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Abstract

The effect of Cu on the reduction behavior and surface properties of supported and unsupported Fe-based Fischer–Tropsch synthesis (FTS) catalysts was investigated using in situX-ray photoelectron spectroscopy (XPS) and in situX-ray absorption spectroscopy (XAS) in combination with ex situ bulk characterization. During exposure to 0.4 mbar CO–H2 above 180 °C, the reduction of CuO to Cu0 marked the onset of the reduction of Fe3O4 to α-Fe. The promotion effects of Cu are explained by a combination of spillover of H2 and/or CO molecules from metallic Cu0 nuclei to closely associated iron oxide species and textural promotion. XAS showed that in the supported catalyst, Cu+ and Fe2+ species were stabilized by SiO2 and, as a result, Fe species were not reduced significantly beyond Fe3O4 and Fe2+, even after treatment at 350 °C. After the reduction treatment, XPS showed that the concentration of oxygen and carbon surface species was higher in the presence of Cu. Furthermore, it was observed that the unsupported, Cu-containing catalyst showed higher CO2 concentration in the product gas stream during and after reduction and Fe surface species were slightly oxidized after prolonged exposure to CO–H2. These observations suggest that, in addition to facilitating the reduction of the iron oxide phase, Cu also plays a direct role in altering the surface chemistry of Fe-based FTS catalysts.. These observations suggest that, in addition to facilitating the reduction of the iron oxide phase, Cu also plays a direct role in altering the surface chemistry of Fe-based FTS catalysts.