• DocumentCode
    1912755
  • Title

    Charge transfer interactions between polyaniline and surface functionalized polymer substrates

  • Author

    Kang, E.T. ; Neoh, K.G. ; Pun, M.Y.

  • Author_Institution
    National University of Singapore
  • fYear
    1994
  • fDate
    24-29 July 1994
  • Firstpage
    694
  • Lastpage
    694
  • Abstract
    Summary form only given. Earlier work has demonstrated that the surface of polyaniline (PAN) films can be rendered self-protonated and conductive via graft copolymerization with acrylic acid (AAc) and styrenesulfonic acid (SSAc). In a parallel development, the surface of conventional polymer films, such as low density polyethylene (LDPE), high-density polyethylene (HDPE), polypropylene (PP), poly(ethylene tetraphthalate) (PET) and poly(tetrafluoroethylene) (PTFE) can be functionalized via graft copolymerization with AAc and SSAc. The as-functionalized hydrocarbon and fluoropolyiner surfaces can thus be rendered conductive when coated with the neutral emeraldine (EM) base. The physicochemical properties, such as composition and protonation level, at the EM-functionalized substrate interface were evaluated by X-ray photoelectron spectroscopy (XPS). It was found that in the presence of surface grafted SSAc polymer, protonation levels in the order of 50% could be readily achieved. Lower protonation levels were observed for EM coated on substrate surfaces grafted with AAc polymer. Other substrate surface funcionalization techniques, such as sulfonation (for LDPE, HDPE and PP) and hydrolysis (for PET) were also expored.
  • Keywords
    Charge transfer; Chemical engineering; Conductive films; Hydrocarbons; Physics; Polyethylene; Polymer films; Positron emission tomography; Rendering (computer graphics); Spectroscopy;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Science and Technology of Synthetic Metals, 1994. ICSM '94. International Conference on
  • Conference_Location
    Seoul, Korea
  • Type

    conf

  • DOI
    10.1109/STSM.1994.836138
  • Filename
    836138