Archived
This content is available here strictly for research, reference, and/or recordkeeping and as such it may not be fully accessible. If you work or study at University of Kentucky and would like to request an accessible version, please use the SensusAccess Document Converter.
Abstract
Iron-based catalysts are the most suitable candidates for converting CO2 or CO2-rich syngas to hydrocarbons. However, several issues about the mechanism of CO2 hydrogenation are still unclear. In this work, we investigated the performance of an iron-based catalyst with H2/CO2, H2/CO/N2 and H2/CO/13CO2/N2 gas mixtures at the same process conditions (T = 270°C, P = 175 psi and SV = 3 NL/h/gcat). The CO2 hydrogenation rate was much lower than that observed for CO hydrogenation. 13CO2 tracer experiments indicated that CO2 is hydrogenated to hydrocarbons via the reverse water-gas shift even when present in small concentration (1.8 vol%). 13C enrichment was observed in both CO and C1-C4 hydrocarbons.
Document Type
Article
Publication Date
1-19-2021
Digital Object Identifier (DOI)
https://doi.org/10.1016/j.catcom.2021.106284
Funding Information
This work was supported by the Commonwealth of Kentucky.
Repository Citation
Badoga, Sandeep; Martinelli, Michela; Gnanamani, Muthu Kumaran; Koh, Young; and Shafer, Wilson D., "New Mechanism Insight for the Hydrogenation of CO/CO2 Gas Mixtures to Hydrocarbons over Iron-Based Catalyst" (2021). Center for Applied Energy Research Faculty and Staff Publications. 38.
https://uknowledge.uky.edu/caer_facpub/38
Graphical abstract

Notes/Citation Information
Published in Catalysis Communications, v. 152, 106284.
© 2021 The Author(s)
This is an open access article under the CC BY license (https://creativecommons.org/licenses/by/4.0/).