Abstract

AbstractThe conversion of synthesis gas to hydrocarbons in the Fischer‐Tropsch (FT) synthesis suffers from a broad product distribution not directly providing high fuel quality. This work, therefore, aims at bifunctional catalysts combining the FT and hydroprocessing (HP) reaction for tailoring the product spectrum. Therefore, we applied a bottom‐up synthesis strategy for bifunctional cobalt/zeolite catalysts and investigated the obtained materials by advanced characterizations such as 3D TEM tomography. Based on the results, descriptors are defined for the acidity and the porosity, which are varied by changing the material preparation parameters. The catalytic properties of the obtained materials are studied in FT experiments at industrially relevant conditions (20 bar, 240 and 260 °C) and are correlated to the material properties by means of the respective descriptors. Therefore, the product distribution was analyzed in detail and distinguished between n‐paraffins and 1‐olefins as typical FT‐products as well as paraffinic and olefinic isomers formed in the HP classified in different fractions. It was found that, apart from the acidity, the pore structure plays a vital role in primary and secondary cracking/isomerization reactions. In addition to that, the particular 3D pore structure and thus the individual transport trajectories of the FT products are strongly affecting the cracking and isomerization probability and consequently the product distribution.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.