• DocumentCode
    63747
  • Title

    Esterification of low molecular weight acids in cellulose

  • Author

    Ese, Marit-helen ; Liland, Knut B. ; Lesaint, Cedric ; Kes, Murside

  • Author_Institution
    Dept. of Electr. Power Eng., Sintef Energy Res., Trondheim, Norway
  • Volume
    21
  • Issue
    2
  • fYear
    2014
  • fDate
    Apr-14
  • Firstpage
    662
  • Lastpage
    665
  • Abstract
    The interaction between low molecular weight acids dissolved in mineral oil with cellulose has been studied. The formation of esters as a function of temperature has been demonstrated using attenuated total reflection infrared (IR) spectroscopy. Higher temperatures lead to a shift towards ester formation compared to lower temperatures. This reaction might be reversed by exposing the cellulose to an excess of water at elevated temperatures. However, this hydrolysis of the esters will not be complete, leaving some of the initially free acids trapped in the paper as esters. Regarding degradation of the cellulose, only free acids with a carbonyl group available will enhance the break-up of the glycosidic bonds in the cellulose polymer. Therefore it seems more appropriate to use cold water extraction in order to quantify the amount of free acids in the paper/pressboard.
  • Keywords
    infrared spectra; minerals; molecular weight; paper; polymers; power transformer insulation; transformer oil; IR spectroscopy; attenuated total reflection infrared spectroscopy; cellulose polymer; cold water extraction; elevated temperatures; ester formation; free acids; glycosidic bonds; hydrolysis; low molecular weight acid esterification; mineral oil; paper insulation; paper-pressboard; power transformers; Aging; Degradation; Educational institutions; Oil insulation; Polymers; Power transformer insulation; ageing; esterification; low molecular weight acids; paper insulation; transformers;
  • fLanguage
    English
  • Journal_Title
    Dielectrics and Electrical Insulation, IEEE Transactions on
  • Publisher
    ieee
  • ISSN
    1070-9878
  • Type

    jour

  • DOI
    10.1109/TDEI.2013.004238
  • Filename
    6783059