• DocumentCode
    760301
  • Title

    Dielectric investigation of β-cyclodextrin hydrates and inclusion complexes

  • Author

    Anagnostopoulou-Konsta, A. ; Apekis, L. ; Tsoukaris, G.

  • Author_Institution
    Dept. of Phys., Nat. Tech. Univ. of Athens, Greece
  • Volume
    27
  • Issue
    4
  • fYear
    1992
  • fDate
    8/1/1992 12:00:00 AM
  • Firstpage
    801
  • Lastpage
    806
  • Abstract
    The dielectric behavior of β-CD hydrates and β-CD inclusion complexes with various organic guest molecules has been studied mainly by the thermally stimulated depolarization current (TSDC) method in the temperature range 80 to 300 K. Some preliminary measurements have also been carried out by conventional AC techniques at room temperature. Results are discussed in relation to the corresponding structure as determined by X-ray diffraction and are compared with differential scanning calorimetry data reported in the literature. The main high-temperature (200 to 280 K) peak recorded with the TSDC method is shown to be directly related to a phase transition occurring near the peak temperature. Water enclosed in the β-CD cavity seems to play a very important role as far as this transition is concerned
  • Keywords
    X-ray diffraction examination of materials; crystal atomic structure of organic compounds; organic compounds; phase transformations; thermally stimulated currents; β-CD hydrates; β-cyclodextrin hydrates; 80 to 300 K; AC techniques; H2O inclusion; TSDC; TSDC method; X-ray diffraction; dielectric behavior; differential scanning calorimetry data; enclosed water; inclusion complexes; organic guest molecules; phase transition; room temperature; thermally stimulated depolarization current; Conductivity; Current measurement; Dielectric measurements; Electrochemical impedance spectroscopy; Flip-flops; Hydrogen; Neutrons; Physics; Temperature distribution; X-ray diffraction;
  • fLanguage
    English
  • Journal_Title
    Electrical Insulation, IEEE Transactions on
  • Publisher
    ieee
  • ISSN
    0018-9367
  • Type

    jour

  • DOI
    10.1109/14.155801
  • Filename
    155801