| Literature DB >> 30070756 |
Ilse K van Ravenhorst1, Charlotte Vogt1, Heiko Oosterbeek2, Koen W Bossers1, José G Moya-Cancino1, Alexander P van Bavel2, Ad M J van der Eerden1, David Vine3, Frank M F de Groot1, Florian Meirer1, Bert M Weckhuysen1.
Abstract
A state-of-the-art operando spectroscopic technique is applied to Co/TiO2 catalysts, which account for nearly half of the world's transportation fuels produced by Fischer-Tropsch catalysis. This allows determination of, at a spatial resolution of approximately 50 nm, the interdependence of formed hydrocarbon species in the inorganic catalyst. Observed trends show intra- and interparticular heterogeneities previously believed not to occur in particles under 200 μm. These heterogeneities are strongly dependent on changes in H2 /CO ratio, but also on changes thereby induced on the Co and Ti valence states. We have captured the genesis of an active FTS particle over its propagation to steady-state operation, in which microgradients lead to the gradual saturation of the Co/TiO2 catalyst surface with long chain hydrocarbons (i.e., organic film formation).Entities:
Keywords: Fischer-Tropsch synthesis; X-ray microspectroscopy; chemical imaging; heterogeneous catalysis; nanoparticles
Year: 2018 PMID: 30070756 DOI: 10.1002/anie.201806354
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336