Conversion of CO 2 to CO over Cu–Fe-Based Catalysts via the Reverse Water–Gas Shift (RWGS) Reaction: A Comparative Study on the Impacts of Synthesis Methods and Operating Parameters

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Authors: Hamid R. Radfarnia, Najmeh Ahledel, Holly A. E. Dole, Ramzi Aoun, Gianni Caravaggio, Kourosh Zanganeh
Cited by: 9
References: 55

Abstract

High Resolution Image Download MS PowerPoint Slide In this work, the performance (i.e., conversion and product selectivity) of various Cu–Fe catalysts supported on samarium-doped ceria (Cu–Fe/SDC) was evaluated for the RWGS reaction under different reaction conditions. In order to determine the effect of synthesis methods, the catalysts were synthesized using several techniques, including incipient wetness impregnation (IWI), polyol reduction (PR), ultrasound-assisted polyol reduction (UPR), ultrasound-assisted impregnation (UI), and ultrasound-assisted coprecipitation (UCP). Among these, the UCP method produced catalysts with superior activity and thermal stability, achieving CO 2 conversion near thermodynamic equilibrium above 550 °C (e.g., CO 2 conversion of ∼35% at 600 °C, with a gas hourly space velocity (GHSV) of ∼1.2 × 10 5 mL·g cat –1 ·h –1 ) and nearly 100% CO selectivity. Characterization results revealed that this enhanced performance stems from improved metal dispersion, smaller active particle sizes, and synergistic interactions among Cu, Fe, and the SDC support, contributing to enhanced redox properties and resistance to sintering. Stability tests further confirmed the UCP catalyst’s suitability for sustained RWGS operation at moderate temperatures (∼600 °C), highlighting a potential trade-off between energy consumption and CO production efficiency. This opens opportunities to implement energy-efficient RWGS processes and eliminates the need for expensive superalloy materials in RWGS reactor designs.

Fields of Study & Subjects

Catalysts for Methane Reforming CO2 Reduction Techniques and Catalysts Chemical Looping and Thermochemical Processes

Publication details

Journal / source
Energy & Fuels
Publisher
American Chemical Society (ACS)
Volume
40
Issue
2
Pages
1317–1333
Publication date
2 January 2026
Language
EN