Oxidation of cobalt based Fischer–Tropsch catalysts as a deactivation mechanism
2000; Elsevier BV; Volume: 58; Issue: 4 Linguagem: Inglês
10.1016/s0920-5861(00)00265-0
ISSN1873-4308
AutoresP.J. van Berge, J. van de Loosdrecht, S. Barradas, A. M. van der Kraan,
Tópico(s)Nanoporous metals and alloys
ResumoThe oxidation of supported cobalt based slurry bed Fischer–Tropsch catalysts by means of water was studied. Water is one of the Fischer–Tropsch reaction products and can probably cause oxidation and deactivation of a reduced cobalt catalyst. Model experiments using Mössbauer emission spectroscopy and thermogravimetry as well as realistic Fischer–Tropsch synthesis runs were performed. It was demonstrated that Mössbauer emission spectroscopy can successfully be applied to the investigation of high cobalt loading Fischer–Tropsch catalysts. Strong indications were found that oxidation of reduced cobalt catalysts occurs under realistic Fischer–Tropsch conditions. Mössbauer emission spectroscopy and thermogravimetry results showed that the oxidation depends on the PH2/PH2O ratio, and that oxidation proceeds to less than complete extents under certain conditions. The formation of both reducible and less reducible cobalt oxide species was observed, and the relative ratio between these species depends on the severity of the oxidation conditions.
Referência(s)