• DocumentCode
    3147237
  • Title

    Ferroelectric behavior in Poly(trimethylene terephthalate)

  • Author

    Nakano, Gaku ; Matsuda, Yasuhiro ; Tasaka, Shigeru

  • Author_Institution
    Dept. of Mater. Sci., Shizuoka Univ., Hamamatsu
  • fYear
    2008
  • fDate
    15-17 Sept. 2008
  • Abstract
    Poly(trimethylene terephthalate) (PTT), a flexible polymer containing C=O dipoles in its main chain is synthesized by the polycondensation of 1,3-propanediol and terephthalic acid. Numerous studies on the crystal structure of PTT have been reported. Analysis of crystalline structure of PTT shows that the trimethylene glycol unit in PTT takes a highly coiled structure of trans-gauche-gauche-trans conformation. PTT has a triclinic crystalline structure, each cell of which contains two chemical repeat units. The physical properties of PTT are known to be quite different from those of PET and PBT, since PTT has odd number of methylene units. The crystal structure is nonpolar because of the antiparallel crystal packing of C=O dipoles. However external treatments such as poling and stretching can change the conformation of the PTT chains, to have ferroelectricity. In this study, we investigated the ferroelectric structural change of PTT upon application of an external electric field treatment.
  • Keywords
    crystal structure; dielectric hysteresis; dielectric polarisation; polymers; 1,3-propanediol; C=O dipoles; antiparallel crystal packing; crystal structure; external electric field treatment; ferroelectric behavior; flexible polymer; hysteresis loop; poling; poly(trimethylene terephthalate); polycondensation; remanent poarization; terephthalic acid; transgauche-gauche-trans conformation; Chemicals; Crystallization; Electrodes; Ferroelectric films; Ferroelectric materials; Hysteresis; Ice; Polymer films; Positron emission tomography; Temperature;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Electrets, 2008. ISE-13. 13th International Symposium on
  • Conference_Location
    Tokyo
  • Print_ISBN
    978-1-4244-1850-3
  • Electronic_ISBN
    978-1-4244-1851-0
  • Type

    conf

  • DOI
    10.1109/ISE.2008.4814042
  • Filename
    4814042