Energy & Fuels, Vol.12, No.4, 682-688, 1998
Study of the oxidation of oil shale and kerogen by Fourier transform infrared emission spectroscopy
Infrared emission spectroscopy has been used to monitor the chemical modifications taking place during the oxidation of bitumen-free Kerosene Creek shale, the bitumen-carbonate-free shale, and the bitumen-carbonate-silicate-free shale (kerogen). The samples were heated, in air, at temperatures in the range 50-700 degrees C at intervals of 50 degrees C. Oxidation of the samples at increasing temperatures showed a steady decrease in the signals due to aliphatic hydrocarbons (3000 cm(-1) to 2700, 1460, and 1375 cm(-1)) as well as in the carbonyl/carboxyl signals (similar to 1710 cm(-1)) and the carbonyl signal at 1740 cm(-1), along with an increase in the anhydride signals at 1775 cm(-1) and at similar to 1850 cm(-1) Constant temperature (300 degrees C) oxidation produced a steady increase in the anhydride peaks at similar to 1775 cm(-1) and at similar to 1850 cm(-1) while the 1710 and 1740 cm-1 peaks slowly decreased. Of the mineral bands, those characteristic of carbonates totally disappeared at 700 degrees C while the other bands remained. The rate of decomposition of organic functionalities is generally fastest for the bitumen-carbonate-free sample. Analysis of the kinetic data clearly showed that the presence of carbonates and silicates lowered the activation energy for the oxidation of aliphatic C-H groups.
Keywords:IN-SITU;FT-IR;THERMAL TRANSFORMATIONS;CLAY-MINERALS;FATTY-ACIDS;COAL;PRODUCTS;SURFACES;RUNDLE