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

Paper ID Volume ID Publish Year Pages File Format Full-Text
54655 47019 2013 10 PDF Available
Title
Insights into the deactivation and reactivation of Ru/TiO2 during Fischer–Tropsch synthesis
Abstract

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 H2, 1.25 MPa CO) that decrease significantly with time-on-stream. To recover the initial catalytic performance, different treatments using H2 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.

Graphical abstractFigure optionsDownload full-size imageDownload high-quality image (153 K)Download as PowerPoint slideHighlights► Ru/TiO2 is a very active catalyst for the production of hydrocarbons. ► The catalytic performance decreases with time-on-stream. ► Carbon deposits are responsible for catalyst deactivation. ► Thermal treatments only lead to partial catalyst regeneration.

Keywords
Ru; Fischer–Tropsch; In situ FTIR; Deactivation; Coke
First Page Preview
Insights into the deactivation and reactivation of Ru/TiO2 during Fischer–Tropsch synthesis
Publisher
Database: Elsevier - ScienceDirect
Journal: Catalysis Today - Volume 214, 1 October 2013, Pages 2–11
Authors
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Subjects
Physical Sciences and Engineering Chemical Engineering Catalysis