CO2 Hydrogenation to Hydrocarbons over Fe/BZY Catalysts: Article No. e202200802

Canan Karakaya, Erick White, Dylan Jennings, Michelle Kidder, Olaf Deutschmann, Robert Kee

Research output: Contribution to journalArticlepeer-review

1 Scopus Citations

Abstract

This manuscript reports a CO2 hydrogenation process in a catalytic laboratory-scale packed-bed reactor using an Fe/BZY15 (BaZr0.8Y0.15O3-d) catalyst to form hydrocarbons (e.g., CH4, C2+) at elevated pressure of 30 bar and temperatures in the range 270 = T = 375 degrees C. The effects of temperature, feed composition (i.e., CO2/H2 ratio, and residence time (i.e., Weight Hourly Space Velocity (WHSV) are studied to understand the relationship between CO2 conversion and carbon selectivity. Catalyst characterization elucidates the relationships between the catalyst structure, surface adsorbates, and reaction pathways. Thermodynamic analyses guide the experimental conditions and assist interpreting results. While the feed composition and temperature influence the product distribution, the results suggest that the higher-carbon (C2+) selectivity and yield depend strongly on residence time. The results suggest that the CO2 hydrogenation reaction pathway is similar to Fischer-Tropsch (FT) synthesis. The reaction begins with CO2 activation to form CO, followed by chain-growth reactions similar to the FT process. The CO2 activation depends on the redox activity of the catalyst. However, the carbon chain growth depends primarily on the residence time. as is the case for the FT synthesis, high residence time (on the orders of hours) is required to achieve high C2+ yield. For such high residence times, catalyst-fouling carbon deposition can be problematic. The coke-resistant BZY15 catalyst support contributes to the catalytic activity and enables a coke-free operation for more than 100 h time-on-stream.
Original languageAmerican English
Number of pages12
JournalChemCatChem
Volume14
Issue number19
DOIs
StatePublished - 2022

NREL Publication Number

  • NREL/JA-5100-82558

Keywords

  • bi-functional catalyst
  • CO2 hydrogenation
  • de-facto Fischer-Tropsch
  • Fe catalyst
  • redox-active support

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