4.7 Article

Insights into the deactivation and reactivation of Ru/TiO2 during Fischer-Tropsch synthesis

Journal

CATALYSIS TODAY
Volume 214, Issue -, Pages 2-11

Publisher

ELSEVIER
DOI: 10.1016/j.cattod.2012.09.018

Keywords

Ru; Fischer-Tropsch; In situ FTIR; Deactivation; Coke

Funding

  1. Ministerio de Educacion of Spain through the Formacion de Profesorado program (FPU)
  2. Ministerio de ciencia en innovacion [ENE2007-67533-C02-02/ALT]
  3. Comunidad de Madrid [S2009ENE-1743]
  4. Programa de Actividades de I + D entre Grupos de Investigacion de Tecnologias

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The catalytic performance of Ru/TiO2 for the production of hydrocarbons via Fischer-Tropsch synthesis (FTS) has been evaluated in this work. Ru/TiO2 exhibits high CO conversion rates (523 K, 2.5 MPa H-2, 1.25 MPa CO) that decrease significantly with time-on-stream. To recover the initial catalytic performance, different treatments using H-2 or air have been tested. The evolution of the catalyst structure during FTS and after the re-activation protocols have been explored by a combination of ex situ and in situ techniques. Ru agglomeration, oxidation, and formation of Ru-volatile species are not responsible for the observed deactivation. However, Raman and infrared (FTIR) spectroscopy have confirmed the presence of coke and alkyl chains on the spent catalysts. These species hinder the adsorption of the reactants on the active sites and are the primary reason for the observed decrease in the catalytic activity. These carbonaceous species can be removed by severe thermal treatments in air. However, this latter treatment drastically alters the morphology of the Ru/TiO2, which leads to a substantial loss of catalytic activity. (C) 2012 Elsevier B.V. All rights reserved.

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