• Title of article

    Novel investigation of enzymatic biodiesel reaction by isothermal calorimetry

  • Author/Authors

    Lene Fjerbaek Sotoft، نويسنده , , Peter Westh، نويسنده , , Knud V. Christensen، نويسنده , , Birgir Norddahl، نويسنده ,

  • Issue Information
    دوهفته نامه با شماره پیاپی سال 2010
  • Pages
    7
  • From page
    84
  • To page
    90
  • Abstract
    Isothermal calorimetry (ITC) was used to investigate solvent-free enzymatic biodiesel production. The transesterification of rapeseed oil with methanol and ethanol was catalyzed by immobilized lipase Novozym 435 at 40 °C. The aim of the study was to determine reaction enthalpy for the enzymatic transesterification and to elucidate the mass transfer and energetic processes taking place. Based on the measured enthalpy and composition change in the system, the heat of reaction at 40 °C for the two systems was determined as −9.8 ± 0.9 kJ/mole biodiesel formed from rapeseed oil and methanol, and −9.3 ± 0.7 kJ/mole when rapeseed oil and ethanol was used. Simple Michaelis–Menten kinetics was not an appropriate choice for describing the kinetics of this heterogeneous system. The experiments demonstrated the possibility of investigating complex reaction mixtures using ITC. Although it is possible to determine thermodynamic properties such as reaction enthalpy and reaction rate, the difficulty in actually measuring the true non-mass-transfer-limited reaction kinetics is exposed by the high time resolution of ITC.
  • Keywords
    Lipase , ITC , Transesterification , Reaction enthalpy , enzyme , Biodiesel
  • Journal title
    Thermochimica Acta
  • Serial Year
    2010
  • Journal title
    Thermochimica Acta
  • Record number

    1199059