a H-bonded switching mechanism. Measurements of dielectric relaxation from 5 to 50 C were carried out on 3 isomeric butanediols which differ in the separation of the two OH groups along the carbon skeleton. The differences in relaxation times among the 3 isomers can be explained by the switching mechanism suggested by the results for the ethanol-cyclohexane solutions. The dielectric relaxation times of n-butanol from 5 to 50 C were determined. The chain-length dependence of the dielectric relaxation time of the normal aliphatic alcohols is discussed in terms of the proposed mechanism. (Author)

Document Details

Document Type
Technical Report
Publication Date
Oct 01, 1961
Accession Number
AD0266376

Entities

People

  • Matthew W. Sagal

Organizations

  • Massachusetts Institute of Technology

Tags

Communities of Interest

  • Advanced Electronics

DTIC Thesaurus Topics

  • Chemical Compounds
  • Cyclic Hydrocarbons
  • Cyclohexanes
  • Hydrocarbons
  • Hydrogen
  • Measurement
  • Organic Compounds
  • Relaxation Time
  • Skeleton
  • Switching

Readers

  • Plasma Physics.
  • Polymer Science and Technology
  • Quantum Chemistry