The effect of Mg location on Co-Mg-Ru/γ-Al 2 O 3 Fischer–Tropsch catalysts
Springer Science and Business Media LLC -- Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences
DOI 10.1098/rsta.2015.0087
  1. Fischer–Tropsch
  2. catalysis
  3. cobalt
  4. alumina
  5. XRD

The effectiveness of Mg as a promoter of Co-Ru/γ-Al2O3 Fischer–Tropsch catalysts depends on how and when the Mg is added. When the Mg is impregnated into the support before the Co and Ru addition, some Mg is incorporated into the support in the form of MgxAl2O3+x if the material is calcined at 550°C or 800°C after the impregnation, while the remainder is present as amorphous MgO/MgCO3 phases. After subsequent Co-Ru impregnation MgxCo3−xO4 is formed which decomposes on reduction, leading to Co(0) particles intimately mixed with Mg, as shown by high-resolution transmission electron microscopy. The process of impregnating Co into an Mg-modified support results in dissolution of the amorphous Mg, and it is this Mg which is then incorporated into MgxCo3−xO4. Acid washing or higher temperature calcination after Mg impregnation can remove most of this amorphous Mg, resulting in lower values of x in MgxCo3−xO4. Catalytic testing of these materials reveals that Mg incorporation into the Co oxide phase is severely detrimental to the site-time yield, while Mg incorporation into the support may provide some enhancement of activity at high temperature.